Nutrition and Metabolic Diseases Research Center, Clinical Sciences Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran; Student Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Nutrition and Dietetics, University of North Florida, Jacksonville, FL, USA.
Cytokine. 2024 Jul;179:156608. doi: 10.1016/j.cyto.2024.156608. Epub 2024 Apr 16.
Mounting evidence revealed that an imbalance of Gut Microbiota (GM) leads to metabolic disorders. Synbiotics through regulation of GM composition can be an effective intervention in the management of metabolic diseases. This study aimed to investigate the effects of multi-species synbiotic supplementation on serum interleukin10 (IL-10) and fecal Short Chain Fatty Acids (SCFAs) in patients with dyslipidemia.
In this double-blind, randomized, placebo-controlled clinical trial, fifty-six adult men with dyslipidemia were randomly allocated to intervention and control groups and received either synbiotic or placebo powder twice a day for 12 weeks. Each synbiotic sachet contained 6 species of probiotic microorganisms with a total dose of 3 × 10 Colony Forming Unit (CFU) and 5 gr inulin and Fructooligosaccharide (FOS) as prebiotics. Blood and stool samples were collected at the baseline and end of the study. Dietary intake, physical activity, anthropometric measurements, serum IL-10, and fecal SCFAs were assessed before and after the intervention.
There were no significant differences between the baseline characteristics of patients in the two groups. Serum IL-10 was increased in the synbiotic group (p < 0.0001). Moreover, synbiotic supplementation increased fecal concentration of acetate (p < 0.0001), butyrate (p = 0.043), propionate (p < 0.0001), and valerate (p < 0.026). A significant positive correlation was observed between the changes in fecal butyrate level and serum IL-10 concentration in the control group (r = 0.48, p = 0.01).
A Twelve-week synbiotic supplementation increased fecal SCFAs and improved inflammation in adult men with dyslipidemia.
越来越多的证据表明,肠道微生物群(GM)失衡会导致代谢紊乱。通过调节 GM 组成,共生元可以成为代谢疾病管理的有效干预措施。本研究旨在探讨多菌种共生元补充对血脂异常患者血清白细胞介素 10(IL-10)和粪便短链脂肪酸(SCFAs)的影响。
在这项双盲、随机、安慰剂对照的临床试验中,56 名血脂异常的成年男性被随机分配到干预组和对照组,并每天接受两次共生元或安慰剂粉末,持续 12 周。每个共生元小袋包含 6 种益生菌微生物,总剂量为 3×10 菌落形成单位(CFU)和 5 克菊粉和低聚果糖(FOS)作为益生元。在研究开始和结束时采集血液和粪便样本。在干预前后评估饮食摄入、体力活动、人体测量学测量、血清 IL-10 和粪便 SCFAs。
两组患者的基线特征无显著差异。共生元组血清 IL-10 升高(p<0.0001)。此外,共生元补充增加了粪便乙酸盐(p<0.0001)、丁酸盐(p=0.043)、丙酸盐(p<0.0001)和戊酸盐(p<0.026)的浓度。对照组粪便丁酸水平的变化与血清 IL-10 浓度呈显著正相关(r=0.48,p=0.01)。
十二周共生元补充增加了粪便 SCFAs,并改善了血脂异常成年男性的炎症。