Abstract

Prediabetes affects 84.1 million adults, and many will progress to type 2 diabetes (T2D). The objective of this proof-of-concept trial was to determine the efficacy of inulin supplementation to improve glucose metabolism and reduce T2D risk. Adults (n = 24; BMI: 31.3 ± 2.9 kg/m2; age: 54.4 ± 8.3 years) at risk for T2D were enrolled in this controlled feeding trial and consumed either inulin (10 g/day) or placebo (maltodextrin, 10 g/day) for six weeks. Assessments included peripheral insulin sensitivity, fasting glucose, and insulin, HOMA-IR, in vivo skeletal muscle substrate preference, Bifidobacteria copy number, intestinal permeability, and endotoxin concentrations. Participant retention was 92%. There were no baseline group differences except for fasting insulin (p = 0.003). The magnitude of reduction in fasting insulin concentrations with inulin (p = 0.003, inulin = Δ-2.9, placebo = Δ2.3) was attenuated after adjustment for baseline concentrations (p = 0.04). After adjusting for baseline values, reduction in HOMA-IR with inulin (inulin = Δ-0.40, placebo=Δ0.27; p = 0.004) remained significant. Bifidobacteria 16s increased (p = 0.04; inulin = Δ3.1e9, placebo = Δ-8.9e8) with inulin supplementation. Despite increases in gut Bifidobacteria, inulin supplementation did not improve peripheral insulin sensitivity. These findings question the need for larger investigations of inulin and insulin sensitivity in this population.

Highlights

  • The prevalence of type 2 diabetes (T2D) among U.S adults is estimated to be 13%, and it is the 7th leading cause of deaths in the US [1]

  • All participants met 1 or more of the following criteria established for elevated T2D risk: American Diabetes Association (ADA) risk screener score ≥5; hemoglobin A1c (HbA1c) between 5.7–6.4 mg/dL; fasting blood glucose (FBG) between 100–125 mg/dL; or 2-h oral glucose tolerance test (OGTT) value between 140–200 mg/dL [2,25]

  • There were no group differences in participant characteristics at baseline except fasting insulin concentration was higher (p = 0.027) in the inulin compared with the placebo group

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Summary

Introduction

The prevalence of type 2 diabetes (T2D) among U.S adults is estimated to be 13%, and it is the 7th leading cause of deaths in the US [1]. Prediabetes is a condition defined by impaired glucose tolerance (IGT), impaired fasting glucose (IFG), or a hemoglobin. In 2018, the estimated number of U.S adults with prediabetes was 88 million, and of these individuals, only 15.3% reported that a healthcare provider informed them of this diagnosis [1]. Individual awareness of prediabetes has more than doubled from 6.5% since 2005, most people remain unaware of their metabolic condition [1,3,4,5]. T2D prevention strategies [1,3,4]. Lifestyle modification strategies for prevention of T2D include weight loss of 5–10%

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