此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Impact of Hypoglycemia Unawareness on Brain Metabolism Cognition in T1DM

2020年3月31日 更新者:Yale University
The research study is designed to examine the impact of low blood sugar on brain function in individuals with Type 1 Diabetes who have frequent and severe hypoglycemia (low blood sugar) compared to those who do not.

研究概览

地位

完全的

详细说明

During the course of treating diabetes (for example, after an insulin injection), blood sugar levels will sometimes drop too low. This condition is known as hypoglycemia. Normally, a healthy body responds to hypoglycemia by producing a number of "anti-insulin" hormones which raise blood sugar levels. In addition, these hormones provide the individual with warning signals of hypoglycemia, including hunger, sweating, shaking and heart palpitations. These warning signals allow diabetics to correct low blood sugar levels by eating sugar tablets or by having a snack.

Unfortunately, and for unclear reasons, many people with longstanding diabetes lose their ability to recognize low blood sugar levels-a condition called "hypoglycemia unawareness." The brain, in particular, is extremely sensitive to hypoglycemia. Unable to sense and respond to low blood sugar levels, these individuals may experience a sudden onset of blurred vision, confusion, seizures, coma, or even death.

In recent years, a new technique called "islet cell transplantation" has been developed as an alternate means of treating insulin-dependent diabetes. Pancreatic islet cells (the cells that produce insulin), from human donors, are injected into the diabetic patient's liver where the cells are capable of making insulin and can regulate blood sugar levels without the need for insulin injections. Currently, this technique is used primarily in patients with severe hypoglycemia unawareness.

While it is known that islet cell transplantation can reduce the risk of severe hypoglycemia, the effects of transplantation on hypoglycemia unawareness are unknown. This study is designed to investigate why hypoglycemia unawareness happens and the impact it has on brain function in individuals with type 1 diabetes.

研究类型

观察性的

注册 (预期的)

51

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Connecticut
      • New Haven、Connecticut、美国、06520
        • Yale University School of Medicine

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 49年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Group 1A) T1DM subjects with severe hypoglycemia unawareness and awaiting islet cell transplantation will be referred by participating islet transplantation centers.

Group 1B) T1DM subjects with severe hypoglycemia unawareness but not awaiting islet cell transplantation will be from the greater New Haven, CT area.

Group 2)T1DM, not optimally controlled and without hypoglycemia unawareness will be from the greater New Haven, CT area.

Group 3) Non-Diabetics from the greater New Haven CT area.

描述

Inclusion Criteria:

  • Inclusion Criteria for all subjects:

    • Age 18-49
    • > 85 kg
    • BMI <27female <28 male
    • able to provide written informed consent
    • able to speak and read English fluently
    • must meet Magnetic Resonance safety evaluation

Inclusion criteria for Group 1A:

  • T1DM undergoing intensive clinical management and currently on the islet transplant list
  • History of severe hypoglycemia

Inclusion criteria for Group 1B:

  • T1DM undergoing intensive clinical management
  • History of severe hypoglycemia unawareness

Inclusion criteria for Group 2:

  • T1DM with poor glycemic control, HbA1c > 8%
  • no episodes of hypoglycemia requiring assistance from another person for at least 1 yr, no episodes in last 4 weeks, and hypoglycemia aware

Exclusion Criteria:

Group 1A: (T1DM subjects being considered for islet cell transplantation)

  • Detectable c-peptide level
  • Untreated proliferative retinopathy
  • Creatinine clearance < 65 ml/min/1.73 m2
  • Serum creatinine ≥1.5 mg/dL
  • Previous pancreas or islet transplant
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Active infection including hepatitis C, hepatitis B, HIV, or TB (or under treatment for suspected TB ), or subjects with a positive PPD performed within 1 yr. of enrollment, and no history of adequate prophylaxis
  • Invasive aspergillus infection within year prior to study entry
  • Any history of malignancy except for adequately treated squamous or basal cell carcinoma of the skin
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • History of non-adherence to prescribed regimens
  • Psychiatric disorder making the subject not a suitable candidate for transplantation
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males; lymphopenia (<1,000/μL), or leukopenia (< 3,000 total leukocytes/μL), or an absolute CD4+ count < 500/μL
  • History of coagulopathy or medical condition requiring long-term anticoagulant therapy (e.g., warfarin) after transplantation (low-dose aspirin treatment is allowed) or patient with INR >1.5
  • Severe co-existing cardiac disease, as determined by referring center
  • Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Severe unremitting diarrhea or other gastrointestinal disorders potentially interfering with the ability to absorb oral medications
  • Addison's disease as determined by clinical history
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Group 1 B: (T1DM with Severe Hypoglycemia Unawareness not on the Transplant List)

  • Detectable C-peptide level
  • Serum creatinine ≥1.5 mg/dL
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • Psychiatric disorder making the subject not a suitable candidate for transplantation
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males
  • Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Group 2: (T1DM control subjects)

  • Detectable C-peptide level
  • Serum creatinine ≥1.5 mg/dL
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Any history of malignancy except for adequately treated squamous or basal cell carcinoma of the skin
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Addison's disease as determined by clinical history
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Group 3: (Normal Controls)

  • FBG > 100 mg/dL
  • Serum creatinine ≥1.5 mg/dL
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Any history of malignancy except for adequately treated squamous or basal cell carcinoma of the skin
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males
  • Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
1A, 1B

Type 1 diabetic subjects with a history of severe hypoglycemia and hypoglycemia unawareness who:

1A) meet criteria for islet cell transplantation and are referred by a participating islet cell transplantation center

1B) meet similar criteria but are not currently planning islet cell transplantation

2
Type 1 diabetics who are not optimally controlled (>8% HbA1c) and rarely experience hypoglycemia
3
Healthy non-diabetics

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Robert Sherwin, MD、Yale University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2005年8月1日

研究完成 (实际的)

2008年8月1日

研究注册日期

首次提交

2007年12月14日

首先提交符合 QC 标准的

2007年12月17日

首次发布 (估计)

2007年12月18日

研究记录更新

最后更新发布 (实际的)

2020年4月2日

上次提交的符合 QC 标准的更新

2020年3月31日

最后验证

2020年3月1日

更多信息

与本研究相关的术语

其他研究编号

  • 0505000077_B
  • R01DK072409 (美国 NIH 拨款/合同)
  • HIC# 0505000077

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

3
订阅