“…At present, many genes are reported to be related to the occurrence and development of OA by increasing susceptibility, enhancing cartilaginous matrix degradation, preventing cartilage from repair, increasing the expression of inflammatory factors, or promoting fibroblast transformation. First, the susceptibility genes of OA mainly include ASPN ( Wang et al, 2018 ), ADIPOQ ( Shang et al, 2019 ), AKNA ( Zhao et al, 2020a ), DPEP1 ( Zhang et al, 2021a ), rs1065080 ( Lu et al, 2019a ), TLR7 ( Wang et al, 2020a ), RTP4 ( Wang et al, 2020a ), CRIP1 ( Wang et al, 2020a ), ZNF688 ( Wang et al, 2020a ), TOP1 ( Wang et al, 2020a ), EIF1AY ( Wang et al, 2020a ), RAB2A ( Wang et al, 2020a ), ZNF281 ( Wang et al, 2020a ), UIMC1 ( Wang et al, 2020a ), and PRKACB ( Zhao, 2021 ). Second, the genes that promote the degradation of cartilage mainly include ADAMTS5 ( Jiang et al, 2021 ), ADAM12 ( Lv et al, 2017 ), JUN ( Rhee et al, 2017 ), PTGS2 ( Zhou et al, 2019a ), MMP1 ( Zhou et al, 2019a ), MMP3 ( Zhou et al, 2019a ), MMP13 ( Zhou et al, 2019a ), AGT ( Wang et al, 2020b ), and rs2830585 ( Zhou et al, 2019b ).…”