2013
DOI: 10.1007/s11926-013-0374-7
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Spondyloarthritis with Onset After Age 45

Abstract: The ASAS (Assessment in SpondyloArtrhritis international Society) classification criteria for axial and peripheral spondyloarthritis permit to classify patients with age at disease onset less than 45 years. Nevertheless, these two forms of spondyloarthritis may begin after the age of 45. With the longer duration of the life expectancy, patients with this late-onset form of spondyloarthritis may be more frequently recognized in the near future. A small percentage (ranging from 3.5 to 6 %) of patients with axial… Show more

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Cited by 36 publications
(31 citation statements)
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“…Aktif infeksiyon, kanser ve dev hücreli arterit sıklıkla, kronik inflamatuvar eklem hastalıkları (RA, spondiloartropatiler, kristal depo hastalıkları vb) ise az da olsa PMR bulgularına eşlik eder. [6][7][8] Ayırıcı tanı zordur ve nadirde olsa birlikteliği bildirilmiştir. [9] Hastalar kortikosteroide yanıt verebilir.…”
Section: Discussionunclassified
“…Aktif infeksiyon, kanser ve dev hücreli arterit sıklıkla, kronik inflamatuvar eklem hastalıkları (RA, spondiloartropatiler, kristal depo hastalıkları vb) ise az da olsa PMR bulgularına eşlik eder. [6][7][8] Ayırıcı tanı zordur ve nadirde olsa birlikteliği bildirilmiştir. [9] Hastalar kortikosteroide yanıt verebilir.…”
Section: Discussionunclassified
“…34 Late-onset USpA has the same wide spectrum of manifestations as in early onset USpA including enthesitis, dactylitis, and uveitis in various combinations. 28 It can mimic PMR, RS3PE (Remitting Seronegative Symmetric Synovitis with Pitting Edema), and even reflex sympathetic dystrophy at onset. 28,[35][36][37] Late-onset PsA presents more commonly with peripheral manifestations than axial.…”
Section: Clinical Featuresmentioning
confidence: 99%
“…28 It can mimic PMR, RS3PE (Remitting Seronegative Symmetric Synovitis with Pitting Edema), and even reflex sympathetic dystrophy at onset. 28,[35][36][37] Late-onset PsA presents more commonly with peripheral manifestations than axial. Unilateral sacroiliitis and silent axial involvement is more common than bilateral sacroiliitis, while isolated axial disease is less compared to early onset PsA.…”
Section: Clinical Featuresmentioning
confidence: 99%
“…AS and SpA are usually observed in young patients and a clinical onset after 50 years is uncommon [3]. As we are in the context of an aging population and a longer life expectancy, one may believe that the prevalence of patients with late-onset AS or SpA will rise.…”
Section: Introductionmentioning
confidence: 99%