Department of Clinical Dietetics, Faculty of Health Sciences, Medical University of Warsaw, E Ciołka 27, 01-445 Warsaw, Poland.
Mass Spectrometry Laboratory, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106 Warsaw, Poland.
Nutrients. 2024 Jan 16;16(2):266. doi: 10.3390/nu16020266.
The main objective of this cross-sectional study was to analyze the influence of lifestyle factors (diet, physical activity, sleep) that can affect the concentration of fecal short-chain fatty acids (SCFAs) and SCFAs' potential role in modulating cardiometabolic disease risk by interacting with biochemical and body composition parameters. The study comprised 77 healthy, non-obese individuals aged 30-45 years who were assessed for the concentration of SCFAs in stool, diet, physical activity level, and sleep duration. Moreover, body composition measurement and patients' biochemical parameters were included in the analysis. We have indicated a significant negative correlation between several SCFAs (especially acetic acid (AA), isobutyric acid (IBA), butyric acid (BA), propionic acid (PA), isovaleric acid (IVA) and valeric acid (VA)) with BMI, VAT/SAT ratio (visceral to subcutaneous fat ratio), and percentage of fat mass in a group of females enrolled in the study as well as with waist circumference (WC) in case of both sexes included in the study. Moreover, the results of our study acknowledged the importance of a diet in shaping the SCFA profile-we noticed significant negative associations between energy and fat intake and some SCFAs in males (IBA, IVA, VA, isocaproic acid (ICA)). Further, we indicated that a high intake of fiber (insoluble and soluble) in both males and females results in an elevated concentration of the vast majority of SCFAs and the amount of SCFAs in total. This effect was particularly noticeable in the case of the soluble fraction of fiber. These correlations reflect the fact that diet shapes the composition of the gut microbiota and SCFAs (main microbial metabolites) are synthesized from dietary fiber. In addition, we noticed that in a group of women, the concentration of AA, PA, and ICA as well as the total concentration of SCFAs showed a significant positive association with their sleep duration. We concluded that SCFAs can have a potential role in modulating cardiometabolic disease risk by interacting with adiposity parameters and diet. In addition, this potential direct link between diet and SCFAs may at least partly contribute to sleep improvement.
本横断面研究的主要目的是分析生活方式因素(饮食、体力活动、睡眠)对粪便短链脂肪酸(SCFA)浓度的影响,以及 SCFA 通过与生化和身体成分参数相互作用在调节心血管代谢疾病风险方面的潜在作用。该研究纳入了 77 名年龄在 30-45 岁之间的健康、非肥胖个体,评估了粪便中 SCFA 的浓度、饮食、体力活动水平和睡眠持续时间。此外,身体成分测量和患者的生化参数也包括在分析中。我们发现,在研究中纳入的一组女性中,几种 SCFA(特别是乙酸(AA)、异丁酸(IBA)、丁酸(BA)、丙酸(PA)、异戊酸(IVA)和戊酸(VA))与 BMI、VAT/SAT 比(内脏与皮下脂肪比)和脂肪质量百分比呈显著负相关,与研究中纳入的两性的腰围(WC)呈负相关。此外,我们的研究结果还承认了饮食在塑造 SCFA 谱方面的重要性——我们注意到能量和脂肪摄入与男性中一些 SCFA 之间存在显著的负相关(IBA、IVA、VA、异己酸(ICA))。此外,我们指出,男性和女性摄入高纤维(不溶性和可溶性)会导致绝大多数 SCFA 浓度升高,总 SCFA 浓度升高。这种影响在可溶性纤维部分尤为明显。这些相关性反映了饮食塑造肠道微生物群组成的事实,以及 SCFA(主要微生物代谢物)是从膳食纤维中合成的。此外,我们注意到,在一组女性中,AA、PA 和 ICA 的浓度以及 SCFA 的总浓度与她们的睡眠持续时间呈显著正相关。我们得出结论,SCFA 通过与肥胖参数和饮食相互作用,可能在调节心血管代谢疾病风险方面发挥潜在作用。此外,饮食和 SCFA 之间的这种潜在直接联系至少可以部分有助于改善睡眠。