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DOI 10.1210/clinem/dgae738

Медицинская библиотека · The Journal of clinical endocrinology and metabolism · 2025

Shared Genetic Architecture and Causal Relationship Between Serum 25-Hydroxyvitamin D and Bone Mineral Density.

Sha Linna, Zhang Li, Zhao Xunying, Xiang Rong, Wu Xueyao, Zhu Jiangbo, Hou Jiaojiao, Deng Qin, Qin Chenjiarui, Xiao Changfeng, Qu Yang, Han Tao, Zhou Jinyu, Zheng Sirui, Yu Ting, Song Xin, Yang Bin, Fan Mengyu, Jiang Xia

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Аннотация

CONTEXT: Despite the well-established regulatory role of vitamin D in maintaining bone health, little is known about the shared genetics and causality of the association between serum 25-hydroxyvitamin D (25OHD) and bone mineral density (BMD).

OBJECTIVE

We aimed to investigate the shared genetic architecture and causal relationship between serum 25OHD and BMD, providing insights into their underlying biological mechanisms.

METHODS

Leveraging individual-level data from the UK Biobank (UKB) cohort and summary-level data from the genome-wide association studies (GWASs) conducted on European individuals for serum 25OHD (N = 417 580) and estimated heel BMD (eBMD, N = 426 824), we systematically elucidated the shared genetic architecture underlying serum 25OHD and eBMD through a comprehensive genome-wide cross-trait design.

RESULTS

Despite a lack of global genetic correlation (rg=-0.001; P = .95), a statistically significant local signal was discovered at 5p11-5q11.9. Two-sample mendelian randomization (MR) indicated no causal association in the overall population (β=.003, 95% CI, -0.04 to 0.03; P = .93), while positive causal effects were observed in males (β=.005, 95% CI, 0.00 to 0.01; P = .03) and older individuals (β=.009, 95% CI, 0.00∼0.02; P = .01) according to one-sample MR. A total of 49 pleiotropic single-nucleotide variations (SNVs), with 4 novel SNVs (rs1077151, rs79873740, rs12150353, and rs4760401), were identified, and a total of 95 gene-tissue pairs exhibited overlap, predominantly enriched in the nervous, digestive, exocrine/endocrine, and cardiovascular systems. Protein-protein interaction analysis identified RPS9 and RPL7A as hub genes.

CONCLUSION

This study illuminates the potential health benefits of enhancing serum 25OHD levels to mitigate the risk of osteoporosis among men and individuals older than 65 years. It also unveils a shared genetic basis between serum 25OHD and eBMD, offering valuable insights into the intricate biological pathways.

Для цитирования: Sha Linna, Zhang Li, Zhao Xunying, Xiang Rong, Wu Xueyao, Zhu Jiangbo, Hou Jiaojiao, Deng Qin, Qin Chenjiarui, Xiao Changfeng, Qu Yang, Han Tao, Zhou Jinyu, Zheng Sirui, Yu Ting, Song Xin, Yang Bin, Fan Mengyu, Jiang Xia. Shared Genetic Architecture and Causal Relationship Between Serum 25-Hydroxyvitamin D and Bone Mineral Density.. The Journal of clinical endocrinology and metabolism. 2025. DOI: 10.1210/clinem/dgae738.

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