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Visceral obesity modulates the impact of apolipoprotein C3 gene variants on liver fat content

Objective: It has not been solved whether subjects carrying the minor alleles of the −455T>C or −482C>T single nucleotide polymorphisms (SNPs) in the apolipoprotein-C3-gene ( APOC3) have an increased risk for developing fatty liver and insulin resistance. We investigated the relationships of t...

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Published in:International Journal of Obesity 2012-06, Vol.36 (6), p.774-782
Main Authors: Peter, A, Kantartzis, K, Machicao, F, Machann, J, Wagner, S, Templin, S, Königsrainer, I, Königsrainer, A, Schick, F, Fritsche, A, Häring, H-U, Stefan, N
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container_issue 6
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container_title International Journal of Obesity
container_volume 36
creator Peter, A
Kantartzis, K
Machicao, F
Machann, J
Wagner, S
Templin, S
Königsrainer, I
Königsrainer, A
Schick, F
Fritsche, A
Häring, H-U
Stefan, N
description Objective: It has not been solved whether subjects carrying the minor alleles of the −455T>C or −482C>T single nucleotide polymorphisms (SNPs) in the apolipoprotein-C3-gene ( APOC3) have an increased risk for developing fatty liver and insulin resistance. We investigated the relationships of the SNPs with hepatic APOC3 expression and hypothesized that visceral obesity may modulate the effects of these SNPs on liver fat and insulin sensitivity (IS). Methods: APOC3 mRNA expression and triglyceride content were determined in liver biopsies from 50 subjects. In a separate group ( N =330) liver fat was measured by 1 H-magnetic resonance spectroscopy. IS was estimated during an oral glucose tolerance test (OGTT) and the euglycemic, hyperinsulinemic clamp ( N =222). Results: APOC3 mRNA correlated positively with triglyceride content in liver biopsies ( r =0.29, P =0.036). Carriers of the minor alleles (−455C and −482T) tended to have higher hepatic APOC3 mRNA expression (1.80 (0.45–3.56) vs 0.77 (0.40–1.64), P =0.09), but not higher triglyceride content ( P =0.76). In 330 subjects the genotype did not correlate with liver fat ( P =0.97) or IS (OGTT: P =0.41; clamp: P =0.99). However, a significant interaction of the genotype with waist circumference in determining liver fat was detected ( P =0.02) in which minor allele carriers had higher liver fat only in the lowest tertile of waist circumference ( P =0.01). In agreement, during a 9-month lifestyle intervention the minor allele carriers of the SNP −482C>T in the lowest tertile also had less decrease in liver fat ( P =0.04). Conclusions: APOC3 mRNA expression is increased in fatty liver and is regulated by SNPs in APOC3 . The impact of the APOC3 SNPs on fatty liver is small and depends on visceral obesity.
doi_str_mv 10.1038/ijo.2011.154
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We investigated the relationships of the SNPs with hepatic APOC3 expression and hypothesized that visceral obesity may modulate the effects of these SNPs on liver fat and insulin sensitivity (IS). Methods: APOC3 mRNA expression and triglyceride content were determined in liver biopsies from 50 subjects. In a separate group ( N =330) liver fat was measured by 1 H-magnetic resonance spectroscopy. IS was estimated during an oral glucose tolerance test (OGTT) and the euglycemic, hyperinsulinemic clamp ( N =222). Results: APOC3 mRNA correlated positively with triglyceride content in liver biopsies ( r =0.29, P =0.036). Carriers of the minor alleles (−455C and −482T) tended to have higher hepatic APOC3 mRNA expression (1.80 (0.45–3.56) vs 0.77 (0.40–1.64), P =0.09), but not higher triglyceride content ( P =0.76). In 330 subjects the genotype did not correlate with liver fat ( P =0.97) or IS (OGTT: P =0.41; clamp: P =0.99). However, a significant interaction of the genotype with waist circumference in determining liver fat was detected ( P =0.02) in which minor allele carriers had higher liver fat only in the lowest tertile of waist circumference ( P =0.01). In agreement, during a 9-month lifestyle intervention the minor allele carriers of the SNP −482C&gt;T in the lowest tertile also had less decrease in liver fat ( P =0.04). Conclusions: APOC3 mRNA expression is increased in fatty liver and is regulated by SNPs in APOC3 . 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Abdomen ; Genes ; Genetic aspects ; Genetic Predisposition to Disease ; Genetic Variation ; Genotype ; Genotype &amp; phenotype ; Glucose ; Glucose Tolerance Test ; Health Promotion and Disease Prevention ; Hormones ; Humans ; Insulin resistance ; Insulin Resistance - genetics ; Internal Medicine ; Lifestyle ; Liver ; Liver - pathology ; Liver diseases ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Magnetic Resonance Spectroscopy ; Male ; Measurement ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; Metabolic Diseases ; Middle Aged ; Nephrology ; Obesity ; Obesity, Abdominal - blood ; Obesity, Abdominal - epidemiology ; Obesity, Abdominal - genetics ; Objectives ; original-article ; Other diseases. 