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. 2026 Feb 26;15(1):15. doi: 10.1007/s13668-025-00722-4

From Husks and Seeds to Health: an Inevitable Outcome Rather than a Fluke

Nevin Sanlier 1,, Ebru Ozler 1
PMCID: PMC12935724  PMID: 41741921

Abstract

Purpose of Review

This review was conducted to examine the promising health benefits of psyllium, its therapeutic potential in relation to various chronic diseases, its mechanisms, and its possible side effects or toxicity; to explore its applications in food systems; to identify the positive and negative effects of its consumption; and to provide perspectives for future research and development efforts for psyllium.

Recent Findings

Psyllium, also known as ispaghula, is a dietary fiber obtained from the shells of Plantago ovata seeds. The most abundant monosaccharides in its composition are xylose and arabinose. Psyllium is a natural alternative to the use of food additives such as gum and hydrocolloid to increase the fiber content in fortified foods. Psyllium may have therapeutic effects on various diseases. In recent years, its potential in the management of conditions such as hypertension, diabetes, and liver disease has been emphasized and multifaceted therapeutic applications have been introduced. Psyllium may help to regulate blood glucose, blood pressure and cholesterol levels. It may also increase feelings of fullness and reduce food intake. Furthermore, psyllium may promote bowel regularity and improve the composition of gut microbiota. Psyllium has been reported to exhibit antioxidant and antimicrobial properties, as well as reducing inflammatory mediators such as TNF-α and nitric oxide. Furthermore, psyllium has been associated with lower creatinine and uric acid levels, as well as a reduced risk of carcinogenesis.

Summary

Studies in the literature support the therapeutic effects of psyllium. However, longer-term clinical trials are needed to determine the effective dose and duration of use. Innovative product development studies should be conducted to enhance the functional benefits of psyllium in the food industry.

Supplementary Information

The online version contains supplementary material available at 10.1007/s13668-025-00722-4.

Keywords: Psyllium, Dietary fiber, Obesity, Diabetes, Constipation

Introduction

The shells or husks of Plantago ovata seeds, also known as psyllium, ispaghula, or isabgol, are attracting attention in recent years due to their health benefits [1, 2]. This plant is native to the Mediterranean region and also frequently grown in India, Iran, and Pakistan [3]. One of the main nutritional properties of psyllium husk is its high fiber content [4, 5].

Psyllium is used as a hydrocolloid in the food industry thanks to its water absorption capabilities [6]. It is used to preserve moisture and extend the shelf life of bakery products [7], as a fat substitute in milk and dairy products [8], as a binder in meat and meat products, to increase the fiber contents of breakfast cereals, and to provide a feeling of satiety in meal replacement shakes and nutritional bars [1].

Psyllium may have beneficial impacts on many health problems. In particular, it may be effective in the management of conditions such as hypertension, diabetes, and liver disease, alongside other potential health benefits, such as its ability to support gastrointestinal health, cardiovascular risk reduction, and metabolic control. It has a therapeutic effect against diabetes by regulating blood glucose, against obesity by reducing energy intake, against cardiovascular diseases by reducing blood pressure and cholesterol levels, and against gastrointestinal system diseases by regulating defecation [9, 10].

In recent years, there has been an increase in the number of studies in the literature highlighting the health effects of psyllium. New publications support the beneficial effects of psyllium on lipid metabolism, blood pressure, and glycemic control. Studies also emphasize its various metabolic and hepatoprotective effects, including the modulation of bile acid metabolism and the activation of pathways associated with the farnesoid X receptor. Therefore, updated reviews are needed to integrate these new findings and comprehensively address the health effects of psyllium.

This review study was conducted to examine the clinical effects and modes of action of psyllium in its relationships with many diseases, as well as its positive and negative effects on health as revealed by in vivo, in vitro, animal, and human studies. Furthermore, suggestions are made for future research.

Methods

This article is a narrative review that examines the effects of psyllium on health. A comprehensive literature review was conducted using the PubMed, Web of Science, Scopus, and Google Scholar databases. Articles published in English between January 2018 and January 2025 were evaluated. The main search terms included combinations of the following keywords: “psyllium,” “psyllium husk,” “Plantago ovata,” “dietary fiber,” “obesity,” “diabetes,” “cardiovascular diseases,” “diarrhea,” “constipation,” “ulcer,” “non-alcoholic fatty liver disease,” “gastritis,” “gastroesophageal reflux,” “irritable bowel syndrome,” “inflammatory bowel diseases,” “cancer,” “kidney diseases,” and “burn.” English-language research articles, systematic reviews, meta-analyses, review articles, clinical human and animal studies, and cell-based research studies were subsequently analyzed. The obtained English-language documents were classified as original research, reviews, meta-analyses, or systematic reviews after being obtained in full-text format. Studies that did not include psyllium were excluded. Since this study is not a systematic review, a formal PRISMA-based screening process was not conducted. The abstracts and full texts of relevant articles in the literature were examined. All analyzed studies were accessed using the databases and keywords specified here. For the years 2017–2025, a total of 143 sources were examined and 15 highlighted articles are listed in Table 2. Studies conducted before 2017 were not included in the present review, as their findings have already been discussed in previously published reviews. However, several key references were cited where necessary to provide historical context.

Table 2.

Studies on the effects of psyllium on health

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ALT Alanine aminotransferase, apoB Apolipoprotein B, BMI Body mass index, BMF Bowel movement frequency, BSS Bristol stool scale score,CCI4 Carbon tetrachloride, FBS fasting blood sugar, FPG Fasting plasma glucose, GF Germ-free, HbA1c Hemoglobin A1c, HeLa Human cervical cancer cell line, HOMA-IR Homeostasis model assessment of insulin resistance, Huh7 Human hepatoma cell line, LDL-C Low-density lipoprotein cholesterol, MASLD Obesity metabolic dysfunction-associated steatotic liver disease, mRNA Messenger RNA,PI3K/Akt Phosphatidylinositol 3-kinase/Akt kinase pathway, PPBG Postprandial blood glucose, RCT Randomized controlled trial, SBP Systolic blood pressure, SPF Specific pathogen free, T2DM Type-2 diabetes mellitus, TNF-α Tumor necrosis factor alpha, URAT1 Uric acid transporter 1, XGB Cholecystectomy

Nutrient Composition of Psyllium

Psyllium husk comprises 84.98% carbohydrates, 6.83% protein, and 4.07% ash [1], while psyllium seed flour contains 78.88% carbohydrates, 13.3% protein, 0.38% fat, and 5.0% ash [11]. Thus, psyllium husk has lower protein and fat contents than psyllium seeds, while its levels of carbohydrates and dietary fiber are higher [12]. The nutrient composition of its seeds consists largely of carbohydrates [9] and the ratio of insoluble fiber to soluble fiber is 30/70 [13]. The polysaccharide fraction of psyllium husk is an important functional component [4, 5]. The polysaccharide that forms mucilage is a heteroxylan consisting of (1→4)-linked β-D-xylose with C-2 or C-3 side chains and containing different proportions of xylose and arabinose [4]. In addition, its potassium, phosphorus, and sodium contents are higher compared to other minerals [9]. Psyllium seeds and husks also contain bioactive components such as flavonoids and polyphenols [13]. Table 1 provides detailed information about the nutritional composition of psyllium husk [1416].

Table 1.

Nutritional composition of psyllium husk and psyllium seed [1416]

Nutritional components Psyllium husk Psyllium seed
Moisture (%) 4.9 1.91
Ash (%) 4.1 1.0
Crude fat (%) 1.2 3.75
Crude protein (%) 3.9 17.70
Nitrogen free extract (%) 78.2 -
Total dietary fibre (%) 77.24 24.77
Arabinose (%) 46.8 -
Xylose (%) 24.1 -
Glucose (%) 11.2 1.89
Galactose (%) 2.09 -
Mannose (%) 4.24 -
Rhamnose (%) 2.39 -
Calcium (mg/100 g) 104 -
Potassium (mg/100 g) 805 687
Sodium (mg/100 g) 62.3 -
Iron (mg/100 g) 9.3 6.75
Copper (mg/100 g) 0.36 2.39
Manganese (mg/100 g) 1.15 1.06
Zinc (mg/100 g) ND 3.15

ND: not detected

Bioavailability and Mechanisms of Action of Psyllium

Since psyllium is not fermented in the intestine, its structure and its functions are not impaired in the gastrointestinal system. This increases the bioavailability and effectiveness of psyllium for various health applications. Psyllium consists of 65% insoluble and 35% soluble polysaccharides, and the hemicellulose present in psyllium contributes to its gelling and water retention capacities [17]. When psyllium is diluted, it forms a viscous gel that slows nutrient absorption, increases chyme viscosity, and increases the feeling of satiety [18]. Therefore, psyllium may support intestinal health and may have positive effects on health through various mechanisms of action, potentially reducing inflammation, helping to regulate the intestinal microbiota and its motility, and exerting anti-inflammatory effects in conditions such as irritable bowel syndrome (IBS) and colitis. Psyllium may contribute to the growth of beneficial bacteria, which may positively influence the composition of the intestinal microbiota [19]. In an animal study conducted with rats, psyllium was found to have antioxidant and anti-inflammatory effects [20]. In another animal study, psyllium was reported to significantly reduce colon damage and inflammation in mice [21]. In a food formulation study, the addition of psyllium to rye bread was found to increase the antioxidant activity of the bread by two-fold [5]. Psyllium may support intestinal health and may increase antimicrobial protein expression by neutralizing pathogenic microorganisms [22]. In an in vitro study, a nanoemulsion formed by adding Cuminum cyminum essential oil to Plantago psyllium seed gum inhibited the growth of Staphylococcus aureus [23]. In murine models, psyllium was found to upregulate antimicrobial proteins such as small proline-rich protein 2 A (SPRR2A) and resistin-like beta (RELMβ) in the small intestines of mice [22]. In an experimental study using in vitro assays and a rat wound model, psyllium and Carbopol-based frankincense essential oil were observed to suppress microbial growth and increase microbial death [24]. In an in vitro experimental study, psyllium-based polymeric antimicrobial agents showed antibacterial activity against gram-positive bacteria such as Staphylococcus aureus and Bacillus anthracis [25]. Psyllium may help improve constipation and may help normalize stool consistency via its capabilities for intestinal regulation [19]. It forms a viscous gel that binds bile acids, slows the absorption of cholesterol and glucose, creates a feeling of satiety, and increases the release of glucagon-like peptide-1(GLP-1). However, to fully utilize these significant health benefits, personalized approaches are needed while using psyllium as a dietary supplement due to individual differences in gut microbiota compositions and diets [22].

When examining the mechanism of action of psyllium, it is observed that the findings are generally based on preclinical evidence, including animal and in vitro studies. These studies provide valuable mechanistic hypotheses; however, the findings need to be confirmed in human clinical trials.

