POSSIBLE FACTORS INFLUENCING THE HEMOGLOBIN AND FETAL HEMOGLOBIN LEVELS IN PATIENTS WITH BETA-THALASSEMIA DUE TO A HOMOZYGOSITY FOR THE IVS-I-6 (T-]C) MUTATION

被引:23
作者
EFREMOV, DG
DIMOVSKI, AJ
BAYSAL, E
YE, Z
ADEKILE, AD
RIBEIRO, MLS
SCHILIRO, G
ALTAY, C
GURGEY, A
EFREMOV, GD
HUISMAN, THJ
机构
[1] MED COLL GEORGIA,DEPT BIOCHEM & MOLEC BIOL,AUGUSTA,GA 30912
[2] CTR HOSP COIMBRA,DEPT HAEMATOL,COIMBRA,PORTUGAL
[3] UNIV CATANIA,CATTEDRA EMATOL PEDIAT,IST CLIN PEDIAT 1,CATANIA,ITALY
[4] HACETTEPE UNIV,CHILDRENS MED CTR,DEPT PAEDIAT,ANKARA,TURKEY
[5] MACEDONIAN ACAD SCI & ARTS,NEW TECHNOL RES CTR,SKOPJE,MACEDONIA
关键词
BETA-THALASSEMIA; HEMOGLOBIN; FETAL HEMOGLOBIN; IVS-I-6 (T-]C) MUTATION; HOMOZYGOSITY;
D O I
10.1111/j.1365-2141.1994.tb04837.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have collected haematological, haemoglobin (Hb) and DNA sequence data for 29 patients with a homozygosity for the IVS-I-6 (T-->C) mutation with the intention of identifying factors contributing to the observed variability in the severity of the disease. None of the patients had received blood transfusion therapy for at least 6 months prior to the study. Hb levels varied from 5.0 to 9.9 g/dl. Patients with high Hb F (more than 1.5 g/dl or >20%) had high total Hb levels (7.5-9.7 g/dl) but some with low Hb F also had high total Hb levels; two had a concomitant alpha-thalassaemia-2 (alpha-thal-2) heterozygosity. An inverse correlation between the Hb F and Hb A(2) levels was observed. The majority of the patients were homozygous for haplotype VI (49/58 chromosomes) but haplotypes IV (2/58) and VII (7/58) were also present. The only haplotype IV homozygote had high Hb F levels with high G(gamma) values and the C-->T mutation at position -158 in the G(gamma) promoter, while both high and low Hb F levels were observed among patients with haplotypes VI and VII. Analysis of sequence variations in regulatory regions included the 5'hypersensitive sites (HS) 4, 3 and 2 of the locus control region (LCR), the G(gamma) and A(gamma) 5' flanking regions, the second intervening sequence (IVS-II), and the 5' beta-globin gene region in two patients with high Hb F (one homozygote each for haplotypes VI and IV), and in two patients with low Hb F levels (one homozygote each for haplotypes VI and VII). Haplotype specific differences were observed in the LCR 5' HS-2 and in the G(gamma) and A(gamma) flanking and IVS-II regions; however, no differences were present between the low and high Hb F-producing haplotype VI chromosomes, suggesting a major role for factors which are not linked to the beta-globin gene cluster in mediating gamma-globin gene expression in patients with this type of beta-thal.
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页码:824 / 830
页数:7
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