Volume 11, Issue 3 (Aug 2026)                   JNFS 2026, 11(3): 416-424 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Shokrani S, Nazarpour V, Sangouni A A, Mohammad Hosseini Azar M R, Alizadeh M. The Effect of Garlic Powder Supplementation on Appetite Control and Cardiometabolic Indices in Patients with Non-Alcoholic Fatty Liver Disease: A Double-Blind Randomized Controlled Clinical Trial. JNFS 2026; 11 (3) :416-424
URL: http://jnfs.ssu.ac.ir/article-1-1523-en.html
Food and Beverages Safety Research Center, Urmia University of Medical Sciences, Urmia, Iran
Full-Text [PDF 548 kb]   (55 Downloads)     |   Abstract (HTML)  (598 Views)
Full-Text:   (18 Views)
The Effect of Garlic Powder Supplementation on Appetite Control and Cardiometabolic Indices in Patients with Non-Alcoholic Fatty Liver Disease: A Double-Blind Randomized Controlled Clinical Trial

Sina Shokrani; MD1, Vahid Nazarpour; BSc2,3, Abbas Ali Sangouni; PhD3, Mohammad Reza Mohammad Hosseini Azar; MD4, Mohammad Alizadeh; PhD*5,6
1 Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran; 2 Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran; 3 Department of Nutrition and Food Hygiene, Faculty of Health, Baqiyatallah University of Medical Sciences, Tehran, Iran; 4 Gastroenterology and Hepatology Subdivision of Internal Medicine Department, Imam Khomeini Hospital, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran; 5 Food and Beverages Safety Research Center, Urmia University of Medical Sciences, Urmia, Iran; 6 Department of Nutrition, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
ARTICLE INFO ABSTRACT
ORIGINAL ARTICLE Background: Non-alcoholic fatty liver disease (NAFLD) has become a serious health care challenge. The authors evaluated the effect of garlic powder supplementation on appetite control and cardiometabolic indices in patients with NAFLD. Methods: This double-blind randomized controlled clinical trial was conducted for 12 weeks in ninety patients with NAFLD. The participants were randomly assigned to receive 1600 mg/d garlic powder (treatment group) or 1600 mg/d starch (placebo group). Appetite and cardiometabolic indices such as atherogenic index of plasma (AIP), castelli risk index II (CRI-II), atherogenic coefficient (AC), and cardiometabolic index (CMI) were assessed at baseline, middle and after intervention. Results: A total of 88 participants completed the trial. No difference was found between groups in baseline values of appetite parameters, AIP, AC and CMI. Only CRI-II was significantly higher in the treatment group (P=0.01). After intervention, the treatment group compared to the placebo group showed significant improvements in hunger (P<0.001), fullness (P=0.001), desire to eat (P=0.002), ability to eat (P<0.001), AIP (P<0.001), CRI-II (P<0.001), AC (P<0.001), and CMI (P<0.001). Conclusions: Garlic improves appetite and cardiometabolic indices.
Article history:
Received:20 Nov 2025
Revised: 21 Feb 2026
Accepted: 21 May 2026
*Corresponding author
alizade85@yahoo.com
Food and Beverages Safety Research Center, Department of Nutrition, Urmia University of Medical Sciences, Serow Highway, Nazloo, Urmia, Iran.
Postal code: 5756115111
Tel: +98 4432752372
Keywords
Non-alcoholic fatty liver disease; Garlic; Appetite;
Cardiometabolic risk.

