胰高血糖素受体拮抗剂评价胰外胰高血糖素在全胰切除个体中的生理作用:一项随机对照试验。

IF 10.2 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Caroline Trunk-Black Juel,Asger B Lund,Sofie Hædersdal,Maria M Andersen,Carsten P Hansen,Jan H Storkholm,Gerrit van Hall,Bolette Hartmann,Mette M Rosenkilde,Camilla J Kibsgaard,Flemming Dela,Nicolai J Wewer Albrechtsen,Jens J Holst,Tina Vilsbøll,Filip K Knop
{"title":"胰高血糖素受体拮抗剂评价胰外胰高血糖素在全胰切除个体中的生理作用:一项随机对照试验。","authors":"Caroline Trunk-Black Juel,Asger B Lund,Sofie Hædersdal,Maria M Andersen,Carsten P Hansen,Jan H Storkholm,Gerrit van Hall,Bolette Hartmann,Mette M Rosenkilde,Camilla J Kibsgaard,Flemming Dela,Nicolai J Wewer Albrechtsen,Jens J Holst,Tina Vilsbøll,Filip K Knop","doi":"10.1007/s00125-025-06534-z","DOIUrl":null,"url":null,"abstract":"AIMS/HYPOTHESIS\r\nPrevious studies have indicated that 29-amino-acid glucagon (i.e. 'pancreatic' glucagon) circulates in totally pancreatectomised individuals and that a postprandial glucagon response can be detected. Using a glucagon receptor antagonist (GRA), we investigated the possible role of extrapancreatic glucagon on glucose, lipid and amino acid metabolism in totally pancreatectomised individuals.\r\n\r\nMETHOD\r\nIn a randomised, crossover study, nine totally pancreatectomised individuals and nine matched healthy control individuals were given, in randomised order (planned on the website www.random.org ), 300 mg GRA (LY2409021; Eli Lilly) or placebo 10 h before two 3 h OGTTs. The experiment was double-masked (i.e. both participants and investigator were masked for the type of the experimental day [day A vs day B]). The key inclusion criteria for the healthy control participants were age >18 years, normal fasting plasma glucose and HbA1c 31-44 mmol/mol (6.0-7.2%), haemoglobin >7.0 mmol/l (men) / >6.5 mmol/l (women) and informed consent. Key inclusion criteria for the pancreatectomised individuals were age >18 years, haemoglobin in the normal range and informed consent. The primary endpoint was the difference in plasma glucose excursions between study days.\r\n\r\nRESULTS\r\nGlucagon concentrations remained unchanged from fasting concentrations during the OGTT in the totally pancreatectomised individuals on both study days and circulating glucose, lipids and amino acid levels were unaffected by treatment with LY2409021 compared with placebo. In the control group, LY2409021 resulted in relevant pharmacodynamic effects, including lower fasting plasma glucose (4.7 [0.1] vs 5.2 [0.1] mmol/l, p=0.001) and augmented concentrations of amino acids in plasma, compared with placebo.\r\n\r\nCONCLUSIONS/INTERPRETATION\r\nWe conclude that inhibition of the glucagon receptor using LY2409021 during OGTT in totally pancreatectomised individuals does not produce detectable effects on glucose, lipid or amino acid metabolism, ruling out metabolic effects of extrapancreatic glucagon.\r\n\r\nTRIAL REGISTRATION\r\nClinicalTrials.gov (NCT02944110).\r\n\r\nFUNDING\r\nThis study was supported by grants from the Aase and Ejnar Danielsen's Foundation and the Novo Nordisk Foundation.","PeriodicalId":11164,"journal":{"name":"Diabetologia","volume":"2 1","pages":""},"PeriodicalIF":10.2000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Using glucagon receptor antagonism to evaluate the physiological effects of extrapancreatic glucagon in totally pancreatectomised individuals: a randomised controlled trial.