亚亚种 AP-32、MH-68 和 CP-9 的益生菌辅助治疗可降低 1 型糖尿病患者的血糖水平和炎症细胞因子。

Adjuvant Probiotics of subsp. AP-32, MH-68, and subsp. CP-9 Attenuate Glycemic Levels and Inflammatory Cytokines in Patients With Type 1 Diabetes Mellitus.

机构信息

Division of Medical Genetics, Pediatric Endocrinology & Metabolism, China Medical University Children's Hospital, China Medical University, Taichung, Taiwan.

School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan.

出版信息

Front Endocrinol (Lausanne). 2022 Mar 1;13:754401. doi: 10.3389/fendo.2022.754401. eCollection 2022.

Abstract

INTRODUCTION

Type 1 diabetes mellitus (T1DM) is characterized by autoimmune destruction of pancreatic β cells. Previous study has discovered that probiotic strains residing in the gut play essential roles in host immune regulation. However, few clinical results demonstrated probiotic would actually benefit in attenuating glycated hemoglobin (HbA1c) along with inflammatory cytokine levels of the T1DM patients and analyzed their gut microbiota profile at the same time. In this clinical trial, we evaluated the therapeutic efficacy of probiotics on HbA1c along with inflammatory cytokine levels of T1DM patients to determine an alternative administration mode for T1DM medication. The probiotics changed T1DM gut microbiota profile will be measured by next-generation sequencing (NGS).

RESEARCH DESIGN AND METHODS

A randomized, double-blind, placebo-controlled trial was performed at China Medical University Hospital. T1DM patients between 6 and 18 years of age were enrolled. 27 patients were administered regular insulin therapy plus capsules containing probiotic strains subsp. AP-32, MH-68, and subsp. CP-9 daily for 6 months, and 29 patients were administered insulin therapy without extra probiotic supplement as placebo group. The variations of fasting blood glucose and HbA1c in these patients were analyzed. In addition, serum levels of inflammatory cytokines and anti-inflammatory cytokine were assessed using enzyme-linked immunosorbent assay. Patients' stool microbiota were all subjects to NGS analysis.

RESULTS

NGS data showed elevated populations of and in the gut of patients with T1DM who were taking probiotics. Patients with T1DM who were administered probiotics showed significantly reduced fasting blood glucose levels compared with the before-intervention levels. The HbA1c levels of the patients also improved after administration of probiotics. The concentrations of IL-8, IL-17, MIP-1β, RANTES, and TNF-α were significantly reduced and were associated with an increased TGF-β1 expression after probiotic intervention. The persistence effect of glycemic control and immunomodulation were observed even 3 months after discontinuation of the probiotics.

CONCLUSIONS

Here, we found that conventional insulin therapy plus probiotics supplementation attenuated T1DM symptoms than receiving insulin treatment only. Probiotics supplementation with insulin treatment changed gut microbiota and revealed better outcome in stabilizing glycemic levels and reducing HbA1c levels in patients with T1DM through beneficial regulation of immune cytokines.

CLINICAL TRIAL REGISTRATION

ClinicalTrials.gov, identifier NCT03880760.

摘要

简介

1 型糖尿病(T1DM)的特征是胰岛β细胞的自身免疫破坏。先前的研究发现,肠道中存在的益生菌菌株在宿主免疫调节中起着重要作用。然而,很少有临床研究结果表明益生菌实际上可以减轻 T1DM 患者的糖化血红蛋白(HbA1c)和炎症细胞因子水平,并同时分析他们的肠道微生物组谱。在这项临床试验中,我们评估了益生菌对 T1DM 患者 HbA1c 和炎症细胞因子水平的治疗效果,以确定 T1DM 药物的替代给药方式。通过下一代测序(NGS)测量益生菌改变 T1DM 肠道微生物组谱。

研究设计和方法

在中国医科大学附属医院进行了一项随机、双盲、安慰剂对照试验。招募了 6 至 18 岁的 T1DM 患者。27 名患者接受常规胰岛素治疗,并每天服用含有益生菌亚种 AP-32、MH-68 和亚种 CP-9 的胶囊,持续 6 个月,29 名患者接受胰岛素治疗,不额外补充益生菌作为安慰剂组。分析这些患者空腹血糖和 HbA1c 的变化。此外,使用酶联免疫吸附试验评估血清炎症细胞因子和抗炎细胞因子的水平。所有患者的粪便微生物组均进行 NGS 分析。

结果

NGS 数据显示,接受益生菌治疗的 T1DM 患者肠道中的和种群数量增加。与干预前相比,接受益生菌治疗的 T1DM 患者的空腹血糖水平显著降低。患者的 HbA1c 水平也在接受益生菌治疗后得到改善。益生菌干预后,IL-8、IL-17、MIP-1β、RANTES 和 TNF-α 的浓度降低,TGF-β1 的表达增加。即使在停止益生菌治疗 3 个月后,仍观察到血糖控制和免疫调节的持续效果。

结论

在这里,我们发现常规胰岛素治疗加益生菌补充治疗比单独接受胰岛素治疗更能减轻 T1DM 症状。益生菌补充治疗加胰岛素治疗改变了肠道微生物群,并通过对免疫细胞因子的有益调节,显示出在稳定血糖水平和降低 T1DM 患者的 HbA1c 水平方面更好的效果。

临床试验注册

ClinicalTrials.gov,标识符 NCT03880760。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e654/8921459/db467c35ce89/fendo-13-754401-g001.jpg

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