Pancreatin Added to Standard Antihyperglycemic Therapy in Patients With Type 2 Diabetes
The Effect of Pancreatin Added to Standard Antihyperglycemic Therapy on Metabolic Control in Patients With Type 2 Diabetes
Medications that enhance the incretin effect (GLP-1 receptor agonists, tirzepatide (GIP/GLP-1 receptor agonist) and DPP-4 inhibitors) are used in treatment of patients with type 2 diabetes. GLP-1 agonists and tirzepatide not only effectively lower blood glucose levels but also promote weight loss-primarily by stimulating the satiety center in the central nervous system - and reduce cardiovascular risk. Evidence suggests that oral pancreatin supplementation also enhances the incretin effect by increasing GIP and GLP-1 concentrations, and consequently insulin levels, which translates into a reduction in postprandial glycemia in patients with cystic fibrosis or chronic pancreatitis. In our study we aim to evaluate the impact of pancreatin on the incretin effect and glycemic control in patients with type 2 diabetes without exocrine pancreatic insufficiency.
研究概览
详细说明
Glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are the two primary incretin hormones secreted from the small intestine on ingestion of glucose or nutrients to stimulate insulin secretion from pancreatic β cells. They play a role in regulation of blood glucose levels, particularly postprandial glycemia. Lipids and carbohydrates are the most potent stimulators of incretin hormone secretion. Pancreatin is a mixture of digestive enzymes naturally produced by the pancreas, which is used as a medication supporting macronutrient digestion, especially in cases of exocrine pancreatic insufficiency. Evidence suggests that oral pancreatin supplementation enhances the incretin effect by increasing GIP and GLP-1 concentrations, and consequently insulin levels, which translates into a reduction in postprandial glycemia in patients with cystic fibrosis or chronic pancreatitis. Based on a randomized, placebo-controlled, double-blind study, we aim to evaluate the effect of pancreatin on the incretin effect and glycemic control in patients with type 2 diabetes without exocrine pancreatic insufficiency.
We plan to recruit a total of 100 patients with type 2 diabetes treated with oral antihyperglycemic drugs or insulin, either as monotherapy or in combination. Patients will be randomly divided into 2 groups:
- Group of 50 patients receiving pancreatin 25 000 U with up to 3 main meals daily for 3 months
- Group of 50 patients receiving placebo with up to 3 main meals daily for 3 months
Baseline assessment:
- Anthropometric parameters: body weight, height, waist-to-hip ratio, body composition (bioelectrical impedance analysis)
- Laboratory tests: aspartate aminotransferase, alanine aminotransferase, serum amylase, lipid profile, HbA1c, selected cytokines, average glucose concentration from the last 7 days before study start (glucometer - 4 measurements per day), data from the FreeStyle Libre2 continuous glucose monitoring system (2 weeks prior to study start): assessment of TIR (Time in Range 70-180 mg/dL), glycemic variability coefficient (CV), standard deviation (SD), mean glucose concentration, frequency and severity of hypoglycemia; daily insulin requirements from the last 7 days (for insulin-treated patients)
Assessment after study completion:
- Anthropometric parameters: body weight, height, waist-to-hip ratio, body composition (bioelectrical impedance analysis)
- Laboratory tests: aspartate aminotransferase, alanine aminotransferase, serum amylase, lipid profile, HbA1c, selected cytokines, average glucose concentration from the last 7 days before study end (glucometer - 4 measurements per day), data from the FreeStyle Libre 2 continuous glucose monitoring system (last 2 weeks of study): assessment of TIR, CV, SD, mean glucose concentration, frequency and severity of hypoglycemia; daily insulin requirements from the last 7 days (for insulin-treated patients).
Should pancreatin demonstrate a beneficial effect on glycemic homeostasis, these formulations could serve as a valuable adjunctive therapy for type 2 diabetes.
