TY - JOUR
T1 - Predictors of severe hemolytic anemia and its impact on major outcomes in systemic lupus erythematosus
T2 - Data from a multiethnic Latin American cohort
AU - González, Luis Alonso
AU - Alarcón, Graciela S.
AU - Harvey, Guillermina B.
AU - Quintana, Rosana
AU - Pons-Estel, Guillermo J.
AU - Ugarte-Gil, Manuel F.
AU - Vásquez, Gloria
AU - Catoggio, Luis J.
AU - García, Mercedes A.
AU - Borba, Eduardo F.
AU - Da Silva, Nilzio A.
AU - Tavares Brenol, João C.
AU - Toledano, Marlene Guibert
AU - Massardo, Loreto
AU - Neira, Oscar
AU - Pascual-Ramos, Virginia
AU - Amigo, Mary Carmen
AU - Barile-Fabris, Leonor A.
AU - De La Torre, Ignacio García
AU - Alfaro-Lozano, José
AU - Segami, María I.
AU - Chacón-Díaz, Rosa
AU - Esteva-Spinetti, María H.
AU - Iglesias-Gamarra, Antonio
AU - Pons-Estel, Bernardo A.
N1 - Publisher Copyright:
© The Author(s) 2023.
PY - 2023/4
Y1 - 2023/4
N2 - Objective: To determine the predictors of the occurrence of severe autoimmune hemolytic anemia (AIHA) and its impact on damage accrual and mortality in SLE patients. Methods: Factors associated with time to severe AIHA (hemoglobin level ≤7 g/dL) occurring from the onset of SLE symptoms were examined by Cox proportional hazards regressions. The association of severe AIHA with mortality was examined by logistic regression analyses while its impact on damage was by negative binomial regression. Results: Of 1,349 patients, 49 (3.6%) developed severe AIHA over a mean (SD) follow-up time of 5.4 (3.8) years. The median time from the first clinical manifestation to severe AIHA was 111 days (IQR 43–450). By multivariable analysis, male sex (HR 2.26, 95% CI 1.02–4.75, p = 0.044), and higher disease activity at diagnosis (HR 1.04, 95% CI 1.01–1.08, p = 0.025) were associated with a shorter time to severe AIHA occurrence. Of the SLEDAI descriptors, only hematologic (leukopenia and/or thrombocytopenia) showed a certain trend toward significance in the multivariable analysis (HR 2.36, 95% CI 0.91–6.13, p = 0.0772). Severe AIHA contributed neither to damage nor to mortality. Conclusions: Severe AIHA occurs during the early course of SLE. Male sex and higher disease activity at diagnosis emerged as independent predictors of a shorter time to severe AIHA occurrence. Although not statistically significant, hematological abnormalities at SLE diagnosis could predict the occurrence of severe AIHA in a shorter time. Damage and mortality did not seem to be impacted by the occurrence of severe AIHA.
AB - Objective: To determine the predictors of the occurrence of severe autoimmune hemolytic anemia (AIHA) and its impact on damage accrual and mortality in SLE patients. Methods: Factors associated with time to severe AIHA (hemoglobin level ≤7 g/dL) occurring from the onset of SLE symptoms were examined by Cox proportional hazards regressions. The association of severe AIHA with mortality was examined by logistic regression analyses while its impact on damage was by negative binomial regression. Results: Of 1,349 patients, 49 (3.6%) developed severe AIHA over a mean (SD) follow-up time of 5.4 (3.8) years. The median time from the first clinical manifestation to severe AIHA was 111 days (IQR 43–450). By multivariable analysis, male sex (HR 2.26, 95% CI 1.02–4.75, p = 0.044), and higher disease activity at diagnosis (HR 1.04, 95% CI 1.01–1.08, p = 0.025) were associated with a shorter time to severe AIHA occurrence. Of the SLEDAI descriptors, only hematologic (leukopenia and/or thrombocytopenia) showed a certain trend toward significance in the multivariable analysis (HR 2.36, 95% CI 0.91–6.13, p = 0.0772). Severe AIHA contributed neither to damage nor to mortality. Conclusions: Severe AIHA occurs during the early course of SLE. Male sex and higher disease activity at diagnosis emerged as independent predictors of a shorter time to severe AIHA occurrence. Although not statistically significant, hematological abnormalities at SLE diagnosis could predict the occurrence of severe AIHA in a shorter time. Damage and mortality did not seem to be impacted by the occurrence of severe AIHA.
KW - Systemic lupus erythematosus
KW - autoimmune hemolytic anemia
KW - ethnicity
KW - predictors
UR - http://www.scopus.com/inward/record.url?scp=85150832057&partnerID=8YFLogxK
U2 - 10.1177/09612033231163745
DO - 10.1177/09612033231163745
M3 - Artículo
C2 - 36916674
AN - SCOPUS:85150832057
SN - 0961-2033
VL - 32
SP - 658
EP - 667
JO - Lupus
JF - Lupus
IS - 5
ER -