利拉鲁tid和胰岛素抵抗1例

Stefan Farsky
{"title":"利拉鲁tid和胰岛素抵抗1例","authors":"Stefan Farsky","doi":"10.18103/mra.v11i10.4614","DOIUrl":null,"url":null,"abstract":"Weight reduction in patients with cardiovascular (CV) diseases and concurrent overweight or obesity brings a fundamental improvement in health and prognosis of such diseases, a proven reduction in mortality and morbidity, and is associated with a reduction in pharmacotherapy and the number of hospitalizations, therefore, it is also economically effective. With the current growing trend in population, obesity also becomes a population risk factor that is more significant than smoking, and a leading cause of preventable diseases. From this point of view, the availability of a new effective anti-obesity medication is very welcome, in particular, liraglutide elegantly interferes with the physiological mechanisms regulating food intake. In addition, it reduces the risk of developing diabetes and has anti- atherogenic effects. At the obese diabetic 2 type patients on insulin treatment often resistance develops and in spite of high insuline dosage inadequate control of glucose and HbA1c levels are obvious. We present the extreme case on this topic down: May 2013: first examination dated in our database of cardiology care dept. for out patients, 65 years old man, weight 144 kg, height 178 cm, waist circumferrence 143cm. His history: arterial hypertension since 1993, diabetes 2 type since 2008 on peroral treatment, paroxysmal atrial fibrilation since March 2013, diameter of the left atrium 50mm on ECHO, invasive coronarography negat. Therapy: telmisartan, metoprolol, nitrendipin, warfarin, propafenon, digoxin, spironolacton, statin. November 2013: effect of therapeutic lifestyle changes: regular sinus rhythm, weight 133kg, waist circumferrence 134cm, spironolacton substituted by eplerenon (asymetric gynecomastia), digoxin ex May 2014: weight 126kg, September 2014: atrial fibrilation, propafenon substituted by flekainid, then atrial flutter, switch from flekainid to amiodaron and digoxin, warfarin substituted by apixaban February 2015: sinus rhythm , weight 129kg December 2015: weight 140kg, BP 170/90 mmHg, atrial flutter with a-v blockage 4:1, ankle oedema on both sides, Hb 115g/l, urinary acid 499umol/l, creatinin 119 umol/l, added allopurinol, urapidil, furosemid May 2017: intensification of the diabetes treatment, added insulin application, dosage escalation during the next years, on ECHO: left atriium diameter 52mm, left ventricle diameter 62mm, systolic function of the left ventricle preserved, moderate mitral and tricuspidal regurgitation December 2017: sinus bradycardia 46/min, amiodaron and digoxin ex, sick sinus syndrom brady-tachycardia form, hepatomegaly July 2018: bariatric procedure contraindicated by surgeon because of age and health status December 2018: creatinin 169umol/l, urinary acid 652umol/l October 2019: weight 158 kg, hospitalisation for heart failúre, confirmed by increased NT- BNP level, therapeutic changes from sartan to ARNI, from warfarin to apixaban, increased furosemid dosage. February 2021: weight 159kg, O2 peripheral saturation 93%, start of partial fasting (8:16) May 2021: signifficant dyspnoe, NYHA III, ECHO: left atrium diameter 56mm, left ventricle diameter 70mm, EF of the left ventricle 0,50, E/A 0,7 March 2022: attempt to implantate permanent cardiostimulation device unsuccesfull because of anatomic venous abnormalities. Brain MRI: postischemic frontal area defect right side Creatinin 220 umol/l, kalium 5,4 mmol/l, Hb 121 g/l, diabetic nephropathy. Weight 160kg. Added iron supplement. In spite of high insulin dosage (Humalog 3x20 units and basal 2x50 units) 160 units per day the glucose level were around 20mmol/l July 2022: weight 161 kg, starting of liraglutid daily application of 0,6mg s.c., dosage escalation every week to 1,2, 2,4, 3,0 mg. October 2022: hunger feeling was signifficantly reduced, eating of smaller portions, without craving between main time