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NCT Number: NCT02306005

Insulin Therapy and Lipoproteins' Profile in Type 1 Diabetes.

The aim of the study is to evaluate the effect of insulin therapy in patients with newly diagnosed type 1 diabetes on quantitative and qualitative changes of plasma lipoproteins, with particular emphasis on HDL metabolism, and analysis of the factors determining the effect of insulin therapy on lipid profile.The study is planned to cover a minimum of 100 people with newly diagnosed type 1 diabetes and lead prospective observation of this group (for a minimum of 5-10 years). Patients will be assessed: during the first hospitalization in the moment of diagnosis (prior to introduction of insulin treatment), after 3 weeks, after 6 months and after 12 months of insulin therapy. Further observations planned in the annual intervals. In addition, the study group will be under constant monitoring of metabolic evaluation every three months in the Outpatient Clinic.

During each follow-up will be assessed parameters evaluating the metabolism of plasma lipoprotein fractions and subfractions of HDL:

1. The concentration of apolipoprotein: including A-I, A-II, A-IV, C (II and III), D and E 2. Electrophoresis of plasma lipoproteins 3. Electrophoresis of HDL 4. The activity of enzymes: acyltransferase lecithin: cholesterol (LCAT) and plasma lipoprotein lipase Moreover, evaluation of factors which may potentially modify the relation between insulin therapy and lipoproteins will be assessed

1. Anthropometric data and markers of insulin resistance (such as BMI, waist-hip ratio, the estimated rate of glucose distribution, VAI index, body fat, blood pressure), 2. Metabolic management of diabetes,, 3. Protein glycation end products 4. The concentration of plasma adipokines.

Expected impact of the research project on the development of science, civilization and society The obtained results allow to assess the impact of exogenous insulin on quantitative and qualitative changes and metabolism of lipoproteins in the serum of patients with type 1 diabetes. Understanding the etiopathogenesis of this phenomenon and the factors affecting it seem to be very important in the treatment of patients with type 1 diabetes, where insulin is the treatment of choice and dosage adjustment appears to be extremely important. Remains unknown whether the changes in the lipoprotein profile result from the beginning of insulin therapy or other factors influence it. Selecting a group of patients with less favorable lipoprotein profile may allow better metabolic control, and thus will affect the quality and length of life of our patients. These studies will assess the impact of our therapeutic actions on the diagnosis of the disease on long-term consequences, such as the development of chronic complications.

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Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Internal Medicine and Diabetiology Poznan University of Medical Sciences

Poznan, 60-834, Poland

Location status: Recruiting

Location contact

Aleksandra Uruska, PhD

CONTACT

[email protected]

607620750 ext. +48

Dorota Zozulinska-Ziolkiewicz, Prof

CONTACT

[email protected]

618474579 ext. +48

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • New onset type 1 diabetes and treatment with insulin.
  • Written consent to participate in the study.
  • There are no other medical conditions, and with no other additional drugs beyond insulin

Exclusion criteria

  • any other medical conditions, and any other additional drugs beyond insulin

Treatment and study plan

Primary outcomes

  1. Changes in lipoproteins' metabolism

    Time frame: Change from Baseline in lipoproteins' metabolism at 6 and 12 months

    Evaluation of HDL levels, subfractions and enzymes connected with HDL metabolism (LCAT, lipoprotein lipase)

  2. Factors influencing relationship between insulin treatment and lipoproteins

    Time frame: 1 year

    Metabolic control, presence of remission, insulin resistance, adipokines, daily insulin requirement

Secondary outcomes

  1. Changes in apolipoproteins

    Time frame: Change from baseline in apolipoproteins' at 6 and 12 months

    Evaluation of apolipoproteins: A-I, A-II, A-IV, C (II i III), D i E

  2. Presence of insulin resistance

    Time frame: 1 year

    Evaluation of lipid tissue content, VAI, triglycerides/HDL ratio and estimated glucose disposal rate

  3. Development of Retinopathy

    Time frame: 1 year

    Evaluation of retinopathy (ophthalmology assessment)

  4. Development of Neuropathy

    Time frame: 1 year

    Evaluation of presence of neuropathy peripheral and autonomic (clinical examination and ProsciCard)

  5. Development of Diabetic kidney disease

    Time frame: 1 year

    Evaluation of presence of diabetic kidney disease (albuminuria, GFR)

Study contacts

Contact information is provided by the study sponsor or research team.

Aleksandra Uruska, PhD

CONTACT

[email protected]

607620750 ext. +48

Dorota Zozulinska-Ziolkiewicz, Prof

CONTACT

[email protected]

618474579 ext. +48

Sponsors and collaborators

Lead sponsor

Poznan University of Medical Sciences

Other

Registry information

Official study title

Insulin Therapy and Quantitive and Qualitive Changes of Plasma Lipoproteins in Patients With Newly Diagnosed Type 1 Diabetes.

Acronym: InLipoDiab1

Important dates

Study start
2014
Primary completion
2028
Study completion
2028
First posted
Dec 3, 2014
Registry last updated
Dec 5, 2024

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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