Use of Psyllium in Food Products

Awareness of healthy nutrition is steadily increasing worldwide and a wide variety of functional foods are being produced for this purpose. Considering its potential health effects, psyllium may be used in the food sector in the production of items such as gluten-free breads, cakes, biscuits, pasta, noodles, pizza, and ice cream [13]. The use of psyllium in food products serves two main purposes. First, it may constitute an alternative to the use of gum and hydrocolloid as food additives, and second, it may enrich the nutritional content of food products. Psyllium has high water absorption capacity; in food production, it may contribute to product quality by reducing the water and fat contents of foods [3].

Psyllium may increase dough viscosity and gas retention during baking; may help prevent the loss of softness, moisture, and elasticity during the storage of baked goods; may improve volume; and may increase water-binding capabilities. For these reasons, it is commonly used in a wide range of bakery products. It may improve the texture and structure of gluten-free bread and may extend its shelf life. In addition, it may enrich fiber contents and may reduce the glycemic index [7]. Researchers have found that adding psyllium to gluten-free bread improves the color and textural properties of the bread, increases the gas retention capacity of the psyllium, and exerts a gluten-like effect; thus, this approach can be used in the production of bread with low glycemic index values [26]. In another study, it was reported that adding psyllium to whole wheat bread reduces hardness, increases flexibility, and increases acceptability and nutritional quality [27]. Psyllium may also be added to breakfast cereals due to its fiber contents. It may be used in meal replacement shakes because of its abilities to increase satiety, decrease appetite, and regulate body weight control. It may be used in meat products such as sausages and meatballs to help retain moisture, prevent cooking loss, maintain the texture of the product, and increase the binding capabilities [1]. It was reported that adding water and Plantago ovata to minced chicken increased production efficiency and reduced the hardness of the product [28]. In a study in which psyllium was added to phosphate-free meat at different rates, 1.5% psyllium husk powder was found to increase product quality [29]. Psyllium may be used as a thickener in milk to improve the consistency and texture of dairy products such as yogurt and ice cream [1]. The addition of Plantago psyllium mucilage to Doogh, a yogurt-based fermented product, increased viscosity, reduced phase separation, and improved the stability of the product [30]. Furthermore, adding psyllium as a fat replacer in yogurt production provided appropriate viscosity, created less syneresis, and increased the water retention capacity [8].

However, the interactions of psyllium with other macronutrients and micronutrients in foods are not fully understood. More research is needed to reduce undesirable effects in foods to which psyllium is added, such as gummy textures, and to increase psyllium’s positive effects on foods [3]. The applications of psyllium in food products are shown in Fig. 1.

Fig. 1.

Fig. 1

Use of psyllium in food products [1, 7, 8, 27, 28]

Therapeutic Effects of Psyllium

In addition to its use as a laxative to support intestinal health, psyllium has various other therapeutic applications. In recent years, it has been used in the treatment of many diseases. Psyllium may help reduce cholesterol levels and absorption by binding bile acids in the intestine [31, 32]. It may have beneficial effects for diabetic patients by providing glycemic control as a result of its soluble fiber contents. The antihypertensive properties of psyllium may positively affect cardiovascular health [13]. Psyllium may help relieve diarrhea symptoms and may exert therapeutic effects in cases of gastrointestinal disorders. Furthermore, it may increase the therapeutic potential of various drugs, including antibiotics and anticancer drugs, and may be used to form hydrogels for sustained drug delivery [33, 34]. However, alongside these positive effects in a variety of therapeutic areas, it should be taken into account that dietary fibers may cause different side effects for different individuals.

Effects of Psyllium on Health

Psyllium has positive effects on a wide variety of health problems as it creates feelings of satiety, lowers cholesterol levels, and possesses prebiotic properties. Constipation, diarrhea, cancer, diabetes, obesity, inflammatory bowel diseases (IBD), and hypercholesterolemia are among the health problems that psyllium may positively affect [9].

Obesity

It is predicted that approximately 20% of the female population and 14% of the male population will be obese worldwide by 2030 [35]. As a possible solution, dietary fiber is negatively associated with body weight and body mass index (BMI). Psyllium may play important roles in body weight management and the treatment of obesity-related diseases. Its gel-forming properties may support intestinal health and metabolic functions, making it a suitable dietary supplement for overweight and obese individuals [18]. Psyllium may affect body composition through mechanisms such as intestinal hormones like cholecystokinin, satiety, and gastric emptying [36]. It has been reported that psyllium may alleviate obesity-related inflammation through mechanisms independent of fermentation and intestinal microbiota interactions [37]. However, debates regarding the effect of psyllium on obesity are still ongoing [36].

A meta-analysis study found that psyllium supplementation at an average dose of 10.8 g/day before meals led to reductions in body weight (2.1 kg), BMI (0.8 kg/m2), and waist circumference (2.2 cm) in overweight and obese participants [18]. Another meta-analysis study concluded that there was moderate evidence that psyllium provided a small improvement in body weight loss [38]. Obese adults with genetic polymorphisms including at least one minor allele of the melanocortin 4 receptor (MC4R), fat mass and obesity-associated gene (FTO), leptin receptor (LEPR), and leptin (LEP) polymorphisms were given fiber supplements containing psyllium, glucomannan, and inulin for 180 days and the intervention was shown to achieve significant reductions in body weight, BMI, fat mass, and visceral fat ratio [39]. In another study, psyllium supplementation of 5 g three times daily (15 g/day) for 52 weeks administered to obese and overweight adults was found to have reduced zinc, sodium, folate, and magnesium intake after 3 months, which could be attributed to the satiating effect of dietary fiber and the reduction of food intake, while there was no significant difference in serum micronutrient concentrations [40]. It was also found that psyllium reduced waist circumference and BMI in obese adolescents without any side effects [41]. In adults with central obesity, the combination of psyllium husk pulp and lifestyle changes was found to reduce gastrointestinal system symptoms but did not affect sleep quality [42]. Furthermore, a supplement containing psyllium, glucomannan, inulin, and apple pulp reduced BMI, fat mass, visceral fat, and C-reactive protein levels together with energy restriction in overweight and obese individuals [43]. In a study investigating the effectiveness of an herbal formulation containing a mixture of Plantago psyllium, Portulaca oleracea, and peanut oil in overweight and obese adult individuals for 8 weeks, the product was shown to reduce body weight and suppress appetite [44]. In a single-blind randomized controlled study, patients with BMI values of 20–47 kg/m2 were given cookies containing 10 g of psyllium twice a day for 12 weeks and it was reported that their body weights decreased [45].

Many meta-analyses and clinical studies have reported that psyllium supplementation leads to reductions in BMI and body weight. However, some studies have shown that these effects were not statistically significant or resulted in only minimal changes. These inconsistencies among studies may be attributed to differences in study design, evaluated parameters, individual characteristics of participants, psyllium dose or form, and intervention duration. However, while it shows promise in applications for body weight management, its effects may vary between individuals. It should be considered as one part of broader lifestyle change strategies for obesity management.

Diabetes Mellitus

Diabetes affects 537,000,000 individuals worldwide (10.5%) between the ages of 20 and 79 [46]. Lifestyle changes, nutrition, and exercise are all crucial in the management of diabetes. It is known that dietary fiber reduces the risk of diabetes, and psyllium, a type of dietary fiber, has beneficial effects in controlling blood sugar levels and improving insulin sensitivity in diabetes management. The effects of dietary fiber on glycemic control vary [47].

There are studies in the literature demonstrating that psyllium has beneficial effects on fasting blood glucose [48, 49]. However, consensus has not been reached regarding the psyllium dosage to be used for positive effects in cases of diabetes [47]. Psyllium supplementation may reduce fasting blood sugar, hemoglobin A1c (HbA1c), and homeostasis model assessment of insulin resistance (HOMA-IR) levels, and it does not significantly affect insulin levels [50]. In C57BL/KsJ db/db diabetic mice, psyllium supplementation has been reported to decrease fasting glucose level while increasing insulin levels [51]. It has also been found that psyllium slows glucose absorption and may be beneficial when added to low glycemic index foods such as fortified chapati to reduce postprandial glucose levels [52]. In a meta-analysis study, it was concluded that psyllium fiber reduces HbA1c levels [53]. Another meta-analysis study showed that psyllium supplementation reduced fasting blood sugar and HbA1c levels in diabetic individuals but did not have significant effects on BMI, body weight, or HDL-C levels [47]. In individuals with diabetes, the most effective interventions for fasting blood glucose and HOMA-IR were found to involve the administration of β-glucan and psyllium [49]. It was reported that 16 weeks of psyllium supplementation and lifestyle changes among obese adults reduced HOMA-IR and fasting blood glucose levels [48]. Furthermore, the administration of flaxseed and psyllium (10 g/day) to diabetic individuals for 12 weeks improved glycemia and lipid profiles [54]. Psyllium at 5.1 g/day or 7.7 g/day was not found to have an effect on postprandial glycemia in individuals with cystic fibrosis-associated diabetes [55]. In another study, however, it was reported that vildagliptin-loaded psyllium-alginate nanoparticles exhibited antidiabetic properties [56]. It was also reported that exercise and Plantago psyllium administration improved glucose tolerance in diabetic rats [57].

Metabolic syndrome is a condition characterized by metabolic irregularities such as dyslipidemia, central obesity, hypertension, and insulin resistance [58]. A meta-analysis study on the effectiveness of psyllium against metabolic syndrome reported that it reduced fasting blood glucose and systolic blood pressure while causing a nonsignificant decrease in triglyceride levels and nonsignificant increases in diastolic blood pressure, HDL-C, and waist circumference [59]. It was reported that the administration of an herbal compound (aloe vera leaf gel, 1 g/day psyllium seed, 1.8 g/day black cumin, 300/day mg garlic, 2.5 g/day fenugreek seed, and 500 mg/day milk thorn seed) once daily for 12 weeks in patients with type 2 diabetes and dyslipidemia despite the use of statin-derived drugs reduced triglyceride, total cholesterol, low-density lipoprotein cholesterol (LDL-C), and HbA1c levels but did not affect fasting blood glucose [60]. Obesity and metabolic syndrome cause inflammation in many organ tissues, including the intestines. It has been reported that psyllium reduces intestinal inflammation in obese mice fed high-fat diets [37].

Many meta-analyses and clinical studies have shown that psyllium lowers fasting blood glucose, HOMA-IR, and HbA1c levels. However, some studies have reported limited or non-significant effects on insulin level. These differences among studies may be attributed to variations in psyllium dose and type, duration of intervention, and individual characteristics of participants.

While psyllium shows promise in managing diabetes and its complications, it is important to consider individual dietary needs and possible gastrointestinal effects. Integrating psyllium into a balanced diet, possibly in conjunction with other therapeutic strategies, may optimize its benefits for patients with diabetes. It is often used in conjunction with lifestyle and dietary changes to enhance its therapeutic effects. Further research is needed to examine its long-term effects and interactions with other dietary components.

