The Stability of Metabolic Syndrome in Children and Adolescents

Unit on Growth and Obesity, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, 9000 Rockville Pike, Hatfield Clinical Research Center, Bethesda, Maryland 20892-1103, USA.
The Journal of Clinical Endocrinology and Metabolism (Impact Factor: 6.21). 10/2009; 94(12):4828-34. DOI: 10.1210/jc.2008-2665
Source: PubMed


Some studies suggest the presence of metabolic syndrome before adulthood may identify those at high risk for later cardiovascular morbidity, but there are few data examining the reliability of pediatric metabolic syndrome.
To examine the short- and long-term stability of pediatric metabolic syndrome.
Metabolic syndrome was defined as having at least three of the following: waist circumference, blood pressure, and fasting serum triglycerides in the 90th or higher percentile for age/sex; high-density lipoprotein-cholesterol 10th or lower percentile for age/sex; and fasting serum glucose of at least 100 mg/dl. Short-term metabolic syndrome stability (repeated measurements within 60 d) was assessed in obese youth ages 6-17 yr. Long-term metabolic syndrome stability (repeated measurements more than 1.5 yr apart) was studied in 146 obese and nonobese children age 6-12 yr at baseline.
Convenience samples of obese and nonobese youth ages 6-17 yr participating in research studies were collected at a clinical research hospital.
Short-term metabolic syndrome stability (repeat measurements performed 19.7 +/- 13.1 d apart) was assessed in 220 children. The diagnosis of metabolic syndrome was unstable in 31.6% of cases. At their short-term follow-up visit, incidence of metabolic syndrome among participants who did not have metabolic syndrome at baseline was 24%. In the long term (repeat measurements performed 5.6 +/- 1.9 yr apart), the diagnosis of metabolic syndrome was unstable in 45.5% of cases.
Cutoff-point-based definitions for pediatric metabolic syndrome have substantial instability in the short and long term. The value of making a cutoff-point-based diagnosis of metabolic syndrome during childhood or adolescence remains in question.

Download full-text


Available from: Jack A Yanovski, Nov 09, 2015
  • Source
    • "Metabolic syndrome defined using age-and sex-specific percentile-based cut-off definition commonly used in previous reports (Gustafson et al., 2009; Vikram et al., 2006): values of at least 90 th percentile for waist circumference, systolic or diastolic blood pressure, and triglycerides (Biltoft & Muir, 2009) and no higher than 10 th percentile for HDL cholesterol, and a fasting glucose value of at least 100 mg/dL was used to indicate impaired fasting glucose. Metabolic syndrome was considered present when a child met the cut-points for at least three of these factors. "
    [Show abstract] [Hide abstract]
    ABSTRACT: Preliminary data in adults suggest that binge eating is associated with greater prevalence of metabolic syndrome (MetS) components. However, there are limited data in youth, and little is known of the role of binge episode size in these relationships. We examined the relationship between loss of control eating and metabolic characteristics in a convenience sample of 329 treatment-seeking and non-treatment-seeking adolescent boys and girls. The sample was enriched by design with adolescents who were overweight or obese and with individuals who reported episodes of loss of control over their eating (either objectively large binge episodes, OBEs or subjectively large binge episodes, SBEs, in the past month), as assessed by clinical interview. MetS components (blood pressure, lipids, glucose, and waist circumference) were the primary variables of interest. 46% of the cohort reported loss of control eating; among those, 53% reported SBEs only and 47% reported OBEs. Youth with loss of control eating had higher systolic blood pressure (p=.001) and higher low-density lipoprotein cholesterol (LDL-c) (p=.002) compared to those without loss of control eating, in analyses adjusted for intervention-seeking status, fat mass and sociodemographic characteristics. Youth reporting OBEs had higher LDL-c (p=.013) compared to those reporting only SBEs. Adolescents reporting loss of control episodes had greater dysfunction in some components of the MetS compared to youth without loss of control; episode size may contribute to metabolic dysfunction. Published by Elsevier Ltd.
    Full-text · Article · Jul 2015 · Eating Behaviors
  • Source
    • "However, the clinical utility of the metabolic syndrome in pediatrics remains unclear (Daniels, 2009). There is also quite limited stability for the diagnosis of metabolic syndrome among children and adolescents (Goodman, Daniels, Meigs, & Dolan, 2007; Goodman et al., 2009; Gustafson et al., 2009; Stanley, Chen, & Goodman, 2014). A detailed scientific statement appraising the evidence for utility of the metabolic syndrome in pediatrics is available from the American Heart Association (Steinberger et al., 2009). "
    [Show abstract] [Hide abstract]
    ABSTRACT: The prevalence of child and adolescent obesity in the United States increased dramatically between 1970 and 2000, and there are few indications that the rates of childhood obesity are decreasing. Obesity is associated with myriad medical, psychological, and neurocognitive abnormalities that impact children's health and quality of life. Genotypic variation is important in determining the susceptibility of individual children to undue gains in adiposity; however, the rapid increase in pediatric obesity prevalence suggests changes to children's environments and/or to their learned behaviors may dramatically affect body weight regulation. This paper presents an overview of the epidemiology, consequences, and etiopathogenesis of pediatric obesity, serving as a general introduction to the subsequent papers in this Special Issue that address aspects of childhood obesity and cognition in detail. Copyright © 2015. Published by Elsevier Ltd.
    Full-text · Article · Mar 2015 · Appetite
  • Source
    • "Plasma glucose and insulin were measured from blood samples drawn after 12-h overnight fast as previously described [39]. HOMA-IR was calculated as fasting serum insulin (mU/L)×plasma glucose (mmol/L)/22.5. "
    [Show abstract] [Hide abstract]
    ABSTRACT: Brain pathways, including those in hypothalamus and nucleus of the solitary tract, influence food intake, nutrient preferences, metabolism and development of obesity in ways that often differ between males and females. Branched chain amino acids, including leucine, can suppress food intake, alter metabolism and change vulnerability to obesity. The SLC6A15 (v7-3) gene encodes a sodium-dependent transporter of leucine and other branched chain amino acids that is expressed by neurons in hypothalamus and nucleus of the solitary tract. We now report that SLC6A15 knockout attenuates leucine's abilities to reduce both: a) intake of normal chow and b) weight gain produced by access to a high fat diet in gender-selective fashions. We identify SNPs in the human SLC6A15 that are associated with body mass index and insulin resistance in males. These observations in mice and humans support a novel, gender-selective role for brain amino acid compartmentalization mediated by SLC6A15 in diet and obesity-associated phenotypes.
    Full-text · Article · Sep 2013 · PLoS ONE
Show more