Association analysis between nutritional factors within the genome and the risk of osteoarthritis

Osteoarthritis (OA) is a multifactorial disease influenced by both genetic and environmental factors. Recent studies suggest that genetic variants involved in nutrient metabolism may interact with dietary factors to modulate OA risk. Understanding these gene-nutrient interactions could inform person...

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Main Authors: Liangming Kang, Guihua Wu, Pengfei Lin, Wenjuan Dai, Miao Huang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-06-01
Series:Frontiers in Nutrition
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Online Access:https://www.frontiersin.org/articles/10.3389/fnut.2025.1592974/full
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author Liangming Kang
Guihua Wu
Pengfei Lin
Wenjuan Dai
Miao Huang
author_facet Liangming Kang
Guihua Wu
Pengfei Lin
Wenjuan Dai
Miao Huang
author_sort Liangming Kang
collection DOAJ
description Osteoarthritis (OA) is a multifactorial disease influenced by both genetic and environmental factors. Recent studies suggest that genetic variants involved in nutrient metabolism may interact with dietary factors to modulate OA risk. Understanding these gene-nutrient interactions could inform personalized prevention strategies for OA. We conducted a cross-sectional study involving 500 participants to explore associations between specific genetic variants and OA susceptibility, considering dietary intake. Genotyping focused on polymorphisms in the FADS1 gene (rs174537) related to omega-3 fatty acid metabolism, the VDR gene (rs2228570) involved in vitamin D metabolism, and the IL-6 gene (rs1800795), a marker of inflammation. Dietary intake of omega-3 fatty acids, vitamin D, and antioxidants was assessed using validated food frequency questionnaires. Gene-nutrient interactions were evaluated using multivariable logistic regression models, adjusting for potential confounders. Individuals carrying the G allele of FADS1 who reported low omega-3 fatty acid intake exhibited a significantly increased risk of OA [Odds Ratio (OR) = 1.45; 95% Confidence Interval (CI): 1.10–1.90; p = 0.01]. Similarly, participants with the TT genotype of VDR and insufficient vitamin D intake had a higher OA risk (OR = 1.55; 95% CI: 1.15–2.10; p = 0.005). Furthermore, carriers of the IL-6 GG genotype with low antioxidant consumption showed elevated inflammatory markers and an increased OA risk (OR = 1.60; 95% CI: 1.20–2.15; p = 0.002). Our findings indicate that specific genetic variants in FADS1, VDR, and IL-6 genes interact with dietary factors to influence OA susceptibility. These gene-nutrient interactions underscore the importance of personalized dietary interventions in mitigating OA risk. Future longitudinal studies are warranted to confirm these associations and develop tailored prevention strategies.
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spelling doaj-art-ba15c78e9e01446eafdfbc5d73ce211e2025-08-20T02:23:35ZengFrontiers Media S.A.Frontiers in Nutrition2296-861X2025-06-011210.3389/fnut.2025.15929741592974Association analysis between nutritional factors within the genome and the risk of osteoarthritisLiangming KangGuihua WuPengfei LinWenjuan DaiMiao HuangOsteoarthritis (OA) is a multifactorial disease influenced by both genetic and environmental factors. Recent studies suggest that genetic variants involved in nutrient metabolism may interact with dietary factors to modulate OA risk. Understanding these gene-nutrient interactions could inform personalized prevention strategies for OA. We conducted a cross-sectional study involving 500 participants to explore associations between specific genetic variants and OA susceptibility, considering dietary intake. Genotyping focused on polymorphisms in the FADS1 gene (rs174537) related to omega-3 fatty acid metabolism, the VDR gene (rs2228570) involved in vitamin D metabolism, and the IL-6 gene (rs1800795), a marker of inflammation. Dietary intake of omega-3 fatty acids, vitamin D, and antioxidants was assessed using validated food frequency questionnaires. Gene-nutrient interactions were evaluated using multivariable logistic regression models, adjusting for potential confounders. Individuals carrying the G allele of FADS1 who reported low omega-3 fatty acid intake exhibited a significantly increased risk of OA [Odds Ratio (OR) = 1.45; 95% Confidence Interval (CI): 1.10–1.90; p = 0.01]. Similarly, participants with the TT genotype of VDR and insufficient vitamin D intake had a higher OA risk (OR = 1.55; 95% CI: 1.15–2.10; p = 0.005). Furthermore, carriers of the IL-6 GG genotype with low antioxidant consumption showed elevated inflammatory markers and an increased OA risk (OR = 1.60; 95% CI: 1.20–2.15; p = 0.002). Our findings indicate that specific genetic variants in FADS1, VDR, and IL-6 genes interact with dietary factors to influence OA susceptibility. These gene-nutrient interactions underscore the importance of personalized dietary interventions in mitigating OA risk. Future longitudinal studies are warranted to confirm these associations and develop tailored prevention strategies.https://www.frontiersin.org/articles/10.3389/fnut.2025.1592974/fullosteoarthritisgene-nutrient interactionsFADS1 genevitamin D receptorinflammatory markers
spellingShingle Liangming Kang
Guihua Wu
Pengfei Lin
Wenjuan Dai
Miao Huang
Association analysis between nutritional factors within the genome and the risk of osteoarthritis
Frontiers in Nutrition
osteoarthritis
gene-nutrient interactions
FADS1 gene
vitamin D receptor
inflammatory markers
title Association analysis between nutritional factors within the genome and the risk of osteoarthritis
title_full Association analysis between nutritional factors within the genome and the risk of osteoarthritis
title_fullStr Association analysis between nutritional factors within the genome and the risk of osteoarthritis
title_full_unstemmed Association analysis between nutritional factors within the genome and the risk of osteoarthritis
title_short Association analysis between nutritional factors within the genome and the risk of osteoarthritis
title_sort association analysis between nutritional factors within the genome and the risk of osteoarthritis
topic osteoarthritis
gene-nutrient interactions
FADS1 gene
vitamin D receptor
inflammatory markers
url https://www.frontiersin.org/articles/10.3389/fnut.2025.1592974/full
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