4.4 Article

Oxidative stress and nitric oxide are increased in obese children and correlate with cardiometabolic risk and renal function

期刊

BRITISH JOURNAL OF NUTRITION
卷 116, 期 5, 页码 805-815

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114516002804

关键词

Paediatric obesity; Oxidative stress; Nitric oxide; Risk factors; Glomerular filtration rate

资金

  1. Fundo Europeu de Desenvolvimento Regional (FEDER) funds from Programa Operacional Factores de Competitividade - COMPETE [FCOMP-01-0124-FEDER-028751]
  2. Portuguese Foundation for Science and Technology (FCT), Lisbon, Portugal [PTDC/DTP-PIC/0239/2012]
  3. Calouste Gulbenkian Foundation
  4. FCT [SFRH/SINTD/95898/2013]
  5. Programa Operacional Potencial Humano (POPH)/Fundo Social Europeu (FSE) (EC) [SFRH/BPD/112005]
  6. European Renal Association - European Dialysis and Transplant Association Research Programme, Parma, Italy
  7. KfH Foundation for Preventive Medicine, Neu-Isenburg, Germany
  8. COMPETE
  9. POPH/FSE (EC)
  10. European Renal Association
  11. KfH Foundation for Preventive Medicine
  12. Fundação para a Ciência e a Tecnologia [PTDC/DTP-PIC/0239/2012] Funding Source: FCT

向作者/读者索取更多资源

Oxidative stress and nitric oxide (NO) appear to represent important links between obesity and cardiovascular, metabolic and/or renal disease. We investigated whether oxidative stress and NO production/metabolism are increased in overweight and obese prepubertal children and correlate with cardiometabolic risk and renal function. We performed a cross-sectional evaluation of 313 children aged 8-9 years. Anthropometrics, 24-h ambulatory blood pressure, pulse wave velocity (PWV), insulin resistance (homoeostasis model assessment index (HOMA-IR)), inflammatory/metabolic biomarkers, estimated glomerular filtration rate (eGFR), plasma total antioxidant status (TAS), plasma and urinary isoprostanes (P-Isop, U-Isop), urinary hydrogen peroxide (U-H2O2), and plasma and urinary nitrates and nitrites (P-NOx, U-NOx) were compared among normal weight, overweight and obese groups, according to WHO BMI z-score reference. U-Isop were increased in the obese group, whereas U-NOx were increased in both overweight and obese children. U-Isop were positively correlated with U-H2O2, myeloperoxidase (MPO), high-sensitivity C-reactive protein, HOMA-IR and TAG. TAS correlated negatively with U-Isop and MPO and positively with PWV. HOMA-IR and U-H2O2 were associated with higher U-Isop, independently of BMI and eGFR, and total cholesterol and U-H2O2 were associated with U-NOx, independently of BMI, eGFR values and P-NOx concentration. In overweight and obese children, eGFR decreased across P-NOx tertiles (median: 1393 (25th, 75th percentile 1280, 1465), 1280 (25th, 75th percentile 1215, 1404), 1295 (25th, 75th percentile 1194, 1383), P-for linear trend=0003). We conclude that oxidant status and NO are increased in relation to fat accumulation and, even in young children, they translate into higher values of cardiometabolic risk markers and affect renal function.

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