A Continuous Metabolic Syndrome Score Is Associated with Specific Biomarkers of Inflammation and CVD Risk in Prepubertal Children

被引:39
作者
Olza, Josune [1 ]
Aguilera, Concepcion M. [1 ]
Gil-Campos, Mercedes [2 ,3 ]
Leis, Rosaura [4 ]
Bueno, Gloria [5 ]
Valle, Miguel [6 ]
Canete, Ramon [2 ,3 ]
Tojo, Rafael [4 ]
Moreno, Luis A. [7 ]
Gil, Angel [1 ]
机构
[1] Univ Granada, Dept Biochem & Mol Biol 2, Inst Nutr & Food Technol, ES-18016 Granada, Spain
[2] Reina Sofia Univ Hosp, Paediat Res & Metab Unit, Maimonides Inst Biomed Res, Cordoba, Spain
[3] Reina Sofia Univ Hosp, Unit Paediat Endocrinol, Cordoba, Spain
[4] Univ Santiago Compostela, Clin Univ Hosp Santiago, Dept Paediat, Unit Invest Nutr Growth & Human Dev Galicia, Santiago De Compostela, Spain
[5] Univ Zaragoza, Lozano Blesa Univ Hosp, Dept Paediat, Zaragoza, Spain
[6] Valle Pedroches Hosp, Unit Clin Analyses, Pozoblanco, Spain
[7] Univ Zaragoza, Sch Hlth Sci, Zaragoza, Spain
关键词
Obesity; Metabolic syndrome X; Child; Cardiovascular diseases; INTIMA-MEDIA THICKNESS; BODY-MASS INDEX; INSULIN-RESISTANCE; CARDIORESPIRATORY FITNESS; ENDOTHELIAL DYSFUNCTION; CARDIOVASCULAR-DISEASE; PHYSICAL-ACTIVITY; OBESITY; ADOLESCENTS; YOUTH;
D O I
10.1159/000369981
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: We aimed to evaluate the use of a continuous metabolic syndrome (MetS) score and to assess the associations of this score with risk biomarkers of inflammation, endothelial damage and cardiovascular disease (CVD) in prepubertal children. Methods: A total of 677 prepubertal children (295 obese, 146 overweight, and 236 normal-weight) were recruited. MetS traits, markers of inflammation, endothelial damage and CVD risk were measured, and a continuous MetS score was calculated, consisting of the sum/5 of the standardised scores of the MetS components. Results: The continuous MetS score was significantly associated with active plasminogen activator inhibitor-1 (r = 0.406, p < 0.001), adiponectin (r = -0.212, p < 0.001), resistin (r = 0.263, p < 0.001), C-reactive protein (r = 0.254, p < 0.001), tumour necrosis factor alpha (r = 0.120, p = 0.003), myeloperoxidase (r = 0.188, p < 0.001) and sE-selectin (r = 0.278, p < 0.001). Children in the normal-weight, overweight and obese groups with MetS totalled 0 (0%), 1 (0.7%) and 24 (8.7%), respectively, whereas the at-risk children identified using the continuous MetS score in each group totalled 2 (0.85%), 17 (11.6%) and 167 (56.6%), respectively. Conclusions: The association of the continuous MetS score with specific risk biomarkers of inflammation, endothelial damage and CVD supports its use in the early identification of children at increased risk of metabolic dysfunction. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:72 / 79
页数:8
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