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Novel Platelet Membrane Glycoprotein VI Dimorphism Is a Risk Factor for Myocardial Infarction

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TLDR
The GP VI 13254CC genotype increases the risk of myocardial infarction, particularly in older individuals, and the interaction of the GPVI 13254C allele with other candidate risk alleles may accentuate this risk.
Abstract
Background Glycoprotein (GP) VI plays a crucial role in platelet activation and aggregation. We investigated whether polymorphic variation at the GP VI locus confers an increased risk of myocardial infarction (MI). Methods and Results Coding and 5′ and 3′ non-coding regions of the GP VI gene were analyzed by polymerase chain reaction and conformation sensitive gel electrophoresis in 21 healthy subjects. Ten dimorphisms, 5 of which predicted amino acid substitutions (T13254C, A19871G, A21908G, A22630T, C22644A), were identified. Two core haplotypes involving 7 dimorphisms (C10781A and G10873A and all those predicting amino acid substitutions) were apparent. The contribution of the T13254C dimorphism, which predicted the substitution of serine 219 by proline, to risk of MI was assessed in 525 patients with acute MI and 474 controls, all aged <75 years. The allelic odds ratio (OR) for MI associated with the 13254C allele was 1.16 (95% CI, 0.91 to 1.46; P=0.23). Compared with corresponding control subgroups, ...

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Journal ArticleDOI

Platelet-collagen interaction: is GPVI the central receptor?

Bernhard Nieswandt, +1 more
- 15 Jul 2003 - 
TL;DR: Recent developments in understanding platelet-collagen interactions are discussed and possible mechanisms for how GPVI acts in concert with other receptors and signaling pathways to initiate hemostasis and arterial thrombosis are proposed.
Journal ArticleDOI

The role of collagen in thrombosis and hemostasis.

TL;DR: The role of collagen in the regulation of hemostasis, embracing both coagulation and platelet aggregation is reviewed, with ample evidence that collagen is one of the major activators of the platelet response after injury.
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Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists

TL;DR: In this paper, the authors identified associations of seven loci with platelet aggregation near or within GP6 (P=4.6x10(-13), PEAR1(P=3.4x10-12), ADRA2A (P =3.3x10 -11), PIK3CG (P < 0.1x10−1), MRVI1 (P 2.0x10 −8), MRVC (P 1.6×10−8), SHH (P 4.5x10)-8), and MR
Journal ArticleDOI

Platelet glycoprotein VI: its structure and function

TL;DR: GPVI is widely recognized as a requisite factor for the formation of platelet aggregates on a collagen surface under blood flow, however, individuals with GPVI-deficient or null platelets do not exhibit any strong bleeding tendency, and Analyzing this apparent dichotomy should provide a more precise understanding of the mechanism of thrombus formation.
Journal ArticleDOI

Anti-GPVI–associated ITP: an acquired platelet disorder caused by autoantibody-mediated clearance of the GPVI/FcRγ-chain complex from the human platelet surface

TL;DR: A patient with a mild bleeding disorder and a moderately reduced platelet count whose platelets fail to become activated in response to collagen or CRP and inefficiently adhere to and form thrombi on immobilized collagen under conditions of arterial shear is described.
References
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Journal ArticleDOI

Haemostatic function and ischaemic heart disease: principal results of the northwick park heart study

TL;DR: The Northwick Park Heart Study has investigated the thrombotic component of ischaemic heart disease by the inclusion of measures of haemostatic function, finding that the biochemical disturbance leading to IHD may lie at least as much in the coagulation system as in the metabolism of cholesterol.
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Genetic Susceptibility to Death from Coronary Heart Disease in a Study of Twins

TL;DR: The findings suggest that at younger ages, death from coronary heart disease is influenced by genetic factors in both women and men, and implies that the genetic effect decreases at older ages.
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The Platelet Collagen Receptor Glycoprotein VI Is a Member of the Immunoglobulin Superfamily Closely Related to FcαR and the Natural Killer Receptors

TL;DR: The ability of the cloned GPVI cDNA to code for a functional platelet collagen receptor was demonstrated in the megakaryocytic cell line Dami, and it inhibited collagen-induced platelet aggregation.
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Characteristics affecting fibrinolytic activity and plasma fibrinogen concentrations.

TL;DR: In this article, characteristics influencing fibrinolytic activity (FA) and plasma fibrinogen concentrations were examined in 1601 men aged 18-64 and 707 women aged 18 -59 in several occupational groups in North-west London.
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Glycoprotein VI is the collagen receptor in platelets which underlies tyrosine phosphorylation of the Fc receptor γ-chain

TL;DR: Results support a model where GPVI couples collagen‐stimulation of platelets to phosphorylation of the Fc receptor γ‐chain leading to activation of Syk and phospholipase Cγ2.
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