Department of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Division of Joint Surgery and Sports Medicine, Department of Orthopedic Surgery, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Nutrients. 2023 Nov 15;15(22):4787. doi: 10.3390/nu15224787.
The prior observational research on the impact of polyunsaturated fatty acid (PUFA) supplementation on osteoarthritis (OA) patients had yielded inclusive outcomes. This study utilized the Mendelian randomization (MR) approach to explore potential causal relationships between PUFAs and OA. The MR study was performed using GWAS summary statistics for PUFAs, encompassing omega-3 and omega-6 fatty acids, and for knee OA (KOA) and hip OA (HOA). The primary inverse-variance-weighted (IVW) method and two supplementary MR approaches were used to establish robust causality. Heterogeneity and horizontal pleiotropy were assessed using Cochrane's Q and MR-Egger intercept tests. Additionally, a range of sensitivity analyses were conducted to strengthen the precision and reliability of the results. The IVW method indicated a potential genetic association between omega-3 fatty acids and KOA risk (odd ratio (OR) = 0.94, 95% confidence interval (CI): 0.89-1.00, = 0.048). No significant correlation was found between omega-3 levels and HOA. Moreover, genetically predicted higher levels of omega-6 fatty acids were associated with a decreased risk of KOA (OR = 0. 93, 95% CI: 0.86-1.00, = 0.041) and HOA (OR = 0.89, 95% CI: 0.82-0.96; = 0.003). The MR-Egger intercept evaluation showed no horizontal pleiotropy affecting the MR analysis (all > 0.05). Our findings supported the causal relationship between PUFAs and OA susceptibility and offered a novel insight that high omega-6 fatty acids may reduce the risk of KOA and HOA. These results underscore the importance of maintaining optimal levels of PUFAs, particularly omega-6 fatty acids, in individuals with a genetic predisposition to OA. Future research is necessary to validate these findings and elucidate the underlying mechanisms involved.
先前关于多不饱和脂肪酸 (PUFA) 补充对骨关节炎 (OA) 患者影响的观察性研究结果不一。本研究采用孟德尔随机化 (MR) 方法探讨 PUFA 与 OA 之间潜在的因果关系。MR 研究使用了 PUFA(包括 omega-3 和 omega-6 脂肪酸)、膝关节骨关节炎 (KOA) 和髋关节骨关节炎 (HOA) 的 GWAS 汇总统计数据。主要采用逆方差加权 (IVW) 方法和两种补充性 MR 方法来建立稳健的因果关系。采用 Cochrane's Q 和 MR-Egger 截距检验评估异质性和水平多效性。此外,还进行了一系列敏感性分析,以增强结果的准确性和可靠性。IVW 方法表明 omega-3 脂肪酸与 KOA 风险之间存在潜在的遗传关联(比值比 (OR) = 0.94,95%置信区间 (CI):0.89-1.00, = 0.048)。omega-3 水平与 HOA 之间无显著相关性。此外,遗传预测的较高水平的 omega-6 脂肪酸与 KOA(OR = 0.93,95% CI:0.86-1.00, = 0.041)和 HOA(OR = 0.89,95% CI:0.82-0.96; = 0.003)风险降低相关。MR-Egger 截距评估表明,MR 分析不受水平多效性影响(均 > 0.05)。我们的研究结果支持了 PUFA 与 OA 易感性之间的因果关系,并提供了一个新的见解,即高 omega-6 脂肪酸可能降低 KOA 和 HOA 的风险。这些结果强调了维持 PUFA,特别是 omega-6 脂肪酸,在具有 OA 遗传易感性个体中最佳水平的重要性。需要进一步的研究来验证这些发现并阐明相关的潜在机制。