Thromb Haemost 1995; 74(06): 1497-1500
DOI: 10.1055/s-0038-1649972
Original Articles
Fibrinolysis
Schattauer GmbH Stuttgart

An Amino Acid Polymorphism in Histidine-rich Glycoprotein (HRG) Explains 59% of the Variance in Plasma HRG Levels

B C Hennis
The Gaublus Laboratory TNO-PG, Leiden, The Netherlands
,
D I Boomsma
1   The Department of Psychonomics, Free University, Amsterdam, The Netherlands
,
P A van Boheemen
The Gaublus Laboratory TNO-PG, Leiden, The Netherlands
,
L Engesser
The Gaublus Laboratory TNO-PG, Leiden, The Netherlands
,
P Kievit
The Gaublus Laboratory TNO-PG, Leiden, The Netherlands
,
G Dooijewaard
The Gaublus Laboratory TNO-PG, Leiden, The Netherlands
,
C Kluft
The Gaublus Laboratory TNO-PG, Leiden, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 08 May 1995

Accepted after resubmission 17 August 1995

Publication Date:
10 July 2018 (online)

Summary

A pedigree-based maximum likelihood method developed by Lange et al. (12) was used to study the contribution of a newly defined di-allelic polymorphism in histidine-rich glycoprotein (HRG) to the plasma levels of HRG. In four families (n = 99) and 20 volunteers we found a heritability of 70%, an age effect of 3% and an effect of individual environmental factors of 27%. These results are remarkably similar to the results found in a previous parent-twin study in which a heritability of 69% and an effect of random environment of 31% was found. The overall genetic influence in the present study can be subdivided into an effect of 59% by the HRG phenotype and 11% by residual genetic factors. The influence of the HRG phenotype of 59% can entirely be explained by adding up the effect of the two alleles that make up the phenotype. These results indicate a codominant inheritance pattern of HRG levels in which the genetic influence can almost completely be ascribed to the additive effect of the di-allelic HRG locus whereas only a small part is due to other loci.

 
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