Abstract
Introduction: Coffee is a popular beverage and the most used psychostimulant worldwide. Habitual coffee consumption has been linked to a growing list of health benefits; however, coffee consumption has been a source of longstanding debate. Recent observational studies have challenged the misconception of caffeine and reported the safety and beneficial effects of coffee intake on a range of cardiovascular (CV) conditions, including coronary artery disease, arrhythmias, heart failure, and stroke, leading to a decreased risk of CVD, all-cause and CVD mortality, and being associated with favorable CV outcomes. However, the mechanisms underlying the protective effects of caffeine remain speculative, and there is a lack of dedicated studies aimed at addressing the impact of different coffee subtypes on clinical outcomes such as CVD, arrhythmia, and mortality.
Study and Results: The study included 449,563 UK Biobank participants, free of cardiovascular problems at enrollment (median age 58 years; 55.3% females). The median follow-up time was 12.5 years. Drinking 4 to 5 cups/day of ground (HR 0.83; 95% CI [0.76–0.91]; P < .0001) or 2 to 3 cups/day of instant (HR, 0.88; 95% CI [0.85–0.92]; P < .0001) coffee (but not decaffeinated coffee) was associated with a significant reduction in incident arrhythmia, including AF. Habitual coffee intake of up to 5 cups/day was associated with significant reductions in the risk of incident CVD, CHD (HR 0.89, CI [0.86–0.91], P < 0.0001), CCF (HR 0.83, CI [0.79–0.87], P < 0.0001), and ischemic stroke (HR 0.84, CI [0.78–0.90], P < 0.0001). Coffee consumption led to significant reductions in all-cause mortality (HR 0.86, CI [0.83–0.89], P < 0.0001) and CV mortality (HR 0.82, CI [0.74–0.90], P < 0.0001). Consumption of ground coffee at all levels significantly reduced the risk of all-cause and CV mortality. There was no significant difference in the incidence of CVD among all intake categories or across all coffee subtypes.
Lessons learned: The results from the UK Biobank indicate that mild-to-moderate consumption of all types of coffee is linked to improved CV outcomes and a lower risk of cardiovascular disease and death, with caffeinated coffee significantly reducing the risk of arrhythmias, including AF. Daily coffee intake should not be discouraged by physicians, even in the presence of a newly developed cardiovascular disease. Whether coffee will be prescribed in the future to prevent CVD and improve cardiovascular health depends on further evaluation of the physiological mechanisms and elucidation of the specific protective effects of coffee consumption.
Introduction
Coffee is a popular beverage and the most commonly used psychostimulant worldwide1. In addition to being a delicious booster of energy levels, habitual coffee consumption has been linked to a growing list of health benefits, including the prevention of chronic and degenerative conditions, including cancer2–4; inflammatory and oxidative stress-related diseases such as obesity5–7, metabolic syndrome7,8, type 2 diabetes mellitus (DM)9–17, and autoimmune diseases including endocrine disease18,19, Parkinson’s21–23 and Alzheimer’s disease24,25 (Figures 1 and 2).
Figure 1. The main compounds of coffee: caffeine, chlorogenic acids, and other phenolics, and their anti-inflammatory and antioxidant effects19.
Figure 2. Summary of all major effects of coffee constituents on glucose and lipid metabolism, blood pressure, and waist circumference.
Coffee contains many biologically active substances, including caffeine, chlorogenic acids (CGAs), and diterpenes as cafestol and kahweol, which exert different metabolic effects. Regarding glucose metabolism, caffeine effect insulin release, predominantly, increasing b-cells secretion and reducing their damage. At the same time, CGAs have different effects on glucose absorption and insulin sensitivity by inhibiting salivary and pancreatic a-amylase, a-1,4-glucosidase, and glucose-6-phosphatase secretion of incretins and by inducing the translocation of GLUT-4, responsible for glucose uptake by peripheral tissues. The acute hypertensive effect of coffee is mainly mediated by caffeine, stimulating sympathetic activation with vasoconstriction, increased aortic stiffness, and cardiac automatism, while in the long-term exposure, CGAs reduce oxidative stress by improving endothelial function and the bioavailability of nitric oxide, resulting in a reduction in blood pressure following chronic coffee intake. Regarding the effect of coffee consumption on waist circumference, caffeine stimulates the sympathetic nervous system increasing resting metabolic rate and energy expenditure, and promotes cellular thermogenesis and lipolysis. Simultaneously, CGAs act to suppress the accumulation of hepatic triglycerides via down-regulation of genes associated with adipogenesis and up-regulation of genes involved in fatty acid oxidation. Finally, about lipid metabolism, caffeine and CGAs have been shown to suppress the activity of enzymes for lipid synthesis, acetyl-CoA carboxylase, fatty acid synthase, and stearoyl-CoA desaturase, and to increase fatty acid b-oxidation by stimulating carnitine palmitoyltransferase and by activating PPAR-a in the liver and adipose tissues. Meanwhile, CGAs alone can control lipogenesis by down-regulating sterol regulatory element-binding protein (SREBP)-1C. Cafestol and kahweol have been shown to increase blood cholesterol levels by inhibiting bile acid synthesis acting on farnesoid X receptors. Therefore, habitual coffee consumption has been associated with a reduction in the risk of diabetes, hypertension, abdominal obesity, a reduction in triglycerides levels, and increased HDL cholesterol levels, resulting in a reduction in the risk of metabolic syndrome overall19.
