scholarly journals 21: Integrase strand transfer inhibitors given to HIV-infected women late in pregnancy decrease HIV viral load more quickly than other antiretroviral therapy (ART)

2016 ◽  
Vol 214 (1) ◽  
pp. S16
Author(s):  
Lisa Rahangdale ◽  
Jordan Cates ◽  
JoNell Potter ◽  
Martina L. Badell ◽  
Dominika Seidman ◽  
...  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Anna Prats ◽  
Ignacio Martínez-Zalacaín ◽  
Beatriz Mothe ◽  
Eugènia Negredo ◽  
Núria Pérez-Álvarez ◽  
...  

AbstractIntegrase strand transfer inhibitors (INSTI) are a main component of the current antiretroviral regimens recommended for treatment of HIV infection. However, little is known about the impact of INSTI on neurocognition and neuroimaging. We developed a prospective observational trial to evaluate the effects of INSTI-based antiretroviral therapy on comprehensive brain outcomes (cognitive, functional, and imaging) according to the time since HIV-1 acquisition. We recruited men living with HIV who initiated antiretroviral therapy with INSTI < 3 months since the estimated date of HIV-1 acquisition (n = 12) and > 6 months since estimated date of HIV-1 acquisition (n = 15). We also recruited a group of matched seronegative individuals (n = 15). Assessments were performed at baseline (before initiation of therapy in HIV arms) and at weeks 4 and 48. Baseline cognitive functioning was comparable between the arms. At week 48, we did not find cognitive differences between starting therapy with INSTI earlier than 3 months or later than 6 months after acquisition of HIV-1 infection. Functional status was poorer in individuals diagnosed earlier. This effect recovered 48 weeks after initiation of therapy. Regarding brain imaging, we found that men living with HIV initiating antiretroviral therapy later experienced a greater decrease in medial orbitofrontal cortex over time, with expected negative repercussions for decision-making tasks.


2019 ◽  
Vol 81 (4) ◽  
pp. 379-386 ◽  
Author(s):  
Kirsty Brittain ◽  
Claude A. Mellins ◽  
Robert H. Remien ◽  
Tamsin K. Phillips ◽  
Allison Zerbe ◽  
...  

AIDS ◽  
2018 ◽  
Vol 32 (5) ◽  
pp. 653-661 ◽  
Author(s):  
Sarah J. Willis ◽  
Stephen R. Cole ◽  
Daniel Westreich ◽  
Andrew Edmonds ◽  
Christopher B. Hurt ◽  
...  

2017 ◽  
Vol 76 (3) ◽  
pp. 319-329 ◽  
Author(s):  
Awachana Jiamsakul ◽  
Azar Kariminia ◽  
Keri N. Althoff ◽  
Carina Cesar ◽  
Claudia P. Cortes ◽  
...  

2012 ◽  
Vol 26 (12) ◽  
pp. 714-717 ◽  
Author(s):  
Katarina Westling ◽  
Karin Pettersson ◽  
Anneli Kaldma ◽  
Lars Navér

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Bradley T. Williamson ◽  
Heather A. Leitch

Introduction. In advanced HIV prior to combination antiretroviral therapy (ART), dysplastic marrow changes occurred and resolved with ART. Few reports of myelodysplastic syndromes (MDS) in well-controlled HIV exist and management is undefined.Methods. Patients with well-controlled HIV and higher risk MDS were identified; characteristics, treatment, and outcomes were reviewed.Results. Of 292 MDS patients since 1996, 1 (0.3%) was HIV-positive. A 56-year-old woman presented with cytopenias. CD4 was 1310 cells/mL and HIV viral load <40 copies/mL. Bone marrow biopsy showed RCMD and karyotype included del(5q) and del(7q); IPSS was intermediate-2 risk. She received azacitidine at 75% dose. Cycle 2, at full dose, was complicated by marrow aplasia and possible AML; she elected palliation. Three additional HIV patients with higher risk MDS, aged 56–64, were identified from the literature. All had deletions involving chromosomes 5 and 7. MDS treatment of 2 was not reported and one received palliation; all died of AML.Conclusion. Four higher risk MDS in well-controlled HIV were below the median age of diagnosis for HIV-negative patients; all had adverse karyotype. This is the first report of an HIV patient receiving MDS treatment with azacitidine. Cytopenias were profound and dosing in HIV patients should be considered with caution.


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