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Clinical Significance and Diagnosis of Sarcopenia in Cardiac Patients

M

Medical University of Lodz

Status

Unknown

Conditions

Hypertension
Sarcopenic Obesity
Heart Failure With Preserved Ejection Fraction

Study type

Observational

Funder types

Other

Identifiers

NCT04175080
RNN/80/17/KE

Details and patient eligibility

About

Obesity sarcopenia, characterized by the coexistence of excess fat and muscle mass reduction, may contribute to the pathophysiology of exercise intolerance in patients with heart failure with preserved ejection fraction (HFpEF). The project will examine the impact of selected circulating miRNAs on processes that may form the pathophysiological basis for HFpEF development and obesity sarcopenia in correlation with biochemical markers, echocardiographic assessment and non-invasive assessment of hemodynamic parameters. In addition, the impact of LDL and HDL on these diseases will be assessed. Determinations of selected adipokines and asymmetric dimethylarginine will also be carried out and their effects on the cardiovascular system will be assessed.

Enrollment

190 estimated patients

Sex

All

Ages

35 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • control group: healthy volunteers
  • study groups: patients with HFpEF. Patients in which the results of BNP/NT-proBNP did not confirm the diagnosis of HFpEF were classified as hypertensive group.

Exclusion criteria

  • coronary artery disease
  • unstable hypertension
  • heart failure class IV NYHA
  • condition after percutaneous or surgical revascularization
  • pulmonary hypertension in echocardiography
  • obstructive or restrictive lung diseases
  • congenital heart disease
  • arrhythmias (including atrial fibrillation)
  • pacemaker or implantable cardioverter defibrillator
  • hyperthyroidism or hypothyroidism
  • pregnancy or lactation
  • hemodynamically significant acquired heart defects
  • cardiomyopathies
  • GFR <60 ml/min/1.73 m2
  • other medical conditions such as: cancer, significant anemia, diabetes, alcohol and drug abuse, chronic inflammatory diseases and other
  • the patient's inability to cooperate and / or give informed consent to participate in the study

Trial design

190 participants in 3 patient groups

Control
HFpEF group
Hypertensive group
Description:
Patients in which the results of BNP/NT-proBNP did not confirm the diagnosis of HFpEF were classified as hypertensive group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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