NCT01279161

Brief Summary

The project aims at assessment of the effect of the FTO gene polymorphism and the type of treatment on the development of overweight/obesity and features of metabolic syndrome in children with type 1 diabetes. Gene polymorphism including some genetic variants may predispose to the development of cardiovascular diseases and their complications. The A allele of the FTO gene predisposing to obesity occurs in approximately 40% of the European population and each copy of this allele can increase BMI by 0.1 Z-score i.e. by 0.4 kg/m2. Insulin therapy in diabetic patients may result in excess body weight gain. Therefore we need studies involving large groups of children and assessing cardiovascular risk factors in type 1 diabetes along with their genetic associations. Patients: The study will include 1500 children with type 1 diabetes, aged 6-18 years. Reference group will be made of 1500 children in whom type 1 diabetes was excluded. The following variables will be assessed in the treatment group: 1) Anthropometric data and questionnaire data: age, sex, body height and weight, body mass index (BMI), waist and hip circumferences, arm and thigh circumferences, family history of overweight/obesity, type 1 or 2 diabetes or cardiovascular disease, 2) Primary disease characteristics: age of the disease onset, treatment regimen, mean daily insulin consumption per kg body weight, brands of insulin products, glycated haemoglobin, BMI from the first 3-6 months following diabetes onset, diet, conversion of these data into actual and ideal calorie intake 3) Laboratory data - lipid profile and blood pressure (average of three measurements). Methodology: Gene polymorphism analysis in the extracted DNA will be made with the real-time PCR method using TaqMan 7900 HT by Applied Biosystems. Correlations between the FTO gene polymorphism and clinical variables such as BMI (including BMI increase since the disease onset), body weight and height, waist and hip circumferences, arm and thigh circumferences, and blood pressure will be assessed by a professional statistician with a specially dedicated software. Moreover parameters such as diet and metabolic control will be assessed. As regards insulin therapy the following variables will be analysed: insulin injection device, therapy regimen (intensive versus functional; brands and types of insulin products: human insulin versus insulin analogue), consumption of insulin. All of the above listed variables will be correlated with the genotypes found in the gene polymorphism analysis. The study has been approved by Bioethics Committee of the Medical University in Białystok. Results: The authors of the project expect that the effect of the FTO gene polymorphism on overweight/obesity and features of metabolic syndrome in children with type 1 diabetes will be shown. Moreover the project will enable assessment of the effect of the therapeutic regimen, including the type of insulin product, on body weight increase in the course of type 1 diabetes treatment in the context of the FTO gene polymorphism. Confirmation of the above associations and identification of a group at risk of excess body weight increase in the course of insulin therapy may help physicians, parents and patients to avoid this complication. Therefore clinical benefit of this project will include identification - based on the genetic assays results - of a group of type 1 diabetic children particularly likely to develop overweight, obesity and other cardiovascular risk factors.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2010

Longer than P75 for all trials

Geographic Reach
1 country

6 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2010

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 18, 2011

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 19, 2011

Completed
3.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2014

Completed
Last Updated

December 2, 2014

Status Verified

December 1, 2014

Enrollment Period

4 years

First QC Date

January 18, 2011

Last Update Submit

December 1, 2014

Conditions

Keywords

overweight, obesity, children, insulin, pump therapy, FTO

Outcome Measures

Primary Outcomes (1)

  • Identification of the effect of the FTO gene polymorphism on the development of overweight/obesity in insulin treated children

    one year

Secondary Outcomes (4)

  • • Identification of the effect of the following factors: sex, age, duration of disease, therapy regimen, type of insulin product and degree of metabolic control on the development of overweight/ obesity in insulin treated children

    one year

  • • Identification of the effect of genetic polymorphism of the FTO gene on the incidence of metabolic syndrome features in insulin treated children.

    one year

  • • Identification of the effect of genetic polymorphism of the FTO gene on the incidence of overweight, obesity and metabolic syndrome features in children without diabetes.

    one year

  • • Comparison of frequency distribution of FTO gene polymorphism involved in the pathogenesis of obesity in children with diabetes versus children without diabetes.

    one year

Study Arms (2)

diabetes

The study will include 1500 children with type 1 diabetes, aged 6-18 years. These will be patients from Diabetes Outpatient Clinics and patients hospitalized in Departments of Paediatrics, Endocrinology and Diabetology in University and Municipal Hospitals from Poland (Białystok, Warszawa, Łódź, Gdańsk, Wrocław, Katowice).

control

Reference group will be made of 1500 children from the above mentioned Clinics and Departments in whom type 1 diabetes was excluded. In these children diagnostics procedures will be conducted for reasons other than body weigh related diseases (excluding simple obesity). The children will not receive any treatment that might influence their body weight.

