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Bile acid metabolites and carotid intima media thickness in the Chronic Kidney Disease in Children (CKiD) study

Year: 2026
Type: article
Abstract: Cardiovascular disease is the leading cause of mortality in children with chronic kidney disease (CKD). Children with CKD can have subclinical atherosclerosis as an early manifestation of cardiovascular disease [ 1 ].
DOI: 10.1007/s00467-026-07343-1
Authors: Arthur M. Lee, Mark M. Mitsnefes, Jennifer Roem, Bradley A. Warady, Susan L. Furth, Michelle R. Denburg, For the CKiD Study Investigators
Institutions: Children's Hospital of Philadelphia, University of Pennsylvania, Cincinnati Children's Hospital Medical Center, Johns Hopkins University, Children's Mercy Hospital, University of Missouri–Kansas City
Language: English
Field: Medicine
Open Access status: hybrid
Estimated APC paid: $4,337
Funders: U.S. Department of Health and Human Services, Children's Hospital of Philadelphia, University of Missouri, Children's Mercy Hospital, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: Chronic Kidney Disease (CKD) Biomarkers Consortium Data Coordinating Center, Identifying genetic drivers of circulating metabolites associated with cardiac risk in pediatric chronic kidney disease, Chronic Kidney Disease Biomarkers Consortium (CKD BioCon) U01, CKD Biomarker Consortium-Phase 2: Risk Markers in Blood, Mentoring Early Career Researchers in Patient-Oriented Research in Kidney Disease, The Central Biochemistry Laboratory for the Chronic Kidney Disease in Children Cohort (CKiD), The Kidney Disease in Children Data Management and Analysis Center (KIDMAC), Chronic Kidney Disease in Children (CKiD), Chronic Kidney Disease in Children (CKiD V), A multi-omic investigation of uremic toxin sources and accumulation in children with kidney failure, The Penn-StARR Program for Research in Residency
OpenAlex ID: W7160509149
FWCI:
Cites: 10
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Related to: 10