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极低出生体重儿的生长和身体成分。

Growth and body composition in very young SGA children.

机构信息

Department of Endocrinology, Hospital Infantil Universitario Nino Jesús, 28009 Madrid, Spain.

出版信息

Pediatr Nephrol. 2010 Apr;25(4):679-85. doi: 10.1007/s00467-009-1432-2. Epub 2010 Jan 27.

Abstract

Infants with a very low birth weight are at risk of a reduced number of nephrons predisposing to kidney disorder, hypertension, and metabolic syndrome. Approximately 3% of infants are born small for gestational age (SGA), defined as birth weight and/or length at least 2 SD below the mean for gestational age (GA), independently of whether these children are born prematurely or at term. About 10% of these children do not show postnatal catch-up growth and remain of short stature during childhood. Most of these infants are not growth hormone (GH)-deficient, but may have GH resistance. Although GH-resistant, the majority of patients benefit from GH therapy, normalize height during childhood, maintain a normal growth velocity during puberty, and attain a normal adult height. To date, GH has been shown to be safe and no significant adverse effects have been demonstrated. Children with congenital chronic kidney disease (CKD) are born with subnormal birth weight and length and about 25% are born SGA. Shortness and need for GH treatment is highly correlated with weight at birth and gestational age. Primary renal disorders modify the response to GH treatment. Analysis of whether SGA is an additional risk factor for CKD regarding the development of hypertension, metabolic syndrome and cardiovascular complications is required.

摘要

极低出生体重儿的肾脏单位数量较少,易发生肾脏疾病、高血压和代谢综合征。大约 3%的婴儿为小于胎龄儿(SGA),定义为出生体重和/或身长至少低于胎龄(GA)的平均值 2 个标准差,无论这些儿童是早产还是足月出生。这些儿童中约有 10%的儿童在出生后没有追赶性生长,在儿童期仍身材矮小。这些婴儿大多不是生长激素(GH)缺乏症,但可能存在 GH 抵抗。尽管存在 GH 抵抗,但大多数患者受益于 GH 治疗,可在儿童期使身高正常化,在青春期维持正常生长速度,并达到正常成人身高。迄今为止,GH 已被证明是安全的,没有显示出显著的不良反应。患有先天性慢性肾脏疾病(CKD)的儿童出生时体重和身长低于正常水平,约 25%为 SGA。矮小和需要 GH 治疗与出生体重和胎龄高度相关。原发性肾脏疾病会影响 GH 治疗的反应。需要分析 SGA 是否是 CKD 发展为高血压、代谢综合征和心血管并发症的另一个危险因素。

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