TY - GEN
T1 - Predictors of damage progression in portuguese patients with systemic lupus erythematosus
AU - Santos, Maria José
AU - Vinagre, Filipe
AU - Nero, Patrícia
AU - Barcelos, Filipe
AU - Barcelos, Anabela
AU - Rodrigues, Ana Maria
AU - De Matos, António Alves
AU - Silva, Cândida
AU - Miranda, Luis
AU - Capela, Susana
AU - Marques, Aurora
AU - Branco, Jaime
AU - Da Silva, José Canas
PY - 2009/9
Y1 - 2009/9
N2 - Patients with systemic lupus erythematosus (SLE) have a longer life expectancy. The occurrence of irreversible damage has become a major concern. The present study assessed damage progression in patients with SLE over a 2-year period and identified baseline features associated with damage accrual. Two hundred and twenty-one patients that fulfilled criteria for SLE and had a follow-up longer than 6 months were enrolled. Demographic, clinical, and immunological data were collected at baseline. Accumulated organ damage was scored using the Systemic Lupus International Collaborating Clinics/American College of Rheumatology damage index (SDI). Patients were prospectively followed and SDI assessment repeated at 2 years. At baseline 72 patients (33%) presented some irreversible damage, and after 2 years 53 had accrued new damage. The mean SDI for the whole cohort increased from 0.582 to 0.980. Damage progression was higher in ocular, cardiovascular, and musculoskeletal systems. Older age OR = 1.045; 95% confidence interval (CI) 1.021-1.069; P = 0.03, presence of antiphospholipid antibodies (OR = 3.047; 95% CI 1.169-7.941; P = 0.02), steroid use (OR = 6.401; 95% CI 1.601-25.210; P = 0.008), azathioprine use (OR = 3.501; CI 1.224-10.012; P = 0.01), and hypertension (OR = 3.825; 95% CI 1.490-9.820; P = 0.005) were predictors of damage progression in multivariate analysis. Overall SDI increased over time, with some systems being affected more frequently. Demographic and clinical characteristics, co-morbidity, and treatment options may contribute to irreversible damage. It is necessary to determine whether the control of modifiable factors (e.g., hypertension and judicious use of medications) might prevent damage progression in SLE patients.
AB - Patients with systemic lupus erythematosus (SLE) have a longer life expectancy. The occurrence of irreversible damage has become a major concern. The present study assessed damage progression in patients with SLE over a 2-year period and identified baseline features associated with damage accrual. Two hundred and twenty-one patients that fulfilled criteria for SLE and had a follow-up longer than 6 months were enrolled. Demographic, clinical, and immunological data were collected at baseline. Accumulated organ damage was scored using the Systemic Lupus International Collaborating Clinics/American College of Rheumatology damage index (SDI). Patients were prospectively followed and SDI assessment repeated at 2 years. At baseline 72 patients (33%) presented some irreversible damage, and after 2 years 53 had accrued new damage. The mean SDI for the whole cohort increased from 0.582 to 0.980. Damage progression was higher in ocular, cardiovascular, and musculoskeletal systems. Older age OR = 1.045; 95% confidence interval (CI) 1.021-1.069; P = 0.03, presence of antiphospholipid antibodies (OR = 3.047; 95% CI 1.169-7.941; P = 0.02), steroid use (OR = 6.401; 95% CI 1.601-25.210; P = 0.008), azathioprine use (OR = 3.501; CI 1.224-10.012; P = 0.01), and hypertension (OR = 3.825; 95% CI 1.490-9.820; P = 0.005) were predictors of damage progression in multivariate analysis. Overall SDI increased over time, with some systems being affected more frequently. Demographic and clinical characteristics, co-morbidity, and treatment options may contribute to irreversible damage. It is necessary to determine whether the control of modifiable factors (e.g., hypertension and judicious use of medications) might prevent damage progression in SLE patients.
KW - Organ damage
KW - Outcome
KW - Portugal
KW - SLICC
KW - Systemic lupus erythematosus
UR - http://www.scopus.com/inward/record.url?scp=69949134076&partnerID=8YFLogxK
U2 - 10.1111/j.1749-6632.2009.04669.x
DO - 10.1111/j.1749-6632.2009.04669.x
M3 - Conference contribution
C2 - 19758234
AN - SCOPUS:69949134076
SN - 9781573317627
T3 - Annals of the New York Academy of Sciences
SP - 822
EP - 828
BT - Contemporary Challenges in Autoimmunity
PB - Blackwell Publishing Inc.
ER -