TY - JOUR
T1 - Elevated visfatin levels in overweight and obese children and adolescents with metabolic syndrome
AU - Kolsgaard, Magnhild L.
AU - Wangensteen, Teresia
AU - Brunborg, Cathrine
AU - Joner, Geir
AU - Holven, Kirsten B.
AU - Halvorsen, Bente
AU - Aukrust, Pål
AU - Tonstad, Serena
N1 - Funding Information:
The study was supported by grants from the Norwegian Foundation for Health and Rehabilitation, The Norwegian Women’s Public Health Association, Ullevaal University Hospital Scientific Advisory Committee, the South-Eastern Norway Regional Health Authority, The Norwegian Ministry of health and care services and the Norwegian Directorate of Health. We gratefully thank the patients and their families, and the rest of the ‘Oslo Adiposity Intervention Study’ team.
PY - 2009/8
Y1 - 2009/8
N2 - Objective: Adipokines have been implicated in the pathogenesis of metabolic syndrome (MetS) and insulin resistance. We investigated the association between these conditions and serum levels of visfatin, adiponectin and leptin. Material and methods: 175 overweight and obese boys and girls aged 317 years. MetS was defined as presence of at least three of the following: triglycerides ≥ 1.24 mmol/L, high-density lipoprotein cholesterol ≤ 1.03 mmol/L, fasting glucose ≥ 6.1 mmol/L, elevated waist circumference and systolic or diastolic blood pressure ≥ 90th percentile. Results: After adjustment for age and gender visfatin levels were significantly higher (median 19.0 [25th, 75th percentiles 11.9 , 37.1] vs. 15.2 [11.6 , 21.1] ng/ml; padjusted0.02) in subjects with MetS (n = 41) compared to subjects without (n =134). There were no significant differences in adiponectin or leptin levels between the two groups after adjustment for age and gender. Visfatin levels increased proportionally with number of MetS components (β 0.16, 95%CI 0.04, 0.28; p adjusted 0.01), and adiponectin levels decreased proportionally with number of components (β = -0.11, 95%CI -0.18, -0.04; padjusted = 0.002). Leptin levels were not related to number of components of MetS. Unlike visfatin, both adiponectin (β = -0.24, 95%CI -0.33, -0.15; p adjusted < 0.001) and leptin (β 0.14, 95%CI 0.01, 0.28; padjusted = 0.03) were associated with insulin resistance. Conclusion: The elevation of visfatin observed in children and adolescents with MetS was proportionate to number of components of MetS but was not associated with insulin resistance. The increase in visfatin may contribute to low-grade systemic inflammation associated with MetS. © 2009 Informa UK Ltd.
AB - Objective: Adipokines have been implicated in the pathogenesis of metabolic syndrome (MetS) and insulin resistance. We investigated the association between these conditions and serum levels of visfatin, adiponectin and leptin. Material and methods: 175 overweight and obese boys and girls aged 317 years. MetS was defined as presence of at least three of the following: triglycerides ≥ 1.24 mmol/L, high-density lipoprotein cholesterol ≤ 1.03 mmol/L, fasting glucose ≥ 6.1 mmol/L, elevated waist circumference and systolic or diastolic blood pressure ≥ 90th percentile. Results: After adjustment for age and gender visfatin levels were significantly higher (median 19.0 [25th, 75th percentiles 11.9 , 37.1] vs. 15.2 [11.6 , 21.1] ng/ml; padjusted0.02) in subjects with MetS (n = 41) compared to subjects without (n =134). There were no significant differences in adiponectin or leptin levels between the two groups after adjustment for age and gender. Visfatin levels increased proportionally with number of MetS components (β 0.16, 95%CI 0.04, 0.28; p adjusted 0.01), and adiponectin levels decreased proportionally with number of components (β = -0.11, 95%CI -0.18, -0.04; padjusted = 0.002). Leptin levels were not related to number of components of MetS. Unlike visfatin, both adiponectin (β = -0.24, 95%CI -0.33, -0.15; p adjusted < 0.001) and leptin (β 0.14, 95%CI 0.01, 0.28; padjusted = 0.03) were associated with insulin resistance. Conclusion: The elevation of visfatin observed in children and adolescents with MetS was proportionate to number of components of MetS but was not associated with insulin resistance. The increase in visfatin may contribute to low-grade systemic inflammation associated with MetS. © 2009 Informa UK Ltd.
KW - Adipokines
KW - Inflammation
KW - Insulin resistance
KW - Pediatrics
KW - Adiponectin/blood
KW - Leptin/blood
KW - Nicotinamide Phosphoribosyltransferase/blood
KW - Humans
KW - Insulin/blood
KW - Insulin Resistance
KW - Child, Preschool
KW - Male
KW - Metabolic Syndrome/blood
KW - Adolescent
KW - Obesity/blood
KW - Female
KW - Child
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UR - https://www.mendeley.com/catalogue/eb0ee0bd-396d-3ffb-b98f-2a546ba5461e/
U2 - 10.3109/00365510903348677
DO - 10.3109/00365510903348677
M3 - Article
C2 - 19929281
SN - 0036-5513
VL - 69
SP - 858
EP - 864
JO - Scandinavian Journal of Clinical and Laboratory Investigation
JF - Scandinavian Journal of Clinical and Laboratory Investigation
IS - 8
ER -