生长激素缺乏症诊断的最新进展。

Georgiana Roxana Gabreanu
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引用次数: 3

摘要

生长激素缺乏症(GHD)是一种内分泌紊乱,可能是孤立的,也可能与其他垂体激素缺乏症有关。在儿童中,身材矮小是GHD的一个有用的临床标志。相比之下,成人的症状并不总是那么明显,现有的检测方法可能是不准确和不精确的,特别是在缺乏暗示性临床特征的情况下。由于被诊断为GHD的患者的生活质量也可能受到显著影响,无论是儿童还是成人,因此正确准确的诊断对于选择那些可以从GH治疗中受益的患者非常重要。一般来说,内分泌疾病在诊断方面具有挑战性,简单测量激素基础水平不足以区分生理和病理状况。传统上,临床专业指南考虑了几种刺激试验,如胰岛素耐量试验(ITT)、ghrh -精氨酸刺激试验和胰高血糖素刺激试验,它们都有各自的优点和局限性。最近(2017年12月),FDA批准了一种生长激素分泌素受体激动剂macimorelin用于成人GHD的诊断。马西莫瑞林的明显优势是口服给药简单,对于器质性疾病和胰岛素样生长因子(IGF-I)水平低的患者,与胰岛素耐量试验高度一致。然而,对于儿童人群和极度肥胖或病态肥胖的成年人,安全性和诊断价值尚未确定。此外,应避免马西莫瑞林与延长QT间期的药物和CYP3A4诱导剂同时使用。基因筛查显然可以对GHD的病理有很好的了解。然而,将其纳入GHD患者的常规评估是否也具有成本效益仍然是一个悬而未决的问题。虽然在这一领域取得了重大进展,但基因检测仍然难以获得,主要原因是其费用高昂,特别是在低收入和中等收入国家。
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An update on the diagnosis of growth hormone deficiency.

Growth hormone deficiency (GHD) is an endocrine disorder, which may be either isolated or associated with other pituitary hormone deficiencies. In children, short stature is a useful clinical marker for GHD. In contrast, symptomatology is not always so obvious in adults, and the existing methods of testing might be inaccurate and imprecise, especially in the lack of a suggestive clinical profile. Since the quality of life of patients diagnosed with GHD could also be significantly affected, in both children and adults, a correct and accurate diagnosis is therefore tremendously important to select those patients that can benefit from the GH treatment. In general, the endocrine diseases are challenging in terms of diagnosis, the simple measurement of the basal level of hormones is not sufficient for distinguishing between the physiological and pathological conditions. Traditionally, several stimulation tests have been considered by professional clinical guidelines, such as insulin tolerance test (ITT), GHRH-arginine stimulation test and the glucagon stimulation test, and all of them have both advantages and limitations. More recently (December 2017), FDA approved a growth hormone secretagogue receptor agonist, macimorelin, for the diagnosis of adults with GHD. The obvious advantage for macimorelin is the simple oral administration and the high level of agreement with the insulin tolerance test for those patients with organic disease and low levels of insulin-like growth factor (IGF-I). However, the safety profile and the diagnostic value was not yet established for the pediatric population and for those adults with extreme or morbid obesity. In addition, administration of macimorelin with drugs that prolong QT interval and CYP3A4 inducers should be avoided. Genetic screening could obviously bring a great insight in the GHD pathology. However, it remains an open question if it would be also cost effective to include it in the routine evaluation of the patients with GHD. Although major progresses have been made in this area, genetic testing continues to be difficult to access, mostly because of its high costs, especially in the low-income and middle-income countries.

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