Coffee contains more than 100 different biological agents and many beneficial compounds for health. Caffeine, the most commonly studied compound in coffee, exerts positive effects on kidney function, and daily coffee consumption is associated with a lower risk of chronic kidney disease26 and lower risk of incident acute kidney injury (AKI), presenting an opportunity for cardiorenal protection through diet27. Although other compounds in coffee are less studied, compounds such as chlorogenic acid and trigonelline are known to reduce generalized inflammation and oxidative stress28.
Nevertheless, the health benefits and risks of coffee consumption have been a source of longstanding debate. Moreover, coffee and caffeine are often considered by the general population to be ‘bad’ for the heart owing to their association with palpitations and high blood pressure, and up to 80% of health practitioners recommend avoiding caffeine use in the presence of cardiovascular disease (CVD)29.
Increasing public awareness of modifiable lifestyle risk factors has encouraged more information on the health benefits and CVD risks associated with coffee consumption. Recent observational studies have challenged the misconception of caffeine and reported the safety and beneficial effects of coffee intake30–32. Light-to-moderate coffee consumption(0.5–3 cups per day) has been shown to be beneficial for a range of cardiovascular conditions, including coronary artery disease(CHD)33–35, arrhythmias33,36,37 heart failure20,33,38 and stroke30,32,37–41 leading to a decreased risk of CVD30–34,38,42,43, all-cause40,42,44–47 and CVD mortality48–51 and being associated with favorable CVD outcomes (Figure 3).
Figure 3. Physiological effects of habitual caffeine consumption on the cardiovascular system. Adapted from33.
Importantly, caffeine consumption has been shown to be unlikely related to the incidence or the risk of developing atrial fibrillation52,53, even possibly offering a protective effect54. In addition, moderate and habitual consumption of coffee (1–3 cups per day) has recently been shown to have a significant protective effect on hypertension55–59 and does not adversely affect blood pressure in most people, including those with arterial hypertension60.
These results have led to the consideration of antioxidant rich beverages (e.g., coffee) as potentially helpful choices in supporting healthy blood pressures by The European Society of Hypertension (ESH)61 and promoting coffee consumption(3–4 cups/day) for the prevention of CVD in the 2021 European Society of Cardiology Guidelines62.
However, the mechanisms underlying the protective effects of caffeine remain speculative, and there is a lack of dedicated studies aimed at addressing the impact of different coffee subtypes on clinical outcomes such as CVD, arrhythmia, and mortality.
The study
The UK Biobank is a large-scale biomedical database and research resource that contains in-depth genetic and health information from over 502,521 UK participants aged between 40 and 69 years63. The aim of this study was to provide insights into the impact of coffee on cardiovascular (CV) outcomes, mainly the relationship between coffee consumption and coffee subtypes and new-onset arrhythmias, CVD, and mortality64.
Survey and questionnaire responses on lifestyle risk factors and physical examination findings were collected at baseline. Participants were followed up long term to assess health outcomes. Participants with baseline AF, a previous diagnosis of CVD, or missing data regarding coffee intake, coffee type, tea intake, and body mass index (BMI)/smoking/alcohol status were excluded.
Coffee consumption, including type of coffee (instant coffee, ground coffee and/or decaffeinated coffee) and number of cups per day was self-reported on a touchscreen questionnaire. Participants could only select one type of coffee and were grouped into six daily intake categories, consisting of 0, <1, 1, 2–3, 4–5, and >5 cups/day.
Cardiovascular disease was defined as a composite of coronary heart disease (CHD), congestive cardiac failure (CCF), and ischemic stroke. Arrhythmia included ectopy, atrial fibrillation/atrial flutter (AF/ flutter), supraventricular tachycardia (SVT), and ventricular tachycardia (VT)/ventricular fibrillation (VF). Mortality outcomes included all-cause mortality, CV mortality, and sudden cardiac death.
The study adjusted for covariables, including age, gender, alcohol intake, tea intake, obesity, diabetes, hypertension, obstructive sleep apnea, and smoking status. The outcomes of interest were ascertained using the International Classification of Diseases, Tenth Revision (ICD-10) codes available from medical and death records.
Results of the study
The study included a total of 449,563 UK Biobank participants, free of cardiovascular problems at enrollment (median age 58 years; 55.3% female), of which 100 510 (22.35%) were controls (non-coffee drinkers). The median follow-up time was 12.5 years. The type of coffee, in order of popularity, was instant in 44.1% (n = 198,062), ground in 18.4% (n = 82,575), and decaffeinated in 15.2% (n = 68,416) (Figure 4).
