The Association of COL1A2 rs17166249 and rs412777 Polymorphisms on the Bone Mineral Density in Polish Postmenopausal Women
Adam Kamiński, Mateusz Gutowski, Anna Bogacz, Marta Podralska, Izabela Uzar, Michał Soczawa, Maciej Brązert, Bogusław Czerny

TL;DR
This study investigates the impact of two genetic variations in the COL1A2 gene on bone density in Polish postmenopausal women, finding no strong evidence of their influence.
Contribution
The study explores the potential role of COL1A2 gene polymorphisms in osteoporosis risk among Polish women.
Findings
No significant differences in rs412777 genotype or allele distribution were found between groups.
The rs17166249 T allele was more common in the osteoporosis group but not statistically significant after adjustment.
No significant correlations were found between the SNPs and bone mineral density measurements.
Abstract
Background: Osteoporosis is a chronic metabolic condition characterized by progressive loss of bone mass and disruption of the bone spatial architecture. Pathological changes are influenced by multiple factors, including genetic predispositions. Identifying risk factors for osteoporosis is crucial for recognizing at-risk populations, implementing preventive strategies, and supporting diagnostics. Type I collagen, composed of two chains—α1(I) and α2(I), encoded by the COL1A1 and COL1A2 genes, respectively—plays a key role in the mechanical strength of tissues, including bones. The aim of this study was to assess the effect of the rs17166249 and rs412777 polymorphisms in the COL1A2 gene on bone mineral density (BMD) in postmenopausal women. Methods: The study included 570 unrelated women: 119 diagnosed with osteoporosis, 96 with osteopenia, and 355 healthy controls. Polymorphisms in the…
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Taxonomy
TopicsBone health and osteoporosis research · Bone health and treatments · Connective tissue disorders research
