Evidence map›Paper›PMID 29228317›Full record

ArticleThe Journal of infectious diseases2018

Leukocyte Telomere Length at Birth and During the Early Life of Children Exposed to but Uninfected With HIV After In Utero Exposure to Antiretrovirals.

Abhinav Ajaykumar, Hugo Soudeyns, Fatima Kakkar, Jason Brophy, Ari Bitnun, Ariane Alimenti, Arianne Y K Albert, Deborah M Money, Hélène C F Côté, CIHR Team in Cellular Aging and HIV Comorbidities in Women and Children and 1 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Biomarkers of Aging in HIV-Infected Children on Suppressive Antiretroviral Therapy.Journal of acquired immune deficiency syndromes (1999) · 2018
    Observational
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

11 authors.

Abhinav AjaykumarDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Hugo SoudeynsUnité d'immunopathologie virale, Centre de Recherche du CHU Sainte-Justine, Montreal, Canada.
Fatima KakkarDepartment of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Canada.
Jason BrophyDepartment of Pediatrics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada.
Ari BitnunDepartment of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Canada.
Ariane AlimentiDepartment of Pediatrics, University of British Columbia, Vancouver, Canada.
Arianne Y K AlbertBC Women's Hospital and Health Centre, Vancouver, Canada.
Deborah M MoneyDepartment of Obstetrics and Gynecology, University of British Columbia, Vancouver, Canada.
Hélène C F CôtéDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
CIHR Team in Cellular Aging and HIV Comorbidities in Women and Children
CIHR Team in Cellular Aging and HIV Comorbidities in Women and Children

Funding

CIHR
6 · The paper itself

Abstract

Background: Maternal combination antiretroviral therapy (cART) during pregnancy could impact the health of human immunodeficiency virus (HIV)-exposed, HIV-uninfected (HEU) children, because some antiretrovirals cross the placenta and can inhibit telomerase. Our objective was to compare leukocyte telomere length (LTL) in HEU children and HIV-unexposed, HIV-uninfected (HUU) children at birth and in early life and to investigate any relationship with cART exposure. Methods: HEU and HUU children's blood LTL was compared cross-sectionally at birth, and during the first three years of life. Longitudinal HEU LTL dynamics was evaluated over that same period. Results: At birth, the LTL in HEU children (n = 114) was not shorter than that in HUU children (n = 86), but female infants had longer LTL than male infants. Maternal cART (duration or type) showed no association with shorter infant LTL. Among 214 HEU children age- and sex-matched at a 1:1 ratio to HUU children, LTL declined similarly in both groups. In a longitudinal analysis, LTL attrition in HEU children was rapid from birth to 1 year of age and gradual thereafter. Zidovudine prophylaxis did not significantly alter LTL. Conclusions: Our results indicate that from birth to 3 years of age, the LTL in HEU children is not negatively affected by exposure to maternal HIV infection and cART, at least not to the regimens used within this Canadian cohort, a reassuring finding.

Indexed as

Maternal-Fetal ExchangeTelomereAdolescentAnti-Retroviral AgentsChildChild, PreschoolFemaleHIV InfectionsHumansInfantInfant, NewbornLeukocytesLongitudinal StudiesMalePregnancyPregnancy Complications, InfectiousAnti-Retroviral Agentscombination antiretroviral therapyHIV-exposed uninfectedLeukocyte telomere lengthlongitudinal LTL attritionmaternal smoking during pregnancy

Identifiers

PMID29228317
PMCPMC5853286

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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.