\",\"authors\":\"Caroline Trunk-Black Juel,Asger B Lund,Sofie Hædersdal,Maria M Andersen,Carsten P Hansen,Jan H Storkholm,Gerrit van Hall,Bolette Hartmann,Mette M Rosenkilde,Camilla J Kibsgaard,Flemming Dela,Nicolai J Wewer Albrechtsen,Jens J Holst,Tina Vilsbøll,Filip K Knop\",\"doi\":\"10.1007/s00125-025-06534-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AIMS/HYPOTHESIS\\r\\nPrevious studies have indicated that 29-amino-acid glucagon (i.e. 'pancreatic' glucagon) circulates in totally pancreatectomised individuals and that a postprandial glucagon response can be detected. Using a glucagon receptor antagonist (GRA), we investigated the possible role of extrapancreatic glucagon on glucose, lipid and amino acid metabolism in totally pancreatectomised individuals.\\r\\n\\r\\nMETHOD\\r\\nIn a randomised, crossover study, nine totally pancreatectomised individuals and nine matched healthy control individuals were given, in randomised order (planned on the website www.random.org ), 300 mg GRA (LY2409021; Eli Lilly) or placebo 10 h before two 3 h OGTTs. The experiment was double-masked (i.e. both participants and investigator were masked for the type of the experimental day [day A vs day B]). The key inclusion criteria for the healthy control participants were age >18 years, normal fasting plasma glucose and HbA1c 31-44 mmol/mol (6.0-7.2%), haemoglobin >7.0 mmol/l (men) / >6.5 mmol/l (women) and informed consent. Key inclusion criteria for the pancreatectomised individuals were age >18 years, haemoglobin in the normal range and informed consent. The primary endpoint was the difference in plasma glucose excursions between study days.\\r\\n\\r\\nRESULTS\\r\\nGlucagon concentrations remained unchanged from fasting concentrations during the OGTT in the totally pancreatectomised individuals on both study days and circulating glucose, lipids and amino acid levels were unaffected by treatment with LY2409021 compared with placebo. In the control group, LY2409021 resulted in relevant pharmacodynamic effects, including lower fasting plasma glucose (4.7 [0.1] vs 5.2 [0.1] mmol/l, p=0.001) and augmented concentrations of amino acids in plasma, compared with placebo.\\r\\n\\r\\nCONCLUSIONS/INTERPRETATION\\r\\nWe conclude that inhibition of the glucagon receptor using LY2409021 during OGTT in totally pancreatectomised individuals does not produce detectable effects on glucose, lipid or amino acid metabolism, ruling out metabolic effects of extrapancreatic glucagon.\\r\\n\\r\\nTRIAL REGISTRATION\\r\\nClinicalTrials.gov (NCT02944110).\\r\\n\\r\\nFUNDING\\r\\nThis study was supported by grants from the Aase and Ejnar Danielsen's Foundation and the Novo Nordisk Foundation.\",\"PeriodicalId\":11164,\"journal\":{\"name\":\"Diabetologia\",\"volume\":\"2 1\",\"pages\":\"\"},\"PeriodicalIF\":10.2000,\"publicationDate\":\"2025-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diabetologia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00125-025-06534-z\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diabetologia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00125-025-06534-z","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

摘要

