Evidence map›Paper›PMID 31343987›Full record

ArticleJCI insight2019

A distinct glycerophospholipid metabolism signature of acute graft versus host disease with predictive value.

Yue Liu, Aijie Huang, Qi Chen, Xiaofei Chen, Yang Fei, Xiaoming Zhao, Weiping Zhang, Zhanying Hong, Zhenyu Zhu, Jianmin Yang and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  13. Biomarkers for Allogeneic HCT Outcomes.Frontiers in immunology · 2020
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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

13 authors at 2 institutions in 1 country.

Yue LiuDepartment of Pharmaceutical Analysis, School of Pharmacy.
Aijie HuangDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Qi ChenDepartment of Health Statistics, Second Military Medical University, Shanghai, China.
Xiaofei ChenDepartment of Pharmaceutical Analysis, School of Pharmacy.
Yang FeiDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Xiaoming ZhaoDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Weiping ZhangDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Zhanying HongDepartment of Pharmaceutical Analysis, School of Pharmacy.
Zhenyu ZhuDepartment of Pharmaceutical Analysis, School of Pharmacy.
Jianmin YangDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Yifeng ChaiDepartment of Pharmaceutical Analysis, School of Pharmacy.
Jianmin WangDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Xiaoxia HuDepartment of Hematology, Institute of Hematology, Changhai Hospital, and.
Second Military Medical University · CNChanghai Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute graft-versus-host disease (aGvHD) is a major factor that limits the successful outcomes of allogeneic hematopoietic cell transplantation (alloHSCT). Currently there are few validated biomarkers that can help predict the risk of aGvHD in clinical settings.

methodsWe performed an integrated metabolomics and transcriptomics study and identified biomarkers that distinguish alloHSCT recipients with aGvHD from alloHSCT recipients without aGvHD in two separate cohorts.

resultsPathway analysis of 38 significantly altered metabolites and 1148 differentially expressed genes uncovered a distinctly altered glycerophospholipid (GPL) metabolism network. Subsequently, we developed an aGvHD risk score (GRS) based on 5 metabolites markers from GPL metabolism to predict the risk of aGvHD. GRS showed a positive predictive value of 92.2% and 89.6% in the training and validation cohorts, respectively. In addition, high GRS was correlated with poor overall survival. Gene expressions of GPL-related lipases were significantly altered in aGvHD samples, leading to dysregulated GPLs.

conclusionsUsing integrative "Omic" analysis, we unraveled a comprehensive view of the molecular perturbations underlying the pathogenesis of aGvHD. Our work represents an initial investigation of a unique metabolic and transcriptomic network that may help identify aGvHD at an early stage and facilitate preemptive therapy.

fundingNational Natural Science Foundation of China (NSFC; 81530047, 81870143, 81470321, 81770160, 81270567, 81270638, 81573396, 81703674). Shanghai Sailing Program from Science and Technology Commission Shanghai Municipality (17YF1424700). Scholarship from Shanghai Municipal Health and Family Planning Commission (2017BR012). Special Clinical Research in Health Industry in Shanghai (20184Y0054).

Indexed as

BiomarkersMetabolomicsAdolescentAdultAnimalsChinaDisease Models, AnimalFemaleGlycerophospholipidsGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedTranscriptomeYoung AdultBiomarkersGlycerophospholipidsBone marrow transplantationMetabolismTransplantation

Identifiers

PMID31343987
PMCPMC6777804
OpenAlexW2962863030

What OpenQuestion holds

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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.