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NCT Number: NCT03976271

Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nordsjællands University Hospital, Hillerød, Nordsjaelland, Denmark

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

hyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

Procedure

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.

Other names: hypoglycaemic clamp

Primary outcomes

  1. Inflammatory responses of hypoglycaemia by measuring the cytokine production of isolated monocytes using ELISA

    Time frame: 1.5 year

    Cytokine production (TNF-alfa, IL-6, IL-10 and IL-1β) of isolated and stimulated monocytes

Secondary outcomes

  1. Atherogenic responses of (recurrent) hypoglycaemia using foam cell formation.

    Time frame: 1.5 year

    Measurement of Ox-LDL uptake by measuring intracellular apolipoproteine B

  2. Metabolomics profile of each group

    Time frame: 1.5 year

    Un-targeted metabolomics and identification of metabolites based on exact mass using metabolomics library

  3. Epigenetic modifications

    Time frame: 1.5 year

    Epigenetic modifications due to hypoglycaemia in the promoter regions of the pro-inflammatory cytokines in monocytes

  4. Cardiac function responses to hypoglycaemia using echocardiography

    Time frame: 1.5 year

    Cardiac function responses to hypoglycaemia using echocardiography

  5. Cognitive function responses to hypoglycaemia using cognitive function tests (TAP, PASAT)

    Time frame: 1.5 year

    Amount of correct answers

  6. Oxidative stress responses using oxidative stress marker

    Time frame: 1.5 year

    Excretion of guanine nucleosides in urine (ng/mL)

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Collaborators

  • Rigshospitalet, Denmark

Registry information

Official study title

Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses in Patients With Diabetes Mellitus Type 1, Type 2 and Healthy Volunteers

Acronym: HCIR

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Jun 6, 2019
Registry last updated
May 12, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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