Introduction
Non-alcoholic fatty liver disease (NAFLD) is defined as a range between hepatic steatosis and non-alcoholic steatohepatitis (NASH) (Han et al., 2023). Hepatic steatosis is characterized by 5% fat accumulation in the liver evidence of inflammation or significant alcohol consumption, while, in NASH, inflammation and hepatocellular damage occur along with liver fat accumulation (Han et al., 2023). Recently, a new definition for this disease was suggested as metabolic dysfunction-associated fatty liver disease (MAFLD) (Eslam et al., 2020). This disease is associated with obesity, type 2 diabetes, metabolic syndrome and insulin resistance (Eslam et al., 2020, Han et al., 2023). More than 25% of the global population suffers from NAFLD, and it is increasing worldwide (Younossi et al., 2016). Patients with NAFLD are more likely to develop diabetes due to impaired glucose metabolism (Godoy-Matos et al., 2020). Moreover, abnormal lipid metabolism, obesity, altered gut microbiota and oxidative stress are some important factors that contribute to the occurrence and progression of NAFLD (Godoy-Matos et al., 2020). There is a close relationship between NAFLD and progression of cardiovascular disease (CVD) (Targher et al., 2020). Some indices including atherogenic index of plasma (AIP), castelli risk index II (CRI-II), atherogenic coefficient (AC), and cardiometabolic index (CMI) are used to assess cardiometabolic risk (Fernandez-Macias et al., 2019, Sujatha and Kavitha, 2017, Wakabayashi and Daimon, 2015). Unhealthy dietary patterns are associated with the development of NAFLD (Lv et al., 2023). On the other hand, healthy dietary patterns such as plant-based diets can improve hepatic steatosis, obesity, and also prevent cardiovascular disorders, which is a very important approach for management of NAFLD (Lv et al., 2023, Sangouni et al., 2022).
Garlic (Allium sativum L.), due to its many medicinal properties, helps greatly in reducing blood pressure, improving lipid profile, and regulating glucose metabolism (Zhao et al., 2024). Garlic contains organosulfur compounds such as allicin, ajoene, and diallyl disulfide, which are primarily responsible for its health benefits (De Greef et al., 2021). These compounds have demonstrated a variety of positive effects, particularly on metabolic health, cardiovascular function, and immune modulation (De Greef et al., 2021, El-Saadony et al., 2024). In addition, garlic contains saponins, phenolic and flavonoid compounds, alliin and oil-soluble sulfur compounds (De Greef et al., 2021). Allicin, one of the most studied active compounds, has been shown to reduce oxidative stress and inflammation, which are key contributors to the progression of both NAFLD and CVD (El-Saadony et al., 2024). Other sulfur compounds in garlic, such as diallyl trisulfide, have also been found to improve lipid metabolism and reduce fat accumulation in the liver (El-Saadony et al., 2024). Furthermore, garlic has shown promising effects on promoting weight loss (Ettehad-Marvasti et al., 2022).
To the best of the authors’ knowledge, the effects of garlic on appetite and cardiometabolic indices have not been investigated in patients with NAFLD. This study aims to determine the effect of garlic powder supplementation on appetite control and cardiometabolic indices in patients with NAFLD. This research could provide valuable insights into the potential role of garlic supplementation as an adjunctive approach in managing appetite and cardiometabolic risk in patients with NAFLD.
Materials and Methods
Participant selection
Adult patients diagnosed with NAFLD were recruited from a clinical center in Urmia, Iran. Eligibility criteria were being ≥18 years and ultrasound-confirmed hepatic steatosis graded between 1 and 3. Exclusion criteria comprised diabetes mellitus, viral hepatitis, liver malignancies, untreated hypothyroidism, psychiatric or renal disorders, pregnancy, lactation, hypotension, garlic allergy, use of antihypertensive medications, or unwillingness to participate. Following initial screening, 90 eligible individuals were enrolled in the study.
