Literature DB >> 31399369

Obese Individuals with and without Type 2 Diabetes Show Different Gut Microbial Functional Capacity and Composition.

Louise B Thingholm1, Malte C Rühlemann1, Manja Koch2, Brie Fuqua3, Guido Laucke1, Ruwen Boehm4, Corinna Bang1, Eric A Franzosa5, Matthias Hübenthal6, Ali Rahnavard5, Fabian Frost7, Jason Lloyd-Price5, Melanie Schirmer5, Aldons J Lusis3, Chris D Vulpe8, Markus M Lerch7, Georg Homuth9, Tim Kacprowski10, Carsten O Schmidt11, Ute Nöthlings12, Tom H Karlsen13, Wolfgang Lieb14, Matthias Laudes15, Andre Franke16, Curtis Huttenhower5.   

Abstract

Obesity and type 2 diabetes (T2D) are metabolic disorders that are linked to microbiome alterations. However, their co-occurrence poses challenges in disentangling microbial features unique to each condition. We analyzed gut microbiomes of lean non-diabetic (n = 633), obese non-diabetic (n = 494), and obese individuals with T2D (n = 153) from German population and metabolic disease cohorts. Microbial taxonomic and functional profiles were analyzed along with medical histories, serum metabolomics, biometrics, and dietary data. Obesity was associated with alterations in microbiome composition, individual taxa, and functions with notable changes in Akkermansia, Faecalibacterium, Oscillibacter, and Alistipes, as well as in serum metabolites that correlated with gut microbial patterns. However, microbiome associations were modest for T2D, with nominal increases in Escherichia/Shigella. Medications, including antihypertensives and antidiabetics, along with dietary supplements including iron, were significantly associated with microbiome variation. These results differentiate microbial components of these interrelated metabolic diseases and identify dietary and medication exposures to consider in future studies.
Copyright © 2019. Published by Elsevier Inc.

Entities:  

Keywords:  dietary supplements; iron; magnesium; medication; metabolic disease; microbiome; nutrition; obesity; type 2 diabetes

Mesh:

Substances:

Year:  2019        PMID: 31399369      PMCID: PMC7720933          DOI: 10.1016/j.chom.2019.07.004

Source DB:  PubMed          Journal:  Cell Host Microbe        ISSN: 1931-3128            Impact factor:   21.023


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