Features associated with hematologic abnormalities and their impact in patients with systemic lupus erythematosus: Data from a multiethnic Latin American cohort.

OBJECTIVE: To examine hematological manifestations' correlates and their impact on damage accrual and mortality in SLE patients from the multiethnic, Latin American, GLADEL cohort. METHODS: In patients with recent SLE diagnosis (≤2 years), the association between follow-up hematological manifestations (per ACR criteria) and socio-demographic and clinical variables was examined by univariable and multivariable logistic regressions; their impact on damage accrual and mortality was examined by Poisson and Cox proportional-hazards regression analyses, respectively. RESULTS: Of 1437 patients, 948 (66.0%) developed ≥1 hematological manifestation [5.5% hemolytic anemia (AHA), 16.3% thrombocytopenia, and 56.4% lymphopenia] over 4.3 (3.3) follow-up years. Younger age, Mestizo ethnicity, hematologic disorder (at/or before SLE diagnosis), and first damage recorded were associated with hematological manifestations while antimalarials were negatively associated. AHA (at/or before SLE diagnosis), anti-Sm, and anti-RNP antibodies were associated with subsequent AHA occurrence while musculoskeletal involvement was negatively associated. Thrombocytopenia (at/or before SLE diagnosis), AHA, anti-phospholipid antibodies (aPLs), anti-SSA/Ro, anti-SSB/La antibodies, and first damage recorded were associated with later thrombocytopenia occurrence. Lymphopenia (at/or before SLE diagnosis), younger age at diagnosis, Mestizo ethnicity, having medical insurance, and first damage recorded were associated with subsequent lymphopenia occurrence while antimalarials and azathioprine treatment were negatively associated. AHA was associated with damage accrual and mortality after adjusting for variables known to affect these outcomes. CONCLUSIONS: Mestizo ethnicity and early hematological manifestations are risk factors for their subsequent occurrence while antimalarials have a protective effect. The associations between AHA and aPLs and thrombocytopenia were corroborated. AHA contributes independently to damage accrual and diminished survival.

Manifestaciones reumáticas de la infección por el virus de inmunodeficiencia humana (VIH) / Rheumatological manifestations of HIV infection

Con la aparición del VIH/SIDA se ha puesto de manifiesto un espectro de manifestaciones clínicas reumáticas. El compromiso articular incluye las artralgias, la artritis por VIH, el síndrome de Reiter, la artritis psoriásica y la espondiloartropatía indiferenciada. También se ha documentado una miopatía inducida por el VIH en cuyo diagnóstico diferencial se deben tener en cuenta la miopatía inducida por zidovudina y la debida a toxoplasmosis, cuya presentación clínica es más parecida a la miopatía inducida por el VIH que a otras afecciones musculares. El síndrome de linfocitosis con infiltración difusa es una entidad parecida al síndrome de Sjõgren, que es exclusiva de los pacientes VIH positivos, con algunas diferencias en la presentación clínica e inmunológica. Por último, es frecuente la presencia de fenómenos autoinmunes el más común de los cuales es la hipergamaglobulinemia policlonal. También se han descrito diferentes tipos de vasculitis como parte de esta enfermedad