Switching from boosted PIs to dolutegravir decreases soluble CD14 and adiponectin in high cardiovascular risk people living with HIV


Por: Gonzalez-Cordon, A, Assoumou, L, Moyle, G, Waters, L, Johnson, M, Domingo, P, Fox, J, Stellbrink, H, Guaraldi, G, Masia, M, Gompels, M, De Wit, S, Florence, E, Esser, S, Raffi, F, Behrens, G, Pozniak, A, Gatell, J, Martinez, E and NEAT022 Study Grp

Publicada: 1 sep 2021 Ahead of Print: 1 jun 2021
Resumen:
Background: Switching from boosted PIs to dolutegravir in people living with HIV (PLWH) with high cardiovascular risk improved plasma lipids at 48 weeks in the NEAT022 trial. Whether this strategy may have an impact on cardiovascular biomarkers is unknown. Methods: We assessed 48 week changes in biomarkers associated with inflammation, endothelial dysfunction, monocyte immune activation, oxidation, insulin resistance, hypercoagulability, heart failure, myocardial injury, and glomerular and tubular kidney injury. Results: Of 415 PLWH randomized in the NEAT022 study, 313 (75.4%) remained on allocated therapy and had paired samples available. Soluble CD14 (-11%, P< 0.001) and adiponectin (-11%, P < 0.001) significantly declined and high-sensitive C-reactive protein (-13%, P=0.069) and oxidized LDL (-13%, P=0.084) tended to decrease with dolutegravir. Switching to dolutegravir remained significantly associated with soluble CD14 and adiponectin reductions after adjustment for baseline variables. There were inverse correlations between soluble CD14 and CD4 count changes (P= 0.05), and between adiponectin and BMI changes (P< 0.001). Conclusions: Switching from boosted PIs to dolutegravir in PLWH with high cardiovascular risk Led to soluble CD14 and adiponectin reductions at 48 weeks. While decreasing soluble CD14 may entail favourable health effects in PLWH, adiponectin reduction may reflect less insulin sensitivity associated with weight gain.

Filiaciones:
Gonzalez-Cordon, A:
 Univ Barcelona, Hosp Clin IDIBAPS, Barcelona, Spain

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

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

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

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

Domingo, P:
 Hosp Santa Creu & Sant Pau, Barcelona, Spain

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

Stellbrink, H:
 Infekt Med Ctr, Hamburg, Germany

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

:
 Hosp Gen Univ Elche, Elche, Spain

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

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

Florence, E:
 Univ Ziekenhuis Antwerpen, Antwerp, Belgium

Esser, S:
 Univ Klinikum Essen, Essen, Germany

Raffi, F:
 CHU Nantes, Nantes, France

Behrens, G:
 Hannover Med Sch, Hannover, Germany

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

Gatell, J:
 Univ Barcelona, Hosp Clin IDIBAPS, Barcelona, Spain

 ViiV Healthcare, Brentford, England

Martinez, E:
 Univ Barcelona, Hosp Clin IDIBAPS, Barcelona, Spain
ISSN: 03057453





JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Editorial
OXFORD UNIV PRESS, GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 76 Número: 9
Páginas: 2380-2393
WOS Id: 000692561500023
ID de PubMed: 34120186
imagen Open Access

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