Figure 4. The impact of coffee subtypes on incident cardiovascular disease, arrhythmias, and mortality: long-term outcomes from the UK Biobank.
Arrhythmia was diagnosed in 6.7% (n = 30,100) participants, which included AF/flutter in 3.4% (n = 15,302), SVT in 0.7% (n = 3032), and VT/VF in 0.4% (n = 2008). Compared to non-drinkers, a U-shaped relationship was observed between increasing levels of coffee consumption and the incidence of any arrhythmia.
The lowest risk for arrhythmias was seen in those who consumed 2–3 coffee cups/day (HR 0.91, CI [0.88–0.94]; P < 0.0001). A similar relationship was observed for AF/flutter and SVT (HR 0.88, CI [0.83–0.94], P < 0.0001) and VT/VF (HR 0.83, CI [0.70–0.97], P = 0.0201) as significant risk reductions were seen in those who consumed 1–5 cups/day, with the lowest risk seen in 4–5 cups/day.
Drinking 1–5 cups/day of ground or instant coffee (but not decaffeinated coffee) was associated with a significant reduction in incident arrhythmia, including AF. The lowest risk was at 4–5 cups/day for ground coffee (HR 0.83; 95% CI [0.76–0.91]; P <0.0001) and 2–3 cups/day for instant coffee (HR, 0.88; 95% CI [0.85–0.92]; P <0.0001).
Cardiovascular disease was diagnosed in 9.6% (n = 43,173) participants during follow-up. A total of 7.7% (n = 34,677) participants were diagnosed with incident CHD, 2.8% (n= 12,966) with incident CCF, and 1.5% (n = 6767) with incident stroke.
Habitual coffee intake of up to 5 cups/day was associated with significant reductions in the risk of incident CVD and CHD (with the lowest risk in those who consumed 2–3 cups/day (HR 0.89, CI [0.86–0.91], P < 0.0001), when compared with non-drinkers.
Coffee consumption at all levels was associated with significant reduction in the risk of CCF (lowest risks in those who consumed 2–3 cups/day (HR 0.83, CI [0.79–0.87], P < 0.0001) and ischemic stroke (HR 0.84, CI [0.78–0.90], P < 0.0001) (Table 1).
Table 1. Cardiovascular outcomes and risk reduction in different coffee subtypes and overall coffee intake.
| Cardiovascular Outcomes | Ground Coffee | Instant Coffee | Decaffeinated Coffee | Overall Coffee Intake | |||
|---|---|---|---|---|---|---|---|
| n = 82575 | % | n = 198062 | % | n = 68416 | % | n = 349053 | |
| Arrhythmia | 5872 | 7.0 | 16696 | 8.4 | 6737 | 9.8 | |
| AF/flutter | 3269 | 3.9 | 9273 | 4.7 | 3889 | 5.7 | |
| CVD | 8670 | 10.5 | 29751 | 15 | 9904 | 14.5 | |
| CHD | 7154 | 8.6 | 25051 | 12.6 | |||
| CCF | 1976 | 2.3 | 7029 | 3.5 | 2263 | 3.3 | |
| Stroke | 1114 | 1.3 | 3707 | 1.8 | 1224 | 1.7 | |
| Mortality | 4511 | 5.5 | 15365 | 7.7 | 7434 | 10.9 | |
| Risk reduction effect | |||||||
| Arrhythmia | 1–5 cups/day | 2–3 cups/day 0.85–0.92 (HR 0.88, CI [0.85–0.92] | 2–3 cups/day (HR 0.91, CI [0.88–0.94], P < 0.0001) | ||||
| AF/flutter | 1–5 cups/day | 4–5 cups/day (HR 0.85, CI [0.79–0.91], P < 0.0001) | 4–5 cups/day (HR 0.88, CI [0.83–0.94], P < 0.0001) | ||||
| SVT | 2–5 cups/day | 4–5 cups/day (HR 0.75, CI [0.63–0.88], P = 0.0005) | |||||
| VT/VF | 2–5 cups/day | 4–5 cups/day (HR 0.83, CI [0.70–0.97], P = 0.0201) | |||||
| CVD | up to 5 cups/day | 2–3 cups/day (HR 0.91, CI [0.88–0.94], P < 0.0001) | 2–3 cups/day (HR 0.94, CI [0.90–0.99], P = 0.0093) | 5 cups/day | |||
| CHD | up to 5 cups/day | 2–3 cups/day (HR 0.91, CI [0.88–0.94], P < 0.0001) | 2–3 cups/day (HR 0.94, CI [0.89–0.99], P = 0.0127) | 2–3 cups/day (HR 0.89, CI [0.86–0.91], P < 0.0001). | |||
| CCF | up to 5 cups/day | 2–3 cups/day (HR 0.86, CI [0.79–0.94], P = 0.0004) | 2–3 cups/day (HR 0.83, (CI [0.79–0.87], P < 0.0001) | ||||
| All-cause mortality | 2–3 cups/day (HR 0.73, CI [0.69–0.78], P < 0.0001) | 2–3 cups/day (HR 0.89, CI [0.86–0.93], P < 0.0001) | 2–3 cups/day (HR 0.86, CI [0.80–0.91], P < 0.0001) | 2–3 cups/day (HR 0.86, CI [0.83–0.89], P < 0.0001) | |||
| CV mortality | 4–5 cups/day (HR 0.65, CI [0.51–0.83], P < 0.0001) | 1–3 cups/day (HR 0.74, CI [0.61–0.89], P = 0.0012) | 1 cup/day (HR 0.82, CI [0.74–0.90], P 0.0001) | ||||
A total of 6.2% (n = 27,809) participants died during long-term follow-up, including 1.0% (n = 4402) from CV causes. A significant reduction in all-cause mortality was associated with coffee consumption up to 5 cups/day, with the greatest effect seen with 2–3 cups/day (HR 0.86, CI [0.83–0.89], P < 0.0001).
