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Cardiometabolic Parameters 3 Years After Switch to Dolutegravir/Lamivudine vs Maintenance of Tenofovir Alafenamide-Based Regimens.
Batterham, Rachel L; Espinosa, Nuria; Katlama, Christine; McKellar, Mehri; Scholten, Stefan; Smith, Don E; Ait-Khaled, Mounir; George, Nisha; Wright, Jonathan; Gordon, Lori A; Moodley, Riya; Wynne, Brian; van Wyk, Jean.
Afiliación
  • Batterham RL; Department of Medicine, Centre for Obesity Research, University College London, London, UK.
  • Espinosa N; National Institute of Health Research, University College London Hospitals Biomedical Research Centre, London, UK.
  • Katlama C; Hospital Universitario Virgen del Rocío, Sevilla, Andalucía, Spain.
  • McKellar M; Service de Maladies Infectieuses et Tropicales, AP-HP, Hôpital Pitié-Salpêtrière, INSERM-Sorbonne Universités, Paris, France.
  • Scholten S; Department of Medicine, School of Medicine, Duke University, Durham, North Carolina, USA.
  • Smith DE; Praxis Hohenstaufenring, Cologne, Germany.
  • Ait-Khaled M; Albion Centre, Sydney, Australia.
  • George N; ViiV Healthcare, Brentford, UK.
  • Wright J; GSK, Bangalore, India.
  • Gordon LA; GSK, Brentford, UK.
  • Moodley R; ViiV Healthcare, Durham, North Carolina, USA.
  • Wynne B; ViiV Healthcare, Brentford, UK.
  • van Wyk J; ViiV Healthcare, Durham, North Carolina, USA.
Open Forum Infect Dis ; 10(7): ofad359, 2023 Jul.
Article en En | MEDLINE | ID: mdl-37520420
Background: Cardiometabolic outcomes were investigated 3 years after switching to the 2-drug regimen dolutegravir/lamivudine (DTG/3TC) vs continuing 3-/4-drug tenofovir alafenamide (TAF)-based regimens in a multicenter phase 3 noninferiority study based on an open-label randomized design. Method: Adults with virologically suppressed HIV-1 switched to once-daily DTG/3TC (n = 369) or continued TAF-based regimens (n = 372). Cardiometabolic health parameters were assessed through week 144 via mixed-model repeated measures or logistic regression analyses, adjusting for baseline variables. Results: At week 144, 13% (42/316) of the DTG/3TC group and 12% (37/303) of the TAF-based regimen group had ≥10% weight gain from baseline (adjusted odds ratio, 1.11; 95% CI, .68-1.80). Adjusted change from baseline in serum leptin, a surrogate marker of adiposity, was similar between groups (treatment ratio, 1.00; 95% CI, .89-1.13). The lipid profile generally favored DTG/3TC in the baseline boosted subgroup. Adjusted odds revealed no clinically meaningful differences between groups: homeostatic model assessment of insulin resistance ≥2 (adjusted odds ratio, 0.79; 95% CI, .50-1.26), metabolic syndrome (International Diabetes Federation criteria, 0.99; .59-1.68), hepatic fibrosis (fibrosis-4 index score ≥1.45, 1.39; .63-3.06), and coronary artery disease risk (Framingham risk score ≥10%, 0.92; .56-1.49). Baseline variables and characteristics associated with odds of each cardiometabolic parameter outcome were consistent with known risk factors, including age, sex, race, and some disease characteristics. Conclusions: Cardiometabolic health 3 years after switching to DTG/3TC was comparable to that for individuals continuing TAF-based regimens, further supporting DTG/3TC as a robust switch option with a stable metabolic profile. Trial registration: ClinicalTrials.gov NCT03446573.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Open Forum Infect Dis Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Open Forum Infect Dis Año: 2023 Tipo del documento: Article