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The Prevalence of Polyneuropathy in Type 2 Diabetes Subgroups Based on HOMA2 Indices of b-Cell Function and Insulin Sensitivity

Kristensen, Frederik Pagh Bredahl (författare)
Aarhus University Hospital
Christensen, Diana Hedevang (författare)
Aarhus University Hospital
Callaghan, Brian Christopher (författare)
University of Michigan
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Stidsen, Jacob Volmer (författare)
Odense University Hospital
Nielsen, Jens Steen (författare)
University of Southern Denmark,Odense University Hospital
Højlund, Kurt (författare)
University of Southern Denmark,Odense University Hospital
Beck-Nielsen, Henning (författare)
Odense University Hospital
Jensen, Troels Staehelin (författare)
Aarhus University Hospital
Andersen, Henning (författare)
Aarhus University Hospital
Vestergaard, Peter (författare)
Steno Diabetes Center Copenhagen
Jessen, Niels (författare)
Aarhus University Hospital
Olsen, Michael Hecht (författare)
Holbæk Hospital,University of Southern Denmark
Hansen, Torben (författare)
Novo Nordisk Foundation Centre for Basic Metabolic Research
Brøns, Charlotte (författare)
Steno Diabetes Center Copenhagen
Vaag, Allan (författare)
Lund University,Lunds universitet,Translationell diabetesforskning,Forskargrupper vid Lunds universitet,Translational Diabetes Research,Lund University Research Groups,Steno Diabetes Center Copenhagen
Sørensen, Henrik Toft (författare)
Aarhus University Hospital
Thomsen, Reimar Wernich (författare)
Aarhus University Hospital
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 (creator_code:org_t)
2023
2023
Engelska 10 s.
Ingår i: Diabetes Care. - 0149-5992. ; 46:8, s. 1546-1555
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • OBJECTIVE Metabolic syndrome components may cumulatively increase the risk of diabetic polyneuropathy (DPN) in type 2 diabetes mellitus (T2DM) patients, driven by insulin resistance and hyperinsulinemia. We investigated the prevalence of DPN in three T2DM subgroups based on indices of b-cell function and insulin sensitivity. RESEARCH DESIGN AND METHODS We estimated b-cell function (HOMA2-B) and insulin sensitivity (HOMA2-S) in 4,388 Danish patients with newly diagnosed T2DM. Patients were categorized into subgroups of hyperinsulinemic (high HOMA2-B, low HOMA2-S), classical (low HOMA2-B, low HOMA2-S), and insulinopenic (low HOMA2-B, high HOMA2-S) T2DM. After a median follow-up of 3 years, patients filled the Michigan Neuropathy Screening Instrument questionnaire (MNSIq) to identify DPN (score ‡ 4). We used Poisson regression to calculate adjusted prevalence ratios (PRs) for DPN, and spline models to examine the association with HOMA2-B and HOMA2-S. RESULTS A total of 3,397 (77%) patients filled in the MNSIq. The prevalence of DPN was 23% among hyperinsulinemic, 16% among classical, and 14% among insulinopenic pa-tients. After adjusting for demographics, diabetes duration and therapy, lifestyle behaviors, and metabolic syndrome components (waist circumference, triglycer-ides, HDL cholesterol, hypertension, and HbA1c), the PR of DPN was 1.35 (95% CI 1.15–1.57) for the hyperinsulinemic compared with the classical patients. In spline analyses, we observed a linear relation of higher DPN prevalence with increasing HOMA2-B, independent of both metabolic syndrome components and HOMA2-S. CONCLUSIONS Hyperinsulinemia marked by high HOMA2-B is likely an important risk factor for DPN beyond metabolic syndrome components and insulin resistance. This should be considered when developing interventions to prevent DPN.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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