Department of Pelvic and Acetabular Surgery, HongHui Hospital, Xi'an Jiaotong University, Xi'an, China.
Sci Rep. 2024 Oct 10;14(1):23716. doi: 10.1038/s41598-024-73205-1.
Growing research has suggested an association between chronic inflammation and Intervertebral disc degeneration (IVDD), but whether there is a causal effect remains unknown. This study adopted two-sample Mendelian randomization (MR) approach to explore the etiological role of chronic inflammation in IVDD risk. Here, summary statistics for C-reactive protein (CRP), interleukin (IL)-1 , IL-1 , IL-6 expression and IVDD were obtained from genome-wide association studies (GWAS) of European ancestry. MR analyses were conducted by using inverse variance weighted (IVW), Wald Ratio, weighted median, and MR-Egger method. Sensitivity analyses were conducted to assess the robustness of the results. The MR analyses suggested a lack of causal association of CRP, IL-6 , and IL-1 levels on IVDD (CRP-IVDD: odds ratio [OR] = 0.97, 95% confidence interval [CI] 0.86-1.09, P = 0.583; IL-6-IVDD: OR = 1.04, 95% CI 0.86-1.27, P = 0.679; IL-1 -IVDD: OR = 1.09, 95%CI 1.00-1.18, P = 0.058). However, there was a sign of a connection between genetically elevated IL-1 levels and a decreased IVDD incidence (OR = 0.87, 95%CI 0.77-0.99, P = 0.03). Our findings suggest a connection between IL-1 levels and the risk of IVDD. However, due to the support of only one SNP, heterogeneity and pleiotropy tests cannot be performed, the specific underlying mechanisms warrant further investigation.
越来越多的研究表明,慢性炎症与椎间盘退变(IVDD)之间存在关联,但因果关系尚不清楚。本研究采用两样本 Mendelian 随机化(MR)方法探讨慢性炎症在 IVDD 风险中的病因作用。这里,从欧洲血统的全基因组关联研究(GWAS)中获得了 C 反应蛋白(CRP)、白细胞介素(IL)-1 、IL-1 、IL-6 表达和 IVDD 的汇总统计数据。采用逆方差加权(IVW)、 Wald 比值、加权中位数和 MR-Egger 方法进行 MR 分析。进行敏感性分析以评估结果的稳健性。MR 分析表明,CRP、IL-6 和 IL-1 水平与 IVDD 之间不存在因果关联(CRP-IVDD:比值比 [OR] = 0.97,95%置信区间 [CI] 0.86-1.09,P = 0.583;IL-6-IVDD:OR = 1.04,95%CI 0.86-1.27,P = 0.679;IL-1 -IVDD:OR = 1.09,95%CI 1.00-1.18,P = 0.058)。然而,遗传上升高的 IL-1 水平与 IVDD 发生率降低之间存在关联的迹象(OR = 0.87,95%CI 0.77-0.99,P = 0.03)。我们的研究结果表明 IL-1 水平与 IVDD 风险之间存在关联。然而,由于仅支持一个 SNP,无法进行异质性和多效性检验,具体的潜在机制需要进一步研究。