A significant reduction in CV mortality was observed in coffee drinkers of 1–5 cups/day (lowest risk 1 cup/day; HR 0.82, CI [0.74–0.90], P < 0.0001). Coffee intake was not associated with a risk of sudden cardiac death. Consumption of ground coffee at all levels significantly reduced the risk of all-cause and CV mortality.
A sensitivity analysis on coffee drinkers only found no significant difference in the incidence of CVD at all intake categories and across all coffee subtypes. Coffee drinking was associated with a reduction in incident CVD in participants who had normotension (HR 0.90, CI [0.86–0.94], P < 0.0001), hypertension (HR 0.91, CI [0.89–0.94], P < 0.0001), DM (HR 0.92, CI [0.88–0.97], P = 0.001), non-diabetics (HR 0.91, CI [0.88–0.93], P < 0.0001), obstructive sleep apnea (OSA) (HR 0.87, CI [0.78–0.96], P = 0.008), as well as non-OSA (HR 0.91, CI [0.89–0.94], P < 0.0001) when compared with non-drinkers.
Discussion
This study shows that habitual consumption of all types of coffee reduces the incidence of CVD and all-cause and cardiovascular mortality, with the largest risk reduction of CVD, CHD, CCF, and all-cause mortality seen with the consumption of 2–3 cups of coffee per day. Caffeinated (ground/instant) coffee, but not decaffeinated coffee, was associated with a reduction in new-onset arrhythmias, including AF, with the greatest benefit seen at 4–5 cups/day.
The findings of this study corroborate the beneficial association of habitual coffee intake reported in recent population studies17,33,34,45,52,65–67 regarding the risk of stroke41 and the reduction in AF incidence52,53, CVD/CHD risk33,34, and all-cause mortality40,42,44–47.
The beneficial effects of coffee on the cardiovascular system might be due to caffeine, which increases endothelial nitric oxide release, downregulates lipogenesis, reduces insulin sensitivity, and has antioxidant properties48,68,69.
However, the risk reduction for incidence of CVD, CHD, heart failure, and all-cause and cardiovascular mortality was seen both in the consumption of caffeinated as well as decaffeinated beverages. These results are similar to previous data on the effect of coffee on type-2 DM risk17, hypertension58,59, all-cause and CV mortality reduction49–51.
This finding suggests the importance of the non-caffeinated constituents of coffee, which are likely responsible for the beneficial effects of coffee consumption on CVD and longevity. Interestingly, caffeinated coffee has been associated with a reduction in arrhythmias through unknown mechanisms. Further research is needed to elucidate the protective mechanisms of coffee and the impact of the non-caffeinated constituents of coffee on clinical outcomes.
Study limitations
The main study limitation is that coffee consumption was self-reported by the study participants, which carries a potential risk of reporting bias. Furthermore, participants could only select one type of coffee in the questionnaire, although some participants might have consumed more than one subtype of coffee over time. Additionally, participants’ coffee consumption was assumed to not change from baseline to follow-up. However, the type of coffee and coffee consumption might have varied throughout the day and over time.
The system used to assess outcomes and track participants’ health (ICD-10 codes) is susceptible to measurement and reporting errors. Furthermore, certain arrhythmias, particularly atrial/ventricular ectopy, may have gone undetected owing to the absence of routine monitoring.
Participants’ alcohol and tea intake were considered in the analysis, but other unaccounted confounding factors, including dietary factors, may have impacted health outcomes. Finally, because the UK Biobank population is predominantly Caucasian, the study conclusions may not be entirely applicable to populations of other ethnicities.
Lessons learned
The newly published findings indicate that mild-to-moderate consumption of all types of coffee is linked to improved CV outcomes and lower risk of cardiovascular disease and death, with caffeinated coffee significantly reducing the risk of arrhythmias, including AF. Daily coffee intake should not be discouraged by physicians but rather considered part of a healthy lifestyle, even in the presence or newly development of cardiovascular disease, unless there are specific coffee-related personal symptoms.
