Evidence map›Paper›PMID 33513838›Full record

ArticleCancers2021

Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations.

Yan Jiang, Jean-Richard Eveillard, Marie-Anne Couturier, Benoit Soubise, Jian-Min Chen, Sujun Gao, Audrey Basinko, Frédéric Morel, Nathalie Douet-Guilbert, Marie-Bérengère Troadec

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 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

10 authors at 3 institutions in 2 countries.

Yan JiangUniv Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, France.ORCID 0000-0002-5005-0642
Jean-Richard EveillardCHRU Brest, Service d'Hématologie, F-29200 Brest, France.
Marie-Anne CouturierCHRU Brest, Service d'Hématologie, F-29200 Brest, France.
Benoit SoubiseUniv Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, France.
Jian-Min ChenUniv Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, France.ORCID 0000-0002-2424-3969
Sujun GaoDepartment of Hematology, The First Hospital of Jilin University, Changchun 130021, China.
Audrey BasinkoCHRU Brest, Service de Génétique, Laboratoire de Génétique Chromosomique, F-29200 Brest, France.
Frédéric MorelUniv Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, France.
Nathalie Douet-GuilbertUniv Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, France.
Marie-Bérengère TroadecUniv Brest, Inserm, EFS, UMR 1078, GGB, F-29200 Brest, France.ORCID 0000-0003-2668-9670
Inserm · FRCentre Hospitalier Régional Universitaire de Brest · FRJilin University · CN

Funding

Association Gaetan Saleun MBTAssociation Halte au Cancer MBTLigue Contre le Cancer comités 22, 29, 35, 56, 79, 41
6 · The paper itself

Abstract

This study explores the hypothesis that genetic differences related to an ethnic factor may underlie differences in phenotypic expression of myelodysplastic syndrome (MDS). First, to identify clear ethnic differences, we systematically compared the epidemiology, and the clinical, biological and genetic characteristics of MDS between Asian and Western countries over the last 20 years. Asian MDS cases show a 2- to 4-fold lower incidence and a 10-year younger age of onset compared to the Western cases. A higher proportion of Western MDS patients fall into the very low- and low-risk categories while the intermediate, high and very high-risk groups are more represented in Asian MDS patients according to the Revised International Prognostic Scoring System. Next, we investigated whether differences in prognostic risk scores could find their origin in differential cytogenetic profiles. We found that 5q deletion (del(5q)) aberrations and mutations in

Indexed as

Asiacytogeneticsdel(20q), TET2del(5q), trisomy 8ETV6EuropeIDH1/2myelodysplastic syndromeprognosisRUNX1SF3B1SRSF2survivaltreatmentsU2AF1

Identifiers

PMID33513838
PMCPMC7865620
OpenAlexW3124594379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.