Small Dense Low-density Lipoprotein in Patients With Prediabetes and Type 2 Diabetes

NCT ID: NCT01584856

Last Updated: 2012-04-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-05-31

Study Completion Date

2013-01-31

Brief Summary

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It is known that small dense LDL particles are associated with an increased cardiovascular risk. LDL particles can be separated by gradient gel electrophoresis (GGE) according to their size. The risk to suffer from coronary heart disease is 3-7 fold elevated in subjects with small dense LDL particles compared to subjects with large LDL particles. This study aims at evaluating the predictive value of small dense LDL particles in patients with prediabetes and type 2 diabetes mellitus concerning future changes in intima media thickness, flow-mediated dilation and other risk factors of atherosclerosis (e.g. insulin resistance). 60 patients with prediabetes or type 2 diabetes will be recruited for the study. Assessment will include medical history (risk factors), physical examination (blood pressure, BMI, waist-to-hip ratio), collection of serum, oral glucose tolerance test, measurement of intima media thickness and endothelial dysfunction by ultrasound. All measurements will be repeated after 2 years. Data will be analysed to assess whether the amount of small dense LDL particles can predict further structural and functional changes of the cardiovascular system or changes in the severity of the disease (insulin resistance).

Detailed Description

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Conditions

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Prediabetes / Type 2 Diabetes

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* impaired fasting glucose OR type 2 diabetes (ADA criteria)
* BMI \> 25 kg/m2
* given informed consent

Exclusion Criteria

* insulin therapy
* fasting glucose \> 11mmol/l
* total cholesterol \> 6.5 mmol/l OR triglycerides \> 2.5 mmol/l
* malignant or severe renal, hepatic, pulmonary, neurological or psychiatric disease
* alcohol or drug abuse
* HIV infection.
Minimum Eligible Age

20 Years

Maximum Eligible Age

90 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Kaspar Berneis, Prof. MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Zurich, Endocrinology and Diabetology

Locations

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University Hospital Zurich, Endocrinology and Diabetology

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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EK-1267

Identifier Type: -

Identifier Source: org_study_id

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