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Effects of Hormonal Anabolic Deficiency and Neurovascular Alterations on Mortality in Male Patients With Heart Failure

Hormonal Anabolic Deficiency Associated With Neurovascular Alterations Predict Poor Prognosis in Male Patients With Heart Failure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03463226
Acronym
TestoHF
Enrollment
169
Registered
2018-03-13
Start date
2016-06-30
Completion date
2020-12-30
Last updated
2021-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

Testosterone Deficiency, Sympathetic overactivity, Exercise Intolerance

Brief summary

Heart failure (HF) has been associated with chronic deleterious effects on skeletal muscle, endocrine system, vasculature and sympathetic nervous system. These alterations have a significant impact on quality of life, leading to a reduction in functional capacity and limited symptoms, which involve dyspnea and fatigue. The investigators tested the hypothesis that hormonal anabolic deficiency associated with neurovascular alterations may worsen the prognosis of patients with heart failure.

Detailed description

One hundred and fifty six patients have been enrolled so far. Methods were as described below: * Muscle sympathetic nerve activity (MSNA) was directly recorded from the peroneal nerve using the microneurography technique ; * All patients underwent symptom-limited cardiopulmonary exercise test performed on a cycle ergometer, using a ramp protocol with workload increments of 5 or 10 Watts per minute; * Body composition measurements were performed using dual-energy X-ray absorptiometry (DXA); * Muscle strength was assessed by handgrip dynamometer using the mean value of three attempts; * Blood samples were drawn in the morning after 12h overnight fasting. The laboratory tests included B-type natriuretic peptide (BNP; pg/mL) plasma level, serum sodium (mEq/L), serum potassium (mEq/L), creatinine (mg/dL), haemoglobin level (g/dL), high-sensitivity C-reactive protein (CRP; mg/L), lipid profile (triglyceride, total cholesterol, high-density lipoprotein, and low-density lipoprotein; mg/dL), and fasting glucose (mg/dL). Blood sample to assess hormone plasma levels were also drawn at the same time: total testosterone (TT), free testosterone (FT), sex hormone binding globulin (SHBG), dehydroepiandrosterone sulfate (DHEAS), luteinizing hormone (LH), follicle-stimulating hormone (FSH), thyroid stimulating hormone (TSH) and insulin-like growth factor 1 (IGF1).

Interventions

Dual-energy X-ray absorptiometry (DXA) scan was used to measure total lean mass, body fat and bone mineral content.

Venous occlusion plethysmography was used to assess non-invasively blood flow.

DIAGNOSTIC_TESTBlood sample collection

Blood samples were drawn in the morning after 12h overnight fasting.

DIAGNOSTIC_TESTDynamometers for Handgrip Strength

Muscle strength was assessed by handgrip dynamometer using the mean value of three attempts.

DIAGNOSTIC_TESTCardiopulmonary exercise test

Oxygen consumption (VO2) and carbon dioxide output (VCO2) were measured by means of gas exchange on a breath-by-breath basis. The patients were initially monitored for 2 minutes at rest when seated on the ergometer, after that they were instructed to pedal at a pace of 60-70 rpm and the completion of the test occurred when, in spite of verbal encouragement, the patient reached maximal volitional fatigue.

DIAGNOSTIC_TESTMuscle Sympathetic Nerve Activity

Multiunit post-ganglionic muscle sympathetic nerve recordings were made using a tungsten microelectrode placed in the peroneal nerve near the fibular head. Nerve signals were amplified by a factor of 50,000 to 100,000 and band-pass filtered (700 to 2000 Hz). For recording and analysis, nerve activity was rectified and integrated (time constant 0.1 seconds) to obtain a mean voltage display of sympathetic nerve activity.

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* age between 18 and 65 years old; * at least1 year of diagnosed HF; * left ventricular ejection fraction (LVEF) lower than 40% measured by echocardiography; * non-ischaemic and ischaemic aetiologies; * compensated HF with optimal medication for at least 3 months prior the study; * New York Heart Association (NYHA) class of I to IV.

Exclusion criteria

* patients with autonomic diabetic neuropathy; * patients with chronic renal failure with haemodialysis; * heart transplantation; * presence of pacemaker; * patients with muscular dystrophy (i.e. Duchenne muscular dystrophy); * patients submitted to any hormonal treatment; * history of cancer; * ongoing infection; * myocardial infarction with percutaneous coronary intervention or revascularization 6 months prior to the study entry.

Design outcomes

Primary

MeasureTime frameDescription
Impact of testosterone deficiency on mortality2 yearsBlood sample was collected in the morning (between 8:00-10:00 a.m.) after 12 hours fasting.
Impact of muscle sympathetic nerve activity on mortality2 yearsMicroneurography was used to assess the sympathetic nervous system.
Impact of neurovascular alterations on mortality2 yearsVenous occlusion pletysmography was used to evaluate vasodilation.

Secondary

MeasureTime frameDescription
Impact of testosterone deficiency on body composition2 yearsBody composition measurements were performed using dual-energy X-ray absorptiometry.
Impact of testosterone deficiency on functional capacity2 yearsAll patients underwent symptom-limited cardiopulmonary exercise test to measure functional capacity.
Impact of testosterone deficiency on strength2 yearsMuscle strength was assessed by handgrip dynamometer using the mean value of three attempts.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026