Evidence map›Paper›PMID 40160402›Full record

ArticleAdvances in laboratory medicine2025

Evaluating the research parameters available on the Sysmex

Vicente Aguadero, María López, Míriam Ruíz, Diana Regidor, Gemma Celma

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Article in Advances in laboratory medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Vicente AguaderoLaboratory of Sant Joan Despí Moisès Broggi Hospital, Consorci del Laboratori Intercomarcal de l'Alt Penedès, l'Anoia i el Garraf (CLILAB Diagnòstics), Vilafranca del Penedès, Barcelona, Spain.
María LópezLaboratory of Sant Joan Despí Moisès Broggi Hospital, Consorci del Laboratori Intercomarcal de l'Alt Penedès, l'Anoia i el Garraf (CLILAB Diagnòstics), Vilafranca del Penedès, Barcelona, Spain.
Míriam RuízLaboratoy of Vilafranca Del Penedès, Consorci del Laboratori Intercomarcal de l'Alt Penedès, l'Anoia i el Garraf (CLILAB Diagnòstics), Vilafranca del Penedès, Barcelona, Spain.
Diana RegidorLaboratoy of Vilafranca Del Penedès, Consorci del Laboratori Intercomarcal de l'Alt Penedès, l'Anoia i el Garraf (CLILAB Diagnòstics), Vilafranca del Penedès, Barcelona, Spain.
Gemma CelmaLaboratory of Sant Joan Despí Moisès Broggi Hospital, Consorci del Laboratori Intercomarcal de l'Alt Penedès, l'Anoia i el Garraf (CLILAB Diagnòstics), Vilafranca del Penedès, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Myelodysplastic syndromes (MDS) are clonal hematopoietic disorders characterized by peripheral blood cytopenias, cellular dysplasia and risk for progression into acute leukemia. Recent studies reveal that some research parameters available on Sysmex XN-1000 Methods: Seventy-five patients older than 60 years with anemia, leukopenia or thrombocytopenia, without vitamin B12 and folate deficiency or hematological diseases underwent testing with the Sysmex XN-1000 analyzer. Results: Dysplasia was confirmed in 32 % of patients, with significant differences in Neu-GI, PDW and IPF count between the groups of patients with and without dysplasia. Neu-GI was the parameter with the highest predictive value (AUC=0.98), with such value not increasing significantly after the addition of PDW or PIF. A Neu-GI value≤146ch predicts dysplasia with a positive predictive value=90 %. Conclusions: Neu-GI is the parameter most strongly associated with dysplasia. A Neu-GI value≤146ch indicates a high probability of dysplasia and supports indication for a blood smear review. Additionally, values>152ch indicate a low probability of dysplasia.

Indexed as

dysplasiaimmature platelet fraction (IPF)neutrophil granularity index (neu-Gi)platelet distribution width (PDW)Sysmex

Identifiers

PMID40160402
PMCPMC11949553

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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.