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口服葡萄糖负荷试验前给予二肽基肽酶-4 抑制剂可使肢端肥大症患者的生长激素水平升高。

Acromegaly Cases Exhibiting Increased Growth Hormone Levels during Oral Glucose Loading with Preadministration of Dipeptidyl Peptidase-4 Inhibitor.

机构信息

Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Japan.

Division of Diabetes and Obesity, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Japan.

出版信息

Intern Med. 2021;60(15):2375-2383. doi: 10.2169/internalmedicine.4755-20. Epub 2021 Aug 1.

DOI:10.2169/internalmedicine.4755-20
PMID:34334589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8381171/
Abstract

Objective Glucose-dependent insulinotropic polypeptide (GIP) is speculated to worsen growth hormone (GH) hypersecretion in acromegaly and to be a cause of paradoxical increases in GH (PI-GH) during 75-g oral glucose tolerance testing (75-g OGTT). Dipeptidyl peptidase-4 inhibitors (DPP4is), which increase the circulating concentration of active GIP, are frequently administered to diabetic patients, including those with acromegaly. We aimed to determine whether or not the administration of a DPP4i increases GH concentration, especially in patients demonstrating PI-GH during a DPP4i-OGTT, in which a DPP4i was administered immediately before 75-g OGTT. Methods This prospective cross-sectional study was carried out on acromegalic patients admitted to Hokkaido University hospital between June 2011 and May 2018. The participants underwent both 75-g OGTT and DPP4i-OGTT. For those who underwent surgery, immunohistochemical staining and quantitative polymerase chain reaction (PCR) for the GIP receptor (GIPR) were performed on the resected pituitary adenomas. Results Twenty-five percent of the participants had PI-GH confirmed (3 of 12 cases). Two of the three participants who demonstrated PI-GH exhibited higher circulating GH concentrations during DPP4i-OGTT than during OGTT. The increase in plasma glucose was reduced during DPP4i-OGTT compared to during 75-g OGTT, suggesting that the increase in GH during DPP4i-OGTT was due not to high glucose concentrations but instead increased GIP caused by the administration of DPP4i. The adenoma from one participant with PI-GH displayed positive immunostaining for GIPR and a higher GIPR messenger ribonucleic acid (mRNA) expression than the others. Conclusion DPP4i may enhance the GH secretion response during glucose loading, especially in individuals with PI-GH.

摘要

目的

葡萄糖依赖性胰岛素释放多肽(GIP)被推测会加重肢端肥大症中的生长激素(GH)过度分泌,并且是 75g 口服葡萄糖耐量试验(75g OGTT)期间 GH(PI-GH)反常增加的原因之一。二肽基肽酶-4 抑制剂(DPP4i)会增加循环中活性 GIP 的浓度,常被用于治疗糖尿病患者,包括肢端肥大症患者。我们旨在确定 DPP4i 的给药是否会增加 GH 浓度,特别是在 DPP4i-OGTT 期间表现出 PI-GH 的患者中,即在 75g OGTT 之前立即给予 DPP4i。

方法

这项前瞻性的病例对照研究于 2011 年 6 月至 2018 年 5 月在北海道大学医院收治的肢端肥大症患者中进行。参与者接受了 75g OGTT 和 DPP4i-OGTT。对于接受手术的患者,对切除的垂体腺瘤进行 GIP 受体(GIPR)的免疫组织化学染色和定量聚合酶链反应(PCR)。

结果

25%的参与者(3 例中的 12 例)被证实存在 PI-GH。在表现出 PI-GH 的 3 名参与者中,有 2 名在 DPP4i-OGTT 期间的循环 GH 浓度高于 OGTT。与 75g OGTT 相比,DPP4i-OGTT 期间的血糖升高减少,这表明 DPP4i-OGTT 期间 GH 的增加不是由于高血糖浓度,而是由于 DPP4i 的给药导致 GIP 增加。一名 PI-GH 患者的腺瘤对 GIPR 显示出阳性免疫染色,并且与其他患者相比,GIPR 信使 RNA(mRNA)表达更高。

结论

DPP4i 可能会增强葡萄糖负荷期间的 GH 分泌反应,特别是在存在 PI-GH 的个体中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/6205d85e6a0c/1349-7235-60-2375-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/09f8480a9ae1/1349-7235-60-2375-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/85b93bb0a165/1349-7235-60-2375-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/fdebc3033a2b/1349-7235-60-2375-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/6205d85e6a0c/1349-7235-60-2375-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/09f8480a9ae1/1349-7235-60-2375-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/85b93bb0a165/1349-7235-60-2375-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/fdebc3033a2b/1349-7235-60-2375-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f328/8381171/6205d85e6a0c/1349-7235-60-2375-g004.jpg

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Neuroendocrinology. 2019;108(3):244-255. doi: 10.1159/000497214. Epub 2019 Jan 25.
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Front Endocrinol (Lausanne). 2023 Sep 28;14:1248985. doi: 10.3389/fendo.2023.1248985. eCollection 2023.
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Hypermethylator Phenotype and Ectopic GIP Receptor in GNAS Mutation-Negative Somatotropinomas.GNAS 基因突变阴性生长激素瘤中的高甲基化表型和异位 GIP 受体。
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