Iron deficiency anaemia in young women - A hypothesis on the impact of the platelet collagen receptor GPIaIIa polymorphism GPIa-C807T

被引:3
作者
Carlsson, LE [1 ]
Hempel, S [1 ]
Greinacher, A [1 ]
机构
[1] Univ Greifswald, Dept Immunol & Transfus Med, D-17487 Greifswald, Germany
关键词
anaemia; platelet; collagen receptor; GPIaIIa; integrin alpha 2 beta 1; polymorphism;
D O I
10.1034/j.1600-0609.2002.00679.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives : The expression density of GPIaIIa, the primary platelet collagen receptor (integrin alpha2beta1), is linked to two polymorphisms (GPIa-807C/T and HPA-5a/b). During evolution a gene shift from the genotypes GPIa-807CC-HPA-5bb to the genotypes GPIa-807CT-HPA-5aa has taken place. The aim of the study was to assess whether iron deficiency anaemia (e.g. increased blood loss) in young women could be associated with a specific genotype, indicating a role as potential evolutionary selection factor. Study design : Women between 18 and 40 yr of age presenting for their first blood donation were asked about alimentary habits and use of oral contraception. Haemoglobin and serum ferritin were measured and the GPIa-C807T and HPA-5 genotypes were determined. Results : Two hundred women were included and grouped according to the WHO definition for iron deficiency anaemia (haemoglobin <121 g L-1 and ferritin <15 mug L-1). Eight women fulfilled both WHO-criteria for iron deficiency anaemia, 145 women fulfilled none. No differences regarding age, use of oral contraceptives, alimentary habits, and HPA-5 were found between the groups. The GPIa-807CC genotype was strongly over-represented in the WHO-anaemic women as compared to the non-WHO-anaemic women (87.5% vs. 33.1%, P=0.003). Conclusion: Iron deficiency anaemia in young women might have been the evolutionary disadvantage causing the gene shift from GPIa-807CC to 807CT.
引用
收藏
页码:341 / 344
页数:4
相关论文
共 15 条
[1]   The α2 gene coding sequence T807/A873 of the platelet collagen receptor integrin α2β1 might be a genetic risk factor for the development of stroke in younger patients [J].
Carlsson, LE ;
Santoso, S ;
Spitzer, C ;
Kessler, C ;
Greinacher, A .
BLOOD, 1999, 93 (11) :3583-3586
[2]   Polymorphisms of the human platelet antigens HPA-1, HPA-2, HPA-3, and HPA-5 on the platelet receptors for fibrinogen (GPIIb/IIIa), von Willebrand factor (GPIb/IX), and collagen (GPIa/IIa) are not correlated with an increased risk for stroke [J].
Carlsson, LE ;
Greinacher, A ;
Spitzer, C ;
Walther, R ;
Kessler, C .
STROKE, 1997, 28 (07) :1392-1395
[3]   The number of platelet glycoprotein Ia molecules is associated with the genetically linked 807 C/T and HPA-5 polymorphisms [J].
Corral, J ;
Rivera, J ;
González-Conejero, R ;
Vicente, V .
TRANSFUSION, 1999, 39 (04) :372-378
[4]   Low platelet α2β1 levels in type I von Willebrand disease correlate with impaired platelet function in a high shear stress system [J].
Di Paola, J ;
Federici, AB ;
Mannucci, PM ;
Canciani, FT ;
Kritzik, M ;
Kunicki, TJ ;
Nugent, D .
BLOOD, 1999, 93 (11) :3578-3582
[5]   Rapid typing for human platelet antigen systems -1, -2, -3 and -5 by PCR amplification with sequence-specific primers [J].
Kluter, H ;
Fehlau, K ;
Panzer, S ;
Kirchner, H ;
Bein, G .
VOX SANGUINIS, 1996, 71 (02) :121-125
[6]   Nucleotide polymorphisms in the α2 gene define multiple alleles that are associated with differences in platelet α2β1 density [J].
Kritzik, M ;
Savage, B ;
Nugent, DJ ;
Santoso, S ;
Ruggeri, ZM ;
Kunicki, TJ .
BLOOD, 1998, 92 (07) :2382-2388
[7]  
Kroll H, 2000, THROMB HAEMOSTASIS, V83, P392
[8]   Hereditary variation in platelet integrin alpha(2)beta(1) density is associated with two silent polymorphisms in the alpha(2) gene coding sequence [J].
Kunicki, TJ ;
Kritzik, M ;
Annis, DS ;
Nugent, DJ .
BLOOD, 1997, 89 (06) :1939-1943
[9]  
Lindqvist PG, 1998, THROMB HAEMOSTASIS, V79, P69
[10]   IRON STATUS MARKERS, SERUM FERRITIN AND HEMOGLOBIN IN 1359 DANISH WOMEN IN RELATION TO MENSTRUATION, HORMONAL CONTRACEPTION, PARITY, AND POSTMENOPAUSAL HORMONE-TREATMENT [J].
MILMAN, N ;
KIRCHHOFF, M ;
JORGENSEN, T .
ANNALS OF HEMATOLOGY, 1992, 65 (02) :96-102