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UnknownNCT04886713

Adipose Tissue Inflammation in HFpEF

Adipose Tissue Inflammation in the Development, Maintenance and Functional Impairments in Heart Failure With Preserved Ejection Fraction

Status
Unknown
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
Heart Center Leipzig - University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To evaluate the role of adipose tissue inflammation in patients with heart failure with preserved ejection fraction (HFpEF). Patients undergoing coronary artery bypass grafting with HFpEF and without heart failure will be included in this prospective study. Epicardial, paracardial, paraaortic/paravascular, subcutaneous adipose tissue samples as well as myocardial tissue will be harvested during cardiac surgery. Inflammatory patterns of these tissues and their relation to circulating markers will be investigated.

Detailed description

Heart Failure with preserved Ejection Fraction (HFpEF) is a growing public health concern with an increasing incidence, high morbidity and mortality and no proven therapy to date. Better characterization of individual pathophysiological implications is mandatory to develop effective therapeutic strategies or preventive programs. Obesity is an important risk factor for the development of HFpEF and also modulates its course possibly by its association with systemic inflammation. However, the role of adipose tissue (AT) inflammation in the development, maintenance and functional impairments in HFpEF has been under-investigated. Dysfunctional AT leads to a shift from a protective adipokine profile to an imbalanced production of pro-inflammatory, pro-oxidant and pro-fibrotic adipokines. Besides depot specific paracrine effects, the overall secretory activity or endocrine effect of AT can be evaluated in peripheral plasma. The investigators hypothesize that adipose inflammation distinguishes obese HFpEF patients from obese patients without heart failure and that adipose tissue inflammation is a key driver the maintenance and development of HFpEF and determines functional capacity. In addition the investigators hypothesize that the degree of myocardial inflammatory alterations is more closely related to epicardial tissue alterations than subcutaneous or visceral AT tissue inflammation or peripheral adipokine profiles.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTAdipose and myocardial tissue samplingAfter median sternotomy tissue samples will be collected from the epicardial space, the abdominal wall and the myocardium.
DIAGNOSTIC_TESTCardiac magnetic resonance imagingMagnetic resonance imaging will be performed at 1.5 Tesla ('Intera', Philips Medical Systems, Best, The Netherlands). All subjects will be examined in the supine position with initial anatomy scans to cover the thorax to the first sacral vertebrae. The magnetic resonance imaging protocol is summarized in Figure 4. The following imaging parameters will be acquired: * Biventricular end-diastolic and end-systolic volume, ejection fraction, stroke volume * Biventricular mass, wall thickness * T1 mapping; native and \> 10 minutes post contrast injection as an estimate of left ventricular diffuse fibrosis and extracellular volume * Late enhancement for detection of regional fibrosis and scar * Myocardial feature tracking for analysis of deformation/motion * Epicardial fat volume
DIAGNOSTIC_TESTCardiopulmonary exercise testingAfter completion of a regular cardiac rehabilitation program patients are scheduled to undergo their discharge examination at 3 to 4 weeks after the operation in order to be functionally characterized. Cardiopulmonary exercise testing will be performed, if possible by patients condition, on a mechanically braked bicycle ergometer and respiratory gas exchange analysis via a mouthpiece or facemask.

Timeline

Start date
2019-11-01
Primary completion
2021-12-31
Completion
2022-03-15
First posted
2021-05-14
Last updated
2021-05-14

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04886713. Inclusion in this directory is not an endorsement.