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一种新的矮小症诊断方法。

A new approach to the diagnosis of short stature.

机构信息

Department of Pediatric Endocrinology, National Children's Hospital, San José, Costa Rica.

Department of Pediatric Endocrinology, University of Virginia, Charlottesville, VA, USA -

出版信息

Minerva Pediatr. 2020 Aug;72(4):250-262. doi: 10.23736/S0026-4946.20.05835-1.

DOI:10.23736/S0026-4946.20.05835-1
PMID:33045802
Abstract

Growth is the task of children. We review the normal process of linear growth from the fetus through adolescence and note that growth is the result of age- and gender-dependent interactions among key genetic, environmental, dietary, socioeconomic, developmental, behavioral, nutritional, metabolic, biochemical, and hormonal factors. We then define the wide range of normative data at each stage of growth and note that a pattern within this range is generally indicative of good general health and that growth significantly slower than this range may lead to growth faltering and subsequent short stature. Although not often emphasized, we detail how to properly measure infants and children because height velocity is usually determined from two height measurements (both relatively large values) to calculate the actual height velocity (a relatively much smaller number in comparison). Traditionally the physiology of growth has been taught from an endocrine-centric point-of-view. Here we review the hypothalamic-pituitary-end organ axes for the GH/IGF-1 and gonadal steroid hormones (hypothalamic-pituitary-gonadal axis), both during "mini"-puberty as well as at puberty. However, over the past few decades much more emphasis has been placed on the growth plate and its many interactions with the endocrine system but also with its own intrinsic physiology and gene mutations. These latter, whether individually (large effect size) or in combination with many others including endocrine system-based, may account in toto for meaningful differences in adult height. The clinical assessment of children with short stature includes medical, social and family history, physical exam and importantly proper interpretation of the growth curve. This analysis should lead to judicious use of screening laboratory and imaging tests depending on the pre-test probability (Bayesian inference) of a particular diagnosis in that child. In particular for those with no pathological features in the history and physical exam and a low, but normal height velocity, may lead only to a bone age exam and reevaluation (re-measurement), perhaps 6 months later. he next step depends on the comfort level of the primary care physician, the patient, and the parent; that is, whether to continue with the evaluation with more directed, more sophisticated testing, again based on Bayesian inference or to seek consultation with a subspecialist pediatrician based on the data obtained. This is not necessarily an endocrinologist. The newest area and the one most in flux is the role for genetic testing, given that growth is a complex process with large effect size for single genes but smaller effect sizes for multiple other genes which in the aggregate may be relevant to attained adult height. Genetics is a discipline that is rapidly changing, especially as the cost of exome or whole gene sequencing diminishes sharply. Within a decade it is quite likely that a genetic approach to the evaluation of children with short stature will become the standard, truncating the diagnostic odyssey and be cost effective as fewer biochemical and imaging studies are required to make a proper diagnosis.

摘要

生长是儿童的任务。我们回顾了胎儿到青春期线性生长的正常过程,并指出生长是年龄和性别依赖性的关键遗传、环境、饮食、社会经济、发育、行为、营养、代谢、生化和激素因素相互作用的结果。然后,我们定义了每个生长阶段的广泛规范数据,并指出该范围内的模式通常表明身体健康状况良好,而生长速度明显慢于该范围可能导致生长迟缓,并随后导致身材矮小。尽管这一点并不常被强调,但我们详细说明了如何正确测量婴儿和儿童,因为身高速度通常是通过两次身高测量(都是相对较大的值)来计算实际身高速度(相比之下是一个相对较小的数字)。传统上,生长的生理学是从内分泌中心的角度来教授的。在这里,我们回顾了 GH/IGF-1 和性腺类固醇激素(下丘脑-垂体-性腺轴)的下丘脑-垂体-终末器官轴,包括“迷你”青春期和青春期。然而,在过去几十年中,人们更加关注生长板及其与内分泌系统的许多相互作用,但也关注其自身的内在生理学和基因突变。这些后者,无论是单独的(大效应量)还是与许多其他因素(包括内分泌系统为基础的因素)结合在一起,都可能导致成年身高的显著差异。身材矮小儿童的临床评估包括医学、社会和家庭史、体格检查,重要的是要正确解释生长曲线。这种分析应该根据该儿童特定诊断的预测试概率(贝叶斯推理),明智地使用筛选实验室和影像学检查。特别是对于那些在病史和体检中没有病理特征,且身高速度较低但正常的儿童,可能仅需要进行骨龄检查和重新评估(重新测量),可能在 6 个月后。下一步取决于初级保健医生、患者和家长的舒适度;也就是说,是继续进行更有针对性、更复杂的测试,再次基于贝叶斯推理,还是根据所获得的数据咨询儿科专家。这不一定是内分泌学家。最新的领域也是最不稳定的领域是基因检测的作用,因为生长是一个复杂的过程,单个基因的效应量较大,但其他多个基因的效应量较小,这些基因加在一起可能与成年身高有关。遗传学是一个发展迅速的学科,尤其是随着外显子或全基因测序成本的急剧下降。在十年内,很可能通过基因方法来评估身材矮小的儿童将成为标准,缩短诊断的探索过程,并具有成本效益,因为需要更少的生化和影像学研究来做出正确的诊断。

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