Whether coffee will be prescribed in the future for the prevention CVD and improvement of cardiovascular health depends on further evaluation of the physiological mechanisms and elucidation of the specific protective effects of coffee consumption.
References
- 1.Ferré S. Mechanisms of the psychostimulant effects of caffeine: implications for substance use disorders. Psychopharmacology (Berl) 2016;233(10):1963–1979. doi: 10.1007/s00213-016-4212-2. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Setiawan VW, Wilkens LR, Lu SC, Hernandez BY, le Marchand L, Henderson BE. Association of coffee intake with reduced incidence of liver cancer and death from chronic liver disease in the US multiethnic cohort. Gastroenterology. 2015;148(1):118–125. doi: 10.1053/j.gastro.2014.10.005. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Oh J-K, Sandin S, Ström P, Löf M, Adami H-O, Weiderpass E. Prospective study of breast cancer in relation to coffee, tea and caffeine in Sweden. Int J Cancer. 2015;137(8):1979–1989. doi: 10.1002/ijc.29569. doi: [DOI] [PubMed] [Google Scholar]
- 4.Bravi F, Tavani A, Bosetti C, Boffetta P, la Vecchia C. Coffee and the risk of hepatocellular carcinoma and chronic liver disease: a systematic review and meta-analysis of prospective studies. European Journal of Cancer Prevention. 2017;26(5):368–377. doi: 10.1097/CEJ.0000000000000252. doi: [DOI] [PubMed] [Google Scholar]
- 5.Gökcen BB, Şanlier N. Coffee consumption and disease correlations. Crit Rev Food Sci Nutr. 2019;59(2):336–348. doi: 10.1080/10408398.2017.1369391. doi: [DOI] [PubMed] [Google Scholar]
- 6.Lee A, et al. Coffee intake and obesity: A meta-analysis. Nutrients. 2019;11(6) doi: 10.3390/nu11061274. doi: MDPI AG. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Kim HJ, et al. Caffeine inhibits adipogenesis through modulation of mitotic clonal expansion and the AKT/GSK3 pathway in 3T3-L1 adipocytes. BMB Rep. 2016;49(2):111–115. doi: 10.5483/BMBRep.2016.49.2.128. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Shang F, Li X, Jiang X. Coffee consumption and risk of the metabolic syndrome: a meta-analysis. Diabetes Metab. 2016;42(2):80–87. doi: 10.1016/j.diabet.2015.09.001. doi: [DOI] [PubMed] [Google Scholar]
- 9.Kolb H, Martin S, Kempf K. Coffee and lower risk of type 2 diabetes: arguments for a causal relationship. Nutrients. 2021;13(4) doi: 10.3390/nu13041144. doi: MDPI AG. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Huxley R. Coffee, Decaffeinated Coffee, and Tea consumption in relation to incident type 2 diabetes mellitus. Arch Intern Med. 2009;169(22):2053. doi: 10.1001/archinternmed.2009.439. doi: [DOI] [PubMed] [Google Scholar]
- 11.Jin T, et al. Interactions of habitual coffee consumption by genetic polymorphisms with the risk of prediabetes and type 2 diabetes combined. Nutrients. 2020;12(8):2228. doi: 10.3390/nu12082228. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Salazar-Martinez E, et al. Coffee consumption and risk for type 2 diabetes mellitus. Ann Intern Med. 2004;140(1):1. doi: 10.7326/0003-4819-140-1-200401060-00005. doi: [DOI] [PubMed] [Google Scholar]
- 13.Sartorelli DS, et al. Differential effects of coffee on the risk of type 2 diabetes according to meal consumption in a French cohort of women: the E3N/EPIC cohort study. Am J Clin Nutr. 2010;91(4):1002–1012. doi: 10.3945/ajcn.2009.28741. doi: [DOI] [PubMed] [Google Scholar]
- 14.Ghavami HS, Khoshtinat M, Sadeghi-Farah S, Kalimani AB, Ferrie S, Faraji H. The relationship of coffee consumption and CVD risk factors in elderly patients with T2DM, BMC. Cardiovasc Disord. 2021;21(1):241. doi: 10.1186/s12872-021-02058-7. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Moura-Nunes N, Perrone D, Farah A, Donangelo CM. The increase in human plasma antioxidant capacity after acute coffee intake is not associated with endogenous non-enzymatic antioxidant components. Int J Food Sci Nutr. 2009;60(sup6):173–181. doi: 10.1080/09637480903158893. doi: [DOI] [PubMed] [Google Scholar]
- 16.Paiva C, Beserra B, Reis C, Dorea J, da Costa T, Amato A. Consumption of coffee or caffeine and serum concentration of inflammatory markers: a systematic review. Crit Rev Food Sci Nutr. 2019;59(4):652–663. doi: 10.1080/10408398.2017.1386159. doi: [DOI] [PubMed] [Google Scholar]
