Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy

The objective of this study was to compare red blood cell indices among normal, α-thalassemia-1 trait, and hemoglobin (Hb) Bart's fetuses at mid-pregnancy. A total of 87 pregnancies (88 fetuses) at risk of homozygous α-thalassemia-1, who underwent cordocentesis including the measurement of Hb l...

Full description

Saved in:
Bibliographic Details
Main Authors: Srisupundit K., Piyamongkol W., Tongsong T.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-56749130072&partnerID=40&md5=bdc2cdb99750a5c64a23d2179f717505
http://cmuir.cmu.ac.th/handle/6653943832/2307
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-2307
record_format dspace
spelling th-cmuir.6653943832-23072014-08-30T02:00:42Z Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy Srisupundit K. Piyamongkol W. Tongsong T. The objective of this study was to compare red blood cell indices among normal, α-thalassemia-1 trait, and hemoglobin (Hb) Bart's fetuses at mid-pregnancy. A total of 87 pregnancies (88 fetuses) at risk of homozygous α-thalassemia-1, who underwent cordocentesis including the measurement of Hb level and red blood cell indices of fetuses at 18-22 weeks of gestation at Maharaj Nakorn Chiang Mai Hospital, were recruited into this study. The final outcome was based on the fetal DNA analysis using PCR technique for SEA type α-thalassemia-1. Fetuses were divided into three groups: normal, α-thalassemia-1 trait, and homozygous athalassemia-1 (Hb Bart's disease). The mean gestational age of the 87 pregnant women recruited into the study was 18.7 ± 0.8 weeks. According to the DNA analysis, the incidence of Hb Bart's disease, α-thalassemia-1 trait, and normal fetuses were 29.5%, 45.5%, and 25%, respectively. The mean Hb level, mean corpuscular volume, mean corpuscular Hb, and mean cell Hb concentration were significantly different in all three groups of fetuses. Moreover, these differences were also found among fetuses with the α-thalassemia-1 trait and those that were normal. Ninety-two percent of fetuses with Hb Bart's disease had some degree of anemia at mid-pregnancy. However, two Hb Bart's fetuses did not have anemia. Furthermore, two fetuses in the α-thalassemia-1 trait group were mildly anemic, but most (95%) were not. There is a highly significant difference in red blood cell indices among normal, α-thalassemia-1 trait, and Hb Bart's fetuses, and most fetuses with Hb Bart's disease have some degree of anemia from mid-pregnancy. © 2008 Wiley-Liss, Inc. 2014-08-30T02:00:42Z 2014-08-30T02:00:42Z 2008 Article 03618609 10.1002/ajh.21287 18932192 AJHED http://www.scopus.com/inward/record.url?eid=2-s2.0-56749130072&partnerID=40&md5=bdc2cdb99750a5c64a23d2179f717505 http://cmuir.cmu.ac.th/handle/6653943832/2307 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description The objective of this study was to compare red blood cell indices among normal, α-thalassemia-1 trait, and hemoglobin (Hb) Bart's fetuses at mid-pregnancy. A total of 87 pregnancies (88 fetuses) at risk of homozygous α-thalassemia-1, who underwent cordocentesis including the measurement of Hb level and red blood cell indices of fetuses at 18-22 weeks of gestation at Maharaj Nakorn Chiang Mai Hospital, were recruited into this study. The final outcome was based on the fetal DNA analysis using PCR technique for SEA type α-thalassemia-1. Fetuses were divided into three groups: normal, α-thalassemia-1 trait, and homozygous athalassemia-1 (Hb Bart's disease). The mean gestational age of the 87 pregnant women recruited into the study was 18.7 ± 0.8 weeks. According to the DNA analysis, the incidence of Hb Bart's disease, α-thalassemia-1 trait, and normal fetuses were 29.5%, 45.5%, and 25%, respectively. The mean Hb level, mean corpuscular volume, mean corpuscular Hb, and mean cell Hb concentration were significantly different in all three groups of fetuses. Moreover, these differences were also found among fetuses with the α-thalassemia-1 trait and those that were normal. Ninety-two percent of fetuses with Hb Bart's disease had some degree of anemia at mid-pregnancy. However, two Hb Bart's fetuses did not have anemia. Furthermore, two fetuses in the α-thalassemia-1 trait group were mildly anemic, but most (95%) were not. There is a highly significant difference in red blood cell indices among normal, α-thalassemia-1 trait, and Hb Bart's fetuses, and most fetuses with Hb Bart's disease have some degree of anemia from mid-pregnancy. © 2008 Wiley-Liss, Inc.
format Article
author Srisupundit K.
Piyamongkol W.
Tongsong T.
spellingShingle Srisupundit K.
Piyamongkol W.
Tongsong T.
Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy
author_facet Srisupundit K.
Piyamongkol W.
Tongsong T.
author_sort Srisupundit K.
title Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy
title_short Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy
title_full Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy
title_fullStr Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy
title_full_unstemmed Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy
title_sort comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin bart's fetuses at mid-pregnancy
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-56749130072&partnerID=40&md5=bdc2cdb99750a5c64a23d2179f717505
http://cmuir.cmu.ac.th/handle/6653943832/2307
_version_ 1681419834107101184