Oxford Brookes Centre for Nutrition and Health (OxBCNH), Department of Sport, Health Sciences and Social Work, Faculty of Health and Life Sciences, Oxford Brookes University, OxfordOX3 0BP, UK.
Nutritional Health Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran.
Br J Nutr. 2024 Apr 14;131(7):1225-1235. doi: 10.1017/S000711452300288X. Epub 2023 Dec 19.
Niacin has been investigated for its potential impact on lipid metabolism and cardiovascular health. This meta-analysis aims to systematically evaluate the effects of niacin interventions on apo A1 and apo B levels, key regulators of lipoprotein metabolism and markers of cardiovascular risk. A comprehensive search of the literature was performed on five databases of PubMed, Scopus, Web of Science, Embase and Cochrane library, from inception up to 15 July 2023. This search identified 1452 publications, from which twelve randomised controlled trials met the inclusion criteria. The intervention dosages ranged from 500 to 3000 mg/d, and the study durations spanned from 6 to 102·8 weeks. The niacin intervention demonstrated a significant reduction in apo B levels (weighted mean differences (WMD): -24·37 mg/dl, = 0·01). Subgroup analyses indicated that intervention duration played a role, with trials of ≤ 16 weeks showing a greater reduction in apo B. Regarding apo A1, niacin significantly increased its levels (WMD: 8·23 mg/dl, < 0·001). Subgroup analyses revealed that the beneficial effects of niacin on apo A1 were observed at a dosage of > 1500 mg/d ( < 0·001), and extended-release niacin was more effective compared with other forms ( < 0·001). According to the Begg's regression test, no publication bias was observed in this systematic review and meta-analysis. This meta-analysis highlights niacin's potential role in improving lipid profiles and cardiovascular health. Further well-designed clinical trials are needed to elucidate and confirm optimal dosages and durations of niacin interventions for influencing apo A1 and B.
烟酸已被研究其对脂质代谢和心血管健康的潜在影响。本荟萃分析旨在系统评估烟酸干预对载脂蛋白 A1 和载脂蛋白 B 水平的影响,载脂蛋白 A1 和载脂蛋白 B 是脂蛋白代谢的关键调节剂和心血管风险的标志物。我们在五个数据库(PubMed、Scopus、Web of Science、Embase 和 Cochrane library)中全面检索了文献,检索时间从建库到 2023 年 7 月 15 日。此次检索共识别出 1452 篇文献,其中 12 项随机对照试验符合纳入标准。干预剂量范围为 500 至 3000mg/d,研究持续时间为 6 至 102.8 周。烟酸干预显著降低了载脂蛋白 B 水平(加权均数差(WMD):-24.37mg/dl, = 0.01)。亚组分析表明,干预持续时间发挥了作用,≤16 周的试验显示载脂蛋白 B 降低幅度更大。关于载脂蛋白 A1,烟酸显著增加了其水平(WMD:8.23mg/dl, < 0.001)。亚组分析显示,烟酸对载脂蛋白 A1 的有益作用出现在剂量>1500mg/d( < 0.001)时,与其他形式相比,缓释烟酸更为有效( < 0.001)。根据贝叶斯回归检验,本系统评价和荟萃分析未观察到发表偏倚。本荟萃分析强调了烟酸在改善血脂谱和心血管健康方面的潜在作用。需要进一步设计良好的临床试验来阐明和证实烟酸干预影响载脂蛋白 A1 和 B 的最佳剂量和持续时间。