Women's and Children's Hospital, Adelaide, South Australia, Australia.
Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Pediatr Diabetes. 2021 May;22(3):425-433. doi: 10.1111/pedi.13178. Epub 2021 Feb 1.
We aimed to characterize associations between diet and the gut microbiome and short chain fatty acid (SCFA) products in youth with islet autoimmunity or type 1 diabetes (IA/T1D) in comparison with controls.
Eighty participants (25 diagnosed with T1D, 17 with confirmed IA, 38 sibling or unrelated controls) from the Australian T1D Gut Study cohort were studied (median [IQR] age 11.7 [8.9, 14.0] years, 43% female). A Food Frequency Questionnaire characterized daily macronutrient intake over the preceding 6 months. Plasma and fecal SCFA were measured by gas chromatography; gut microbiome composition and diversity by 16S rRNA gene sequencing.
A 10 g increase in daily carbohydrate intake associated with higher plasma acetate in IA/T1D (adjusted estimate +5.2 (95% CI 1.1, 9.2) μmol/L p = 0.01) and controls (adjusted estimate +4.1 [95% CI 1.7, 8.5] μmol/L p = 0.04). A 5 g increase in total fat intake associated with lower plasma acetate in IA/T1D and controls. A 5% increase in noncore (junk) food intake associated with reduced richness (adjusted estimate -4.09 [95%CI -7.83, -0.35] p = .03) and evenness (-1.25 [95% CI -2.00, -0.49] p < 0.01) of the gut microbiome in IA/T1D. Fiber intake associated with community structure of the microbiome in IA/T1D.
Modest increments in carbohydrate and fat intake associated with plasma acetate in all youth. Increased junk food intake associated with reduced diversity of the gut microbiome in IA/T1D alone. These associations with the gut microbiome in IA/T1D support future efforts to promote SCFA by using dietary interventions.
我们旨在比较胰岛自身免疫或 1 型糖尿病(IA/T1D)患儿与对照组之间饮食与肠道微生物组和短链脂肪酸(SCFA)产物之间的关联。
对来自澳大利亚 T1D 肠道研究队列的 80 名参与者(25 名确诊为 T1D,17 名确认为 IA,38 名兄弟姐妹或无亲缘关系的对照组)进行了研究(中位[IQR]年龄 11.7[8.9,14.0]岁,43%为女性)。食物频率问卷用于评估过去 6 个月的日常宏量营养素摄入量。通过气相色谱法测量血浆和粪便中的 SCFA;通过 16S rRNA 基因测序测量肠道微生物组的组成和多样性。
IA/T1D 和对照组中,每日碳水化合物摄入量增加 10 g 与血浆乙酸水平升高相关(调整后的估计值分别为+5.2(95%CI 1.1,9.2)μmol/L,p=0.01 和+4.1(95%CI 1.7,8.5)μmol/L,p=0.04)。IA/T1D 和对照组中,总脂肪摄入量增加 5 g 与血浆乙酸水平降低相关。IA/T1D 中,非核心(垃圾)食物摄入量增加 5%与肠道微生物组丰富度降低(调整后的估计值-4.09[95%CI-7.83,-0.35],p=0.03)和均匀度降低(调整后的估计值-1.25[95%CI-2.00,-0.49],p<0.01)相关。IA/T1D 中,膳食纤维摄入量与微生物组群落结构相关。
在所有儿童中,碳水化合物和脂肪摄入量的适度增加与血浆乙酸水平相关。在 IA/T1D 中,垃圾食品摄入量增加与肠道微生物组多样性降低相关。这些与 IA/T1D 肠道微生物组的关联支持未来通过饮食干预促进 SCFA 的努力。