Guo Fa-Qi, Deng Min
a Department of Emergency Medicine, First Affiliated Hospital , Henan University of Science and Technology , Luoyang , China.
b Department of Functional Inspection , The Sixth People's Hospital of Luoyang , Luoyang , China.
J Invest Surg. 2019 Mar;32(2):118-126. doi: 10.1080/08941939.2017.1385663. Epub 2017 Nov 9.
Steroid-induced osteonecrosis of the femoral head (ONFH) in young adults is a challenging disorder that can impairs the quality of life of a patient. The disease also leads to frequent occurrences of collapse of the femoral head and resultant dysfunction of the hip joint. In recent years, some scholars have studied steroid-induced lipid metabolism disorder and achieved the effect of steroid-induced ONFH treatment. This study aims to review the investigations on the hepatic CYP3A (cytochrome P4503A enzyme) genetic polymorphisms in steroid-induced ONFH patients. We then further explore its activity correlation with the development of steroid-induced ONFH in a rabbit model.
A systematic literature search of articles was conducted in PubMed, Web of Science, Google Scholar, Springerlink, and the Chinese National Knowledge Infrastructure database up to February 2017. Twelve relevant articles were retrieved. The odds ratios, standard mean difference, and 95% confidence intervals were calculated to assess the effect of hepatic CYP3A activity on the rabbit model with steroid-induced ONFH. Fixed-effects and random-effects models were used to analyze the heterogeneity. Begg's funnel plot was used to assess publication bias.
High hepatic CYP3A activity significantly decreased the risk for steroid-induced ONFH in the rabbit model (p <. 05). The CYP3A gene may be potentially associated with increased risk of steroid-induced ONFH in the human allele model.
The study suggests that high hepatic CYP3A activity decreases the risk of steroid-induced ONFH.
年轻成年人的类固醇诱导性股骨头坏死(ONFH)是一种具有挑战性的疾病,会损害患者的生活质量。该疾病还会导致股骨头频繁塌陷以及髋关节功能障碍。近年来,一些学者研究了类固醇诱导的脂质代谢紊乱,并在类固醇诱导性ONFH的治疗方面取得了成效。本研究旨在回顾对类固醇诱导性ONFH患者肝脏CYP3A(细胞色素P4503A酶)基因多态性的研究。然后,我们在兔模型中进一步探讨其活性与类固醇诱导性ONFH发展的相关性。
截至2017年2月,在PubMed、科学网、谷歌学术、Springerlink和中国知网数据库中对文章进行了系统的文献检索。检索到12篇相关文章。计算比值比、标准平均差和95%置信区间,以评估肝脏CYP3A活性对类固醇诱导性ONFH兔模型的影响。采用固定效应和随机效应模型分析异质性。使用Begg漏斗图评估发表偏倚。
在兔模型中,高肝脏CYP3A活性显著降低了类固醇诱导性ONFH的风险(p <.05)。在人类等位基因模型中,CYP3A基因可能与类固醇诱导性ONFH风险增加潜在相关。
该研究表明,高肝脏CYP3A活性可降低类固醇诱导性ONFH的风险。