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发育性髋关节发育不良(DDH)中 GDF5 的 DNA 高甲基化。

DNA hypermethylation of GDF5 in developmental dysplasia of the hip (DDH).

机构信息

Department of Orthopedic Surgery, Tehran University of Medical Sciences, Tehran, IR Iran.

Joint Reconstruction Research Center, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, IR Iran.

出版信息

Mol Genet Genomic Med. 2019 Sep;7(9):e887. doi: 10.1002/mgg3.887. Epub 2019 Jul 23.

Abstract

INTRODUCTION & OBJECTIVE: Developmental Dysplasia of the Hip (DDH) is one of the most common congenital skeletal anomalies. Body of evidence suggests that genetic variations in GDF5 are associated with susceptibility to DDH. DDH is a multifactorial disease and its etiology has not been entirely determined. Epigenetic changes such as DNA methylation could be linked to DDH. In this scheme, we hypothesized that changes in GDF5 DNA methylation could predispose a susceptible individual to DDH.

METHODS

This study consisted of 45 DDH patients and 45 controls with healthy femoral neck cartilage, who underwent hemi-, or total arthroplasty for the femoral neck fracture. A cartilage sample of 1 cm in diameter and 1 mm in the thickness was obtained for DNA extraction. DNA was extracted and DNA methylation of GDF5 was evaluated by metabisulfite method.

RESULTS

Methylation analysis showed that the promoter of GDF5 in cartilage samples from DDH patients was hypermethylated in comparison to healthy controls (p = .001).

CONCLUSION

Our study showed that the methylation status of the GDF5 in patients with DDH is dysregulated. This dysregulation indicates that adjustment in the methylation might modify the expression of this gene. Since this gene plays an essential role in cartilage and bone development, thus reducing its expression can contribute to the pathogenesis of DDH. Further studies are needed to elucidate the role of GDF5 in this disease.

摘要

介绍与目的

发育性髋关节发育不良(DDH)是最常见的先天性骨骼畸形之一。有证据表明,GDF5 中的遗传变异与 DDH 的易感性有关。DDH 是一种多因素疾病,其病因尚未完全确定。表观遗传变化,如 DNA 甲基化,可能与 DDH 有关。在本研究中,我们假设 GDF5 DNA 甲基化的变化可能使易感个体易患 DDH。

方法

本研究纳入了 45 名 DDH 患者和 45 名因股骨颈骨折行半髋关节或全髋关节置换术的健康股骨颈软骨患者。采集直径 1cm、厚度 1mm 的软骨样本用于提取 DNA。提取 DNA 后,采用亚硫酸氢盐测序法检测 GDF5 的 DNA 甲基化。

结果

甲基化分析显示,与健康对照组相比,DDH 患者软骨样本中 GDF5 的启动子呈超甲基化(p=0.001)。

结论

我们的研究表明,DDH 患者 GDF5 的甲基化状态失调。这种失调表明,甲基化的调节可能会改变该基因的表达。由于该基因在软骨和骨骼发育中起着至关重要的作用,因此降低其表达可能有助于 DDH 的发病机制。需要进一步的研究来阐明 GDF5 在该疾病中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9394/6732267/059d17d16d8a/MGG3-7-e887-g001.jpg

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