Phagocytic activity in Familial Mediterranean fever

Citation
G. Keskin et al., Phagocytic activity in Familial Mediterranean fever, YONSEI MED, 41(4), 2000, pp. 441-444
Citations number
26
Categorie Soggetti
General & Internal Medicine
Journal title
YONSEI MEDICAL JOURNAL
ISSN journal
05135796 → ACNP
Volume
41
Issue
4
Year of publication
2000
Pages
441 - 444
Database
ISI
SICI code
0513-5796(200008)41:4<441:PAIFMF>2.0.ZU;2-#
Abstract
Familial Mediterranean fever (FMF) is an autosomal recessive disease. Altho ugh the possibility of multiple immunologic mechanisms have been studied, t he actual mechanism is still unresolved. Forty-one patients with FMF (24 ma les and 17 females with a mean age and disease duration of 17.8+/-4.1 and 4 .7+/-2.3 years, respectively) and 14 healthy controls (10 males and 4 femal es with a mean age 23.2+/-5.1) were involved in the study. A phagotest was studied in both the patients and control groups with a FACScalibur Flow. Al l patients were in the acute stages of the disease and had not undergone co lchicine treatment for 2 months. The percentage blood phagocytic activity o f both granulocytes and monocytes were 84.23+/-8.76 and 67.28+/-10.15 in th e patient group and 94.68+/-3.24 and 76.23+/-5.7 in the control group, resp ectively. There was no statistically significant difference in the percenta ge of phagocytic activity of the granulocytes and monocytes between the FMF patients and healthy controls (p>0.05 and p>0.05, respectively).