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小于胎龄儿:身材矮小及其他情况。

Small for gestational age: short stature and beyond.

作者信息

Saenger Paul, Czernichow Paul, Hughes Ieuan, Reiter Edward O

机构信息

Department of Pediatrics, Albert Einstein College of Medicine, Bronx, New York 10467, USA.

出版信息

Endocr Rev. 2007 Apr;28(2):219-51. doi: 10.1210/er.2006-0039. Epub 2007 Feb 23.

Abstract

Depending on the definitions used, up to 10% of all live-born neonates are small for gestational age (SGA). Although the vast majority of these children show catch-up growth by 2 yr of age, one in 10 does not. It is increasingly recognized that those who are born SGA are at risk of developing metabolic disease later in life. Reduced fetal growth has been shown to be associated with an increased risk of insulin resistance, obesity, cardiovascular disease, and type 2 diabetes mellitus. The majority of pathology is seen in adults who show spontaneous catch-up growth as children. There is evidence to suggest that some of the metabolic consequences of intrauterine growth retardation in children born SGA can be mitigated by ensuring early appropriate catch-up growth, while avoiding excessive weight gain. Implicitly, this argument questions current infant formula feeding practices. The risk is less clear for individuals who do not show catch-up growth and who are treated with GH for short stature. Recent data, however, suggest that long-term treatment with GH does not increase the risk of type 2 diabetes mellitus and the metabolic syndrome in young adults born SGA.

摘要

根据所采用的定义,高达10%的活产新生儿为小于胎龄儿(SGA)。尽管这些儿童中的绝大多数在2岁时会出现追赶生长,但十分之一的儿童不会。人们越来越认识到,出生时为SGA的儿童在生命后期有患代谢性疾病的风险。胎儿生长受限已被证明与胰岛素抵抗、肥胖、心血管疾病和2型糖尿病的风险增加有关。大多数病理情况出现在儿童期有自发追赶生长的成年人中。有证据表明,对于出生时为SGA的儿童,通过确保早期适当的追赶生长,同时避免体重过度增加,可以减轻宫内生长迟缓的一些代谢后果。不言而喻,这一观点对当前的婴儿配方奶喂养做法提出了质疑。对于没有出现追赶生长且因身材矮小而接受生长激素治疗的个体,风险尚不明确。然而,最近的数据表明,对出生时为SGA的年轻成年人长期使用生长激素治疗不会增加患2型糖尿病和代谢综合征的风险。

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