Study design 
The study design was completely reported in previous articles (Sangouni et al., 2020a, b). Participants were randomly assigned to either the garlic powder supplementation group (SG) or the placebo group (PG) using a computer-generated sequence. Each garlic tablet contained 400 mg of garlic powder standardized to 1.5 mg allicin (equivalent to ~2 g fresh garlic). According to the optimal dose of allicin suggested by Lawson et al. (Lawson and Hunsaker, 2018) participants consumed four tablets daily-two before lunch and two before dinner. Placebo tablets were starch-based and identical in appearance and coating. All participants received general advice on weight management, although no structured dietary or behavioral intervention was implemented. Garlic and placebo tablets were given to participants every three weeks. Participants were instructed to take the tablets one hour before meals to optimize allicin absorption and minimize protein-related interference (Lawson and Hunsaker, 2018). Both types of tablets were manufactured by Amin Pharmaceuticals Co. in Isfahan, Iran. Adherence was monitored at each visit, and participants with <80% compliance were excluded from analysis.
Measurements
Body weight, height, waist circumference (WC), and body mass index (BMI) were measured at baseline, middle and after intervention using standardized equipment. Dietary intake was assessed using a 24-hour food recall questionnaire on three non-consecutive days (including one weekend day) at weeks 0, 6, and 12. Physical activity was also evaluated using the metabolic equivalent of task (MET) questionnaire at the same intervals.
Laboratory tests were performed at weeks 0, 6, and 12 to determine serum concentrations of alanine transaminase (ALT) and aspartate transaminase (AST), as well as lipid profile components including triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), and low-density lipoprotein cholesterol (LDL-c). Blood samples were collected after a 12-hour overnight fasting and centrifuged for 10 minutes at 3600 rpm. Then, serum samples were evenly poured into microtubes and immediately stored at −80 °C. All biochemical parameters were measured using routine enzymatic assays with commercial kits (Pars Azmoon, Iran) and analyzed by an autoanalyzer (Siemens, United Kingdom). Moreover, laboratory assessments were conducted in the Nutrition Department laboratory using standard procedures, and the participants and the researchers were blinded during study.
Appetite-related parameters including hunger, fullness, desire to eat, and ability to eat were evaluated using a visual analogue scale (VAS) (Sangouni et al., 2021a) at baseline, week 6, and week 12. 
Cardiometabolic risk was assessed using the following indices:
AIP = log (TG/HDL−c) (Fernandez-Macias et al., 2019)
CRI-II = LDL−c/HDL−c (Sangouni et al., 2021b)
AC = (TC−HDL−c)/HDL−c (Sujatha and Kavitha, 2017)
CMI = (TG/HDL-c) × waist to height ratio (WHtR) (Wakabayashi and Daimon, 2015)
Ethical considerations
This 12-week randomized, double-blind, placebo-controlled clinical trial was approved by the Ethics Committee of Urmia University of Medical Sciences and registered at the Iranian Registry of Clinical Trials (IRCT20170206032417N4, https://irct.behdasht.gov.ir/trial/34737).
Data analysis and sample size
Sample size was calculated to be 90 based on values of HDL-c in the study of Ashraf et al. (Ashraf et al., 2005) to ensure 95% power with α=0.05, which accounted for a 20% dropout rate. Baseline characteristics were compared using independent samples t-test for continuous variables and chi-square test for categorical variables. To assess appetite-related parameters between the two groups at weeks 0, 6, and 12, independent samples t-test was applied separately at each time point. For cardiometabolic and atherogenic indices, general linear model was used to evaluate differences. Additionally, univariate analysis of covariance (ANCOVA) was performed to compare mean changes between groups, adjusting for changes in energy intake. All statistical analyses were conducted using SPSS version 24, and P-values less than 0.05 were considered statistically significant.
Results
Baseline characteristics of participants
This was a randomized, controlled clinical trial conducted from August 2018 to March 2019. A total of 90 eligible participants were randomly assigned to either the SG and PG. During the follow-up period, two participants were excluded-one due to surgery and one due to loss to follow-up. Ultimately, 88 participants completed the study (45 in the SG and 43 in the PG, Figure 1). At baseline, demographic, anthropometric, physical activity, and dietary intake variables showed no statistically significant differences between the two groups (P>0.05, Table 1). No adverse effect related to the intervention was reported throughout the study.
Table 1. Baseline characteristics of patients with NAFLD.