研究类型
注册 (估计的)
阶段
- 第四阶段
联系人和位置
学习联系方式
- 姓名:Marta Wróbel, PhD
- 电话号码:48606873060
- 邮箱:mwrobel@sum.edu.pl
研究联系人备份
- 姓名:Paulina Piekarz-Ząbek, MD
- 电话号码:+48 604 223 652
- 邮箱:k_bielawa@poczta.fm
学习地点
-
-
Silesian Voivodeship
-
Zabrze、Silesian Voivodeship、波兰、41-800
- 招聘中
- Department of Internal Medicine, Diabetology and Cardiometabolic Disorders, Faculty of Medical Sciences Zabrze
-
接触:
- Paulina Piekarz-Ząbek, MD
- 电话号码:+48 604 223 652
- 邮箱:k_bielawa@poczta.fm
-
接触:
- Marta Wróbel, PhD
- 电话号码:+48606873060
- 邮箱:mwrobel@sum.edu.pl
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Type 2 diabetes diagnosed for at least 12 months
- Patients treated with oral antihyperglycemic agents and/or insulin as monotherapy or combination therapy
- Age between 35 and 75 years
- HbA1c: 6.5% - 9.0%
Exclusion Criteria:
- Type 1 diabetes
- Use of incretin-based drugs (GLP-1 receptor agonists, dual GIP and GLP-1 receptor agonists, DPP-4 inhibitors) currently or within the last 3 months
- History of pancreatic surgery
- History of chronic pancreatitis
- History of acute pancreatitis
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Pancreatin
Participants receiving pancreatin |
Pancreatin 25 000 U with each of the 3 main meals daily for 3 months
其他名称:
|
|
安慰剂比较:Control
Participants receiving placebo |
Placebo capsule with each of the 3 main meals daily for 3 months
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Glycemic control
大体时间:3 months
|
HbA1c value |
3 months
|
|
Time in range
大体时间:3 months
|
Time in range (glucose 70-180 mg/dl) |
3 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Body weight
大体时间:3 months
|
Body weight measurement |
3 months
|
|
Lipid profile
大体时间:3 months
|
Total cholesterol, LDL-cholesterol, HDL-cholesterol, Triglicerides |
3 months
|
合作者和调查者
调查人员
- 首席研究员:Marta Wróbel, PhD、Department of Internal Medicine, Diabetology and Cardiometabolic Disorders
出版物和有用的链接
一般刊物
- Perano SJ, Couper JJ, Horowitz M, Martin AJ, Kritas S, Sullivan T, Rayner CK. Pancreatic enzyme supplementation improves the incretin hormone response and attenuates postprandial glycemia in adolescents with cystic fibrosis: a randomized crossover trial. J Clin Endocrinol Metab. 2014 Jul;99(7):2486-93. doi: 10.1210/jc.2013-4417. Epub 2014 Mar 26.
- Knop FK, Vilsboll T, Larsen S, Hojberg PV, Volund A, Madsbad S, Holst JJ, Krarup T. Increased postprandial responses of GLP-1 and GIP in patients with chronic pancreatitis and steatorrhea following pancreatic enzyme substitution. Am J Physiol Endocrinol Metab. 2007 Jan;292(1):E324-30. doi: 10.1152/ajpendo.00059.2006. Epub 2006 Sep 5.
- Ebert R, Creutzfeldt W. Reversal of impaired GIP and insulin secretion in patients with pancreatogenic steatorrhea following enzyme substitution. Diabetologia. 1980 Sep;19(3):198-204. doi: 10.1007/BF00275269.
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
关键字
其他研究编号
- Pancreatin - type 2 diabetes
- BNW-1-089/N/5/K (其他赠款/资助编号:Medical University of Silesia, Katowice, Poland)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Deidentified individual participant data and the study protocol will be made available upon reasonable request.
IPD 共享时间框架
after publication, till 5 yrs
IPD 共享访问标准
via email:mwrobel@sum.edu.pl
IPD 共享支持信息类型
- 研究方案
- 树液
- 国际碳纤维联合会
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