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Frontiers in Immunology logoLink to Frontiers in Immunology
. 2024 May 10;15:1393378. doi: 10.3389/fimmu.2024.1393378

The role of different nutrients in the prevention and treatment of cardiovascular diseases

Zhi Tu 1, Jinfu Yang 1, Chengming Fan 1,*
PMCID: PMC11116626  PMID: 38799425

Abstract

Cardiovascular health is a hot topic around the world, and as the incidence of cardiovascular disease increases each year, people are increasingly focusing on the management of their heart health. Dietary and lifestyle changes as non-pharmacological treatments have been increasingly recognized as important in the prevention of cardiovascular disease and in reducing the risk of cardiovascular accidents. Awareness of different nutrients and their effects on cardiovascular health is important for establishing a good dietary pattern. This review summarizes the effects of the five major nutrients in the daily diet, namely carbohydrates, proteins, dietary fats, vitamins, and minerals, on cardiovascular health, and aims to provide a more comprehensive understanding of the effects of a healthy dietary pattern on cardiovascular health.

Keywords: cardiovascular disease, nutrient, diet, antioxidant, omega-3 fat acid, fibre, antioxidants

Introduction

As the global incidence of heart disease continues to increase year on year, more people are becoming aware of their heart health management (1). Dietary and lifestyle changes, in addition to pharmacological interventions for those who already have the disease or are at risk of developing it, are increasingly recognized as a means of preventing and delaying the onset of the disease (2). The Mediterranean diet, a dietary pattern closely related to cardiovascular health, has been shown to reduce the burden of cardiovascular disease, cancer, diabetes, and obesity, as well as play a preventive role (3). The Mediterranean diet includes fish, monounsaturated fats in olive oil, fruits, vegetables, whole grains, legumes/nuts, and moderate alcohol consumption. Related studies have reported that this dietary pattern can also improve surrogate indicators of cardiovascular disease, such as waist-to-hip ratio, blood lipids, and inflammatory markers, and can even have the same effect as cardiovascular prevention and treatment drugs (4). Although the Mediterranean diet pattern it is currently unclear whether the Mediterranean diet confers cardiovascular disease benefits from its individual components or overall components, some studies have shown that increasing the intake of foods such as fruits, vegetables and dietary fibre and reducing the intake of saturated fatty acids, red meat and sugar can effectively reduce the risk of cardiovascular disease (5). At the same time, several studies have shown that the biologically active parts of many dietary components can be directly or indirectly involved in regulating biological metabolic and influencing the expression of hormones, receptors and other proteins (6). Diet is the main source of nutrient intake, and different dietary structures contain different nutrients, which can lead to individual differences in cardiovascular health (7). A low-fat diet reduces the risk of death and non-fatal myocardial infarction in people at increased cardiovascular risk, as demonstrated in a systematic review (8). Apart from this, dietary fibre (9) and antioxidants (10) are also closely related to the development of cardiovascular disease. These evidences suggest that, in addition to the study of dietary patterns, the role of different food nutrients in the treatment and prevention of cardiovascular diseases is a unique and valuable direction, and the study of the role and influence of different nutrients in the occurrence and development of cardiovascular diseases is of great significance for the prevention and treatment of cardiovascular diseases. In this review, we highlight the role of nutrients in the development, prevention, and treatment of cardiovascular diseases and discuss the epidemiological evidence on the relationship between nutrients and different types of cardiovascular diseases.

The main nutrients found in the human body and how they relate to cardiovascular diseases

We know that the six essential nutrients in the human body are carbohydrates, proteins, fats, water, inorganic salts, and vitamins, and these nutrients are categorized into macronutrients and micronutrients based on their content (11). Carbohydrates, proteins and fats are the three main nutrients involved in supplying the body with energy and regulating metabolism. Carbohydrates serve as an important component that helps keep the body functioning and active (12); proteins, as nitrogenous organic compounds, are closely linked to growth, development and metabolism (13); dietary fat also serves as an essential nutrient in the growth and development of the body and is closely associated with a number of diseases (14). Similarly, vitamins and minerals are present in most foods as trace elements, and although they are small in proportion, they still play an important regulatory role in the organism (15). According to a scientific statement from the American Heart Association, dietary patterns are closely related to cardiovascular health (16). Many studies have shown that excessive weight gain during pregnancy increases the incidence of non-genetic obesity in the offspring (17). Meanwhile, according to a global review of food-based dietary guidelines (18), as we can see in the recognized healthy diets, their dietary structure has similar characteristics, such as the consumption of fibre-rich foods, the consumption of more fruit and vegetables, the control of processed foods and the reduction of salt intake. This highlights the importance of diet in improving cardiovascular health. We will review the nutrient components behind these dietary guidelines for healthy eating and their preventive and therapeutic effects on cardiovascular disease, and briefly describe some of the mechanisms that may be involved.

Carbohydrates

In general, 50% to 70% of the energy required for human life is provided by the oxidative breakdown of sugars, and carbohydrates, as the main component of the general dietary structure (19), take on the role of providing sugars. Sugars in our daily diet include monosaccharides, disaccharides and complex sugars consisting of starch glycogen fibres (12). Starch, for example, is found in large quantities in staple foods such as cereals and wheat, and is broken down into glucose ( Figure 1 ) by digestive enzymes in the digestive tract and absorbed as monosaccharides in the small intestine after the body has ingested such foods (20). The absorption of glucose in the small intestine is an energy-consuming process accompanied by the transport of sodium ions called sodium-driven sugar cotransporters (SGLTs) (21). There is another class of glucose transport proteins called concentration gradient dependent glucose transporters (GLUTs) (22). They are now known to be 12 in number and function in different parts of the body and are closely related to the development of disease (23).

Figure 1.

Figure 1

Common chemical formulae for nutrients.

Unbalanced dietary intake as well as some diseases can upset the metabolic balance in the body and may lead to metabolic syndrome (24). The metabolic syndrome, also known as the X-syndrome, was first used to describe the relationship between abdominal obesity and metabolic abnormalities, and subsequently it was proposed that the metabolic effects of aging, obesity, and sex hormone-related effects are associated with the risk of cardio genesis (25). A meta-analysis also confirmed that metabolic syndrome increases the risk of cardiovascular-related adverse events (26). Key features of the metabolic syndrome include dyslipidaemia, insulin resistance, hypertension, abdominal obesity and elevated levels of various inflammatory markers (27). Different types of carbohydrates have different effects on cardiovascular disease risk, and one study suggests that increasing intake of dietary fibre, as well as grains, in place of highly refined carbohydrates may have cardiovascular protective effects (28). Dietary fibre is a complex group of carbohydrates that are generally not digested and absorbed by the body due to the lack of enzymes in the body to digest fibre (29). But in fact, dietary fibre consists of both soluble and insoluble fibre fractions, which are intact in plants, whereas soluble dietary fibre is absorbed in the form of short-chain fatty acids out of the large intestine and the insoluble fraction cannot be digested (9). Whether soluble or insoluble, fibre plays an important role in cardiovascular health (30). The main roles that dietary fibre may play include bile acid salt metabolism, enzyme-substrate interactions, nutrient encapsulation, interactions with the mucus layer, and microbial degradation (31). The effect of these factors may improve blood glucose, lipid and insulin levels by influencing increased intestinal viscosity, faecal distension, etc., which reduces energy intake and promotes satiety, ultimately influencing cardiovascular disease occurrence (32). In addition, a class of functional dietary fibres, such as prebiotics, can lead to specific changes in the composition and/or activity of the gastrointestinal microbiota, which can benefit the health and wellbeing of the host (33). In addition to the effects of dietary fibre on cardiovascular health, many studies have focused on the relationship between carbohydrates on blood glucose, diabetes and obesity and have proposed a carbohydrate-insulin model (34). According to the Carbohydrate-Insulin Model (CIM) of obesity, a high-carbohydrate diet including refined grains and sugar intake produces a similar postprandial hyperinsulinaemia. Elevated insulin reduces all major metabolic fuels such as glucose, stimulates tissue uptake of glucose, inhibits the release of fatty acids from adipose tissue, inhibits hepatic production of ketone bodies, and promotes the deposition of fats and glycogen, thereby decreasing insulin levels and circulating fatty acid concentrations. This will result in promoting calorie deposition in fat cells rather than oxidation of lean tissue, thus increasing hunger, slowing the metabolic rate, or both, thus predisposing to weight gain (35). A randomized controlled trial showed that low-carbohydrate and low-calorie diets similarly reduced weight, waist circumference, fasting glucose, insulin, postprandial glucose changes, monocyte chemotactic protein-1, free fatty acids and fibroblast growth factor 21 (36). In another randomized controlled trial of carbohydrate diets and glycaemic control in people with diabetes, moderate carbohydrate restriction modestly improved glycaemic control and reduced circulating and intrahepatic triglyceride levels over and above the effects of weight loss itself (37). Blood glucose levels determine much of the impact of carbohydrates on cardiovascular disease. Through the tricarboxylic acid cycle, we know that when we consume more energy than our body needs, the excess sugar is stored in the body by being converted to fat, which in turn leads to obesity, one of the risk factors for cardiovascular disease (38). Blood glucose levels also affect the regulation of insulin, which is closely related to blood pressure. It influences the regulation of blood pressure by increasing sodium and water reabsorption in the kidneys and by affecting the diastolic function of vascular smooth muscle as well as the sympathetic nervous system (39). For diabetic patients, the intake of carbohydrates will be more cautious, because cardiovascular disease is one of the major complications of diabetes mellitus. In addition to the cardiovascular disease caused by hyperglycaemia mentioned above, diabetic patients are also accompanied by abnormalities in lipid metabolism and oxidative stress and other factors, which will gradually damage the endothelium of blood vessels as well as the heart itself, increasing the burden on the heart (40). Overall carbohydrates affect the health of the body, although there is no direct evidence that improving the quality of carbohydrate intake or simply consuming a low-carbohydrate diet improves cardiovascular health, both in terms of the type and quantity of carbohydrates consumed, carbohydrates are not only involved in the metabolism of substances, such as the tricarboxylic acid cycle. At the same time, carbohydrates influence endocrine functions, and some unabsorbed carbohydrates, such as dietary fibre, are involved in the absorption of substances, which also indirectly influences substance metabolism.

Fats

Lipid is a general term for fats and lipids. Fat is often referred to as triglyceride, which is formed through the esterification of the hydroxyl group of glycerol with three identical or different fatty acids and is an important energy supply and energy storage substance in our body (41). Lipids include sterols, phospholipids, glycolipids and so on (42). Phospholipid molecules have unique hydrophilic and hydrophobic structures which form the basis of biological membranes, and phosphatidylinositol is a precursor of second messengers involved in intracellular signalling (43). Cholesterol is the precursor of a variety of biologically functional steroids, which, like phospholipids, is a fundamental structural component of cell membranes, and serves as a raw material for the synthesis of steroid hormones as well as being involved in the synthesis of vitamin D in the body (44).

Fatty acids are important components of fats, cholesterol esters and phospholipids, and are also an important component of food. Like other nutrients, fatty acids are classified as essential or non-essential, and essential fatty acids, such as linoleic acid and linolenic acid, cannot be synthesized due to the lack of the enzyme that desaturates these fatty acids in the human body (45). Fatty acids can also be classified according to their molecular structure, i.e. whether there are double bonds on the carbon chain of the fatty acid and can be classified as saturated fatty acids, unsaturated fatty acids, and polyunsaturated fatty acids (11). Currently, dietary unsaturated fatty acids (TFA) have been the focus of the effects of dietary fats on cardiovascular disease, including the effects of trans fatty acids (TFA) and polyunsaturated fatty acids (PUFA) on cardiovascular health.

Regarding the mechanism of cardiovascular protection by PUFA ( Figure 2 ), the main ideas include the regulation of blood lipid levels to improve atherosclerosis (46), participation in the production of anti-inflammatory substances (47), and the maintenance of biofilm stability (48). Hyperlipidaemia is an important risk factor for cardiovascular disease, and studies have shown that patients with hyperlipidaemia who take omega-3FAs, including DHA and EPA ( Figure 1 ), have significantly lower triglyceride levels (49). And there is evidence that the use of prescription (EPA DHA or EPA only) doses of 4 g/d (>3 g/d total EPA and DHA) is an effective and safe option for lowering triglycerides, either as monotherapy or as adjunctive therapy to other lipid-lowering agents (49). The role of EPA and DHA in reducing hepatic VLDL-TG synthesis, as well as enhancing TG clearance, may be related to the reduction of VLDL-TG synthesis in the liver, which has been demonstrated in relevant studies (50). Although the molecular mechanisms underlying this significant reduction are not fully understood, potential mechanisms may be related to the regulation of transcription factors involved in hepatic fatty acid uptake, synthesis, and oxidation, as well as transcription factors involved in TG synthesis and VLDL assembly (51).

Figure 2.

Figure 2

The mechanism of cardiovascular protection by PUFA. (A) PUFA may be involved in the regulation of transglutaminating factors to reduce VLDL-TG synthesis and improve atherosclerosis. (B) Metabolised by pro-inflammatory lipid mediators in the arachidonic acid (AA) cascade, but their active metabolites are thought to be weaker than the active metabolites of AA, thus tipping the balance in favour of inhibition of inflammation. (C) Omega-3 PUFA prevents arrhythmias caused by sustained sodium spillage in cardiomyocytes after myocardial infarction.

High dietary intake of omega-3 fatty acids leads to appropriate accumulation of these fatty acids in cell membranes and circulating lipids, and phagocytosis by cell membranes affects the fluidity and biophysical properties of lipid rafts (52), they act as modulators of protein function and are also involved in signalling pathways (53). The mechanisms of anti-inflammatory effects of EPA and DHA may include alteration of cell membrane phospholipid fatty acid composition, disruption of lipid rafts, inhibition of pro-inflammatory transcription factor NF-κB activation, resulting in reduced expression of inflammatory genes and activation of the anti-inflammatory transcription factor peroxisome proliferator-activated receptor γ (54). Specifically, cell membranes enriched with omega-3 PUFA disrupted recruitment and initiation of toll-like receptor-4, which triggers anti-inflammatory effects through downregulation of the NF-κB pathway, and inhibition of the pro-inflammatory cytokines in aortas (IL6, TNFα, IL1, and c-cytokine). IL6, TNF-α, IL1, and c-reactive protein (CRP)) in the aorta, reducing the infiltration of inflammatory cells (macrophages) into the intima, thereby reducing atherosclerosis and plaque formation (55). At the same time omega-3 fatty acid, may have an effect on platelet aggregation as well as anticoagulant function (56). Thromboxane A2 (TXA2) and prostaglandin E2 (PGE2) produced by platelets in physiological haemostasis promote platelet aggregation and contraction, thereby promoting coagulation as well as thrombosis (57). Prostacyclin 2 (PGI2), which is produced by the endothelial cells of blood vessels, inhibits the formation of blood clots (58). Whereas prostacyclin 2 production by vascular endothelial cells inhibits thrombosis, EPA appears to reduce the ability of endothelial cells to produce PGI2 in two ways: by lowering arachidonic acid levels in the cellular pool of phospholipid precursors, and by acting as an inhibitor of prostaglandin production (59), which is thought to be important evidence that consumption of EPA-enriched seawater fish can reduce the risk of myocardial infarction (60). A cohort study analysed a dose-response relationship between higher TFA intake and increased risk of cardiovascular disease (61). Another meta-analysis showed that higher concentrations of marine-derived omega-3 PUFA biomarkers were associated with significant reductions in cardiovascular disease, coronary heart disease, and total mortality (62). Several studies appear to support this claim, (63) showed that the effect of TFA on cardiovascular disease may affect the cardiovascular system by lowering HDL. Another study found that introducing or replacing saturated and trans fats with unsaturated fatty acids in obese or overweight non-diabetic older adults was beneficial in reducing cardiovascular risk (64). Omega-3 fatty acids including docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) have been shown to significantly reduce the risk of sudden cardiovascular death and all-cause mortality, as well as being used to treat hyperlipidaemia and hypertension (65). The importance of essential fatty acids (EFAs) has been recognized in the fields of cardiac science and cardiology, and polyunsaturated fatty acids are considered important multifunctional mediators for improving and maintaining human health throughout the life cycle (66). In general, dietary fatty acids have an impact on the development and progression of cardiovascular disease in a number of ways. Fat intake influences lipid metabolism. Excessive fat intake is also associated with a higher incidence of obesity. Some fatty acids, such as saturated and trans fatty acids, may be associated with atherosclerosis through oxidative stress and metabolic effects. Fatty acids can also affect the stability of cell membranes and some of the ion channels in the membranes, which can lead to electrophysiological abnormalities in cardiomyocytes and ultimately to cardiac arrhythmias. On the other hand, some of the anti-inflammatory, anti-thrombotic and membrane stability-enhancing properties of unsaturated fatty acids may play a role in the prevention of cardiovascular disease.

Proteins

Proteins are composed of amino acids as the basic unit, the process of absorbing proteins in food needs to hydrolyse proteins into oligopeptides and amino acids under the action of digestive enzymes in order to be absorbed by the human body, and this process of proteins will lose the original structure and function, so we can think that the actual value of proteins is determined by the type and amount of amino acids they contain (67). Amino acids are classified as essential or non-essential according to whether they can be synthesized by the body itself (68). Essential amino acids include leucine, isoleucine, threonine, valine, lysine, methionine, phenylalanine, tryptophan, and histidine (69). In addition, although arginine can be synthesized by the human body, studies have reported that long-term insufficient intake can cause negative nitrogen balance, so it is also classified as an essential amino acid (70). Amino acids are organic compounds that are essential for sustaining life, providing raw materials for biosynthesis and energy for living activities. In addition to being raw materials for biomass and sources of energy, amino acids are involved in key pathways for cell growth, metabolism and immunity (71). An important mechanism for regulating protein synthesis is the mammalian target of rapamycin (mTOR) signalling pathway. The mTOR system includes the rapamycin-sensitive complex 1 (mTORC1), which is activated by glutamine (Gln)( Figure 1 ), arginine (Arg) and leucine (Leu) and activates protein synthesis by phosphorylating eIF4E-binding protein 1 (4E-BP1) and ribosomal protein S6 kinase 1 (S6K1) to activate protein synthesis (72). Arginine is involved in a wide range of biological processes. The synthesis of urea and creatine uses arginine to balance nitrogen and meet the metabolic needs of muscle. As a free amino acid, arginine is a precursor for the formation of nitric oxides(NO) and Gln, important neurotransmitters that regulate vascular tension and nerve conduction (73). The process of methylation of arginine is catalysed by protein arginine methyltransferases (PRMTs).Increased PRMT activity leads to enhancement of the metabolite asymmetric dimethylarginine (ADMA), both of which are associated with an increased risk of cardiovascular disease because they tend to inhibit nitric oxide synthase (NOS) (74). Accumulation of the endogenous NOS inhibitor ADMA (significantly reduces the synthesis of the potent vasodilator NO and contributes to the development of cardiovascular disease. Glutamine is structurally similar to glutamic acid, with the carboxylic acid group of the side chain replaced by an amide, and is an amino acid used in protein synthesis (75). Glutamine is a dietary non-essential amino acid and is the most abundant amino acid involved in the synthesis of all non-essential amino acids and proteins. Muscle tissue produces the most glutamine in the body, accounting for approximately 90% of all glutamine synthesised. Although the liver also synthesises glutamine, its main function is to regulate glutamine levels. The brain and lungs also produce small amounts of glutamine (76). Gln is a key amino acid in the regulation of glucose stability and insulin sensitivity, and Gln levels affect the inflammatory response in skeletal muscle and regulate the expression of the adaptor protein GRB10, an inhibitor of insulin signalling. In addition, systemic elevation of Gln improves insulin sensitivity and restores glucose homeostasis in a mouse model of obesity (77). Gln levels influence the inflammatory response in skeletal muscle and modulate the expression of the adaptive protein GRB10, which inhibits insulin signalling. Furthermore, systemic elevation of Gln improves insulin sensitivity and restoration of glucose homeostasis (77). The anthracycline antibiotic doxorubicin (DOX) is a cardiotoxic antineoplastic drug that can cause free radical and oxidative stress. Gln supplementation significantly reduces cardiac lipid peroxide levels and increases peroxidase and glutathione levels, thereby protecting cardiac function (78).

The amount of protein in foods varies greatly and is commonly found in animal sources such as meat, dairy products, and eggs. Some plants also contain significant amounts of protein such as legumes. The effects of protein on human health, especially on cardiovascular health, have been controversial, and there is no definitive conclusion on the merits of animal and plant sources of protein (79). The benefits of plant-based sources of protein began to spread among vegetarians, and prospective studies have shown that consumption of a vegetarian diet is associated with a reduced risk of coronary artery disease (80) and other cardiovascular disease (81). However, plant-based proteins also have limitations. For example, most plant-based proteins are deficient in some essential amino acids, such as lysine in cereals and tryptophan in legumes (82). Vegan diets may also be deficient in certain nutrients such as vitamin B12, iron and zinc (83). The role of animal proteins is also twofold. On the one hand, animal-derived amino acids provide a sufficiently complete range of essential amino acids, which are thought to promote muscle growth and development (84). On the other hand, the intake of proteins of animal origin, especially red meat, and processed meat products, can lead to an increased risk of cardiovascular disease (85). A cohort study demonstrated that higher intake of processed meat, unprocessed red meat or poultry was significantly associated with a small increase in the risk of developing cardiovascular disease (86). More evidence is needed on the advantages and disadvantages of plant and animal proteins and their relationship to cardiovascular disease, and the selection of proteins in the daily diet needs to be based on a combination of factors and individualized dietary regimens.

Micronutrients

Micronutrients include vitamins and minerals, which are present in the human body at very low levels compared to the macronutrients mentioned above (87). Most micronutrients cannot be synthesized by the human body, and the body obtains them mainly through the daily diet or nutritional supplements, etc. There are also micronutrients that can be synthesized and utilized by human beings under certain circumstances. In the case of vitamin D, for example, 7-dehydrocholesterol in the skin under solar ultraviolet conditions is eventually converted to vitamin D3 and metabolized in the liver to 25-hydroxyvitamin D3, which is ultimately present and biologically active in the kidneys as 1,25-dihydroxyvitamin D3 (88). Although nutrients such as vitamin D can be synthesized and utilized on their own, because they require the involvement of ultraviolet light, factors such as the season, the amount of time spent in the sun during the day, age, and the use of sunscreens can affect the skin’s production of vitamin D3 (89). Therefore, although some of the nutrients can be utilized synthetically on their own, it is still necessary to obtain adequate nutrients through food, subject to several factors (90).

Vitamins are a diverse group of micronutrients that are broadly classified into lipid-soluble (91) and water-soluble vitamins (92) based on their physicochemical properties. Fat-soluble vitamins include vitamins A, D, E, and K. These vitamins are soluble in lipids and organic solvents and are absorbed and stored in the body along with lipids, usually in the liver (93). It has been suggested that impaired lipid absorption may cause deficiencies in these vitamins (94). Water-soluble vitamins include the B vitamins (e.g. B1, B2, folic acid, etc.) (95) and vitamin C (96). These vitamins are more dependent on dietary sources than fat-soluble vitamins due to their physio-chemical properties and the fact that they rarely accumulate in the body, and in case of excess they are excreted in the urine (97). The specific classification of vitamins and their corresponding physiological functions and sources of acquisition have been described in detail in other studies (11), and in this paper, we will focus on some of these vitamins, which are common and supported by reliable evidence, and analyse their role in the treatment and prevention of cardiovascular disease.

