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鉴定生长激素缺乏症患者接受低剂量生长激素替代治疗的新生物标志物。

Identification of new biomarkers of low-dose GH replacement therapy in GH-deficient patients.

机构信息

Edison Biotechnology Institute, Ohio University, College of Osteopathic Medicine, Athens, Ohio 45701, USA.

出版信息

J Clin Endocrinol Metab. 2011 Jul;96(7):2089-97. doi: 10.1210/jc.2011-0197. Epub 2011 May 4.

Abstract

CONTEXT

GH secretion peaks at puberty and continues to be secreted in adulthood, albeit at a declining rate. Profound GH deficiency (GHD) in adults with pituitary disease is associated with symptoms that improve with GH substitution, but it is important to tailor the GH dose to avoid overtreatment. Measurement of serum IGF-I levels is an important clinical tool in this regard, but it is well recognized that some patients receiving GH treatment do not show an increase in IGF-I.

OBJECTIVE

The objective of the study was to identify novel serum biomarkers of GH treatment in adults with GHD.

DESIGN AND PATIENTS

Eight patients with profound GHD as a consequence of a pituitary adenoma or its treatment were evaluated before and 3 months after GH replacement therapy (0.2-0.4 mg/d).

MAIN OUTCOME MEASURES

Serum proteomic changes were studied using two-dimensional gel electrophoresis and mass spectrometry. Protein profiles were analyzed and compared in serum samples obtained before and after GH treatment.

RESULTS

The levels of six serum protein spots were significantly altered after GH substitution. These proteins were identified as five isoforms of haptoglobin (decreased in posttreatment samples) and one isoform of apolipoprotein A-I (increased in posttreatment samples). Importantly, changes in the levels of the identified proteins were associated with decreases in fat mass and increases in lean mass in all patients. These results were independent of serum IGF-I levels.

CONCLUSIONS

Evaluation of the identified proteins provides a novel alternative to traditional markers of GH status, such as serum IGF-I levels, to assess GH therapy in GH deficient adults.

摘要

背景

生长激素(GH)在青春期达到峰值,并在成年后继续分泌,尽管分泌速率逐渐降低。患有垂体疾病的成年人中,严重的 GH 缺乏症(GHD)与改善 GH 替代治疗相关的症状有关,但重要的是要调整 GH 剂量以避免过度治疗。测量血清 IGF-I 水平是这方面的重要临床工具,但众所周知,一些接受 GH 治疗的患者 IGF-I 水平没有增加。

目的

本研究的目的是确定成人 GHD 患者接受 GH 治疗后的新型血清生物标志物。

设计和患者

评估了 8 例因垂体腺瘤或其治疗而导致严重 GHD 的患者在接受 GH 替代治疗(0.2-0.4mg/d)前后 3 个月的情况。

主要观察指标

使用二维凝胶电泳和质谱法研究血清蛋白质组学变化。分析和比较 GH 治疗前后获得的血清样本中的蛋白质谱。

结果

GH 替代治疗后,6 种血清蛋白斑点的水平显著改变。这些蛋白质被鉴定为结合珠蛋白的 5 种同工型(治疗后样本中减少)和载脂蛋白 A-I 的 1 种同工型(治疗后样本中增加)。重要的是,鉴定出的蛋白质水平变化与所有患者的脂肪量减少和瘦体重增加相关。这些结果与血清 IGF-I 水平无关。

结论

评估鉴定出的蛋白质提供了一种替代传统 GH 状态标志物(如血清 IGF-I 水平)的新方法,可用于评估 GH 缺乏的成年患者的 GH 治疗。

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