- 17.Ding M, Bhupathiraju SN, Chen M, van Dam RM, Hu FB. Caffeinated and decaffeinated coffee consumption and risk of type 2 diabetes: a systematic review and a dose-response meta-analysis. Diabetes Care. 2014;37(2):569–586. doi: 10.2337/dc13-1203. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Barrea L, et al. Nutritional status and follicular-derived thyroid cancer: an update. Crit Rev Food Sci Nutr. 2021;61(1):25–59. doi: 10.1080/10408398.2020.1714542. doi: [DOI] [PubMed] [Google Scholar]
- 19.Barrea L, et al. Critical Reviews in Food Science and Nutrition. Taylor and Francis Ltd; 2021. Coffee consumption, health benefits and side effects: a narrative review and update for dietitians and nutritionists. doi: [DOI] [PubMed] [Google Scholar]
- 20.Ross GW. Association of coffee and caffeine intake with the risk of parkinson disease. JAMA. 2000;283(20):2674. doi: 10.1001/jama.283.20.2674. doi: [DOI] [PubMed] [Google Scholar]
- 21.Hong CT, Chan L, Bai C-H. The effect of caffeine on the risk and progression of parkinson’s disease: a meta-analysis. Nutrients. 2020;12(6):1860. doi: 10.3390/nu12061860. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Ren X, Chen J-F. Caffeine and Parkinson’s disease: multiple benefits and emerging mechanisms. Front Neurosci. 2020;14 doi: 10.3389/fnins.2020.602697. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Eskelinen MH, Kivipelto M. Caffeine as a protective factor in dementia and Alzheimer’s disease. Journal of Alzheimer’S Disease. 2010;20(s1):S167–S174. doi: 10.3233/JAD-2010-1404. doi: [DOI] [PubMed] [Google Scholar]
- 24.Gardener SL, et al. Higher coffee consumption is associated with slower cognitive decline and less cerebral Aβ-amyloid accumulation over 126 months: data from the Australian imaging, biomarkers, and lifestyle study. Front Aging Neurosci. 2021;13 doi: 10.3389/fnagi.2021.744872. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Hu EA, Selvin E, Grams ME, Steffen LM, Coresh J, Rebholz CM. Coffee consumption and incident kidney disease: results from the atherosclerosis risk in communities (ARIC) study. American Journal of Kidney Diseases. 2018;72(2):214–222. doi: 10.1053/j.ajkd.2018.01.030. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Tommerdahl KL, et al. Coffee consumption may mitigate the risk for acute kidney injury: results from the atherosclerosis risk in communities study. Kidney Int Rep. 2022;7(7):1665–1672. doi: 10.1016/j.ekir.2022.04.091. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Iglesias-Aguirre CE, et al. Main drivers of (poly)phenol effects on human health: metabolite production and/or gut microbiota-associated metabotypes? Food Funct. 2021;12(21):10324–10355. doi: 10.1039/D1FO02033A. doi: [DOI] [PubMed] [Google Scholar]
- 28.Hughes JR, Amori G, Hatsukami DK. A survey of physician advice about caffeine. J Subst Abuse. 1988;1(1):67–70. doi: 10.1016/S0899-3289(88)80009-9. doi: [DOI] [PubMed] [Google Scholar]
- 29.van Dam RM, Hu FB. Caffeine consumption and cardiovascular health. Nat Rev Cardiol. 2022;19(7):429–430. doi: 10.1038/s41569-022-00719-4. doi: [DOI] [PubMed] [Google Scholar]
- 30.van Dam RM, Hu FB, Willett WC. Coffee, caffeine, and health. New England Journal of Medicine. 2020;383(4):369–378. doi: 10.1056/NEJMRA1816604/SUPPL_FILE/NEJMRA1816604_DISCLOSURES.PDF. doi: [DOI] [PubMed] [Google Scholar]
- 31.O’Keefe JH, Di Nicolantonio JJ, Lavie CJ. Coffee for cardioprotection and longevity. Prog Cardiovasc Dis. 2018;61(1):38–42. doi: 10.1016/j.pcad.2018.02.002. doi: [DOI] [PubMed] [Google Scholar]
- 32.Voskoboinik A, Koh Y, Kistler PM. Cardiovascular effects of caffeinated beverages. Trends Cardiovasc Med. 2019;29(6):345–350. doi: 10.1016/j.tcm.2018.09.019. doi: [DOI] [PubMed] [Google Scholar]
