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Ugandan Non-Communicable Diseases and Aging Cohort

Epidemiology of Atherosclerosis Among Older-Age People in Southwestern Uganda

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02445079
Acronym
UGANDAC
Enrollment
309
Registered
2015-05-15
Start date
2013-12-31
Completion date
2018-05-31
Last updated
2019-03-07

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

Conditions

Atherosclerosis, Cardiovascular Disease, Chronic Obstructive Pulmonary Disease, Diabetes Mellitus, HIV, Hypertension

Brief summary

Longitudinal cohort study of older-aged people living with HIV infection in southwestern Uganda and age and gender-matched HIV uninfected controls with the primary aim of measuring the epidemiology of cardiovascular and pulmonary disease in this study setting, and particularly the contribution of HIV infection to it.

Detailed description

This study recruits people living with HIV/AIDS (PLWH) aged 40 and older; and an HIV-uninfected age and gender-matched, community-based comparison group in the HIV clinic catchment area. Study investigators will collect sociodemographic, clinical, immune activation, systemic inflammation, plasma and stool microbiome, and clinical pulmonary and cardiovascular disease measures. Our outcomes of interest are measures of carotid atherosclerosis, including carotid intima media thickness and presence of plaque, prior ischemic heart disease (as measured by electrocardiograms), peripheral arterial disease (as measured by ankle-branchial index), and lung function as measured by pulmonary function testing. Our exposures of interest are traditional cardiovascular disease risk factors (e.g. age, gender, family history of cardiovascular disease, smoking history, diet, activity, body mass index, prevalence of diabetes, and prevalence of hypertension) and HIV-related cardiovascular risk factors (e.g. nadir CD4 count, ART duration and regimen, gut and plasma microbiome composition, and markers of both immune activation and systemic inflammation). Investigators will collect this data to accomplish the following aims: Aim 1: Compare the prevalence of atherosclerosis, measured by cIMT, ankle-brachial index, and presence of q-waves on electrocardiogram, in PLWH taking ART aged 40 and older and age and gender-matched, population-based HIV-uninfected controls. This study aims to be among the first to capture high-quality measures of atherosclerotic disease among a population of PLWH in sub-Saharan Africa. The study aims to test the hypothesis that older-age Ugandans on ART will have thicker carotid intima media, higher prevalence of peripheral arterial disease, and higher prevalence of pathologic q-waves on electrocardiogram than age and gender-matched, HIV-uninfected controls. Aim 2: Evaluate correlates of atherosclerosis in older-age PLWH on ART, including both traditional (age, gender, smoking, diabetes and hypertension prevalence) and HIV-related risk factors (immune activation, systemic inflammation, and stool and plasma microbiome composition). The study will leverage a collaboration with the Ragon Institute to perform immunologic and molecular testing for microbial translocation and markers of immune activation and systemic inflammation (e.g. soluble CD163, C-reactive protein, IL-6, CD8+ T-lymphocyte activation). Aim 3: Compare the progression of atherosclerosis in PLWH versus HIV-uninfected individuals over five years of observation time. The study aims to test the hypothesis that the rate of change in carotid intima media thickness will be faster in among PLWH over 45 on ART than age and gender-matched HIV-uninfected controls, and that rates of change in carotid intima media thickness among the HIV-infected cohort will be associated with markers of microbial translocation, immune activation, and systemic inflammation. Aim 4: Compare the prevalence and incidence of abnormal pulmonary function (FEV1, FVC, FEV1/FVC) in PLWH on ART and age- and gender-matched, population-based HIV-uninfected controls, utilizing handheld spirometry with bronchodilator challenge. The study aims to test the hypothesis that pulmonary function is worse and COPD is more common among people living with HIV/AIDS than age- and gender-match HIV-uninfected controls.

Interventions

OTHERThis is an observational study only

Observational study only

Sponsors

Mbarara University of Science and Technology
CollaboratorOTHER
University of California, San Francisco
CollaboratorOTHER
Ragon Institute of MGH, MIT and Harvard
CollaboratorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
Harvard University
CollaboratorOTHER
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Group 1 Inclusion Criteria: * HIV infected * Age \> 40 years old at enrollment * Minimum 2 years of antiretroviral therapy Group 1

Exclusion criteria

* Decline informed consent Group 2 Inclusion Criteria: * Living in catchment area of Mbarara Regional Referral Hospital (greater Mbarara) * Age \> 40 years old * Age and gender matched to a participant in group 1 Group 2

Design outcomes

Primary

MeasureTime frameDescription
Baseline prevalence and incident change in carotid intima media thicknessOutcomes will be collected at baseline and every 12 months (i.e. months 12, 24, 36, 48, and 60) for study duration (planned 60 months)Measured by carotid ultrasonography

Secondary

MeasureTime frameDescription
Baseline prevalence and incident change in carotid plaqueOutcomes will be collected at baseline and every 12 months (i.e. months 12, 24, 36, 48, and 60) for study duration (planned 60 months)Measured by carotid ultrasonography
Baseline prevalence and incident change in ischemic heart diseaseOutcomes will be collected at baseline and every 12 months (i.e. months 12, 24, 36, 48, and 60) for study duration (planned 60 months)Measured by electrocardiography
Baseline prevalence and incident change in peripheral arterial diseaseOutcomes will be collected at baseline and every 12 months (i.e. months 12, 24, 36, 48, and 60) for study duration (planned 60 months)Measured by ankle branchial index
Baseline prevalence and incident change in chronic obstructive pulmonary diseaseOutcomes will be collected at baseline and every 12 months (i.e. months 12, 24, 36, 48, and 60) for study duration (planned 60 months)Measured by pulmonary function testing

Countries

Uganda

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026