I. Krause et al., Behcet's disease in Israel: The influence of ethnic origin on disease expression and severity, J RHEUMATOL, 28(5), 2001, pp. 1033-1036
Objective. To evaluate the relationship between ethnic origin and manifesta
tions of Behcet's disease (BD) in Israel.
Methods. We studied 100 Israeli patients with ED, 66 Jews and 34 Arabs. The
3 largest ethnic groups of Jewish patients originated from Iran/Iraq (n =
21), Turkey (n = 12), and North African countries (n = 21). Patients were e
valuated with respect to the entire spectrum of disease manifestations, and
a systemic severity score for ED was calculated for each patient, Disease
expression was compared between Jewish and Arab patients and among Jewish e
thnic groups.
Results, There were no statistically significant differences between Jewish
and Arab patients with respect to male:female ratio. prevalence of HLA-B5,
age of disease onset, or disease duration, Disease expression and severity
score were also similar in the 2 groups, but Arab patients had a higher ra
te of posterior uveitis (20.6 vs 4.6%; p < 0.03), Among the 3 largest Jewis
h ethnic groups, patients of North African origin had a significantly highe
r rate of ocular disease (p < 0.01), mainly in the form of anterior uveitis
(p < 0.01). These patients also had higher rates of arthritis, overall vas
cular disease, deep vein thrombosis, and neuro-Behcet without reaching stat
istical significance. The disease severity score in this group was signific
antly higher compared to the other Jewish ethnic groups (p < 0.02).
Conclusion, The expression of ED is similar in Israeli Jewish and Arab pati
ents but the latter have more severe eye. disease. The disease in Israeli J
ewish patients is most severe in those originating from North African count
ries.