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Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study

Nonalcoholic fatty liver is associated with obesity‐related metabolic disturbances, but little is known about the metabolic perturbations preceding fatty liver disease. We performed comprehensive metabolic profiling to assess how circulating metabolites, such as lipoprotein lipids, fatty acids, amin...

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Autores principales: Kaikkonen, Jari E., Würtz, Peter, Suomela, Emmi, Lehtovirta, Miia, Kangas, Antti J., Jula, Antti, Mikkilä, Vera, Viikari, Jorma S.A., Juonala, Markus, Rönnemaa, Tapani, Hutri‐Kähönen, Nina, Kähönen, Mika, Lehtimäki, Terho, Soininen, Pasi, Ala‐Korpela, Mika, Raitakari, Olli T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5299457/
https://www.ncbi.nlm.nih.gov/pubmed/27775848
http://dx.doi.org/10.1002/hep.28899
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author Kaikkonen, Jari E.
Würtz, Peter
Suomela, Emmi
Lehtovirta, Miia
Kangas, Antti J.
Jula, Antti
Mikkilä, Vera
Viikari, Jorma S.A.
Juonala, Markus
Rönnemaa, Tapani
Hutri‐Kähönen, Nina
Kähönen, Mika
Lehtimäki, Terho
Soininen, Pasi
Ala‐Korpela, Mika
Raitakari, Olli T.
author_facet Kaikkonen, Jari E.
Würtz, Peter
Suomela, Emmi
Lehtovirta, Miia
Kangas, Antti J.
Jula, Antti
Mikkilä, Vera
Viikari, Jorma S.A.
Juonala, Markus
Rönnemaa, Tapani
Hutri‐Kähönen, Nina
Kähönen, Mika
Lehtimäki, Terho
Soininen, Pasi
Ala‐Korpela, Mika
Raitakari, Olli T.
author_sort Kaikkonen, Jari E.
collection PubMed
description Nonalcoholic fatty liver is associated with obesity‐related metabolic disturbances, but little is known about the metabolic perturbations preceding fatty liver disease. We performed comprehensive metabolic profiling to assess how circulating metabolites, such as lipoprotein lipids, fatty acids, amino acids, and glycolysis‐related metabolites, reflect the presence of and future risk for fatty liver in young adults. Sixty‐eight lipids and metabolites were quantified by nuclear magnetic resonance metabolomics in the population‐based Young Finns Study from serum collected in 2001 (n = 1,575), 2007 (n = 1,509), and 2011 (n = 2,002). Fatty liver was diagnosed by ultrasound in 2011 when participants were aged 34‐49 years (19% prevalence). Cross‐sectional associations as well as 4‐year and 10‐year risks for fatty liver were assessed by logistic regression. Metabolites across multiple pathways were strongly associated with the presence of fatty liver (P < 0.0007 for 60 measures in age‐adjusted and sex‐adjusted cross‐sectional analyses). The strongest direct associations were observed for extremely large very‐low‐density lipoprotein triglycerides (odds ratio [OR] = 4.86 per 1 standard deviation, 95% confidence interval 3.48‐6.78), other very‐low‐density lipoprotein measures, and branched‐chain amino acids (e.g., leucine OR = 2.94, 2.51‐3.44). Strong inverse associations were observed for high‐density lipoprotein measures, e.g., high‐density lipoprotein size (OR = 0.36, 0.30‐0.42) and several fatty acids including omega‐6 (OR = 0.37, 0.32‐0.42). The metabolic associations were attenuated but remained significant after adjusting for waist, physical activity, alcohol consumption, and smoking (P < 0.0007). Similar aberrations in the metabolic profile were observed already 10 years before fatty liver diagnosis. Conclusion: Circulating lipids, fatty acids, and amino acids reflect fatty liver independently of routine metabolic risk factors; these metabolic aberrations appear to precede the development of fatty liver in young adults. (Hepatology 2017;65:491‐500).
