Association between angiotensin-converting enzyme (ACE) gene I/D polymorphism with the risk of knee OA: A systematic review, meta-analysis, and meta-regression [version 1; peer review: awaiting peer review]

• Published in: F1000 research Vol. 13; p. 146
• Main Authors: Mustari, M. Nasser, Massi, Muh. Nasrum, Usman, Muh. Andry, Bukhari, Agussalim, Idris, Irfan, Zainuddin, Alfian, Adnan, Endy, Bakri, Syakib, Hatta, Mizwar, Rasyid, Haerani, Fikry, Achmad, Soetjipto, Audrey Suryani
• Format: Journal Article
• Language: English
• Published: England Faculty of 1000 Ltd 2024; F1000 Research Limited; F1000 Research Ltd
• Subjects: ACE; ACE protein; Angiotensin; Arthritis; Cartilage; Case-Control Studies; eng; Enzymes; Ethnicity; Female; Gene polymorphism; Genetic analysis; Genetic Association Studies; genetic models; Genetic Predisposition to Disease; Genotype & phenotype; Health care; Humans; INDEL Mutation; Knee; Male; Meta-analysis; Minority & ethnic groups; Nitric-oxide synthase; Osteoarthritis; Osteoarthritis, Knee - genetics; Peptidyl-dipeptidase A; Peptidyl-Dipeptidase A - genetics; Polymorphism; Polymorphism, Genetic; Population studies; Risk Factors; Systematic Review; South Korea; Turkey; Kuwait; China; Taiwan; India; knee; polymorphism; ACE; genetic models; osteoarthritis
• ISSN: 2046-1402; 2046-1402
• DOI: 10.12688/f1000research.140233.1

Background Previous studies have linked genetics to knee osteoarthritis. Angiotensin-converting enzyme (ACE) gene I/D polymorphism may cause OA. However, evidence remains inconsistent. This study examines knee OA risk and ACE gene I/D polymorphism. Methods We explored Europe PMC, Medline, Scopus, and Cochrane Library using keywords. Three assessment bias factors were assessed using the Newcastle-Ottawa Scale (NOS). Criteria for inclusion: (1) Split the study population into knee OA patients and healthy controls; (2) Analysed the ACE gene I/D polymorphism; (3) Case-control or cross-sectional surveys. Studies with non-knee OA, incomplete data, and no full-text were excluded. The odds ratio (OR) and 95% confidence intervals (95% CI) were calculated using random-effect models. Results A total of 6 case-control studies consist of 1,226 patients with knee OA and 1,145 healthy subjects as controls were included. Our pooled analysis revealed that a significant association between ACE gene I/D polymorphism and risk of knee OA was only seen in the dominant (DD + ID vs. II) [OR 1.69 (95% CI 1.14 - 2.50), p = 0.009, I2 = 72%], and ID vs. II [OR 1.37 (95% CI 1.01- 1.86), p = 0.04, I2 = 43%] genotype models. Other genotype models, including recessive (DD vs. ID + II), alleles (D vs. I), DD vs. ID, and DD vs. II models did not show a significant association with knee OA risk. Further regression analysis revealed that ethnicity and sex may influence those relationships in several genotype models. Conclusions Dominant and ID vs. II ACE gene I/D polymorphism models increased knee OA risk significantly. More research with larger samples and different ethnic groups is needed to confirm our findings. After ethnicity subgroup analysis, some genetic models in our study showed significant heterogeneities, and most studies are from Asian countries with Asian populations, with little evidence on Arabs.