Variable SG PG P-valuec
Sex 0.08
   Male 33 (73.3)a 24 (55.8)
   Female 12 (26.7) 19 (44.2)
Smoking status 0.31
   Current smoker 16 (35.6) 11 (25.6)
   Nonsmoker 29 (64.4) 32 (74.4)
Age (y) 45.2 ± 12.4b 44.2 ± 11.1 0.68
Weight (kg) 89.8 ± 11.9 90.0 ± 13.6 0.95
MET (h/d) 28.8 ± 3.8 27.8 ± 3.6 0.23
Energy intake (kcal/d) 2041 ± 123 2034 ± 136 0.80
ALT (iu/l) 30.9 ± 15.7 24.9 ± 15.4 0.07
AST (iu/l) 22.8 ± 11.1 21.2 ± 7.3 0.41
AIP 0.24 ± 0.21 0.20 ± 0.22 0.48
CRI-II 2.81 ± 0.67 2.46 ± 0.65 0.01
AC 3.69 ± 0.97 3.33 ± 1.19 0.12
CMI 1.29 ± 0.69 1.19 ± 0.78 0.88
a: n (%); b: Mean± standard deviation; c: P-values were computed by independent t-test for continuous variables and by chi-square for categorical variables; NAFLD: Non-alcoholic fatty liver disease; MET: Metabolic equivalent task hours; ALT: Alanine transaminase; AST: Aspartate transaminase; AIP: Atherogenic index of plasma; CRI: Castelli risk index; AC: Atherogenic index; CMI: cardiometabolic index; SG: Supplemnetd group; PG: Placebo group.
Outcome
At baseline, no significant differences were observed between the SG and PG in hunger (58.2±15.1 vs 57.9±13.7; P=0.91), fullness (48.0±12.1 vs 44.8±14.6; P=0.28), desire to eat (48.0±10.5 vs −47.20±10.0; P=0.72), and ability to eat (55.3±11.5 vs 57.9±12.8; P=0.32, Table 2).
After the intervention, the SG compared to the PG showed significant improvements in hunger (mean changes: −10.9±11.6 vs +1.8±11.5; P<0.001), fullness (mean changes: 9.3±10.9 vs 0.0± 12.1; P=0.001), desire to eat (mean changes: −6.0±12.3 vs 1.9±10.0; P=0.002), and ability to eat was (mean changes: −11.5±13.4 vs −0.5±10.6; P<0.001, Table 2).
There was no significant difference between groups in baseline values of AIP (0.24±0.21 vs 0.20±0.22; P=0.48), AC (3.69±0.97 vs 3.33±1.19; P=0.12) and CMI (1.21±0.69 vs 1.19±0.78; P=0.01). Only CRI-II showed a significant difference between groups at baseline (2.81±0.67 vs 2.46±0.65; P=0.01, Table 1). The SG compared to the PG demonstrated a significant reduction in AIP (mean change: −0.13±0.13 vs 0.03±0.12; P<0.001), CRI-II (mean change: −0.47±0.34 vs 0.01±0.36; P<0.001), AC (mean change: −0.65±0.54 vs 0.14±0.51; P<0.001), and CMI (mean change: −0.32±0.37 vs 0.06±0.31; P<0.001, Table 3) after 12 weeks.
Table 2. Effect of garlic on appetite control.