schedule of eating. Weight reduced to 151kg during first 3 months of liraglutid application (cca minus 100g per day), insulin dosage was reduced to 60 units daily (Humalog ex, basal insulin reduced to 60 units) what was accompanied by signifficant glucose level reduction to around 8 mmol/l. Creatinin level was 166 umol/l, acidum uricum level was 323 umol/l. January 2023: weight 157kg, fat content 50%, water content 40%. ECHO: left ventricle diameter 60mm, EF 0,5, left atrium diameter 54mm, tricuspidal regurgitation not detected, E/A 0,7. creatinin 128 umol/l , kalium 4,5 mmol/l.","PeriodicalId":18641,"journal":{"name":"Medical Research Archives","volume":"426 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Case report Liraglutid and insuline resistance\",\"authors\":\"Stefan Farsky\",\"doi\":\"10.18103/mra.v11i10.4614\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Weight reduction in patients with cardiovascular (CV) diseases and concurrent overweight or obesity brings a fundamental improvement in health and prognosis of such diseases, a proven reduction in mortality and morbidity, and is associated with a reduction in pharmacotherapy and the number of hospitalizations, therefore, it is also economically effective. With the current growing trend in population, obesity also becomes a population risk factor that is more significant than smoking, and a leading cause of preventable diseases. From this point of view, the availability of a new effective anti-obesity medication is very welcome, in particular, liraglutide elegantly interferes with the physiological mechanisms regulating food intake. In addition, it reduces the risk of developing diabetes and has anti- atherogenic effects. At the obese diabetic 2 type patients on insulin treatment often resistance develops and in spite of high insuline dosage inadequate control of glucose and HbA1c levels are obvious. We present the extreme case on this topic down: May 2013: first examination dated in our database of cardiology care dept. for out patients, 65 years old man, weight 144 kg, height 178 cm, waist circumferrence 143cm. His history: arterial hypertension since 1993, diabetes 2 type since 2008 on peroral treatment, paroxysmal atrial fibrilation since March 2013, diameter of the left atrium 50mm on ECHO, invasive coronarography negat. Therapy: telmisartan, metoprolol, nitrendipin, warfarin, propafenon, digoxin, spironolacton, statin. November 2013: effect of therapeutic lifestyle changes: regular sinus rhythm, weight 133kg, waist circumferrence 134cm, spironolacton substituted by eplerenon (asymetric gynecomastia), digoxin ex May 2014: weight 126kg, September 2014: atrial fibrilation, propafenon substituted by flekainid, then atrial flutter, switch from flekainid to amiodaron and digoxin, warfarin substituted by apixaban February 2015: sinus rhythm , weight 129kg December 2015: weight 140kg, BP 170/90 mmHg, atrial flutter with a-v blockage 4:1, ankle oedema on both sides, Hb 115g/l, urinary acid 499umol/l, creatinin 119 umol/l, added allopurinol, urapidil, furosemid May 2017: intensification of the diabetes treatment, added insulin application, dosage escalation during the next years, on ECHO: left atriium diameter 52mm, left ventricle diameter 62mm, systolic function of the left ventricle preserved, moderate mitral and tricuspidal regurgitation December 2017: sinus bradycardia 46/min, amiodaron and digoxin ex, sick sinus syndrom brady-tachycardia form, hepatomegaly July 2018: bariatric procedure contraindicated by surgeon because of age and health status December 2018: creatinin 169umol/l, urinary acid 652umol/l October 2019: weight 158 kg, hospitalisation for heart failúre, confirmed by increased NT- BNP level, therapeutic changes from sartan to ARNI, from warfarin to apixaban, increased furosemid dosage. February 2021: weight 159kg, O2 peripheral saturation 93%, start of partial fasting (8:16) May 2021: signifficant dyspnoe, NYHA III, ECHO: left atrium diameter 56mm, left