The response of skin perfusion and of rheological and immunological variables to intravenous prostanoid administration in Raynaud's phenomenon secondary to collagenosis

Vasa. 2005 Nov;34(4):243-9. doi: 10.1024/0301-1526.34.4.243.

Abstract

Background: Prostanoids are used in the treatment of Raynaud's phenomenon and acral perfusion disorders secondary to collagenosis. In subjective terms, intravenous administration of these agents produces success in more than 50% of patients. The therapeutic outcome of clinical administration of alprostadil or iloprost may vary from individual to individual.

Patients and methods: The following variables were analysed in a cross-over study in 27 patients with collagenosis and Raynaud's phenomenon: plasma viscosity and erythrocyte aggregation (rheological variables), partial pressure of oxygen and laser Doppler flowmetry in the finger region, and lymphocyte phenotyping and interleukin (IL) determinations (immunological variables).

Results: Laser Doppler flowmetry revealed significant differences between patients with secondary Raynaud's phenomenon and a control group of 25 healthy subjects. Laser Doppler readings did not change significantly as a result of the treatments. Therapy with iloprost produced a reduction in IL-1beta, L-selectin (CD 62 L) and IL-6.

Conclusion: The change in immunological variables due to iloprost may explain the long-term effects of prostaglandins in the treatment of Raynaud's phenomenon. From our results it is not possible to infer any preference for iloprost or alprostadil.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Blood Flow Velocity / drug effects
  • Collagen Diseases / complications
  • Collagen Diseases / drug therapy*
  • Collagen Diseases / physiopathology*
  • Cross-Over Studies
  • Cytokines / immunology
  • Female
  • Humans
  • Injections, Intravenous
  • Male
  • Middle Aged
  • Prostaglandins / administration & dosage*
  • Raynaud Disease / drug therapy*
  • Raynaud Disease / etiology
  • Raynaud Disease / physiopathology*
  • Skin / blood supply*
  • Skin / drug effects*
  • Skin / immunology
  • Treatment Outcome

Substances

  • Cytokines
  • Prostaglandins