Variable SG (n = 45) PG(n = 43) P-baseline P-valueb P-valuec P-valued
Change in hunger score 0.91 < 0.001 < 0.001 < 0.001
   Baseline 58.2 ± 15.1a 57.9 ± 13.7
   Week 6 50.2 ± 13.0 60.0 ± 12.1
   Week 12 47.3 ± 12.8 59.7 ± 10.5
   Mean change -10.9 ± 11.6 1.8 ± 11.5
Change in fullness  score 0.28 < 0.001 < 0.001 0.001
   Baseline 48.0 ± 12.1 44.8 ± 14.6
   Week 6 54.2 ± 13.7 44.4 ± 10.5
   Week 12 57.3 ± 12.3 44.8 ± 10.9
   Mean change 9.3 ± 10.9 0.0 ± 12.1
Change in desire to eat score 0.72 0.002 < 0.001 0.002
   Baseline -48.0 ± 10.5 -47.2 ± 10.0
   Week 6 -52.6 ± 11.5 -45.8 ± 8.2
   Week 12 -54.0 ± 10.9 -45.3 ± 9.8
   Mean change -6.0 ± 12.3 1.9 ± 10.0
Change in ability to eat score 0.32 < 0.001 < 0.001 < 0.001
   Baseline 55.3 ± 11.5 57.9 ± 12.8
   Week 6 47.1 ± 10.3 58.1 ± 9.8
   Week 12 43.7 ± 11.7 57.4 ± 8.7
   Mean difference -11.5 ± 13.4 -0.5 ± 10.6
a: Mean± standard deviation; b: Comparisons between treatment and control groups at week 6; c: Comparisons between treatment and control groups at week 12; d: Mean change comparisons between groups; SG: Supplemnetd group; PG: Placebo group.
Table 3. Effect of garlic on cardiometabolic indices.
Variable SG (n = 45) PG (n = 43) PTime PGroup PTime×Group P-valueb
AIP 0.001 0.31 < 0.001 < 0.001
   Baseline 0.24 ± 0.21a 0.20 ± 0.22
   Week 6 0.16 ± 0.21 0.21 ± 0.21
   Week 12 0.11 ± 0.20 0.23 ± 0.20
   Mean change -0.13 ± 0.13 0.03 ± 0.12
CRI-II < 0.001 0.24 < 0.001 < 0.001
   Baseline 2.81 ± 0.67 2.46 ± 0.65
   Week 6 2.49 ± 0.64 2.45 ± 0.58
   Week 12 2.34 ± 0.57 2.47 ± 0.63
   Mean change -0.47 ± 0.34 0.01 ± 0.36
AC 0.002 0.68 < 0.001 < 0.001
   Baseline 3.69 ± 0.97 3.33 ± 1.19
   Week 6 3.20 ± 0.92 3.40 ± 1.10
   Week 12 3.04 ± 0.85 3.47 ± 1.12
   Mean change -0.65 ± 0.54 0.14 ± 0.51
CMI < 0.001 0.24 < 0.001 < 0.001
   Baseline 1.21 ± 0.69 1.19 ± 0.78
   Week 6 1.03 ± 0.66 1.19 ± 0.72
   Week 12 0.89 ± 0.50 1.25 ± 0.76
   Mean change -0.32 ± 0.37 0.06 ± 0.31
a: Mean± standard deviation; b: P-values were computed by univariate analysis of covariance (ANCOVA) for parameters after controlling baseline values of indices and mean changes of energy intake; AIP: Atherogenic index of plasma; CRI: Castelli risk index; AC: Atherogenic index; CMI: cardiometabolic index; SG: Supplemnetd group; PG: Placebo group.

Discussion
The present study showed that garlic can be effective in management of appetite and cardiometabolic indices. Previously, a clinical trial demonstrated that garlic powder supplementation for 12 weeks improved appetite scores in individuals with metabolic syndrome (Sangouni et al., 2021a). Some animal studies also support the appetite-modulating effects of garlic. In an experimental study, Masjedi (Masjedi et al., 2013) found that garlic extract reduced food intake in streptozotocin-induced diabetic rats. A study conducted on mice provided a high-fat diet and induced type 2 diabetes; it showed decreased energy intake and improved cardiometabolic risk factors such as abnormal lipid metabolism after receiving garlic powder (Islam and Choi, 2008). Cardiometabolic improvement may be due to the beneficial effect of appetite control on cardiometabolic risk factors such as dyslipidemia, obesity, and insulin resistance, in addition to the direct effects of garlic bioactive compounds on metabolic risk factors (Islam and Choi, 2008). However, more studies investigating the relationship between appetite control and cardiometabolic risk are needed to reach a clear vision.
