No impact of a high‐fat meal coupled with intermittent hypoxemia on acute kidney injury biomarkers in adults with and without obstructive sleep apnea

Author:

Goulet Nicholas12ORCID,Tetzlaff Emily J.2ORCID,Morin Renée1ORCID,Mauger Jean‐François1ORCID,Amaratunga Ruwan3,Kenny Glen P.2ORCID,Imbeault Pascal13ORCID

Affiliation:

1. Behavioural and Metabolic Research Unit, School of Human Kinetics, Faculty of Health Sciences University of Ottawa Ottawa Ontario Canada

2. Human and Environmental Physiology Research Unit, School of Human Kinetics, Faculty of Health Sciences University of Ottawa Ottawa Ontario Canada

3. Institut du Savoir Montfort Montfort Hospital Ottawa Ontario Canada

Abstract

AbstractObstructive sleep apnea (OSA) is characterized by chronic intermittent hypoxemia, which is associated with progressive loss of kidney function, where postprandial fluctuations in renal physiology may further compromise oxygen supply and kidney function. Therefore, we measured biomarkers of acute kidney injury (AKI) following a high‐fat meal with and without intermittent hypoxemia. Eighteen healthy young men (mean age [SD]: 22.7 years [3.1]) and seven middle‐aged to older individuals with OSA (54.4 years [6.4]) consumed a high‐fat meal during normoxia or intermittent hypoxemia (~15 hypoxic cycles per hour, ~85% oxyhemoglobin saturation) for 6 h. We observed no changes in estimated glomerular filtration rate and plasma concentrations of creatinine, neutrophil gelatinase‐associated lipocalin (NGAL), and kidney injury molecule‐1 (KIM‐1) at any measured time points. In both groups, plasma concentrations of interleukin‐18 (IL‐18) increased after 6 h during normoxia only (p = 0.033, ηp2 = 0.122), and plasma concentrations of liver‐type fatty acid‐binding protein (L‐FABP) transiently decreased after 3 h in both conditions (p = 0.008, ηp2 = 0.152). These findings indicate that AKI biomarkers are not acutely elevated during the postprandial state with or without intermittent hypoxemia, suggesting that other mechanisms may play more important roles in the progression of kidney disease in OSA.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Physiology (medical),Physiology

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