Department of Internal and Vascular Medicine, Amsterdam University Medical Centers, 1105 AZ Amsterdam, The Netherlands.
HorAIzon BV, 2625 GZ Delft, The Netherlands.
Nutrients. 2021 Sep 21;13(9):3289. doi: 10.3390/nu13093289.
It is currently unknown whether associations between gut microbiota composition and type 2 diabetes (T2D) differ according to the ethnic background of individuals. Thus, we studied these associations in participants from two ethnicities characterized by a high T2D prevalence and living in the same geographical area, using the Healthy Life In Urban Settings (HELIUS) study. We included 111 and 128 T2D participants on metformin (Met-T2D), 78 and 49 treatment-naïve T2D (TN-T2D) participants, as well as a 1:1 matched group of healthy controls from, respectively, African Surinamese and South-Asian Surinamese descent. Fecal microbiome profiles were obtained through 16S rRNA gene sequencing. Univariate and machine learning analyses were used to explore the associations between T2D and the composition and function of the gut microbiome in both ethnicities, comparing Met-T2D and TN-T2D participants to their respective healthy control. We found a lower α-diversity for South-Asian Surinamese TN-T2D participants but no significant associations between TN-T2D status and the abundance of bacterial taxa or functional pathways. In African Surinamese participants, we did not find any association between TN-T2D status and the gut microbiome. With respect to Met-T2D participants, we identified several bacterial taxa and functional pathways with a significantly altered abundance in both ethnicities. More alterations were observed in South-Asian Surinamese. Some altered taxa and pathways observed in both ethnicities were previously related to metformin use. This included a strong negative association between the abundance of and Met-T2D status. Other bacterial taxa were consistent with previous observations in T2D, including reduced butyrate producers such as . Hence, our results highlighted both shared and unique gut microbial biomarkers of Met-T2D in individuals from different ethnicities but living in the same geographical area. Future research using higher-resolution shotgun sequencing is needed to clarify the role of ethnicity in the association between T2D and gut microbiota composition.
目前尚不清楚肠道微生物组成与 2 型糖尿病(T2D)之间的关联是否因个体的种族背景而异。因此,我们使用 Healthy Life In Urban Settings(HELIUS)研究,在具有高 T2D 患病率且生活在同一地理区域的两种族裔参与者中研究了这些关联。我们纳入了分别来自非洲苏里南裔和南亚苏里南裔的 111 名和 128 名接受二甲双胍(Met-T2D)治疗的 T2D 患者、78 名和 49 名未经治疗的 T2D(TN-T2D)患者,以及各自的 1:1 匹配健康对照组。通过 16S rRNA 基因测序获得粪便微生物组谱。使用单变量和机器学习分析来探索两种族裔中 T2D 与肠道微生物组组成和功能之间的关联,将 Met-T2D 和 TN-T2D 参与者与各自的健康对照组进行比较。我们发现南亚苏里南裔 TN-T2D 参与者的 α-多样性较低,但 TN-T2D 状态与细菌分类群或功能途径的丰度之间没有显著关联。在非洲苏里南裔参与者中,我们没有发现 TN-T2D 状态与肠道微生物组之间存在任何关联。对于 Met-T2D 参与者,我们在两个种族中都发现了一些细菌分类群和功能途径的丰度发生了显著改变。在南亚苏里南裔中观察到更多的改变。在两个种族中观察到的一些改变的分类群和途径与二甲双胍的使用有关。这包括在丰度上与 Met-T2D 状态之间存在强烈的负相关。其他细菌分类群与 T2D 的先前观察结果一致,包括减少的丁酸产生菌,如 。因此,我们的研究结果突出了来自不同种族但生活在同一地理区域的 Met-T2D 个体的肠道微生物生物标志物的共享和独特性。需要使用更高分辨率的 shotgun 测序进行进一步研究,以阐明种族在 T2D 与肠道微生物组成之间的关联中的作用。