Evidence map›Paper›PMID 32337220›Full record

ArticleBioMed research international2020

Levels of Soluble CD30 and CD26 and Their Clinical Significance in Patients with Primary Immune Thrombocytopenia.

Honghui Wang, Xueping Gu, Huiyuan Li, Lingmei Yin, Wei Tao, Jingxing Yu, Qiyuan Zhou, Hongli Mu, Yu Shen, Jin Yao and 4 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 96% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 3 institutions in 2 countries.

Honghui WangDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.ORCID https://orcid.org/0000-0003-0438-0234
Xueping GuDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Huiyuan LiState Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Lingmei YinDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Wei TaoDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Jingxing YuDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Qiyuan ZhouCollege of Biological Sciences, University of California, Davis, CA, USA.
Hongli MuDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Yu ShenDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Jin YaoDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Lin LiuDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Hui BiDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.ORCID https://orcid.org/0000-0002-4532-9948
Renchi YangState Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Zeping ZhouDepartment of Hematology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.ORCID https://orcid.org/0000-0002-7698-7695
Kunming Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNUniversity of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundsCD30 and sCD26 are correlated with autoimmune diseases. However, little research has been done on the relationship between them and primary immune thrombocytopenia (ITP).

methodsThis study enrolled 47 patients diagnosed with ITP in the Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences (Tianjin, China), from January 2015 to August 2015. The peripheral blood of all subjects was collected. The mRNA expression of CD30 was quantified by RT-PCR, and concentrations of sCD30 and sCD26 were measured by ELISA. Patient characteristics, CD30 mRNA levels, and sCD30 and sCD26 concentrations were analyzed.

resultsThe concentration of sCD30 was higher in active ITP patients (median, 35.82 ng/mL) than in remission ITP patients (median, 23.12 ng/mL;

conclusionSince sCD30 levels and sCD26/sCD30 ratios may contribute to the activity of the disease, they may be used to assess ITP disease activity.

Indexed as

AdolescentAdultAgedBiomarkersCase-Control StudiesDipeptidyl Peptidase 4FemaleHumansKi-1 AntigenMaleMiddle AgedPurpura, Thrombocytopenic, IdiopathicYoung AdultBiomarkersDipeptidyl Peptidase 4DPP4 protein, humanKi-1 Antigen

Identifiers

PMID32337220
PMCPMC7152940
OpenAlexW3014938785

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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.