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spelling pubmed-52994572017-02-22 Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study Kaikkonen, Jari E. Würtz, Peter Suomela, Emmi Lehtovirta, Miia Kangas, Antti J. Jula, Antti Mikkilä, Vera Viikari, Jorma S.A. Juonala, Markus Rönnemaa, Tapani Hutri‐Kähönen, Nina Kähönen, Mika Lehtimäki, Terho Soininen, Pasi Ala‐Korpela, Mika Raitakari, Olli T. Hepatology Steatohepatitis/Metabolic Liver Disease Nonalcoholic fatty liver is associated with obesity‐related metabolic disturbances, but little is known about the metabolic perturbations preceding fatty liver disease. We performed comprehensive metabolic profiling to assess how circulating metabolites, such as lipoprotein lipids, fatty acids, amino acids, and glycolysis‐related metabolites, reflect the presence of and future risk for fatty liver in young adults. Sixty‐eight lipids and metabolites were quantified by nuclear magnetic resonance metabolomics in the population‐based Young Finns Study from serum collected in 2001 (n = 1,575), 2007 (n = 1,509), and 2011 (n = 2,002). Fatty liver was diagnosed by ultrasound in 2011 when participants were aged 34‐49 years (19% prevalence). Cross‐sectional associations as well as 4‐year and 10‐year risks for fatty liver were assessed by logistic regression. Metabolites across multiple pathways were strongly associated with the presence of fatty liver (P < 0.0007 for 60 measures in age‐adjusted and sex‐adjusted cross‐sectional analyses). The strongest direct associations were observed for extremely large very‐low‐density lipoprotein triglycerides (odds ratio [OR] = 4.86 per 1 standard deviation, 95% confidence interval 3.48‐6.78), other very‐low‐density lipoprotein measures, and branched‐chain amino acids (e.g., leucine OR = 2.94, 2.51‐3.44). Strong inverse associations were observed for high‐density lipoprotein measures, e.g., high‐density lipoprotein size (OR = 0.36, 0.30‐0.42) and several fatty acids including omega‐6 (OR = 0.37, 0.32‐0.42). The metabolic associations were attenuated but remained significant after adjusting for waist, physical activity, alcohol consumption, and smoking (P < 0.0007). Similar aberrations in the metabolic profile were observed already 10 years before fatty liver diagnosis. Conclusion: Circulating lipids, fatty acids, and amino acids reflect fatty liver independently of routine metabolic risk factors; these metabolic aberrations appear to precede the development of fatty liver in young adults. (Hepatology 2017;65:491‐500). John Wiley and Sons Inc. 2016-12-24 2017-02 /pmc/articles/PMC5299457/ /pubmed/27775848 http://dx.doi.org/10.1002/hep.28899 Text en © 2016 The Authors. Hepatology published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Steatohepatitis/Metabolic Liver Disease
Kaikkonen, Jari E.
Würtz, Peter
Suomela, Emmi
Lehtovirta, Miia
Kangas, Antti J.
Jula, Antti
Mikkilä, Vera
Viikari, Jorma S.A.
Juonala, Markus
Rönnemaa, Tapani
Hutri‐Kähönen, Nina
Kähönen, Mika
Lehtimäki, Terho
Soininen, Pasi
Ala‐Korpela, Mika
Raitakari, Olli T.
Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study
title Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study
title_full Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study
title_fullStr Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study
title_full_unstemmed Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study
title_short Metabolic profiling of fatty liver in young and middle‐aged adults: Cross‐sectional and prospective analyses of the Young Finns Study
title_sort metabolic profiling of fatty liver in young and middle‐aged adults: cross‐sectional and prospective analyses of the young finns study
topic Steatohepatitis/Metabolic Liver Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5299457/
https://www.ncbi.nlm.nih.gov/pubmed/27775848
http://dx.doi.org/10.1002/hep.28899
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