# VDR Gene Polymorphisms and Inter-Individual Variability in Response to Resistance Training

**Authors:** Chen Yang, Yanchun Li

PMC · DOI: 10.3390/genes17020137 · Genes · 2026-01-27

## TL;DR

This study explores how genetic variations in the VDR gene affect how people respond to resistance training, with different results for men and women.

## Contribution

The study identifies sex-specific associations between VDR gene polymorphisms and resistance training outcomes in Chinese Han adults.

## Key findings

- The AG genotype of rs731236 and CT genotype of rs1544410 were linked to greater gains in bone mineral content.
- In women, the rs731236-AA genotype correlated with better strength and power gains, while AG genotype improved body composition.
- In men, the rs1544410-CC genotype was associated with greater lower-limb muscle growth.

## Abstract

Background: Vitamin D receptor (VDR) gene polymorphisms are linked to muscle and bone physiology, yet their influence on individual differences in resistance training adaptations, especially between sexes, is not well understood. Methods: In total, 191 healthy Chinese Han adults (94 men, 97 women) completed a 12-week, twice-weekly resistance training program (squat and bench press). Key indicators of strength, power, body composition, and muscle morphology were assessed before and after the intervention. Participants were genotyped for VDR polymorphisms (rs731236/TaqI, rs7975232/ApaI, rs1544410/BsmI, rs2228570/FokI). Data were analyzed to compare responses across genotype groups. Results: Training induced significant improvements in multiple outcomes. Overall, the AG genotype of rs731236 and the CT genotype of rs1544410 were associated with greater gains in bone mineral content. Sex-specific analyses revealed distinct patterns: in women, the rs731236-AA genotype correlated with better strength and power gains, while the AG genotype linked to greater body composition improvements. In men, the rs1544410-CC genotype was associated with superior lower-limb muscle growth. The rs7975232 showed no significant overall effect, and rs2228570 deviated from Hardy–Weinberg equilibrium. Conclusions: VDR gene polymorphisms, particularly rs731236 and rs1544410, are associated with inter-individual variability in resistance training responses among Chinese Han adults, demonstrating clear sex and phenotype specificity. These findings offer preliminary support for genotype-informed personalized training.

## Linked entities

- **Genes:** VDR (vitamin D receptor) [NCBI Gene 7421]

## Full-text entities

- **Genes:** Vdr (vitamin D (1,25-dihydroxyvitamin D3) receptor) [NCBI Gene 22337] {aka Nr1i1}, Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, Mstn (myostatin) [NCBI Gene 17700] {aka Cmpt, Gdf8}, CYP27B1 (cytochrome P450 family 27 subfamily B member 1) [NCBI Gene 1594] {aka CP2B, CYP1, CYP1alpha, CYP27B, P450c1, PDDR}, MKNK1 (MAPK interacting serine/threonine kinase 1) [NCBI Gene 8569] {aka MNK1}
- **Diseases:** reduced bone mass (MESH:D001847), weight loss (MESH:D015431), osteoporosis (MESH:D010024), hypertension (MESH:D006973), muscle hypertrophy (MESH:C536106), central obesity (MESH:D056128), heart disease (MESH:D006331), hyperextension (MESH:C563315), injury to (MESH:D014947), sarcopenia (MESH:D055948), fat loss (MESH:D004620), bone mineral density reduction (MESH:D001851), weight gain (MESH:D015430), obese (MESH:D009765)
- **Chemicals:** 25-hydroxyvitamin D (MESH:C104450), calcium (MESH:D002118), 1,25-dihydroxyvitamin D3 (MESH:D002117), EDTA (MESH:D004492), phosphate (MESH:D010710), oxygen (MESH:D010100), Vitamin D (MESH:D014807), ethanol (MESH:D000431), cholesterol (MESH:D002784), isopropanol (MESH:D019840), Testosterone (MESH:D013739), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** rs2228570, rs1544410, rs7975232, rs731236

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## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940962/full.md

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Source: https://tomesphere.com/paper/PMC12940962