(1)Be Active Sleep and Eat (BASE) Facility, Department of Nutrition, Dietetics and Food, Monash University, Notting Hill, Australia.
(2)Department of Gastroenterology, Central Clinical School, Monash University and Alfred Hospital, Melbourne, Victoria, Australia.
J Acad Nutr Diet. 2021 May;121(5):895-914. doi: 10.1016/j.jand.2020.12.002. Epub 2021 Jan 9.
Acetic acid is a short-chain fatty acid that has demonstrated biomedical potential as a dietary therapeutic agent for the management of chronic and metabolic illness comorbidities. In human beings, its consumption may improve glucose regulation and insulin sensitivity in individuals with cardiometabolic conditions and type 2 diabetes mellitus. Published clinical trial evidence evaluating its sustained supplementation effects on metabolic outcomes is inconsistent.
This systematic review and meta-analysis summarized available evidence on potential therapeutic effects of dietary acetic acid supplementation via consumption of acetic acid-rich beverages and food sources on metabolic and anthropometric outcomes.
A systematic search was conducted in Medline, Scopus, EMBASE, CINAHL Plus, and Web of Science from database inception until October 2020. Randomized controlled trials conducted in adults evaluating the effect of dietary acetic acid supplementation for a minimum of 1 week were included. Meta-analyses were performed using a random-effects model on fasting blood glucose (FBG), triacylglycerol (TAG), high-density lipoprotein (HDL), low-density lipoprotein (LDL), glycated hemoglobin (HbA1c), body mass index (BMI), and body fat percentage. Statistical heterogeneity was assessed by calculation of Q and I statistics, and publication bias was assessed by calculation of Egger's regression asymmetry and Begg's test.
Sixteen studies were included, involving 910 participants who consumed between 750 and 3600 mg acetic acid daily in interventions lasting an average of 8 weeks. Dietary acetic acid supplementation resulted in significant reductions in TAG concentrations in overweight and obese but otherwise healthy individuals (mean difference [MD] = -20.51 mg/dL [95% confidence intervals = -32.98, -8.04], P = .001) and people with type 2 diabetes (MD = -7.37 mg/dL [-10.15, -4.59], P < .001). Additionally, acetic acid supplementation significantly reduced FBG levels (MD = -35.73 mg/dL [-63.79, -7.67], P = .01) in subjects with type 2 diabetes compared with placebo and low-dose comparators. No other changes were seen for other metabolic or anthropometric outcomes assessed. Five of the 16 studies did not specify the dose of acetic acid delivered, and no studies measured blood acetate concentrations. Only one study controlled for background acetic acid-rich food consumption during intervention periods. Most studies had an unclear or high risk of bias.
Supplementation with dietary acetic acid is well tolerated, has no adverse side effects, and has clinical potential to reduce plasma TAG and FBG concentrations in individuals with type 2 diabetes, and to reduce TAG levels in people who are overweight or obese. No significant effects of dietary acetic acid consumption were seen on HbA1c, HDL, or anthropometric markers. High-quality, longer-term studies in larger cohorts are required to confirm whether dietary acetic acid can act as an adjuvant therapeutic agent in metabolic comorbidities management.
乙酸是一种短链脂肪酸,已被证明具有作为膳食治疗剂用于管理慢性和代谢疾病合并症的生物医学潜力。在人类中,其摄入可能会改善患有心脏代谢疾病和 2 型糖尿病的个体的葡萄糖调节和胰岛素敏感性。已发表的评估其持续补充对代谢结果影响的临床试验证据并不一致。
本系统评价和荟萃分析总结了通过食用富含乙酸的饮料和食物来源来补充膳食乙酸对代谢和人体测量结果的潜在治疗效果的现有证据。
从数据库建立到 2020 年 10 月,在 Medline、Scopus、EMBASE、CINAHL Plus 和 Web of Science 中进行了系统搜索。纳入了至少 1 周内评估膳食乙酸补充对代谢影响的成年人的随机对照试验。使用随机效应模型对空腹血糖(FBG)、三酰甘油(TAG)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、糖化血红蛋白(HbA1c)、体重指数(BMI)和体脂百分比进行荟萃分析。通过计算 Q 和 I 统计量评估统计异质性,并通过计算 Egger 回归不对称和 Begg 检验评估发表偏倚。
纳入了 16 项研究,涉及 910 名参与者,他们在平均持续 8 周的干预中每天摄入 750 至 3600 毫克乙酸。膳食乙酸补充对超重和肥胖但健康的个体(平均差异 [MD] = -20.51mg/dL [95%置信区间 = -32.98,-8.04],P =.001)和 2 型糖尿病患者(MD = -7.37mg/dL [-10.15,-4.59],P <.001)的 TAG 浓度有显著降低。此外,与安慰剂和低剂量对照相比,乙酸补充可显著降低 2 型糖尿病患者的 FBG 水平(MD = -35.73mg/dL [-63.79,-7.67],P =.01)。未观察到其他代谢或人体测量结果的变化。16 项研究中有 5 项未具体说明提供的乙酸剂量,也没有研究测量血液乙酸浓度。只有一项研究在干预期间控制了背景富含乙酸的食物摄入。大多数研究的偏倚风险为不确定或高。
膳食乙酸补充剂耐受性良好,无不良反应,具有降低 2 型糖尿病患者血浆 TAG 和 FBG 浓度以及降低超重或肥胖个体 TAG 水平的临床潜力。膳食乙酸摄入对 HbA1c、HDL 或人体测量标志物没有显著影响。需要高质量、长期的更大规模队列研究来证实膳食乙酸是否可以作为代谢合并症管理的辅助治疗剂。