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Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses (HCIR)

Primary Purpose

Hypoglycemia, Inflammatory Response, Diabetes Mellitus, Type 1

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Hypoglycemia

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Overall inclusion criteria

  • Ability to provide written informed consent
  • Must be able to speak and read Danish (for Hillerød-site) and Dutch (for Nijmegen-site)
  • Insulin treatment according to basal-bolus insulin regimen (injections or insulin pump) (except for group 5)
  • Body-Mass Index: 19-40 kg/m2
  • Age ≥18 years, ≤ 80 years
  • Blood pressure: <140/90 mmHg
  • Duration of diabetes > 1 year (except for group 5)
  • HbA1c < 100 mmol/mol

Group specific

  • Group 1: HbA1c >64 mmol/mol
  • Group 2: impaired awareness of hypoglycaemia (IAH) as assessed by a score of ≥3 on the modified Clarke questionnaire, ≥4 on the Gold questionnaire and a positive score on the Pedersen-Bjergaard questionnaire.
  • Group 3: normal awareness of hypoglycaemia (NAH) as assessed by a score of <3 on the modified Clarke questionnaire, <4 on the Gold questionnaire and a negative score on the Pedersen-Bjergaard.
  • Group 4: Insulin treatment for at least 1 year
  • Group 5/6: HbA1c <42 mmol/mol

Exclusion Criteria:

  • - Severe medical or psychological conditions interfering with the perception of hypoglycaemia other than IAH such as brain injuries, epilepsy, a major cardiovascular disease event or anxiety disorders
  • Use of immune-modifying drugs or antibiotics
  • Treatment with glucose-modifying (other than insulin, SGLT-2 inhibitors and metformin) agents (e.g. prednisolon)
  • Use of anti-depressive drugs
  • Pregnancy or breastfeeding or unwillingness to undertake measures for birth control
  • Use of statins (e.g. stop statins >2 weeks before performing blood sampling. This can be safely done in the context of primary prevention)
  • Any event of cardiovascular disease in the past 5 years (e.g. myocardial infarction, stroke, heart failure, symptomatic peripheral arterial disease)
  • Auto-inflammatory or auto-immune diseases
  • Any infection in past three months
  • Previous vaccination in the past three months
  • Laser coagulation for proliferative retinopathy in the past six months
  • Proliferative retinopathy
  • Diabetic nephropathy as reflected by an albumin-creatinine ratio ˃ 30 mg/gor an estimated glomerular filtration rate (by MDRD) ˂60ml/min/1.73m2
  • History of pancreatitis (acute or chronic) or pancreatic cancer

Sites / Locations

  • Nordsjællands University Hospital
  • Radboudumc

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

T1DM poor glycaemic control

T1DM impaired awareness

T1DM Normal awareness

T2DM + Insulin

Healthy control T2DM

Healthy control T1DM

Arm Description

patients with type 1 diabetes and poor glycaemic control (HbA1c >8% / >64 mmol/mol will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

patients with type 1 diabetes and impaired awareness of hypoglycaemia will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

patients with type 1 diabetes and normal awareness of hypoglycaemia will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

patients with type 2 diabetes with insulin treatment for at least 1 year will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

healthy controls without diabetes and age, gender and BMI matched with diabetes type 2 participants will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

Healthy controls without diabetes and age, gender and BMI matched with diabetes type 1 participants will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

Outcomes

Primary Outcome Measures

Inflammatory responses of hypoglycaemia by measuring the cytokine production of isolated monocytes using ELISA
Cytokine production (TNF-alfa, IL-6, IL-10 and IL-1β) of isolated and stimulated monocytes

