Disease patterns of patients with Behcet's disease demonstrated by factor analysis

Citation
I. Krause et al., Disease patterns of patients with Behcet's disease demonstrated by factor analysis, CLIN EXP RH, 17(3), 1999, pp. 347-350
Citations number
16
Categorie Soggetti
Rheumatology,"da verificare
Journal title
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
ISSN journal
0392856X → ACNP
Volume
17
Issue
3
Year of publication
1999
Pages
347 - 350
Database
ISI
SICI code
0392-856X(199905/06)17:3<347:DPOPWB>2.0.ZU;2-V
Abstract
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.