- 33.Ding M, Bhupathiraju SN, Satija A, van Dam RM, Hu FB. Long-term coffee consumption and risk of cardiovascular disease. Circulation. 2014;129(6):643–659. doi: 10.1161/CIRCULATIONAHA.113.005925. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Mostofsky E, Rice MS, Levitan EB, Mittleman MA. Habitual coffee consumption and risk of heart failure. Circ Heart Fail. 2012;5(4):401–405. doi: 10.1161/CIRCHEARTFAILURE.112.967299. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Kim E, Hoffmann TJ, Nah G, Vittinghoff E, Delling F, Marcus GM. Coffee consumption and incident tachyarrhythmias reported behavior, mendelian randomization, and their interactions. JAMA Intern Med. 2021;181(9):1185–1193. doi: 10.1001/jamainternmed.2021.3616. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Simon J, et al. Association of daily coffee consumption with cardiovascular health - results from the UK Biobank. 2021. (Accessed 14 October 2022) [Online]. Available at https://qmro.qmul.ac.uk/xmlui/handle/123456789/75498. [Google Scholar]
- 37.Stevens LM, Linstead E, Hall JL, Kao DP. Association between coffee intake and incident heart failure risk: a machine learning analysis of the FHS, the ARIC study, and the CHS. Circ Heart Fail. 2021;14(2):E006799. doi: 10.1161/CIRCHEARTFAILURE.119.006799. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Ribeiro EM, Alves M, Costa J, Ferreira JJ, Pinto FJ, Caldeira D. Safety of coffee consumption after myocardial infarction: a systematic review and meta-analysis. Nutrition, Metabolism and Cardiovascular Diseases. 2020;30(12):2146–2158. doi: 10.1016/j.numecd.2020.07.016. doi: [DOI] [PubMed] [Google Scholar]
- 39.Svatun ÅL, Løchen M-L, Thelle DS, Wilsgaard T. Association between espresso coffee and serum total cholesterol: the Tromsø Study 2015–2016. Open Heart. 2022;9(1):e001946. doi: 10.1136/openhrt-2021-001946. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Simon J, et al. Light to moderate coffee consumption is associated with lower risk of death: a UK Biobank study. Eur J Prev Cardiol. 2022;29(6):982–991. doi: 10.1093/eurjpc/zwac008. doi: [DOI] [PubMed] [Google Scholar]
- 41.D’Elia L, Cairella G, Garbagnati F, Scalfi L, Strazzullo P. Moderate coffee consumption is associated with lower risk of stroke: meta-analysis of prospective studies. J Hypertens. 2012;30:e107. [Google Scholar]
- 42.Crippa A, Discacciati A, Larsson SC, Wolk A, Orsini N. Coffee consumption and mortality from all causes, cardiovascular disease, and cancer: a dose-response meta-analysis. Am J Epidemiol. 2014;180(8):763–775. doi: 10.1093/aje/kwu194. doi: [DOI] [PubMed] [Google Scholar]
- 43.Rodríguez-Artalejo F, López-García E. Coffee consumption and cardiovascular disease: a condensed review of epidemiological evidence and mechanisms. J Agric Food Chem. 2018;66(21):5257–5263. doi: 10.1021/acs.jafc.7b04506. doi: [DOI] [PubMed] [Google Scholar]
- 44.Malerba S, et al. A meta-analysis of prospective studies of coffee consumption and mortality for all causes, cancers and cardiovascular diseases. Eur J Epidemiol. 2013;28(7):527–539. doi: 10.1007/s10654-013-9834-7. doi: [DOI] [PubMed] [Google Scholar]
- 45.Kim Y, Je Y, Giovannucci E. Coffee consumption and all-cause and cause-specific mortality: a meta-analysis by potential modifiers. Eur J Epidemiol. 2019;34(8):731–752. doi: 10.1007/s10654-019-00524-3. doi: [DOI] [PubMed] [Google Scholar]
- 46.Freedman ND, Park Y, Abnet CC, Hollenbeck AR, Sinha R. Association of coffee drinking with total and cause-specific mortality. New England Journal of Medicine. 2012;366(20):1891–1904. doi: 10.1056/NEJMoa1112010. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Loftfield E, Cornelis MC, Caporaso N, Yu K, Sinha R, Freedman N. Association of coffee drinking with mortality by genetic variation in caffeine metabolism. JAMA Intern Med. 2018;178(8):1086. doi: 10.1001/jamainternmed.2018.2425. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Chieng D, Kistler PM. Coffee and tea on cardiovascular disease (CVD) prevention. Trends Cardiovasc Med. 2022;32(7):399–405. doi: 10.1016/j.tcm.2021.08.004. doi: [DOI] [PubMed] [Google Scholar]
- 49.Lopez-Garcia E. The relationship of coffee consumption with mortality. Ann Intern Med. 2008;148(12):904. doi: 10.7326/0003-4819-148-12-200806170-00003. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Freedman ND, Park Y, Abnet CC, Hollenbeck AR, Sinha R. Association of coffee drinking with total and cause-specific mortality. New England Journal of Medicine. 2012;366(20):1891–1904. doi: 10.1056/NEJMoa1112010. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Lopez-Garcia E. The relationship of coffee consumption with mortality. Ann Intern Med. 2008;148(12):904. doi: 10.7326/0003-4819-148-12-200806170-00003. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Cheng M, Hu Z, Lu X, Huang J, Gu D. Caffeine intake and atrial fibrillation incidence: dose response meta-analysis of prospective cohort studies. Canadian Journal of Cardiology. 2014;30(4):448–454. doi: 10.1016/j.cjca.2013.12.026. doi: [DOI] [PubMed] [Google Scholar]
