Methods
Sixty-eight ED patients were studied. The following disease manifestations
were used for the factor analysis. genital ulcerations, typical skin lesion
s (erythema nodosum, folliculitis or papulo-pustular rash), uveitis, CNS in
volvement, joint disease, deep vein and superficial vein thrombosis, and ga
strointestinal manifestations. The results were further analyzed according
to sex, HLA typing, and childhood vs. adult-onset disease.
Results
Five factors were derived, which accounted for 69% of the variance of the m
atrix. Factor 1 represented the association between folliculitis and genita
l ulceration. Factor 2 represented the association between papulopustular r
ash and gastrointestinal symptoms. Factor 3 represented the inverse associa
tion between superficial vein thrombosis and erythema nodosum. Factor 4 rep
resented the correlation between deep vein thrombosis and neuro-Behcet. Fac
tor 5 represented joint disease. No difference was found between males and
females in relation to factors 1, 2 or 5, but factors 3 and 4 had higher sc
ores in male patients (p = 0.1 and p = 0.07 respectively). Factor 3 was sig
nificantly higher in patients with HLA-B5, compared to HLA-B5-negative ED p
atients (p < 0.001). Factors 2 and 3 were higher in patients with adult ons
et of the disease (p = 0.07 and p = 0.003, respectively), while factor 2 wa
s higher in patients with childhood-onset BD (p = 0.07).
Conclusions
The application of factor analysis revealed possible associations between d
istinct types of skin lesions, or venous thrombosis, and other disease mani
festations of Behcet's syndrome, some of which were sex, age at onset, or H
LA-related.