Vitamin C ( Figure 1 ) is a familiar antioxidant with reducing properties that protect cells from oxidative damage by counteracting oxidative stress and help improve cardiovascular health. In order to understand the mechanisms of oxidative stress on cellular damage, we need to recognize the process of biological oxidation (98). We know that the process of oxidative breakdown of chemicals in living organisms is called biological oxidation, most typically in the mitochondrial oxidation system, where the main products are water and carbon dioxide, a process that requires the consumption of oxygen and the production of ATP as well as heat (99). The purpose of biological oxidation is the complete oxidation of nutrients such as sugars, fats, and proteins in food, which is a process in which hydrogen is removed and eventually transferred to oxygen molecules to form water molecules, which will be briefly outlined (100). Firstly, biological oxidation requires a variety of hydrogen and electron transferring components, including nicotinamide adenine dinucleotides, flavin nucleotide derivatives, as well as ubiquinone, also known as coenzyme Q, and cytochromes (101). The transfer of electrons and hydrogen from the above substances is also dependent on the oxidative respiratory chain consisting of a complex of proteins with the ability to transfer electrons, NADH, FADH2, which passes through a series of oxidoreductase systems in the oxidative respiratory chain. Firstly, oxidative respiration requires a variety of hydrogen- and electron-transferring components, including nicotinamide adenine dinucleotide, flavin nucleotide derivatives, as well as ubiquinone and cytochromes. The transfer of electrons and hydrogen from the above-mentioned substances is also dependent on the oxidative respiration chain consisting of a complex of proteins with the ability to transfer electrons, NADH, FADH2, which passes through a series of oxidoreductase systems in the oxidative respiration chain. Firstly - the release of electrons from NADH, FADH2 on the stromal side of the mitochondrial membrane, the electrons pass through the oxidative respiratory chain (this process includes complexes I-IV), these complexes receive and release energy through the function of the proton pump of the complexes to transport H+ from the mitochondrial matrix to the cytoplasmic side, as protons are not free to pass through the inner membrane of the mitochondria to return to the stroma, which in turn creates an electrochemical gradient and drives the complexes V, i.e. ATP synthase, to synthesize ATP. at the same time the oxidative respiratory chain ultimately transfers electrons to oxygen and reduces oxygen to water at complex IV (101). In the process of biological oxidation, the mitochondria exist but the electron transfer process, when a single electron is directly transferred to the oxygen will generate reactive oxygen species rather than simply through the oxidative respiratory chain to oxygen to generate water, so that a series of products such as superoxide anion, hydrogen peroxide, hydroxyl radicals collectively known as the reaction reactive oxygen species (102). For reactive oxygen species (ROS), a large number of studies have demonstrated their effects on cellular function (103), and although there are reports showing that small amounts of ROS, and under specific circumstances, promote cell proliferation (104), there is more evidence that accumulation of large amounts of ROS impairs cellular function and leads to cell death (105). In most studies we have found that the cardiovascular effects of reactive oxygen species (ROS) focus on damage to the vascular endothelium (106). On the one hand, the increase in ROS due to oxidative stress can lead directly to the oxidation of proteins and nucleic acids, which can directly damage the cellular structure and lead to direct damage to the endothelium (107). On the other hand, ROS can oxidize nitric oxide, thereby reducing its bioavailability, nitric oxide is an important vasodilatory factor (108), while peroxynitrite a product of nitric oxide oxidation, also belongs to the category of ROS and further damages the normal structure and function of cells (109). In addition, oxidative stress can cause apoptosis and necrosis of cardiomyocytes through direct damage to cardiomyocytes (110), and may also promote the proliferation of fibroblasts leading to diastolic and contractile dysfunction of the myocardium and fibrosis of the myocardium ultimately leading to the development of heart failure (111). Oxidative stress is also strongly implicated in atherosclerosis. Oxidative stress increases the risk of cardiovascular events by oxidising LDL so that it can more readily cross the arterial endothelium and induces the formation of lipid plaques leading to an inflammatory response in the vessel wall (112). Oxidative stress can also activate platelet formation, increasing the risk of thrombosis (113). Although there are antioxidant systems in the body such as superoxide dismutase (SOD) (114), glutathione peroxidase (GPx) (115), etc., which are capable of scavenging oxygen radicals and other oxidative substances to maintain the redox balance in the body, but subject to the individual’s level of health, living habits, living environment and other influences, the body itself oxidative stress generated by free radicals may exceed the scavenging capacity of antioxidant enzymes (116), which at this point requires additional supplementation of antioxidants in order to meet the body’s needs (117) ( Figure 3 ). Vitamins are used in many dietary guidelines and health recommendations as excellent antioxidants, and the convenience of their role as antioxidants against oxidative stress may be related to their own structure as well as their reducing properties (118). Firstly, vitamins as antioxidants can neutralize the activity of free radicals by directly donating electrons to them, e.g. vitamin C (Ascorbic acid) (119), and in addition, e.g. vitamin E, which reacts with oxidized lipids and prevents the lipid peroxidation chain reaction, protects cell membranes from damage (120). In addition, vitamin C regenerates oxidized vitamin E and vitamins modulate the activity of antioxidant enzymes indirectly affecting the antioxidant capacity of cells (121). In general, vitamins, as a class of antioxidants, help cells to remove reactive oxygen species generated by oxidative stress by donating electrons to eliminate oxidative regenerative oxidants and by increasing the activity of the body’s own antioxidant enzyme system, which maintains the redox balance of the cells and protects the cells from the damage caused by oxidative stress. It is worth mentioning that although many clinical studies have shown that the consumption of vitamin-rich foods such as vegetables and fruits can reduce cardiovascular disease incidence and mortality, however there is only limited evidence to support the benefits of vitamin and mineral supplementation in the prevention of cancer or cardiovascular disease (122).

Figure 3.

Figure 3

The increase of ROS caused by oxidative stress directly leads to the oxidation of proteins and nucleic acids, which directly destroys the cellular structure and leads to the direct damage of endothelial cells. ROS can oxidize nitric oxide and produce peroxynitrite, which further damages the normal cellular structure and function. Oxidative stress oxidises LDL (ox LDL), which can more easily penetrate the endothelium of the arteries and induce the formation of lipid plaques, which can lead to inflammatory reactions in the vessel wall, and thus increase the risk of cardiovascular events. inflammatory response, thus increasing the risk of cardiovascular events. Oxidative stress can lead to apoptosis and necrosis of cardiomyocytes through direct damage to cardiomyocytes, and promote fibroblast proliferation, leading to diastolic and systolic dysfunction as well as myocardial fibrosis, which ultimately leads to the development of heart failure.

Minerals are also an important class of micronutrients that play an important role in metabolism, growth and development (123). The 10 essential metal elements include sodium (Na), potassium (K), magnesium (Mg), calcium (Ca), manganese (Mn), iron (Fe), cobalt (Co), copper (Cu), zinc (Zn), and molybdenum (Mo) (124). Sodium and potassium are important substances involved in the metabolism of substances in the body. In addition, they are important components in maintaining homeostasis in the body’s internal environment (125). Sodium and potassium are distributed differently in the body. Sodium is mainly distributed in the extracellular fluid, whereas potassium is distributed more in the intracellular fluid, and the intracellular potassium concentration is as high as 140-150 mmol/L, which accounts for 98% of the total amount of potassium in the body (126). The main reason for the different ionic compositions in the cell is the presence of a sodium pump (known also as Sodium–Potassium-ATP-ase) in the cell membrane, in which hydrolysis of one molecule of ATP is accompanied by pumping three sodium ions out of the cell and two potassium ions into the cell (127). Sodium and potassium metabolism is regulated by blood pressure, the antidiuretic hormone aldosterone system and activation of β2-adrenergic receptors (125). Sodium, as an essential nutrient in our daily diet, is not only an inorganic salt necessary for the maintenance of life activities, but it is also closely related to the occurrence and prevention of cardiovascular disease (128). We consume sodium ions through salt in our daily diet, and related studies have reported the mode of sodium ions in the regulation of blood pressure and concluded that imbalance of sodium balance is the main cause of hypertension, and in some salt-sensitive people, plasma sodium levels are even more strongly correlated with blood pressure (129). Potassium ions may influence the regulation of blood pressure in relation to the homeostasis of sodium ions in the body (130). Calcium and magnesium are often compared together due to their physicochemical characteristics. Mg2+ is not only a cofactor for a number of enzymes in the body it also acts as a regulator of potassium and calcium ion channels and antagonises the function of calcium (131). Calcium ions are involved in the regulation of a variety of ion channels, such as small conductance Ca2+-activated K (SK) channels These channels play a key role in the regulation of cardiac excitability, and SK channels play a key role not only in the healthy heart but also in diseases such as atrial fibrillation (AF), ventricular arrhythmias and heart failure (HF) (132). In addition to its role in influencing blood pressure, related animal experiments suggest that modulation of Ca processing may be one of the molecular mechanisms underlying the effects of salt intake on myocardial function in hypertensive patients (133). It has also been shown that a high salt diet is associated with an increase in salt-induced expression of kinase 1, which may be associated with the activation of genes involved in left ventricular hypertrophy leading to alterations in myocardial mechanical properties (134). Reports have also shown that potassium, magnesium, and calcium intake also have an effect on blood pressure (135). Magnesium ions may be involved in the regulation of the vasodilator prostaglandin E1, and reduced synthesis of this substance under low magnesium conditions may induce cardiovascular disease (136). These ions may also affect the diastolic function of the myocardium which can lead to heart failure (137). Clinical results may contradict current theories, such as one study that showed insufficient evidence to support the use of potassium, magnesium, and calcium ions to effectively lower blood pressure (138). A prospective cohort study of 28,886 U.S. women showed a potential role for calcium intake in the primary prevention of hypertension and cardiovascular complications, but there was no direct evidence of changes in blood pressure with calcium supplementation (139). A prospective cohort study of 28,886 U.S. women showed a potential role for calcium intake in the primary prevention of hypertension and cardiovascular complications, but there was no direct evidence of changes in blood pressure with calcium supplementation (139).

In addition to the metal ions mentioned above, among the metal ions essential to the human body, the elements iron and zinc play an essential role in the human body, even though the elements in front of their content in the human body are small. Iron in food is mainly absorbed through heme iron in animal meat and non-heme iron in some plants and grains (140). Iron absorption occurs mainly in the duodenum and the upper part of the jejunum. Iron is absorbed by the body mainly in the form of divalent iron ions. Vitamin C can reduce trivalent iron to divalent iron due to its strong reducing properties, thus promoting iron absorption (141). Iron is a key metal element in the synthesis of haemoglobin. When there is an imbalance in iron intake, circulation, storage and loss, iron deficiency anaemia results, which is associated with a decrease in haemoglobin, myoglobin and cytochrome levels (142). Iron imbalances in the body include iron deficiency and iron overload and are present in a variety of cardiovascular diseases such as heart failure and myocardial infarction (143). Zinc is a component of many enzymes in the body and is involved in the metabolism of substances as well as other life activities (144). Also, zinc is found in a structure called zinc finger and binds to specific sequences of DNA or RNA to regulate biological processes such as gene expression, DNA replication and repair (145). Zinc deficiency increases the formation of ROS and causes significant oxidative damage to all important biological macromolecules such as DNA, proteins and membrane lipids, so the maintenance of a certain concentration of zinc in the body by an organism is closely related to heart health (146).

Epidemiology of nutrients in CVD

We have described the role played by different nutrients in cardiovascular disease and analysed some of the possible mechanisms involved, and then we will further analyse their relationship from an epidemiological point of view ( Table 1 ).

Table 1.

Human epidemiological studies showing associations between nutrients and CVD.

