Department of Toxicology and Nutrition, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, China.
Department of Nutrition, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
Food Funct. 2021 Jan 7;12(1):30-40. doi: 10.1039/d0fo01976c. Epub 2020 Nov 24.
The purpose of the systematic review and meta-analysis was to determine if low-ratio n-6/n-3 long-chain polyunsaturated fatty acid (PUFA) supplementation affects serum inflammation markers based on the current studies.
PubMed, Embase and The Cochrane library databases were systematically searched to find randomized controlled trials (RCTs) on the effect of low-ratio n-6/n-3 PUFA intervention on inflammation markers up to July 2020. Data were pooled using standardized mean difference (SMD) and 95% confidence intervals (95% CI), with P value ≦ 0.05 as statistical significance.
Thirty-one RCTs were included in the meta-analysis. The analysis indicated that increasing low-ratio n-6/n-3 PUFA supplementation decreased the level of tumor necrosis factor-α (TNF-α) (SMD = -0.270; 95% CI: -0.433, -0.106; P = 0.001) and interleukin 6 (IL-6) (SMD = -0.153; 95% CI: -0.260, -0.045; P = 0.005). There were no significant effects on C-reactive protein (CRP) (SMD = -0.027; 95% CI: -0.189: 0.135; P = 0.741). Subgroup analysis indicated that there was a significant reduction in TNF-α serum concentration in subjects from Asia (SMD: -0.367; 95% CI: -0.579, -0.155; P = 0.001) and in subjects with diseases (SMD: -0.281; 95% CI: -0.436, -0.127; P < 0.001). In the subgroup of the n-6/n-3 ratio ≦5, low-ratio n-6/n-3 PUFA supplementation could decrease the level of TNF-α (SMD: -0.335; 95% CI: -0.552, -0.119; P = 0.002). Serum IL-6 decreased significantly in patients from the Europe subgroup (SMD: -0.451; 95% CI: -0.688, -0.214; P < 0.001), but not in Asia (SMD: -0.034; 95% CI: -0.226, 0.157; P = 0.724), North America (SMD: -0.115; 95% CI: -0.274, 0.044; P = 0.157) and Oceania (SMD: 0.142; 95% CI: -0.557, 0.842; P = 0.690).
Low-ratio n-6/n-3 PUFA supplementation could decrease significantly the concentration of serum TNF-α and IL-6, but not decrease CRP concentration.
本系统评价和荟萃分析的目的是根据现有研究确定低 n-6/n-3 长链多不饱和脂肪酸(PUFA)比值补充是否会影响血清炎症标志物。
系统检索 PubMed、Embase 和 The Cochrane library 数据库,以查找截至 2020 年 7 月关于低 n-6/n-3 PUFA 干预对炎症标志物影响的随机对照试验(RCT)。使用标准化均数差(SMD)和 95%置信区间(95%CI)合并数据,P 值≤0.05 为统计学意义。
荟萃分析纳入了 31 项 RCT。分析表明,增加低 n-6/n-3 PUFA 补充可降低肿瘤坏死因子-α(TNF-α)水平(SMD=-0.270;95%CI:-0.433,-0.106;P=0.001)和白细胞介素 6(IL-6)(SMD=-0.153;95%CI:-0.260,-0.045;P=0.005)。对 C-反应蛋白(CRP)(SMD=-0.027;95%CI:-0.189:0.135;P=0.741)没有显著影响。亚组分析表明,亚洲人群的 TNF-α 血清浓度明显降低(SMD:-0.367;95%CI:-0.579,-0.155;P=0.001),疾病患者的 TNF-α 血清浓度明显降低(SMD:-0.281;95%CI:-0.436,-0.127;P<0.001)。在 n-6/n-3 比值≤5 的亚组中,低 n-6/n-3 PUFA 补充可降低 TNF-α 水平(SMD:-0.335;95%CI:-0.552,-0.119;P=0.002)。欧洲亚组的患者血清 IL-6 明显下降(SMD:-0.451;95%CI:-0.688,-0.214;P<0.001),但亚洲亚组(SMD:-0.034;95%CI:-0.226,0.157;P=0.724)、北美亚组(SMD:-0.115;95%CI:-0.274,0.044;P=0.157)和大洋洲亚组(SMD:0.142;95%CI:-0.557,0.842;P=0.690)则无明显变化。
低 n-6/n-3 PUFA 补充可显著降低血清 TNF-α 和 IL-6 浓度,但不能降低 CRP 浓度。