Assuntos
Anemia Falciforme/sangue , Anemia Falciforme/diagnóstico , Sistema do Grupo Sanguíneo Duffy/sangue , Úlcera da Perna/diagnóstico , Receptores de Superfície Celular/sangue , Índice de Gravidade de Doença , Adolescente , Adulto , Idoso , Anemia Falciforme/complicações , Estudos de Coortes , Feminino , Humanos , Úlcera da Perna/sangue , Úlcera da Perna/etiologia , Masculino , Pessoa de Meia-Idade , Adulto JovemRESUMO
Studies have questioned whether renal dysfunction in sickle cell disease is linked to hemolysis-associated vasculopathy. We have investigated renal function and markers of hemolysis in a cohort of 424 adult African-British patients with sickle cell disease. While significant associations were found in HbSS and HbSß(0) (sickle cell anemia) patients with and without controlling for covariates between hemolytic markers and albuminuria, the associations were not significant in patients with HbSC. Estimated glomerular filtration rate, a marker of renal function, correlated significantly with reticulocyte count and bilirubin. Alpha thalassemia, present in 34% of the sickle cell anaemia patients, had a protective effect against albuminuria in this group. Altogether, the incidence of hyperfiltration was 71% and microalbuminuria 37%, making nephropathy a common complication of sickle cell anemia.
