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过氧化物酶体增殖物激活受体γ基因多态性与韩国人群股骨头坏死无关。

Peroxisome proliferator-activated receptor-gamma gene polymorphisms are not associated with osteonecrosis of the femoral head in the Korean population.

作者信息

Kim Tae-Ho, Hong Jung Min, Park Eui Kyun, Kim Shin-Yoon

机构信息

Skeletal Diseases Genome Research Center, Kyungpook National University Hospital, Daegu 700-412, Korea.

出版信息

Mol Cells. 2007 Dec 31;24(3):388-93.

Abstract

Osteonecrosis of the femoral head (ONFH) is a multifactorial disease to which certain individuals are more at risk. Altered lipid metabolism is one of the major risk factors for osteonecrosis, especially corticosteroid therapy and alcoholism. Peroxisome Proliferator-Activated Receptor-gamma (PPARgamma) plays a crucial role in differentiation of mesenchymal cells to adipocytes, lipid homeostasis, and bone metabolism. To investigate the possible association between PPARgamma gene variants and susceptibility to ONFH, we genotyped three common polymorphisms (-796A > G, +34C > G[Pro12Ala], and +82466C > T[His477His]) in 448 ONFH patients and 336 control subjects. Genotypes, allele frequencies, and haplotypes of the polymorphisms in the complete set of patients as well as in subgroups by sex or etiology were not significantly different from those in the control group. This suggests that the examined polymorphisms and haplotypes of the PPARgamma gene are unlikely to be associated with susceptibility to ONFH.

摘要

股骨头坏死(ONFH)是一种多因素疾病,某些个体更易患病。脂质代谢改变是骨坏死的主要危险因素之一,尤其是皮质类固醇治疗和酗酒。过氧化物酶体增殖物激活受体γ(PPARγ)在间充质细胞向脂肪细胞的分化、脂质稳态和骨代谢中起关键作用。为了研究PPARγ基因变异与ONFH易感性之间的可能关联,我们对448例ONFH患者和336例对照受试者的三种常见多态性(-796A>G、+34C>G[Pro12Ala]和+82466C>T[His477His])进行了基因分型。在全部患者以及按性别或病因划分的亚组中,这些多态性的基因型、等位基因频率和单倍型与对照组相比无显著差异。这表明所检测的PPARγ基因多态性和单倍型不太可能与ONFH易感性相关。

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