Division of Pediatric and Public Health, Adams School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
J Pain. 2022 Oct;23(10):1724-1736. doi: 10.1016/j.jpain.2022.05.008. Epub 2022 Jun 10.
Preclinical studies demonstrate opposing effects of long-chain polyunsaturated fatty acid (PUFA) metabolites on inflammation and nociception. Omega-6 (n-6) PUFAs amplify both processes while omega-3 (n-3) PUFAs inhibit them. This cross-sectional study examined relationships between PUFAs in circulating erythrocytes and 2 chronic idiopathic pain conditions: temporomandibular disorder (TMD) and low back pain in a community-based sample of 503 U.S. adults. Presence or absence of TMD and low back pain, respectively, were determined by clinical examination and by responses to established screening questions. Liquid chromatography-tandem mass spectrometry quantified PUFAs. In multivariable logistic regression models, a higher ratio of n-6/n-3 long-chain PUFAs was associated with greater odds of TMD (odds ratio ((OR) = 1.75, 95% confidence limits (CL): 1.16, 2.64) and low back pain (OR = 1.63, 95% CL: 1.07, 2.49). Higher levels of the pronociceptive n-6 long-chain arachidonic acid (AA) were associated with a greater probability of both pain conditions for women, but not men. Higher levels of the antinociceptive long-chain n-3 PUFAs eicosapentaenoic and docosahexaenoic acids were associated with a lower probability of both pain conditions for men, but not women. As systemic inflammation is not a hallmark of these conditions, PUFAs may influence idiopathic pain through other mechanisms. PERSPECTIVE: This cross-sectional clinical study found that a higher ratio of circulating n-6/n-3 long-chain PUFAs was associated with greater odds of 2 common chronic overlapping pain conditions. This suggests that the pro and antinociceptive properties of n-6 and n-3 PUFAs, respectively, influence pain independently of their well-established inflammatory pathways.
临床前研究表明,长链多不饱和脂肪酸(PUFA)代谢物对炎症和痛觉过敏有相反的影响。ω-6(n-6)PUFA 放大这两个过程,而 ω-3(n-3)PUFA 则抑制它们。本横断面研究检查了循环红细胞中 PUFAs 与两种常见慢性重叠性疼痛状况之间的关系:颞下颌关节紊乱症(TMD)和下腰痛,研究对象是美国 503 名成年人的社区样本。TMD 和下腰痛的存在与否分别通过临床检查和对既定筛查问题的回答来确定。液相色谱-串联质谱法定量了 PUFAs。在多变量逻辑回归模型中,n-6/n-3 长链 PUFAs 比值较高与 TMD(比值比(OR)=1.75,95%置信区间(CL):1.16,2.64)和下腰痛(OR=1.63,95%CL:1.07,2.49)的可能性更大相关。促痛觉 n-6 长链花生四烯酸(AA)水平较高与女性两种疼痛状况的可能性更大相关,但与男性无关。镇痛性长链 n-3 PUFAs 二十碳五烯酸和二十二碳六烯酸水平较高与男性两种疼痛状况的可能性较小相关,但与女性无关。由于系统性炎症不是这些疾病的特征,因此 PUFAs 可能通过其他机制影响特发性疼痛。观点:这项横断面临床研究发现,循环中 n-6/n-3 长链 PUFAs 比值较高与两种常见慢性重叠性疼痛状况的可能性更大相关。这表明,n-6 和 n-3 PUFAs 的促和抗痛觉特性分别独立于其既定的炎症途径影响疼痛。