Evidence map›Paper›PMID 32766884›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2021

Shorter Granulocyte Telomeres Among Children and Adolescents With Perinatally Acquired Human Immunodeficiency Virus Infection and Chronic Lung Disease in Zimbabwe.

Abhinav Ajaykumar, Glenn C Wong, Louis-Marie Yindom, Grace McHugh, Ethel Dauya, Edith Majonga, Hilda Mujuru, Rashida A Ferrand, Sarah L Rowland-Jones, Hélène C F Côté

Open access · hybridAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 48% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Trial
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

10 authors at 5 institutions in 3 countries.

Abhinav AjaykumarDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Glenn C WongNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Louis-Marie YindomNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Grace McHughBiomedical Research and Training Institute, Harare, Zimbabwe.
Ethel DauyaBiomedical Research and Training Institute, Harare, Zimbabwe.
Edith MajongaBiomedical Research and Training Institute, Harare, Zimbabwe.
Hilda MujuruUniversity of Zimbabwe, Harare, Zimbabwe.
Rashida A FerrandBiomedical Research and Training Institute, Harare, Zimbabwe.
Sarah L Rowland-JonesNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Hélène C F CôtéDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Biomedical Research and Training Institute · ZWUniversity of Oxford · GBUniversity of British Columbia · CALondon School of Hygiene & Tropical Medicine · GBUniversity of Zimbabwe · ZW

Funding

Wellcome Trust 206316/Z/17/Z
6 · The paper itself

Abstract

backgroundChronic lung disease (CLD) has been reported among African children with perinatally acquired human immunodeficiency virus (HIV) infection (C-PHIV), despite combination antiretroviral therapy (cART). In adults, shorter telomere length (TL) has been reported in association with both CLD and HIV. As little is known in children, our objective was to compare TL in HIV-positive (cART-naive or -treated) and HIV-negative children with and without CLD.

methodsParticipants included Zimbabwean C-PHIV, aged 6-16, who were either newly diagnosed and cART-naive, or on cART for >6 months, and HIV-negative controls of similar age and sex. Packed blood cell (granulocyte) TLs from 621 children were compared cross-sectionally between groups. For a subset of newly diagnosed C-PHIV, changes in TL following cART initiation were evaluated.

resultsC-PHIV had shorter granulocyte TL compared with uninfected peers, regardless of cART. Among 255 C-PHIV without CLD, TL was shorter in cART-naive participants. In multivariable analyses adjusted for age, sex, CLD, and HIV/cART status, shorter TL was independently associated with older age, being HIV positive, and having reduced forced vital capacity (FVC). Last, cART initiation increased TL.

conclusionsIn this cohort, C-PHIV and those with reduced FVC have shorter granulocyte TL, possibly the result of increased immune activation and cellular turnover due to longstanding HIV infection with delayed cART initiation.

Indexed as

HIV InfectionsLung DiseasesAdolescentAgedChildGranulocytesHumansTelomereZimbabwechronic lung diseasecombination antiretroviral therapygranulocyte telomere lengthlung functionperinatal HIV infection

Identifiers

PMID32766884
PMCPMC8492138
OpenAlexW3048141088

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Registered trials

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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.