Secondary Outcome Measures

Atherogenic responses of (recurrent) hypoglycaemia using foam cell formation.
Measurement of Ox-LDL uptake by measuring intracellular apolipoproteine B
Metabolomics profile of each group
Un-targeted metabolomics and identification of metabolites based on exact mass using metabolomics library
Epigenetic modifications
Epigenetic modifications due to hypoglycaemia in the promoter regions of the pro-inflammatory cytokines in monocytes
Cardiac function responses to hypoglycaemia using echocardiography
Cardiac function responses to hypoglycaemia using echocardiography
Cognitive function responses to hypoglycaemia using cognitive function tests (TAP, PASAT)
Amount of correct answers
Oxidative stress responses using oxidative stress marker
Excretion of guanine nucleosides in urine (ng/mL)

Full Information

First Posted
November 8, 2018
Last Updated
May 11, 2021
Sponsor
Radboud University Medical Center
Collaborators
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT03976271
Brief Title
Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses
Acronym
HCIR
Official Title
Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses in Patients With Diabetes Mellitus Type 1, Type 2 and Healthy Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
August 12, 2019 (Actual)
Primary Completion Date
March 31, 2021 (Actual)
Study Completion Date
March 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
Rigshospitalet, Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
People with Type 1 diabetes (T1DM), type 2 diabetes (T2DM) and healthy volunteers will undergo a hypoglycaemic clamp to to investigate the effect of hypoglycaemia on cardiovascular and inflammatory responses.
Detailed Description
Objectives: The overall aim of the present study is to investigate the effect of hypoglycaemia on cardiovascular and inflammatory responses, molecular mechanisms and epigenetic profiles in various groups of people with diabetes type 1, type 2 and healthy volunteers. Study design: Intervention study Intervention: All subjects will undergo a hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp (nadir 2.8 mmol/L), during and after which blood and urine will be sampled for further examination for up to one week.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoglycemia, Inflammatory Response, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
All subjects will undergo a hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp (nadir 2.8 mmol/L), during and after which blood and urine will be sampled for further examination for up to one week.
Allocation
Non-Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
T1DM poor glycaemic control
Arm Type
Active Comparator
Arm Description
patients with type 1 diabetes and poor glycaemic control (HbA1c >8% / >64 mmol/mol will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Arm Title
T1DM impaired awareness
Arm Type
Active Comparator
Arm Description
patients with type 1 diabetes and impaired awareness of hypoglycaemia will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Arm Title
T1DM Normal awareness
Arm Type
Active Comparator
Arm Description
patients with type 1 diabetes and normal awareness of hypoglycaemia will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Arm Title
T2DM + Insulin
Arm Type
Active Comparator
Arm Description
patients with type 2 diabetes with insulin treatment for at least 1 year will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Arm Title
Healthy control T2DM
Arm Type
Active Comparator
Arm Description
healthy controls without diabetes and age, gender and BMI matched with diabetes type 2 participants will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Arm Title
Healthy control T1DM
Arm Type
Active Comparator
Arm Description
Healthy controls without diabetes and age, gender and BMI matched with diabetes type 1 participants will undergo hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Intervention Type
Procedure
Intervention Name(s)
hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp
Other Intervention Name(s)
hypoglycaemic clamp
Intervention Description
For this study, a hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp will be conducted to investigate the effect of hypoglycaemia. This means that subjects will receive an intravenous insulin infusion, at a continuous rate of 60 mU∙m-2∙min-1, as well as glucose 20% w/w intravenously at a variable rate, adjusted by arterial plasma glucose levels, measured at 5 minute intervals.
Primary Outcome Measure Information:
Title
