Instability in the diagnosis of metabolic syndrome in adolescents

被引:166
作者
Goodman, Elizabeth
Daniels, Stephen R.
Meigs, James B.
Dolan, Lawrence M.
机构
[1] Floating Hosp Children, Tufts New England Med Ctr, Boston, MA USA
[2] Denver Childrens Hosp, Dept Pediat, Denver, CO USA
[3] Univ Colorado, Sch Med, Denver, CO 80202 USA
[4] Massachusetts Gen Hosp, Dept Med, Div Gen Med, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Boston, MA 02115 USA
[6] Cincinnati Childrens Hosp, Med Ctr, Div Endocrinol, Cincinnati, OH USA
关键词
adolescents; insulin; obesity; syndrome X;
D O I
10.1161/CIRCULATIONAHA.106.669994
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Factor analyses suggest that the structure underlying metabolic syndrome is similar in adolescents and adults. However, adolescence is a period of intense physiological change, and therefore stability of the underlying metabolic structure and clinical categorization based on metabolic risk is uncertain. Methods and Results - We analyzed data from 1098 participants in the Princeton School District Study, a school-based study begun in 2001 - 2002, who were followed up for 3 years. We performed factor analyses of 8 metabolic risks at baseline and follow-up to assess stability of factor patterns and clinical categorization of metabolic syndrome. Metabolic syndrome was defined using the current American Heart Association/ National Heart, Lung, and Blood Institute definition for adults (AHA), a modified AHA definition used in prior pediatric metabolic syndrome studies ( pediatric AHA), and the International Diabetes Federation (IDF) guidelines. We found that factor structures were essentially identical at both time points. However, clinical categorization was not stable. Approximately half of adolescents with baseline metabolic syndrome lost the diagnosis at follow-up regardless of the definitions used: pediatric AHA = 56% (95% confidence interval [CI], 42% to 69%), AHA = 49% ( 95% CI, 32% to 66%), IDF = 53% ( 95% CI, 38% to 68%). In addition to loss of the diagnosis, new cases were identified. Cumulative incidence rates were as follows: pediatric AHA = 3.8% ( 95% CI, 2.8% to 5.2%); AHA = 4.4% ( 95% CI, 3.3% to 5.9%); IDF = 5.2% ( 95% CI, 4.0% to 6.8%). Conclusions - During adolescence, metabolic risk factor clustering is consistent. However, marked instability exists in the categorical diagnosis of metabolic syndrome. This instability, which includes both gain and loss of the diagnosis, suggests that the syndrome has reduced clinical utility in adolescence and that metabolic syndrome - specific pharmacotherapy for youth may be premature.
引用
收藏
页码:2316 / 2322
页数:7
相关论文
共 44 条
  • [1] The metabolic syndrome - a new worldwide definition
    Alberti, KGMM
    Zimmet, P
    Shaw, J
    [J]. LANCET, 2005, 366 (9491) : 1059 - 1062
  • [2] The incidence and persistence of the NCEP (National Cholesterol Education Program) metabolic syndrome.: The French DESIR study
    Balkau, B
    Vernay, M
    Mhamdi, L
    Novak, M
    Arondel, D
    Vol, S
    Tichet, J
    Eschwège, E
    [J]. DIABETES & METABOLISM, 2003, 29 (05) : 526 - 532
  • [3] Age-belated patterns of the clustering of cardiovascular risk variables of Syndrome X from childhood to young adulthood in a population made up of black and white subjects - The Bogalusa Heart Study
    Chen, W
    Bao, WH
    Begum, S
    Elkasabany, A
    Srinivasan, SR
    Berenson, GS
    [J]. DIABETES, 2000, 49 (06) : 1042 - 1048
  • [4] Definition of metabolic syndrome in preadolescent girls
    Chi, Carolyn H.
    Wang, Yun
    Wilson, Darrell M.
    Robinson, Thomas N.
    [J]. JOURNAL OF PEDIATRICS, 2006, 148 (06) : 788 - 792
  • [5] 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)
    Cleeman, JI
    Grundy, SM
    Becker, D
    Clark, LT
    Cooper, RS
    Denke, MA
    Howard, WJ
    Hunninghake, DB
    Illingworth, DR
    Luepker, RV
    McBride, P
    McKenney, JM
    Pasternak, RC
    Stone, NJ
    Van Horn, L
    Brewer, HB
    Ernst, ND
    Gordon, D
    Levy, D
    Rifkind, B
    Rossouw, JE
    Savage, P
    Haffner, SM
    Orloff, DG
    Proschan, MA
    Schwartz, JS
    Sempos, CT
    Shero, ST
    Murray, EZ
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19): : 2486 - 2497
  • [6] Prevalence of a metabolic syndrome phenotype in adolescents - Findings from the Third National Health and Nutrition Examination Survey, 1988-1994
    Cook, S
    Weitzman, M
    Auinger, P
    Nguyen, M
    Dietz, WH
    [J]. ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 2003, 157 (08): : 821 - 827
  • [7] The metabolic syndrome in overweight Hispanic youth and the role of insulin sensitivity
    Cruz, ML
    Weigensberg, MJ
    Huang, TTK
    Ball, G
    Shaibi, GQ
    Goran, MI
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (01) : 108 - 113
  • [8] Prevalence of the metabolic syndrome in American adolescents - Findings from the Third National Health and Nutrition Examination Survey
    de Ferranti, SD
    Gauvreau, K
    Ludwig, DS
    Neufeld, EJ
    Newburger, JW
    Rifai, N
    [J]. CIRCULATION, 2004, 110 (16) : 2494 - 2497
  • [9] Frequency of abnormal carbohydrate metabolism and diabetes in a population-based screening of adolescents
    Dolan, LM
    Bean, J
    D'Alessio, D
    Cohen, RM
    Morrison, JA
    Goodman, E
    Daniels, SR
    [J]. JOURNAL OF PEDIATRICS, 2005, 146 (06) : 751 - 758
  • [10] Prevalence and trends of a metabolic syndrome phenotype adolescents, 1999-2000
    Duncan, GE
    Li, SM
    Zhou, XH
    [J]. DIABETES CARE, 2004, 27 (10) : 2438 - 2443