ventricle diameter 70mm, EF of the left ventricle 0,50, E/A 0,7 March 2022: attempt to implantate permanent cardiostimulation device unsuccesfull because of anatomic venous abnormalities. Brain MRI: postischemic frontal area defect right side Creatinin 220 umol/l, kalium 5,4 mmol/l, Hb 121 g/l, diabetic nephropathy. Weight 160kg. Added iron supplement. In spite of high insulin dosage (Humalog 3x20 units and basal 2x50 units) 160 units per day the glucose level were around 20mmol/l July 2022: weight 161 kg, starting of liraglutid daily application of 0,6mg s.c., dosage escalation every week to 1,2, 2,4, 3,0 mg. October 2022: hunger feeling was signifficantly reduced, eating of smaller portions, without craving between main time schedule of eating. Weight reduced to 151kg during first 3 months of liraglutid application (cca minus 100g per day), insulin dosage was reduced to 60 units daily (Humalog ex, basal insulin reduced to 60 units) what was accompanied by signifficant glucose level reduction to around 8 mmol/l. Creatinin level was 166 umol/l, acidum uricum level was 323 umol/l. January 2023: weight 157kg, fat content 50%, water content 40%. ECHO: left ventricle diameter 60mm, EF 0,5, left atrium diameter 54mm, tricuspidal regurgitation not detected, E/A 0,7. creatinin 128 umol/l , kalium 4,5 mmol/l.\",\"PeriodicalId\":18641,\"journal\":{\"name\":\"Medical Research Archives\",\"volume\":\"426 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical Research Archives\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18103/mra.v11i10.4614\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Research Archives","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18103/mra.v11i10.4614","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

心血管(CV)疾病合并超重或肥胖患者的体重减轻从根本上改善了这些疾病的健康状况和预后,证实了死亡率和发病率的降低,并与药物治疗和住院次数的减少有关,因此,它在经济上也是有效的。随着目前人口的增长趋势,肥胖也成为比吸烟更重要的人口危险因素,是导致可预防疾病的主要原因。从这个角度来看,一种新的有效的抗肥胖药物的可用性是非常受欢迎的,特别是利拉鲁肽巧妙地干扰了调节食物摄入的生理机制。此外,它还能降低患糖尿病的风险,并具有抗动脉粥样硬化的作用。肥胖的2型糖尿病患者在接受胰岛素治疗时经常出现抵抗,尽管胰岛素剂量很高,但血糖和糖化血红蛋白水平的控制明显不足。我们在2013年5月提出了这个主题的极端案例:在我们的心脏病护理部门数据库中首次检查门诊患者,65岁男性,体重144公斤,身高178厘米,腰围143厘米。病史:1993年开始动脉高血压,2008年开始口服治疗2型糖尿病,2013年3月开始阵发性心房颤动,超声左心房直径50mm,有创冠状造影阴性。治疗:替米沙坦,美托洛尔,尼群地平,华法林,普罗帕南,地高辛,螺内酯,他汀类药物。2013年11月:治疗性生活方式改变效果:窦性心律正常,体重133kg,腰围134cm,安替乐酮(不对称型男性乳房发育),地高辛停用,2014年5月:体重126kg, 2014年9月:房颤,用氟来卡因替代普帕酮,然后心房扑动,由氟来卡因改用胺碘酮和地高辛,华法林替代阿哌沙班2015年2月:窦性心律,体重129kg 2015年12月:体重140kg,血压170/ 90mmhg,心房扑动合并a-v阻塞4:1,双侧踝关节水肿,Hb 115g/l,尿酸499umol/l,创造素119 umol/l,添加别嘌呤醇、乌拉地尔、速尿,2017年5月:糖尿病治疗强化,添加胰岛素应用,未来几年剂量增加,ECHO:左心房直径52mm,左心室直径62mm,左心室收缩功能保留,二尖瓣和三尖瓣中度反流2017年12月:2018年7月:由于年龄和健康状况,外科医生禁止进行减肥手术2018年12月:创造素169umol/l,尿酸652umol/l 2019年10月:体重158 kg,因心脏住院failúre,证实NT- BNP水平升高,治疗从沙坦到ARNI,从华法林到阿哌沙班,尿速减慢剂量增加。2021年2月:体重159kg,外周血氧饱和度93%,开始部分禁食(8:16)2021年5月:明显呼吸困难,NYHA III, ECHO:左心房直径56mm,左心室直径70mm,左心室EF 0.50, E/A 0.70, 2022年3月7日:由于解剖性静脉异常,尝试植入永久性心脏刺激装置失败。脑MRI:右侧脑额区缺血后缺损创素220 μ mol/l,钾5,4 mmol/l,血红蛋白121 g/l,糖尿病肾病。体重160公斤。添加铁补充剂。尽管胰岛素剂量很高(Humalog 3x20单位和basal 2x50单位),每天160单位,血糖水平约为20mmol/l, 2022年7月:体重161 kg,开始利拉鲁tid每日应用0.6 mg s.c,剂量每周增加到1,2,2,4,3,0 mg。2022年10月:饥饿感明显减少,吃得更少了,没有了想吃主食的时间安排。在利拉鲁tid应用的前3个月,体重减少到151公斤(cca每天减100克),胰岛素剂量减少到每天60单位(Humalog ex,基础胰岛素减少到60单位),同时血糖水平显著降低到8 mmol/l左右。血凝素为166 umol/l,尿酸为323 umol/l。2023年1月:体重157kg,脂肪含量50%,水分含量40%。ECHO:左心室内径60mm, EF 0.5,左心房内径54mm,未见三尖瓣反流,E/A 0.7。创造素128 mmol/l,钾4.5 mmol/l。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case report Liraglutid and insuline resistance