Cardiovascular Diseases

Cardiovascular diseases are among the leading causes of death worldwide [61]. It is estimated that 35.6 million people will die globally from cardiovascular diseases, 20 million from ischemic heart diseases, and 18.9 million from high systolic blood pressure in 2050 [61, 62]. Dietary fiber exerts protective effects against cardiovascular diseases by lowering total cholesterol and LDL-C [63]. In particular, the seed coats of Plantago ovata may have antioxidant, anti-inflammatory, and blood lipid-lowering effects [64]. It is thought that psyllium can significantly reduce cardiovascular risk factors including blood pressure, cholesterol levels, and blood glucose level [65]. In one study, supplementation with 3.4 g of psyllium per day for eight weeks in men was reported to reduce total cholesterol and LDL-C levels [66]. Psyllium intake has been reported to reduce systolic blood pressure by a mean of 2.24 mmHg with no significant effect on diastolic blood pressure, making it effective in the management of hypertension [67]. It was also shown to reduce total cholesterol by 9.05 mg/dL and LDL-C by 8.55 mg/dL [65]. These changes in lipid profiles suggest that psyllium may serve as an effective dietary intervention for hyperlipidemia, which is an important risk factor for cardiovascular diseases [13]. Psyllium was shown to increase the antioxidant capacity of the blood and reduce oxidative stress markers such as cardiac malondialdehyde [68]. It was also found to regulate inflammatory pathways that support cardiovascular health [13].

According to a meta-analysis study, psyllium achieved a mean reduction of 2.04 mmHg in systolic blood pressure [69], while other meta-analyses found that Plantago ovata consumption reduced LDL-C and triglyceride levels [64] and provided a reduction in LDL-C equivalent to that achieved by doubling the dose of statin while reducing the side effects caused by high-dose intake of statin group drugs [70]. Psyllium husk ethanol extract was shown to reduce total cholesterol, triglyceride, malondialdehyde, and atherogenic index values in hyperlipidemic rats; to increase superoxide dismutase and catalase levels [71]. In another study, male rats were fed a high-cholesterol diet for 8 weeks and 2.5% and 5% psyllium seed powder supplements were administered, and it was reported that the intervention significantly impacted lipid profiles while significantly increasing HDL-C [72]. A review study concluded that psyllium intake could significantly improve blood pressure levels and a dose of 10.5 g/day for 6 months could provide significant reductions in systolic and diastolic blood pressure [13].

Although numerous meta-analyses and clinical studies have reported that psyllium lowers LDL-C and systolic blood pressure levels, some studies have found no significant effects on HDL-C and diastolic blood pressure levels. The inconsistencies observed across studies may be attributed to differences in participants’ individual characteristics, variations in psyllium dose and form, and the duration of the intervention.

Although psyllium appears promising in improving cardiovascular health, individual differences in response to dietary interventions need to be considered. This suggests that psyllium should be considered not as a standalone treatment but as part of a comprehensive lifestyle approach. It would be helpful to investigate the long-term effects of psyllium on cardiovascular health and optimal dosages in more detail in future studies.

Gastrointestinal System Diseases

Psyllium is known to have beneficial effects on gastrointestinal diseases. It may be used as a laxative to relieve constipation, as well as to help manage diarrhea and IBS symptoms, and it may have positive effects on gastrointestinal symptoms due to its high water absorption capacity and resistance to fermentation [73]. However, individual patient responses and possible interactions with other dietary fibers should be taken into account. When psyllium is combined with inulin, it reduces intestinal gas production but does not directly reduce fermentation [74].

Nonalcoholic fatty liver disease (NAFLD) increases in parallel with obesity and causes an increase in the risk of cirrhosis and liver cancer. Nutrition plays a very important role in chronic liver diseases such as NAFLD [75]. It is assumed that dietary fiber reduces the risk of NAFLD through its effects on obesity [76]. In a meta-analysis study, it was stated that 10–16 g/day fiber consumption for 10–12 weeks, particularly including psyllium, inulin, basil (Ocimum basilicum), and oligofructose, reduced BMI, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, HOMA-IR, and fasting insulin providing beneficial effects for NAFLD patients [77]. Another study reported that psyllium reduced hepatic lipogenesis [78]. The effectiveness of psyllium husk and that of weight loss medication were compared in mice fed a high-fat diet. In that study, psyllium husk had a better effect on serum and liver cholesterol and triglyceride levels and provided better results than weight loss drugs in the treatment of NAFLD. In contrast, weight loss drugs had a better effect on body weight loss, and both interventions exerted similar effects on body fat ratio [79]. Psyllium husk mucilage (100 mg/kg) was also found to reduce the harmful effects of carbon tetrachloride (CCl4) in rat liver and TNF-α expression in rats [80]. It was determined that in rats given fiber supplementation (psyllium, cellulose, pectin, and inulin) in addition to a diet enriched with copper nanoparticles, reductions of fat, cholesterol, and triglyceride levels in the liver were achieved together with reduced cyclooxygenase-2 (COX-2), peroxisome proliferator-activated receptor gamma (PPAR-γ), and sterol regulatory element-binding protein 1 (SREBP-1) gene expression and liver inflammation [81]. Psyllium (100 mg/kg) was also found to reduce hepatic inflammation and alcohol absorption in mice given a single high alcohol dose (4 g/kg), and it may have protective properties against liver damage [82].

Dietary modifications can alleviate the symptoms of gastroesophageal reflux disease, and increasing the intake of dietary fiber is among these modifications [83]. A meta-analysis study reported that psyllium can reduce gastroesophageal reflux symptoms [84]. Another study found that 5 g of psyllium supplementation administered to gastroesophageal reflux patients with low fiber intake reduced heartburn and gastroesophageal reflux disease questionnaire (GERD-Q) scores and increased resting lower esophageal sphincter pressure [85]. A similar study concluded that psyllium supplementation reduced esophageal motility from 71.4% to 14.3% [86]. It was also determined that psyllium seed extract (400 mg/kg) reduced ulcer index values and lipid peroxidation in rats, protected the integrity of the gastric mucosa, and increased the levels of antioxidant enzymes such as catalase, glutathione, and superoxide dismutase [87].

Soluble fiber is not recommended for gastroparesis patients as it can exacerbate symptoms such as nausea, abdominal pain, bloating, and vomiting. However, low-viscosity soluble fiber can be tolerated by gastroparesis patients [88]. It was reported that psyllium husk regulates blood glucose in gastroparesis patients and does not have a significant effect on its passage through the gastrointestinal system [89].

Low fiber consumption may be a risk factor for gallstones, and adequate fiber intake may have a protective effect against them [90]. In a study conducted on obese individuals, supplementation with psyllium (15 g/day) alongside a low-energy diet was found to have a similar effect to ursodeoxycholic acid in preventing gallstone formation [91]. In a study conducted on mice, it was reported that psyllium induced the expression of genes regulating bile acid secretion, activated the farnesoid X receptor that suppresses proinflammatory signals, and exerted a protective effect against colitis by altering bile acid metabolism [92]. Another study found that a 1:2 ratio of whey protein/psyllium tripled the binding ability of bile acid compared to psyllium alone [93].

Irritable bowel syndrome (IBS) is a chronic condition accompanied by abdominal pain and disrupted bowel movements [94]. A systematic review reported that psyllium can reduce IBS symptom [95]. It was also found that psyllium reduced the severity of IBS in pediatric IBS patients and may have positive effects on treatment [96]. Psyllium was shown to reduce pain attacks in children with IBS and functional abdominal pain disorder [97]. Another study demonstrated that psyllium reduced the colon gas caused by inulin in individuals with IBS and increased the tolerability of prebiotics in that patient population [74]. Low intake levels of vegetables, fruits, and fiber are among the factors that cause IBD. Dietary fiber has a positive effect on IBD by reducing inflammation and protecting the intestinal epithelial barrier [98]. However, a systematic review reported conflicting results on the effects of psyllium on IBD symptoms [99]. In one study, it was determined that claudin 2, claudin 3, claudin 8, and occludin gene expression levels were higher among mice with dextran sodium sulfate-induced colitis given psyllium compared to a control group, and the authors concluded that psyllium may have protective effects against colitis [100]. In another study investigating the effects of psyllium, cellulose, and inulin on the microbiota in individuals with IBD, it was reported that there were differences between participants in the interactions of psyllium and inulin with the microbiota and that the administered treatment reduced proinflammation [101].

In a meta-analysis study evaluating the effect of adding different dietary fibers to enteral nutrition on diarrhea, the effect of psyllium on diarrhea was found to be unclear [102]. Another study evaluated the effectiveness of a low fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAP) diet or psyllium at 6 g/day for 4 weeks in adults with episodes of fecal incontinence. Both interventions were found to reduce episodes of fecal incontinence in individuals with loose stools [103].

Dietary fiber also may play an effective role in the treatment of chronic constipation [104]. Psyllium may have a positive effect on constipation by increasing bowel movements and stool water, facilitating defecation, and altering the colonic content [105, 106]. In a systematic review, it was stated that psyllium increased stool water content and stool softness in individuals with chronic idiopathic constipation [107]. A meta-analysis study reported that psyllium supplementation at a dose of > 10 g/day for at least 4 weeks was the most effective method for treating constipation [108]. One study concluded that psyllium increased bowel movements and reduced constipation symptoms in individuals with chronic constipation [109]. Similarly, in another study, psyllium was shown to increase stool water in individuals with constipation [105]. Yang et al. [110] reported that psyllium may reduce constipation symptoms. However, it was found that agave fructans and Plantago psyllium did not have an effect on intestinal transit time in individuals with functional constipation [111]. Other researchers demonstrated that psyllium (3.5 g) and lactitol (10 g) supplementation for 4 weeks increased intestinal motility in individuals with constipation, but the difference compared to the placebo group was not significant [112]. In a study conducted by Xu et al. [113] it was found that the administration of psyllium and Ligilactobacillus salivarius Li01 to mice increased the water content of their feces, improved the rate of gastrointestinal transit, and provided protection against constipation. Psyllium may help regulate intestinal function and may be used as a laxative in cases of constipation [32]. Although psyllium has many health benefits, it is necessary to take into account individual dietary requirements and possible side effects; in particular, excessive intake can lead to gastrointestinal symptoms.

Cancer

It is predicted that there will be 35 million new cancer cases worldwide in 2050 [114]. Psyllium may help protect the intestinal structure and may inhibit carcinogenesis by reducing the levels of inflammatory mediators such as TNF-α and NO. It also may increase stool volume, may accelerate intestinal transit, and may reduce the concentration of carcinogens. Psyllium may reduce cell proliferation in the distal colon via butyric acid and may help prevent the transformation of colonic epithelial cells into cancer [115].

