Relationship of vitamin D receptor gene polymorphism with sarcopenia and muscle traits based on propensity score matching
J Clin Lab Anal. 2020 Jul 22;e23485. doi: 10.1002/jcla.23485
Xuemei Yao 1, Lei Yang 1, Meiyan Li 1, Hui Xiao 1
Sarcopenia (muscle loss) and Vitamin D many studies in VitaminDWiki
- Better handgrip strength if some good vitamin D genes (or if supplement) – April 2022
- Sarcopenia (muscle loss) is 1.6X more likely if poor Vitamin D receptor – July 2020
- Reduced muscle function in mice lacking Vitamin D Receptors in muscles – June 2019
- Mechanisms of vitamin D action in skeletal muscle – June 2019
- Weaker hand grip if poor Vitamin D Receptor (15 percent) – Nov 2016
- Intense exercise increases vitamin D receptor activation
The risk of 44 diseases at least double with poor Vitamin D Receptor as of Oct 2019
Vitamin D Receptor activation can be increased by any of: Resveratrol, Omega-3, Magnesium, Zinc, Quercetin, non-daily Vit D, Curcumin, intense exercise, Ginger, Essential oils, etc Note: The founder of VitaminDWiki uses 10 of the 12 known VDR activators
Background: Vitamin D receptor (VDR) gene polymorphism is reported to be associated with muscle mass and muscle strength. Loss of skeletal muscle mass and decreased muscle strength are the main characteristics of sarcopenia. In this study, the relationship of VDR gene polymorphism with muscle traits (muscle mass, muscle strength, and physical performance) and sarcopenia were studied in Xinjiang, China.
Methods: Totally, 205 sarcopenia patients were enrolled. Propensity score method was used to match control group. FokI and BsmI polymorphisms were genotyped using improved multiplex ligation detection reaction (iMLDR).
Results: Fok1, but not Bsm1, polymorphism was significantly associated with sarcopenia. Patients with Fok1 GG genotype were more likely to have sarcopenia. Both Bsm1 and Fok1 polymorphism were related to muscle traits. Patients with Bsm1 CT genotype had lower gait speed (GS) but higher skeletal mass index. Patients with Fok1 GG genotype had lower GS, and female subjects with the Fok1 GG genotype had lower handgrip strength (HS). GS was decreased in Bsm1 CT genotype than CC carriers. HS and GS were decreased in Fok1 GG genotype than AA carriers.
Conclusion: Fok1, but not Bsm1, polymorphism is associated with sarcopenia. Both Bsm1 and Fok1 polymorphism affect both HS and GS.