Erythroid progenitors in the peripheral blood of children with sickle cell disease.

T B West, K Ohene-Frempong, C J Stoeckert, S Surrey
{"title":"Erythroid progenitors in the peripheral blood of children with sickle cell disease.","authors":"T B West,&nbsp;K Ohene-Frempong,&nbsp;C J Stoeckert,&nbsp;S Surrey","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>The goals of this study were (a) to determine the number of peripheral blood burst forming units-erythroid (BFU-E); (b) to define the relationship between circulating BFU-E number and fetal hemoglobin (HbF) level; and (c) to define the relationship between BFU-E number and age in pediatric sickle cell disease (SCD) patients.</p><p><strong>Patients and methods: </strong>Fetal hemoglobin (HbF) level and peripheral blood BFU-E number were determined in children < 18 years of age with SCD in a steady state of their disease. These data were compared with those of normal children.</p><p><strong>Results: </strong>An increased number of BFU-E was observed in the peripheral blood of children with SCD compared with normals (30.7 vs. 15.7 per 10(5) mononuclear cells, respectively; p = 0.009). Overall there was the suggestion of a direct relationship between HbF level and peripheral blood BFU-E number (regression coefficient = 0.445; p = 0.06). Additionally, a strong inverse relationship between BFU-E number and age (regression coefficient = -0.671; p < 0.0001) was observed.</p><p><strong>Conclusions: </strong>In children with SCD (a) there are an increased number of peripheral blood BFU-E compared with normal children; (b) the inverse relationship between HbF level and BFU-E number observed in adult SCD patients is not seen in children; and (c) there is a strong inverse relationship between age and BFU-E number. This information may help to further clarify the relationship between peripheral blood BFU-E and erythropoietic stress.</p>","PeriodicalId":22558,"journal":{"name":"The American journal of pediatric hematology/oncology","volume":"16 2","pages":"116-9"},"PeriodicalIF":0.0000,"publicationDate":"1994-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The American journal of pediatric hematology/oncology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: The goals of this study were (a) to determine the number of peripheral blood burst forming units-erythroid (BFU-E); (b) to define the relationship between circulating BFU-E number and fetal hemoglobin (HbF) level; and (c) to define the relationship between BFU-E number and age in pediatric sickle cell disease (SCD) patients.

Patients and methods: Fetal hemoglobin (HbF) level and peripheral blood BFU-E number were determined in children < 18 years of age with SCD in a steady state of their disease. These data were compared with those of normal children.

Results: An increased number of BFU-E was observed in the peripheral blood of children with SCD compared with normals (30.7 vs. 15.7 per 10(5) mononuclear cells, respectively; p = 0.009). Overall there was the suggestion of a direct relationship between HbF level and peripheral blood BFU-E number (regression coefficient = 0.445; p = 0.06). Additionally, a strong inverse relationship between BFU-E number and age (regression coefficient = -0.671; p < 0.0001) was observed.

Conclusions: In children with SCD (a) there are an increased number of peripheral blood BFU-E compared with normal children; (b) the inverse relationship between HbF level and BFU-E number observed in adult SCD patients is not seen in children; and (c) there is a strong inverse relationship between age and BFU-E number. This information may help to further clarify the relationship between peripheral blood BFU-E and erythropoietic stress.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
镰状细胞病患儿外周血中的红系祖细胞。
目的:本研究的目的是:(a)测定外周血破裂形成单位-红细胞(BFU-E)的数量;(b)确定循环BFU-E数与胎儿血红蛋白(HbF)水平的关系;(c)确定小儿镰状细胞病(SCD)患者BFU-E数与年龄的关系。患者和方法:对年龄< 18岁、病情稳定的SCD患儿进行胎儿血红蛋白(HbF)水平和外周血BFU-E数测定。这些数据与正常儿童的数据进行了比较。结果:与正常人相比,SCD患儿外周血中BFU-E的数量增加(30.7比15.7 / 10(5)单个核细胞;P = 0.009)。总体而言,HbF水平与外周血BFU-E数有直接关系(回归系数= 0.445;P = 0.06)。BFU-E值与年龄呈显著负相关(回归系数= -0.671;P < 0.0001)。结论:与正常儿童相比,SCD儿童(a)外周血BFU-E数量增加;(b)在成人SCD患者中观察到的HbF水平和BFU-E数之间的负相关关系在儿童中未见;(c)年龄与BFU-E值呈较强的负相关。这一信息可能有助于进一步阐明外周血BFU-E与红细胞生成应激之间的关系。
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
期刊最新文献
Increased cytokine levels and abnormal response of myeloid progenitor cells to granulocyte colony-stimulating factor in a case of severe congenital neutropenia. In vitro effects of stem cell factor. Recombinant human granulocyte colony stimulating factor in cyclic neutropenia: use of a new 3-day-a-week regimen. Maternal malignancy involving the products of conception: a report of malignant melanoma and medulloblastoma. Secondary acute promyelocytic leukemia in a child treated with epipodophyllotoxins. Transient abnormal myelopoiesis in Down's syndrome neonates.
×
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