Psyllium has been used to develop hydrogels for the sustained delivery of anticancer drugs. Hydrogels offer valuable properties such as mucoadhesion, non-hemolytic structures, and antioxidant activity, indicating that they can be used in the treatment of cancers of the gastrointestinal system [33]. In an animal study, the combination of psyllium husk, guar gum, and wheat bran was found to increase hydrated feces mass and may reduce constipation, indirectly lowering the risk of colorectal cancer [116]. Psyllium capecitabine-loaded core-shell nanoparticles have shown high cytotoxicity against the HCT-15 colon cancer cell line and may exert significant anticancer activities [117]. In a study investigating the effects of psyllium, pectin, inulin, and cellulose fiber on high-fructose diet-induced chronic colitis and colitis-associated colorectal neoplasia in male C57BL/6J mice, it was determined that these dietary fiber sources significantly suppressed the increase in colorectal tumor incidence, number, and size [118]. Furthermore, psyllium, cellulose, and inulin pulp delayed tumor growth and significantly reduced tumor size in C57BL/6 mice with bladder cancer [119]. A bionanogel combined with caffeic acid and IR-820 carrying a nanocomplex comprising psyllium mucilage polysaccharide and bacterial gellan gum was described as a potential new approach for drug delivery in the treatment of epidermoid tumors [120]. It was found that high-fructose diets increased tumor formation in cases of colitis in mice but psyllium supplementation exerted protective effects against tumor formation [121]. Furthermore, the addition of psyllium supplementation was shown to increase the treatment efficacy of the MR-HIFU method used for uterine myoma [122]. Although psyllium thus shows promise in cancer treatment, it is important to consider the broader context of its use. The majority of existing studies on the anticancer effects of psyllium consist of preclinical research conducted in vitro and in animal models. More research is needed to fully understand and optimize the contributions of psyllium in cancer treatment. The efficacy of psyllium in clinical settings needs to be evaluated comprehensively.

Other Diseases

Evidence on the effects of psyllium on kidney disease is quite limited, and the available data are mostly derived from animal models. One previous study reported that psyllium seed husk reduced blood urea nitrogen and serum creatinine levels in the 5/6 nephrectomy rat model, alleviated renal tubular interstitial damage, downregulated indoxyl sulfate, lowered the levels of interleukin-6 (IL-6) and interleukin-1 (IL-1), regulated the intestinal microbiota, and may have therapeutic effects in the treatment of chronic kidney disease [123].

Burns constitute the fourth most common type of injury worldwide. Moist wounds cause microorganisms to multiply, leading to infection [124]. Applied with the aim of reducing the moisture in burn wounds, Plantago ovata mucilage was also found to significantly reduce wound size [125]. The health effects of psyllium are shown in Fig. 2.

Fig. 2.

Fig. 2

Use of psyllium in food products

Meta-analysis, in vivo, in vitro, animal, and human studies conducted to evaluate the health effects of psyllium are summarized in Table 2.

Safe Intake Level and Toxic Effects

The European Food Safety Authority has reported that the amount of psyllium seed husk providing a feeling of satiety and helping to control body weight is 1–3 g/day [138]. Other important aspects of the safety of psyllium supplementation are the purity and degree of processing of the psyllium. The US Food and Drug Administration has stated that psyllium with purity of at least 95% at 10.2 g/day is safe and offers therapeutic effects. The literature suggests that the appropriate dosage for therapeutic effects is 3.4–5 g three times a day before main meals, totaling 10–15 g/day. In cases other than constipation, it is recommended to start at 3.4 g/day and increase the dose every week to reach 10.2 g/day [115]. Researchers report that psyllium supplementation at 10 g does not cause any side effects in individuals with type 2 diabetes [54]. It has also been stated that psyllium husk does not cause side effects in women with chronic constipation [110]. In addition to its beneficial effects on health, some common and, though rare, serious adverse effects of psyllium have also been observed [11]. In a case report, the use of psyllium for the treatment of constipation was reported to cause severe dizziness, wheezing, and loss of consciousness [139]. High doses of psyllium can also lead to increased intestinal gas production and abdominal bloating, which are among the most commonly reported mild side effects [134]. Serious adverse effects of psyllium are generally rare; however, in some individuals, it may cause allergic reactions, gastrointestinal symptoms, anaphylaxis, and skin reactions. It can act as a strong inhalant allergen and cause asthma symptoms [11]. In a case report, psyllium was observed to potentially exacerbate asthma symptoms [140], while another case report documented allergic rhinitis in a bakery worker due to exposure to a psyllium-containing product [141]. If sufficient fluids are not consumed while taking psyllium powder and the powder is not swallowed completely, it causes bloating of the throat and obstruction of the esophagus. Therefore, it is recommended to drink a glass of water with each dose of psyllium powder [115]. Several case reports have described intestinal obstruction associated with insufficient fluid intake during psyllium use [142, 143]. Thus, although psyllium has beneficial effects for many individuals, it is necessary to pay attention to its potential toxic effects, especially in individuals with gastrointestinal sensitivity [82]. Adequate fluid intake is essential when using psyllium, and this should be emphasized as a critical public health message to prevent gastrointestinal obstruction.

Limitations and Strengths

A significant limitation of this review is that the types of psyllium (e.g., powder, shell, or seed) and the doses used in the studies in the literature differ. This makes it difficult to draw general conclusions. Furthermore, the fact that these studies were conducted among different populations also limits the generalizability of the results to some extent. There are differences in the methods and follow-up periods of the studies in the literature, and that prevents clear results from being obtained in the long term.

However, psyllium appears to have beneficial effects for many health problems, including obesity, cardiovascular diseases, diabetes mellitus, cancer, and gastrointestinal diseases. These positive effects highlight the multifaceted benefits that psyllium provides thanks to its soluble fiber contents and different biological mechanisms of action. This review of the literature has confirmed that psyllium is an effective ingredient with wide potential for use in the field of health as both a complementary and a preventive compound.

Future studies should compare the effects of different psyllium types and doses with more homogeneous study designs, taking into account differences across populations. With such planning, the effects of psyllium on health can be revealed more clearly and more effective usage strategies can be developed in clinical practice.

Conclusion and Future Perspective

Psyllium may have beneficial effects on metabolic, cardiovascular, gastrointestinal, renal and inflammatory pathways. While the current scientific evidence highlights its benefits, variations in formulation, dosage and study duration limit the comparability of studies. Future research should prioritise standardising psyllium forms and dosages, and conducting long-term randomised controlled trials examining outcomes such as glycaemic control, lipid metabolism, blood pressure, NAFLD, and gastrointestinal function. Mechanistic studies focusing on bile acid dynamics, appetite-related hormones and microbiota–host interactions will further clarify the underlying pathways of psyllium’s effects. Additionally, research related to functional food applications should address parameters such as texture, sensory acceptability, stability and real-world effectiveness. Overall, psyllium is a promising functional ingredient with potential applications in health and industry, and more comprehensive research will facilitate its optimal use.

Key References

  • Gholami Z, Clark CCT, Paknahad Z. The effect of psyllium on fasting blood sugar, HbA1c, HOMA IR, and insulin control: A GRADE-assessed systematic review and meta-analysis of randomized controlled trials. BMC Endocr Disord. 2024;24(1):82. 10.1186/s12902-024-01608-2.
    • ○ This article is a systematic review and meta-analysis of randomized controlled trials investigating the effects of psyllium on fasting blood sugar, HbA1c, HOMA-IR, and insulin levels. It was shown that psyllium significantly reduces fasting blood sugar, HbA1c, and HOMA-IR levels, but has no significant effect on insulin levels.
  • Gholami Z, Paknahad Z. The effect of psyllium consumption on blood pressure: Systematic review and dose-response meta-analysis of randomized controlled trials. Food Sci Nutr. 2024;12(10):7075–87. 10.1002/fsn3.3863.
    • ○ This article is a systematic review and meta-analysis of randomized controlled trials investigating the effects of psyllium on blood pressure. It was reported that psyllium significantly reduces systolic blood pressure, while it has no significant effect on diastolic blood pressure.
  • Xu L, Qiu B, Ba F, Zhang S, Han S, Chen H, et al. Synergistic effects of Ligilactobacillus salivarius Li01 and psyllium husk prevent mice from developing loperamide-induced constipation. Food Funct. 2024;15(24):11934–48. 10.1039/d4fo04444d.
    • ○ This article is an animal study investigating the effects of the combined use of psyllium and Ligilactobacillus salivarius Li01 on constipation. It was shown that this combination provides protection against constipation by improving gastrointestinal transit rate and increasing fecal water content.

Supplementary Information

Below is the link to the electronic supplementary material.

ESM 1 (380.7KB, pdf)

(PDF 380 KB)

Abbreviations

ALT

Alanine aminotransferase

AST

Aspartate aminotransferase

BMI

Body mass index

COX-2

Cyclooxygenase-2

FODMAP

Fermentable oligosaccharides, disaccharides, monosaccharides, and polyols

FTO

Fat mass and obesity-associated gene

GERD-Q

Gastroesophageal reflux disease questionnaire

GLP-1

Glucagon-like peptide-1

HbA1c

Hemoglobin A1c

HDL-C

High-density lipoprotein cholesterol

HOMA-IR

Homeostasis model assessment of insulin resistance

IBD

Inflammatory bowel diseases

IBS

Irritable bowel syndrome

IL-1

Interleukin-1

IL-6

Interleukin-6

LDL-C

Low-density lipoprotein cholesterol

LEP

Leptin

LEPR

Leptin receptor

MC4R

Melanocortin 4 receptor

NAFLD

Non-alcoholic fatty liver disease

NO

Nitric oxide

PPAR-γ

Peroxisome proliferator-activated receptor gamma

RELMβ

Resistin-like beta

SPRR2A

Small proline-rich protein 2 A

SREBP-1

Sterol regulatory element-binding protein 1

TNF-α:

Tumor necrosis factor alpha

Author Contributions

N.S and E.O wrote the main manuscript text and table. N.S. and E.O prepared the figure. N.S. overviewed the selection of the literature and reviewed the draft, finalized the final version of the manuscript.

Funding

Open access funding provided by the Scientific and Technological Research Council of Türkiye (TÜBİTAK). This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Data Availability

All data needed to evaluate the conclusions in this article are included in the article. Additional data related to this article may be requested from the authors.

Declarations

Competing interests

The authors declare no competing interests.