- 53.Kim E, Hoffmann TJ, Nah G, Vittinghoff E, Delling F, Marcus GM. Coffee consumption and incident tachyarrhythmias. JAMA Intern Med. 2021;181(9):1185. doi: 10.1001/jamainternmed.2021.3616. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Cai L, Ma D, Zhang Y, Liu Z, Wang P. The effect of coffee consumption on serum lipids: a meta-analysis of randomized controlled trials. Eur J Clin Nutr. 2012;66(8):872–877. doi: 10.1038/ejcn.2012.68. doi: [DOI] [PubMed] [Google Scholar]
- 55.Xie C, Cui L, Zhu J, Wang K, Sun N, Sun C. Coffee consumption and risk of hypertension: a systematic review and dose–response meta-analysis of cohort studies. J Hum Hypertens. 2018;32(2):83–93. doi: 10.1038/s41371-017-0007-0. doi: [DOI] [PubMed] [Google Scholar]
- 56.D’Elia L, la Fata E, Galletti F, Scalfi L, Strazzullo P. Coffee consumption and risk of hypertension: a dose–response meta-analysis of prospective studies. Eur J Nutr. 2019;58(1):271–280. doi: 10.1007/s00394-017-1591-z. doi: [DOI] [PubMed] [Google Scholar]
- 57.Miranda AM, Goulart AC, Benseñor IM, Lotufo PA, Marchioni DM. Coffee consumption and risk of hypertension: a prospective analysis in the cohort study. Clinical Nutrition. 2021;40(2):542–549. doi: 10.1016/j.clnu.2020.05.052. doi: [DOI] [PubMed] [Google Scholar]
- 58.Rhee JJ, et al. Coffee and caffeine consumption and the risk of hypertension in postmenopausal women. Am J Clin Nutr. 2016;103(1):210–217. doi: 10.3945/ajcn.115.120147. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.O’Keefe JH, Bhatti SK, Patil HR, Di Nicolantonio JJ, Lucan SC, Lavie CJ. Effects of habitual coffee consumption on cardiometabolic disease, cardiovascular health, and all-cause mortality. J Am Coll Cardiol. 2013;62(12):1043–1051. doi: 10.1016/j.jacc.2013.06.035. doi: [DOI] [PubMed] [Google Scholar]
- 60.Surma S, Oparil S. Coffee and arterial hypertension. Curr Hypertens Rep. 2021;23(7):38. doi: 10.1007/s11906-021-01156-3. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Borghi C, et al. Nutraceuticals and blood pressure control: a European Society of Hypertension position document. J Hypertens. 2020;38(5):799–812. doi: 10.1097/HJH.0000000000002353. doi: [DOI] [PubMed] [Google Scholar]
- 62.Visseren FLJ, et al. ESC Guidelines on cardiovascular disease prevention in clinical practice. Eur Heart J. 2021;42(34):3227–3337. doi: 10.1093/eurheartj/ehab484. doi: [DOI] [PubMed] [Google Scholar]
- 63.UK Biobank - UK Biobank. https://www.ukbiobank.ac.uk/ (Accessed 14 October 2022) [Google Scholar]
- 64.Chieng D, et al. The impact of coffee subtypes on incident cardiovascular disease, arrhythmias, and mortality: long-term outcomes from the UK Biobank. Eur J Prev Cardiol. 2022 doi: 10.1093/eurjpc/zwac189. doi: [DOI] [PubMed] [Google Scholar]
- 65.Wu J, et al. Coffee consumption and risk of coronary heart diseases: a meta-analysis of 21 prospective cohort studies. Int J Cardiol. 2009;137(3):216–225. doi: 10.1016/j.ijcard.2008.06.051. doi: [DOI] [PubMed] [Google Scholar]
- 66.Larsson SC, Orsini N. Coffee consumption and risk of stroke: a dose-response meta-analysis of prospective studies. Am J Epidemiol. 2011;174(9):993–1001. doi: 10.1093/aje/kwr226. doi: [DOI] [PubMed] [Google Scholar]
- 67.Cicco S. Diet as a cornerstone of cardiovascular prevention: the key role of coffee consumption. Eur J Prev Cardiol. 2022;29(6):979–981. doi: 10.1093/eurjpc/zwac030. doi: [DOI] [PubMed] [Google Scholar]
- 68.Konstantinidi M, Koutelidakis AE. Functional foods and bioactive compounds: a review of its possible role on weight management and obesity’s metabolic consequences. Medicines. 2019;6(3):94. doi: 10.3390/medicines6030094. doi: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Keijzers GB, de Galan BE, Tack CJ, Smits P. Caffeine can decrease insulin sensitivity in humans. Diabetes Care. 2002;25(2):364–369. doi: 10.2337/diacare.25.2.364. doi: [DOI] [PubMed] [Google Scholar]




