Türk Medline
ADR Yönetimi
ADR Yönetimi

IMPACT OF AGE AT DISEASE ONSET ON CLINICAL MANIFESTATIONS AND PROGNOSIS IN SYSTEMIC LUPUS ERYTHEMATOSUS

DİDEM ŞAHİN, BUĞU BULAT, EMİNE USLU, NİLGÜN GÖVEÇ GIYNAŞ, GÖRKEM TURHAN, MUSTAFA KADER, MEHMET LEVENT YÜKSEL, EMİNE GÖZDE AYDEMİR GÜLÖKSÜZ, MÜÇTEBA ENES YAYLA, TAHSİN MURAT TURGAY, GÜLAY KINIKLI, AŞKIN ATEŞ

Ulusal Romatoloji Dergisi - 2025;17(2):60-67

Ankara University Faculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Ankara, Türkiye

 

OBJECTIVE To assess age-related differences in demographic, clinical, and treatment characteristics of systemic lupus erythematosus (SLE) patients and evaluate outcomes based on age at disease onset. METHODS Patients diagnosed with SLE who met 2012 Systemic Lupus International Collaborating Clinics (SLICC) criteria were retrospectively evaluated. Patients were classified based on age at onset: adult-onset (18-49 years) and late-onset (≥50 years). Demographic, clinical, laboratory characteristics and outcomes of adult and late-onset groups were compared. Disease damage was evaluated with the SLICC/American College of Rheumatology damage index (SDI). To assess the effect of age on mortality, Cox regression analysis was performed with the selected variables that were causally associated with the outcome. RESULTS Among 519 patients, 88.1% were female, with a mean diagnosis age of 36.6 years. Adult-onset SLE represented 82.3% of cases, while 17.7% had late-onset disease. Neurological involvement was more frequent in adult-onset SLE (25.8% vs. 16.3%), as was renal involvement (41.1% vs. 26.1%). Anti-ribonucleoprotein antibodies were more prevalent in adult-onset SLE (24.7% vs. 7.1%, p<0.001). Damage accrual was observed in 40.3% of patients, without significant differences in SDI scores between groups. After a median follow-up of 9.2 years, 10.8% of patients died, with a higher mortality rate in late-onset SLE (20.7% vs. 8.7%, p=0.001). Cox regression showed age at SLE onset was independently associated with increased mortality (hazard ratio: 1.09, 95% confidence interval: 1.06-1.11, p<0.001). CONCLUSION Age at SLE onset is associated with distinct clinical features and outcomes. Late-onset SLE patients experience higher mortality, emphasizing the need for age-specific approaches in SLE management.