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Impaired -Oxidation and Altered Complex Lipid Fatty Acid Partitioning with Advancing CKD.

Citation
Afshinnia, F., et al. “Impaired -Oxidation And Altered Complex Lipid Fatty Acid Partitioning With Advancing Ckd.”. Journal Of The American Society Of Nephrology : Jasn, pp. 295-306.
Center University of Michigan
Author Farsad Afshinnia, Thekkelnaycke M Rajendiran, Tanu Soni, Jaeman Byun, Stefanie Wernisch, Kelli M Sas, Jennifer Hawkins, Keith Bellovich, Debbie Gipson, George Michailidis, Subramaniam Pennathur, Michigan Kidney Translational Core CPROBE Investigator Group
Keywords acylcarnitines, free fatty acids, Chronic kidney disease, complex lipids, lipids
Abstract

Studies of lipids in CKD, including ESRD, have been limited to measures of conventional lipid profiles. We aimed to systematically identify 17 different lipid classes and associate the abundance thereof with alterations in acylcarnitines, a metric of -oxidation, across stages of CKD. From the Clinical Phenotyping Resource and Biobank Core (CPROBE) cohort of 1235 adults, we selected a panel of 214 participants: 36 with stage 1 or 2 CKD, 99 with stage 3 CKD, 61 with stage 4 CKD, and 18 with stage 5 CKD. Among participants, 110 were men (51.4%), 64 were black (29.9%), and 150 were white (70.1%), and the mean (SD) age was 60 (16) years old. We measured plasma lipids and acylcarnitines using liquid chromatography-mass spectrometry. Overall, we identified 330 different lipids across 17 different classes. Compared with earlier stages, stage 5 CKD associated with a higher abundance of saturated C16-C20 free fatty acids (FFAs) and long polyunsaturated complex lipids. Long-chain-to-intermediate-chain acylcarnitine ratio, a marker of efficiency of -oxidation, exhibited a graded decrease from stage 2 to 5 CKD (<0.001). Additionally, multiple linear regression revealed that the long-chain-to-intermediate-chain acylcarnitine ratio inversely associated with polyunsaturated long complex lipid subclasses and the C16-C20 FFAs but directly associated with short complex lipids with fewer double bonds. We conclude that increased abundance of saturated C16-C20 FFAs coupled with impaired -oxidation of FFAs and inverse partitioning into complex lipids may be mechanisms underpinning lipid metabolism changes that typify advancing CKD.

Year of Publication
2018
Journal
Journal of the American Society of Nephrology : JASN
Volume
29
Issue
1
Number of Pages
295-306
Date Published
12/2018
ISSN Number
1533-3450
DOI
10.1681/ASN.2017030350
Alternate Journal
J. Am. Soc. Nephrol.
PMID
29021384
PMCID
PMC5748913
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