Limited Weight Impact After Switching From Boosted Protease Inhibitors to Dolutegravir in Persons With Human Immunodeficiency Virus With High Cardiovascular Risk: A Post Hoc Analysis of the 96-Week NEAT-022 Randomized Trial


Por: Waters, L, Assoumou, L, Gonzalez-Cordon, A, Rusconi, S, Domingo, P, Gompels, M, de Wit, S, Raffi, F, Stephan, C, Masia, M, Rockstroh, J, Katlama, C, Behrens, GMN, Moyle, G, Johnson, M, Fox, J, Stellbrink, HJ, Guaraldi, G, Florence, E, Esser, S, Gatell, JM, Pozniak, A, Martinez, E

Publicada: 1 mar 2023 Ahead of Print: 1 oct 2022
Resumen:
Background In the NEAT022 trial, virologically suppressed persons with human immunodeficiency virus (HIV) at high cardiovascular risk switching from protease inhibitors to dolutegravir either immediately (DTG-I) or after 48 weeks (DTG-D) showed noninferior virological suppression and significant lipid and cardiovascular disease risk reductions on switching to dolutegravir relative to continuing protease inhibitors. Methods In post hoc analysis, major endpoints were 48-week and 96-week weight and body mass index (BMI) changes. Factors associated with weight/BMI changes within the first 48 weeks of DTG exposure, proportion of participants by category of percentage weight change, proportions of BMI categories over time, and impact on metabolic outcomes were also assessed. Results Between May 2014 and November 2015, 204 (DTG-I) and 208 (DTG-D) participants were included. Weight significantly increased (mean, +0.810 kg DTG-I arm, and +0.979 kg DTG-D arm) in the first 48 weeks postswitch, but remained stable from 48 to 96 weeks in DTG-I arm. Switching from darunavir, White race, total to high-density lipoprotein cholesterol ratio <3.7, and normal/underweight BMI were independently associated with higher weight/BMI gains. The proportion of participants with >= 5% weight change increased similarly in both arms over time. The proportions of BMI categories, use of lipid-lowering drugs, diabetes and/or use of antidiabetic agents, and hypertension and/or use of antihypertensive agents did not change within or between arms at 48 and 96 weeks. Conclusions Switching from protease inhibitors to dolutegravir in persons with HIV with high cardiovascular risk led to modest weight gain limited to the first 48 weeks, which involved preferentially normal-weight or underweight persons and was not associated with negative metabolic outcomes. Switching from protease inhibitors to dolutegravir in persons with HIV with high cardiovascular risk led to modest weight gain limited to the first 48 weeks, which involved preferentially normal-weight or underweight persons and was not associated with negative metabolic outcomes.

Filiaciones:
Waters, L:
 Cent & North West London NHS Fdn Trust, Mortimer Market Ctr, London, England

Assoumou, L:
 Sorbonne Univ, Inst Pierre Louis Epidemiol & Sante Publ, INSERM, Paris, France

Gonzalez-Cordon, A:
 Univ Barcelona, Hosp Clin, Consorci Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain

 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Infecciosas, Madrid, Spain

Rusconi, S:
 Azienda Socio Sanit Terr Ovest Milanese, Unita Operat Malattie Infett, Osped Civile Legnano, Legnano, MI, Italy

Domingo, P:
 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Infecciosas, Madrid, Spain

 Hosp Santa Creu & Sant Pau, Barcelona, Spain

Gompels, M:
 North Bristol NHS Trust, Bristol, Avon, England

de Wit, S:
 Ctr Hosp Univ St Pierre, Brussels, Belgium

Raffi, F:
 Ctr Hosp Univ, Nantes, France

Stephan, C:
 Goethe Univ, Univ Klinikum, Abt Infektionskrankheiten, Frankfurt, Germany

Masia, M:
 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Infecciosas, Madrid, Spain

 Hosp Gen Univ Elche, Alicante, Spain

Rockstroh, J:
 Univ Klinikum, Bonn, Germany

Katlama, C:
 Hop Univ Pitie Salpetriere, Paris, France

Behrens, GMN:
 Med Hsch, Hannover, Germany

Moyle, G:
 Chelsea & Westminster Hosp NHS Fdn Trust, London, England

Johnson, M:
 Royal Free London NHS Fdn Trust, London, England

Fox, J:
 Kings Coll London, Guys & St Thomas NHS Fdn Trust, London, England

Stellbrink, HJ:
 Infektionsmed Ctr, Hamburg, Germany

Guaraldi, G:
 Univ Modena & Reggio Emilia, Modena, Italy

Florence, E:
 Inst Trop Geneeskunde, Antwerp, Belgium

Esser, S:
 Univ Klinikum, Essen, Germany

Gatell, JM:
 ViiV Healthcare, Barcelona, Spain

Pozniak, A:
 Chelsea & Westminster Hosp NHS Fdn Trust, London, England

Martinez, E:
 Univ Barcelona, Hosp Clin, Consorci Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain

 Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Infecciosas, Madrid, Spain
ISSN: 10584838
Editorial
OXFORD UNIV PRESS INC, JOURNALS DEPT, 2001 EVANS RD, CARY, NC 27513 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 76 Número: 5
Páginas: 861-875
WOS Id: 000878301600001
ID de PubMed: 36259527
imagen Green Submitted, All Open Access; Green

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