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Erschienen in: Diabetologia 6/2009

01.06.2009 | Short Communication

A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans

verfasst von: A. Kotronen, L. E. Johansson, L. M. Johansson, C. Roos, J. Westerbacka, A. Hamsten, R. Bergholm, P. Arkkila, J. Arola, T. Kiviluoto, R. M. Fisher, E. Ehrenborg, M. Orho-Melander, M. Ridderstråle, L. Groop, H. Yki-Järvinen

Erschienen in: Diabetologia | Ausgabe 6/2009

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Abstract

Aims/hypothesis

It has recently been suggested that the rs738409 G allele in PNPLA3, which encodes adiponutrin, is strongly associated with increased liver fat content in three different ethnic groups. The aims of the present study were as follows: (1) to try to replicate these findings in European individuals with quantitative measures of hepatic fat content; (2) to study whether the polymorphism influences hepatic and adipose tissue insulin sensitivity; and (3) to investigate whether PNPLA3 expression is altered in the human fatty liver.

Methods

We genotyped 291 Finnish individuals in whom liver fat had been measured using proton magnetic resonance spectroscopy. Hepatic PNPLA3 expression was measured in 32 participants. Hepatic and adipose tissue insulin sensitivities were measured using a euglycaemic–hyperinsulinaemic (insulin infusion 0.3 mU kg−1 min−1) clamp technique combined with infusion of [3-3H]glucose in 109 participants.

Results

The rs738409 G allele in PNPLA3 was associated with increased quantitative measures of liver fat content (p = 0.011) and serum aspartate aminotransferase concentrations (p = 0.002) independently of age, sex and BMI. Fasting serum insulin and hepatic and adipose tissue insulin sensitivity were related to liver fat content independently of genotype status. PNPLA3 mRNA expression in the liver was positively related to obesity (r = 0.62, p < 0.0001) and to liver fat content (r = 0.58, p = 0.025) in participants who were not morbidly obese (BMI < 40 kg/m2).