The authors demonstrated the efficacy of 1600 mg/d garlic powder on some cardiometabolic indices. The clinical trials examining the effect of garlic on cardiometabolic indices are scarce. A clinical trial reported that garlic powder improves AIP, AC and CMI in subjects with metabolic syndrome (Sangouni et al., 2023). Furthermore, cardiometabolic indices are based on body composition and lipid profile (Fernandez-Macias et al., 2019, Wakabayashi and Daimon, 2015). Previous studies have suggested the beneficial effects of garlic on metabolic parameters in individuals with chronic conditions. It has been reported that garlic powder intake for 12 weeks reduced triglyceride (TG), total cholesterol (TC), LDL-c, and increased HDL-c in patients with NAFLD (Sangouni et al., 2020a). Another study observed significant decreases in TG and LDL-c levels after garlic intake for 12 weeks in patients with dyslipidemia (Ashraf et al., 2005). Similarly, Kojuri et al. (Kojuri et al., 2007) showed that garlic improved lipid profile in individuals with hypercholesterolemia. In a study, a reduction in WC after 12-week garlic supplementation was reported (Sangouni et al., 2020b), which aligns with the present findings. Another clinical trial that was conducted in patients with NAFLD, reported improvement of obesity after 15-week garlic powder supplementation (Soleimani et al., 2016). In line with this study’s findings, a systematic review and meta-analysis showed that garlic supplementation significantly improved some cardiovascular risk factors, although the magnitude of effect depended on dosage and intervention duration (Fu et al., 2023).
The potential mechanisms underlying garlic’s effects on cardiometabolic indices may be attributed to its bioactive compounds, particularly allicin (El-Saadony et al., 2024, Melguizo-Rodriguez et al., 2022). Allicin exhibits anti-inflammatory, antioxidant, and lipid-regulating properties (Melguizo-Rodriguez et al., 2022). Studies have shown that it may inhibit key enzymes in lipid synthesis, reduce intestinal fat absorption, and enhance cholesterol excretion (El-Saadony et al., 2024, Melguizo-Rodriguez et al., 2022). Garlic reduces intestinal absorption of triglycerides, inhibits gene expressions related to the lipid production, and consequently, attenuates human preadipocyte differentiation and lipid accumulation in differentiated preadipocyte (Joo et al., 2013, Keophiphath et al., 2009). Garlic may also improve insulin resistance and lipid metabolism by increasing adiponectin levels and activating the AMP-activated protein kinase (AMPK) pathway (Melguizo-Rodriguez et al., 2022, Padiya et al., 2011).
The present study is a part of this project. In accordance with ethical principles in research, the authors declare that the effect of garlic powder supplementation on hepatic steatosis, liver enzymes, lipid profile, insulin resistance, oxidative stress, and body composition has previously been reported (Sangouni et al., 2020a, b). To facilitate better understanding and interpretation, some key information from previous publications has been incorporated into the present article.
One limitation of this study was the lack of long-term intervention. As another important limitation, lack of mechanistic biomarkers limits causal interpretation. In addition, ultrasonography was used to detect NAFLD (Hernaez et al., 2011). Fibroscan has higher accuracy than ultrasonography in detecting NAFLD (Eddowes et al., 2019).
Conclusion
In conclusion, a 12-week supplementation with garlic powder led to improvements in appetite and cardiometabolic indices among individuals with NAFLD. To establish definitive conclusions, future studies should be rigorously designed to examine the effect of raw, extract, or black garlic.
Acknowledgments
The authors would like to thank the contribution of the participants and co-researchers.
