The PNPLA3-I148M Variant Confers an Antiatherogenic Lipid Profile in Insulin-resistant Patients
The PNPLA3-I148M Variant Confers an Antiatherogenic Lipid Profile in Insulin-resistant Patients
AbstractContextThe I148M (rs738409-G) variant in PNPLA3 increases liver fat content but may be protective against cardiovascular disease. Insulin resistance (IR) amplifies the effect of PNPLA3-I148M on liver fat.ObjectiveTo study whether PNPLA3-I148M confers an antihyperlipidemic effect in insulin-resistant patients.DesignCross-sectional study comparing the impact of PNPLA3-I148M on plasma lipids and lipoproteins in 2 cohorts, both divided into groups based on rs738409-G allele carrier status and median HOMA-IR.SettingTertiary referral center.PatientsA total of 298 obese patients who underwent a liver biopsy during bariatric surgery (bariatric cohort: age 49 ± 9 years, body mass index [BMI] 43.2 ± 6.8 kg/m2), and 345 less obese volunteers in whom liver fat was measured by proton magnetic resonance spectroscopy (nonbariatric cohort: age 45 ± 14 years, BMI 29.7 ± 5.7 kg/m2).Main Outcome MeasuresNuclear magnetic resonance profiling of plasma lipids, lipoprotein particle subclasses and their composition.ResultsIn both cohorts, individuals carrying the PNPLA3-I148M variant had significantly higher liver fat content than noncarriers. In insulin-resistant and homozygous carriers, PNPLA3-I148M exerted a distinct antihyperlipidemic effect with decreased very-low-density lipoprotein (VLDL) and low-density lipoprotein (LDL) particles and their constituents, and increased high-density lipoprotein particles and their constituents, compared with noncarriers. VLDL particles were smaller and LDL particles larger in PNPLA3-I148M carriers. These changes were geometrically opposite to those due to IR. PNPLA3-I148M did not have a measurable effect in patients with lower IR, and its effect was smaller albeit still significant in the less obese than in the obese cohort.ConclusionsPNPLA3-I148M confers an antiatherogenic plasma lipid profile particularly in insulin-resistant individuals.
- Minerva Foundation Institute for Medical Research
- Yale University United States
- University of Helsinki Finland
- Lund University Sweden
- Helsinki University Hospital Finland
Male, Steatosis, Cohort Studies, Methionine, insulin resistance, rasvamaksatauti, genetics, metabolinen oireyhtymä, aineenvaihdunta, Finland, Disease Resistance, rasvamaksa, Middle Aged, General medicine, internal medicine and other clinical medicine, non-alcoholic fatty liver, Female, Adult, ateroskleroosi, genetiikka, ei-alkoholiperäinen rasvamaksatauti, lipoproteiinit, Lipoproteins, metabolic syndrome, TM6SF2, steatoosi, NAFLD, metabolia, Humans, Isoleucine, PNPLA3, Genetic Association Studies, fatty liver, dyslipidemia, non-alcoholic fatty liver disease, Membrane Proteins, Lipase, insuliiniresistenssi, Atherosclerosis, Lipid Metabolism, patatin-like phospholipase domain containing 3, lipoproteins, Cross-Sectional Studies, Amino Acid Substitution, Lipidomics, fatty liver disease, atherosclerosis, Insulin Resistance, metabolism
Male, Steatosis, Cohort Studies, Methionine, insulin resistance, rasvamaksatauti, genetics, metabolinen oireyhtymä, aineenvaihdunta, Finland, Disease Resistance, rasvamaksa, Middle Aged, General medicine, internal medicine and other clinical medicine, non-alcoholic fatty liver, Female, Adult, ateroskleroosi, genetiikka, ei-alkoholiperäinen rasvamaksatauti, lipoproteiinit, Lipoproteins, metabolic syndrome, TM6SF2, steatoosi, NAFLD, metabolia, Humans, Isoleucine, PNPLA3, Genetic Association Studies, fatty liver, dyslipidemia, non-alcoholic fatty liver disease, Membrane Proteins, Lipase, insuliiniresistenssi, Atherosclerosis, Lipid Metabolism, patatin-like phospholipase domain containing 3, lipoproteins, Cross-Sectional Studies, Amino Acid Substitution, Lipidomics, fatty liver disease, atherosclerosis, Insulin Resistance, metabolism
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