Ref. Nutritional conditions Population Results
Heart failure
(147) Breakfast cereal intake Individuals from the Physicians' Health Study I(n=21376) A higher intake of whole grain breakfast cereals is associated with a lower risk of HF
(148) High-protein diet Individuals from a randomized controlled study(n=76) A high-protein diet may be more effective in reducing cardiometabolic risk in this population
(149) Omega-3 PUFAs supplements Individuals from double-blind, placebo controlled, cross-over trial (n=31) Short term treatment with omega-3 PUFAs in subjects with stable ischemic HF improved inflammatory and fibrotic status as well as endothelial function in parallel with systolic and diastolic performance of left ventricle
(150) 4000 IU vitamin D daily Individuals from an investigator-initiated, multicenter, prospective, randomized, placebo-controlled trial (n=73) A daily vitamin D dose of 4000 IU for chronic HF appears to be safe and did improve the 6-min walk distance, symptoms, and left atrial diameter at 6 months.
Hypertension
(151) Very low carbohydrate (VLC) Adults with a triple multimorbidity (hypertension, prediabetes, or type 2 diabetes, and overweight or obesity) the VLC diet resulted in greater improvements in systolic blood pressure, glycemic control, and weight over a 4-month period compared with the DASH diet
(152) Fiber and protein An 8-week factorial study of parallel design (n=41) Dietary protein and soluble fiber supplements lower blood pressure additively in hypertensives.
(153) Sodium reduction Of 412 participants, 57% were women, and 57% were black; mean age was 48 years, and mean SBP/diastolic BP was 135/86 mm Hg. The combination of reduced sodium intake and the DASH diet lowered SBP throughout the range of pre- and stage 1 hypertension, with progressively greater reductions at higher levels of baseline SBP.
Coronary artery disease
(154) Fish intake Postmenopausal women enrolled in the Estrogen Replacement and Atherosclerosis Trial (n = 229) Consumption of fish is associated with a significantly reduced progression of coronary artery atherosclerosis in women with coronary artery disease.
(155) Vegetable intake Men who were free of heart disease, stroke, or cancer (n=15220) A negative association between vegetable intake and risk of coronary heart disease.
(156) 300 000 IU of vitamin D was administered orally 12 hours before PCI Patients undergoing elective PCI (n=99) Mean difference in CK-MB between 8 hours and 24 hours was significantly lower in the vitamin D group. The mean difference in hs-CRP was significantly lower in the vitamin D group
(157) Recommended daily allowance (RDA) of dietary calcium, zinc, and iron Individuals from an matched case-control study which was carried out at Shahid Gangalal National Heart Center (n=466) A significant inverse association of dietary zinc intake above RDA indicates the potential protective effect of higher dietary zinc against CAD. However, causal odds of CAD are inconsistent across the median or RDA of calcium and iron intakes.
Arrhythmia
(158) Antioxidants Antioxidants might be useful as adjuvants in controlling reperfusion induced arrhythmias following therapeutic alteplase thrombolysis
(159) Marine omega-3 fatty acids and vitamin D An ancillary study of a 2 × 2 factorial randomized clinical trial involving 25 119 women and men aged 50 years or older without prior cardiovascular disease, cancer, or atrial fibrillation (AF) Treatment with EPA-DHA or vitamin D3, compared with placebo, resulted in no significant difference in the risk of incident AF over a median follow-up of more than 5 years
Inherited cardiovascular conditions
(160) Multivitamin Individuals from a population-based Atlanta Birth Defects Case-Control Study Periconceptional multivitamin use is associated with a reduced risk for conotruncal defects

HF, Heart failure; PUFA, polyunsaturated fatty acid; DASH, Dietary Approaches to Stop Hypertension; SBP, Systolic Pressure; PCI, percutaneous coronary intervention; CAD, Coronary Artery Disease; EPA, eicosapentaenoic Acid; DHA, docosahexaenoic acid.

Heart failure

Different nutrients all have an important impact on cardiovascular health. A study evaluated prospectively the association between breakfast cereal intake and incident HF among 21 376 participants of the Physicians’ Health Study I. The result demonstrate that a higher intake of whole grain breakfast cereals is associated with a lower risk of HF (147). In a randomized controlled study, results suggest that a high-protein (30% protein, 40% carbohydrates, and 30% fat) diet may be more effective in reducing cardiometabolic risk (148). In a double-blind, placebo-controlled crossover trial with 31 patients with ischaemic heart failure, the intervention group was given Omega-3 PUFAs (2 g daily for 8 weeks). The results showed improvements in the inflammatory and fibrotic state of the left ventricle, as well as endothelial function, and left ventricular systolic and diastolic function in the intervention group (149). Vitamin D intake at safe doses showed no improvement in endothelial cells in a randomised controlled trial, but improved 6-minute walking distance, symptoms and left atrial internal diameter at 6 months in patients with heart failure (150). The development of chronic heart failure is a long-lasting process, and although there has been growing evidence that a healthy diet can improve symptoms as well as cardiac function in patients with heart failure, more evidence is needed to confirm this.

Hypertension

Low-carbohydrate diets show relevance in improving blood pressure in hypertensive patients. A randomized trial comparing a very low-carbohydrate (VLC) diet vs a Dietary Approaches to Stop Hypertension (DASH) diet. And the study showed the VLC diet resulted in greater improvements in systolic blood pressure, glycaemic control, and weight over a 4-month period compared with the DASH diet (151). In addition, dietary protein and soluble fibre supplementation was found to further reduce blood pressure in hypertensive patients in an 8-week, parallel-design, factorisation study (152). In a study of DASH-sodium (dietary patterns, sodium intake and blood pressure), the low-sodium-DASH diet was effective in reducing systolic blood pressure in prehypertension and stage 1 hypertension, and the reduction was greater at higher baseline systolic blood pressure levels (153).

Coronary artery disease

A prospective cohort study of postmenopausal women (n = 229) participating in the Estrogen Replacement and Atherosclerosis trial showed higher fish consumption was also associated with smaller decreases in minimum coronary artery diameter and fewer new lesions (154). In addition some studies have reported vegan diet significantly reduces high-sensitivity C-reactive protein, an indicator of risk for adverse outcomes, by 32% compared to the American Heart Association diet (161). Although there was also no significant difference in glycaemic control measures between the two dietary groups. LDL cholesterol was 13% lower on the vegan diet compared with the American Heart Association diet. There were no significant differences in other lipid parameters. 15,220 men who were free of heart disease, stroke or cancer at baseline were investigated in a 12-year follow-up. The study showed men who consumed at least 2.5 servings/day of vegetables had a relative risk (RR) of 0.77 (95% CI: 0.60-0.98) for CHD (155). The results suggest an inverse association between vegetable intake and risk of CHD. In a randomized clinical trial investigating the role of vitamin D in preventing myocardial injury after selective percutaneous coronary intervention, we found that the mean difference in CK-MB between 8 hours and 24 hours was significantly lower in the vitamin D group. The mean difference in hs-CRP was significantly lower in the vitamin D group (156). For the study of dietary mineral intake for cardiovascular disease, a matched case-control study which was conducted to determine the causal effect of dietary intake of calcium, zinc and iron on coronary artery disease in Nepalese men showed a significant inverse association of dietary zinc intake above recommended daily allowance (RDA) indicates the potential protective effect of higher dietary zinc against CAD (157). Interestingly, the causal odds of CAD being caused by different median or RDA values for calcium and iron intake were not consistent. This may require cohort studies with larger sample sizes and randomised clinical trial studies.

Arrhythmia

Arrhythmias involve excitability of cardiac machine cells, electrolyte abnormalities, and abnormalities in the cardiac conduction system. Although the number of related literature reports is smaller than that of other cardiovascular diseases, many studies have shown the correlation between diet and arrhythmia. A research showed the effect of antioxidant vitamins on biochemical changes and arrhythmias induced by reperfusion before and after therapeutic thrombolysis (Actilyse). Compared with patients taking placebo, patients taking antioxidants had significantly lower rates of premature ventricular contractions, atrial fibrillation, ventricular tachycardia, and first-degree atrioventricular block and increased plasma antioxidant properties. These findings suggest that antioxidants might be useful as adjuvants in controlling reperfusion induced arrhythmias following therapeutic alteplase thrombolysis (158). Another randomised clinical trial on the effects of supplementation with marine Omega-3 fatty acids and vitamin D on the incidence of atrial fibrillation showed no significant difference in the incidence of atrial fibrillation at a median follow-up of more than 5 years with EPA-DHA or vitamin D3 treatment compared to a placebo group in adults aged 50 years or older (159).

Inherited cardiovascular conditions

Inherited cardiovascular diseases (CVDs) are a complex group of diseases that are caused by genetic mutations or hereditary factors. The effect of folic acid ( Figure 1 ) on congenital heart disease has been the main subject of research on the relationship between cardiovascular disease and nutrients. A study in 1964 showed a higher rate of congenital malformations in infants of folic acid-deficient mothers (3.0%) than in a control group (1.6%) (162). Folate transfers and processes one-carbon unit coenzymes and synthetes thymidine nucleotides, which are essential for de novo DNA construction or repair, and are required for cell division and cell maintenance. In addition, folate is a key factor in “site-specific” methylation of cytosine bases in DNA, which regulates the expression of epigenetic genes (163). Folic acid has a preventive effect on reducing congenital heart disease, as has been reported in other studies (164). From a population-based Atlanta Birth Defects Case-Control Study showed mothers who reported periconceptional multivitamin use had a 43% lower risk of having infants with conotruncal defects (odds ratio [OR], 0.57; 95% confidence interval [CI], 0.33 to 1.00) than did mothers who reported no use (160). In a study of folic acid antagonists during pregnancy and the risk of birth defects, folic acid antagonists not only increased the risk of neural tube defects, but also increased the risk of cardiovascular defects. A multivitamin folic acid component may reduce the risk of these defects (165). In a systematic review of observational studies, the authors evaluated the effects of eight maternal micronutrients - vitamin D, vitamin B12, folate, vitamin A, zinc, copper, selenium, and ferritin - on congenital heart disease (166). Unfortunately, there is insufficient evidence to conclude with confidence whether maternal micronutrient deficiencies increase the risk of foetal CHD. Although further large-scale prospective studies are needed to confirm this contention, available data support that folic acid and multivitamins are essential for proper foetal heart development during early embryonic development and that supplementation of these substances during the peri-pregnancy or early pregnancy may reduce the risk of congenital heart disease (167). Other nutrients such as carbohydrate, protein and fat may not have direct evidence of their relationship with hereditary heart disease, but the deficiency of some nutrients may lead to impaired heart function, abnormal blood pressure and heart rhythm, which may affect the progression and symptoms of hereditary heart disease. Therefore, for patients with hereditary heart disease, it is still necessary to correct the nutrient deficiency by proper diet. This will improve symptoms and promote heart health.

Conclusions

This review describes the types of macronutrients and micronutrients commonly found in the human body, their physicochemical properties and their metabolic characteristics. The pathogenesis of different nutrients in cardiovascular diseases is discussed and the effects of different nutrients on cardiovascular diseases are analysed ( Figure 4 ). At the same time, we provide epidemiological evidences on the therapeutic and preventive roles of nutrients in different types of cardiovascular diseases, which is believed to be helpful in analysing and comparing the effects of different nutrients on different types of cardiovascular diseases. In addition to cardiovascular disease in general, an attempt has been made to analyse the role of nutrients in hereditary heart disease, and although there is only a small amount of evidence, we have been able to find a relationship between nutrient deficiencies and hereditary heart disease. Although we have analysed the effects of different nutrients on cardiovascular disease, the analysis has been limited to a single nutrient or food group. There is still a great deal of room for research on the effects of different food groups and nutrient ratios in the daily diet on cardiovascular health. In addition, although the metabolism of nutrients in the human body is very complex and is not described in this paper, it is interesting to see whether the interactions of different nutrients in human metabolism are involved in the development of cardiovascular diseases. In conclusion, nutrients have a very important impact on the occurrence, prevention and treatment of cardiovascular diseases, while the mechanisms of nutrients in cardiovascular diseases, as well as dietary patterns, nutrient combinations for cardiovascular health diets need to be further studied.

Figure 4.

Figure 4

Impact of different nutrients on cardiovascular disease.

