Department of Nutrition, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, 27599, USA; AdventHealth Translational Research Institute, Orlando, 32804, USA.
Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, 27599, USA.
Nutr Metab Cardiovasc Dis. 2023 Feb;33(2):388-398. doi: 10.1016/j.numecd.2022.11.017. Epub 2022 Nov 17.
Disordered eating (DE) in type 1 diabetes (T1D) includes insulin restriction for weight loss with serious complications. Gut microbiota-derived short chain fatty acids (SCFA) may benefit host metabolism but are reduced in T1D. We evaluated the hypothesis that DE and insulin restriction were associated with reduced SCFA-producing gut microbes, SCFA, and intestinal microbial diversity in adults with T1D.
We collected stool samples at four timepoints in a hypothesis-generating gut microbiome pilot study ancillary to a weight management pilot in young adults with T1D. 16S ribosomal RNA gene sequencing measured the normalized abundance of SCFA-producing intestinal microbes. Gas-chromatography mass-spectrometry measured SCFA (total, acetate, butyrate, and propionate). The Diabetes Eating Problem Survey-Revised (DEPS-R) assessed DE and insulin restriction. Covariate-adjusted and Bonferroni-corrected generalized estimating equations modeled the associations. COVID-19 interrupted data collection, so models were repeated restricted to pre-COVID-19 data. Data were available for 45 participants at 109 visits, which included 42 participants at 65 visits pre-COVID-19. Participants reported restricting insulin "At least sometimes" at 53.3% of visits. Pre-COVID-19, each 5-point DEPS-R increase was associated with a -0.34 (95% CI -0.56, -0.13, p = 0.07) lower normalized abundance of genus Anaerostipes; and the normalized abundance of Lachnospira genus was -0.94 (95% CI -1.5, -0.42), p = 0.02 lower when insulin restriction was reported "At least sometimes" compared to "Rarely or Never".
DE and insulin restriction were associated with a reduced abundance of SCFA-producing gut microbes pre-COVID-19. Additional studies are needed to confirm these associations to inform microbiota-based therapies in T1D.
1 型糖尿病(T1D)中的饮食障碍(DE)包括为减轻体重而限制胰岛素,这会带来严重的并发症。肠道微生物衍生的短链脂肪酸(SCFA)可能有益于宿主代谢,但在 T1D 中会减少。我们评估了这样一个假设,即在 T1D 成人中,DE 和胰岛素限制与产生 SCFA 的肠道微生物减少、SCFA 减少和肠道微生物多样性减少有关。
我们在一项针对年轻 T1D 成人的体重管理试验的辅助性肠道微生物组先导研究中,在四个时间点收集了粪便样本。16S 核糖体 RNA 基因测序测量了产生 SCFA 的肠道微生物的归一化丰度。气相色谱-质谱法测量了 SCFA(总、乙酸盐、丁酸盐和丙酸盐)。糖尿病饮食问题调查修订版(DEPS-R)评估了 DE 和胰岛素限制。协变量调整和 Bonferroni 校正的广义估计方程对关联进行建模。由于 COVID-19 中断了数据收集,因此仅对 COVID-19 前的数据重复了模型。在 109 次就诊中,有 45 名参与者的数据可用,其中包括 42 名参与者在 COVID-19 前的 65 次就诊中有数据。参与者报告在 53.3%的就诊中“至少有时”限制胰岛素。在 COVID-19 前,DEPS-R 每增加 5 分,与产生 Anaerostipes 属的归一化丰度降低 0.34(95%CI -0.56,-0.13,p=0.07)相关;当报告“至少有时”而不是“很少或从不”限制胰岛素时,Lachnospira 属的归一化丰度降低 0.94(95%CI -1.5,-0.42),p=0.02。
在 COVID-19 前,DE 和胰岛素限制与产生 SCFA 的肠道微生物丰度降低有关。需要进一步的研究来确认这些关联,以便为 T1D 提供基于微生物组的治疗。