Published online Jun 6, 2020. doi: 10.12998/wjcc.v8.i11.2280
Peer-review started: December 11, 2019
First decision: January 7, 2020
Revised: March 6, 2020
Accepted: April 24, 2020
Article in press: April 24, 2020
Published online: June 6, 2020
Processing time: 179 Days and 13.1 Hours
Osteoarthritis (OA) is the combined result of complex pathogenic factors, including mechanical, biochemical, environmental, endocrine, metabolic, and genetic factors, which account for nearly 50% of the risk of OA development. Although the pathogenesis and etiology of OA are not known, it is likely that interleukin-17 (IL-17) might play an important role in OA development.
To date, several studies have explored the relationship between polymorphisms of the IL-17 gene and OA susceptibility. The association between IL-17 gene single nucleotide polymorphisms and OA susceptibility may provide novel research directions for OA studies. However, the results of previous studies are inconclusive and conflicting due to clinical heterogeneity, different ethnic populations and small sample sizes.
We meta-analyzed relevant articles regarding the association between the polymorphisms of IL-17 gene and OA susceptibility.
We systematically conducted the literature search using the following electronic databases: PubMed, EMBASE, MEDLINE, Cochrane Library, and Google Scholar to identify epidemiological studies published up to September 2019 to retrieve genetic association studies on OA. Pooled odds ratios with 95% confidence intervals were calculated. Subgroup analyses were carried based on ethnicity and type of OA. Furthermore, false-positive report probability was conducted to evaluate the significant findings and rule out any false associations due to multiple tests.
In a total of 6 citations involving 8 studies (2131 cases and 2299 controls), 4 single nucleotide polymorphisms were identified. Of these 4 polymorphisms, 2 (rs2275913, rs763780) were common in five case-control studies. Together, the pooled results revealed that the A allele and genotype AA/GA of the rs2275913 polymorphism, and the C allele and genotype CC of the rs763780 polymorphism in the IL-17 gene increased the risk of OA. Furthermore, stratification analyses by ethnicity and OA type showed that the rs2275913 polymorphism increased the risk of OA among Asians and in knee/hip OA, respectively. In addition, stratification analyses also revealed that the rs763780 polymorphism increased OA risk among both Asians and Caucasians in knee/hip OA.
The rs763780 polymorphism of the IL-17F gene increased the risk of OA, whereas the rs2275913 polymorphism of the IL-17A gene increased the risk of OA only among Asians. Due to the limitations of this study, these findings should be validated in future studies.