Author contributions

ZT: Data curation, Formal analysis, Writing – original draft. JY: Methodology, Writing – review & editing. CF: Conceptualization, Supervision, Writing – review & editing.

Funding Statement

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was financially supported by the Science and Technology Innovation Program of Hunan Province (2021RC2106 to CF, 2023SK2031 to JY), the Natural Science Foundation of Hunan Province (2022JJ20088 to CF, 2023JJ30793 to JY), the National Natural Science Foundation of China (82200323 to CF), and the Scientific Research Launch Project for new employees of the Second Xiangya Hospital of Central South University (to CF).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1. Roth GA, Mensah GA, Johnson CO, Addolorato G, Ammirati E, Baddour LM, et al. Global burden of cardiovascular diseases and risk factors 1990-2019: update from the GBD 2019 study. J Am Coll Cardiol. (2020) 76:2982–3021. doi:  10.1016/j.jacc.2020.11.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Kaminsky LA, German C, Imboden M, Ozemek C, Peterman JE, Brubaker PH. The importance of healthy lifestyle behaviors in the prevention of cardiovascular disease. Prog Cardiovasc Dis. (2022) 70:8–15. doi:  10.1016/j.pcad.2021.12.001 [DOI] [PubMed] [Google Scholar]
  • 3. Kiani AK, Medori MC, Bonetti G, Aquilanti B, Velluti V, Matera G, et al. Modern vision of the Mediterranean diet. J Prev Med Hyg. (2022) 63:E36–e43. doi:  10.15167/2421-4248/jpmh2022.63.2S3.2745 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Widmer RJ, Flammer AJ, Lerman LO, Lerman A. The Mediterranean diet, its components, and cardiovascular disease. Am J Med. (2015) 128:229–38. doi:  10.1016/j.amjmed.2014.10.014 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Chen W, Zhang S, Hu X, Chen F, Li D. A review of healthy dietary choices for cardiovascular disease: from individual nutrients and foods to dietary patterns. Nutrients. (2023) 15:(23). doi:  10.3390/nu15234898 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Lal MK, Sharma E, Tiwari RK, Devi R, Mishra UN, Thakur R, et al. Nutrient-mediated perception and signalling in human metabolism: A perspective of nutrigenomics. Int J Mol Sci. (2022) 23:(19). doi:  10.3390/ijms231911305 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Tapsell LC, Neale EP, Probst Y. Dietary patterns and cardiovascular disease: insights and challenges for considering food groups and nutrient sources. Curr Atheroscler Rep. (2019) 21:9. doi:  10.1007/s11883-019-0770-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Karam G, Agarwal A, Sadeghirad B, Jalink M, Hitchcock CL, Ge L, et al. Comparison of seven popular structured dietary programmes and risk of mortality and major cardiovascular events in patients at increased cardiovascular risk: systematic review and network meta-analysis. Bmj. (2023) 380:e072003. doi:  10.1136/bmj-2022-072003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Soliman GA. Dietary fiber, atherosclerosis, and cardiovascular disease. Nutrients. (2019) 11:(5). doi:  10.3390/nu11051155 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Toledo-Ibelles P, Mas-Oliva J. Antioxidants in the fight against atherosclerosis: is this a dead end? Curr Atheroscler Rep. (2018) 20:36. doi:  10.1007/s11883-018-0737-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Zohoori FV. Chapter 1: nutrition and diet. Monogr Oral Sci. (2020) 28:1–13. doi:  10.1159/000455365 [DOI] [PubMed] [Google Scholar]
  • 12. Clemente-Suárez VJ, Mielgo-Ayuso J, Martín-Rodríguez A, Ramos-Campo DJ, Redondo-Flórez L, Tornero-Aguilera JF. The burden of carbohydrates in health and disease. Nutrients. (2022) 14:(18). doi:  10.3390/nu14183809 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Hudson JL, Baum JI, Diaz EC, Børsheim E. Dietary protein requirements in children: methods for consideration. Nutrients. (2021) 13. doi:  10.3390/nu13051554 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Lifshitz F, Tarim O. Considerations about dietary fat restrictions for children. J Nutr. (1996) 126:1031s–41s. doi:  10.1093/jn/126.suppl_4.1031S [DOI] [PubMed] [Google Scholar]
  • 15. Sutter DO, Bender N. Nutrient status and growth in vegan children. Nutr Res. (2021) 91:13–25. doi:  10.1016/j.nutres.2021.04.005 [DOI] [PubMed] [Google Scholar]
  • 16. Lichtenstein AH, Appel LJ, Vadiveloo M, Hu FB, Kris-Etherton PM, Rebholz CM, et al. 2021 dietary guidance to improve cardiovascular health: A scientific statement from the american heart association. Circulation. (2021) 144:e472–87. doi:  10.1161/cir.0000000000001031 [DOI] [PubMed] [Google Scholar]
  • 17. Skrypnik D, Bogdański P, Zawiejska A, Wender-Ożegowska E. Role of gestational weight gain, gestational diabetes, breastfeeding, and hypertension in mother-to-child obesity transmission. Pol Arch Intern Med. (2019) 129:267–75. doi:  10.20452/pamw.4426 [DOI] [PubMed] [Google Scholar]
  • 18. Herforth A, Arimond M, Álvarez-Sánchez C, Coates J, Christianson K, Muehlhoff E. A global review of food-based dietary guidelines. Adv Nutr. (2019) 10:590–605. doi:  10.1093/advances/nmy130 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Sahyoun NR, Jacques PF, Zhang XL, Juan W, McKeown NM. Whole-grain intake is inversely associated with the metabolic syndrome and mortality in older adults. Am J Clin Nutr. (2006) 83:124–31. doi:  10.1093/ajcn/83.1.124 [DOI] [PubMed] [Google Scholar]
  • 20. Wright EM, M. n. G, Turk E. Intestinal absorption in health and disease—sugars. Best Pract Res Clin Gastroenterol. (2003) 17:943–56. doi:  10.1016/S1521-6918(03)00107-0 [DOI] [PubMed] [Google Scholar]
  • 21. Qi X, Tester RF. Fructose, galactose and glucose - In health and disease. Clin Nutr ESPEN. (2019) 33:18–28. doi:  10.1016/j.clnesp.2019.07.004 [DOI] [PubMed] [Google Scholar]
  • 22. Wright EM, Sala-Rabanal M, Loo DDF, Hirayama BA. Chapter 58 - Sugar Absorption. In: Johnson LR, Ghishan FK, Kaunitz JD, Merchant JL, Said HM, Wood JD, editors. Physiology of the Gastrointestinal Tract, Fifth. Academic Press, Boston: (2012). p. 1583–93. doi:  10.1016/B978-0-12-382026-6.00058-0 [DOI] [Google Scholar]
  • 23. Chadt A, Al-Hasani H. Glucose transporters in adipose tissue, liver, and skeletal muscle in metabolic health and disease. Pflugers Arch. (2020) 472:1273–98. doi:  10.1007/s00424-020-02417-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Pitsavos C, Panagiotakos D, Weinem M, Stefanadis C. Diet, exercise and the metabolic syndrome. Rev Diabetes Stud. (2006) 3:118–26. doi:  10.1900/rds.2006.3.118 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Phillips GB. Sex hormones, risk factors and cardiovascular disease. Am J Med. (1978) 65:7–11. doi:  10.1016/0002-9343(78)90685-X [DOI] [PubMed] [Google Scholar]
  • 26. Li X, Zhai Y, Zhao J, He H, Li Y, Liu Y, et al. Impact of metabolic syndrome and it's components on prognosis in patients with cardiovascular diseases: A meta-analysis. Front Cardiovasc Med. (2021) 8:704145. doi:  10.3389/fcvm.2021.704145 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Haffner SM. The metabolic syndrome: inflammation, diabetes mellitus, and cardiovascular disease. Am J Cardiol. (2006) 97:3a–11a. doi:  10.1016/j.amjcard.2005.11.010 [DOI] [PubMed] [Google Scholar]
  • 28. Kelly RK, Tong TYN, Watling CZ, Reynolds A, Piernas C, Schmidt JA, et al. Associations between types and sources of dietary carbohydrates and cardiovascular disease risk: a prospective cohort study of UK Biobank participants. BMC Med. (2023) 21:34. doi:  10.1186/s12916-022-02712-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Eastwood MA, Kay RM. An hypothesis for the action of dietary fiber along the gastrointestinal tract. Am J Clin Nutr. (1979) 32:364–7. doi:  10.1093/ajcn/32.2.364 [DOI] [PubMed] [Google Scholar]
  • 30. Anderson JW, Baird P, Davis RH, Jr., Ferreri S, Knudtson M, Koraym A, et al. Health benefits of dietary fiber. Nutr Rev. (2009) 67:188–205. doi:  10.1111/nure.2009.67.issue-4 [DOI] [PubMed] [Google Scholar]
  • 31. Grundy MM, Edwards CH, Mackie AR, Gidley MJ, Butterworth PJ, Ellis PR. Re-evaluation of the mechanisms of dietary fibre and implications for macronutrient bioaccessibility, digestion and postprandial metabolism. Br J Nutr. (2016) 116:816–33. doi:  10.1017/s0007114516002610 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. McRae MP. Dietary fiber is beneficial for the prevention of cardiovascular disease: an umbrella review of meta-analyses. J Chiropr Med. (2017) 16:289–99. doi:  10.1016/j.jcm.2017.05.005 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Slavin J. Fiber and prebiotics: mechanisms and health benefits. Nutrients. (2013) 5:1417–35. doi:  10.3390/nu5041417 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Sievenpiper JL. Low-carbohydrate diets and cardiometabolic health: the importance of carbohydrate quality over quantity. Nutr Rev. (2020) 78:69–77. doi:  10.1093/nutrit/nuz082 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Ludwig DS, Ebbeling CB. The carbohydrate-insulin model of obesity: beyond "Calories in, calories out". JAMA Intern Med. (2018) 178:1098–103. doi:  10.1001/jamainternmed.2018.2933 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Dou Y, Jiang Y, Chen X, Zhang Y, Wang Y, Chen H, et al. Intermittent dietary carbohydrate restriction versus calorie restriction and cardiometabolic profiles: A randomized trial. Obes (Silver Spring). (2023) 31:2260–71. doi:  10.1002/oby.23855 [DOI] [PubMed] [Google Scholar]
  • 37. Thomsen MN, Skytte MJ, Samkani A, Carl MH, Weber P, Astrup A, et al. Dietary carbohydrate restriction augments weight loss-induced improvements in glycaemic control and liver fat in individuals with type 2 diabetes: a randomised controlled trial. Diabetologia. (2022) 65:506–17. doi:  10.1007/s00125-021-05628-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Hall KD, Bemis T, Brychta R, Chen KY, Courville A, Crayner EJ, et al. Calorie for calorie, dietary fat restriction results in more body fat loss than carbohydrate restriction in people with obesity. Cell Metab. (2015) 22:427–36. doi:  10.1016/j.cmet.2015.07.021 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Martín-Peláez S, Fito M, Castaner O. Mediterranean diet effects on type 2 diabetes prevention, disease progression, and related mechanisms. A review. Nutrients. (2020) 12:(8). doi:  10.3390/nu12082236 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Gajos G. Diabetes and cardiovascular disease: from new mechanisms to new therapies. Pol Arch Intern Med. (2018) 128:178–86. doi:  10.20452/pamw.4227 [DOI] [PubMed] [Google Scholar]
