Antidiabetic Medication-Induced Acute Interstitial Nephritis: Case Report and Literature Search

IF 0.4 Q4 ENDOCRINOLOGY & METABOLISM
Nadia Chaudhury, Alexandros-Leonidas D Liarakos, K. Gopalakrishnan, W. Ayub, N. Murthy, R. Rao
{"title":"Antidiabetic Medication-Induced Acute Interstitial Nephritis: Case Report and Literature Search","authors":"Nadia Chaudhury, Alexandros-Leonidas D Liarakos, K. Gopalakrishnan, W. Ayub, N. Murthy, R. Rao","doi":"10.15277/bjd.2021.321","DOIUrl":null,"url":null,"abstract":"Introduction Liraglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist, is a recognised treatment for type 2 diabetes mellitus (T2DM). It mimics human GLP-1 and works by augmenting insulin secretion, inhibiting glucagon secretion and inhibiting gastric acid secretion.1 It has been shown to not only improve glycaemic control in people with diabetes, but also result in weight loss, reduced hypoglycaemic episodes, reduced albuminuria, reduced progression to macroalbuminuria and reduced incidence of myocardial infarction and stroke events.2–5 Gastrointestinal upset is the commonest reported side effect, which occurs in up to 56% of patients in clinical trials. Furthermore, BNF recommends avoiding liraglutide treatment in end-stage renal disease/estimated glomerular filtration rate (eGFR) <15 mL/min/1.73 m2 (depending on brand), due to the increased risk of adverse events. We present a rare case of a female with chronic kidney disease (CKD), whose treatment with liraglutide was associated with rapid deterioration of renal function and tubulointerstitial nephritis. Our literature search highlighted one previous case, thus we would like to raise awareness of this potential rare side effect of liraglutide treatment.6 We have further conducted a literature search of all case reports noting associations of glucose-lowering therapies with acute interstitial nephritis to raise awareness of this potential complication.","PeriodicalId":42951,"journal":{"name":"British Journal of Diabetes","volume":null,"pages":null},"PeriodicalIF":0.4000,"publicationDate":"2021-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"British Journal of Diabetes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15277/bjd.2021.321","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 3

Abstract

Introduction Liraglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist, is a recognised treatment for type 2 diabetes mellitus (T2DM). It mimics human GLP-1 and works by augmenting insulin secretion, inhibiting glucagon secretion and inhibiting gastric acid secretion.1 It has been shown to not only improve glycaemic control in people with diabetes, but also result in weight loss, reduced hypoglycaemic episodes, reduced albuminuria, reduced progression to macroalbuminuria and reduced incidence of myocardial infarction and stroke events.2–5 Gastrointestinal upset is the commonest reported side effect, which occurs in up to 56% of patients in clinical trials. Furthermore, BNF recommends avoiding liraglutide treatment in end-stage renal disease/estimated glomerular filtration rate (eGFR) <15 mL/min/1.73 m2 (depending on brand), due to the increased risk of adverse events. We present a rare case of a female with chronic kidney disease (CKD), whose treatment with liraglutide was associated with rapid deterioration of renal function and tubulointerstitial nephritis. Our literature search highlighted one previous case, thus we would like to raise awareness of this potential rare side effect of liraglutide treatment.6 We have further conducted a literature search of all case reports noting associations of glucose-lowering therapies with acute interstitial nephritis to raise awareness of this potential complication.
抗糖尿病药物诱导的急性间质性肾炎病例报告及文献检索
引言利拉鲁肽是一种胰高血糖素样肽-1(GLP-1)受体激动剂,是公认的2型糖尿病(T2DM)的治疗方法。它模仿人类GLP-1,通过增加胰岛素分泌、抑制胰高血糖素分泌和抑制胃酸分泌发挥作用。1研究表明,它不仅能改善糖尿病患者的血糖控制,还能减轻体重、减少低血糖发作、减少蛋白尿,减少大蛋白尿的进展,降低心肌梗死和中风事件的发生率。2-5胃肠道不适是最常见的副作用,在临床试验中,高达56%的患者会出现这种副作用。此外,BNF建议在终末期肾病/估计肾小球滤过率(eGFR)<15 mL/min/1.73 m2(取决于品牌)时避免利拉鲁肽治疗,因为不良事件的风险增加。我们报告了一例罕见的女性慢性肾脏病(CKD)患者,其利拉鲁肽治疗与肾功能快速恶化和肾小管间质性肾炎有关。我们的文献检索强调了以前的一个病例,因此我们希望提高对利拉鲁肽治疗这种潜在罕见副作用的认识。6我们进一步对所有病例报告进行了文献检索,注意到降糖治疗与急性间质性肾炎的关联,以提高对这种潜在并发症的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
British Journal of Diabetes
British Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
16.70%
发文量
15
×
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:481959085
Book学术官方微信