Giriş: Sistemik lupus eritematozus (SLE), kronik, otoimmün karakterli, birçok organ ve sistemi etkileyebilen bir bağ̆ dokusu hastalığıdır. Artralji ve myalji SLE hastalarında sık görülen semptomlardır ve sebebi inflamatuvar olabileceği gibi eklem hipermobilitesi veya fibromyaljiden de kaynaklanabilir. Çalışmamızda SLE hastalarındaki eklem ve kas şikayetlerinin inflamatuvar aktivite dışında hipermobilite veya fibromyalji ile ilişkisinin araştırılması amaçlanmıştır.
Materyal ve Metod: Çalışmamıza 2012 SLE sınıflama kriterlerini karşılayan hastalar dahil edildi. Son 6 ay içerisinde eklem mobilitesini etkileyecek cerrahi girişim geçirmiş olan, eşlik eden romatoid artrit, inflamatuar myozit gibi inflamatuar artritler ile seyredebilen hastalık tanıları bulunan hastalar çalışmadan dışlandı. Muayene esnasındaki hastalık aktivitesi SLE Hastalık Aktivite İndeksi-2000 değerlendirme formuna göre belirlendi. Hipermobilite Beighton Hipermobilite Skoru ile fibromyalji ise 2016 Fibromyalji Tanı Kriterleri ile baz alındı. Hastalar hipermobilitesi olan, fibromyaljisi olan ve her ikisi de olmayan olmak üzere 3 gruba ayrıldı. Demografik özellikler, eşlik eden komorbiditeler, tedavide kullanılan ilaçlar, aktivite ve ağrı skorları değerlendirildi.
Bulgular: Fibromyaljisi ve hipermobilitesi olan 6 hasta çalışmadan çıkartırdı. 120 hasta analize edildi. Hastaların 104’ü (%86.7) kadındı. Hastalık süresi median (min-max) değeri 12 (1-38) yıl idi. Hastaların 25’inde (%20.8) hipermobilite, 28’inde (%23.3) fibromyalji tespit edildi. Tüm grupta hipermobilite veya fibromiyaljisi olan hasta oranı %44.1’idi. Gruplar arasında komorbiditeler açısından istatiksel fark saptanmadı. Fibromiyaljisi olan hastalarda median hasta VAS değeri ve ağrı değerlendirmesi diğer iki gruba göre daha yüksek iken SLEDAI-2K aktivite skoru daha düşüktü. SLEDAI-2K Aktivite Skoru’na göre artrit her ikisi olmayan grupta daha sıktı. Pulse-steroid öyküsü hipermobilitesi olan ve fibromiyaljisi olan grup arasında (p:0.01), fibromiyaljisi olan ve her ikisi olmayan grup arasında (p:0.02) fark saptandı.
Sonuç: Hipermobilitenin neden olduğu, ciddi müsküloskeletal ağrı artralji, artrit ile karışabilmektedir ve klinisyence hastalığın progresyonu olarak algılanabilir. Bu durum gereksiz immünsüpresif tedavi verilmesine sebep olabilir. Bu nedenle SLE seyrinde eşlik edebilecek hipermobilite ve fibromyaljinin ayrıntılı şekilde değerlendirilmesi gerekmektedir.
Aims: Systemic lupus erythematosus (SLE) is a chronic autoimmune connective tissue disease that can affect multiple organs and systems. Arthralgia and myalgia are common symptoms in patients with SLE, and their etiology may be inflammatory or may result from joint hypermobility or fibromyalgia. This study aimed to investigate whether musculoskeletal complaints in SLE patients are attributable solely to inflammatory activity or whether they may also be associated with hypermobility or fibromyalgia.
Methods: Patients who fulfilled the 2012 SLE classification criteria were included. Patients who had undergone surgical procedures affecting joint mobility within the last 6 months, or those with concomitant diseases such as rheumatoid arthritis or inflammatory myositis that may present with inflammatory arthritis, were excluded from the study. Disease activity at the time of examination was assessed using the SLE Disease Activity Index-2000 (SLEDAI-2K). Hypermobility was evaluated using the Beighton Hypermobility Score, and fibromyalgia was assessed according to the 2016 Fibromyalgia Diagnostic Criteria. Patients were divided into three groups: those with hypermobility, those with fibromyalgia, and those with neither condition. Demographic characteristics, comorbidities, medications, disease activity, and pain scores were analyzed.
Results: Six patients with both fibromyalgia and hypermobility were excluded. A total of 120 patients were analyzed, of whom 104 (86.7%) were female. The median (min-max) disease duration was 12 (1-38) years. Hypermobility was detected in 25 patients (20.8%) and fibromyalgia in 28 patients (23.3%). Overall, 44.1% of the cohort had either hypermobility or fibromyalgia. No significant differences were found between groups in terms of comorbidities. Patients with fibromyalgia had higher median patient VAS and pain scores compared with the other two groups, while their SLEDAI-2K activity scores were lower. Arthritis, according to SLEDAI-2K, was more frequent in the group without hypermobility or fibromyalgia. A significant difference in pulse-steroid use was found between the hypermobility and fibromyalgia groups (p=0.01) and between the fibromyalgia and neither group (p=0.02).
Conclusion: Severe musculoskeletal pain due to hypermobility may mimic arthralgia or arthritis and may be misinterpreted by clinicians as disease progression. This could lead to unnecessary immunosuppressive therapy (risk of overtreatment), which could lead to increased risk of infection and liver and kidney dysfunction. Therefore, hypermobility and fibromyalgia, which may coexist in the course of SLE, should be thoroughly evaluated. In our study, a significant frequency (almost half of the patients) of pain was due to non-inflammatory causes.
This study was conducted in accordance with the 2013 revision of the Declaration of Helsinki and was approved by the Hacettepe University Health Sciences Research Ethics Committee (SBA 24/837, 03/09/2024).
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| Primary Language | English |
|---|---|
| Subjects | Rheumatology and Arthritis |
| Journal Section | Original Article |
| Authors | |
| Publication Date | October 25, 2025 |
| Submission Date | August 21, 2025 |
| Acceptance Date | September 7, 2025 |
| Published in Issue | Year 2025 Volume: 8 Issue: 6 |
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