Literature DB >> 26703124

Upper Normal Alanine Aminotransferase Range and Insulin Resistance in Korean Adolescents: Korean National Health and Nutrition Examination Survey, 2009-2010.

Yoon Lee1, Kyung-Do Han2, Jennifer Jaeeun Jung3, Kee-Hyoung Lee1, Kyung-Hwan Cho4, Yang-Hyun Kim5.   

Abstract

BACKGROUND: Alanine aminotransferase (ALT) has been one of the most useful biomarkers reflecting liver damage. Some studies have proposed that serum ALT levels, even those within the conventional normal range, are associated with metabolic syndrome and fatty liver. AIMS: We examined the correlation between ALT levels and insulin resistance (IR) and ALT cutoff value for high IR status in Korean adolescents.
METHODS: A total of 886 subjects (461 boys and 425 girls) who participated in the 2009-2010 Korea National Health and Nutrition Examination Survey were included in this study. Multivariable adjusted logistic regression analyses were used to examine the odds ratios and 95 % confidence intervals (CIs) of the prevalence of the highest quartile of the homeostasis model assessment of IR (HOMA-IR) according to the ALT quartile. The cutoff value of ALT for the highest HOMA-IR quartile (Q4) were obtained using receiver operating characteristic curve analysis.
RESULTS: The mean ALT value increased as the number of metabolic syndrome components increased, but in only boys (p for trend <0.001), while the IR quartile increased in both boys and girls (all p for trends <0.001). The prevalence of IR (Q4) was only increased in ALT (Q4) in boys after the adjustment for age, body mass index, and waist circumference (OR 2.49; 95 % CI 1.05-5.91; p for trend = 0.017). The cutoff values were 17.0 IU/L in boys and 11.0 IU/L in girls.
CONCLUSIONS: The highest ALT quartile was associated with an increased prevalence of the highest quartile of IR in boys but not in girls.

Entities:  

Keywords:  Adolescents; Alanine aminotransferase; Insulin resistance; Korean National Health and Nutrition Examination Survey; Metabolic syndrome

Mesh:

Substances:

Year:  2015        PMID: 26703124     DOI: 10.1007/s10620-015-4009-x

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


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