TY - JOUR
T1 - Mestizos with systemic lupus erythematosus develop renal disease early while antimalarials retard its appearance
T2 - Data from a Latin American cohort
AU - Pons-Estel, G. J.
AU - Alarcón, G. S.
AU - Burgos, P. I.
AU - Hachuel, L.
AU - Boggio, G.
AU - Wojdyla, D.
AU - Nieto, R.
AU - Alvarellos, A.
AU - Catoggio, L. J.
AU - Guibert-Toledano, M.
AU - Sarano, J.
AU - Massardo, L.
AU - Vásquez, G. M.
AU - Iglesias-Gamarra, A.
AU - Costallat, Lt Lavras
AU - Da Silva, N. A.
AU - Alfaro, J. L.
AU - Abadi, I.
AU - Segami, M. I.
AU - Huerta, G.
AU - Cardiel, M. H.
AU - Pons-Estel, B. A.
N1 - Funding Information:
This work was supported by grants from the Federico Wilhelm Agricola Foundation Research (BAPE) and the National Institute of Arthritis and Musculoskeletal and Skin Diseases P01 AR49084 (GSA), and by the STELLAR (Supporting Training Efforts in Lupus for Latin American Rheumatologists) Program funded by Rheuminations Inc (GPE and PIB) and the Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)-Beca de Formació i Contractació de Personal Investigador (GPE). Research grant financed by FONDECYT #1110395 (PIB).
PY - 2013/8
Y1 - 2013/8
N2 - Objectives: The objective of this paper is to assess the predictors of time-to-lupus renal disease in Latin American patients. Methods: Systemic lupus erythematosus (SLE) patients (n = 1480) from Grupo Latino Americano De Estudio de Lupus (GLADEL's) longitudinal inception cohort were studied. Endpoint was ACR renal criterion development after SLE diagnosis (prevalent cases excluded). Renal disease predictors were examined by univariable and multivariable Cox proportional hazards regression analyses. Antimalarials were considered time dependent in alternative analyses. Results: Of the entire cohort, 265 patients (17.9%) developed renal disease after entering the cohort. Of them, 88 (33.2%) developed persistent proteinuria, 44 (16.6%) cellular casts and 133 (50.2%) both; 233 patients (87.9%) were women; mean (SD) age at diagnosis was 28.0 (11.9) years; 12.2% were African-Latin Americans, 42.5% Mestizos, and 45.3% Caucasians (p = 0.0016). Mestizo ethnicity (HR 1.61, 95% CI 1.19-2.17), hypertension (HR 3.99, 95% CI 3.02-5.26) and SLEDAI at diagnosis (HR 1.04, 95% CI 1.01-1.06) were associated with a shorter time-to-renal disease occurrence; antimalarial use (HR 0.57, 95% CI 0.43-0.77), older age at onset (HR 0.90, 95% CI 0.85-0.95, for every five years) and photosensitivity (HR 0.74, 95% CI 0.56-0.98) were associated with a longer time. Alternative model results were consistent with the antimalarial protective effect (HR 0.70, 95% CI 0.50-0.99). Conclusions: Our data strongly support the fact that Mestizo patients are at increased risk of developing renal disease early while antimalarials seem to delay the appearance of this SLE manifestation. These data have important implications for the treatment of these patients regardless of their geographic location.
AB - Objectives: The objective of this paper is to assess the predictors of time-to-lupus renal disease in Latin American patients. Methods: Systemic lupus erythematosus (SLE) patients (n = 1480) from Grupo Latino Americano De Estudio de Lupus (GLADEL's) longitudinal inception cohort were studied. Endpoint was ACR renal criterion development after SLE diagnosis (prevalent cases excluded). Renal disease predictors were examined by univariable and multivariable Cox proportional hazards regression analyses. Antimalarials were considered time dependent in alternative analyses. Results: Of the entire cohort, 265 patients (17.9%) developed renal disease after entering the cohort. Of them, 88 (33.2%) developed persistent proteinuria, 44 (16.6%) cellular casts and 133 (50.2%) both; 233 patients (87.9%) were women; mean (SD) age at diagnosis was 28.0 (11.9) years; 12.2% were African-Latin Americans, 42.5% Mestizos, and 45.3% Caucasians (p = 0.0016). Mestizo ethnicity (HR 1.61, 95% CI 1.19-2.17), hypertension (HR 3.99, 95% CI 3.02-5.26) and SLEDAI at diagnosis (HR 1.04, 95% CI 1.01-1.06) were associated with a shorter time-to-renal disease occurrence; antimalarial use (HR 0.57, 95% CI 0.43-0.77), older age at onset (HR 0.90, 95% CI 0.85-0.95, for every five years) and photosensitivity (HR 0.74, 95% CI 0.56-0.98) were associated with a longer time. Alternative model results were consistent with the antimalarial protective effect (HR 0.70, 95% CI 0.50-0.99). Conclusions: Our data strongly support the fact that Mestizo patients are at increased risk of developing renal disease early while antimalarials seem to delay the appearance of this SLE manifestation. These data have important implications for the treatment of these patients regardless of their geographic location.
KW - antimalarials
KW - ethnicity
KW - nephritis
KW - renal lupus
KW - systemic lupus erythematosus
UR - http://www.scopus.com/inward/record.url?scp=84880885195&partnerID=8YFLogxK
U2 - 10.1177/0961203313496339
DO - 10.1177/0961203313496339
M3 - Article
C2 - 23857989
AN - SCOPUS:84880885195
SN - 0961-2033
VL - 22
SP - 899
EP - 907
JO - Lupus
JF - Lupus
IS - 9
ER -