Author/Authors :
Fallahi, Sasan Internal Medicine Division - Baharloo Hospital - Tehran University of Medical Sciences, Tehran , Mahmoudi, Mahdi Rheumatology Research Center - Shariati Hospital - Tehran University of Medical Sciences, Tehran , Nicknam, Mohammad Hossein Molecular Immunology Research Center - Tehran University of Medical Sciences, Tehran , Gharibdoost, Farhad Rheumatology Research Center - Shariati Hospital - Tehran University of Medical Sciences, Tehran , Farhadi, Elham Department of Haematology - School of Medicine - Tehran University of Medical Sciences, Tehran , Saei, Azad Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Nourijelyani, Keramat Department of Epidemiology and Biostatistics - School of Public Health - Tehran University of Medical Sciences, Tehran , Ahmadzadeh, Noushin Rheumatology Research Center - Shariati Hospital - Tehran University of Medical Sciences, Tehran , Jamshidi, Ahmad Reza Rheumatology Research Center - Shariati Hospital - Tehran University of Medical Sciences, Tehran
Abstract :
The aim of this study was to assess the role of HLA-B*27 and it’s subtypes in determining
severity and clinical manifestations of ankylosing spondylitis (AS).
A total of 163 AS patients were assessed for clinical manifestations and severity using
structured questionnaires. HLA-B*27 screening and B*27 sub-typing were performed by PCR.
One hundred twenty two patients (74.8%) were B*27 positive. The male to female ratio,
peripheral arthritis, steroid use, intense dorsal kyphosis and decrease of cervical slope had a
significantly higher frequency in B*27 positive patients compared to B*27 negative ones
(p=0.01, 0.001, 0.01, 0.04 and 0.04, respectively). However, the age of diagnosis was
significantly lower in B*27 positive patients (p=0.005). Trend in uveitis and some severity
markers including: BASMI and ASQoL were toward higher values in B*27 positive group with
no significant difference. After controlling confounding variables, significant relationship was
found only between B*27 and BASMI (p=0.01). B*27 subtypes in patients were included
B*2705: 48.4%, B*2702: 42.6%, B*2704: 5.7% and B*2707: 3.3%. No significant differences
were seen for severity markers and clinical manifestations between subtypes; although trend
toward lower values of severity markers, less intense dorsal kyphosis and less decrease of
cervical slope were observed in B*2704 and B*2707 versus other polymorphisms.
Clinical features and severity of AS is influenced by HLA-B*27. Trend toward higher
severity markers in B*2705 and B*2702 versus other polymorphisms might be subject of
interest for evaluation in other ethnicities with concentration to other novel susceptibility genes
co-inherited in each B*27 subtype.
Keywords :
Ankylosing Spondylitis , Clinical manifestations , HLA-B*27 , HLA-B*2705