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DOI 10.3858/emm.2012.44.6.045

Медицинская библиотека · Experimental & molecular medicine · 2012

Association of ADIPOR1 polymorphisms with bone mineral density in postmenopausal Korean women.

Kim Ha Young, Hwang Joo-Yeon, Han Bok-Ghee, Lee Jong-Young, Park Eui Kyun, Kim Beom-Jun, Lee Seung Hun, Kim Ghi Su, Kim Shin-Yoon, Koh Jung-Min

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Adiponectin may affect bone through interactions with two known receptors, adiponectin receptors (ADIPOR) 1 and 2. We examined the association between polymorphisms of ADIPOR1 and ADIPOR2 and bone mineral density (BMD) in postmenopausal Korean women. Six polymorphisms in ADIPOR1 and four polymorphisms in ADIPOR2 were selected and genotyped in all study participants (n = 1,329). BMD at the lumbar spine and femur neck were measured using dual-energy X-ray absorptiometry. Lateral thoracolumbar (T4-L4) radiographs were obtained for vertebral fracture assessment and the occurrence of non-vertebral fractures examined using self-reported data. P values were adjusted for multiple testing using Bonferroni correction (P(corr)). ADIPOR1 rs16850799 and rs34010966 polymorphisms were significantly associated with femur neck BMD (P(corr) = 0.036 in the dominant model; P(corr) = 0.024 and P(corr) = 0.006 in the additive and dominant models, respectively). Subjects with the rare allele of each polymorphism had lower BMD, and association of rs34010966 with BMD showed a gene dosage effect. However, ADIPOR2 single nucleotide polymorphisms and haplotypes were not associated with BMD at any site. Our results suggest that ADIPOR1 polymorphisms present a useful genetic marker for BMD in postmenopausal Korean women.

Для цитирования: Kim Ha Young, Hwang Joo-Yeon, Han Bok-Ghee, Lee Jong-Young, Park Eui Kyun, Kim Beom-Jun, Lee Seung Hun, Kim Ghi Su, Kim Shin-Yoon, Koh Jung-Min. Association of ADIPOR1 polymorphisms with bone mineral density in postmenopausal Korean women.. Experimental & molecular medicine. 2012. DOI: 10.3858/emm.2012.44.6.045.

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