Mandatory oral glucose tolerance tests identify more diabetics in stable patients with chronic heart failure: a

An Lm Stevens1, Dominique Hansen1,2, Vincent Vandoren1

  • 1REVAL Rehabilitation Research Centre, Hasselt University, Martelarenlaan 42, BE-3500 Hasselt, Belgium.

Insights

Many chronic heart failure (CHF) patients have undiagnosed diabetes or prediabetes, linked to body fat distribution and heart function. Early detection through glucose tolerance tests is crucial for managing this common comorbidity.

Area of Science:

  • Cardiology
  • Endocrinology
  • Metabolic Health

Background:

  • Undiagnosed diabetes is prevalent in chronic heart failure (CHF) patients, worsening prognosis.
  • A significant portion of stable CHF patients may have unrecognized glucose metabolism disorders.
  • Understanding glucose tolerance in CHF is vital for improving patient outcomes.

Purpose of the Study:

  • To determine the prevalence of impaired glucose tolerance in stable CHF patients.
  • To identify factors associated with glucose intolerance, focusing on body composition and muscle strength.
  • To explore the relationship between glucose metabolism and cardiac function indicators.

Main Methods:

  • Prospective observational study of stable CHF patients without glucose-lowering medication.
  • Utilized 2-hour oral glucose tolerance test (OGTT), isometric leg strength testing, and dual-energy x-ray absorptiometry (DXA).
  • Assessed quality of life and physical activity via questionnaires.

Main Results:

  • 55% prediabetic, 14% diabetic, 20% normal glucose tolerant among 56 participants.
  • Most newly diagnosed diabetics identified by 2-hour OGTT values, not HbA1c.
  • Impaired glucose tolerance correlated with fat distribution (fat trunk/fat limbs) and cardiac measures (E/E').

Conclusions:

  • A substantial majority of CHF patients exhibit impaired glucose tolerance.
  • Fat distribution and left ventricular filling pressures are key determinants of glucose intolerance in CHF.
  • These findings highlight the need for screening glucose metabolism in CHF populations.
Abstract

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