Human and Animal Rights and Informed Consent

Thisarticledoesnot contain any studies with human or animal subjects performed by any of the authors.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Kassa MG, Teferi DA, Asemu AM, Belachew MT, Satheesh N, Abera BD, et al. Review on psyllium husk: nutritional, functional, health benefits, food industry applications, waste treatment, and potential negative effects. CyTA - Journal of Food. 2024;22(1):2409174. 10.1080/19476337.2024.2409174. [Google Scholar]
  • 2.Chan EK, Schroeder DJ. Psyllium in hypercholesterolemia. Ann Pharmacother. 1995;29(6):625–7. 10.1177/106002809502900613. [DOI] [PubMed] [Google Scholar]
  • 3.Belorio M, Gómez M. Psyllium: a useful functional ingredient in food systems. Crit Rev Food Sci Nutr. 2022;62(2):527–38. 10.1080/10408398.2020.1822276. [DOI] [PubMed] [Google Scholar]
  • 4.Kaczmarczyk K, Kruk J, Ptaszek P, Ptaszek A. Plantago ovata husk: an investigation of raw aqueous extracts. osmotic, hydrodynamic and complex rheological characterisation. Molecules. 2023;28(4):1660. 10.3390/molecules28041660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Wojciechowicz-Budzisz A, Pejcz E, Spychaj R, Harasym J. Mixed psyllium fiber improves the quality, nutritional value, polyphenols and antioxidant activity of rye bread. Foods. 2023;12(19):3534. 10.3390/foods12193534. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Noguerol AT, Igual MM, Pagán MJ. Developing psyllium fibre gel-based foods: physicochemical, nutritional, optical and mechanical properties. Food Hydrocoll. 2022;122(2):107108. 10.1016/j.foodhyd.2021.107108. [Google Scholar]
  • 7.Fratelli C, Santos FG, Muniz DG, Habu S, Braga ARC, Capriles VD. Psyllium improves the quality and shelf life of gluten-free bread. Foods. 2021;10(5):954. 10.3390/foods10050954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Tosif MM, Bains A, Goksen G, Rehman MZ, Ali N, Karabulut G, et al. A comparative study on utilization of different plant-derived nano-mucilage as a fat replacer in yogurt: product optimization, physicochemical attributes, shelf-life evaluation, and consumer perception with market orientation. Food Chemistry: X. 2024;24:101920. 10.1016/j.fochx.2024.101920. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Franco EAN, Sanches-Silva A, Ribeiro-Santos R, de Melo NR. Psyllium (Plantago ovata Forsk): from evidence of health benefits to its food application. Trends Food Sci Technol. 2020;96(1):166–75. 10.1016/j.foodhyd.2021.107108. [Google Scholar]
  • 10.Xing LC, Santhi D, Shar AG, Saeed M, Arain MA, Shar AH, et al. Psyllium husk (Plantago ovata) as a potent hypocholesterolemic agent in animal, human and poultry. Int J Pharmacol. 2017;13(7):690–7. 10.3923/ijp.2017.690.697. [Google Scholar]
  • 11.Shah AR, Gour VS, Kothari SL, Sharma P, Dar KB, Ganie SA. Antioxidant, nutritional, structural, thermal and physico-chemical properties of psyllium (Plantago ovata) seeds. Curr Res Nutr Food Sci J. 2020;8(3):727–43. 10.12944/CRNFSJ.8.3.06. [Google Scholar]
  • 12.Shah AR, Sharma P, Longvah T, Gour VS, Kothari SL, Shah YR, et al. Nutritional composition and health benefits of psyllium (Plantago ovata) husk and seed. Nutr Today. 2020;55(6):313–21. 10.1097/NT.0000000000000450. [Google Scholar]
  • 13.Chen C, Shang C, Xin L, Xiang M, Wang Y, Shen Z, et al. Beneficial effects of psyllium on the prevention and treatment of cardiometabolic diseases. Food Funct. 2022;13(14):7473–86. 10.1039/D2FO00560C. [DOI] [PubMed] [Google Scholar]
  • 14.Chong RWW, Ball M, McRae C, Packer NH. Comparing the chemical composition of dietary fibres prepared from sugarcane, psyllium husk and wheat dextrin. Food Chem. 2019;298:125032. 10.1016/j.foodchem.2019.125032. [DOI] [PubMed] [Google Scholar]
  • 15.Sagar S, Goudar G, Sreedhar M, Panghal A, Sharma P. Characterization of nutritional content and in vitro antioxidant properties of Plantago ovata seeds. Int J Food Nutr. 2020;9:27. 10.4103/IJFNS.IJFNS_27_20. [Google Scholar]
  • 16.Waleed M, Saeed F, Afzaal M, Niaz B, Raza MA, Hussain M, et al. Structural and nutritional properties of psyllium husk arabinoxylans with special reference to their antioxidant potential. Int J Food Prop. 2022;25(1):2505–13. 10.1080/10942912.2022.2143522. [Google Scholar]
  • 17.Agrawal R. Psyllium: a source of dietary fiber. In: Waisundara VY, editor. Dietary fibers. London: IntechOpen; 2021. [Google Scholar]
  • 18.Gibb RD, Sloan KJ, McRorie JW Jr. Psyllium is a natural nonfermented gel-forming fiber that is effective for weight loss: a comprehensive review and meta-analysis. J Am Assoc Nurse Pract. 2023;35(8):468–76. 10.1097/JXX.0000000000000882. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Garg P, Garg PK, Bhattacharya K. Psyllium husk positively alters gut microbiota, decreases inflammation, and has bowel-regulatory action, paving the way for physiologic management of irritable bowel syndrome. Gastroenterology. 2024;166(3):545–6. 10.1053/j.gastro.2023.11.019. [DOI] [PubMed] [Google Scholar]
  • 20.Abouzied MM, Mahmoud SM, Wahid A, Ahmed AE, Okasha AM, Soliman HA, et al. A study of the hepatoprotective effect of Plantago psyllium L. seed extract against carbon tetrachloride induced hepatic injury in rats. J Appl Biomed. 2020;18(2–3):80–6. 10.32725/jab.2020.006. [DOI] [PubMed] [Google Scholar]
  • 21.Ogata M, Ogita T, Tari H, Arakawa T, Suzuki T. Supplemental psyllium fibre regulates the intestinal barrier and inflammation in normal and colitic mice. Br J Nutr. 2017;118(9):661–72. 10.1017/S0007114517002586. [DOI] [PubMed] [Google Scholar]
  • 22.Ishii Y, Matsunaga T, Yasui T, Rini DM, Inoue R, Yamamoto Y, et al. Supplemental psyllium fiber increases antimicrobial proteins via the tuft cell-ILC2 circuit and type II immune response in the mouse small intestine. Nutraceuticals. 2024;4(2):307–22. 10.3390/nutraceuticals4020019. [Google Scholar]
  • 23.Mohajeri P, Hematian Sourki A, Mehregan Nikoo A, Ertas YN. Fabrication, characterisation and antimicrobial activity of electrospun Plantago psyllium L. seed gum/gelatine nanofibres incorporated with Cuminum cyminum essential oil nanoemulsion. Int J Food Sci Technol. 2023;58(4):1832–40. 10.1111/ijfs.16324. [Google Scholar]
  • 24.El-Araby E, Raafat A, Elsonbaty SM. Radiation synthesis of psyllium/frankincense essential oil–based wound dressing hydrogels: antimicrobial, antioxidant and wound healing performance. Arab J Nucl Sci Appl. 2021;54(2):19–36. 10.21608/ajnsa.2021.33835.1373. [Google Scholar]
  • 25.Pal P, Banerjee A, Soren K, Chakraborty P, Pandey JP, Sen G, et al. Novel biocide based on cationic derivative of psyllium: surface modification and antibacterial activity. J Polym Environ. 2019;27(5):1178–90. 10.1007/s10924-019-01419-w. [Google Scholar]
  • 26.Gao Z, Wang G, Zhang J, Guo L, Zhao W. Psyllium fibre inclusion in gluten-free buckwheat dough improves dough structure and lowers glycaemic index of the resulting bread. Foods. 2024;13(5):767. 10.3390/foods13050767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Franco M, Gómez M. Effect of psyllium on physical properties, composition and acceptability of whole grain breads. Foods. 2022;11(12):1685. 10.3390/foods11121685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Zając MH. The properties of poultry batters depending on the amount of water and Plantago ovata husk. Acta Sci Pol Technol Aliment. 2020;19(4):475–82. 10.17306/J.AFS.0824. [DOI] [PubMed] [Google Scholar]
  • 29.Zhao N, Sun C, Li C, Kong B, Xia X, Sun F, et al. Application of psyllium husk powder addition on the textural properties, oxidative stability and sensory attributes of non-phosphates luncheon meat. Meat Sci. 2025;222:109760. 10.1016/j.meatsci.2025.109760. [DOI] [PubMed] [Google Scholar]
  • 30.Arabshahi SS, Sedaghati M. Production of synbiotic Doogh enriched with Plantago psyllium mucilage. J Food Sci Technol. 2022;59(10):3819–26. 10.1007/s13197-022-05401-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Alagawany M, Bilal RM, Batool F, Attia YA, Abd El Hack ME, Abdelnour SA, et al. Use of psyllium husk (Plantago ovata) in poultry feeding and possible application in organic production. Antibiotic alternatives in poultry and fish feed. Sharjah: Bentham Science; 2022. pp. 111–23. Chapter 8. [Google Scholar]
  • 32.Pal D. A review of potential health benefits and therapeutic applications of psyllium (Plantago ovata) husk in disease management. Int J Pharm Sci Res. 2023;12(5):120–8. 10.21275/SR23517155336. [Google Scholar]
  • 33.Singh B, Kumar S, Rajneesh, Mohan M, Divya. Synthesis and characterization of psyllium polysaccharide–poly(2-hydroxypropyl methacrylate) – poly(acrylamide) hydrogels for use in sustained drug delivery applications. Polym Sci Ser B. 2020;62(6):685–96. 10.1134/S1560090420330064. [Google Scholar]
  • 34.Singh B, Sharma V, Kumar R, Mohan M. Development of dietary fiber psyllium based hydrogel for use in drug delivery applications. Food Hydrocoll Health. 2022;2(3):100059. 10.1016/j.fhfh.2022.100059. [Google Scholar]
  • 35.Chandrasekaran P, Weiskirchen R. The role of obesity in type 2 diabetes mellitus – an overview. Int J Mol Sci. 2024;25(3):1882. 10.3390/ijms25031882. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Darooghegi Mofrad M, Mozaffari H, Mousavi SM, Sheikhi A, Milajerdi A. The effects of psyllium supplementation on body weight, body mass index and waist circumference in adults: a systematic review and dose-response meta-analysis of randomized controlled trials. Crit Rev Food Sci Nutr. 2020;60(5):859–72. 10.1080/10408398.2018.1553140. [DOI] [PubMed] [Google Scholar]
  • 37.Bretin A, San Yeoh B, Ngo VL, Reddivari L, Pellizzon M, Vijay-Kumar M, et al. Psyllium fiber protects mice against Western diet-induced metabolic syndrome via the gut microbiota-dependent mechanism. Gut Microbes. 2023;15(1):2221095. 10.1080/19490976.2023.2221095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Shahinfar H, Jayedi A, Torabynasab K, Payandeh N, Martami F, Moosavi H, et al. Comparative effects of nutraceuticals on body weight in adults with overweight or obesity: a systematic review and network meta-analysis of 111 randomized clinical trials. Pharmacol Res. 2023;196:106944. 10.1016/j.phrs.2023.106944. [DOI] [PubMed] [Google Scholar]
