Abstract
A Thr789Ala variant in the von Willebrand Factor (vWF) gene is associated with increased
vWF plasma concentrations and might therefore affect the risk of coronary heart disease
(CHD) in the general population. Patients with type 2 diabetes have an increased risk
for premature atherosclerosis and are characterized by alterations of the coagulation
system. However, it is not known whether the Thr789Ala variant in the vWF gene contributes
to the increased CHD risk in patients with type 2 diabetes. We therefore investigated
the potential relationship between the Thr789Ala variant in the vWF gene and the occurrence
of CHD in 356 patients with type 2 diabetes, either with (DM+/CHD+, n = 204) or without
evidence for CHD (DM+/CHD-, n = 152). In addition, two control groups without type
2 diabetes, with (DM-/CHD+, n = 22) or without CHD (DM-/CHD-, n = 100), were investigated.
Individuals with the vWF Thr789Ala variant have significantly higher von Willebrand
factor plasma concentrations (p < 0.001). In addition, ristocetin co-factor was significantly
increased in vWF Thr789Ala variant carriers (p < 0.05). Ristocetin co-factor levels
and collagen binding capacity were also increased in individuals affected with either
type 2 diabetes, CHD or both (DM+/CHD+, DM+/CHD-, DM-/CHD+) as compared to healthy
controls (DM-/CHD-) (p < 0.001). However, we did not find an association between the
vWF Thr789Ala variant and the occurrence of CHD in patient with type 2 diabetes (p
= 0.34). In conclusion, although the Thr789Ala vWF gene variant is associated with
increased plasma concentrations of vWF, ristocetin co factor levels and collagen binding
capacity in patients with type 2 diabetes and CHD, a direct effect of this variant
on the occurrence of CHD in patients with type 2 diabetes, could not be detected.
Key words
vWF - type 2 diabetes - CHD - Thr789Ala variant
References
1
Ballard D J, Humphrey L L, Melton 3rd L J.
Epidemiology of persistent proteinuria in typ II diabetes mellitus. Population based
study in Rochester Minnesota.
Diabetes.
1998;
37
405-412
2
Blüher M, Unger R, Rassoul F, Richter V, Paschke R.
Relation between glycaemic control, hyperinsulinaemia and plasma concentrations of
soluble adhesion molecules in patients with impaired glucose tolerance or Type II
diabetes.
Diabetologia.
2002;
45
210-216
3
Caprio S, Wong S, Alberti K GMM.
Cardiovascular complications of diabetes.
Diabetologia.
1997;
40
B78-B82
4
Carr M E.
Diabetes mellitus A hypercoagulable state.
Journal of Diabetes and its Complications.
2001;
15
44-45
5
Diabetes Control and Complication Trial Research Group .
The effect of intensive treatment of diabetes on the development and progression of
long-term complications in insulin-dependent diabetes mellitus.
N Engl J Med.
1993;
329
977-983
6
The Expert Committee on the Diagnosis and Classification of Diabetes mellitus .
Report the Expert Committee on the Diagnosis and Classification of Diabetes mellitus
(Committee Report).
Diabetes Care.
1998;
21 (Suppl 1)
S5-S19
7
Haffner S M, Lehto S, Ronnemaa T, Pyorala K, Laakso M.
Mortality form coronary heart disease in subjacts with type 2 diabetes and in nondiabetic
subjects with and without prior myocardial infarction.
N Engl J Med.
1998;
339
229-234
8
Hopfner R L, Gopalakrishnan V.
Endothelin: emerging role in diabetic vascular Complications.
Diabetologia.
1999;
42
1383-1394
9
Jager A, van Hinsbergh V W, Kostense P J, Emeis J J, Yudkin J S, Nijpels G, Dekker J M,
Heine R J, Bouter L M, Stehouwer C D.
Von Willebrand factor, C-reactive protein, and 5-year mortality in diabetic and nondiabetic
subjects: the Hoorn Study.
Arterioscler Thromb Vasc Biol.
1999;
19
3071-3078
10
Jansson J H, Nilsson T K, Johnson O.
A novel risk factor for recurrent myocardial infarction and death.
British Heart Journal.
1991;
66
351-355
11
Kunkel G R, Graham J B, Fowlkes D M, Lord S T.
Rsa I polymorphism in von Willebrand factor (vWF) at codon 789.
Nucl Acids Res.
1990;
18
7467
12
Lacquemant C, Gaucher C, Delorme C, Chatellier G, Gallois Y, Rodier M, Passa P, Balkau B,
Mazurier C, Marre M, Froguel P.
For the GENEDIAB Study Group, and the DESIR Study Group: Association between high
von Willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with
nephropathy in type 1 diabetes.
Kidney Int.
2000;
57
1437-1443
13
Leurs P B, Stolk R P, Hamulyak K, Van Oerle R, Grobbee D E, Wolffenbuttel B H.
Tissue factor pathway inhibitor and other endothelium-dependent hemostatic factors
in elderly individuals with normal or impaired glucose tolerance and type 2 diabetes.
Diabetes Care.
2002;
25
1340-1345
14
Lip G, Blann A.
Von Willebrand factor: a marker of endothelial dysfunction in vascular disorders?.
Cardiovasc Res.
1997;
34
255-265
15
Panzram G.
Mortality and survival in Type 2 (non insulin dependent) diabetes mellitus.
Diabetologia.
1987;
30
123-131
16
Pettitt D J, Saad M F, Bennett P H, Nelson R G, Knowler W C.
Familial predisposition to renal disease in two generations of Pima indians with type
II (non-insulin dependent) diabetes mellitus.
Diabetologia.
1990;
33
438-443
17
Rossing P, Rossing K, Jacobsen P.
Unchanged incidence of diabetic nephropathy in IDDM patients.
Diabetes.
1995;
44
739-743
18
Schiekofer S, Balletshofer B, Andrassy M, Bierhaus A, Nawroth P P.
Endothelial dysfunction in diabetes mellitus.
Semin Thromb Hemost.
2000;
26
503-511
19
Seaquist E R, Goetz F C, Rich S, Barbosa J.
Familial clustering of diabetic kidney disease: Evidence for genetic susceptibility
to diabetic nephropathy.
New Engl J Med.
1989;
320
1161-1165
20
Standl E, Balletshofer B, Dahl B, Weichenhain B, Stiegler H, Hörmann A, Holle R.
Predictors of 10-year macrovascular and overall mortality in patients with NIDDM:
the Munich General Practitioner Project.
Diabetologia.
1996;
39
1540-1545
21
Takahashi H, Ito S, Hanano M, Wada K, Niwano H, Seki Y, Shibata A.
Circulating thrombomodulin as a novel endothelial cell marker: comparison of its behavior
with von Willebrand factor and tissue-type plasminogen activator.
Am J Hematol.
1992;
42
32-39
22
Thompson S G, Kienast J, Pyke S DM, Haverkate F, van de Loo J CW.
Hemostatic factors and the risk of myocardial infarction or sudden death in patients
with angina pectoris.
N Engl J Med.
1995;
332
635-641
MD Ralf Paschke
University of Leipzig III. Medical Department
Philipp-Rosenthal-Straße 27
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Fax: + 49 34 19 71 32 09
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