Department of Orthopedics, Zhejiang Chinese Medicine and Western Medicine Integrated Hospital/Hangzhou Red Cross Hospital, 208 East Huancheng Road, Hangzhou, Zhejiang, China.
Department of Orthopaedic Surgery, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, 158 Shangtang Road, Hangzhou, Zhejiang, China
Biosci Rep. 2019 Feb 26;39(2). doi: 10.1042/BSR20181713. Print 2019 Feb 28.
Osteoarthritis (OA) is a degenerative joint disease characterized by joint destruction with cartilage loss and occasional gross derangement of joint integrity. In recent years, several studies have reported the association between angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism and knee OA. However, the results were conflicting. To determine the association between ACE gene I/D polymorphism and knee OA, we conducted a hospital-based case-control study with 282 knee OA cases and 316 controls to investigate the association between ACE gene I/D polymorphism and knee OA susceptibility in a Chinese Han population. The present study found that DD genotype or D allele carriers of ACE gene I/D polymorphism increased the risk of knee OA. Stratification analyses of sex, age, and body mass index (BMI) showed significant associations amongst the groups of females, ≥55 years, and abnormal BMI. In addition, the present study made analysis between ACE I/D polymorphism and some clinical features of OA, and found DD genotype of I/D polymorphism was associated with arthralgia. Furthermore, we undertook a meta-analysis together with the present study between this single nucleotide polymorphism (SNP) and knee OA risk. This meta-analysis found that ACE gene I/D polymorphism was associated with increased risk for OA. Stratification analysis of ethnicity in this meta-analysis indicated that I/D polymorphism increased the risk of knee OA amongst the Asians and Caucasians. In conclusion, this case-control study and meta-analysis suggest that ACE gene I/D polymorphism is associated with increased risk for knee OA.
骨关节炎(OA)是一种退行性关节疾病,其特征为关节破坏伴软骨丢失,偶尔关节完整性严重紊乱。近年来,几项研究报告了血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性与膝骨关节炎之间的关联。然而,结果存在争议。为了确定 ACE 基因 I/D 多态性与膝骨关节炎之间的关联,我们进行了一项基于医院的病例对照研究,共纳入 282 例膝骨关节炎患者和 316 例对照,以探讨 ACE 基因 I/D 多态性与中国汉族人群膝骨关节炎易感性之间的关系。本研究发现,ACE 基因 I/D 多态性的 DD 基因型或 D 等位基因携带者增加了膝骨关节炎的风险。对性别、年龄和体重指数(BMI)进行分层分析显示,在女性、≥55 岁和 BMI 异常的组中存在显著相关性。此外,本研究还分析了 ACE I/D 多态性与 OA 一些临床特征之间的关系,发现 I/D 多态性的 DD 基因型与关节痛有关。此外,我们还与本研究一起进行了一项关于该单核苷酸多态性(SNP)与膝骨关节炎风险的荟萃分析。该荟萃分析发现,ACE 基因 I/D 多态性与 OA 风险增加相关。在该荟萃分析的种族分层分析中,I/D 多态性增加了亚洲人和白种人患膝骨关节炎的风险。总之,本病例对照研究和荟萃分析表明,ACE 基因 I/D 多态性与膝骨关节炎的风险增加有关。