  • 39.Pokushalov E, Ponomarenko A, Garcia C, Pak I, Shrainer E, Seryakova M, et al. The impact of glucomannan, inulin, and psyllium supplementation (SolowaysTM) on weight loss in adults with FTO, LEP, LEPR, and MC4R polymorphisms: a randomized, double-blind, placebo-controlled trial. Nutrients. 2024;16(4):557. 10.3390/nu16040557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Pal S, McKay J, Ho S, Jane M, Gahler RJ, Wood S. Micronutrient status of individuals with overweight and obesity following 3 months’ supplementation with polyglycoplex (PGX®) or psyllium: a randomized controlled trial. BMC Nutr. 2022;8(1):42. 10.1186/s40795-022-00534-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.González AP, Flores-Ramírez A, Gutiérrez-Castro KP, Luévano-Contreras C, Gómez-Ojeda A, Sosa-Bustamante GP, et al. Reduction of small dense LDL and IL-6 after intervention with Plantago psyllium in adolescents with obesity: a parallel, double blind, randomized clinical trial. Eur J Pediatr. 2021;180(8):2493–503. 10.1007/s00431-021-04064-5. [DOI] [PubMed] [Google Scholar]
  • 42.Bacha AA, Suhail M, Awwad FA, Ismail EAA, Ahmad H. Role of dietary fiber and lifestyle modification in gut health and sleep quality. Front Nutr. 2024;11:1324793. 10.3389/fnut.2024.1324793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Jenko Pražnikar Z, Mohorko N, Gmajner D, Kenig S, Petelin A. Effects of four different dietary fibre supplements on weight loss and lipid and glucose serum profiles during energy restriction in patients with traits of metabolic syndrome: a comparative, randomized, placebo-controlled study. Foods. 2023;12(11):2122. 10.3390/foods12112122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Golzar M, Saghi E, Rakhshandeh H, Dehnavi Z, Jafarzadeh Esfehani A, Nematy M. Evaluating the effect of an Iranian traditional medicine-based herbal candy on body composition and appetite in overweight and obese adults: a preliminary study. Avicenna J Phytomed. 2023;13(2):165–76. 10.22038/AJP.2022.21314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Noureddin S, Mohsen J, Payman A. Effects of psyllium vs. placebo on constipation, weight, glycemia, and lipids: a randomized trial in patients with type 2 diabetes and chronic constipation. Complement Ther Med. 2018;40:1–7. 10.1016/j.ctim.2018.07.004. [DOI] [PubMed] [Google Scholar]
  • 46.Kumar A, Gangwar R, Zargar AA, Kumar R, Sharma A. Prevalence of diabetes in India: a review of IDF diabetes atlas 10th edition. Curr Diabetes Rev. 2024;20(1):105–14. 10.2174/1573399819666230413094200. [DOI] [PubMed] [Google Scholar]
  • 47.Xiao Z, Chen H, Zhang Y, Deng H, Wang K, Bhagavathula AS, et al. The effect of psyllium consumption on weight, body mass index, lipid profile, and glucose metabolism in diabetic patients: a systematic review and dose-response meta-analysis of randomized controlled trials. Phytother Res. 2020;34(6):1237–47. 10.1002/ptr.6609. [DOI] [PubMed] [Google Scholar]
  • 48.Bacha AA, Din ZU, Khan I. Effect of psyllium husk fiber and lifestyle modification on human body insulin resistance. Nutr Metab Insights. 2022;15:11786388221107797. 10.1177/11786388221107797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Juhász AE, Greff D, Teutsch B, Gede N, Hegyi P, Horváth EM, et al. Galactomannans are the most effective soluble dietary fibers in type 2 diabetes: a systematic review and network meta-analysis. Am J Clin Nutr. 2023;117(2):266–77. 10.1016/j.ajcnut.2022.12.015. [DOI] [PubMed] [Google Scholar]
  • 50.Gholami Z, Clark CCT, Paknahad Z. The effect of psyllium on fasting blood sugar, HbA1c, HOMA IR, and insulin control: a GRADE-assessed systematic review and meta-analysis of randomized controlled trials. BMC Endocr Disord. 2024;24(1):82. 10.1186/s12902-024-01608-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Watters K, Blaisdell P. Reduction of glycemic and lipid levels in db/db diabetic mice by psyllium plant fiber. Diabetes. 1989;38(12):1528–33. 10.2337/diab.38.12.1528. [DOI] [PubMed] [Google Scholar]
  • 52.Mallikarjunan N, Deshpande R, Maurya DK, Jamdar SN. Modifying rheological properties of psyllium by gamma irradiation enables development of low glycaemic index food with a predicted gastrointestinal tolerance. Int J Biol Macromol. 2024;257(2):128625. 10.1016/j.ijbiomac.2023.128625. [DOI] [PubMed] [Google Scholar]
  • 53.Willcox ML, Elugbaju C, Al-Anbaki M, Lown M, Graz B. Effectiveness of medicinal plants for glycaemic control in type 2 diabetes: an overview of meta-analyses of clinical trials. Front Pharmacol. 2021;12:777561. 10.3389/fphar.2021.777561. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Soltanian N, Janghorbani M. Effect of flaxseed or psyllium vs. placebo on management of constipation, weight, glycemia, and lipids: a randomized trial in constipated patients with type 2 diabetes. Clin Nutr ESPEN. 2019;29:41–8. 10.1016/j.clnesp.2018.11.002. [DOI] [PubMed] [Google Scholar]
  • 55.Lehoux Dubois C, Boudreau V, Potter KJ, Colomba J, Lavoie A, Mailhot M, et al. Acute soluble fibre supplementation has no impact on reducing post-prandial glucose excursions in adults with cystic fibrosis and glucose intolerance. Ann Endocrinol (Paris). 2023;84(6):767–72. 10.1016/j.ando.2023.02.001. [DOI] [PubMed] [Google Scholar]
  • 56.Kumar D, Gautam A, Rohatgi S, Kundu PP. Synthesis of vildagliptin loaded acrylamide-g-psyllium/alginate-based core-shell nanoparticles for diabetes treatment. Int J Biol Macromol. 2022;218:82–93. 10.1016/j.ijbiomac.2022.07.066. [DOI] [PubMed] [Google Scholar]
  • 57.Parsa H, Moradi-Khaligh Z, Rajabi S, Ranjbar K, Komaki A. Swimming training and Plantago psyllium ameliorate cognitive impairment and glucose tolerance in streptozotocin-nicotinamide-induced type 2 diabetic rats. J Physiol Sci. 2021;71(1):37. 10.1186/s12576-021-00823-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Fahed G, Aoun L, Bou Zerdan M, Allam S, Bou Zerdan M, Bouferraa Y, et al. Metabolic syndrome: updates on pathophysiology and management in 2021. Int J Mol Sci. 2022;23(2):786. 10.3390/ijms23020786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Gholami Z, Paknahad Z. Effect of psyllium consumption on metabolic syndrome indices: systematic review and dose–response meta-analysis of randomized controlled trials. J Funct Foods. 2023;107(4):105685. 10.1016/j.jff.2023.105685. [Google Scholar]
  • 60.Ghorbani A, Zarvandi M, Rakhshandeh H. A randomized controlled trial of a herbal compound for improving metabolic parameters in diabetic patients with uncontrolled dyslipidemia. Endocr Metab Immune Disord Drug Targets. 2019;19(7):1075–82. 10.2174/1871530319666190206213420. [DOI] [PubMed] [Google Scholar]
  • 61.Bernatova I, Liskova S, Bartekova M. Hypertension and cardiovascular diseases: from etiopathogenesis to potential therapeutic targets. Int J Mol Sci. 2022;23(14):7742. 10.3390/ijms23147742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Chong B, Jayabaskaran J, Jauhari SM, Chan SP, Goh R, Kueh MTW, et al. Global burden of cardiovascular diseases: projections from 2025 to 2050. Eur J Prev Cardiol. 2024;zwae281. 10.1093/eurjpc/zwae281. [DOI] [PubMed] [Google Scholar]
  • 63.Soliman GA. Dietary fiber, atherosclerosis, and cardiovascular disease. Nutrients. 2019;11(5):1155. 10.3390/nu11051155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Zhu R, Lei Y, Wang S, Zhang J, Lv M, Jiang R, et al. Plantago consumption significantly reduces total cholesterol and low-density lipoprotein cholesterol in adults: A systematic review and meta-analysis. Nutr Res. 2024;126:123–37. 10.1016/j.nutres.2024.03.013. [DOI] [PubMed] [Google Scholar]
  • 65.Gholami Z, Paknahad Z. The beneficial effects of psyllium on cardiovascular diseases and their risk factors: systematic review and dose-response meta-analysis of randomized controlled trials. J Funct Foods. 2023;111(5):105878. 10.1016/j.jff.2023.105878. [Google Scholar]
  • 66.Anderson JW, Zettwoch N, Feldman T, Tietyen-Clark J, Oeltgen P, Bishop CW. Cholesterol-lowering effects of psyllium hydrophilic mucilloid for hypercholesterolemic men. Arch Intern Med. 1988;148(2):292–6. 10.1001/archinte.148.2.292. [PubMed] [Google Scholar]
  • 67.Gholami Z, Paknahad Z. The effect of psyllium consumption on blood pressure: systematic review and dose-response meta-analysis of randomized controlled trials. Food Sci Nutr. 2024;12(10):7075–87. 10.1002/fsn3.3863. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Majewski M, Gromadziński L, Cholewińska E, Ognik K, Fotschki B, Juśkiewicz J. The interaction of dietary pectin, inulin, and psyllium with copper nanoparticle induced changes to the cardiovascular system. Nutrients. 2023;15(16):3557. 10.3390/nu15163557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Clark CCT, Salek M, Aghabagheri E, Jafarnejad S. The effect of psyllium supplementation on blood pressure: a systematic review and meta-analysis of randomized controlled trials. Korean J Intern Med. 2020;35(6):1385–99. 10.3904/kjim.2019.049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Brum J, Ramsey D, McRorie J, Bauer B, Kopecky SL. Meta-analysis of usefulness of psyllium fiber as adjuvant antilipid therapy to enhance cholesterol lowering efficacy of statins. Am J Cardiol. 2018;122(7):1169–74. 10.1016/j.amjcard.2018.06.040. [DOI] [PubMed] [Google Scholar]
  • 71.Hashem MA, Abd-Allah NA, Mahmoud EA, Amer SA, Alkafafy M. A preliminary study on the effect of psyllium husk ethanolic extract on hyperlipidemia, hyperglycemia, and oxidative stress induced by triton X-100 injection in rats. Biology. 2021;10(4):335. 10.3390/biology10040335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Rabeh NM, Refaat OG, Dhaher AGAE. Effect of psyllium seeds and its husk on hypercholesterolemic rats. Int J Health Sci. 2022;6(S1):116–24. 10.53730/ijhs.v6nS1.4750. [Google Scholar]
  • 73.Wang Z, Lv Q, Liu L, Zhu Z. Psyllium husk powder improves constipation by remodeling gut microbiota and improving intestinal metabolites. Food Biosci. 2025;64(7):105828. 10.1016/j.fbio.2025.105828. [Google Scholar]
