Xu J, Gao Y, Yin J, Zhao X, Wang H, Yuan H, Wang F
Hong Yuan, Department of the First Orthopedics, Xinjiang Uygur Autonomous Region People's Hospital, Urumqi, Xinjiang 830001, China, Tel.: 0086-0991- 8563585; E-mail:
J Nutr Health Aging. 2014;18(2):204-8. doi: 10.1007/s12603-013-0383-2.
Osteoporosis is a systemic disease with a strong genetic component. Calcitonin receptors (CTR) are involved in maintaining calcium homeostasis. There is no consensus whether CTR gene polymorphism plays a role in affecting pathogenesis of osteoporosis.
The objective of this study was to investigate genetic susceptibility of calcitonin receptor gene polymorphism (genotypes and allele frequencies) to primary osteoporosis between Han and Uygur patients and healthy controls in the Chinese Xinjiang region.
This was a cross-sectional study conducted in an academic hospital.
Between 2010 and 2012 a total of 404 female patients with primary osteoporosis (200 Han and 204 Uygur) and 316 healthy control subjects (160 Han and 156 Uygur) were recruited to determine the distribution of C/T single nucleotide polymorphism of the CTR gene. PCR-restriction fragment length polymorphism was used at the 1377-bp site.
The frequency of polymorphic C/T alleles of the calcitonin receptor gene in each group fit the Hardy-Weinberg equilibrium model. There was no statistically significant difference in genotypes (P = 0.922) or allele frequency (P = 0.654) between the Xinjiang Han postmenopausal osteoporosis patients and the controls. Similarly, there was no difference in genotypes (P = 0.897) or allele frequency (P = 0.825) between Xinjiang Uygur postmenopausal osteoporosis patients and the controls. Moreover, there was no significant difference (P = 0.86) between the combination of both ethnic groups and controls. In contrast, compared to these two ethnic groups, Han CC type accounted for 67.8%, CT 30.0%, and TT 2.2%, whereas Uighur CC type accounted for 55.6%, CT 33.3%, and TT 11.2%, which is statistically significant between Han and Uygur CTR genotypes (P = 0.006). Allele frequency of C accounted for 82.8% and T for 17.2% in Han, whereas C accounted for 72.2% and T for 27.8% in Uygur (P = 0.001).
There was no statistically significant difference in CTR gene nucleotide sequence polymorphisms at 1377-bp between Chinese Xinjiang Han and Uygur patients with primary osteoporosis, suggesting that this CTR gene polymorphism may not affect incidence of osteoporosis. However, there was a significant difference in CTR gene nucleotide sequence polymorphism at the 1377-bp site between Chinese Xinjiang Han and Uygur, but the importance of this difference needs further study.
骨质疏松症是一种具有很强遗传成分的全身性疾病。降钙素受体(CTR)参与维持钙稳态。关于CTR基因多态性是否在影响骨质疏松症发病机制中起作用尚无定论。
本研究旨在调查中国新疆地区汉族和维吾尔族原发性骨质疏松症患者及健康对照者中降钙素受体基因多态性(基因型和等位基因频率)的遗传易感性。
这是一项在学术医院进行的横断面研究。
2010年至2012年期间,共招募了404例原发性骨质疏松症女性患者(200例汉族和204例维吾尔族)和316例健康对照者(160例汉族和156例维吾尔族),以确定CTR基因C/T单核苷酸多态性的分布。在1377-bp位点采用聚合酶链反应-限制性片段长度多态性方法。
每组降钙素受体基因多态性C/T等位基因频率均符合Hardy-Weinberg平衡模型。新疆汉族绝经后骨质疏松症患者与对照组之间的基因型(P = 0.922)或等位基因频率(P = 0.654)无统计学显著差异。同样,新疆维吾尔族绝经后骨质疏松症患者与对照组之间的基因型(P = 0.897)或等位基因频率(P = 0.825)也无差异。此外,两个民族组合与对照组之间也无显著差异(P = -0.86)。相比之下,与这两个民族相比,汉族CC型占67.8%,CT型占30.0%,TT型占2.2%,而维吾尔族CC型占55.6%,CT型占33.3%,TT型占11.2%,汉族和维吾尔族CTR基因型之间具有统计学显著性差异(P = 0.006)。汉族中C等位基因频率占82.8%,T占17.2%,而维吾尔族中C占72.2%,T占27.8%(P = 0.001)。
中国新疆汉族和维吾尔族原发性骨质疏松症患者在1377-bp处的CTR基因核苷酸序列多态性无统计学显著差异,提示该CTR基因多态性可能不影响骨质疏松症的发病率。然而,中国新疆汉族和维吾尔族在1377-bp位点的CTR基因核苷酸序列多态性存在显著差异,但这种差异的重要性需要进一步研究。