R21TW012644
Project Grant
Overview
Grant Description
Cardiometabolic consequences and pathway of weight gain associated with dolutegravir-based antiretroviral therapy in Haiti. A collaborative study between GHESKIO and CCASANET - Abstract
Haiti has the largest number of persons with HIV (PWH) in the Caribbean. PWH have a higher risk of developing metabolic and cardiovascular disease (CVD), which are leading causes of mortality among Haitians and other residents of low and middle-income countries (LMICs), driven in part by high rates of hypertension, elevated fasting plasma glucose and high body mass index.
Weight gain is common early after starting antiretroviral therapy (ART), particularly among PWH on an integrase strand transfer inhibitor (INSTI)-based regimen. The INSTI-containing combination regimen of tenofovir disoproxil fumarate, lamivudine, and dolutegravir (TLD) is the most commonly prescribed ART regimen in LMICs, but at present there are few data on the consequences of weight gain on ART in these settings.
Consequently, there is a critical need for innovative approaches to 1) determine the features and severity of cardiometabolic disease risk accompanying weight gain among TLD recipients in LMICs, including insulin sensitivity, blood pressure, lipid profiles and systemic inflammation; and 2) determine the metabolic mechanisms underlying weight gain to guide the development and implementation of effective prevention and treatment strategies.
GHESKIO (Groupe Haitien d'Etude du Sarcome et des Infections Opportunités) is the largest HIV clinic in the Americas, a founding member of CCASANET (the Caribbean, Central and South America Network for HIV Epidemiology) and has a 37-year track record of NIH research on HIV and associated comorbidities. Building upon this infrastructure, our multi-disciplinary study will leverage advanced metabolic phenotyping and multiomic data analysis to elucidate the bioenergetic pathways underlying weight gain on TLD and the cardiometabolic consequences among PWH in LMICs, where diet and lifestyle factors differ from higher income countries.
Aim 1 will assess whether weight gain on TLD is associated with increased insulin resistance, blood pressure, dyslipidemia, and inflammation. We will enroll 200 previously ART-naïve patients who initiated TLD at GHESKIO 12 to 24 months previously and gained <3% versus 10% body weight to define the factors associated with weight gain including sociodemographic variables, appetite, food security and physical activity, and whether weight gain is associated with higher HOMA-IR, fasting lipids, systolic and diastolic blood pressure, and inflammatory markers linked to CVD.
Aim 2 will determine the metabolic and lipid pathways associated with weight gain in the first 12 months of TLD exposure using metabolomic and lipidomic profiling. We will enroll 60 ART-naïve patients initiating TLD and perform fasting metabolomic and lipidomic profiling at baseline and 12 months to identify the pre-ART pathways predisposing to weight gain.
This project will develop new capacity for sophisticated cardiometabolic research and analyses at GHESKIO and within CCASANET more broadly, and the results of this study will provide preliminary data on whether weight gain on TLD may represent an emerging threat to health outcomes in the context of the wide implementation of this regimen in LMICs across the world.
Haiti has the largest number of persons with HIV (PWH) in the Caribbean. PWH have a higher risk of developing metabolic and cardiovascular disease (CVD), which are leading causes of mortality among Haitians and other residents of low and middle-income countries (LMICs), driven in part by high rates of hypertension, elevated fasting plasma glucose and high body mass index.
Weight gain is common early after starting antiretroviral therapy (ART), particularly among PWH on an integrase strand transfer inhibitor (INSTI)-based regimen. The INSTI-containing combination regimen of tenofovir disoproxil fumarate, lamivudine, and dolutegravir (TLD) is the most commonly prescribed ART regimen in LMICs, but at present there are few data on the consequences of weight gain on ART in these settings.
Consequently, there is a critical need for innovative approaches to 1) determine the features and severity of cardiometabolic disease risk accompanying weight gain among TLD recipients in LMICs, including insulin sensitivity, blood pressure, lipid profiles and systemic inflammation; and 2) determine the metabolic mechanisms underlying weight gain to guide the development and implementation of effective prevention and treatment strategies.
GHESKIO (Groupe Haitien d'Etude du Sarcome et des Infections Opportunités) is the largest HIV clinic in the Americas, a founding member of CCASANET (the Caribbean, Central and South America Network for HIV Epidemiology) and has a 37-year track record of NIH research on HIV and associated comorbidities. Building upon this infrastructure, our multi-disciplinary study will leverage advanced metabolic phenotyping and multiomic data analysis to elucidate the bioenergetic pathways underlying weight gain on TLD and the cardiometabolic consequences among PWH in LMICs, where diet and lifestyle factors differ from higher income countries.
Aim 1 will assess whether weight gain on TLD is associated with increased insulin resistance, blood pressure, dyslipidemia, and inflammation. We will enroll 200 previously ART-naïve patients who initiated TLD at GHESKIO 12 to 24 months previously and gained <3% versus 10% body weight to define the factors associated with weight gain including sociodemographic variables, appetite, food security and physical activity, and whether weight gain is associated with higher HOMA-IR, fasting lipids, systolic and diastolic blood pressure, and inflammatory markers linked to CVD.
Aim 2 will determine the metabolic and lipid pathways associated with weight gain in the first 12 months of TLD exposure using metabolomic and lipidomic profiling. We will enroll 60 ART-naïve patients initiating TLD and perform fasting metabolomic and lipidomic profiling at baseline and 12 months to identify the pre-ART pathways predisposing to weight gain.
This project will develop new capacity for sophisticated cardiometabolic research and analyses at GHESKIO and within CCASANET more broadly, and the results of this study will provide preliminary data on whether weight gain on TLD may represent an emerging threat to health outcomes in the context of the wide implementation of this regimen in LMICs across the world.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Haiti
Geographic Scope
Foreign
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 108% from $156,331 to $324,477.
LES Centres Gheskio was awarded
Cardiometabolic Consequences of Dolutegravir-based ART in Haiti
Project Grant R21TW012644
worth $324,477
from Fogarty International Center in July 2023 with work to be completed primarily in Haiti.
The grant
has a duration of 2 years and
was awarded through assistance program 93.989 International Research and Research Training.
The Project Grant was awarded through grant opportunity HIV-associated Non-Communicable Diseases Research at Low- and Middle-Income Country Institutions (R21 Clinical Trial Optional).
Status
(Complete)
Last Modified 7/5/24
Period of Performance
7/10/23
Start Date
6/30/25
End Date
Funding Split
$324.5K
Federal Obligation
$0.0
Non-Federal Obligation
$324.5K
Total Obligated
Activity Timeline
Transaction History
Modifications to R21TW012644
Additional Detail
Award ID FAIN
R21TW012644
SAI Number
R21TW012644-2973755297
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Non-Domestic (Non-U.S.) Entity
Awarding Office
75NF00 NIH FOGARTY INTERNATIONAL CENTER
Funding Office
75NF00 NIH FOGARTY INTERNATIONAL CENTER
Awardee UEI
ZKDAZLMSN6S8
Awardee CAGE
SKX25
Performance District
Not Applicable
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Health and Human Services (075-0884) | Health research and training | Grants, subsidies, and contributions (41.0) | $156,331 | 100% |
Modified: 7/5/24