Evidence map›Paper›PMID 34935195›Full record

ArticleJournal of clinical laboratory analysis2022

The expression and clinical significance of CD59 and FLAER in Chinese adult AML patients.

Lijuan Li, Shunjie Yu, Shanshan Liu, Fanqiao Meng, Xiaotong Ren, Zhaoyun Liu, Rong Fu

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 5 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

7 authors at 1 institution in 1 country.

Lijuan LiDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.ORCID https://orcid.org/0000-0001-8913-3915
Shunjie YuDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.
Shanshan LiuDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.
Fanqiao MengDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.
Xiaotong RenDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.
Zhaoyun LiuDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.
Rong FuDepartment of Hematology, General Hospital, Tianjin Medical University, Tianjin, China.
Tianjin Medical University General Hospital · CN

Funding

National Natural Science Fund of China 81770118
6 · The paper itself

Abstract

backgroundThe role of CD59 and fluorescently labeled aerolysin (FLAER) in acute myeloid leukemia (AML) remains unclear and requires further investigation. To explore the relationship between CD59, FLAER, and AML, we investigated CD59 and FLAER expression in AML and analyzed their relationship with clinical characteristics of AML patients.

methodsWe employed flow cytometry (FCM) to analyze CD59 and FLAER expression in 161 AML patients at Tianjin Medical University General Hospital and evaluated its association with sex, white blood cell (WBC) count, platelet (PLT) count, thrombin time (TT), prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen (FIB), D-Dimer(D-D), and lactate dehydrogenase (LDH), followed by analyzing its connection with disease progression and complete remission (CR).

resultsCD59 and FLAER deficiencies were identified in AML patients. Compared with CR group, non-CR group patients revealed more CD59 and FLAER deficiency. Compared with non-acute promyelocytic leukemia (M3) group, M3 group patients had more CD59 and FLAER deficiency. CD59

conclusionsWe demonstrated that the decline in CD59 and FLAER levels was associated with leukemia cell proliferation and abnormal coagulation function in AML, suggesting that they could serve as a predictor of AML coagulation dysfunction, particularly in M3.

Indexed as

AdolescentAdultAgedAged, 80 and overBacterial ToxinsBiomarkers, TumorBlood Coagulation DisordersCD59 AntigensCell ProliferationChinaFemaleFlow CytometryHumansLeukemia, Myeloid, AcuteMaleMiddle AgedaerolysinBacterial ToxinsBiomarkers, TumorCD59 AntigensCD59 protein, humanPore Forming Cytotoxic Proteinsacute myeloid leukemiaCD59coagulation functionFLAER

Identifiers

PMID34935195
PMCPMC8761415
OpenAlexW4200390242

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.