Cyclosporine for Behcet's uveitis: is it associated with an increased risk of neurological involvement?


Akman-Demir G., Ayranci O., Kurtuncu M., Vanli E. N., Mutlu M., Tugal-Tutkun I.

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, sa.4, 2008 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Basım Tarihi: 2008
  • Dergi Adı: CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • İstanbul Üniversitesi Adresli: Evet

Özet

Objective. The immunosuppressant cyclosporine is widely used to treat Behcets disease (BD). The aim of this study was to determine whether cyclosporine increases the risk of neurological involvement in BD. Methods. Patient files from the Ophthalmology Department for the period 2000-2005 were screened retrospectively , and the occurrence of neurological involvement and its relationship to ocular severity were evaluated. Results. A total of 454 patients with BD were seen at the Ophthalmology Department in this period, including, 24 who had been referred from the Neurology Department. Excluded from the study were 47 patients who did not have uveitis and 114 patients with all inadequate follow-up. The remaining 269 patients had been treated with either cyclosporine (Group I, n=92), other immunosuppressants (Group II, n=132), or no treatment other than colchicine (Group III, n=45). Patients with neurological symptoms were sent to the Neurology Department for evaluation: 20 from Group I [10 with primary headache. I with depression, I with sinus thrombosis. and 8 with parenchymal neurological involvement (pNBD)]; 13 from Group II/10 with primary headache. I with premorbid epilepsy, I with sinus thrombosis, and I with pNBD/; and 5 from Group III with primary headache. The frequency of pNBD was significantly higher in Group I, and included such as seizures and MRI lesions as well as the typical symptoms of brainstem involvement and pleocytosis. Eye involvement tended to be more severe in Group I. and the difference remained significant both Q e when milder cases were excluded from the analysis (6 vs. 0; p=0.03) and when severe cases were excluded (p=0.04). pNBD was significantly more frequent in patients on cyclosporine alone than in those receiving cyclosporine phis another agent. Conclusion. In patients with Behcets uveitis, cyclosporine seems to be associated with all increased risk of developing pNBD, although the reason for this is unknown. A prospective trial is needed to shed light onthis problem.