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The Relationship of Alanine Aminotransferase to Metabolic Syndrome in a Korean Population

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Publisher Aves
Specialty Gastroenterology
Date 2018 Feb 3
PMID 29391308
Citations 4
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Abstract

Background/aims: Although associations between serum alanine aminotransferase and metabolic syndrome are well-recognized in Western countries, only a limited number of prospective studies have been performed in Asian populations. The aim of the study was to cross-sectionally and longitudinally examine whether serum alanine aminotransferase levels are associated with metabolic syndrome and its associated components in a Korean population.

Materials And Methods: A total of 31,832 subjects who received health screenings were included in cross-sectional analyses; a subgroup of 4.070 subjects without metabolic syndrome at baseline was included in the longitudinal analyses. The metabolic syndrome definition was based on the National Cholesterol Education Program Third Adult Treatment Panel criteria with modification on waist circumference cut-off to be more appropriate for an Asian population.

Results: In the cross-sectional analyses, serum alanine aminotransferase is positively associated with metabolic syndrome and its components. In the longitudinal analyses, the prevalence of metabolic syndrome increased across serum alanine aminotransferase quartiles in a dose-dependent manner after extensive adjustments (hazard ratios were 1.000, 1.609, 2.601, and 3.015 for quartiles, 1 through quartile 4; P for trend<0.001).

Conclusion: Our study confirmed a positive association between components of metabolic syndrome and elevated serum alanine aminotransferase in a Korean population.

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References
1.
Pratt D, KAPLAN M . Evaluation of abnormal liver-enzyme results in asymptomatic patients. N Engl J Med. 2000; 342(17):1266-71. DOI: 10.1056/NEJM200004273421707. View

2.
Greenfield T . Ways of measuring drinking patterns and the difference they make: experience with graduated frequencies. J Subst Abuse. 2001; 12(1-2):33-49. DOI: 10.1016/s0899-3289(00)00039-0. View

3.
. Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001; 285(19):2486-97. DOI: 10.1001/jama.285.19.2486. View

4.
Garg A, Misra A . Hepatic steatosis, insulin resistance, and adipose tissue disorders. J Clin Endocrinol Metab. 2002; 87(7):3019-22. DOI: 10.1210/jcem.87.7.8736. View

5.
Seppala-Lindroos A, Vehkavaara S, Hakkinen A, Goto T, Westerbacka J, Sovijarvi A . Fat accumulation in the liver is associated with defects in insulin suppression of glucose production and serum free fatty acids independent of obesity in normal men. J Clin Endocrinol Metab. 2002; 87(7):3023-8. DOI: 10.1210/jcem.87.7.8638. View