Evidence map›Paper›PMID 40593283›Full record

ArticleJournal of hematopathology2025

Evaluation of CD200 marker variations and its correlation with clinicopathological features of chronic lymphocytic leukemia patients: a case-control study.

Maryam Valibeigi, Faezeh Gharehchahi, Tahereh Kalantari, Reza Ranjbaran, Gholamreza Rafie Dehbidi, Mani Ramzi, Sedigheh Sharifzadeh

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

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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

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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.

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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

7 authors.

Maryam ValibeigiShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of.
Faezeh GharehchahiShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of.
Tahereh KalantariShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of.
Reza RanjbaranShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of.
Gholamreza Rafie DehbidiShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of.
Mani RamziShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of.
Sedigheh SharifzadehShiraz University of Medical Sciences, Shiraz, Iran, Islamic Republic of. sharifsd@sums.ac.ir.

Funding

Shiraz University of Medical Sciences 7060
6 · The paper itself

Abstract

Given its strong correlation with disease progression and risk stratification, CD200 has emerged as a pivotal biomarker in chronic lymphocytic leukemia (CLL). Elevated CD200 expression, strongly linked to CLL progression, underscores its diagnostic and therapeutic potential. In this case-control study, we evaluated CD200 expression levels in CLL patients and analyzed their correlation with key clinicopathological features, investigating its potential as a critical biomarker for diagnosis and follow-up strategies. Peripheral blood samples from 27 CLL patients and five healthy individuals were stained by fluorochrome-conjugated antibodies against CD19 and CD200 markers, followed by flow cytometry. Data analysis compared CD200 expression levels among CLL patients at four stages and in the healthy control group. CD200 expression levels in CLL patients' lymphocytes significantly exceeded those observed in the healthy control group (P < 0.0001). Within the patient group, expression levels progressively increased from low-risk to high-risk classifications, with statistically significant differences between each category (P < 0.0001). Furthermore, a strong positive association was identified between CD200 expression and disease clinical stage (r = 0.758, P < 0.0001), WBC count (r = 0.705, P < 0.0001), and lymphocyte percentage (r = 0.544, P = 0.009). Conversely, a strong inverse correlation was observed with neutrophil count (r =  - 0.55, P = 0.008). Overall, CD200 assessment may serve as a valuable prognostic marker in CLL, providing insight into disease progression and aiding in treatment monitoring.

Indexed as

Antigens, CDBiomarkers, TumorLeukemia, Lymphocytic, Chronic, B-CellAdultAgedAged, 80 and overCase-Control StudiesFemaleHumansMaleMiddle AgedPrognosisAntigens, CDantigens, CD200Biomarkers, TumorCD200Chronic lymphocytic leukemiaClinical responseFlow cytometryPrognosis

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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.