Evidence map›Paper›PMID 24595021›Full record

ArticlePloS one2014

Select neurocognitive impairment in HIV-infected women: associations with HIV viral load, hepatitis C virus, and depression, but not leukocyte telomere length.

Chantelle J Giesbrecht, Allen E Thornton, Clare Hall-Patch, Evelyn J Maan, Hélène C F Côté, Deborah M Money, Melanie Murray, Neora Pick

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  9. Neurocognitive Impairment and Associated Genetic Aspects in HIV Infection.Current topics in behavioral neurosciences · 2021
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  16. Early life infection, but not breastfeeding, predicts adult blood telomere lengths in the Philippines.American journal of human biology : the official journal of the Human Biology Council · 2017
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Chantelle J GiesbrechtDepartment of Psychology, Simon Fraser University, Burnaby, British Columbia, Canada; British Columbia Mental Health and Addictions Research Institute, Vancouver, British Columbia, Canada.
Allen E ThorntonDepartment of Psychology, Simon Fraser University, Burnaby, British Columbia, Canada; British Columbia Mental Health and Addictions Research Institute, Vancouver, British Columbia, Canada.
Clare Hall-PatchOak Tree Clinic, BC Women's Hospital, Vancouver, British Columbia, Canada; CIHR Emerging Team in HIV Therapy and Aging (CARMA), Vancouver, British Columbia, Canada.
Evelyn J MaanOak Tree Clinic, BC Women's Hospital, Vancouver, British Columbia, Canada; CIHR Emerging Team in HIV Therapy and Aging (CARMA), Vancouver, British Columbia, Canada.
Hélène C F CôtéCIHR Emerging Team in HIV Therapy and Aging (CARMA), Vancouver, British Columbia, Canada; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada; Women's Health Research Institute, Vancouver, British Columbia, Canada.
Deborah M MoneyOak Tree Clinic, BC Women's Hospital, Vancouver, British Columbia, Canada; CIHR Emerging Team in HIV Therapy and Aging (CARMA), Vancouver, British Columbia, Canada; Women's Health Research Institute, Vancouver, British Columbia, Canada; Department of Obstetrics & Gynecology, University of British Columbia, Vancouver, British Columbia, Canada.
Melanie MurrayOak Tree Clinic, BC Women's Hospital, Vancouver, British Columbia, Canada; CIHR Emerging Team in HIV Therapy and Aging (CARMA), Vancouver, British Columbia, Canada; Women's Health Research Institute, Vancouver, British Columbia, Canada; Division of Infectious Disease, University of British Columbia, Vancouver, British Columbia, Canada.
Neora PickOak Tree Clinic, BC Women's Hospital, Vancouver, British Columbia, Canada; CIHR Emerging Team in HIV Therapy and Aging (CARMA), Vancouver, British Columbia, Canada; Women's Health Research Institute, Vancouver, British Columbia, Canada; Division of Infectious Disease, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundThrough implementation of combination antiretroviral therapy (cART) remarkable gains have been achieved in the management of HIV infection; nonetheless, the neurocognitive consequences of infection remain a pivotal concern in the cART era. Research has often employed norm-referenced neuropsychological scores, derived from healthy populations (excluding many seronegative individuals at high risk for HIV infection), to characterize impairments in predominately male HIV-infected populations.

methodsUsing matched-group methodology, we assessed 81 HIV-seropositive (HIV+) women with established neuropsychological measures validated for detection of HIV-related impairments, as well as additional detailed tests of executive function and decision-making from the Cambridge Neuropsychological Test Automated Battery (CANTAB).

resultsOn validated tests, the HIV+ women exhibited impairments that were limited to significantly slower information processing speed when compared with 45 HIV-seronegative (HIV-) women with very similar demographic backgrounds and illness comorbidities. Additionally, select executive impairments in shifting attention (i.e., reversal learning) and in decision-making quality were revealed in HIV+ participants. Modifiers of neurocognition in HIV-infected women included detectable HIV plasma viral load, active hepatitis C virus co-infection, and self-reported depression symptoms. In contrast, leukocyte telomere length (LTL), a marker of cellular aging, did not significantly differ between HIV+ and HIV- women, nor was LTL associated with overall neurocognition in the HIV+ group.

conclusionsThe findings suggest that well-managed HIV infection may entail a more circumscribed neurocognitive deficit pattern than that reported in many norm-referenced studies, and that common comorbidities make a secondary contribution to HIV-related neurocognitive impairments.

Indexed as

Viral LoadAdultCognition DisordersDemographyDepressionFemaleHepacivirusHIV InfectionsHIV SeropositivityHumansLeukocytesMiddle AgedReference StandardsTelomere

Identifiers

PMID24595021
PMCPMC3942358

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.