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胰岛素耐量试验期间出现生化性低血糖是否必要?

Is biochemical hypoglycemia necessary during an insulin tolerance test?

作者信息

Simsek Yasin, Karaca Zuleyha, Diri Halit, Tanriverdi Fatih, Unluhizarci Kursad, Kelestemur Fahrettin

机构信息

Department of Endocrinology, Medical School, Erciyes University, Kayseri, Turkey.

出版信息

Arch Endocrinol Metab. 2020 Feb;64(1):82-88. doi: 10.20945/2359-3997000000200. Epub 2020 Mar 13.

DOI:10.20945/2359-3997000000200
PMID:32187262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10522286/
Abstract

Objective The insulin tolerance test (ITT) has been accepted as the gold standard test for assessing the integrity of the growth hormone (GH) - insulin-like growth factor (IGF-1) axis and the hypothalamic-pituitary-adrenal (HPA) axis. The goal of the test is to achieve clinical and biochemical hypoglycemia at a blood glucose level ≤ 40 mg/dL to effectively and correctly assess the HPA and GH-IGF-1 axes. In this study, the GH and cortisol responses of patients who achieved and failed to achieve biochemical hypoglycemia during an ITT were compared. Subjects and methods One hundred thirty-five patients with pituitary disorders were included in the study. Samples for blood glucose levels were obtained after clear symptoms of clinical hypoglycemia developed. The patients were enrolled in the hypoglycemic and nonhypoglycemic groups according to whether their plasma glucose level ≤ 40 mg/dL or > 40 mg/dL during an ITT, and the groups were compared in terms of their GH and cortisol responses. Results The mean age, body mass index and waist circumference of the two patient groups were found to be similar. The mean blood glucose level was significantly lower in the hypoglycemic group than in the nonhypoglycemic group (19.3 and 52.0 mg/dL, respectively). When the two groups were compared in terms of peak cortisol and GH responses, no statistically significant differences were found. Conclusion The data presented suggest that clinically symptomatic hypoglycemia is as effective as biochemically confirmed hypoglycemia during an ITT. Arch Endocrinol Metab. 2020;64(1):82-8.

摘要

目的 胰岛素耐量试验(ITT)已被公认为评估生长激素(GH)-胰岛素样生长因子(IGF-1)轴及下丘脑-垂体-肾上腺(HPA)轴完整性的金标准试验。该试验的目的是在血糖水平≤40mg/dL时实现临床和生化性低血糖,以有效且正确地评估HPA轴和GH-IGF-1轴。在本研究中,比较了ITT期间实现和未实现生化性低血糖的患者的GH和皮质醇反应。

受试者与方法 本研究纳入了135例垂体疾病患者。在出现明确的临床低血糖症状后采集血糖水平样本。根据ITT期间血浆葡萄糖水平≤40mg/dL或>40mg/dL,将患者分为低血糖组和非低血糖组,并比较两组的GH和皮质醇反应。

结果 发现两组患者的平均年龄、体重指数和腰围相似。低血糖组的平均血糖水平显著低于非低血糖组(分别为19.3和52.0mg/dL)。比较两组的皮质醇峰值和GH反应时,未发现统计学上的显著差异。

结论 所呈现的数据表明,在ITT期间,临床症状性低血糖与生化确诊的低血糖一样有效。《内分泌与代谢档案》。2020;64(1):82-8。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/c405964c307a/2359-4292-aem-64-01-0082-gf02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/0e2798f8bc41/2359-4292-aem-64-01-0082-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/0634f30b86ef/2359-4292-aem-64-01-0082-gf03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/c405964c307a/2359-4292-aem-64-01-0082-gf02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/0e2798f8bc41/2359-4292-aem-64-01-0082-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/0634f30b86ef/2359-4292-aem-64-01-0082-gf03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ea/10522286/c405964c307a/2359-4292-aem-64-01-0082-gf02.jpg

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