4.0 Article

Urinary Polycyclic Aromatic Hydrocarbons in a Longitudinal Cohort of Children with CKD: A Case of Reverse Causation?

Journal

KIDNEY360
Volume 3, Issue 6, Pages 1011-1020

Publisher

AMER SOC NEPHROLOGY
DOI: 10.34067/KID.0000892022

Keywords

chronic kidney disease; children; kidney; polycyclic aromatic hydrocarbon; renal function; reverse causation

Funding

  1. NIH, National Institute of Diabetes and Digestive and Kidney Diseases [R01 DK100307]

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This study aimed to examine the associations between serially measured urinary PAH metabolites and clinical and subclinical measures of kidney function in children with CKD. The results showed that PAH metabolites were associated with certain indicators, such as KIM-1 and 8-OHdG concentrations. Additionally, the study found associations between PHEN metabolites and certain indicators, such as eGFR and proteinuria.
Background Air pollution, which results in the formation of polycyclic aromatic hydrocarbons (PAH), has been identified as a cause of renal function decline and a contributor to chronic kidney disease (CKD). However, the results of cross-sectional studies investigating personal, integrated biomarkers of PAHs have been mixed. Longitudinal studies may be better suited to evaluate environmental drivers of kidney decline. The purpose of this study was to examine associations of serially measured urinary PAH metabolites with clinical and subclinical measures of kidney function over time among children with CKD. Methods This study was conducted among 618 participants in the CKD in Children study, a cohort study of pediatric CKD patients from the US and Canada, between 2005 and 2015. In serially collected urine samples over time, nine PAH metabolites were measured. Clinical outcomes measured annually included estimated glomerular filtration rate (eGFR), proteinuria, and blood pressure. Subclinical biomarkers of tubular injury (kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL)) and oxidant stress (8-hydroxy-2'- deoxyguanosine (8-OHdG) and F-2-isoprostane) were assayed in urine samples. Results Children were followed over an average of 3.0 years (standard deviation (SD)=1.6) and 2469 study visits (mean=4.0, SD=1.6). Hydroxynaphthalene (NAP) or hydroxyphenanthrene (PHEN) metabolites were detected in > 99% of samples and NAP concentrations were greater than PHEN concentrations. PHEN metabolites, driven by 3-PHEN, were associated with increased eGFR and reduced proteinuria, diastolic blood pressure z-score, and NGAL concentrations over time. However, PAH metabolites were consistently associated with increased KIM-1 and 8-OHdG concentrations. Conclusions Among children with CKD, these findings provoke the potential explanation of reverse causation where renal function affects measured biomarker concentrations even in the setting of a longitudinal study. Additional work is needed to determine if elevated KIM-1 and 8-OHdG excretion reflects site-specific injury to the proximal tubule mediated by low-grade oxidant stress.

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