Weight reduction in patients with cardiovascular (CV) diseases and concurrent overweight or obesity brings a fundamental improvement in health and prognosis of such diseases, a proven reduction in mortality and morbidity, and is associated with a reduction in pharmacotherapy and the number of hospitalizations, therefore, it is also economically effective. With the current growing trend in population, obesity also becomes a population risk factor that is more significant than smoking, and a leading cause of preventable diseases. From this point of view, the availability of a new effective anti-obesity medication is very welcome, in particular, liraglutide elegantly interferes with the physiological mechanisms regulating food intake. In addition, it reduces the risk of developing diabetes and has anti- atherogenic effects. At the obese diabetic 2 type patients on insulin treatment often resistance develops and in spite of high insuline dosage inadequate control of glucose and HbA1c levels are obvious. We present the extreme case on this topic down: May 2013: first examination dated in our database of cardiology care dept. for out patients, 65 years old man, weight 144 kg, height 178 cm, waist circumferrence 143cm. His history: arterial hypertension since 1993, diabetes 2 type since 2008 on peroral treatment, paroxysmal atrial fibrilation since March 2013, diameter of the left atrium 50mm on ECHO, invasive coronarography negat. Therapy: telmisartan, metoprolol, nitrendipin, warfarin, propafenon, digoxin, spironolacton, statin. November 2013: effect of therapeutic lifestyle changes: regular sinus rhythm, weight 133kg, waist circumferrence 134cm, spironolacton substituted by eplerenon (asymetric gynecomastia), digoxin ex May 2014: weight 126kg, September 2014: atrial fibrilation, propafenon substituted by flekainid, then atrial flutter, switch from flekainid to amiodaron and digoxin, warfarin substituted by apixaban February 2015: sinus rhythm , weight 129kg December 2015: weight 140kg, BP 170/90 mmHg, atrial flutter with a-v blockage 4:1, ankle oedema on both sides, Hb 115g/l, urinary acid 499umol/l, creatinin 119 umol/l, added allopurinol, urapidil, furosemid May 2017: intensification of the diabetes treatment, added insulin application, dosage escalation during the next years, on ECHO: left atriium diameter 52mm, left ventricle diameter 62mm, systolic function of the left ventricle preserved, moderate mitral and tricuspidal regurgitation December 2017: sinus bradycardia 46/min, amiodaron and digoxin ex, sick sinus syndrom brady-tachycardia form, hepatomegaly July 2018: bariatric procedure contraindicated by surgeon because of age and health status December 2018: creatinin 169umol/l, urinary acid 652umol/l October 2019: weight 158 kg, hospitalisation for heart failúre, confirmed by increased NT- BNP level, therapeutic changes from sartan to ARNI, from warfarin to apixaban, increased furosemid dosage. February 2021: weight 159kg, O2 peripheral saturation 93%, start of partial fasting (8:16) May 2021: signifficant dyspnoe, NYHA III, ECHO: left atrium diameter 56mm, left ventricle diameter 70mm, EF of the left ventricle 0,50, E/A 0,7 March 2022: attempt to implantate permanent cardiostimulation device unsuccesfull because of anatomic venous abnormalities. Brain MRI: postischemic frontal area defect right side Creatinin 220 umol/l, kalium 5,4 mmol/l, Hb 121 g/l, diabetic nephropathy. Weight 160kg. Added iron supplement. In spite of high insulin dosage (Humalog 3x20 units and basal 2x50 units) 160 units per day the glucose level were around 20mmol/l July 2022: weight 161 kg, starting of liraglutid daily application of 0,6mg s.c., dosage escalation every week to 1,2, 2,4, 3,0 mg. October 2022: hunger feeling was signifficantly reduced, eating of smaller portions, without craving between main time schedule of eating. Weight reduced to 151kg during first 3 months of liraglutid application (cca minus 100g per day), insulin dosage was reduced to 60 units daily (Humalog ex, basal insulin reduced to 60 units) what was accompanied by signifficant glucose level reduction to around 8 mmol/l. Creatinin level was 166 umol/l, acidum uricum level was 323 umol/l. January 2023: weight 157kg, fat content 50%, water content 40%. ECHO: left ventricle diameter 60mm, EF 0,5, left atrium diameter 54mm, tricuspidal regurgitation not detected, E/A 0,7. creatinin 128 umol/l , kalium 4,5 mmol/l.
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
自引率
0.00%
发文量
0
×
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