Department of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.
Horm Res Paediatr. 2011;75(3):213-9. doi: 10.1159/000321192. Epub 2011 Feb 10.
BACKGROUND/AIMS: Studies on the association between head circumference (HC) and height or weight have shown variable results.
Using data from the Dutch nationwide survey performed in 1997 (n = 14,500), we calculated correlations for different ages, and fitted a regression model for the estimation of HC. HC versus height charts were created for different age groups. Data from children from other ethnic groups and children with various growth disorders were plotted on the charts and compared with reference data.
Correlations between HC and height or weight showed similar patterns: highest at birth, followed by a rapid decline to a stable level and a peak in adolescence. On charts containing the regression line ±2 standard deviations for subjects aged 0-2 months and 2 months to 21 years, Turkish and Moroccan children, as well as children with idiopathic short stature and small for gestational age, had a normal HC for height, whereas children with an insulin-like growth factor 1 receptor defect or Sotos syndrome showed trends towards a smaller or larger HC for height, respectively.
HC correlates strongly with height and weight. The charts of HC for height may serve as an additional tool to interpret HC in short or tall children.
背景/目的:关于头围(HC)与身高或体重之间关系的研究结果各异。
我们使用了 1997 年进行的荷兰全国性调查的数据(n=14500),计算了不同年龄的相关系数,并拟合了一个回归模型来估计 HC。为不同年龄组创建了 HC 与身高的图表。将来自其他族裔的儿童和患有各种生长障碍的儿童的数据标绘在图表上,并与参考数据进行比较。
HC 与身高或体重之间的相关性呈现出相似的模式:出生时最高,随后迅速下降至稳定水平,青春期达到峰值。在包含 0-2 个月和 2 个月至 21 岁受试者的回归线±2 标准差的图表中,土耳其和摩洛哥儿童以及特发性身材矮小和小于胎龄儿的 HC 与身高相匹配,而胰岛素样生长因子 1 受体缺陷或 Sotos 综合征的儿童的 HC 与身高呈偏小或偏大的趋势。
HC 与身高和体重密切相关。HC 与身高的图表可以作为解释矮或高个子儿童 HC 的附加工具。