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Inflammatory Aspects of Glucose in Hyperlipidemia and Diabetes

Inflammatory Aspects of Glucose in Hyperlipidemia and Diabetes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02130505
Acronym
INFORM
Enrollment
51
Registered
2014-05-05
Start date
2007-06-30
Completion date
2008-06-30
Last updated
2014-05-05

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

Conditions

Atherosclerosis, Leukocyte Activation Disorder, Type 2 Diabetes Mellitus, Familial Combined Hyperlipidemia

Brief summary

In this study, we will investigate both inflammatory systems in healthy volunteers and patients with T2DM on insulin therapy and hyperlipidemia (both familial hyperlipidemia (FH) and familial combined hyperlipidemia (FCH)) during an OGTT.

Detailed description

Cardiovascular disease (CVD) is number one killer in the Netherlands. Insulin resistance and dyslipideima are the main causes of CVD. Recently, we have shown that there is an acute leukocyte activation after an oral glucose tolerance test (OGTT) in patients with newly-diagnosed diabets mellitus type 2 (T2DM). Leukocyte activation is an important and obligatory aspect in the process of atherosclerosis. Complement system is another important inflammatory component in atherosclerosis, which becomes activated in the postprandial phase. In this study, we will investigate both inflammatory systems in healthy volunteers and patients with T2DM on insulin therapy and hyperlipidemia (both familial hyperlipidemia (FH) and familial combined hyperlipidemia (FCH)) during an OGTT.

Interventions

DIETARY_SUPPLEMENTOGTT

Oral glucose tolerance test (OGTT) with 75 g of oral anhydrous glucose

Sponsors

Sint Franciscus Gasthuis
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Provide written informed consent * Aged 45-65 years * BMI \< 35 kg/m2

Exclusion criteria

* Emotionally and intellectually not capable to decide about participation in the study and the consequences of participation. Subjects who are not able to understand the patient information * Diabetes mellitus treated with oral antidiabetic medicine * Type 1 diabetes mellitus * Peripheral artery and/or coronary disease * Untreated hypertension * Alcohol use \> 2 units/day * Aberrations in kidney, liver and thyroid function * Use of any experimental medication within 6 months of the study * The use of immunosuppressive drugs

Design outcomes

Primary

MeasureTime frameDescription
Postprandial change in leukocyte activationarea under the curve during 2 hoursLeukocyte activation is determined by flow cytometry, using fluorescent labelled antibodies: FITC-conjugated anti-CD66b and PE-conjugated anti-CD11b, expressed in mean fluorescence intensity in arbitrary units. The difference in postprandial response, expressed as area under the curve, between patients with T2DM, FCH and healthy controls is determined using ANOVA.

Secondary

MeasureTime frameDescription
Correlation between chronic glycemia and leukocyte activationarea under the curve during 2 hoursTo assess whether chronic hyperglycemia (HbA1c) correlates with postprandial leukocyte activation, correlation between HbA1c and postprandial leukocyte activation (area under the curve) will be determined for the total study group.
Correlation between acute glycemia and leukocyte activationarea under the curve during 2 hoursTo assess whether acute hyperglycemia correlates with postprandial leukocyte activation, correlation between fasting glucose levels and postprandial leukocyte activation (area under the curve) will be determined for the total study group.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026