The role of erythropoietin levels and other hematological factors in the diagnosis of polycythemia vera in Iraqi patients

IF 0.1 Q4 HEMATOLOGY Iraqi Journal of Hematology Pub Date : 2023-01-01 DOI:10.4103/ijh.ijh_8_23
Aseel Al Dayyeni, B. Al-Gailani, M. Mahdi
{"title":"The role of erythropoietin levels and other hematological factors in the diagnosis of polycythemia vera in Iraqi patients","authors":"Aseel Al Dayyeni, B. Al-Gailani, M. Mahdi","doi":"10.4103/ijh.ijh_8_23","DOIUrl":null,"url":null,"abstract":"BACKGROUND: According to the World Health Organization (WHO), erythropoietin (EPO) is only a minor criterion for the diagnosis of polycythemia vera (PV), but its diagnostic validity is controversial. OBJECTIVES: The objective was to assess the diagnostic accuracy of EPO levels and the different combinations of the laboratory and clinical criteria, defined by the latest WHO report, as markers for the diagnosis of PV in Iraqi patients. PATIENTS, MATERIALS AND METHODS: This cross-sectional study included 158 myeloproliferative neoplasm-suspected patients (48 PV, 47 essential thrombocythemia, 25 secondary thrombocytosis, and 35 nonclonal erythrocytosis). Patients were assessed for the presence of Janus Kinase 2 (JAK2) V617F mutation. Subsequently, JAK2V617F-negative patients were evaluated for the presence of JAK2 exon 12 mutations. Plasma EPO was measured in PV and nonclonal erythrocytosis patients. RESULTS: Male was more prevalent among the nonclonal erythrocytosis patients. PV patients were older and had higher levels of all hematological variables examined in the study. Although all obtained EPO levels were normal, PV patients had significantly lower levels of EPO than nonclonal erythrocytosis. In addition, the hemoglobin and hematocrit had a better diagnostic accuracy than EPO levels in both male and female patients with PV. Furthermore, a better diagnostic accuracy was obtained when JAK2 mutation status was added to the evaluation of hemoglobin or hematocrit. CONCLUSION: The low EPO level is not a good predictive marker for PV. Hemoglobin and hematocrit had equal predictive validity in the diagnosis of PV. It is convenient to evaluate JAK2 mutation as one of the major criteria in the diagnosis of PV.","PeriodicalId":53847,"journal":{"name":"Iraqi Journal of Hematology","volume":null,"pages":null},"PeriodicalIF":0.1000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iraqi Journal of Hematology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijh.ijh_8_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND: According to the World Health Organization (WHO), erythropoietin (EPO) is only a minor criterion for the diagnosis of polycythemia vera (PV), but its diagnostic validity is controversial. OBJECTIVES: The objective was to assess the diagnostic accuracy of EPO levels and the different combinations of the laboratory and clinical criteria, defined by the latest WHO report, as markers for the diagnosis of PV in Iraqi patients. PATIENTS, MATERIALS AND METHODS: This cross-sectional study included 158 myeloproliferative neoplasm-suspected patients (48 PV, 47 essential thrombocythemia, 25 secondary thrombocytosis, and 35 nonclonal erythrocytosis). Patients were assessed for the presence of Janus Kinase 2 (JAK2) V617F mutation. Subsequently, JAK2V617F-negative patients were evaluated for the presence of JAK2 exon 12 mutations. Plasma EPO was measured in PV and nonclonal erythrocytosis patients. RESULTS: Male was more prevalent among the nonclonal erythrocytosis patients. PV patients were older and had higher levels of all hematological variables examined in the study. Although all obtained EPO levels were normal, PV patients had significantly lower levels of EPO than nonclonal erythrocytosis. In addition, the hemoglobin and hematocrit had a better diagnostic accuracy than EPO levels in both male and female patients with PV. Furthermore, a better diagnostic accuracy was obtained when JAK2 mutation status was added to the evaluation of hemoglobin or hematocrit. CONCLUSION: The low EPO level is not a good predictive marker for PV. Hemoglobin and hematocrit had equal predictive validity in the diagnosis of PV. It is convenient to evaluate JAK2 mutation as one of the major criteria in the diagnosis of PV.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
红细胞生成素水平和其他血液学因素在伊拉克患者真性红细胞增多症诊断中的作用
背景:根据世界卫生组织(WHO),促红细胞生成素(EPO)只是真性红细胞增多症(PV)诊断的次要标准,但其诊断有效性存在争议。目的:目的是评估EPO水平的诊断准确性和实验室和临床标准的不同组合,由最新的世卫组织报告定义,作为诊断伊拉克患者PV的标志物。患者、材料和方法:这项横断面研究包括158例骨髓增生性肿瘤疑似患者(48例PV, 47例原发性血小板增多症,25例继发性血小板增多症,35例非克隆性红细胞增多症)。评估患者是否存在Janus Kinase 2 (JAK2) V617F突变。随后,评估jak2v617f阴性患者是否存在JAK2外显子12突变。在PV和非克隆性红细胞增多症患者中测定血浆EPO。结果:非克隆性红细胞增多症患者以男性为主。PV患者年龄较大,研究中检查的所有血液学变量水平较高。虽然所有获得的EPO水平都是正常的,但PV患者的EPO水平明显低于非克隆性红细胞增多症。此外,在男性和女性PV患者中,血红蛋白和红细胞压积比EPO水平具有更好的诊断准确性。此外,当将JAK2突变状态添加到血红蛋白或红细胞压积的评估中时,获得了更好的诊断准确性。结论:低EPO水平不是PV的良好预测指标。血红蛋白和红细胞压积对PV的诊断具有相同的预测效度。将JAK2突变作为PV诊断的主要标准之一是方便的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
17 weeks
期刊最新文献
Pathogenicity role of human herpesvirus-8 in patients with acute myeloid leukemia Serum level of human transforming growth factors β3 in Iraqi patient with chronic myeloid leukemia A comparative study to assess diagnostic efficacy of micro typing gel technique versus conventional tube technique in blood cross-match in blood bank at a tertiary care hospital Provisional diagnosis of clinically significant hemoglobinopathies and decision on suitability for marriage as part of the premarital screening program in Iraq: Iraqi Society of Hematology Guidelines Pattern of bacterial infections in neutropenic febrile patients (experience of the Specialized BMT center - Medical city complex - Baghdad, Iraq)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1