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Frequencies of glycosylphosphatidylinositol (GPI)-deficient cells using high-sensitivity flow cytometry as per the 2018 ICCS/ESCCA consensus guideline in patients with hematologic malignancy, aplastic anemia, or cytopenia

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dc.contributor.authorKwoun, Woo-Jae-
dc.contributor.authorLee, Hwan Tae-
dc.contributor.authorAhn, Jeong-Yeal-
dc.date.accessioned2022-04-25T02:40:03Z-
dc.date.available2022-04-25T02:40:03Z-
dc.date.created2022-02-27-
dc.date.issued2022-02-
dc.identifier.issn1747-4086-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/84090-
dc.description.abstractObjectives We examined the frequencies and sizes of glycosylphosphatidylinositol (GPI)-deficient cells as per the International Clinical Cytometry Society/European Society for Clinical Cell Analysis (ICCS/ESCCA) consensus guidelines for the high-sensitivity detection of GPI-deficient cells. Methods In 2018, the ICCS/ESCCA guidelines for the high-sensitivity detection of GPI-deficient cells were published. We evaluated frequencies and sizes of GPI-deficient red blood cells (RBCs), neutrophils, and monocytes as determined using the ICCS/ESCCA guidelines and Clinical and Laboratory Standards Institute (CLSI) guidelines in patients with a hematologic malignancy, aplastic anemia, or cytopenia. Results A total of 106 (38.7%) patients exhibited GPI deficiency in at least one blood cell lineage. GPI-deficient cells of one or more lineages were found in 62.7% of patients with a hematologic malignancy, 51.1% of patients with aplastic anemia, and 23.4% of patients with cytopenia. GPI-deficient monocytes were most frequently detected in all three groups. By population size, GPI-deficient clones (>1%) in monocytes were mostly detected in patients with a hematologic malignancy or aplastic anemia. Rare cells with GPI deficiency (<0.1%) in monocytes were most common among patients with cytopenia. Conclusion High-sensitive flow cytometry analysis including monocytes may be necessary for patients with a hematologic disorder.-
dc.language영어-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.relation.isPartOfEXPERT REVIEW OF HEMATOLOGY-
dc.titleFrequencies of glycosylphosphatidylinositol (GPI)-deficient cells using high-sensitivity flow cytometry as per the 2018 ICCS/ESCCA consensus guideline in patients with hematologic malignancy, aplastic anemia, or cytopenia-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000755415900001-
dc.identifier.doi10.1080/17474086.2022.2038561-
dc.identifier.bibliographicCitationEXPERT REVIEW OF HEMATOLOGY, v.15, no.2, pp.175 - 181-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85125240018-
dc.citation.endPage181-
dc.citation.startPage175-
dc.citation.titleEXPERT REVIEW OF HEMATOLOGY-
dc.citation.volume15-
dc.citation.number2-
dc.contributor.affiliatedAuthorKwoun, Woo-Jae-
dc.contributor.affiliatedAuthorAhn, Jeong-Yeal-
dc.type.docTypeArticle; Early Access-
dc.subject.keywordAuthorParoxysmal nocturnal hemoglobinuria-
dc.subject.keywordAuthorglycosylphosphatidylinositol deficiency-
dc.subject.keywordAuthorhigh-sensitivity flow cytometry-
dc.subject.keywordAuthor2018 ICCS-
dc.subject.keywordAuthorESCCA-
dc.subject.keywordAuthorhematologic disorder-
dc.subject.keywordPlusPAROXYSMAL-NOCTURNAL HEMOGLOBINURIA-
dc.subject.keywordPlusGPI-DEFICIENT CELLS-
dc.subject.keywordPlusMYELODYSPLASTIC SYNDROMES-
dc.subject.keywordPlusANCHORED PROTEIN-
dc.subject.keywordPlusBLOOD-CELLS-
dc.subject.keywordPlusPNH-
dc.subject.keywordPlusDISORDERS-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusFLAER-
dc.subject.keywordPlusCLONES-
dc.relation.journalResearchAreaHematology-
dc.relation.journalWebOfScienceCategoryHematology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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