Genetic polymorphisms of CYP3A4 among Chinese patients with steroid-induced osteonecrosis of the femoral head. Issue 44 (November 2016)

• Record Type: Journal Article
• Authors: Wang, Yuan; Li, Xiuling; Gao, Yaoyu; Li, Zhi; Yu, Lidong; Meng, Qingbo; Sun, Li; Wang, Jianzhong
• Other Names: Zhu. Xiaolin section editor.
• Is Part Of: Medicine. Volume 95:Issue 44(2016)
• Publication Date: 2016-11
• Subjects: case–control study -- CYP3A4 -- gene -- genotype analysis -- single nucleotide polymorphism -- steroid-induced osteonecrosis of femoral head; Medicine -- Periodicals; Medicine -- Periodicals; Médecine -- Périodiques; Geneeskunde; Medicine; Periodicals; Periodicals; 610.5
• DOI: 10.1097/MD.0000000000005332
• Languages: English
• ISSNs: 0025-7974

Abstract

Abstract: Background: Steroid therapy has been an important reason of nontraumatic osteonecrosis of the femoral head (ONFH). Steroids are metabolized by hepatic cytochrome P4503A, a low endogenous activity of this enzyme can contribute to the pathogenesis of ONFH. The aim of this study was to investigate the associations of polymorphisms of cytochrome P4503A4 ( CYP3A4 ) gene with steroid-induced ONFH in Chinese patients. Methods: A total of 150 steroid-induced ONFH patients and 250 healthy controls were enrolled. We evaluated 5 single-nucleotide polymorphisms of the CYP3A4 gene in this case–control study. Results: We identified rs2242480 in the CYP3A4 gene that was potentially associated with an increased risk of steroid-induced ONFH in the allele model ( P = 0.023; odds ratio [OR]: 1.47; 95% confidence intervals [CI]: 1.05–2.04) and in the additive model ( P = 0.028; OR: 1.44; 95% CI: 1.04–1.99) adjusted age + gender. Furthermore, we also observed a protective effect of haplotype "TG" ( P = 0.025; OR: 0.69; 95% CI: 0.49–0.96) and a risk effect of haplotype "CG" ( P = 0.006; OR: 1.81; 95% CI: 1.19–2.77) of the CYP3A4 gene adjusted age + gender. Conclusion: These findings suggested that polymorphisms of CYP3A4 gene may be associated with susceptibility to steroid-induced ONFH.