Ossification of the posterior longitudinal ligament in three geographically and genetically different populations of ankylosing spondylitis and other spondyloarthropathies

STUDY DESIGN Cross sectional. RESEARCH QUESTIONS (a) Is any clinical variable of ankylosing spondylitis (AS) associated with the presence of ossification of the posterior longitudinal ligament (OPLL)? and (b) Is OPLL present in patients with AS from different geographical or genetic backgrounds? MET...

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Veröffentlicht in:Annals of the rheumatic diseases 1998-07, Vol.57 (7), p.429-433
Hauptverfasser: Ramos-Remus, Cesar, Russell, Anthony S, Gomez-Vargas, Amparo, Hernandez-Chavez, Abel, Maksymowych, Walter P, Gamez-Nava, Jorge I, Gonzalez-Lopez, Laura, García-Hernández, Alicia, Meoño-Morales, Esther, Burgos-Vargas, Ruben, Suarez-Almazor, Maria E
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Sprache:eng
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Zusammenfassung:STUDY DESIGN Cross sectional. RESEARCH QUESTIONS (a) Is any clinical variable of ankylosing spondylitis (AS) associated with the presence of ossification of the posterior longitudinal ligament (OPLL)? and (b) Is OPLL present in patients with AS from different geographical or genetic backgrounds? METHODS Three groups were assembled: (1) a prospective group of 103 consecutive AS patients from two community based rheumatology clinics from Guadalajara, who were evaluated using: a questionnaire with disease characteristic variables; clinical assessment by a neurologist; lateral radiographic views of the cervical spine and somatosensory evoked potentials (SSEP). (2) Fifty one spondyloarthropathies (SpA) patients from Mexico city whose cervical spine films were retrospectively reviewed. (3) Thirty nine AS patients from Edmonton, Canada whose cervical spine films were retrospectively reviewed and compared with 72 controls. RESULTS Group 1: 74% of the 103 patients were men and 86% were HLA-B27 positive. The mean age was 35 years, and mean (SD) disease duration 10 (8) years. OPLL was reported in 16 patients (15.5%; 95%C I 9, 22). OPLL was statistically associated with older age (p=0.001), longer disease duration (p=0.001), clinical myelopathy (p=0.03), worst functional index (p=0.042), restricted axial movement measurements (all p
ISSN:0003-4967
1468-2060
DOI:10.1136/ard.57.7.429