Dipartimento Pediatrico Universitario Ospedaliero Bambino Gesù Children's Hospital - Tor Vergata University, Rome, Italy.
Baystate Children's Hosptal, University of Massachusetts Medical School-Baystate, Springfield, Massachusetts, USA.
Horm Res Paediatr. 2019;92(2):71-83. doi: 10.1159/000502901. Epub 2019 Oct 2.
Idiopathic short stature (ISS) comprises a wide range of conditions associated with short stature that elude the conventional diagnostic work-up and are often caused by still largely unknown genetic variants. In the last decade, the improvement of diagnostic techniques has led to the discovery of causal mutations in genes involved in the function of the growth hormone (GH)/insulin-like growth factor-I (IGF-I) axis as well as in growth plate physiology. However, many cases of ISS remain idiopathic. In the future, the more frequent identification of the underlying causes will allow a better stratification of subjects and offer a tailored management. GH therapy has been proposed and approved in some countries for the treatment of children with ISS. To improve the efficacy of GH therapy, trials with GH combined with GnRH agonists, aromatase inhibitors, and even IGF-I have been conducted. This review aims to revise the current definition of ISS and discuss the management of children with ISS on the basis of the most recent evidence.
特发性身材矮小症(ISS)是一组由多种与身材矮小相关的病症组成的病症,这些病症逃避了常规的诊断工作,并且通常是由尚未完全了解的遗传变异引起的。在过去的十年中,诊断技术的改进导致了在涉及生长激素(GH)/胰岛素样生长因子-I(IGF-I)轴功能和生长板生理学的基因中发现了因果突变。然而,许多 ISS 病例仍然是特发性的。在未来,更频繁地识别潜在病因将允许更好地对受试者进行分层,并提供针对性的管理。在一些国家,GH 治疗已被提议并批准用于治疗 ISS 儿童。为了提高 GH 治疗的疗效,已经进行了 GH 与 GnRH 激动剂、芳香酶抑制剂甚至 IGF-I 联合治疗的试验。本综述旨在根据最新证据修订 ISS 的当前定义,并讨论 ISS 儿童的管理。