AI Article Synopsis

  • Herpes virus infections, particularly HSV-1, CMV, and EBV, may contribute to the development of atherosclerosis, as indicated by their presence in atherosclerotic plaques.
  • A study analyzing 48 biopsies showed that HSV-1 DNA was found more frequently in plaques than in control vascular tissues, while CMV and EBV were exclusively present in the plaques.
  • The presence of herpes viral DNA was linked to arterial hypertension, suggesting that these infections could impact vessel health and potentially increase the risk of atherosclerosis or restenosis in grafts used for bypass surgery.

Article Abstract

Background: Herpes virus infections are suspected to be involved in the pathogenesis of atherosclerosis.

Objective And Method: Viral DNA of herpes simplex virus (HSV), Epstein-Barr virus (EBV) and cytomegalovirus (CMV) was analyzed by real-time PCR on 48 biopsies from atherosclerotic plaques extracted by end-arterectomy (46 coronary arteries, 2 carotid arteries), and in tissue from non-atherosclerosis vessels from the same patient as controls (23 internal mammary arteries, 43 saphenous veins).

Results: HSV-1 DNA was detected significantly more frequently in plaques (35%) than in control veins (9%, P = 0.006). However, the frequency of HSV-1 DNA detection in the internal mammary artery grafts was as high as in plaques (22%, P = 0.28). CMV and EBV DNA were exclusively found in plaques but not in controls, with 10% for CMV (P = 0.06 versus veins, P = 0.17 versus graft arteries) and 2% for EBV (P = 1.0), respectively. HSV-2 was neither detected in plaques nor in controls. Herpes viral DNA was significantly associated only with arterial hypertension but not with other classical risk factors (P = 0.02), in accordance with the hypothesis that herpes viral infection may alter the vessel wall.

Conclusion: We conclude that herpes viral infections may have a role in atherosclerosis and that the presence of herpes viral DNA in the grafts used for bypass surgery might constitute a potential risk for atherosclerosis or restenosis.

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Source
http://dx.doi.org/10.1016/j.jcv.2004.06.010DOI Listing

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