Identification of key variants correlated with susceptibility of primary osteoporosis in the Chinese Han group. (8th December 2022)

• Record Type: Journal Article
• Authors: Li, Yanjiao; Liu, Qi; Ma, Qiuye; Ma, Zhaoxia; Chen, Juan; Yu, An; Ma, Changguo; Qiu, Lihua; Shi, Hong; Liang, Hongsuo; Hu, Min
• Is Part Of: Annals of human genetics. Volume 87:Number 1/2(2023)
• Page Start: 63
• Page End: 74
• Publication Date: 2022-12-08
• Subjects: age‐dependent manner -- bMSCs -- CRB2 -- osteoporosis -- TBX3; Human genetics -- Periodicals; 599.935
• DOI: 10.1111/ahg.12490
• Languages: English
• ISSNs: 0003-4800

Abstract

Abstract: Background: Primary osteoporosis is a systemic skeletal disease characterized by reduced bone mass and vulnerability to fractures. The genetics of osteoporosis in the Chinese population remain unclear, which hinders the prevention and treatment of osteoporosis in China. This study aimed to explore the susceptibility genes and the roles played by their variants in osteoporosis. Methods: Blood samples were collected from 45 osteoporosis patients and 30 healthy individuals, and genome‐wide association study was performed on array data. The expression levels of the candidate gene in different genotypes were further determined by using quantitative real‐time PCR. Moreover, the differentiation capacity of bone marrow mesenchymal stem cells under different genotypes from osteoporosis patients was investigated. Results: The most significant variant rs1891632 located in the upstream (918 bp) region of CRB2, which could down‐regulate the expression levels of CRB2 in genotype‐tissue expression database and played an essential role in the regulation of osteoblastic and osteoclastic differentiation during skeletal development. Another significant variant rs1061657 located within the 3′UTR region of TBX3 gene. We found that the mRNA levels of TBX3 decreased in the bMSCs of old osteoporosis patients. Interestingly, osteoblast differentiation capacity and TBX3 mRNA levels were similar between the young healthy individuals carrying derived and ancestral allele of rs1061657, whereas the differentiation capacity and TBX3 mRNA levels dramatically declined in elderly patients with osteoporosis. Conclusions: The variant rs1061657 might affect the osteogenesis of bMSCs in an age‐dependent manner and that TBX3 may be a key susceptibility gene for primary osteoporosis. In conclusion, CRB2 and TBX3 may influence the development of osteoporosis; additionally, rs1891632 and rs1061657, as the key variants first reported to be associated with primary osteoporosis, may potentially contribute to predicting the risk of osteoporosis (especially for older individuals) and may serve as therapeutic targets.