Evidence map›Paper›PMID 31568142›Full record

Trial reportThe Pediatric infectious disease journal2019

Trajectory Analysis of Cognitive Outcomes in Children With Perinatal HIV.

Payal B Patel, Tanakorn Apornpong, Thanyawee Puthanakit, Kulvadee Thongpibul, Pope Kosalaraksa, Rawiwan Hansudewechakul, Suparat Kanjanavanit, Chiawat Ngampiyaskul, Wicharn Luesomboon, Jurai Wongsawat and 10 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Pediatric infectious disease journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Review
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

20 authors.

Payal B PatelFrom the Department of Neurology, Yale University, New Haven, Connecticut.
Tanakorn ApornpongDepartment of Statistics, HIV-NAT, The Thai Red Cross AIDS Research Center, Bangkok, Thailand.
Thanyawee PuthanakitDepartment of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Kulvadee ThongpibulDepartment of Psychology, Faculty of Humanities, Chiang Mai University, Chiang Mai, Thailand.
Pope KosalaraksaDepartment of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Rawiwan HansudewechakulDepartment of Pediatrics, Infectious Diseases, Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.
Suparat KanjanavanitDepartment of Pediatrics, Infectious Diseases, Nakornping Hospital, Chiang Mai, Thailand.
Chiawat NgampiyaskulPrapokklao Hospital, Chantaburi, Thailand.
Wicharn LuesomboonDepartment of Pediatrics, Infectious Diseases, Queen Savang Vadhana Memorial Hospital, Chonburi, Thailand.
Jurai WongsawatDepartment of Pediatrics, Infectious Diseases, Bamrasnaradura Infectious Diseases Institute, Nonthaburi, Thailand.
Ly Penh SunDepartment of Infectious Diseases, Department of Infectious Diseases, National Center for HIV/AIDS Dermatology and STDs, Phnom Penh, Cambodia.
Kea ChettraDepartment of Infectious Diseases, Department of Infectious Diseases, National Center for HIV/AIDS Dermatology and STDs, Phnom Penh, Cambodia.
Vonthanak SaphonnDepartment of Pediatrics, Infectious Diseases, University of Health Sciences, Phnom Pehn, Cambodia.
Claude A MellinsDepartment of Medical Psychology, HIV Center for Clinical and Behavioral Studies, New York State Psychiatric Institute, and Columbia University, New York, New York.
Kathleen MaleeNorthwestern University Feinberg School of Medicine, Department of Psychiatry and Behavioral Science, Chicago, Illinois.
Serena SpudichFrom the Department of Neurology, Yale University, New Haven, Connecticut.
Jintanat AnanworanichDepartment of HIV Therapeutics Research, The Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland.
Stephen J KerrDepartment of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Robert PaulMissouri Institute of Mental Health, University of Missouri-St. Louis, St. Louis, Missouri.
PREDICT/Resilience Study Group

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Treatment of HIV/Tuberculosis Co-DiseaseU19AI053741 · NIAID · HIV-NAT, THE THAI RED CROSS AIDS RCH CTR · PI RUXRUNGTHAM, KIAT · 2004 to 2010
$6.3M
TRAINING IN THE PATHOGENESIS OF INFECTIOUS DISEASEST32AI007517 · NIAID · YALE UNIVERSITY · PI Jaimie Meyer, Albert C Shaw · 1997 to 2026
$6.1M
Determinants of Resilience in Youth with HIV infection and Youth affected by HIVR01MH102151 · NIMH · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI ROBB, MERLIN L · 2014 to 2018
$2.3M
Immunologic Profiles of Distinct Cognitive Trajectories in Adultswith Perinatal HIVK23MH119914 · NIMH · YALE UNIVERSITY · PI PATEL, PAYAL · 2019 to 2023
$881k
Predictors of Immunologic Long-term Non-Progression in Children with HIVR01AI075408 · NIAID · HIV-NAT, THE THAI RED CROSS AIDS RCH CTR · PI ANANWORANICH, JINTANAT · 2007 to 2010
$318k
NCATS NIH HHS UL1 TR001863NIAID NIH HHS R01 AI075408NIAID NIH HHS T32 AI007517NIAID NIH HHS U19 AI053741NIMH NIH HHS K23 MH119914NIMH NIH HHS R01 MH102151
6 · The paper itself

Abstract

backgroundChildren with perinatal HIV (pHIV) may display distinct long-term cognitive phenotypes. We used group-based trajectory modeling to identify clusters of children with pHIV after similar developmental trajectories and predictors of belonging to select cognitive trajectory groups.

methodsParticipants included children, 4-17 years of age, with pHIV in Thailand and Cambodia. Cognitive measures included translated versions of Intelligence Quotient tests, Color Trails Tests and Beery-Buktenica Developmental Test of Visual-Motor Integration conducted semiannually over 3-6 years. The best fit of trajectory groups was determined using maximum likelihood estimation. Multivariate logistic regression identified baseline factors associated with belonging to the lowest scoring trajectory group.

resultsGroup-based trajectory analyses revealed a 3-cluster classification for each cognitive test, labeled as high, medium and low scoring groups. Most trajectory group scores remained stable across age. Verbal IQ declined in all 3 trajectory groups and the high scoring group for Children's Color Trails Test 1 and 2 showed an increase in scores across age. Children in the lowest scoring trajectory group were more likely to present at an older age and report lower household income.

conclusionsGroup-based trajectory modeling succinctly classifies cohort heterogeneity in cognitive outcomes in pHIV. Most trajectories remained stable across age suggesting that cognitive potential is likely determined at an early age with the exception of a small subgroup of children who displayed developmental gains in select cognitive domains and may represent those with better cognitive reserve. Poverty and longer duration of untreated HIV may predispose children with pHIV to suboptimal cognitive development.

Indexed as

AdolescentCambodiaChildChild, PreschoolDevelopmental DisabilitiesFemaleHIV InfectionsHumansInfantMaleNeurocognitive DisordersNeuropsychological TestsPrognosisThailand

Identifiers

PMID31568142
PMCPMC6776249

What OpenQuestion holds

Textmetadata
LicenceTDM
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.