Cardiopulmonary Capacity in Elderly With Different Ranges of Serum Thyroid Stimulating Hormone

Healthy Clinical Trial

Official title: Cardiopulmonary Capacity In Different Quartiles Ranges Of Reference For Serum Thyroid Stimulating Hormone (TSH): Sectional Evaluation And Effect Of The Use Of Methimazole In Elderly Population

Status Recruiting

Clinical Trial Summary

The purpose of this study is to correlate in an elderly population (≥ 65 years), the different levels of serum TSH, with cardiopulmonary capacity, quality of life, depressive symptoms and cognition. And assess whether the increased serum TSH to the upper half of the normal range, through the use of antithyroid drugs, is associated with improvements in these parameters.

Clinical Trial Description

Specific Objectives:

Describe the cardiopulmonary capacity in elderly people with 65 years old or more, in different quartiles of normal range for serum TSH.

Assess the quality of life, mini mental health status and depression scale in seniors aged 65 or older, in different quartiles of normal range for serum TSH.

Quantify the possible effects related to the use of antithyroid drugs in cardiopulmonary capacity, quality of life, mini mental health status and depression scale in elderly people aged 65 or more, with the initial serum TSH at the lower limit of the normal range (1.0 milli-International unit/ml) (mIU/ml).

Justification:

Despite evidence that in the elderly population the mean serum TSH tends to be higher as compared to younger adults, there isn't a curve of normal range of TSH for this specific population (more shifted to the right, which would increase the number of diagnoses for subclinical hyperthyroidism).

Thus, elderly individuals, even when classified as euthyroidism, but presenting TSH in the normal lower range, may present at a greater risk of cardiovascular disease and therefore, may have indication for treatment.

These findings motivate and justify this study design, which may have great clinical relevance in the scientific community for its originality, and important clinical applicability.

Materials and Methods:

If the patient agrees to participate, an appointment will be scheduled at HUCFF that will be made: anamnesis, review of medical records, clinical examination and signing the Informed Consent Form (ICF).

Secondly, they will be guided and directed to: laboratory analysis for serum dosage of TSH and free thyroxine (FT4), cardiopulmonary exercise testing and application of the questionnaires of quality of life, mini mental health status and depression.

The study comprised of two parts:

Phase 1: Sectional:

• Analysis of variables.

• Sample as a whole and according to the quartiles of the reference range for serum TSH, with comparisons between groups.

• 1st Quartile: TSH: 0.4 to 1.0 mIU / ml.

• 2nd Quartile: TSH: 1.0 to 2.0 mIU / ml.

• 3rd Quartile: TSH: 2.0 to 3.0 mIU / ml.

• 4th Quartile: TSH: 3.0 to 4.0 mIU / ml Phase 2: Clinical uncontrolled. Patients with serum TSH initially on the 1st. Quartile (TSH: 0.4 to 1.0 mIU / ml) will receive treatment with Methimazole (initial dose of 5mg/day) with the goal of raising the TSH values to range between 2.0 and 4.0 mIU / ml (the half upper range of normal).

After six months with TSH in the target range (2.0 and 4.0 mIU / ml), these patients will be subjected to the same examination protocol performed at baseline and assessed to the effects of treatment on outcome variables.

Variables considered in this study:

• TSH and FT4

• Questionnaire of Quality of life for older adults (WHOQOL-OLD)

• Mini-Mental State Examination

• Geriatric Depression Scale

• Cardiopulmonary exercise testing - cardiopulmonary capacity Variables to be analyzed at rest, peak of the exercise and recovery: Heart rate, systolic blood pressure and diastolic blood pressure.

Variables to be assessed at peak effort: pulmonary ventilation, oxygen consumption, carbon dioxide production, ventilatory equivalent for oxygen and carbon dioxide, respiratory quotient, oxygen pulse, fraction of expired oxygen and carbon dioxide. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Healthy

• NCT number: NCT01849861
• Study type: Interventional
• Source: Universidade Federal do Rio de Janeiro
• Contact: Dhiãnah SO Chachamovitz
• Phone: +552126203063
• Email: dhianahsantini@gmail.com
• Status: Recruiting
• Phase: Phase 4
• Start date: September 2011
• Completion date: September 2014