头围高度指数(HCH-I)量化儿童相对大头畸形和帮助识别软骨发育不良。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Moira S Cheung, Ruggero Lanzafame, Karen J Low, Tim J Cole
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引用次数: 0

摘要

软骨发育不良(HCH)是一种罕见的骨骼发育不良,由FGFR3基因的致病性变异引起。我们假设HCH的头围和身高的相对不比例可能是诊断信息,并产生一个简单的头身高不比例指数来帮助儿科医生诊断HCH。头围身高指数(HCH-I),基于正式的统计原理,被定义为身高z - 1/2头围z -得分,这里的z -得分基于UK90生长参考。hch - 1低于-2的临界值表明头部高度严重失调。我们通过比较诊断为HCH的儿童(n = 364)和剑桥婴儿生长研究(CIGS)的儿童(n = 4620)来验证该指数,这些儿童使用了最近欧洲HCH生长图表的数据。HCH组的平均(SD) HCH- i为-3.0(1.2),而CIGS组的平均(SD) HCH- i为-0.2(0.9)。HCH- 1低于-2正确识别出78%的HCH- 1儿童,而只有2.4%的CIGS儿童低于临界值。HCH- 1低于-2的儿童头高比例失调,可能患有HCH或其他遗传疾病。该指数故意简单计算,并应证明在临床实践中有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Head Circumference Height Index (HCH-I) to Quantify Relative Macrocephaly and Aid Identification of Hypochondroplasia in Children.

Hypochondroplasia (HCH) is a rare skeletal dysplasia caused by pathogenic variants in the FGFR3 gene. We hypothesized that the relative disproportion between head circumference and height in HCH might be diagnostically informative and generated a simple index of head-stature disproportion to help pediatricians diagnose HCH. The Head Circumference Height Index (HCH-I), based on formal statistical principles, is defined as height Z-score - 1/2 head circumference Z-score, with the Z-scores based here on the UK90 growth reference. An HCH-I below the cut-off of -2 indicates substantial head-height disproportion. We validated the index by comparing children diagnosed with HCH (n = 364), using data from the recent European HCH growth charts, to children from the Cambridge Infant Growth Study (CIGS) (n = 4620). The mean (SD) HCH-I was -3.0 (1.2) in the HCH cohort, compared to -0.2 (0.9) in the CIGS cohort. An HCH-I below -2 correctly identified 78% of children with HCH, while only 2.4% of CIGS children fell below the cut-off. An HCH-I below -2 identifies children with head-height disproportion who may have HCH or another genetic disorder. The index is deliberately simple to calculate and should prove useful in clinical practice.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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