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We investigated the relationships of the SNPs with hepatic APOC3 expression and hypothesized that visceral obesity may modulate the effects of these SNPs on liver fat and insulin sensitivity (IS). Methods: APOC3 mRNA expression and triglyceride content were determined in liver biopsies from 50 subjects. In a separate group ( N =330) liver fat was measured by 1 H-magnetic resonance spectroscopy. IS was estimated during an oral glucose tolerance test (OGTT) and the euglycemic, hyperinsulinemic clamp ( N =222). Results: APOC3 mRNA correlated positively with triglyceride content in liver biopsies ( r =0.29, P =0.036). Carriers of the minor alleles (−455C and −482T) tended to have higher hepatic APOC3 mRNA expression (1.80 (0.45–3.56) vs 0.77 (0.40–1.64), P =0.09), but not higher triglyceride content ( P =0.76). In 330 subjects the genotype did not correlate with liver fat ( P =0.97) or IS (OGTT: P =0.41; clamp: P =0.99). However, a significant interaction of the genotype with waist circumference in determining liver fat was detected ( P =0.02) in which minor allele carriers had higher liver fat only in the lowest tertile of waist circumference ( P =0.01). In agreement, during a 9-month lifestyle intervention the minor allele carriers of the SNP −482C&gt;T in the lowest tertile also had less decrease in liver fat ( P =0.04). Conclusions: APOC3 mRNA expression is increased in fatty liver and is regulated by SNPs in APOC3 . The impact of the APOC3 SNPs on fatty liver is small and depends on visceral obesity.</description><subject>Apolipoprotein C-III - blood</subject><subject>Apolipoprotein C-III - genetics</subject><subject>Apolipoproteins</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Blood glucose</subject><subject>Complications and side effects</subject><subject>Diabetes</subject><subject>Disorders of blood lipids. Hyperlipoproteinemia</subject><subject>Endocrinology</subject><subject>Epidemiology</subject><subject>Fatty Liver - blood</subject><subject>Fatty Liver - epidemiology</subject><subject>Fatty Liver - genetics</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetic Variation</subject><subject>Genotype</subject><subject>Genotype &amp; phenotype</subject><subject>Glucose</subject><subject>Glucose Tolerance Test</subject><subject>Health Promotion and Disease Prevention</subject><subject>Hormones</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - genetics</subject><subject>Internal Medicine</subject><subject>Lifestyle</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver diseases</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Male</subject><subject>Measurement</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metabolic Diseases</subject><subject>Middle Aged</subject><subject>Nephrology</subject><subject>Obesity</subject><subject>Obesity, Abdominal - blood</subject><subject>Obesity, Abdominal - epidemiology</subject><subject>Obesity, Abdominal - genetics</subject><subject>Objectives</subject><subject>original-article</subject><subject>Other diseases. 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We investigated the relationships of the SNPs with hepatic APOC3 expression and hypothesized that visceral obesity may modulate the effects of these SNPs on liver fat and insulin sensitivity (IS). Methods: APOC3 mRNA expression and triglyceride content were determined in liver biopsies from 50 subjects. In a separate group ( N =330) liver fat was measured by 1 H-magnetic resonance spectroscopy. IS was estimated during an oral glucose tolerance test (OGTT) and the euglycemic, hyperinsulinemic clamp ( N =222). Results: APOC3 mRNA correlated positively with triglyceride content in liver biopsies ( r =0.29, P =0.036). Carriers of the minor alleles (−455C and −482T) tended to have higher hepatic APOC3 mRNA expression (1.80 (0.45–3.56) vs 0.77 (0.40–1.64), P =0.09), but not higher triglyceride content ( P =0.76). In 330 subjects the genotype did not correlate with liver fat ( P =0.97) or IS (OGTT: P =0.41; clamp: P =0.99). However, a significant interaction of the genotype with waist circumference in determining liver fat was detected ( P =0.02) in which minor allele carriers had higher liver fat only in the lowest tertile of waist circumference ( P =0.01). In agreement, during a 9-month lifestyle intervention the minor allele carriers of the SNP −482C&gt;T in the lowest tertile also had less decrease in liver fat ( P =0.04). Conclusions: APOC3 mRNA expression is increased in fatty liver and is regulated by SNPs in APOC3 . The impact of the APOC3 SNPs on fatty liver is small and depends on visceral obesity.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>21829161</pmid><doi>10.1038/ijo.2011.154</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Apolipoprotein C-III - blood
Apolipoprotein C-III - genetics
Apolipoproteins
Biological and medical sciences
Biopsy
Blood glucose
Complications and side effects
Diabetes
Disorders of blood lipids. Hyperlipoproteinemia
Endocrinology
Epidemiology
Fatty Liver - blood
Fatty Liver - epidemiology
Fatty Liver - genetics
Female
Gastroenterology. Liver. Pancreas. Abdomen
Genes
Genetic aspects
Genetic Predisposition to Disease
Genetic Variation
Genotype
Genotype & phenotype
Glucose
Glucose Tolerance Test
Health Promotion and Disease Prevention
Hormones
Humans
Insulin resistance
Insulin Resistance - genetics
Internal Medicine
Lifestyle
Liver
Liver - pathology
Liver diseases
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Magnetic Resonance Spectroscopy
Male
Measurement
Medical sciences
Medicine
Medicine & Public Health
Metabolic Diseases
Middle Aged
Nephrology
Obesity
Obesity, Abdominal - blood
Obesity, Abdominal - epidemiology
Obesity, Abdominal - genetics
Objectives
original-article
Other diseases. Semiology
Pathogenesis
Physiological aspects
Polymorphism, Single Nucleotide
Prevalence
Public Health
Single nucleotide polymorphisms
Spectroscopy
Triglycerides - blood
Waist
title Visceral obesity modulates the impact of apolipoprotein C3 gene variants on liver fat content
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