Evidence map›Paper›PMID 35603857›Full record

ArticleJNCI cancer spectrum2022

Sex-Based Differences in Functional Brain Activity During Working Memory in Survivors of Pediatric Acute Lymphoblastic Leukemia.

Kellen Gandy, Matthew A Scoggins, Nicholas Phillips, Ellen van der Plas, Slim Fellah, Lisa M Jacola, Ching-Hon Pui, Melissa M Hudson, Wilburn E Reddick, Ranganatha Sitaram and 1 more

Open access · goldAbstract read
In one paragraph

Article in JNCI cancer spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. [Recent research on cognitive impairment in children with acute lymphoblastic leukemia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Review
  11. Article
  12. 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

11 authors at 3 institutions in 1 country.

Kellen GandyDepartment of Epidemiology and Cancer Control, St. Jude's Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-4769-9114
Matthew A ScogginsDepartment of Diagnostic Imaging, St. Jude's Children's Research Hospital, Memphis, TN, USA.
Nicholas PhillipsDepartment of Epidemiology and Cancer Control, St. Jude's Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-2021-4036
Ellen van der PlasDepartment of Psychiatry, University of Iowa Hospital and Clinics, Iowa City, IA, USA.ORCID 0000-0002-7490-6636
Slim FellahDepartment of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Lisa M JacolaDepartment of Psychology, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-2698-5816
Ching-Hon PuiDepartment of Oncology, St. Jude's Children's Research Hospital, Memphis, TN, USA.
Melissa M HudsonDepartment of Epidemiology and Cancer Control, St. Jude's Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0001-6984-2407
Wilburn E ReddickDepartment of Diagnostic Imaging, St. Jude's Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-1054-1201
Ranganatha SitaramDepartment of Diagnostic Imaging, St. Jude's Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-8577-8035
Kevin R KrullDepartment of Epidemiology and Cancer Control, St. Jude's Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-0476-7001
St. Jude Children's Research Hospital · USUniversity of Iowa Hospitals and Clinics · USWashington University in St. Louis · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
The St. Jude Lifetime CohortU01CA195547 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HUDSON, MELISSA M, NESS, KIRSTEN KIMBERLIE · 2015 to 2024
$14.9M
Risk for Psychopathology and Neurocognitive Impairment in Leukemia SurvivorsR01MH085849 · NIMH · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KRULL, KEVIN R · 2010 to 2014
$2.4M
Training in Pediatric Cancer Survivorship Outcomes and InterventionsT32CA225590 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Kevin R Krull · 2018 to 2026
$2.4M
National Institute of Mental Health (MH085849 to KRK), National Cancer Institute CA195547NCI NIH HHS P30 CA021765NCI NIH HHS T32 CA225590NCI NIH HHS U01 CA195547NIMH NIH HHS R01 MH085849
6 · The paper itself

Abstract

backgroundLong-term survivors of pediatric acute lymphoblastic leukemia are at elevated risk for neurocognitive deficits and corresponding brain dysfunction. This study examined sex-based differences in functional neuroimaging outcomes in acute lymphoblastic leukemia survivors treated with chemotherapy alone.

methodsFunctional magnetic resonance imaging (fMRI) and neurocognitive testing were obtained in 123 survivors (46% male; median [min-max] age = 14.2 years [8.3-26.5 years]; time since diagnosis = 7.7 years [5.1-12.5 years]) treated on the St. Jude Total XV treatment protocol. Participants performed the n-back working memory task in a 3 T scanner. Functional neuroimaging data were processed (realigned, slice time corrected, normalized, smoothed) and analyzed using statistical parametric mapping with contrasts for 1-back and 2-back conditions, which reflect varying degrees of working memory and task load. Group-level fMRI contrasts were stratified by sex and adjusted for age and methotrexate exposure. Statistical tests were 2-sided (P < .05 statistical significance threshold).

resultsRelative to males, female survivors exhibited less activation (ie, reduced blood oxygen dependent-level signals) in the right parietal operculum, supramarginal gyrus and inferior occipital gyrus, and bilateral superior frontal medial gyrus during increased working memory load (family-wise error-corrected P = .004 to .008, adjusting for age and methotrexate dose). Female survivors were slower to correctly respond to the 2-back condition than males (P < .05), though there were no differences in overall accuracy. Performance accuracy was negatively correlated with fMRI activity in female survivors (Pearson's r = -0.39 to -0.29, P = .001 to .02), but not in males.

conclusionsThese results suggest the working memory network is more impaired in female survivors than male survivors, which may contribute to ongoing functional deficits.

Indexed as

Memory, Short-TermPrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentChildFemaleHumansMaleMethotrexatePrefrontal CortexSurvivorsMethotrexate

Identifiers

PMID35603857
PMCPMC9041337
OpenAlexW4223605139

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.