Authors' contributions
Sangouni A and Alizadeh M conceived and designed the study; Shokrani S and Nazarpour V analyzed the data; Mohammad Hosseini Azar M provided material and technical support; Shokrani S and Nazarpour V wrote the manuscript; Alizadeh M critically revised the manuscript for important intellectual content and had primary responsibility. All authors reviewed the final manuscript.
Conflict interests
The authors declared no conflict of interests.
Funding
The study was supported by Urmia University of Medical Sciences, Urmia, Iran. They provided kit and conducted laboratory works.
References
Ashraf R, Aamir K, Shaikh AR & Ahmed T 2005. Effects of garlic on dyslipidemia in patients with type 2 diabetes mellitus. Journal of Ayub Medical College Abbottabad. 17 (3): 60-64.
De Greef D, et al. 2021. Anticancer potential of garlic and its bioactive constituents: A systematic and comprehensive review. Seminars in cancer biology. 73: 219-264.
Eddowes P, et al. 2019. Accuracy of fibroScan controlled attenuation parameter and liver stiffness measurement in assessing steatosis and fibrosis in patients with nonalcoholic fatty liver disease. Gastroenterology. 156 (6): 1717-1730.
El-Saadony M, et al. 2024. Garlic bioactive substances and their therapeutic applications for improving human health: a comprehensive review. Frontiers in jmmunology. 15: 1277074.
Eslam M, Sanyal A, George J & International Consensus P 2020. MAFLD: A consensus-driven proposed nomenclature for metabolic associated fatty liver disease. Gastroenterology. 158 (7): 1999-2014 e1991.
Ettehad-Marvasti F, et al. 2022. Effect of garlic extract on weight loss and gut microbiota composition in obese women: A double-blind randomized controlled trial. Frontiers in nutrition. 9: 1007506.
Fernandez-Macias J, Ochoa-Martinez A, Varela-Silva J & Perez-Maldonado I 2019. Atherogenic index of plasma: novel predictive biomarker for cardiovascular illnesses. Archives of medical research. 50 (5): 285-294.
Fu Z, et al. 2023. Effects of garlic supplementation on components of metabolic syndrome: a systematic review, meta-analysis, and meta-regression of randomized controlled trials. BMC complementary medicine and therapies. 23 (1): 260.
Godoy-Matos A, Silva Junior W & Valerio C 2020. NAFLD as a continuum: from obesity to metabolic syndrome and diabetes. Diabetology and metabolic syndrome. 12: 60.
Han S, Baik S & Kim M 2023. Non-alcoholic fatty liver disease: Definition and subtypes. Clinical and molecular hepatology. 29 (suppl): S5-S16.
Hernaez R, et al. 2011. Diagnostic accuracy and reliability of ultrasonography for the detection of fatty liver: a meta-analysis. Hepatology. 54 (3): 1082-1090.
Islam M & Choi H 2008. Comparative effects of dietary ginger (Zingiber officinale) and garlic (Allium sativum) investigated in a type 2 diabetes model of rats. Journal of medicinal food. 11 (1): 152-159.
Joo H, Kim C, Kim I & Kim Y 2013. Anti-obesity effects of hot water extract and high hydrostatic pressure extract of garlic in rats fed a high-fat diet. Food and chemical toxicology 55: 100-105.
Keophiphath M, Priem F, Jacquemond-Collet I, Clement K & Lacasa D 2009. 1,2-vinyldithiin from garlic inhibits differentiation and inflammation of human preadipocytes. Journal of nutritionr. 139 (11): 2055-2060.
Kojuri J, Vosoughi A & Akrami M 2007. Effects of anethum graveolens and garlic on lipid profile in hyperlipidemic patients. Lipids in health and disease. 6: 5.
Lawson L & Hunsaker S 2018. Allicin bioavailability and bioequivalence from Garlic supplements and Garlic foods. Nutrients. 10 (7).
Lv Y, et al. 2023. Plant-based diets, genetic predisposition and risk of non-alcoholic fatty liver disease. BMC medicine. 21 (1): 351.
