Evidence map›Paper›PMID 40996462›Full record

ArticleAnnals of hematology2025

Comprehensive analysis of the clinical feature, myeloid neoplasm-related gene mutation profiles and T cell diversity acquired pure red cell aplasia.

Yuemin Gong, Xingxing Chai, Xiaoqing Liu, Yawen Zhang, Yue Li, Yunlong Li, Jianping Hao, Guangsheng He

Abstract read
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

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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

8 authors.

Yuemin Gong *Department of Hematology, Jiangsu Province Hospital, Key Laboratory of Hematology of Nanjing, Collaborative Innovation Center for Cancer Personalized Medicine, the First Affiliated Hospital with Nanjing Medical University, Nanjing, 210000, China.
Xingxing Chai *Department of Hematology, the Second People's Hospital of Lianyungang, Lianyungang, 230601, China.
Xiaoqing LiuDepartment of Hematology, the Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, 210037, China.
Yawen ZhangDepartment of Hematology, Jiangsu Province Hospital, Key Laboratory of Hematology of Nanjing, Collaborative Innovation Center for Cancer Personalized Medicine, the First Affiliated Hospital with Nanjing Medical University, Nanjing, 210000, China.
Yue LiDepartment of Hematology, Jiangsu Province Hospital, Key Laboratory of Hematology of Nanjing, Collaborative Innovation Center for Cancer Personalized Medicine, the First Affiliated Hospital with Nanjing Medical University, Nanjing, 210000, China.
Yunlong LiChongqing Hospital of Jiangsu Province Hospital, the People's Hospital of Qijiang District Chongqing, Chongqing, 400800, China.
Jianping HaoDepartment of Hematology, Xinjiang Hematology Clinical Medical Research Center, Xinjiang Institute of Hematology, First Affiliated Hospital of Xinjiang Medical University, No.137 Liyushan Road, Urumqi , 830054, China. 13579876416@163.com.
Guangsheng HeDepartment of Hematology, Jiangsu Province Hospital, Key Laboratory of Hematology of Nanjing, Collaborative Innovation Center for Cancer Personalized Medicine, the First Affiliated Hospital with Nanjing Medical University, Nanjing, 210000, China. heguangsheng1972@sina.com.

Funding

National Natural Science Foundation of China 81900109
6 · The paper itself

Abstract

purposeAcquired pure red cell aplasia (PRCA) is a kind of rare bone marrow failure disease characterized by destruction of erythrocyte by the immune system. However, the diverse etiologies of acquired PRCA make its pathogenesis largely unclear. MATERIALS AND

methodsWe portrayed the clinicopathologic, mutation and TCR rearrangement profiles of 64 primary PRCA cases and 104 large granular lymphocytic leukemia (LGLL)-associated PRCA, and tried to reveal the association factors of CsA response.

resultsWe found that gene mutations were detected in 39.7% of acquired PRCA who were older than 40 years, with DNMT3A, KMT2A and TP53 being the top 3 mutation genes. KMT2A mutation was only detected in patients with normal reticulocyte (Ret)%, while IDH1 mutation only occurred in patients with normal CD3 + CD8+/Lym%. For LGLL-associated PRCA patients, TRBV6_TRBJ2 was the most frequent dominant clonotype and the proportion of each dominant clone decreased following the remission of anemia. The response rate of LGLL-associated PRCA to CsA treatment was lower than primary PRCA (56.4% vs. 77.4%). β2-MG dysregulation, MF dysregulation were unfavorable factors for the response to CsA in PRCA patients, while other clinical information, mutated genes, number of mutated genes, mean VAF, number of TCR clones in PRCA patients did not significantly affect the response to CsA.

conclusionThis study described the clinical features, mutation landscape and TCR rearrangement profile in a relatively larger PRCA cohort, which may contribute to the clear perception of PRCA and the development of more potent treatment approaches.

Indexed as

MutationRed-Cell Aplasia, PureT-LymphocytesAdolescentAdultAgedAged, 80 and overFemaleHumansLeukemia, Large Granular LymphocyticMaleMiddle AgedYoung AdultGene mutationLarge granular lymphocytic leukemiaPure red cell aplasiaT-cell receptor rearrangement

Identifiers

PMID40996462
PMCPMC12552327

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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.