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本文引用的文献

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A self-report measure of pubertal status: Reliability, validity, and initial norms.一种青春期发育状况的自我报告测量方法:信度、效度和初步常模。
J Youth Adolesc. 1988 Apr;17(2):117-33. doi: 10.1007/BF01537962.
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Gender-related differences in muscle injury, oxidative stress, and apoptosis.肌肉损伤、氧化应激和细胞凋亡中的性别差异。
Med Sci Sports Exerc. 2008 Oct;40(10):1772-80. doi: 10.1249/MSS.0b013e31817d1cce.
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Oxidative stress markers, C-reactive protein and heat shock protein 70 levels in subjects with metabolic syndrome.代谢综合征患者的氧化应激标志物、C反应蛋白和热休克蛋白70水平
Clin Chem Lab Med. 2008;46(6):785-90. doi: 10.1515/CCLM.2008.166.
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Human biochemistry of the isoprostane pathway.异前列腺素途径的人体生物化学
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Insulin resistance and oxidative stress in familial combined hyperlipidemia.家族性混合性高脂血症中的胰岛素抵抗与氧化应激
Atherosclerosis. 2008 Aug;199(2):384-9. doi: 10.1016/j.atherosclerosis.2007.11.023. Epub 2007 Dec 31.
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Expert committee recommendations regarding the prevention, assessment, and treatment of child and adolescent overweight and obesity: summary report.专家委员会关于儿童及青少年超重与肥胖的预防、评估和治疗的建议:总结报告
Pediatrics. 2007 Dec;120 Suppl 4:S164-92. doi: 10.1542/peds.2007-2329C.
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Oxidative stress and adverse adipokine profile characterize the metabolic syndrome in children.氧化应激和不良脂肪因子谱是儿童代谢综合征的特征。
J Cardiometab Syndr. 2006 Summer;1(4):248-52. doi: 10.1111/j.1559-4564.2006.05758.x.
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Cellular immunity and inflammatory mediator responses to intense exercise in overweight children and adolescents.超重儿童和青少年对剧烈运动的细胞免疫和炎症介质反应。
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Quantification of F2-isoprostanes as a biomarker of oxidative stress.F2-异前列腺素作为氧化应激生物标志物的定量分析。
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肥胖儿童氧化应激增加及底物代谢改变。

Increased oxidative stress and altered substrate metabolism in obese children.

作者信息

Oliver Stacy R, Rosa Jaime S, Milne Ginger L, Pontello Andria M, Borntrager Holly L, Heydari Shirin, Galassetti Pietro R

机构信息

Department of Pharmacology, School of Medicine, University of California, Irvine, CA 92697, USA.

出版信息

Int J Pediatr Obes. 2010 Oct;5(5):436-44. doi: 10.3109/17477160903545163.

DOI:10.3109/17477160903545163
PMID:20233149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3110748/
Abstract

OBJECTIVE

Pediatric obesity, a major risk factor for cardiovascular diseases and diabetes, has steadily increased in the last decades. Although excessive inflammation and oxidation are possible biochemical links between obesity and cardiovascular events in adults, little information is available in children. Furthermore, effects of gender and fitness on the interaction between dyslipidemia and oxidative/inflammatory stress in children are mostly unknown.

METHODS

Therefore, we measured systemic markers of oxidation (F(2)-isoprostanes [F(2)-IsoP] and antioxidants) and inflammation (interleukin-6 [IL-6] and leukocyte counts) and metabolic variables in 113 peripubertal children (55 obese [Ob] age and gender-adjusted BMI% ≥ 95(th), 25 Females [F]; 15 overweight [OW] BMI% 85(th)-95(th), 8 F; 43 normoweight [NW] 25 F).

RESULTS

When compared with NW, Ob displayed elevated F(2)-IsoP (99 ± 7 vs. 75 ± 4 pg/mL, p<0.005), IL-6 (2.2 ± 0.2 vs. 1.5 ± 0.3 pg/mL, p<0.005), elevated total leukocytes and neutrophils, altered levels of total cholesterol , low- and high-density-lipoprotein cholesterol, triglycerides, free fatty acids, glucose, and insulin (all p<0.005). This pattern was present in both genders and over a broad range of fitness in Ob.

CONCLUSIONS

Our data indicate that alterations in metabolic control and a concomitant increase in inflammation and oxidative stress occur early in life in obese children, likely exposing both genders to a similar degree of increased risk of future cardiovascular diseases.

摘要

目的

儿童肥胖是心血管疾病和糖尿病的主要危险因素,在过去几十年中呈稳步上升趋势。尽管过度炎症和氧化可能是成人肥胖与心血管事件之间的生化联系,但关于儿童的相关信息却很少。此外,性别和健康状况对儿童血脂异常与氧化/炎症应激之间相互作用的影响大多未知。

方法

因此,我们测量了113名青春期前儿童(55名肥胖[Ob],年龄和性别调整后的BMI%≥95(百分位数),25名女性[F];15名超重[OW],BMI%为85(百分位数)-95(百分位数),8名F;43名正常体重[NW],25名F)的氧化系统标志物(F(2)-异前列腺素[F(2)-IsoP]和抗氧化剂)、炎症标志物(白细胞介素-6[IL-6]和白细胞计数)以及代谢变量。

结果

与NW相比,Ob的F(2)-IsoP升高(99±7对75±4 pg/mL,p<0.005),IL-6升高(2.2±0.2对1.5±0.3 pg/mL,p<0.005),总白细胞和中性粒细胞升高,总胆固醇、低密度和高密度脂蛋白胆固醇、甘油三酯、游离脂肪酸、葡萄糖和胰岛素水平改变(均p<0.005)。这种模式在Ob的男女两性以及广泛的健康状况范围内均存在。

结论

我们的数据表明,肥胖儿童在生命早期就出现代谢控制改变以及炎症和氧化应激随之增加,这可能使两性面临未来心血管疾病风险增加的相似程度。