TY  - JOUR
T1  - Between diffuse and limited: the unique identity of systemic sclerosis–overlap syndromes
TT  - Diffüz ve limitli arasında: sistemik skleroz–çakışma sendromlarının kendine özgü kimliği
AU  - Vasi, İbrahim
AU  - Küçük, Hamit
AU  - Karaduman, İbrahim
AU  - Erden, Abdulsamet
PY  - 2025
DA  - October
Y2  - 2025
DO  - 10.38053/acmj.1779330
JF  - Anatolian Current Medical Journal
JO  - Anatolian Curr Med J / ACMJ / acmj
PB  - MediHealth Academy Yayıncılık
WT  - DergiPark
SN  - 2718-0115
SP  - 913
EP  - 918
VL  - 7
IS  - 6
LA  - en
AB  - Aims: Systemic sclerosis–overlap syndrome (SSc-OS) constitutes a distinct clinical phenotype within the spectrum of systemic sclerosis, marked by unique immunological and clinical characteristics that differentiate it from the classical subsets. The present study aimed to characterise the demographic, serological, and organ involvement patterns of patients with SSc-OS, and to assess their disease manifestations and prognostic trajectories in comparison with diffuse cutaneous and limited cutaneous SSc.Methods: This study included patients followed at the Gazi University Hospital Rheumatology Department between January 2010 and July 2025. SSc-OS was defined as patients fulfilling classification criteria for systemic sclerosis together with other autoimmune diseases as rheumatoid arthritis, polymyositis, and or Sjögren’s syndrome. Baseline and 1-year characteristics were compared between SSc and SSc-OS.  Results: A total of 160 patients were included: 68 diffuse cutaneous (dcSSc), 67 limited cutaneous (lcSSc), and 25 SSc-OS. Age at disease onset was lower in dcSSc (42.5±13.7 years) compared with lcSSc (50.6±13.7) and SSc-OS (47.2±13.9; p=0.003). Anti topoisomerase I positivity was highest in dcSSc (83.8%) versus lcSSc (43.3%) and SSc-OS (16%; p=0.001), whereas anti-centromere was most frequent in lcSSc (41.8%; p=0.001) and anti-SSa in SSc-OS (44%; p=0.002). Interstitial lung disease (ILD) occurred in 89.7% of dcSSc, 76% of SSc-OS, and 56.7% of lcSSc (p=0.001), with extensive disease more common in dcSSc (61.7%; p=0.001). Myopathy was higher in SSc-OS (44%) and dcSSc (35.3%) than lcSSc (12.1%; p=0.001). Immunosuppressive therapy was most frequent in dcSSc (88.2% vs. 35.8% lcSSc and 60% SSc-OS; p=0.001). At one year, SSc-OS patients showed greater improvements in force vital capacity (FVC) and diffusing capacity for carbon monoxide (DLco), though not statistically significant. Mortality occurred in 25% of dcSSc, 14.9% of lcSSc, and 8% of SSc-OS (p=0.113); Kaplan–Meier analysis demonstrated numerically better survival in SSc-OS (mean 25.3 years) compared with lcSSc (19.8) and dcSSc (19.5; log-rank p=0.249). Conclusion: This study identified SSc-OS in 15.6% of patients, most commonly SSc–Sjögren’s. Distinct autoantibody profiles and prominent musculoskeletal involvement differentiated SSc-OS from classical subsets. While dcSSc showed the highest ILD burden and lcSSc was linked to pulmonary arterial hypertension, SSc-OS demonstrated intermediate pulmonary disease and numerically better survival, supporting its recognition as a clinically distinct phenotype within the SSc spectrum.
