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Consequences of Hypoglycaemia on Cardiovascular and Inflammatory Responses

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03976271
Acronym
HCIR
Enrollment
110
Registered
2019-06-06
Start date
2019-08-12
Completion date
2021-03-31
Last updated
2021-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Hypoglycemia, Inflammatory Response

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.

Interventions

PROCEDUREhyperinsulinemic normoglycaemic-hypoglycaemic glucose clamp

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.

Sponsors

Rigshospitalet, Denmark
CollaboratorOTHER
Radboud University Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

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.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Inflammatory responses of hypoglycaemia by measuring the cytokine production of isolated monocytes using ELISA1.5 yearCytokine production (TNF-alfa, IL-6, IL-10 and IL-1β) of isolated and stimulated monocytes

Secondary

MeasureTime frameDescription
Metabolomics profile of each group1.5 yearUn-targeted metabolomics and identification of metabolites based on exact mass using metabolomics library
Epigenetic modifications1.5 yearEpigenetic modifications due to hypoglycaemia in the promoter regions of the pro-inflammatory cytokines in monocytes
Atherogenic responses of (recurrent) hypoglycaemia using foam cell formation.1.5 yearMeasurement of Ox-LDL uptake by measuring intracellular apolipoproteine B
Cognitive function responses to hypoglycaemia using cognitive function tests (TAP, PASAT)1.5 yearAmount of correct answers
Oxidative stress responses using oxidative stress marker1.5 yearExcretion of guanine nucleosides in urine (ng/mL)
Cardiac function responses to hypoglycaemia using echocardiography1.5 yearCardiac function responses to hypoglycaemia using echocardiography

Countries

Denmark, Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026