  • 41. Fahy E, Cotter D, Sud M, Subramaniam S. Lipid classification, structures and tools. Biochim Biophys Acta. (2011) 1811(11):637–47. doi:  10.1016/j.bbalip.2011.06.009 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42. Fahy E, Subramaniam S, Brown HA, Glass CK, Merrill AH, Jr., Murphy RC, et al. A comprehensive classification system for lipids. J Lipid Res. (2005) 46:839–61. doi:  10.1194/jlr.E400004-JLR200 [DOI] [PubMed] [Google Scholar]
  • 43. Drzazga A, Sowińska A, Koziołkiewicz M. Lysophosphatidylcholine and lysophosphatidylinosiol–novel promissing signaling molecules and their possible therapeutic activity. Acta Pol Pharm. (2014) 71:887–99. [PubMed] [Google Scholar]
  • 44. SChade DS, Shey L, Eaton RP. Cholesterol review: A metabolically important molecule. Endocr Pract. (2020) 26:1514–23. doi:  10.4158/ep-2020-0347 [DOI] [PubMed] [Google Scholar]
  • 45. Lee JM, Lee H, Kang S, Park WJ. Fatty acid desaturases, polyunsaturated fatty acid regulation, and biotechnological advances. Nutrients. (2016) 8:(1). doi:  10.3390/nu8010023 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Guichardant M, Calzada C, Bernoud-Hubac N, Lagarde M, Véricel E. Omega-3 polyunsaturated fatty acids and oxygenated metabolism in atherothrombosis. Biochim Biophys Acta. (2015) 1851(4):485–95. doi:  10.1016/j.bbalip.2014.09.013 [DOI] [PubMed] [Google Scholar]
  • 47. Chang KJ, Saito H, Tatsuno I, Tamura Y, Yoshida S. Role of 5-lipoxygenase products of arachidonic acid in cell-to-cell interaction between macrophages and natural killer cells in rat spleen. J Leukoc Biol. (1991) 50:273–8. doi:  10.1002/jlb.50.3.273 [DOI] [PubMed] [Google Scholar]
  • 48. Tavazzi L, Maggioni AP, Marchioli R, Barlera S, Franzosi MG, Latini R, et al. Effect of n-3 polyunsaturated fatty acids in patients with chronic heart failure (the GISSI-HF trial): a randomised, double-blind, placebo-controlled trial. Lancet. (2008) 372:1223–30. doi:  10.1016/s0140-6736(08)61239-8 [DOI] [PubMed] [Google Scholar]
  • 49. Rodriguez D, Lavie CJ, Elagizi A, Milani RV. Update on omega-3 polyunsaturated fatty acids on cardiovascular health. Nutrients. (2022) 14:(23). doi:  10.3390/nu14235146 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Miller M, Motevalli M, Westphal D, Kwiterovich PO., Jr. Incorporation of oleic acid and eicosapentaenoic acid into glycerolipids of cultured normal human fibroblasts. Lipids. (1993) 28:1–5. doi:  10.1007/bf02536351 [DOI] [PubMed] [Google Scholar]
  • 51. Harris WS, Miller M, Tighe AP, Davidson MH, Schaefer EJ. Omega-3 fatty acids and coronary heart disease risk: clinical and mechanistic perspectives. Atherosclerosis. (2008) 197:12–24. doi:  10.1016/j.atherosclerosis.2007.11.008 [DOI] [PubMed] [Google Scholar]
  • 52. Rogero MM, Calder PC. Obesity, inflammation, toll-like receptor 4 and fatty acids. Nutrients. (2018) 10:(4). doi:  10.3390/nu10040432 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53. Balta I, Stef L, Pet I, Iancu T, Stef D, Corcionivoschi N. Essential fatty acids as biomedicines in cardiac health. Biomedicines. (2021) 9:(10). doi:  10.3390/biomedicines9101466 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54. Calder PC. Omega-3 fatty acids and inflammatory processes: from molecules to man. Biochem Soc Trans. (2017) 45:1105–15. doi:  10.1042/bst20160474 [DOI] [PubMed] [Google Scholar]
  • 55. Shibabaw T. Omega-3 polyunsaturated fatty acids: anti-inflammatory and anti-hypertriglyceridemia mechanisms in cardiovascular disease. Mol Cell Biochem. (2021) 476:993–1003. doi:  10.1007/s11010-020-03965-7 [DOI] [PubMed] [Google Scholar]
  • 56. von Schacky C, Fischer S, Weber PC. Long-term effects of dietary marine omega-3 fatty acids upon plasma and cellular lipids, platelet function, and eicosanoid formation in humans. J Clin Invest. (1985) 76:1626–31. doi:  10.1172/jci112147 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57. van der Meijden PEJ, Heemskerk JWM. Platelet biology and functions: new concepts and clinical perspectives. Nat Rev Cardiol. (2019) 16:166–79. doi:  10.1038/s41569-018-0110-0 [DOI] [PubMed] [Google Scholar]
  • 58. Vanhoutte PM, Scott-Burden T. The endothelium in health and disease. Tex Heart Inst J. (1994) 21:62–7 [PMC free article] [PubMed] [Google Scholar]
  • 59. Spector AA, Kaduce TL, Figard PH, Norton KC, Hoak JC, Czervionke RL. Eicosapentaenoic acid and prostacyclin production by cultured human endothelial cells. J Lipid Res. (1983) 24:1595–604. doi:  10.1016/S0022-2275(20)37858-5 [DOI] [PubMed] [Google Scholar]
  • 60. Elagizi A, Lavie CJ, O'Keefe E, Marshall K, O'Keefe JH, Milani RV. An update on omega-3 polyunsaturated fatty acids and cardiovascular health. Nutrients. (2021) 13:(1). doi:  10.3390/nu13010204 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61. Zhu Y, Bo Y, Liu Y. Dietary total fat, fatty acids intake, and risk of cardiovascular disease: a dose-response meta-analysis of cohort studies. Lipids Health Dis. (2019) 18:91. doi:  10.1186/s12944-019-1035-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62. Jiang H, Wang L, Wang D, Yan N, Li C, Wu M, et al. Omega-3 polyunsaturated fatty acid biomarkers and risk of type 2 diabetes, cardiovascular disease, cancer, and mortality. Clin Nutr. (2022) 41:1798–807. doi:  10.1016/j.clnu.2022.06.034 [DOI] [PubMed] [Google Scholar]
  • 63. Chardigny JM, Destaillats F, Malpuech-Brugère C, Moulin J, Bauman DE, Lock AL, et al. Do trans fatty acids from industrially produced sources and from natural sources have the same effect on cardiovascular disease risk factors in healthy subjects? Results of the trans Fatty Acids Collaboration (TRANSFACT) study. Am J Clin Nutr. (2008) 87:558–66. doi:  10.1093/ajcn/87.3.558 [DOI] [PubMed] [Google Scholar]
  • 64. de Oliveira PA, Kovacs C, Moreira P, Magnoni D, Saleh MH, Faintuch J. Unsaturated fatty acids improve atherosclerosis markers in obese and overweight non-diabetic elderly patients. Obes Surg. (2017) 27:2663–71. doi:  10.1007/s11695-017-2704-8 [DOI] [PubMed] [Google Scholar]
  • 65. Jain AP, Aggarwal KK, Zhang PY. Omega-3 fatty acids and cardiovascular disease. Eur Rev Med Pharmacol Sci. (2015) 19:441–5. [PubMed] [Google Scholar]
  • 66. Sokoła-Wysoczańska E, Wysoczański T, Wagner J, Czyż K, Bodkowski R, Lochyński S, et al. Polyunsaturated fatty acids and their potential therapeutic role in cardiovascular system disorders-A review. Nutrients. (2018) 10:(10). doi:  10.3390/nu10101561 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67. Watford M, Wu G. Protein. Adv Nutr. (2018) 9:651–3. doi:  10.1093/advances/nmy027 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68. Trumbo P, Schlicker S, Yates AA, Poos M. Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein and amino acids. J Am Diet Assoc. (2002) 102:1621–30. doi:  10.1016/s0002-8223(02)90346-9 [DOI] [PubMed] [Google Scholar]
  • 69. Hoffer LJ. Human protein and amino acid requirements. JPEN J Parenter Enteral Nutr. (2016) 40:460–74. doi:  10.1177/0148607115624084 [DOI] [PubMed] [Google Scholar]
  • 70. Morris CR, Hamilton-Reeves J, Martindale RG, Sarav M, Ochoa Gautier JB. Acquired amino acid deficiencies: A focus on arginine and glutamine. Nutr Clin Pract. (2017) 32:30s–47s. doi:  10.1177/0884533617691250 [DOI] [PubMed] [Google Scholar]
  • 71. Rose AJ. Amino acid nutrition and metabolism in health and disease. Nutrients. (2019) 11:(11). doi:  10.3390/nu11112623 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72. Szwed A, Kim E, Jacinto E. Regulation and metabolic functions of mTORC1 and mTORC2. Physiol Rev. (2021) 101:1371–426. doi:  10.1152/physrev.00026.2020 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73. Wu G, Morris SM., Jr. Arginine metabolism: nitric oxide and beyond. Biochem J. (1998) 336:1–17. doi:  10.1042/bj3360001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74. Böger RH. The emerging role of asymmetric dimethylarginine as a novel cardiovascular risk factor. Cardiovasc Res. (2003) 59:824–33. doi:  10.1016/s0008-6363(03)00500-5 [DOI] [PubMed] [Google Scholar]
  • 75. Tapiero H, Mathé G, Couvreur P, Tew KD. II. Glutamine and glutamate. BioMed Pharmacother. (2002) 56:446–57. doi:  10.1016/s0753-3322(02)00285-8 [DOI] [PubMed] [Google Scholar]
  • 76. Newsholme P, Lima MM, Procopio J, Pithon-Curi TC, Doi SQ, Bazotte RB, et al. Glutamine and glutamate as vital metabolites. Braz J Med Biol Res. (2003) 36:153–63. doi:  10.1590/s0100-879x2003000200002 [DOI] [PubMed] [Google Scholar]
  • 77. Bataglini C, Ramos Mariano I, Azevedo SCF, Freire VN, Natali MRM, Dias Pedrosa MM, et al. Insulin degludec and glutamine dipeptide modify glucose homeostasis and liver metabolism in diabetic mice undergoing insulin-induced hypoglycemia. J Appl BioMed. (2021) 19:210–9. doi:  10.32725/jab.2021.025 [DOI] [PubMed] [Google Scholar]
  • 78. Todorova VK, Kaufmann Y, Hennings L, Klimberg VS. Oral glutamine protects against acute doxorubicin-induced cardiotoxicity of tumor-bearing rats. J Nutr. (2010) 140:44–8. doi:  10.3945/jn.109.113415 [DOI] [PubMed] [Google Scholar]
  • 79. Richter CK, Skulas-Ray AC, Champagne CM, Kris-Etherton PM. Plant protein and animal proteins: do they differentially affect cardiovascular disease risk? Adv Nutr. (2015) 6:712–28. doi:  10.3945/an.115.009654 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80. Satija A, Bhupathiraju SN, Spiegelman D, Chiuve SE, Manson JE, Willett W, et al. Healthful and unhealthful plant-based diets and the risk of coronary heart disease in U.S. Adults. J Am Coll Cardiol. (2017) 70:411–22. doi:  10.1016/j.jacc.2017.05.047 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81. Naghshi S, Sadeghi O, Willett WC, Esmaillzadeh A. Dietary intake of total, animal, and plant proteins and risk of all cause, cardiovascular, and cancer mortality: systematic review and dose-response meta-analysis of prospective cohort studies. Bmj. (2020) 370:m2412. doi:  10.1136/bmj.m2412 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82. Pinckaers PJM, Trommelen J, Snijders T, van Loon LJC. The anabolic response to plant-based protein ingestion. Sports Med. (2021) 51:59–74. doi:  10.1007/s40279-021-01540-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83. Wang T, Masedunskas A, Willett WC, Fontana L. Vegetarian and vegan diets: benefits and drawbacks. Eur Heart J. (2023) 44:3423–39. doi:  10.1093/eurheartj/ehad436 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84. Ewy MW, Patel A, Abdelmagid MG, Mohamed Elfadil O, Bonnes SL, Salonen BR, et al. Plant-based diet: is it as good as an animal-based diet when it comes to protein? Curr Nutr Rep. (2022) 11:337–46. doi:  10.1007/s13668-022-00401-8 [DOI] [PubMed] [Google Scholar]