Conclusions/interpretation

A common variant in PNPLA3 increases the risk of hepatic steatosis in humans.
Literatur
1.
Zurück zum Zitat Neuschwander-Tetri BA, Caldwell SH (2003) Nonalcoholic steatohepatitis: summary of an AASLD Single Topic Conference. Hepatology 37:1202–1219PubMedCrossRef Neuschwander-Tetri BA, Caldwell SH (2003) Nonalcoholic steatohepatitis: summary of an AASLD Single Topic Conference. Hepatology 37:1202–1219PubMedCrossRef
2.
Zurück zum Zitat Szczepaniak LS, Nurenberg P, Leonard D et al (2005) Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am J Physiol Endocrinol Metab 288:E462–E468PubMedCrossRef Szczepaniak LS, Nurenberg P, Leonard D et al (2005) Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am J Physiol Endocrinol Metab 288:E462–E468PubMedCrossRef
3.
Zurück zum Zitat Charlton M (2004) Nonalcoholic fatty liver disease: a review of current understanding and future impact. Clin Gastroenterol Hepatol 2:1048–1058PubMedCrossRef Charlton M (2004) Nonalcoholic fatty liver disease: a review of current understanding and future impact. Clin Gastroenterol Hepatol 2:1048–1058PubMedCrossRef
4.
Zurück zum Zitat Romeo S, Kozlitina J, Xing C et al (2008) Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat Genet 40:1461–1465PubMedCrossRef Romeo S, Kozlitina J, Xing C et al (2008) Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat Genet 40:1461–1465PubMedCrossRef
5.
Zurück zum Zitat Kotronen A, Westerbacka J, Bergholm R, Pietilainen KH, Yki-Jarvinen H (2007) Liver fat in the metabolic syndrome. J Clin Endocrinol Metab 92:3490–3497PubMedCrossRef Kotronen A, Westerbacka J, Bergholm R, Pietilainen KH, Yki-Jarvinen H (2007) Liver fat in the metabolic syndrome. J Clin Endocrinol Metab 92:3490–3497PubMedCrossRef
6.
Zurück zum Zitat Jenkins CM, Mancuso DJ, Yan W, Sims HF, Gibson B, Gross RW (2004) Identification, cloning, expression, and purification of three novel human calcium-independent phospholipase A2 family members possessing triacylglycerol lipase and acylglycerol transacylase activities. J Biol Chem 279:48968–48975PubMedCrossRef Jenkins CM, Mancuso DJ, Yan W, Sims HF, Gibson B, Gross RW (2004) Identification, cloning, expression, and purification of three novel human calcium-independent phospholipase A2 family members possessing triacylglycerol lipase and acylglycerol transacylase activities. J Biol Chem 279:48968–48975PubMedCrossRef
7.
Zurück zum Zitat Johansson LE, Hoffstedt J, Parikh H et al (2006) Variation in the adiponutrin gene influences its expression and associates with obesity. Diabetes 55:826–833PubMedCrossRef Johansson LE, Hoffstedt J, Parikh H et al (2006) Variation in the adiponutrin gene influences its expression and associates with obesity. Diabetes 55:826–833PubMedCrossRef
8.
Zurück zum Zitat Kotronen A, Vehkavaara S, Seppala-Lindroos A, Bergholm R, Yki-Jarvinen H (2007) Effect of liver fat on insulin clearance. Am J Physiol Endocrinol Metab 293:E1709–E1715PubMedCrossRef Kotronen A, Vehkavaara S, Seppala-Lindroos A, Bergholm R, Yki-Jarvinen H (2007) Effect of liver fat on insulin clearance. Am J Physiol Endocrinol Metab 293:E1709–E1715PubMedCrossRef
9.
Zurück zum Zitat Kotronen A, Juurinen L, Tiikkainen M, Vehkavaara S, Yki-Jarvinen H (2008) Increased liver fat, impaired insulin clearance, and hepatic and adipose tissue insulin resistance in type 2 diabetes. Gastroenterology 135:122–130PubMedCrossRef Kotronen A, Juurinen L, Tiikkainen M, Vehkavaara S, Yki-Jarvinen H (2008) Increased liver fat, impaired insulin clearance, and hepatic and adipose tissue insulin resistance in type 2 diabetes. Gastroenterology 135:122–130PubMedCrossRef
10.
Zurück zum Zitat Yuan X, Waterworth D, Perry JR et al (2008) Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. Am J Hum Genet 83:520–528PubMedCrossRef Yuan X, Waterworth D, Perry JR et al (2008) Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. Am J Hum Genet 83:520–528PubMedCrossRef
11.
Zurück zum Zitat Lake AC, Sun Y, Li JL et al (2005) Expression, regulation, and triglyceride hydrolase activity of adiponutrin family members. J Lipid Res 46:2477–2487PubMedCrossRef Lake AC, Sun Y, Li JL et al (2005) Expression, regulation, and triglyceride hydrolase activity of adiponutrin family members. J Lipid Res 46:2477–2487PubMedCrossRef
12.
Zurück zum Zitat Baulande S, Lasnier F, Lucas M, Pairault J (2001) Adiponutrin, a transmembrane protein corresponding to a novel dietary- and obesity-linked mRNA specifically expressed in the adipose lineage. J Biol Chem 276:33336–33344PubMedCrossRef Baulande S, Lasnier F, Lucas M, Pairault J (2001) Adiponutrin, a transmembrane protein corresponding to a novel dietary- and obesity-linked mRNA specifically expressed in the adipose lineage. J Biol Chem 276:33336–33344PubMedCrossRef
13.
Zurück zum Zitat Liu YM, Moldes M, Bastard JP et al (2004) Adiponutrin: A new gene regulated by energy balance in human adipose tissue. J Clin Endocrinol Metab 89:2684–2689PubMedCrossRef Liu YM, Moldes M, Bastard JP et al (2004) Adiponutrin: A new gene regulated by energy balance in human adipose tissue. J Clin Endocrinol Metab 89:2684–2689PubMedCrossRef
Metadaten
Titel
A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans
verfasst von
A. Kotronen
L. E. Johansson
L. M. Johansson
C. Roos
J. Westerbacka
A. Hamsten
R. Bergholm
P. Arkkila
J. Arola
T. Kiviluoto
R. M. Fisher
E. Ehrenborg
M. Orho-Melander
M. Ridderstråle
L. Groop
H. Yki-Järvinen
Publikationsdatum
01.06.2009
Verlag
Springer-Verlag
Erschienen in
Diabetologia / Ausgabe 6/2009
Print ISSN: 0012-186X
Elektronische ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-009-1285-z

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