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Effects of PNPLA3 I148M on hepatic lipid and very-low-density lipoprotein metabolism in humans

Authors :
Aarno Palotie
Elias Björnson
Sanni Söderlund
Marja-Riitta Taskinen
Stefano Romeo
Antti Hakkarainen
Samuli Ripatti
Pietari Ripatti
Chris J. Packard
Mari Ainola
Martin Adiels
Marcus Henricsson
Niina Matikainen
Joel T. Rämö
Rosellina Margherita Mancina
Jan Borén
HUS Abdominal Center
Clinicum
CAMM - Research Program for Clinical and Molecular Metabolism
Endokrinologian yksikkö
Institute for Molecular Medicine Finland
Genomics of Neurological and Neuropsychiatric Disorders
Complex Disease Genetics
Helsinki Institute of Life Science HiLIFE
Samuli Olli Ripatti / Principal Investigator
Doctoral Programme in Social Sciences
Centre of Excellence in Complex Disease Genetics
Department of Public Health
Faculty Common Matters (Faculty of Social Sciences)
Biostatistics Helsinki
Research Programs Unit
Aarno Palotie / Principal Investigator
INDIVIDRUG - Individualized Drug Therapy
HUS Internal Medicine and Rehabilitation
HUS Medical Imaging Center
Marja-Riitta Taskinen Research Group
Source :
Journal of internal medicineReferences. 291(2)
Publication Year :
2021

Abstract

Background The phospholipase domain-containing 3 gene (PNPLA3)-148M variant is associated with liver steatosis but its influence on the metabolism of triglyceride-rich lipoproteins remains unclear. Here, we investigated the kinetics of large, triglyceride-rich very-low-density lipoprotein (VLDL), (VLDL1), and smaller VLDL2 in homozygotes for the PNPLA3-148M variant. Methods and results The kinetics of apolipoprotein (apo) B100 (apoB100) and triglyceride in VLDL subfractions were analysed in nine subjects homozygous for PNPLA3-148M and nine subjects homozygous for PNPLA3-148I (controls). Liver fat was >3-fold higher in the 148M subjects. Production rates for apoB100 and triglyceride in VLDL1 did not differ significantly between the two groups. Likewise, production rates for VLDL2-apoB100 and -triglyceride, and fractional clearance rates for both apoB100 and triglyceride in VLDL1 and VLDL2, were not significantly different. Conclusions Despite the higher liver fat content in PNPLA3 148M homozygotes, there was no increase in VLDL production. Equally, VLDL production was maintained at normal levels despite the putative impairment in cytosolic lipid hydrolysis in these subjects.

Details

ISSN :
13652796
Volume :
291
Issue :
2
Database :
OpenAIRE
Journal :
Journal of internal medicineReferences
Accession number :
edsair.doi.dedup.....3fc0a49e73ac513cd8f6d6a59089e5a5