The role of obesity in altering the effects of short chain fatty acids (SCFA) on metabolic hormone regulation: A systematic review and meta-analysis

Q3 Nursing
Andi Faradilah , Agussalim Bukhari , Aminuddin Aminuddin , Andi Yasmin Syauki
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引用次数: 0

Abstract

Background

Current studies suggest that supplementing SCFA producers may have beneficial effects in preventing and treating obesity. Plasma SCFAs play a significant role in modulating metabolic hormones, thereby positively influencing metabolism. This review explores the connection between plasma SCFAs and metabolic hormones associated with obesity.

Methods

We collected data from PubMed, EBSCO, and EMBASE using MESH keywords [(short-chain fatty acids) AND (overweight OR obesity OR obese) AND (GLP-1) OR (glucagon-like peptide 1) OR (insulin) OR (ghrelin) OR (leptin) OR (PYY)]. Studies published between 2012 and 2024 were included, involving both genders, filtered for human studies, and published in English. Studies without full-text access were excluded. Risk of bias was assessed using the ROB-2 tool for clinical trials and the Joanna Briggs Institute (JBI) Critical Appraisal Tools for cohort and cross-sectional studies. This study was registered in PROSPERO with the number CRD42021284687.

Results

We identified 52 studies, comprising a total of 3,552 overweight or obese individuals, including adults (aged 18–78 years) and adolescents (aged 11–12 years), that met the inclusion criteria. These studies reported on circulating SCFAs, GLP-1, PYY, insulin, leptin, and ghrelin. We found no significant differences in acetate (-2.05 [-37.54, 33.44]), propionate (-0.17 [-3.28, 2.93]), butyrate (-0.23 [1.46, 1.00]), GLP-1 (-0.36 [-1.36, 0.64]), or insulin (1.71 [-9.65, 13.06]) between the placebo and intervention groups in the clinical trials. However, PYY levels showed a significant difference (-0.91 [-1.64, -0.71]) in the placebo compared to the intervention group. Methodological variations prevented us from assessing leptin and ghrelin levels, as well as analyzing observational studies related to SCFAs and metabolic hormones. The impact of dietary fiber, SCFA infusion, prebiotic supplementation, and dietary modifications varied concerning GLP-1, PYY, and insulin. We hypothesize that the characteristics of the intervention and participant variability regarding obesity and its comorbidities influenced the study outcomes.

Conclusion

The dietary intervention had no effect on plasma SCFAs and metabolic hormones, considering obesity-related conditions. We recommend that future research investigate mediating variables when exploring the association between plasma SCFAs and metabolic hormones in obesity.
肥胖在改变短链脂肪酸(SCFA)对代谢激素调节的作用中的作用:一项系统综述和荟萃分析
背景:目前的研究表明,补充短链脂肪酸可能对预防和治疗肥胖有有益的作用。血浆SCFAs在调节代谢激素中发挥重要作用,从而积极影响代谢。这篇综述探讨了血浆SCFAs与肥胖相关的代谢激素之间的联系。方法采用MESH关键词[(短链脂肪酸)和(超重或肥胖或肥胖)和(GLP-1)或(胰高血糖素样肽1)或(胰岛素)或(胃饥饿素)或(瘦素)或(PYY)]从PubMed、EBSCO和EMBASE中收集数据。2012年至2024年间发表的研究被纳入其中,涉及男女,经过筛选以进行人类研究,并以英语发表。未获得全文的研究被排除在外。使用rob2工具对临床试验和乔安娜布里格斯研究所(JBI)关键评估工具对队列和横断面研究进行偏倚风险评估。本研究已在PROSPERO注册,编号为CRD42021284687。结果我们确定了52项研究,共包括3552名超重或肥胖个体,包括成人(18-78岁)和青少年(11-12岁),符合纳入标准。这些研究报告了循环SCFAs、GLP-1、PYY、胰岛素、瘦素和胃饥饿素。我们发现在临床试验中,安慰剂组和干预组在醋酸盐(-2.05[-37.54,33.44])、丙酸盐(-0.17[-3.28,2.93])、丁酸盐(-0.23[1.46,1.00])、GLP-1(-0.36[-1.36, 0.64])和胰岛素(1.71[-9.65,13.06])方面无显著差异。然而,与干预组相比,安慰剂组PYY水平有显著差异(-0.91[-1.64,-0.71])。方法上的差异使我们无法评估瘦素和胃饥饿素水平,也无法分析与SCFAs和代谢激素相关的观察性研究。膳食纤维、短链脂肪酸输注、益生元补充和饮食调整对GLP-1、PYY和胰岛素的影响各不相同。我们假设干预的特点和参与者肥胖及其合并症的可变性影响了研究结果。结论考虑到肥胖相关情况,饮食干预对血浆SCFAs和代谢激素无影响。我们建议未来的研究在探讨血浆SCFAs与肥胖代谢激素之间的关系时,研究中介变量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Nutrition Open Science
Clinical Nutrition Open Science Nursing-Nutrition and Dietetics
CiteScore
2.20
自引率
0.00%
发文量
55
审稿时长
18 weeks
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