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Relationship of asymmetric dimethylarginine and homocysteine to vascular aging in systemic lupus erythematosus patients

✍ Scribed by Michelle Perna; Mary J. Roman; Deborah R. Alpert; Mary K. Crow; Michael D. Lockshin; Lisa Sammaritano; Richard B. Devereux; John P. Cooke; Jane E. Salmon


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
64 KB
Volume
62
Category
Article
ISSN
0004-3591

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✦ Synopsis


Abstract

Objective

Systemic lupus erythematosus (SLE) is independently associated with accelerated atherosclerosis and premature arterial stiffening. Asymmetric dimethylarginine (ADMA) and homocysteine are mechanistically interrelated mediators of endothelial dysfunction and correlates of atherosclerosis in the general population. The aim of this study was to assess the relationship of ADMA and homocysteine to subclinical vascular disease in patients with SLE.

Methods

One hundred twenty‐five patients with SLE who were participating in a study of cardiovascular disease underwent clinical and laboratory assessment, carotid artery ultrasonography to detect atherosclerosis, and radial artery applanation tonometry to measure arterial stiffness.

Results

Neither ADMA nor homocysteine correlated with the presence or extent of carotid atherosclerosis. In contrast, ADMA was significantly related to the arterial stiffness index. Independent correlates of arterial stiffening included the ADMA concentration, the presence of diabetes mellitus, older age at the time of diagnosis, longer disease duration, and the absence of anti‐Sm or anti‐RNP antibodies. A secondary multivariable analysis substituting homocysteine for ADMA demonstrated comparable relationships with arterial stiffness (r^2^ = 0.616 for homocysteine and r^2^ = 0.595 for ADMA).

Conclusion

ADMA and homocysteine are biomarkers for and may be mediators of premature arterial stiffening in patients with SLE. Because arterial stiffness has independent prognostic value for cardiovascular morbidity and mortality, its predictors may identify patients who are at increased risk of cardiovascular disease.


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