目的/假设先前的研究表明29-氨基酸型胰高血糖素(即;胰高血糖素在完全切除胰腺的个体中循环,并且可以检测到餐后胰高血糖素反应。使用胰高血糖素受体拮抗剂(GRA),我们研究了胰外胰高血糖素对全胰切除个体的葡萄糖、脂质和氨基酸代谢的可能作用。方法在一项随机交叉研究中,9名完全胰腺切除的个体和9名匹配的健康对照者,在2次3小时ogtt治疗前10小时,按随机顺序(网站www.random.org计划)给予300 mg GRA (LY2409021; Eli Lilly)或安慰剂。实验是双掩码的(即参与者和研究者都被掩码为实验日的类型[A日与B日])。健康对照参与者的主要纳入标准为年龄>8岁,空腹血糖和HbA1c 31-44 mmol/mol(6.0-7.2%)正常,血红蛋白>7.0 mmol/l(男性)/ >6.5 mmol/l(女性)和知情同意。胰腺切除术患者的主要纳入标准是年龄在18岁至18岁之间,血红蛋白在正常范围内,知情同意。主要终点是研究期间血浆葡萄糖漂移的差异。结果在研究期间,胰高血糖素浓度与OGTT期间的空腹浓度保持不变,LY2409021治疗与安慰剂相比,循环葡萄糖、脂质和氨基酸水平未受影响。在对照组中,LY2409021产生了相关的药效学效应,包括与安慰剂相比,空腹血糖降低(4.7 [0.1]vs 5.2 [0.1] mmol/l, p=0.001),血浆氨基酸浓度增加。结论/解释:我们得出结论,在全胰切除个体的OGTT期间,使用LY2409021抑制胰高血糖素受体不会对葡萄糖、脂质或氨基酸代谢产生可检测到的影响,从而排除了胰外胰高血糖素的代谢影响。临床试验注册(NCT02944110)。本研究得到了Aase和Ejnar Danielsen基金会以及诺和诺德基金会的资助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using glucagon receptor antagonism to evaluate the physiological effects of extrapancreatic glucagon in totally pancreatectomised individuals: a randomised controlled trial.
AIMS/HYPOTHESIS Previous studies have indicated that 29-amino-acid glucagon (i.e. 'pancreatic' glucagon) circulates in totally pancreatectomised individuals and that a postprandial glucagon response can be detected. Using a glucagon receptor antagonist (GRA), we investigated the possible role of extrapancreatic glucagon on glucose, lipid and amino acid metabolism in totally pancreatectomised individuals. METHOD In a randomised, crossover study, nine totally pancreatectomised individuals and nine matched healthy control individuals were given, in randomised order (planned on the website www.random.org ), 300 mg GRA (LY2409021; Eli Lilly) or placebo 10 h before two 3 h OGTTs. The experiment was double-masked (i.e. both participants and investigator were masked for the type of the experimental day [day A vs day B]). The key inclusion criteria for the healthy control participants were age >18 years, normal fasting plasma glucose and HbA1c 31-44 mmol/mol (6.0-7.2%), haemoglobin >7.0 mmol/l (men) / >6.5 mmol/l (women) and informed consent. Key inclusion criteria for the pancreatectomised individuals were age >18 years, haemoglobin in the normal range and informed consent. The primary endpoint was the difference in plasma glucose excursions between study days. RESULTS Glucagon concentrations remained unchanged from fasting concentrations during the OGTT in the totally pancreatectomised individuals on both study days and circulating glucose, lipids and amino acid levels were unaffected by treatment with LY2409021 compared with placebo. In the control group, LY2409021 resulted in relevant pharmacodynamic effects, including lower fasting plasma glucose (4.7 [0.1] vs 5.2 [0.1] mmol/l, p=0.001) and augmented concentrations of amino acids in plasma, compared with placebo. CONCLUSIONS/INTERPRETATION We conclude that inhibition of the glucagon receptor using LY2409021 during OGTT in totally pancreatectomised individuals does not produce detectable effects on glucose, lipid or amino acid metabolism, ruling out metabolic effects of extrapancreatic glucagon. TRIAL REGISTRATION ClinicalTrials.gov (NCT02944110). FUNDING This study was supported by grants from the Aase and Ejnar Danielsen's Foundation and the Novo Nordisk Foundation.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Diabetologia
Diabetologia 医学-内分泌学与代谢
CiteScore
18.10
自引率
2.40%
发文量
193
审稿时长
1 months
期刊介绍: Diabetologia, the authoritative journal dedicated to diabetes research, holds high visibility through society membership, libraries, and social media. As the official journal of the European Association for the Study of Diabetes, it is ranked in the top quartile of the 2019 JCR Impact Factors in the Endocrinology & Metabolism category. The journal boasts dedicated and expert editorial teams committed to supporting authors throughout the peer review process.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信