Evidence map›Paper›PMID 34446917›Full record

ArticleThe pharmacogenomics journal2022

Genetic factors contributing to late adverse musculoskeletal effects in childhood acute lymphoblastic leukemia survivors.

A Shalmiev, G Nadeau, M Aaron, E Ouimet-Grennan, S Drouin, L Bertout, P Beaulieu, P St-Onge, L-N Veilleux, F Rauch and 6 more

Abstract read
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In one paragraph

Article in The pharmacogenomics journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

A ShalmievUniversity of Montreal, Montreal, QC, Canada.
G NadeauUniversity of Montreal, Montreal, QC, Canada.
M AaronUniversity of Montreal, Montreal, QC, Canada.
E Ouimet-GrennanUniversity of Montreal, Montreal, QC, Canada.
S DrouinSainte-Justine University Hospital Research Centre, Montreal, QC, Canada.
L BertoutSainte-Justine University Hospital Research Centre, Montreal, QC, Canada.ORCID http://orcid.org/0000-0003-0120-7882
P BeaulieuSainte-Justine University Hospital Research Centre, Montreal, QC, Canada.
P St-OngeSainte-Justine University Hospital Research Centre, Montreal, QC, Canada.
L-N VeilleuxMontreal Shriners Hospital for Children, Montreal, QC, Canada.ORCID http://orcid.org/0000-0001-7672-8477
F RauchMontreal Shriners Hospital for Children, Montreal, QC, Canada.
A RezguiUniversity of Montreal, Montreal, QC, Canada.
K PetrykeyUniversity of Montreal, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-5865-3907
C LaverdièreUniversity of Montreal, Montreal, QC, Canada.
D SinnettUniversity of Montreal, Montreal, QC, Canada.ORCID http://orcid.org/0000-0003-3625-6676
N Alos *University of Montreal, Montreal, QC, Canada.
M Krajinovic *University of Montreal, Montreal, QC, Canada. maja.krajinovic@umontreal.ca.ORCID http://orcid.org/0000-0003-4772-7031
Centre Hospitalier Universitaire Sainte-Justine · CAUniversité de Montréal · CAShriners Hospitals for Children - Canada · CA

Funding

CIHR
6 · The paper itself

Abstract

backgroundA substantial number of survivors of childhood acute lymphoblastic leukemia (ALL) suffer from treatment-related late adverse effects. While multiple studies have identified the effects of chemotherapeutics and radiation therapy on musculoskeletal outcomes, few have investigated their associations with genetic factors.

methodsHere we analyzed musculoskeletal complications in relation to common and rare genetic variants derived through whole-exome sequencing of the PETALE cohort. Top-ranking associations were further assessed through stratified and multivariate analyses.

resultsDUOX2 variant was associated with skeletal muscle function deficit, as defined by peak muscle power Z score ≤ -2 SD (P = 4.5 × 10

conclusionThis exploratory study identified novel genetic variants associated with long-term musculoskeletal impairments in childhood ALL survivors. Replication in an independent cohort is needed to confirm the association found in this study.

Indexed as

AdolescentAdultAnatomy, Cross-SectionalBone DensityChemoradiotherapyChildChild, PreschoolCohort StudiesDual OxidasesExome SequencingFemaleGenetic VariationGenotypeHumansInfantLumbar VertebraeDual OxidasesDUOX2 protein, human

Identifiers

PMID34446917
OpenAlexW3195824168

What OpenQuestion holds

Textmetadata
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.