Effect of Zingiber officinale Supplementation on Obesity Management with Respect to the Uncoupling Protein 1 ‐3826A>G and ß3‐adrenergic Receptor Trp64Arg Polymorphism
Abstract
The present study aimed to investigate the effect of ginger (Zingiber officinale) supplementation on some obesity-associated parameters, with nutrigenetics approach. Accordingly, 80 eligible obese women (aged 18-45 years) were randomly assigned to receive either ginger (2-g ginger rhizomes powder as two 1-g tablets per day) or placebo supplements (corn starch with the same amount) for 12 weeks. Subjects were tested for changes in body weight, body mass index, waist and hip circumferences, body composition, appetite score, and dietary intake. Moreover, participants were genotyped for the -3826A>G and Trp64Arg polymorphisms of uncoupling protein 1 and ß3-adrenergic receptor genes, respectively. Over 12 weeks, ginger supplementation resulted in a slight but statistically significant decrease in all anthropometric measurements and total appetite score as compared with placebo group, which were more pronounced in subjects with the AA genotype for uncoupling protein 1 and Trp64Trp genotype for ß3-adrenergic receptor gene. However, there was no significant difference in changes of body composition and total energy and macronutrients intake between groups. In conclusion, our findings suggest that ginger consumption has potential in managing obesity, accompanying with an intervention-genotype interaction effect. However, further clinical trials need to explore ginger's efficacy as an anti-obesity agent in the form of powder, extract, or its active components.
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Ginger and placebo tablets were identical in package, size, shape, and color, and a small amount of ginger powder was added to placebo bottles to give ginger odor.
“It is noteworthy that ginger and placebo tablets were exactly the same in package, size, shape, and color. Moreover, a very small amount of ginger powder was added to bottles containing placebo tablets to give ginger odor, as previously done by Mahluji et al. [21] and Ebrahimzadeh Attari et al. [22].”
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Wang, J., Ke, W., Bao, R., Hu, X., & Chen, F. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13375 · Cited by 167 · see citing works
Maharlouei, N., Tabrizi, R., Lankarani, K. B., Rezaianzadeh, A., Akbari, M., Kolahdooz, F., Rahimi, M., Keneshlou, F., & Asemi, Z. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1427044 · Cited by 99 · see citing works
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Foshati, S., Poursadeghfard, M., Heidari, Z., & Amani, R. (2023) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-023-04227-x · Cited by 11 · see citing works
- Authors
- Ebrahimzadeh Attari, V., Asghari Jafarabadi, M., Zemestani, M., & Ostadrahimi, A.
- Affiliations
- Nutrition Research Center Tabriz University of Medical Sciences Tabriz Iran
- Road Traffic Injury Research Center Tabriz University of Medical Sciences Tabriz Iran
- Tabriz University of Medical Sciences (IR)
- Corresponding author
- Ostadrahimi, Alireza
- ORCID
- Ostadrahimi, Alireza
- Venue
- Phytotherapy Research
- Publisher
- Wiley
- Published
- 2015-04-21
- Volume
- 29
- Issue
- 7
- Pages
- 1032-1039
- ISSN
- 0951-418X (ISSN-L)
- 1099-1573
- OpenAlex
- W1952424389
- Cited by
- 42
- References
- 0
- Citations by year
- 2025: 4 · 2024: 3 · 2023: 8 · 2022: 6 · 2021: 2 · 2020: 3 · 2019: 3 · 2018: 4 · 2017: 8 · 2015: 1
- FWCI
- 5.05
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Phytotherapy Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Research Vice-Chancellor and Nutrition Research Center, Tabriz University of Medical Sciences (5/71/1353)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Ginger and Zingiberaceae research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Garlic and Onion Studies
- Keywords
- ginger supplementation, ginger, obesity treatment, UCP1, beta3-adrenergic receptor, Trp64Arg polymorphism, nutrigenetics, obese women, appetite, body composition, anthropometric measures, dietary intake
- MeSH terms
- Uncoupling Protein 1, Adult, Body Weight, Double-Blind Method, Female, Genotype, Humans, Ion Channels, Obesity, Polymorphism, Genetic, Powders, Body Mass Index, Anti-Obesity Agents, Dietary Supplements, Zingiber officinale, Receptors, Adrenergic, beta-3, Mitochondrial Proteins, Rhizome
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