Homocysteine is a risk factor for cerebral small vessel disease, acting via endothelial dysfunction
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Open Access
- 1 January 2004
- journal article
- research article
- Published by Oxford University Press (OUP) in Brain
- Vol. 127 (1) , 212-219
- https://doi.org/10.1093/brain/awh023
Abstract
Cerebral small vessel disease (SVD) causes focal lacunar infarction and more diffuse ischaemia, referred to as leukoaraiosis. Endothelial dysfunction has been proposed as a causal mechanism in the disease. Homocysteine is toxic to endothelium. We determined whether elevated homocysteine levels and the methylene tetrahydrofolate reductase (MTHFR) C677T polymorphism are risk factors for SVD as a whole, and for two different SVD subtypes: isolated lacunar infarction and ischaemic leukoaraiosis. We also determined whether any association was mediated by endothelial dysfunction, as assessed by circulating endothelial markers. One hundred and seventy‐two Caucasian patients with SVD and 172 community controls of similar age and sex were studied. Serum homocysteine measurement and MTHFR genotyping was performed. Levels of intercellular adhesion molecule 1 (ICAM1) and thrombomodulin were measured in a subgroup. Mean homocysteine levels were higher in SVD than controls [14.55 µmol/l [95% confidence interval (CI) 13.78–15.35] versus 12.01 µmol/l (95% CI 11.42–12.64), P < 0.0005]. Homocysteine was a stronger risk factor in those with ischaemic leukoaraiosis [12.92 (95% CI 4.40–37.98), P < 0.0005) per µmol increase in log homocysteine concentration (P < 0.0005)] in comparison with isolated lacunar infarction [4.22 (95% CI 1.29–13.73), P = 0.02] after controlling for both conventional risk factors and age. The MTHFR 677T allele was a risk factor only in the ischaemic leukoaraiosis group [odds ratio (OR) 2.02 (95% CI 1.31–3.1), P = 0.001]. Inclusion of the endothelial markers ICAM1 and thrombomodulin in a logistic regression model resulted in the association between homocysteine and SVD no longer being significant. In conclusion, hyperhomocysteinaemia is an independent risk factor for SVD, particularly ischaemic leukoaraiosis, and this effect may be mediated via endothelial dysfunction. Homocysteine‐lowering therapy may be particularly effective in this subgroup.Keywords
This publication has 12 references indexed in Scilit:
- Markers of endothelial dysfunction in lacunar infarction and ischaemic leukoaraiosisBrain, 2003
- Two Types of Lacunar InfarctsStroke, 2002
- Homocysteine, silent brain infarcts, and white matter lesions: The Rotterdam scan studyAnnals of Neurology, 2002
- Plasma Homocysteine as a Risk Factor for Dementia and Alzheimer's DiseaseNew England Journal of Medicine, 2002
- Homocysteine Elicits a DNA Damage Response in Neurons That Promotes Apoptosis and Hypersensitivity to ExcitotoxicityJournal of Neuroscience, 2000
- Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment.Stroke, 1993
- Practical statistics for medical research. Douglas G. Altman, Chapman and Hall, London, 1991. No. of pages: 611. Price: £32.00Statistics in Medicine, 1991
- Incidental subcortical lesions identified on magnetic resonance imaging in the elderly. II. Postmortem pathological correlations.Stroke, 1986
- Homocysteine-induced endothelial cell injury in vitro: A model for the study of vascular injuryThrombosis Research, 1980
- Capsular InfarctsArchives of Neurology, 1979