  • 85. Mariotti F. Animal and plant protein sources and cardiometabolic health. Adv Nutr. (2019) 10:S351–s366. doi:  10.1093/advances/nmy110 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86. Zhong VW, Van Horn L, Greenland P, Carnethon MR, Ning H, Wilkins JT, et al. Associations of processed meat, unprocessed red meat, poultry, or fish intake with incident cardiovascular disease and all-cause mortality. JAMA Intern Med. (2020) 180:503–12. doi:  10.1001/jamainternmed.2019.6969 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87. Shenkin A. Micronutrients in health and disease. Postgrad Med J. (2006) 82:559–67. doi:  10.1136/pgmj.2006.047670 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 88. Holick MF. Sunlight and vitamin D for bone health and prevention of autoimmune diseases, cancers, and cardiovascular disease. Am J Clin Nutr. (2004) 80:1678s–88s. doi:  10.1093/ajcn/80.6.1678S [DOI] [PubMed] [Google Scholar]
  • 89. Holick MF. McCollum award lecture 1994: vitamin D–new horizons for the 21st century. Am J Clin Nutr. (1994) 60:619–30. doi:  10.1093/ajcn/60.4.619 [DOI] [PubMed] [Google Scholar]
  • 90. Chang SW, Lee HC. Vitamin D and health - The missing vitamin in humans. Pediatr Neonatol. (2019) 60:237–44. doi:  10.1016/j.pedneo.2019.04.007 [DOI] [PubMed] [Google Scholar]
  • 91. Osman DE, Phon BWS, Kamarudin MNA, Ponnampalam SN, Radhakrishnan AK, Bhuvanendran S. Biomarkers regulated by lipid-soluble vitamins in glioblastoma. Nutrients. (2022) 14:(14). doi:  10.3390/nu14142873 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92. Kędzierska-Kapuza K, Szczuko U, Stolińska H, Bakaloudi DR, Wierzba W, Szczuko M. Demand for water-soluble vitamins in a group of patients with CKD versus interventions and supplementation-A systematic review. Nutrients. (2023) 15:(4). doi:  10.3390/nu15040860 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93. Pop TL, Sîrbe C, Benţa G, Mititelu A, Grama A. The role of vitamin D and vitamin D binding protein in chronic liver diseases. Int J Mol Sci. (2022) 23:(18). doi:  10.3390/ijms231810705 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94. Muñoz SJ, Heubi JE, Balistreri WF, Maddrey WC. Vitamin E deficiency in primary biliary cirrhosis: gastrointestinal malabsorption, frequency and relationship to other lipid-soluble vitamins. Hepatology. (1989) 9:525–31. doi:  10.1002/hep.1840090403 [DOI] [PubMed] [Google Scholar]
  • 95. Hanna M, Jaqua E, Nguyen V, Clay J. B vitamins: functions and uses in medicine. Perm J. (2022) 26:89–97. doi:  10.7812/tpp/21.204 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96. Lykkesfeldt J, Tveden-Nyborg P. The pharmacokinetics of vitamin C. Nutrients. (2019) 11:(10). doi:  10.3390/nu11102412 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97. Levine M, Conry-Cantilena C, Wang Y, Welch RW, Washko PW, Dhariwal KR, et al. Vitamin C pharmacokinetics in healthy volunteers: evidence for a recommended dietary allowance. Proc Natl Acad Sci U.S.A. (1996) 93:3704–9. doi:  10.1073/pnas.93.8.3704 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98. Arrigoni O, De Tullio MC. Ascorbic acid: much more than just an antioxidant. Biochim Biophys Acta. (2002) 1569:1–9. doi:  10.1016/s0304-4165(01)00235-5 [DOI] [PubMed] [Google Scholar]
  • 99. Tamma G, Valenti G, Grossini E, Donnini S, Marino A, Marinelli RA, et al. Aquaporin membrane channels in oxidative stress, cell signaling, and aging: recent advances and research trends. Oxid Med Cell Longev. (2018) 2018:1501847. doi:  10.1155/2018/1501847 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100. Nolfi-Donegan D, Braganza A, Shiva S. Mitochondrial electron transport chain: Oxidative phosphorylation, oxidant production, and methods of measurement. Redox Biol. (2020) 37:101674. doi:  10.1016/j.redox.2020.101674 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101. Zhao RZ, Jiang S, Zhang L, Yu ZB. Mitochondrial electron transport chain, ROS generation and uncoupling (Review). Int J Mol Med. (2019) 44:3–15. doi:  10.3892/ijmm.2019.4188 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102. Brieger K, Schiavone S, Miller FJ, Jr., Krause KH. Reactive oxygen species: from health to disease. Swiss Med Wkly. (2012) 142:w13659. doi:  10.4414/smw.2012.13659 [DOI] [PubMed] [Google Scholar]
  • 103. Zhang B, Pan C, Feng C, Yan C, Yu Y, Chen Z, et al. Role of mitochondrial reactive oxygen species in homeostasis regulation. Redox Rep. (2022) 27:45–52. doi:  10.1080/13510002.2022.2046423 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104. Kidwell CU, Casalini JR, Pradeep S, Scherer SD, Greiner D, Bayik D, et al. Transferred mitochondria accumulate reactive oxygen species, promoting proliferation. Elife. (2023) 12. doi:  10.7554/eLife.85494 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105. Lambeth JD. Nox enzymes, ROS, and chronic disease: an example of antagonistic pleiotropy. Free Radic Biol Med. (2007) 43:332–47. doi:  10.1016/j.freeradbiomed.2007.03.027 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106. Shaito A, Aramouni K, Assaf R, Parenti A, Orekhov A, Yazbi AE, et al. Oxidative stress-induced endothelial dysfunction in cardiovascular diseases. Front Biosci (Landmark Ed). (2022) 27:105. doi:  10.31083/j.fbl2703105 [DOI] [PubMed] [Google Scholar]
  • 107. Quan Y, Xin Y, Tian G, Zhou J, Liu X. Mitochondrial ROS-modulated mtDNA: A potential target for cardiac aging. Oxid Med Cell Longev. (2020) 2020:9423593. doi:  10.1155/2020/9423593 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108. Lundberg JO, Weitzberg E. Nitric oxide signaling in health and disease. Cell. (2022) 185:2853–78. doi:  10.1016/j.cell.2022.06.010 [DOI] [PubMed] [Google Scholar]
  • 109. Radi R. Oxygen radicals, nitric oxide, and peroxynitrite: Redox pathways in molecular medicine. Proc Natl Acad Sci U.S.A. (2018) 115:5839–48. doi:  10.1073/pnas.1804932115 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110. Ren BC, Zhang YF, Liu SS, Cheng XJ, Yang X, Cui XG, et al. Curcumin alleviates oxidative stress and inhibits apoptosis in diabetic cardiomyopathy via Sirt1-Foxo1 and PI3K-Akt signalling pathways. J Cell Mol Med. (2020) 24:12355–67. doi:  10.1111/jcmm.15725 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111. Purnomo Y, Piccart Y, Coenen T, Prihadi JS, Lijnen PJ. Oxidative stress and transforming growth factor-β1-induced cardiac fibrosis. Cardiovasc Hematol Disord Drug Targets. (2013) 13:165–72. doi:  10.2174/1871529x11313020010 [DOI] [PubMed] [Google Scholar]
  • 112. Marchio P, Guerra-Ojeda S, Vila JM, Aldasoro M, Victor VM, Mauricio MD. Targeting early atherosclerosis: A focus on oxidative stress and inflammation. Oxid Med Cell Longev. (2019) 2019:8563845. doi:  10.1155/2019/8563845 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113. El Haouari M. Platelet oxidative stress and its relationship with cardiovascular diseases in type 2 diabetes mellitus patients. Curr Med Chem. (2019) 26:4145–65. doi:  10.2174/0929867324666171005114456 [DOI] [PubMed] [Google Scholar]
  • 114. Carillon J, Rouanet JM, Cristol JP, Brion R. Superoxide dismutase administration, a potential therapy against oxidative stress related diseases: several routes of supplementation and proposal of an original mechanism of action. Pharm Res. (2013) 30:2718–28. doi:  10.1007/s11095-013-1113-5 [DOI] [PubMed] [Google Scholar]
  • 115. Handy DE, Loscalzo J. The role of glutathione peroxidase-1 in health and disease. Free Radic Biol Med. (2022) 188:146–61. doi:  10.1016/j.freeradbiomed.2022.06.004 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116. Pingitore A, Lima GP, Mastorci F, Quinones A, Iervasi G, Vassalle C. Exercise and oxidative stress: potential effects of antioxidant dietary strategies in sports. Nutrition. (2015) 31:916–22. doi:  10.1016/j.nut.2015.02.005 [DOI] [PubMed] [Google Scholar]
  • 117. Tomasello G, Mazzola M, Leone A, Sinagra E, Zummo G, Farina F, et al. Nutrition, oxidative stress and intestinal dysbiosis: Influence of diet on gut microbiota in inflammatory bowel diseases. BioMed Pap Med Fac Univ Palacky Olomouc Czech Repub. (2016) 160:461–6. doi:  10.5507/bp.2016.052 [DOI] [PubMed] [Google Scholar]
  • 118. Higgins MR, Izadi A, Kaviani M. Antioxidants and exercise performance: with a focus on vitamin E and C supplementation. Int J Environ Res Public Health. (2020) 17:(22). doi:  10.3390/ijerph17228452 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119. Gęgotek A, Skrzydlewska E. Ascorbic acid as antioxidant. Vitam Horm. (2023) 121:247–70. doi:  10.1016/bs.vh.2022.10.008 [DOI] [PubMed] [Google Scholar]
  • 120. Mustacich DJ, Bruno RS, Traber MG. Vitamin E. Vitam Horm. (2007) 76:1–21. doi:  10.1016/s0083-6729(07)76001-6 [DOI] [PubMed] [Google Scholar]
  • 121. Carr AC, Maggini S. Vitamin C and immune function. Nutrients. (2017) 9:(11). doi:  10.3390/nu9111211 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122. Fortmann SP, Burda BU, Senger CA, Lin JS, Whitlock EP. Vitamin and mineral supplements in the primary prevention of cardiovascular disease and cancer: An updated systematic evidence review for the U.S. Preventive Services Task Force. Ann Intern Med. (2013) 159:824–34. doi:  10.7326/0003-4819-159-12-201312170-00729 [DOI] [PubMed] [Google Scholar]
  • 123. Kusumi K, Kremsdorf R, Kakajiwala A, Mahan JD. Pediatric mineral and bone disorder of chronic kidney disease and cardiovascular disease. Adv Chronic Kidney Dis. (2022) 29:275–82. doi:  10.1053/j.ackd.2022.04.002 [DOI] [PubMed] [Google Scholar]
  • 124. Zoroddu MA, Aaseth J, Crisponi G, Medici S, Peana M, Nurchi VM. The essential metals for humans: a brief overview. J Inorg Biochem. (2019) 195:120–9. doi:  10.1016/j.jinorgbio.2019.03.013 [DOI] [PubMed] [Google Scholar]
  • 125. Pohl HR, Wheeler JS, Murray HE. Sodium and potassium in health and disease. Met Ions Life Sci. (2013) 13:29–47. doi:  10.1007/978-94-007-7500-8_2 [DOI] [PubMed] [Google Scholar]
  • 126. Kettritz R, Loffing J. Potassium homeostasis - Physiology and pharmacology in a clinical context. Pharmacol Ther. (2023) 249:108489. doi:  10.1016/j.pharmthera.2023.108489 [DOI] [PubMed] [Google Scholar]
