The effect of eight different gene polymorphisms on osteopenia and osteoporosis in the Turkish population.

Revista da Associacao Medica Brasileira (1992) Pub Date : 2025-05-02 eCollection Date: 2025-01-01 DOI:10.1590/1806-9282.20241624
Naim Uzun, Ahmet Kiziltunc, Adem Keskin
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Abstract

Objective: Bone mineral density is affected by many gene regions. Osteoporosis is a disease that occurs due to decreased bone mineral density and has a polygenetic multifactorial pathogenesis. The aim of this study was to examine the effect of gene variants in eight gene regions related to bone mineral density in patients diagnosed with osteopenia or osteoporosis.

Methods: A total of 60 patients diagnosed with osteoporosis, 50 patients diagnosed with osteopenia, and 40 healthy volunteers (control group) were included in the study. Collagen type I alpha 1 1997G/T, estrogen receptor α PvuII, estrogen receptor α XbaI, vitamin D receptor BsmI, lactase gene, osteoprotegerin G209A, osteoprotegerin T245G, and interleukin-6 G174C gene variants were analyzed.

Results: No important difference was found in the distribution of collagen type I alpha 1 1997G/T, estrogen receptor α PvuII, estrogen receptor α XbaI, vitamin D receptor BsmI, lactase gene T13910C, osteoprotegerin T245G, and interleukin-6 G174C gene variants between groups. A significant difference was detected between the distribution of osteoprotegerin G209A gene variants in the patient groups and the distribution of osteoprotegerin G209A gene variants in the control group. On the other hand, no important difference was detected in the distribution of osteoprotegerin G209A gene variants between patient groups.

Conclusion: The osteoprotegerin G209A gene variant may be associated with the risk of osteopenia and osteoporosis in the Turkish population. Other gene variants analyzed that affect bone mineral density were not associated with the risk of osteopenia and osteoporosis.

土耳其人群中8种不同基因多态性对骨质减少和骨质疏松症的影响
目的:骨密度受多个基因区域的影响。骨质疏松症是一种由于骨密度降低而发生的疾病,具有多基因、多因素的发病机制。本研究的目的是检查与骨质疏松症或骨质疏松症患者骨密度相关的8个基因区域的基因变异的影响。方法:选取60例骨质疏松患者、50例骨质减少患者和40例健康志愿者(对照组)作为研究对象。分析I型胶原α 1 1997G/T、雌激素受体α PvuII、雌激素受体α XbaI、维生素D受体BsmI、乳糖酶基因、骨保护素G209A、骨保护素T245G、白细胞介素6 G174C基因变异。结果:组间ⅰ型胶原α 1 1997G/T、雌激素受体α PvuII、雌激素受体α XbaI、维生素D受体BsmI、乳糖酶基因T13910C、骨保护素T245G、白细胞介素6 G174C基因变异分布无明显差异。患者组骨保护素G209A基因变异分布与对照组骨保护素G209A基因变异分布差异有统计学意义。另一方面,骨保护素G209A基因变异在患者组间的分布无明显差异。结论:在土耳其人群中,骨保护素G209A基因变异可能与骨质减少和骨质疏松的风险相关。经分析,其他影响骨矿物质密度的基因变异与骨质减少和骨质疏松的风险无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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