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Prediction of future risk of insulin resistance and metabolic syndrome based on Korean boy’s metabolite profiing
  • Date2018-02-13 12:43
  • Update2018-02-13 12:43
  • CountersignatureDivision of Research Planning
  • Tel043-719-8033
Obesity Research and Clinical Practice, 2015, 01, 336─345

Prediction of future risk of insulin resistance and metabolic syndrome based on Korean boy’s metabolite profiing

AeJin Lee, Han Byul Jang, Moonjin Ra, Youngshim Choi, Hye-Ja Lee, Ju Yeon Park, Jae Heon Kang, Kyung-Hee Park, Sang Ick Park, Jihyun Song

Abstract

    Objective
    Childhood obesity is strongly related to future insulin resistance and metabolic syndrome. Thus, identifying early biomarkers of obesity-related diseases based on metabolic pro-ling is useful to control future metabolic disorders. We compared metabolic proles between obese and normal-weight children and inves- tigated speci?c biomarkers of future insulin resistance and metabolic syndrome.
    Methods
    In all, 186 plasma metabolites were analysed at baseline and after 2 years in 109 Korean boys (age 10.5 ± 0.4 years) from the Korean Child Obesity Cohort Study using the AbsoluteIDQTM p180 Kit.
    Results
    We observed that levels of 41 metabolites at baseline and 40 metabolites at follow-up were signi?cantly altered in obese children (p < 0.05). Obese children showed signi?cantly higher levels of branched-chain amino acids (BCAAs) and sev- eral acylcarnitines and lower levels of acyl―alkyl phosphatidylcholines. Also, baseline BCAAs were signi?cantly positively correlated with both homeostasis model assess- ment for insulin resistance (HOMA-IR) and continuous metabolic risk score at the 2-year follow-up. In logistic regression analyses with adjustments for degree of obe- sity at baseline, baseline BCAA concentration, greater than the median value, was identi?ed as a predictor of future risk of insulin resistance and metabolic syndrome.
    Conclusion
    High BCAA concentration could be ‘‘early’’ biomarkers for predicting future metabolic diseases.


  • ISBN or ISSN: 1871-403X

  • 본 연구는 질병관리본부 연구개발과제(과제번호 2012-NG64001-00) 연구비를 지원받아 수행되었습니다.
  • This research was supported by a fund(code 2012-NG64001-00) by Research of Korea Centers for Disease Control and Prevention.


This public work may be used under the terms of the public interest source + commercial use prohibition + nonrepudiation conditions This public work may be used under the terms of the public interest source + commercial use prohibition + nonrepudiation conditions
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