  • 127. Weaver CM. Potassium and health. Adv Nutr. (2013) 4:368s–77s. doi:  10.3945/an.112.003533 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 128. Kirabo A. A new paradigm of sodium regulation in inflammation and hypertension. Am J Physiol Regul Integr Comp Physiol. (2017) 313:R706–r710. doi:  10.1152/ajpregu.00250.2017 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 129. Houston MC. Sodium and hypertension. A review. Arch Intern Med. (1986) 146:179–85. doi:  10.1001/archinte.146.1.179 [DOI] [PubMed] [Google Scholar]
  • 130. Panza JA, Quyyumi AA, Brush JE, Jr., Epstein SE. Abnormal endothelium-dependent vascular relaxation in patients with essential hypertension. N Engl J Med. (1990) 323:22–7. doi:  10.1056/nejm199007053230105 [DOI] [PubMed] [Google Scholar]
  • 131. Saris NE, Mervaala E, Karppanen H, Khawaja JA, Lewenstam A. Magnesium. An update on physiological, clinical and analytical aspects. Clin Chim Acta. (2000) 294:1–26. doi:  10.1016/s0009-8981(99)00258-2 [DOI] [PubMed] [Google Scholar]
  • 132. Zhang XD, Thai PN, Lieu DK, Chiamvimonvat N. Cardiac small-conductance calcium-activated potassium channels in health and disease. Pflugers Arch. (2021) 473:477–89. doi:  10.1007/s00424-021-02535-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133. Berger RCM, Benetti A, Girardi ACC, Forechi L, de Oliveira RM, Vassallo PF, et al. Influence of long-term salt diets on cardiac ca2+ Handling and contractility proteins in hypertensive rats. Am J Hypertens. (2018) 31:726–34. doi:  10.1093/ajh/hpy023 [DOI] [PubMed] [Google Scholar]
  • 134. Popov S, Venetsanou K, Chedrese PJ, Pinto V, Takemori H, Franco-Cereceda A, et al. Increases in intracellular sodium activate transcription and gene expression via the salt-inducible kinase 1 network in an atrial myocyte cell line. Am J Physiol Heart Circ Physiol. (2012) 303:H57–65. doi:  10.1152/ajpheart.00512.2011 [DOI] [PubMed] [Google Scholar]
  • 135. Burgess E, Lewanczuk R, Bolli P, Chockalingam A, Cutler H, Taylor G, et al. Lifestyle modifications to prevent and control hypertension. 6. Recommendations on potassium, magnesium and calcium. Canadian Hypertension Society, Canadian Coalition for High Blood Pressure Prevention and Control, Laboratory Centre for Disease Control at Health Canada, Heart and Stroke Foundation of Canada. Cmaj. (1999) 160:S35–45 [PMC free article] [PubMed] [Google Scholar]
  • 136. Das UN. Nutrients, essential fatty acids and prostaglandins interact to augment immune responses and prevent genetic damage and cancer. Nutrition. (1989) 5:106–10. [PubMed] [Google Scholar]
  • 137. Ferreira JP, Butler J, Rossignol P, Pitt B, Anker SD, Kosiborod M, et al. Abnormalities of potassium in heart failure: JACC state-of-the-art review. J Am Coll Cardiol. (2020) 75:2836–50. doi:  10.1016/j.jacc.2020.04.021 [DOI] [PubMed] [Google Scholar]
  • 138. Sacks FM, Brown LE, Appel L, Borhani NO, Evans D, Whelton P. Combinations of potassium, calcium, and magnesium supplements in hypertension. Hypertension. (1995) 26:950–6. doi:  10.1161/01.hyp.26.6.950 [DOI] [PubMed] [Google Scholar]
  • 139. Wang L, Manson JE, Buring JE, Lee IM, Sesso HD. Dietary intake of dairy products, calcium, and vitamin D and the risk of hypertension in middle-aged and older women. Hypertension. (2008) 51:1073–9. doi:  10.1161/hypertensionaha.107.107821 [DOI] [PubMed] [Google Scholar]
  • 140. Hurrell R, Egli I. Iron bioavailability and dietary reference values. Am J Clin Nutr. (2010) 91:1461s–7s. doi:  10.3945/ajcn.2010.28674F [DOI] [PubMed] [Google Scholar]
  • 141. Lynch SR, Cook JD. Interaction of vitamin C and iron. Ann N Y Acad Sci. (1980) 355:32–44. doi:  10.1111/j.1749-6632.1980.tb21325.x [DOI] [PubMed] [Google Scholar]
  • 142. DeLoughery TG. Iron deficiency anemia. Med Clin North Am. (2017) 101:319–32. doi:  10.1016/j.mcna.2016.09.004 [DOI] [PubMed] [Google Scholar]
  • 143. Sawicki KT, De Jesus A, Ardehali H. Iron metabolism in cardiovascular disease: physiology, mechanisms, and therapeutic targets. Circ Res. (2023) 132:379–96. doi:  10.1161/circresaha.122.321667 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144. Stiles LI, Ferrao K, Mehta KJ. Role of zinc in health and disease. Clin Exp Med. (2024) 24:38. doi:  10.1007/s10238-024-01302-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 145. Cassandri M, Smirnov A, Novelli F, Pitolli C, Agostini M, Malewicz M, et al. Zinc-finger proteins in health and disease. Cell Death Discovery. (2017) 3:17071. doi:  10.1038/cddiscovery.2017.71 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146. Prasad AS. Zinc: role in immunity, oxidative stress and chronic inflammation. Curr Opin Clin Nutr Metab Care. (2009) 12:646–52. doi:  10.1097/MCO.0b013e3283312956 [DOI] [PubMed] [Google Scholar]
  • 147. Djoussé L, Gaziano JM. Breakfast cereals and risk of heart failure in the physicians' health study I. Arch Intern Med. (2007) 167:2080–5. doi:  10.1001/archinte.167.19.2080 [DOI] [PubMed] [Google Scholar]
  • 148. Evangelista LS, Jose MM, Sallam H, Serag H, Golovko G, Khanipov K, et al. High-protein vs. standard-protein diets in overweight and obese patients with heart failure and diabetes mellitus: findings of the Pro-HEART trial. ESC Heart Fail. (2021) 8:1342–8. doi:  10.1002/ehf2.13213 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 149. Oikonomou E, Vogiatzi G, Karlis D, Siasos G, Chrysohoou C, Zografos T, et al. Effects of omega-3 polyunsaturated fatty acids on fibrosis, endothelial function and myocardial performance, in ischemic heart failure patients. Clin Nutr. (2019) 38:1188–97. doi:  10.1016/j.clnu.2018.04.017 [DOI] [PubMed] [Google Scholar]
  • 150. Woo JS, Woo Y, Jang JY, Ha SJ. Effect of vitamin D on endothelial and ventricular function in chronic heart failure patients: A prospective, randomized, placebo-controlled trial. Med (Baltimore). (2022) 101:e29623. doi:  10.1097/md.0000000000029623 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 151. Saslow LR, Jones LM, Sen A, Wolfson JA, Diez HL, O'Brien A, et al. Comparing very low-carbohydrate vs DASH diets for overweight or obese adults with hypertension and prediabetes or type 2 diabetes: A randomized trial. Ann Fam Med. (2023) 21:256–63. doi:  10.1370/afm.2968 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 152. Burke V, Hodgson JM, Beilin LJ, Giangiulioi N, Rogers P, Puddey IB. Dietary protein and soluble fiber reduce ambulatory blood pressure in treated hypertensives. Hypertension. (2001) 38:821–6. doi:  10.1161/hy1001.092614 [DOI] [PubMed] [Google Scholar]
  • 153. Juraschek SP, Miller ER, Weaver CM, Appel LJ. Effects of sodium reduction and the DASH diet in relation to baseline blood pressure. J Am Coll Cardiol. (2017) 70:2841–8. doi:  10.1016/j.jacc.2017.10.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 154. Erkkilä AT, Lichtenstein AH, Mozaffarian D, Herrington DM. Fish intake is associated with a reduced progression of coronary artery atherosclerosis in postmenopausal women with coronary artery disease. Am J Clin Nutr. (2004) 80:626–32. doi:  10.1093/ajcn/80.3.626 [DOI] [PubMed] [Google Scholar]
  • 155. Liu S, Lee IM, Ajani U, Cole SR, Buring JE, Manson JE. Intake of vegetables rich in carotenoids and risk of coronary heart disease in men: The Physicians' Health Study. Int J Epidemiol. (2001) 30:130–5. doi:  10.1093/ije/30.1.130 [DOI] [PubMed] [Google Scholar]
  • 156. Aslanabadi N, Jafaripor I, Sadeghi S, Hamishehkar H, Ghaffari S, Toluey M, et al. Effect of vitamin D in the prevention of myocardial injury following elective percutaneous coronary intervention: A pilot randomized clinical trial. J Clin Pharmacol. (2018) 58:144–51. doi:  10.1002/jcph.989 [DOI] [PubMed] [Google Scholar]
  • 157. Basnet TB, Srijana GC, Basnet R, Neupane B, Thapa G. Causal effects of dietary calcium, zinc and iron intakes on coronary artery disease in men: G-estimation and inverse probability of treatment weighting (IPTW) analyses. Clin Nutr ESPEN. (2021) 42:73–81. doi:  10.1016/j.clnesp.2020.12.030 [DOI] [PubMed] [Google Scholar]
  • 158. Hicks JJ, Montes-Cortes DH, Cruz-Dominguez MP, Medina-Santillan R, Olivares-Corichi IM. Antioxidants decrease reperfusion induced arrhythmias in myocardial infarction with ST-elevation. Front Biosci. (2007) 12:2029–37. doi:  10.2741/2208 [DOI] [PubMed] [Google Scholar]
  • 159. Albert CM, Cook NR, Pester J, Moorthy MV, Ridge C, Danik JS, et al. Effect of marine omega-3 fatty acid and vitamin D supplementation on incident atrial fibrillation: A randomized clinical trial. Jama. (2021) 325:1061–73. doi:  10.1001/jama.2021.1489 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 160. Botto LD, Khoury MJ, Mulinare J, Erickson JD. Periconceptional multivitamin use and the occurrence of conotruncal heart defects: results from a population-based, case-control study. Pediatrics. (1996) 98:911–7. doi:  10.1542/peds.98.5.911 [DOI] [PubMed] [Google Scholar]
  • 161. Shah B, Newman JD, Woolf K, Ganguzza L, Guo Y, Allen N, et al. Anti-inflammatory effects of a vegan diet versus the American heart association-recommended diet in coronary artery disease trial. J Am Heart Assoc. (2018) 7:e011367. doi:  10.1161/jaha.118.011367 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 162. Hibbard BM. The role of folic acid in pregnancy; with particular reference to anaemia, abruption and abortion. J Obstet Gynaecol Br Commonw. (1964) 71:529–42. doi:  10.1111/j.1471-0528.1964.tb04317.x [DOI] [PubMed] [Google Scholar]
  • 163. Shulpekova Y, Nechaev V, Kardasheva S, Sedova A, Kurbatova A, Bueverova E, et al. The concept of folic acid in health and disease. Molecules. (2021) 26:(12). doi:  10.3390/molecules26123731 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 164. Czeizel AE, Tóth M, Rockenbauer M. Population-based case control study of folic acid supplementation during pregnancy. Teratology. (1996) 53:345–51. doi:  [DOI] [PubMed] [Google Scholar]
  • 165. Hernández-Díaz S, Werler MM, Walker AM, Mitchell AA. Folic acid antagonists during pregnancy and the risk of birth defects. N Engl J Med. (2000) 343:1608–14. doi:  10.1056/nejm200011303432204 [DOI] [PubMed] [Google Scholar]
  • 166. Mires S, Caputo M, Overton T, Skerritt C. Maternal micronutrient deficiency and congenital heart disease risk: A systematic review of observational studies. Birth Defects Res. (2022) 114:1079–91. doi:  10.1002/bdr2.2072 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167. Czeizel AE, Dudás I, Vereczkey A, Bánhidy F. Folate deficiency and folic acid supplementation: the prevention of neural-tube defects and congenital heart defects. Nutrients. (2013) 5:4760–75. doi:  10.3390/nu5114760 [DOI] [PMC free article] [PubMed] [Google Scholar]

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