Masjedi F, Gol A & Dabiri S 2013. Preventive effect of Garlic (Allium sativum L.) on serum biochemical factors and histopathology of pancreas and liver in streptozotocin-induced diabetic rats. Iranian journal of pharmaceutical sciences 12 (3): 325-338.
Melguizo-Rodriguez L, et al. 2022. Biological properties and therapeutic applications of garlic and its components. Food & Function. 13 (5): 2415-2426.
Padiya R, Khatua T, Bagul P, Kuncha M & Banerjee S 2011. Garlic improves insulin sensitivity and associated metabolic syndromes in fructose fed rats. Nutrition & Metabolism. 8: 53.
Sangouni A, Alizadeh M, Jamalzehi A, Hosseinzadeh M & Parastouei K 2023. Garlic supplementation improves intestinal transit time, lipid accumulation product and cardiometabolic indices in subjects with metabolic syndrome: A randomized controlled trial. Phytotherapy research. 37 (6): 2305-2314.
Sangouni A, Alizadeh M, Jamalzehi A & Parastouei K 2021a. Effects of garlic powder supplementation on metabolic syndrome components, insulin resistance, fatty liver index, and appetite in subjects with metabolic syndrome: A randomized clinical trial. Phytotherapy research 35 (8): 4433-4441.
Sangouni A, Hassani Zadeh S, Mozaffari-Khosravi H & Hosseinzadeh M 2022. Effect of Mediterranean diet on liver enzymes: a systematic review and meta-analysis of randomised controlled trials. British journal of nutrition. 128 (7): 1231-1239.
Sangouni A, Mohammad Hosseini Azar M & Alizadeh M 2020a. Effect of garlic powder supplementation on hepatic steatosis, liver enzymes and lipid profile in patients with non-alcoholic fatty liver disease: a double-blind randomised controlled clinical trial. British journal of nutrition. 124 (4): 450-456.
Sangouni A, Mohammad Hosseini Azar M & Alizadeh M 2020b. Effects of garlic powder supplementation on insulin resistance, oxidative stress, and body composition in patients with non-alcoholic fatty liver disease: A randomized controlled clinical trial. Complementary therapies in medicine. 51: 102428.
Sangouni A, Sasanfar B, Ghadiri-Anari A & Hosseinzadeh M 2021b. Effect of l-carnitine supplementation on liver fat content and cardiometabolic indices in overweight/obese women with polycystic ovary syndrome: A randomized controlled trial. Clinical nutrition ESPEN i. 46: 54-59.
Soleimani D, Paknahad Z, Askari G, Iraj B & Feizi A 2016. Effect of garlic powder consumption on body composition in patients with nonalcoholic fatty liver disease: A randomized, double-blind, placebo-controlled trial. Advanced biomedical research. 5: 2.
Sujatha R & Kavitha S 2017. Atherogenic indices in stroke patients: A retrospective study. Iranian journal of neurology. 16 (2): 78-82.
Targher G, Byrne C & Tilg H 2020. NAFLD and increased risk of cardiovascular disease: clinical associations, pathophysiological mechanisms and pharmacological implications. Gut. 69 (9): 1691-1705.
Wakabayashi I & Daimon T 2015. The "cardiometabolic index" as a new marker determined by adiposity and blood lipids for discrimination of diabetes mellitus. Clinica chimica Acta. 438: 274-278.
Younossi Z, et al. 2016. Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology. 64 (1): 73-84.
Zhao X, Cheng T, Xia H, Yang Y & Wang S 2024. Effects of Garlic on glucose parameters and lipid profile: A systematic review and meta-analysis on randomized controlled trials. Nutrients. 16 (11).


 
Type of article: orginal article | Subject: public specific
Received: 2025/11/20 | Published: 2026/08/19 | ePublished: 2026/08/19

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2026 CC BY-NC 3.0 | Journal of Nutrition and Food Security

Designed & Developed by : Yektaweb