Men, HIV-associated lipodystrophy syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult subjects; male; stable weight for 3 months; body mass index between 18.5 and 29.9 kg / m2; in the case of HIV seropositive patients group using antiretroviral therapy for at least 6 months; T-CD4 cell count greater than 200 cells / mm3; undetectable viral load
Exclusion criteria
Exclusion criteria: Changes of thyroid function; use of glucocorticoids in the last 6 months; use of lipid-lowering drugs; use of oral anti-diabetics; use of beta-blockers; use of benzodiazepines; signs and symptoms of opportunistic diseases in the case of HIV seropositive patients
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Primary
| Measure | Time frame |
|---|---|
| Expected Outcome 1: increase in UCP1 gene expression assessed by the real-time polymerase chain reaction method based on the finding by previously published studies of a variation of at least 10% in measurements between groups with HIV with lipodystrophy and the control group (healthy). Measurements will be taken after the end of the study.;Expected Outcome 2: increased resting energy expenditure assessed by indirect calorimetry based on the finding by previously published studies of a variation of at least 8% in measurements between HIV-positive and lipodystrophy groups. Measurements will be taken after the end of the study. | — |
Countries
Brazil
Contacts
Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo