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胚系 VWF/MPRIP 和体腔 FGA 变体协同赋予非创伤性股骨头坏死易感性。

Germline VWF/MPRIP and somatoplasm FGA variants synergically confer susceptibility to non-traumatic osteonecrosis of the femoral head.

机构信息

Department of Orthopedic Surgery, Liaocheng People's Hospital, Liaocheng, 252000, Shandong, China.

Joint Laboratory for Translational Medicine Research, Liaocheng People's Hospital, Liaocheng, 252000, Shandong, China.

出版信息

Sci Rep. 2023 Feb 22;13(1):3112. doi: 10.1038/s41598-023-30260-4.

Abstract

Non-traumatic osteonecrosis of the femoral head (ONFH) relies on multiple pathogenic factors, including intravascular coagulation, osteoporosis and lipid metabolism disorders. Despite extensively explored from various aspects, genetic mechanism underlying non-traumatic ONFH has not been fully elucidated. We randomly collected blood and necrotic tissue samples from 32 patients with non-traumatic ONFH as well as blood samples from 30 healthy individuals for whole exome sequencing (WES). Germline mutation and somatic mutation were analyzed to identify new potential pathogenic genes responsible for non-traumatic ONFH. Three genes might correlate with non-traumatic ONFH: VWF, MPRIP (germline mutations) and FGA (somatic mutations). Germline or somatic mutations in VWF, MPRIP and FGA correlate with intravascular coagulation, thrombosis, and consequently, ischemic necrosis of the femoral head.

摘要

非创伤性股骨头坏死(ONFH)依赖于多种致病因素,包括血管内凝血、骨质疏松症和脂代谢紊乱。尽管从多个方面进行了广泛的探索,但非创伤性 ONFH 的遗传机制尚未完全阐明。我们随机收集了 32 例非创伤性 ONFH 患者的血液和坏死组织样本以及 30 名健康个体的血液样本进行全外显子组测序(WES)。分析种系突变和体细胞突变,以鉴定新的潜在致病基因,这些基因可能与非创伤性 ONFH 有关。有三个基因可能与非创伤性 ONFH 相关:VWF、MPRIP(种系突变)和 FGA(体细胞突变)。VWF、MPRIP 和 FGA 的种系或体细胞突变与血管内凝血、血栓形成有关,进而导致股骨头缺血性坏死。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea00/9946931/822671a9c937/41598_2023_30260_Fig1_HTML.jpg

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