KW  - Mortality
KW  - overlap syndrome
KW  - prognosis
KW  - systemic sclerosis
N2  - Amaç: Sistemik skleroz–Çakışma Sendromu (SSk-ÇS), sistemik skleroz spektrumu içinde, klasik alt tiplerden ayıran özgün immünolojik ve klinik özelliklerle karakterize ayrı bir klinik fenotip oluşturmaktadır. Bu çalışmanın amacı, SSk-ÇS hastalarının demografik, serolojik ve organ tutulum paternlerini tanımlamak ve bunların klinik yansımalarını ve prognostik seyirlerini diffüz kutanöz ve limitli kutanöz SSk ile karşılaştırmaktır.Yöntem: Bu çalışmaya Ocak 2010–Temmuz 2025 tarihleri arasında Gazi Üniversitesi Tıp Fakültesi Romatoloji Anabilim Dalı’nda takip edilen hastalar dahil edildi. SSK-ÇS, sistemik skleroz sınıflama kriterleri ile birlikte romatoid artrit, polimiyozit veya Sjögren sendromu gibi diğer otoimmün hastalıkların kriterlerini de karşılayan hastalar olarak tanımlandı. Başlangıç ve 1. yıl özellikleri SSk ve SSk-ÇS grupları arasında karşılaştırıldı.Bulgular: Çalışmaya toplam 160 hasta dahil edildi: 68 diffüz kutanöz (dkSSk), 67 limitli kutanöz (lkSSk) ve 25 SSk-ÇS. Hastalık başlangıç yaşı dkSSk’de (42,5 ± 13,7 yıl), lkSSk (50,6 ± 13,7) ve SSk-ÇS’e (47,2 ± 13,9) kıyasla daha düşüktü (p = 0,003). Anti-topoizomeraz I pozitifliği dkSSk’de (%83,8), lkSSk (%43,3) ve SSk-ÇS’e (%16) kıyasla daha yüksekti (p = 0,001); anti-sentromer en sık lkSSk’de (%41,8; p = 0,001) ve anti-SSa antikoru en sık SSk-ÇS’da (%44; p = 0,002) görüldü. İnterstisyel akciğer hastalığı (İAH), dkSSk’de %89,7, SSk-ÇS’da %76 ve lkSSk’de %56,7 oranında görüldü (p = 0,001); yaygın tutulum dkSSk’de (%61,7) daha sıktı (p = 0,001). Miyopati, SSk-ÇS (%44) ve dkSSk’de (%35,3) lkSSk’ye (%12,1) göre daha yüksekti (p = 0,001). İmmünsüpresif tedavi dkSSk’de (%88,2) lkSSk (%35,8) ve SSk-ÇS’a (%60) göre daha sık kullanıldı (p = 0,001). Birinci yılda, SSk-ÇS hastaları FVC ve DLco’da daha büyük iyileşme gösterdi ancak bu fark istatistiksel olarak anlamlı değildi. Mortalitenin dağılımı dkSSk’de %25, lkSSk’de %14,9 ve SSk-ÇS’da %8 idi (p = 0,113); Kaplan–Meier analizi SSk-ÇS’de (ortalama 25,3 yıl) lkSSk (19,8 yıl) ve dkSSk’ye (19,5 yıl) kıyasla daha iyi sağkalımı göstermesine rağmen fark istatistiksel olarak anlamlı değildi (log-rank p = 0,249).Sonuç: Bu çalışmada hastaların %15,6’sında SSk-ÇS saptandı, en sık SSk–Sjögren’s alt tipi görüldü. Özgün otoantikor profilleri ve belirgin kas-iskelet tutulumları SSk-ÇS’u klasik alt tiplerden ayırdı. dkSSk en yüksek İAH yükü ile ilişkiliyken, lkSSk pulmoner arteriyel hipertansiyon ile ilişkili bulundu. SSk-ÇS ise orta düzeyde pulmoner tutulum ve sayısal olarak daha iyi sağkalım gösterdi; bu da SSk spektrumu içinde klinik olarak ayrı bir fenotip olarak tanınmasını desteklemektedir.
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UR  - https://doi.org/10.38053/acmj.1779330
L1  - https://dergipark.org.tr/tr/download/article-file/5219951
ER  -