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身材矮小:世界卫生组织与国家身高生长标准/参考值的比较

Short Stature: Comparison of WHO and National Growth Standards/References for Height.

作者信息

Christesen Henrik Thybo, Pedersen Birgitte Tønnes, Pournara Effie, Petit Isabelle Oliver, Júlíusson Pétur Benedikt

机构信息

Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.

Epidemiology, Novo Nordisk A/S, Søborg, Denmark.

出版信息

PLoS One. 2016 Jun 9;11(6):e0157277. doi: 10.1371/journal.pone.0157277. eCollection 2016.

Abstract

The use of appropriate growth standards/references is of significant clinical importance in assessing the height of children with short stature as it may determine eligibility for appropriate therapy. The aim of this study was to determine the impact of using World Health Organization (WHO) instead of national growth standards/references on height assessment in short children. Data were collected from routine clinical practice (1998-2014) from nine European countries that have available national growth references and were enrolled in NordiNet® International Outcome Study (IOS) (NCT00960128), a large-scale, non-interventional, multinational study. The patient cohort consisted of 5996 short pediatric patients diagnosed with growth hormone deficiency (GHD), Turner syndrome (TS) or born small for gestational age (SGA). The proportions of children with baseline height standard deviation score (SDS) below clinical cut-off values (-2 SDS for GHD and TS; -2.5 SDS for SGA) based on national growth references and WHO growth standards/references were compared for children aged <5 years and children aged ≥5 years. In seven of the countries evaluated, significantly fewer children aged ≥5 years with GHD (22%; P<0.0001), TS (21%; P<0.0001) or born SGA (32%; P<0.0001) had height below clinical cut-off values using WHO growth references vs. national references. Likewise, among children aged <5 years in the pooled analysis of the same seven countries, a significantly lower proportion of children with GHD (8%; P<0.0001), TS (12%; P = 0.0003) or born SGA (12%; P<0.0001) had height below clinical cut-off values using WHO growth standards vs. national references. In conclusion, in NordiNet® IOS the number of patients misclassified using WHO growth standards/references was significantly higher than with national references. This study highlights that, although no growth reference has 100% sensitivity for identifying growth disorders, the most recent national or regional growth charts may offer the most appropriate tool for monitoring childhood growth in Europe.

摘要

在评估身材矮小儿童的身高时,使用适当的生长标准/参考值具有重要的临床意义,因为这可能决定是否适合接受适当的治疗。本研究的目的是确定使用世界卫生组织(WHO)生长标准而非国家生长标准/参考值对矮小儿童身高评估的影响。数据收集自九个拥有国家生长参考值且参与了NordiNet®国际结局研究(IOS)(NCT00960128)的欧洲国家的常规临床实践(1998 - 2014年),这是一项大规模、非干预性的跨国研究。患者队列包括5996名被诊断为生长激素缺乏症(GHD)、特纳综合征(TS)或小于胎龄儿(SGA)的矮小儿科患者。比较了基于国家生长参考值和WHO生长标准/参考值,年龄<5岁和年龄≥5岁儿童中基线身高标准差评分(SDS)低于临床临界值(GHD和TS为 - 2 SDS;SGA为 - 2.5 SDS)的儿童比例。在七个评估国家中,使用WHO生长参考值时,年龄≥5岁的GHD患儿(22%;P<0.0001)、TS患儿(21%;P<0.0001)或SGA出生患儿(32%;P<0.0001)身高低于临床临界值的人数明显少于使用国家参考值时。同样,在这七个国家的汇总分析中,年龄<5岁的儿童中,使用WHO生长标准时,GHD患儿(8%;P<0.0001)、TS患儿(12%;P = 0.0003)或SGA出生患儿(12%;P<0.0001)身高低于临床临界值的比例明显低于使用国家参考值时。总之,在NordiNet® IOS中,使用WHO生长标准/参考值误分类的患者数量明显高于使用国家参考值。本研究强调,尽管没有生长参考值对识别生长障碍具有100%的敏感性,但最新的国家或地区生长图表可能为监测欧洲儿童生长提供最合适的工具。

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