| Literature DB >> 32253519 |
Pepe M Ekulu1,2, Agathe B Nkoy3, Oyindamola C Adebayo4, Orly K Kazadi3, Michel N Aloni3, Fanny O Arcolino4, Rene M Ngiyulu3, Jean-Lambert E Gini3, François B Lepira5, Lamberthus P Van den Heuvel4,6, Elena N Levtchenko7.
Abstract
Individuals of African origin have an increased risk of developing various progressive chronic kidney diseases (CKD). This risk has been attributed to genetic variants (G1, G2) in apolipoprotein-L1 (APOL1) gene. In the pediatric population, especially in children affected by sickle cell disease (SCD), by human immunodeficiency virus (HIV), or with various glomerular diseases, APOL1 risk variants have been associated with the development of hypertension, albuminuria, and more rapid decline of kidney function. The present review focuses on existing APOL1-related epidemiological data in children with CKD. It also includes data from studies addressing racial disparities in CKD, the APOL1-related innate immunity, and the relationship between APOL1 and CKD and pathogenic pathways mediating APOL1-related kidney injury.Entities:
Keywords: APOL1; Children; Chronic kidney disease; Genetics; HIV-associated nephropathy; Sickle cell disease
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Year: 2020 PMID： 32253519 DOI： 10.1007/s00467-020-04553-z
Source DB: PubMed Journal: Pediatr Nephrol ISSN： 0931-041X Impact factor: 3.714