  • 74.Gunn D, Abbas Z, Harris HC, Major G, Hoad C, Gowland P, et al. Psyllium reduces inulin-induced colonic gas production in IBS: MRI and in vitro fermentation studies. Gut. 2022;71(5):919–27. 10.1136/gutjnl-2021-324784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Guo W, Ge X, Lu J, Xu X, Gao J, Wang Q, et al. Diet and risk of non-alcoholic fatty liver disease, cirrhosis, and liver cancer: a large prospective cohort study in UK biobank. Nutrients. 2022;14(24):5335. 10.3390/nu14245335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Zhu Y, Yang H, Zhang Y, Rao S, Mo Y, Zhang H, et al. Dietary fiber intake and non-alcoholic fatty liver disease: the mediating role of obesity. Front Public Health. 2023;10:1038435. 10.3389/fpubh.2022.1038435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Stachowska E, Portincasa P, Jamioł-Milc D, Maciejewska-Markiewicz D, Skonieczna-Żydecka K. The relationship between prebiotic supplementation and anthropometric and biochemical parameters in patients with NAFLD: a systematic review and meta-analysis of randomized controlled trials. Nutrients. 2020;12(11):3460. 10.3390/nu12113460. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Pontifex MG, Mushtaq A, Le Gall G, Rodriguez-Ramiro I, Blokker BA, Hoogteijling MEM, et al. Differential influence of soluble dietary fibres on intestinal and hepatic carbohydrate response. Nutrients. 2021;13(12):4278. 10.3390/nu13124278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Deng Z, Meng C, Huang H, Song S, Fu L, Fu Z. The different effects of psyllium husk and Orlistat on weight control, the amelioration of hypercholesterolemia and non-alcohol fatty liver disease in obese mice induced by a high-fat diet. Food Funct. 2022;13(17):8829–49. 10.1039/d2fo01161a. [DOI] [PubMed] [Google Scholar]
  • 80.Wahid A, Mahmoud SMN, Attia EZ, Yousef AS, Okasha AMM, Soliman HA. Dietary fiber of psyllium husk (Plantago ovata) as a potential antioxidant and hepatoprotective agent against CCl₄-induced hepatic damage in rats. S Afr J Bot. 2020;130:208–14. 10.1016/j.sajb.2020.01.007. [Google Scholar]
  • 81.Marzec A, Fotschki B, Napiórkowska D, Fotschki J, Cholewińska E, Listos P, et al. The effect of copper nanoparticles on liver metabolism depends on the type of dietary fiber. Nutrients. 2024;16(21):3645. 10.3390/nu16213645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Yang K, Ryu T, Chung BS. Psyllium fiber improves hangovers and inflammatory liver injury by inhibiting intestinal drinking. Front Pharmacol. 2024;15:1378653. 10.3389/fphar.2024.1378653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Newberry C, Lynch K. The role of diet in the development and management of gastroesophageal reflux disease: why we feel the burn. J Thorac Dis. 2019;11(S12):S1594–601. 10.21037/jtd.2019.06.42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Martin Z, Spry G, Hoult J, Maimone IR, Tang X, Crichton M, et al. What is the efficacy of dietary, nutraceutical, and probiotic interventions for the management of gastroesophageal reflux disease symptoms? A systematic literature review and meta-analysis. Clin Nutr ESPEN. 2022;52:340–52. 10.1016/j.clnesp.2022.09.015. [DOI] [PubMed] [Google Scholar]
  • 85.Morozov S, Isakov V, Konovalova M. Fiber-enriched diet helps to control symptoms and improves esophageal motility in patients with non-erosive gastroesophageal reflux disease. World J Gastroenterol. 2018;24(21):2291–9. 10.3748/wjg.v24.i21.2291. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Morozov S, Isakov V. The effect of diet composition change on high-resolution oesophageal manometry metrics in non-erosive gastroesophageal reflux disease patients. Curr Dev Nutr. 2020;4(Suppl 2):54. [Google Scholar]
  • 87.Khedher A, Dhibi S, Bouzenna H, Akermi S, El Feki A, Teles PHV, et al. Antiulcerogenic and antioxidant activities of Plantago ovata ethanolic extract in rats. Braz J Biol. 2022;84:e255120. 10.1590/1519-6984.255120. [DOI] [PubMed] [Google Scholar]
  • 88.Suresh H, Ho V, Zhou J. Rheological characteristics of soluble fibres during chemically simulated digestion and their suitability for gastroparesis patients. Nutrients. 2020;12(8):2479. 10.3390/nu12082479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Suresh H, Zhou J, Ho V. The short-term effects and tolerability of low-viscosity soluble fibre on gastroparesis patients: a pilot clinical intervention study. Nutrients. 2021;13(12):4298. 10.3390/nu13124298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Di Ciaula A, Garruti G, Frühbeck G, De Angelis M, de Bari O, Wang DQ, et al. The role of diet in the pathogenesis of cholesterol gallstones. Curr Med Chem. 2019;26(19):3620–38. 10.2174/0929867324666170530080636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Orán S, Uribe M, Prado ME, de la Mora G, Muñoz RM, Pérez MF, et al. Efecto de La administración de fibra En La prevención de litiasis vesicular En obesos sometidos a Dieta de reducción. Rev Gastroenterol Mex. 1997;62(4):266–72. [PubMed] [Google Scholar]
  • 92.Bretin A, Zou J, San Yeoh B, Ngo VL, Winer S, Winer DA, et al. Psyllium fiber protects against colitis via activation of bile acid sensor farnesoid X receptor. Cell Mol Gastroenterol Hepatol. 2023;15(6):1421–42. 10.1016/j.jcmgh.2023.02.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Niu Y, Xia Q, Jung W, Yu L. Polysaccharides–protein interaction of psyllium and whey protein with their texture and bile acid binding activity. Int J Biol Macromol. 2019;126:215–20. 10.1016/j.ijbiomac.2018.12.221. [DOI] [PubMed] [Google Scholar]
  • 94.Galica AN, Galica R, Dumitrașcu DL. Diet, fibers, and probiotics for irritable bowel syndrome. J Med Life. 2022;15(2):174–9. 10.25122/jml-2022-0028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Moayyedi P, Andrews CN, MacQueen G, Korownyk C, Marsiglio M, Graff L, et al. Canadian Association of Gastroenterology clinical practice guideline for the management of irritable bowel syndrome (IBS). J Can Assoc Gastroenterol. 2019;2(1):6–29. 10.1093/jcag/gwy071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Menon J, Thapa BR, Kumari R, Puttaiah Kadyada S, Rana S, Lal SB. Efficacy of oral psyllium in pediatric irritable bowel syndrome: a double-blind randomized control trial. J Pediatr Gastroenterol Nutr. 2023;76(1):14–9. 10.1097/MPG.0000000000003622. [DOI] [PubMed] [Google Scholar]
  • 97.So SY, Badu S, Wu Q, Yalcinkaya N, Mirabile Y, Castaneda R, et al. Sex-dependent efficacy of dietary fiber in pediatric functional abdominal pain. Gastroenterology. 2024;166(4):645–e5714. 10.1053/j.gastro.2023.12.011. [DOI] [PubMed] [Google Scholar]
  • 98.Christensen C, Knudsen A, Arnesen EK, Hatlebakk JG, Sletten IS, Fadnes LT. Diet, food, and nutritional exposures and inflammatory bowel disease or progression of disease: an umbrella review. Adv Nutr. 2024;15(5):100219. 10.1016/j.advnut.2024.100219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Peters V, Dijkstra G, Campmans-Kuijpers MJE. Are all dietary fibers equal for patients with inflammatory bowel disease? A systematic review of randomized controlled trials. Nutr Rev. 2022;80(5):1179–93. 10.1093/nutrit/nuab062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Lin CY, Lee AH, Chiu KK, Vieson MD, Steelman AJ, Swanson KS. Saccharomyces cerevisiae fermentation product did not attenuate clinical signs, but psyllium husk has protective effects in a murine dextran sulfate sodium–induced colitis model. Curr Dev Nutr. 2020;4(11):nzaa159. 10.1093/cdn/nzaa159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Bonazzi E, Bretin A, Vigué L, Hao F, Patterson AD, Gewirtz AT, et al. Individualized microbiotas dictate the impact of dietary fiber on colitis sensitivity. Microbiome. 2024;12(1):5. 10.1186/s40168-023-01724-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Kaewdech A, Sripongpun P, Wetwittayakhlang P, Churuangsuk C. The effect of fiber supplementation on the prevention of diarrhea in hospitalized patients receiving enteral nutrition: a meta-analysis of randomized controlled trials with the GRADE assessment. Front Nutr. 2022;9:1008464. 10.3389/fnut.2022.1008464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Menees SB, Jackson K, Baker JR, Fenner DE, Eswaran S, Nojkov B, et al. A randomized pilot study to compare the effectiveness of a low FODMAP diet vs psyllium in patients with fecal incontinence and loose stools. Clin Transl Gastroenterol. 2022;13(3):e00454. 10.14309/ctg.0000000000000454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Bellini M, Tonarelli S, Barracca F, Rettura F, Pancetti A, Ceccarelli L, et al. Chronic constipation: is a nutritional approach reasonable? Nutrients. 2021;13(10):3386. 10.3390/nu13103386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Jalanka J, Major G, Murray K, Singh G, Nowak A, Kurtz C, et al. The effect of psyllium husk on intestinal microbiota in constipated patients and healthy controls. Int J Mol Sci. 2019;20(2):433. 10.3390/ijms20020433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Lai H, Li Y, He Y, Chen F, Mi B, Li J, et al. Effects of dietary fibers or probiotics on functional constipation symptoms and roles of gut microbiota: a double-blinded randomized placebo trial. Gut Microbes. 2023;15(1):2197837. 10.1080/19490976.2023.2197837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.McRorie JW Jr, Fahey GC Jr, Gibb RD, Chey WD. Laxative effects of wheat bran and psyllium: resolving enduring misconceptions about fiber in treatment guidelines for chronic idiopathic constipation. J Am Assoc Nurse Pract. 2020;32(1):15–23. 10.1097/JXX.0000000000000346. [DOI] [PubMed] [Google Scholar]
  • 108.van der Schoot A, Drysdale C, Whelan K, Dimidi E. The effect of fiber supplementation on chronic constipation in adults: an updated systematic review and meta-analysis of randomized controlled trials. Am J Clin Nutr. 2022;116(4):953–69. 10.1093/ajcn/nqac184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Chey SW, Chey WD, Jackson K, Eswaran S. Exploratory comparative effectiveness trial of green kiwifruit, psyllium, or prunes in US patients with chronic constipation. Am J Gastroenterol. 2021;116(6):1304–12. 10.14309/ajg.0000000000001149. [DOI] [PubMed] [Google Scholar]
