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本文引用的文献

1
The IDF Diabetes Atlas: providing evidence, raising awareness and promoting action.国际糖尿病联盟糖尿病地图集:提供证据、提高认识并促进行动。
Diabetes Res Clin Pract. 2010 Jan;87(1):2-3. doi: 10.1016/j.diabres.2009.11.006. Epub 2009 Dec 4.
2
Size at birth, weight gain in infancy and childhood, and adult blood pressure in 5 low- and middle-income-country cohorts: when does weight gain matter?5个低收入和中等收入国家队列中的出生体重、婴幼儿及儿童期体重增加与成人血压:体重增加在何时起重要作用?
Am J Clin Nutr. 2009 May;89(5):1383-92. doi: 10.3945/ajcn.2008.27139. Epub 2009 Mar 18.
3
Life course weight gain and C-reactive protein levels in young adults: findings from a Brazilian birth cohort.年轻成年人的生命历程体重增加与C反应蛋白水平:来自巴西出生队列的研究结果
Am J Hum Biol. 2009 Mar-Apr;21(2):192-9. doi: 10.1002/ajhb.20852.
4
Intrauterine growth restriction and adult disease: the role of adipocytokines.宫内生长受限与成人疾病:脂肪细胞因子的作用
Eur J Endocrinol. 2009 Mar;160(3):337-47. doi: 10.1530/EJE-08-0621. Epub 2008 Dec 18.
5
Adult metabolic syndrome and impaired glucose tolerance are associated with different patterns of BMI gain during infancy: Data from the New Delhi Birth Cohort.成人代谢综合征和糖耐量受损与婴儿期不同的体重指数增长模式相关:来自新德里出生队列的数据。
Diabetes Care. 2008 Dec;31(12):2349-56. doi: 10.2337/dc08-0911. Epub 2008 Oct 3.
6
C-reactive protein and coronary heart disease: a critical review.C反应蛋白与冠心病:批判性综述
J Intern Med. 2008 Oct;264(4):295-314. doi: 10.1111/j.1365-2796.2008.02015.x.
7
Low birth weight and markers of inflammation and endothelial activation in adulthood: the ARIC study.低出生体重与成年期炎症和内皮细胞活化标志物:ARIC 研究。
Int J Cardiol. 2009 May 29;134(3):371-7. doi: 10.1016/j.ijcard.2008.02.024. Epub 2008 Jun 27.
8
Early life growth and hemostatic factors: the Barry Caerphilly Growth study.早期生命成长与止血因素:巴里卡菲利成长研究
Am J Epidemiol. 2008 Jul 15;168(2):179-87. doi: 10.1093/aje/kwn106. Epub 2008 May 20.
9
Size at birth, weight gain over the life course, and low-grade inflammation in young adulthood: northern Finland 1966 Birth Cohort study.出生时的体型、一生的体重增加情况以及青年期的低度炎症:芬兰北部1966年出生队列研究
Eur Heart J. 2008 Apr;29(8):1049-56. doi: 10.1093/eurheartj/ehn105. Epub 2008 Apr 9.
10
Is birth weight a risk factor for ischemic heart disease in later life?出生体重是日后患缺血性心脏病的风险因素吗?
Am J Clin Nutr. 2007 May;85(5):1244-50. doi: 10.1093/ajcn/85.5.1244.

儿童时期的体重指数与成人促炎和促血栓形成的风险因素:来自新德里出生队列的研究数据。

Childhood body mass index and adult pro-inflammatory and pro-thrombotic risk factors: data from the New Delhi birth cohort.

机构信息

Department of Cardiac Biochemistry, Department of Endocrinology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Int J Epidemiol. 2011 Feb;40(1):102-11. doi: 10.1093/ije/dyq121. Epub 2010 Jul 26.

DOI:10.1093/ije/dyq121
PMID:20660641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428891/
Abstract

OBJECTIVE

Weight gain and growth in early life may influence adult pro-inflammatory and pro-thrombotic cardiovascular risk factors.

METHODS

Follow-up of a birth cohort in New Delhi, India, whose weight and height were measured every 6 months until age 21 years. Body mass index (BMI) at birth, during infancy (2 years), childhood (11 years) and adulthood (26-32 years) and BMI gain between these ages were analysed in 886 men and 640 women with respect to adult fibrinogen, high-sensitivity C-reactive protein (hsCRP) and plasminogen activator inhibitor-1 (PAI-1) concentrations.

RESULTS

All the pro-inflammatory/pro-thrombotic risk factors were higher in participants with higher adiposity. In women, BMI at birth and age 2 years was inversely related to fibrinogen (P = 0.002 and 0.05) and, after adjusting for adult adiposity, to hsCRP (P = 0.02 and 0.009). After adjusting for adult adiposity, BMI at 2 years was inversely related to hsCRP and PAI-1 concentrations (P < 0.001 and 0.02) in men. BMI gain between 2 and 11 years and/or 11 years to adulthood was positively associated with fibrinogen and hsCRP in women and with hsCRP and PAI-1 in men.

CONCLUSIONS

Thinness at birth or during infancy, and accelerated BMI gain during childhood/adolescence are associated with a pro-inflammatory/pro-thrombotic state in adult life. An altered inflammatory state could be one link between small newborn/infant size and adult cardiovascular disease. Associations between pro-inflammatory markers and childhood/adolescent BMI gain are probably mediated through adult adiposity.

摘要

目的

生命早期的体重增加和生长可能会影响成年后的促炎和促血栓形成的心血管危险因素。

方法

对印度新德里的一个出生队列进行随访,在 21 岁之前每 6 个月测量一次体重和身高。分析了 886 名男性和 640 名女性的出生时、婴儿期(2 岁)、儿童期(11 岁)和成年期(26-32 岁)的体重指数(BMI)以及这些年龄段之间的 BMI 增长与成年时纤维蛋白原、高敏 C 反应蛋白(hsCRP)和纤溶酶原激活物抑制剂-1(PAI-1)浓度的关系。

结果

所有促炎/促血栓形成的危险因素在肥胖程度较高的参与者中更高。在女性中,出生时和 2 岁时的 BMI 与纤维蛋白原呈负相关(P=0.002 和 0.05),并且在调整成年肥胖后与 hsCRP 呈负相关(P=0.02 和 0.009)。在调整成年肥胖后,2 岁时的 BMI 与 hsCRP 和 PAI-1 浓度呈负相关(P<0.001 和 0.02)在男性中。2 岁至 11 岁之间和/或 11 岁至成年期间的 BMI 增长与女性的纤维蛋白原和 hsCRP 以及男性的 hsCRP 和 PAI-1 呈正相关。

结论

出生时或婴儿期的消瘦,以及儿童期/青春期 BMI 的快速增长,与成年后的促炎/促血栓形成状态有关。改变的炎症状态可能是新生儿/婴儿期体型较小和成年心血管疾病之间的一个联系。促炎标志物与儿童/青少年 BMI 增长之间的关联可能是通过成年肥胖来介导的。