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Examining the influence of DPP4 inhibitors and sulphonyureas in combination with metformin on the Type II Diabetes gut microbiome: a pilot study

Published online by Cambridge University Press:  17 August 2021

P. Cronin ,
P.W. O'Toole  and
E.M. O’ Connor
P. Cronin
Affiliation:
Department of Biological Sciences, University of Limerick, Limerick, Ireland APC Microbiome Ireland, University College Cork, National University of Ireland, Cork, Ireland
P.W. O'Toole
Affiliation:
APC Microbiome Ireland, University College Cork, National University of Ireland, Cork, Ireland
E.M. O’ Connor
Affiliation:
Department of Biological Sciences, University of Limerick, Limerick, Ireland APC Microbiome Ireland, University College Cork, National University of Ireland, Cork, Ireland Health Research Institute, University of Limerick, Limerick, Ireland
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Abstract

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Proceedings of the Nutrition Society , Volume 80 , Issue OCE3: Irish Section Conference, 22–24 June 2021, Nutrition, health and ageing — translating science into practice – Part A , 2021 , E115
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Copyright © The Authors 2021

Type II Diabetes Mellitus (T2DM) has increased in prevalence globally over the last number of decades particularly in industrialised nations. This is primarily due to the Western diet, which is high in saturated fat and low in dietary fibre. Evidence has shown the gut microbiome to be altered in patients with T2DM when compared to healthy controls(Reference Qin, Li and Cai1). Given T2DM is characterized by elevated blood glucose levels due to insulin resistance and inadequate insulin secretion, a wide range of metabolic pathways are implicated by this pathogenesis(Reference Saltiel and Kahn2). As a result, numerous medications have been developed in order to combat this disease. Indeed, the mechanism of action of the most widely prescribed, first line antidiabetic therapy, metformin, has been shown to alter gut microbiota composition(Reference Wu, Esteve and Tremaroli3). Other commonly prescribed drugs include sulphonylurea and dipeptidyl peptidase 4 (DPP4) inhibitors (often prescribed in addition to metformin as second line therapies) which have been poorly studied in terms of potential microbiome impact.

Thus, we conducted a pilot study (n = 20) on T2D patients, all of whom were prescribed metformin in addition to either a DPP4 inhibitor (n = 6), a sulphonylurea (n = 8) or a combination of the latter two therapies (n = 6). Faecal samples were collected and the gut microbiota profiled using 16S rRNA gene amplicon sequencing.

Beta-diversity measures (Weighted Unifrac – measure of inter-individual species diversity) revealed significant differences between all groups examined. Individuals prescribed sulphonylurea had lower alpha-diversity (Shannon Index - measure of species diversity between specific communities) while this group also differed when comparing the log2-fold differences of the most abundant amplicon sequence variants (representing sequence-based bacterial divisions).

This pilot study provides evidence that these medications may exert an influence on the gut microbiota and the efficacy of these medications when used with first line therapy may depend on microbiome interactions.

References

Qin, J, Li, Y, Cai, Z, et al. (2012) Nature 490(7418), 55–60.10.1038/nature11450CrossRefGoogle Scholar
Saltiel, AR & Kahn, CR (2001) Nature 414(6865), 799–806.10.1038/414799aCrossRefGoogle Scholar
Wu, H, Esteve, E, Tremaroli, V, et al. (2017) Nat Med 23(7), 50.10.1038/nm.4345CrossRefGoogle Scholar