  • 110.Yang C, Liu S, Li H, Bai X, Shan S, Gao P, et al. The effects of psyllium husk on gut microbiota composition and function in chronically constipated women of reproductive age using 16S rRNA gene sequencing analysis. Aging. 2021;13(1):15366–83. 10.18632/aging.203095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Coss-Adame E, Arenas-Martínez JS, García-Cedillo MF, Nosthas LC, Bustillo-Armendriz G. The effect of fiber supplementation with agave fructans or psyllium Plantago in symptoms of constipation and its relation with whole and regional transit time and pH. Neurogastroenterol Motil. 2024;36(11):e14908. 10.1111/nmo.14908. [DOI] [PubMed] [Google Scholar]
  • 112.Cheng J, Tennilä J, Stenman L, Ibarra A, Kumar M, Gupta KK, et al. Influence of lactitol and psyllium on bowel function in constipated Indian volunteers: a randomized, controlled trial. Nutrients. 2019;11(5):1130. 10.3390/nu11051130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Xu L, Qiu B, Ba F, Zhang S, Han S, Chen H, et al. Synergistic effects of Ligilactobacillus salivarius Li01 and psyllium husk prevent mice from developing loperamide-induced constipation. Food Funct. 2024;15(24):11934–48. 10.1039/d4fo04444d. [DOI] [PubMed] [Google Scholar]
  • 114.Bray F, Laversanne M, Sung H, Ferlay J, Siegel RL, Soerjomataram I, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229–63. 10.3322/caac.21834. [DOI] [PubMed] [Google Scholar]
  • 115.Przybyszewska J, Kuźmiński A, Przybyszewski M, Popławski C. The role and therapeutic effectiveness of Plantago ovata seed husk (psyllium husk) in the prevention and non-pharmacological treatment of gastrointestinal diseases. Part 1. Clinical use of psyllium husk in the treatment of irritable bowel syndrome, ulcerative colitis, and colorectal cancer. Gastroenterology Review. 2024;19(2):121–6. 10.5114/pg.2024.139209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Monro JA. Quantitative management of human faecal bulking response to combinations of functionally distinct dietary fibers, using functional equivalents and a validated rat model. Int J Food Sci Nutr. 2024;75(5):518–26. 10.1080/09637486.2024.2370348. [DOI] [PubMed] [Google Scholar]
  • 117.Kumar D, Gautam A, Kundu PP. Synthesis of acrylamide-g-melanin/itaconic acid-g-psyllium based nanocarrier for capecitabine delivery: in vivo and in vitro anticancer activity. Int J Pharm. 2023;635:122735. 10.1016/j.ijpharm.2023.122735. [DOI] [PubMed] [Google Scholar]
  • 118.Basu S, Nishiguchi R, Montrose DC, Staab H, Zhou XK, Wang H, et al. Psyllium protects against high Fructose diet induced exacerbation of colitis and colitis associated colorectal carcinogenesis. Cancer Res. 2020;80(16Supplement):3461. 10.1158/1538-7445.AM2020-3461.32878865 [Google Scholar]
  • 119.Then CK, Paillas S, Moomin A, Misheva MD, Moir RA, Hay SM, et al. Dietary fibre supplementation enhances radiotherapy tumour control and alleviates intestinal radiation toxicity. Microbiome. 2024;12(1):89. 10.1186/s40168-024-01804-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 120.Razack SA, Lee Y, Bose S, Shin H, Jung WK, Kang HW. Photo-triggered caffeic acid delivery via psyllium polysaccharide-gellan gum-based injectable bionanogel for epidermoid carcinoma treatment. Int J Biol Macromol. 2024;267(1):131166. 10.1016/j.ijbiomac.2024.131166. [DOI] [PubMed] [Google Scholar]
  • 121.Nishiguchi R, Basu S, Staab HA, Ito N, Zhou XK, Wang H, et al. Dietary interventions to prevent high-fructose diet-associated worsening of colitis and colitis-associated tumorigenesis in mice. Carcinogenesis. 2021;42(6):842–52. 10.1093/carcin/bgab007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122.Verpalen IM, van ‘t Veer-Ten Kate M, de Boer E, van den Hoed RD, Schutte JM, Dijkstra JR, et al. Development and clinical evaluation of a 3-step modified manipulation protocol for MRI-guided high-intensity focused ultrasound of uterine fibroids. Eur Radiol. 2020;30(7):3869–78. 10.1007/s00330-020-06780-2. [DOI] [PubMed] [Google Scholar]
  • 123.Hu D, Liu W, Yu W, Huang L, Ji C, Liu X, et al. Psyllium seed husk regulates the gut microbiota and improves mucosal barrier injury in the colon to attenuate renal injury in 5/6 nephrectomy rats. Ren Fail. 2023;45(1):2197076. 10.1080/0886022X.2023.2197076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Markiewicz-Gospodarek A, Kozioł M, Tobiasz M, Baj J, Radzikowska-Büchner E, Przekora A. Burn wound healing: clinical complications, medical care, treatment, and dressing types: the current state of knowledge for clinical practice. Int J Environ Res Public Health. 2022;19(3):1338. 10.3390/ijerph19031338. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 125.Jalilimanesh M, Azhdari M, Mirjalili A, Mozaffari MA, Hekmatimoghaddam S. The comparison of clinical and histopathological effects of topical psyllium (Plantago ovata) powder and silver sulfadiazine on second-degree burn wound healing in rats. World J Plast Surg. 2021;10(1):96–103. 10.29252/wjps.10.1.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.McRae MP. Dietary fiber intake and type 2 diabetes mellitus: an umbrella review of meta-analyses. J Chiropr Med. 2018;17(1):44–53. 10.1016/j.jcm.2017.11.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Kamalpour M, Ghalandari H, Nasrollahzadeh J. Short-term supplementation of a moderate carbohydrate diet with psyllium reduces fasting plasma insulin and tumor necrosis factor-α in patients with type 2 diabetes mellitus. J Diet Suppl. 2018;15(4):507–15. 10.1080/19390211.2017.1358791. [DOI] [PubMed] [Google Scholar]
  • 128.Wang Z, Cai Q, Liu L, Zhu Z. Psyllium husk powder enhances the management of type 2 diabetes by modulating gut microbiota and their metabolic products. Food Res Int. 2025;211:116393. 10.1016/j.foodres.2025.116393. [DOI] [PubMed] [Google Scholar]
  • 129.Jovanovski E, Yashpal S, Komishon A, Zurbau A, Blanco Mejia S, Ho HVT, et al. Effect of psyllium (Plantago ovata) fiber on LDL cholesterol and alternative lipid targets, non-HDL cholesterol and apolipoprotein B: a systematic review and meta-analysis of randomized controlled trials. Am J Clin Nutr. 2018;108(5):922–32. 10.1093/ajcn/nqy115. [DOI] [PubMed] [Google Scholar]
  • 130.Khan K, Jovanovski E, Ho HVT, Marques ACR, Zurbau A, Mejia SB, et al. The effect of viscous soluble fiber on blood pressure: a systematic review and meta-analysis of randomized controlled trials. Nutr Metab Cardiovasc Dis. 2018;28(1):3–13. 10.1016/j.numecd.2017.09.007. [DOI] [PubMed] [Google Scholar]
  • 131.Hosseini M, Salari R, Akbari Rad M, Salehi M, Birjandi B, Salari M. Comparing the effect of psyllium seed on gastroesophageal reflux disease with oral omeprazole in patients with functional constipation. J Evid Based Integr Med. 2018;23:2515690X18763294. 10.1177/2515690X18763294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 132.Alexander C, Ridlon J, Swanson K. Cholecystectomy and postprandial psyllium husk fiber consumption alter the gastrointestinal microbiota community in a post-menopausal mouse model (P20-028-19). Curr Dev Nutr. 2019;3:1790. 10.1093/cdn/nzz040.P20-028-19. [Google Scholar]
  • 133.Llewellyn SR, Britton GJ, Contijoch EJ, Vennaro OH, Mortha A, Colombel JF, et al. Interactions between diet and the intestinal microbiota alter intestinal permeability and colitis severity in mice. Gastroenterology. 2018;154(4):1037–e462. 10.1053/j.gastro.2017.11.030. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 134.Lertpipopmetha K, Kongkamol C, Sripongpun P. Effect of psyllium fiber supplementation on diarrhea incidence in enteral tube-fed patients: a prospective, randomized, and controlled trial. JPEN J Parenter Enteral Nutr. 2019;43(6):759–67. 10.1002/jpen.1489. [DOI] [PubMed] [Google Scholar]
  • 135.Major G, Murray K, Singh G, Nowak A, Hoad CL, Marciani L, et al. Demonstration of differences in colonic volumes, transit, chyme consistency, and response to psyllium between healthy and constipated subjects using magnetic resonance imaging. Neurogastroenterol Motil. 2018;30(9):e13400. 10.1111/nmo.13400. [DOI] [PubMed] [Google Scholar]
  • 136.Patel MK, Tanna B, Mishra A, Jha B. Physicochemical characterization, antioxidant and anti-proliferative activities of a polysaccharide extracted from psyllium (P. ovata) leaves. Int J Biol Macromol. 2018;118(Pt A):976–87. 10.1016/j.ijbiomac.2018.06.139. [DOI] [PubMed] [Google Scholar]
  • 137.Yang F, Shi W, Wang L, Qin N, Wang C, Guo Y, et al. Lipidomics study of the therapeutic mechanism of plantaginis semen in potassium oxonate-induced hyperuricemia rat. BMC Complement Med Ther. 2021;21(1):175. 10.1186/s12906-021-03350-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 138.EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA). Scientific opinion on the substantiation of health claims related to dietary fibre (ID 744, 745, 746, 748, 749, 753, 803, 810, 855, 1415, 1416, 4308, 4330) pursuant to Article 13(1) of Regulation (EC) No 1924/2006. EFSA J. 2010;8(10):1735. 10.2903/j.efsa.2010.1735. [Google Scholar]
  • 139.Sussman GL, Dorian W. Psyllium anaphylaxis. Allergy Proc. 1990;11(5):241–2. 10.2500/108854190778879828. [DOI] [PubMed] [Google Scholar]
  • 140.Marwaha AS, Cockcroft D, Philipenko B. Psyllium husk (Metamucil®) induced perennial asthma: a case report. Respir Med Case Rep. 2024;52:102110. 10.1016/j.rmcr.2024.102110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 141.Jungewelter S, Suomela S, Airaksinen L. Occupational IgE-mediated psyllium allergy in contemporary gluten-free and vegan baking: a case of allergic rhinitis. Am J Ind Med. 2021;64(5):431–4. 10.1002/ajim.23238. [DOI] [PubMed] [Google Scholar]
  • 142.Hefny AF, Ayad AZ, Matev N, Bashir MO. Intestinal obstruction caused by a laxative drug (psyllium): a case report and review of the literature. Int J Surg Case Rep. 2018;52:59–62. 10.1016/j.ijscr.2018.10.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 143.Tominaga Y, Hirayama I, Nonaka M, Yano T, Ishii M. Intestinal obstruction caused by consuming diet food containing psyllium. Acute Med Surg. 2023;10(1):e846. 10.1002/ams2.846. [DOI] [PMC free article] [PubMed] [Google Scholar]

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