Copy-Years Viremia and Risk of Virological Failure in Long-Term-Treated HIV Patients.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 04 2019
Historique:
pubmed: 12 12 2018
medline: 19 12 2019
entrez: 12 12 2018
Statut: ppublish

Résumé

Viremia copy-years (VCY) is associated with mortality and disease outcome prediction. This study evaluated the association of VCY with virological failure (VF), defined as a plasma viral load (pVL) >400 copies/mL, and with single levels of viremia. Eight hundred and fifty antiretroviral therapy (ART)-treated patients with pVL < 37 copies/mL [target not detected or target detected (TD)] or >37, but less than 200 copies/mL (low-level viremia), and at least 6-pVL measures during 54 months of follow-up were selected. VCY was calculated individually over the follow-up as the area under pVL curve. Pearson's χ test was used to analyze differences in VCY quartiles distribution between groups. Higher VCY values were detected in patients with low-level viremia {294 copy-years [interquartile range (IQR): 99-1870]} than in TD [52 copy-years (IQR: 53-153)] and target not detected groups [19 copy-years (IQR: 8-54)]. VCY was also significantly different between patients with undetectable viremia and patients with basal pVL TD (P < 0.001). Pearson's χ test revealed a significant association between VCY and basal levels of viremia (P < 0.0001). In addition, the risk of VF rose with increasing VCY (Hazard ratio 1.01, 95% confidence interval: 1.01 to 1.02). This study revealed the association of VCY with VF and with single levels of viremia suggesting that, despite the success of ART, minimal residual viremia may cause the cumulative viral burden to rise. Full viral load suppression during ART is crucial to limit the increase in VCY.

Sections du résumé

BACKGROUND
Viremia copy-years (VCY) is associated with mortality and disease outcome prediction. This study evaluated the association of VCY with virological failure (VF), defined as a plasma viral load (pVL) >400 copies/mL, and with single levels of viremia.
METHODS
Eight hundred and fifty antiretroviral therapy (ART)-treated patients with pVL < 37 copies/mL [target not detected or target detected (TD)] or >37, but less than 200 copies/mL (low-level viremia), and at least 6-pVL measures during 54 months of follow-up were selected. VCY was calculated individually over the follow-up as the area under pVL curve. Pearson's χ test was used to analyze differences in VCY quartiles distribution between groups.
RESULTS
Higher VCY values were detected in patients with low-level viremia {294 copy-years [interquartile range (IQR): 99-1870]} than in TD [52 copy-years (IQR: 53-153)] and target not detected groups [19 copy-years (IQR: 8-54)]. VCY was also significantly different between patients with undetectable viremia and patients with basal pVL TD (P < 0.001). Pearson's χ test revealed a significant association between VCY and basal levels of viremia (P < 0.0001). In addition, the risk of VF rose with increasing VCY (Hazard ratio 1.01, 95% confidence interval: 1.01 to 1.02).
CONCLUSIONS
This study revealed the association of VCY with VF and with single levels of viremia suggesting that, despite the success of ART, minimal residual viremia may cause the cumulative viral burden to rise. Full viral load suppression during ART is crucial to limit the increase in VCY.

Identifiants

pubmed: 30531307
doi: 10.1097/QAI.0000000000001931
doi:

Substances chimiques

Anti-Retroviral Agents 0
RNA, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

423-428

Auteurs

Francesca Falasca (F)

Department of Molecular Medicine, "Sapienza" University of Rome, Italy.

Corrado De Vito (C)

Department of Public Health and Infectious Diseases, "Sapienza" University of Rome, Italy.

Laura Mazzuti (L)

Department of Molecular Medicine, "Sapienza" University of Rome, Italy.

Daniele di Carlo (D)

Department of Molecular Medicine, "Sapienza" University of Rome, Italy.

Luigi Celani (L)

Department of Public Health and Infectious Diseases, "Sapienza" University of Rome, Italy.

Caterina Fimiani (C)

Department of Infectious Diseases, Umberto I University Hospital, Rome, Italy.

Gabriella dʼEttorre (G)

Department of Public Health and Infectious Diseases, "Sapienza" University of Rome, Italy.

Ivano Mezzaroma (I)

Department of Translational and Precision Medicine, "Sapienza" University of Rome, Italy.

Guido Antonelli (G)

Department of Molecular Medicine, "Sapienza" University of Rome, Italy.

Ombretta Turriziani (O)

Department of Molecular Medicine, "Sapienza" University of Rome, Italy.

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Classifications MeSH