2019
DOI: 10.4103/ijn.ijn_40_18
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Early predictors of renal dysfunction in pediatric patients with sickle cell disease

Abstract: Sickle cell disease (SCD) is a hereditary hemoglobinopathy characterized by abnormal hemoglobin production which leads to hemolytic anemia and intermittent occlusion of small blood vessels, which further leads to tissue ischemia, chronic organ damage, and organ dysfunction including urinary system. To measure the serum levels of cystatin-C and beta 2 microglobulin in pediatric patients with SCDand to investigate their significance as early biomarkers of glomerular and/or renal tubular dysfunction. This study w… Show more

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Cited by 4 publications
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“…(23) Furthermore, a study conducted among sickle cell disease patients reported that β2 microglobulin had a higher sensitivity and specificity than serum creatinine. (24) Similarly, in the present study, β2 microglobulin had a higher sensitivity and specificity than serum creatinine. The results of the ROC analysis revealed that serum β2 microglobulin had a better diagnostic accuracy than serum creatinine.…”
Section: Discussionsupporting
confidence: 73%
“…(23) Furthermore, a study conducted among sickle cell disease patients reported that β2 microglobulin had a higher sensitivity and specificity than serum creatinine. (24) Similarly, in the present study, β2 microglobulin had a higher sensitivity and specificity than serum creatinine. The results of the ROC analysis revealed that serum β2 microglobulin had a better diagnostic accuracy than serum creatinine.…”
Section: Discussionsupporting
confidence: 73%