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(i) existing NIH-funded research infrastructure in SA and (ii) the NIH large R01 mechanism to enroll 1900 pregnant women in the 1st trimester (633 WLHIV initiating DTG in pregnancy, 633 WLHIV continuing DTG use from pre-pregnancy, and 633 women without HIV) and their children, following them to two years. Within this cohort, we will first examine how HIV and/or DTG use (HIV/DTG) impacts longitudinal changes in weight and adipose tissue mass in pregnancy using air displacement plethysmography. We will further investigate pathways of excess gestational weight gain and adipose accrual by evaluating: a) the balance between caloric intake and resting energy expenditure, b) markers of systemic and adipose inflammation, gut integrity, and satiety/hunger, and c) subcutaneous adipose tissue (SAT) function and homeostasis. Following this, we will go on to examine how HIV/DTG use in pregnancy and postpartum affects maternal metabolic health postpartum (postpartum weight retention, adiposity, dysglycemia, insulin resistance, and dyslipidemia) as well as neonatal and child metabolic health (weight, adiposity, insulin resistance and dyslipidemia). To understand whether signature clusters of metabolites and lipid subspecies are associated with maternal and child metabolic health, we will apply widely targeted metabolomics techniques to measure maternal (in pregnancy) and cord blood metabolites, lipid subspecies, and eicosanoids. To address the different specific aims we will use a series of nested substudies, including smaller nested cohorts and efficient case-cohort designs, within the main cohort. This study will play a pivotal role in defining the obesogenic mechanisms and clinical consequences of DTG use in pregnancy in WLHIV and their children. The results of our study will provide insights into metabolic disease risk reduction in the context of HIV/ART, identify potential targets for interventions, and inform public health approaches to diminish chronic co-morbidities over the life course for WLHIV and their children.
(i) existing NIH-funded research infrastructure in SA and (ii) the NIH large R01 mechanism to enroll 1900 pregnant women in the 1st trimester (633 WLHIV initiating DTG in pregnancy, 633 WLHIV continuing DTG use from pre-pregnancy, and 633 women without HIV) and their children, following them to two years. Within this cohort, we will first examine how HIV and/or DTG use (HIV/DTG) impacts longitudinal changes in weight and adipose tissue mass in pregnancy using air displacement plethysmography. We will further investigate pathways of excess gestational weight gain and adipose accrual by evaluating: a) the balance between caloric intake and resting energy expenditure, b) markers of systemic and adipose inflammation, gut integrity, and satiety/hunger, and c) subcutaneous adipose tissue (SAT) function and homeostasis. Following this, we will go on to examine how HIV/DTG use in pregnancy and postpartum affects maternal metabolic health postpartum (postpartum weight retention, adiposity, dysglycemia, insulin resistance, and dyslipidemia) as well as neonatal and child metabolic health (weight, adiposity, insulin resistance and dyslipidemia). To understand whether signature clusters of metabolites and lipid subspecies are associated with maternal and child metabolic health, we will apply widely targeted metabolomics techniques to measure maternal (in pregnancy) and cord blood metabolites, lipid subspecies, and eicosanoids. To address the different specific aims we will use a series of nested substudies, including smaller nested cohorts and efficient case-cohort designs, within the main cohort. This study will play a pivotal role in defining the obesogenic mechanisms and clinical consequences of DTG use in pregnancy in WLHIV and their children. The results of our study will provide insights into metabolic disease risk reduction in the context of HIV/ART, identify potential targets for interventions, and inform public health approaches to diminish chronic co-morbidities over the life course for WLHIV and their children.
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论文共 566 篇作者统计合作学者相似作者
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Yoseph Gutema,Sileshi Lulseged,Mirtie Getachew, Meklit Getahun,Zenebe Melaku, Michael Tilahun,Mesfin Shimelis, Chanie Temesgen, Tsegaye Asres, Adinew Dereje, Alemu Assefa, Esayas Tewoldebirhan,Wondimu Teferi,Alemayehu Mekonnen,Ruby Fayorsey,Allison Zerbe, Jayleen Gunn,Amy Medley,Jessica Gross,Susan Hrapcak,Elaine J. Abrams
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMESno. 1 (2025): 57-63
Tamsin K Phillips, Yolanda Gomba, Pheposadi Mogoba,Florence Phelanyane,Kim Anderson,Benjamin H Chi, Kate Clouse,Mary-Ann Davies, Jonathan Euvrard,Lucia Knight,Landon Myer,Elaine J Abrams
AIDS and behavior (2025)
The Lancet Global health (2025)
Allison Hsu, Joana Falcao, Ricardino Zandamela,Allison Zerbe,Jennifer M Zech, Eduarda Pimentel de Gusmao, Elizabeth Stephanz,Mirriah Vitale,Elaine J Abrams
PLOS global public healthno. 6 (2025): e0004746-e0004746
Pharmaceuticsno. 1 (2025)
PloS oneno. 12 (2024): e0315047-e0315047
CLINICAL INFECTIOUS DISEASESno. 3 (2024): 727-733
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMESno. 2 (2024): 107-116
Keolebogile N. Mmasa, Yishan Liu,Jennifer Jao,Kathleen Malee,Justine Legbedze,Shan Sun, Sam Kgole,Gosego Masasa,Mompati Mmalane,Joseph Makhema, Nelly Mafa,Elaine J. Abrams,Kathleen M. Powis,Lauren B. Bonner
AIDS Carepp.1-6, (2024)
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#Papers: 566
#Citation: 19906
H-Index: 73
G-Index: 112
Sociability: 8
Diversity: 4
Activity: 51
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