Inflammatory responses of hypoglycaemia by measuring the cytokine production of isolated monocytes using ELISA
Description
Cytokine production (TNF-alfa, IL-6, IL-10 and IL-1β) of isolated and stimulated monocytes
Time Frame
1.5 year
Secondary Outcome Measure Information:
Title
Atherogenic responses of (recurrent) hypoglycaemia using foam cell formation.
Description
Measurement of Ox-LDL uptake by measuring intracellular apolipoproteine B
Time Frame
1.5 year
Title
Metabolomics profile of each group
Description
Un-targeted metabolomics and identification of metabolites based on exact mass using metabolomics library
Time Frame
1.5 year
Title
Epigenetic modifications
Description
Epigenetic modifications due to hypoglycaemia in the promoter regions of the pro-inflammatory cytokines in monocytes
Time Frame
1.5 year
Title
Cardiac function responses to hypoglycaemia using echocardiography
Description
Cardiac function responses to hypoglycaemia using echocardiography
Time Frame
1.5 year
Title
Cognitive function responses to hypoglycaemia using cognitive function tests (TAP, PASAT)
Description
Amount of correct answers
Time Frame
1.5 year
Title
Oxidative stress responses using oxidative stress marker
Description
Excretion of guanine nucleosides in urine (ng/mL)
Time Frame
1.5 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Overall inclusion criteria Ability to provide written informed consent Must be able to speak and read Danish (for Hillerød-site) and Dutch (for Nijmegen-site) Insulin treatment according to basal-bolus insulin regimen (injections or insulin pump) (except for group 5) Body-Mass Index: 19-40 kg/m2 Age ≥18 years, ≤ 80 years Blood pressure: <140/90 mmHg Duration of diabetes > 1 year (except for group 5) HbA1c < 100 mmol/mol Group specific Group 1: HbA1c >64 mmol/mol Group 2: impaired awareness of hypoglycaemia (IAH) as assessed by a score of ≥3 on the modified Clarke questionnaire, ≥4 on the Gold questionnaire and a positive score on the Pedersen-Bjergaard questionnaire. Group 3: normal awareness of hypoglycaemia (NAH) as assessed by a score of <3 on the modified Clarke questionnaire, <4 on the Gold questionnaire and a negative score on the Pedersen-Bjergaard. Group 4: Insulin treatment for at least 1 year Group 5/6: HbA1c <42 mmol/mol Exclusion Criteria: - Severe medical or psychological conditions interfering with the perception of hypoglycaemia other than IAH such as brain injuries, epilepsy, a major cardiovascular disease event or anxiety disorders Use of immune-modifying drugs or antibiotics Treatment with glucose-modifying (other than insulin, SGLT-2 inhibitors and metformin) agents (e.g. prednisolon) Use of anti-depressive drugs Pregnancy or breastfeeding or unwillingness to undertake measures for birth control Use of statins (e.g. stop statins >2 weeks before performing blood sampling. This can be safely done in the context of primary prevention) Any event of cardiovascular disease in the past 5 years (e.g. myocardial infarction, stroke, heart failure, symptomatic peripheral arterial disease) Auto-inflammatory or auto-immune diseases Any infection in past three months Previous vaccination in the past three months Laser coagulation for proliferative retinopathy in the past six months Proliferative retinopathy Diabetic nephropathy as reflected by an albumin-creatinine ratio ˃ 30 mg/gor an estimated glomerular filtration rate (by MDRD) ˂60ml/min/1.73m2 History of pancreatitis (acute or chronic) or pancreatic cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bastiaan E de Galan, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ulrik Pedersen-Bjergaard, MD, PhD
Organizational Affiliation
Nordsjællands University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nordsjællands University Hospital
City
Hillerød
State/Province
Nordsjaelland
ZIP/Postal Code
3400
Country
Denmark
Facility Name
Radboudumc
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525 GA
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No IPD sharing plan necessary
Citations:
PubMed Identifier
35876660
Citation
Verhulst CEM, Fabricius TW, Nefs G, Kessels RPC, Pouwer F, Teerenstra S, Tack CJ, Broadley MM, Kristensen PL, McCrimmon RJ, Heller S, Evans ML, Pedersen-Bjergaard U, de Galan BE. Consistent Effects of Hypoglycemia on Cognitive Function in People With or Without Diabetes. Diabetes Care. 2022 Sep 1;45(9):2103-2110. doi: 10.2337/dc21-2502.
Results Reference
derived

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Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses

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