Cardiovascular disease (CVD) is a well-established co-morbidity of psoriasis, although
the precise unifying mechanisms remain unknown. The activity of T-cell populations
contribute to the expression of inflammatory cytokines and chemokines, endothelial
adhesion molecules, and other factors that underlie the psoriatic disease process
and also determine balances in lipid metabolism, cell trafficking, and angiogenesis.
Therefore, it has been proposed that abnormal T-cell activity may play a role in the
pathogenesis of both the psoriatic and atherosclerotic plaques [
[1]
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References
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Article info
Publication history
Published online: March 08, 2016
Accepted:
March 7,
2016
Received in revised form:
March 2,
2016
Received:
November 3,
2015
Identification
Copyright
© 2016 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.