The effect of propylthiouracil on plasma adenosine deaminase activity in patients with psoriasis Psoriazisli hastalarda, propiltiourasil'in plazma adenozin deaminaz aktivitesi uzerine etkisi


KÖSE S. K., Utas S., YAZICI C., Akdas A., Kelestimur F., Dogan P.

Turkderm Deri Hastaliklari ve Frengi Arsivi, cilt.32, sa.2, ss.111-115, 1998 (ESCI) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 32 Sayı: 2
  • Basım Tarihi: 1998
  • Dergi Adı: Turkderm Deri Hastaliklari ve Frengi Arsivi
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, Academic Search Premier, CINAHL, EMBASE, Directory of Open Access Journals
  • Sayfa Sayıları: ss.111-115
  • Erciyes Üniversitesi Adresli: Evet

Özet

Background and Design: The point of view that T lymphocyte activation may be correlated to the pathogenesis of psoriasis has been considered important during last years. Adenosine deaminase (ADA) activity has been accepted as a nonspecific marker for the activation of T cells. In this study, the presence of T cell activation and also the effectiveness of propylthiouracil (PTU), suggested as an antioxidant ammunomodulatory, for therapeutic purpose were investigated in psoriasis. Materials and Methods: ADA activity was measured in the plasma of 30 psoriatic patients resistant to conventional therapy and compared with that of healthy control subjects (n:15). Thereafter, plasma ADA activity was measured again in 16 of those patients orally administrated PTU (3x100 mg/day) for two months. The severity of the disease was evaluated in the pre- and post-treatment cases according to PASI scores. Results: Plasma ADA activity was found to be higher in those patients (20.66±5.88 U/L) than that of controls (16.68±3.32 U/L). It was observed that plasma ADA activity (21.34±5.89 U/L) was lowered after PTU treatment (15.56±3.31 U/L). PASI scores of patients were found to be lower after PTU treatment. Conclusion: It may be suggested that T lymphocyte activation may play an important role in the pathogenesis of psoriasis, and also PTU may be effective on the supression of T cell activation and therefore on the achievement of clinical improvement in psoriasis.