Wu Zuyou, Yang Yang, Ning Caibo, Li Jiali, Cai Yimin, Li Yanmin, Cao Zilong, Tian Shuangshuang, Peng Jingyi, Ma Qianying, He Chunyi, Xia Shuting, Chen Jun, Miao Xiaoping, Li Zhen, Zhu Ying, Chu Qian, Tian Jianbo
Department of Epidemiology and Biostatistics, School of Public Health, State Key Laboratory of Metabolism and Regulation in Complex Organisms, TaiKang Center for Life and Medical Sciences, Wuhan University, Wuhan, China.
Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Nat Commun. 2025 Aug 12;16(1):7490. doi: 10.1038/s41467-025-62826-3.
Bone marrow adipose tissue, as a distinct adipose subtype, has been implicated in the pathophysiology of skeletal, metabolic, and hematopoietic disorders. To identify its underlying genetic factors, we utilized a deep learning algorithm capable of quantifying bone marrow fat fraction (BMFF) in the vertebrae and proximal femur using magnetic resonance imaging data of over 38,000 UK Biobank participants. Genome-wide association analyses uncovered 373 significant BMFF-associated variants (P-value < 5 × 10), with enrichment in bone remodeling, metabolism, and hematopoiesis pathway. Furthermore, genetic correlation highlighted a significant association between BMFF and skeletal disease. In about 300,000 individuals, polygenic risk scores derived from three proximal femur BMFF were significantly associated with increased osteoporosis risk. Notably, Mendelian randomization analyses revealed a causal link between proximal femur BMFF and osteoporosis. Here, we show critical insights into the genetic determinants of BMFF and offer perspectives on the biological mechanisms driving osteoporosis development.
骨髓脂肪组织作为一种独特的脂肪亚型,已被认为与骨骼、代谢和造血系统疾病的病理生理学有关。为了确定其潜在的遗传因素,我们利用一种深度学习算法,该算法能够使用超过38000名英国生物银行参与者的磁共振成像数据来量化椎骨和股骨近端的骨髓脂肪分数(BMFF)。全基因组关联分析发现了373个与BMFF显著相关的变异(P值<5×10),这些变异在骨重塑、代谢和造血途径中富集。此外,遗传相关性突出了BMFF与骨骼疾病之间的显著关联。在大约30万人中,来自三个股骨近端BMFF的多基因风险评分与骨质疏松症风险增加显著相关。值得注意的是,孟德尔随机化分析揭示了股骨近端BMFF与骨质疏松症之间的因果关系。在此,我们展示了对BMFF遗传决定因素的关键见解,并提供了关于驱动骨质疏松症发展的生物学机制的观点。