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Metabolic Determinants of Cardiac Function

Completed
Conditions
Diabetes Mellitus
Heart Failure
Registration Number
NCT03386864
Lead Sponsor
German Diabetes Center
Brief Summary

Assessment of cardiac energy metabolism in patients with impaired glucose tolerance

Detailed Description

Insulin resistance, hepatocellular lipids (HCL) and plasma concentrations of free fatty acids (FFA) are predictors of heart failure, the leading cause of mortality in patients suffering from type 2 diabetes mellitus (T2DM). Epidemiological data suggest that diabetic cardiomyopathy (DC) presents as ventricular dysfunction in patients with T2DM independent of coronary artery disease. The underlying cellular mechanisms are poorly understood. Reduced mitochondrial activity and insulin resistance of skeletal muscle relates to liver steatosis, possibly due to higher substrate flux to the liver. High oxidation rates in the liver result in oxidative stress, damage of mitochondria and apoptosis. The investigators hypothesize that (i) HCL and impaired liver energy metabolism correlate with ventricular dysfunction, (ii) impaired glucose uptake and mitochondrial capacity in skeletal muscle relates to enhanced oxidative capacity, oxidative stress and lipid deposition in heart tissue (iii) reduced myocardial oxidative capacity limits recovery of myocardial function in patients with acute heart failure.

The investigators aim to assess (i) liver energy metabolism and heart function, (ii) respiration and lipid metabolites in skeletal muscle and heart tissue in humans with advanced heart failure and (iii) the prognostic impact of these factors in humans with acute heart failure.

This study will improve the understanding of mechanisms underlying the development of DC and the identification of patients at risk for poor outcome in heart failure.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
400
Inclusion Criteria
  • age ≥ 20 and ≤85 years
  • myocardial biopsy for medical reason
Exclusion Criteria
  • acute infection
  • autoimmune disease
  • pregnancy
  • cancer

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
mitochondrial oxygen fluxUp to 36 months

measured using high resolution respirometry. Unit: pmol/(s\*mg)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

German Diabetes Center

🇩🇪

Düsseldorf, NRW, Germany

German Diabetes Center
🇩🇪Düsseldorf, NRW, Germany
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