4.1 Article

HLA-A gene polymorphisms contribute to osteoporosis susceptibility in postmenopausal Han Chinese women

Journal

GENETICS AND MOLECULAR RESEARCH
Volume 14, Issue 3, Pages 10322-10330

Publisher

FUNPEC-EDITORA
DOI: 10.4238/2015.August.28.18

Keywords

Human leukocyte antigen-A; Polymorphisms; Polymerase chain reaction-sequence-based typing; Postmenopausal osteoporosis; Bone mineral density

Funding

  1. National Natural Science Funds of China [81273018, 30700654]
  2. Science Funding of the Health Department, Shaanxi Province [2012D58]
  3. Natural Science Funding of Shaanxi Province [2015JM8436]
  4. Fundamental Research Funds for the Central University [XJJ 2011024]

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Osteoporosis is a common disease characterized by low bone mineral density, deterioration in bone microarchitecture, and increased fracture risk and is more prevalent in postmenopausal women. HLA is a complex gene family; previous studies have shown that it plays an important role in the pathogenesis of osteoporosis among Japanese and Greek populations. Prompted by these findings, this study was designed to explore the associations between HLA-A gene polymorphisms and postmenopausal osteoporosis in the Han Chinese population. The polymerase chain reaction-sequence-based typing method was used for DNA genotyping at the HLA-A locus in 70 patients with postmenopausal osteoporosis and 73 healthy controls. We identified 17 HLA-A alleles in patients with postmenopausal osteoporosis and 20 HLA-A alleles in control subjects. Furthermore, we found that the frequency of the HLA-A* 02:07 allele was significantly higher in patients with postmenopausal osteoporosis than in control subjects (P = 0.023), and the relative risk was 4.065 (95% confidence interval = 1.109-14.893). Our study provides supportive evidence for the contribution of HLA-A gene polymorphisms to the susceptibility to postmenopausal osteoporosis and suggests that HLA-A* 02: 07 is likely an important genetic risk factor for postmenopausal osteoporosis in the Han Chinese population.

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