Eligibility Criteria

Age6 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

The study will include 1500 children with type 1 diabetes, aged 6-18 years. These will be patients from Diabetes Outpatient Clinics and patients hospitalized in Departments of Paediatrics, Endocrinology and Diabetology in University and Municipal Hospitals from all over Poland (Białystok, Warszawa, Gdańsk, Katowice, Wrocław). Reference group will be made of 1500 children from the above mentioned Clinics and Departments in whom type 1 diabetes was excluded. In these children diagnostics procedures will be conducted for reasons other than body weigh related diseases (excluding simple obesity). The children will not receive any treatment that might influence their body weight.

You may qualify if:

  • children of Polish origin
  • diagnosed with type 1 diabetes (defined according to the ADA 2010)
  • treated with insulin therapy for at least 1 year
  • aged ≥ 6 \< 18 years
  • receiving the same treatment regimen for at least one year
  • insulin requirement of \> 0.5 U/kg/daily

You may not qualify if:

  • no consent given by parents/guardians
  • chromosome disorders
  • autoimmune diseases
  • coeliac disease (biopsy-proven)
  • thyroid hormone disorders (but not the presence of antithyroid antibodies)
  • treatment that might influence body weight
  • newly diagnosed diabetes (either type 1, 2, 3 or other types of diabetes)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (6)

Department of Pediatrics, Endocrinology and Diabetology, Medical University

Wroclaw, Lower Silesian Voivodeship, 50-376, Poland

Location

Department of Pediatrics, Medical University

Warsaw, Masovian Voivodeship, 01-184, Poland

Location

Department of Pediatrics, Endocrinology, Diabetology with Cardiology Division, Medical University

Bialystok, Podlaskie Voivodeship, 15-089, Poland

Location

Department of Pediatrics, Hematology, Oncology and Endocrinology, Medical University

Gdansk, Pomeranian Voivodeship, 80-211, Poland

Location

Department of Pediatrics, Endocrinology and Diabetology, Medical University

Katowice, Silesian Voivodeship, 40-752, Poland

Location

Department of Pediatrics, Oncology, Hematology and Diabetology, Medical University

Lodz, Łódź Voivodeship, 91-738, Poland

Location

Related Publications (5)

  • Timpson NJ, Emmett PM, Frayling TM, Rogers I, Hattersley AT, McCarthy MI, Davey Smith G. The fat mass- and obesity-associated locus and dietary intake in children. Am J Clin Nutr. 2008 Oct;88(4):971-8. doi: 10.1093/ajcn/88.4.971.

    PMID: 18842783BACKGROUND
  • Frayling TM, Timpson NJ, Weedon MN, Zeggini E, Freathy RM, Lindgren CM, Perry JR, Elliott KS, Lango H, Rayner NW, Shields B, Harries LW, Barrett JC, Ellard S, Groves CJ, Knight B, Patch AM, Ness AR, Ebrahim S, Lawlor DA, Ring SM, Ben-Shlomo Y, Jarvelin MR, Sovio U, Bennett AJ, Melzer D, Ferrucci L, Loos RJ, Barroso I, Wareham NJ, Karpe F, Owen KR, Cardon LR, Walker M, Hitman GA, Palmer CN, Doney AS, Morris AD, Smith GD, Hattersley AT, McCarthy MI. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science. 2007 May 11;316(5826):889-94. doi: 10.1126/science.1141634. Epub 2007 Apr 12.

    PMID: 17434869BACKGROUND
  • Reinehr T, Holl RW, Roth CL, Wiesel T, Stachow R, Wabitsch M, Andler W; DPV-Wiss Study Group. Insulin resistance in children and adolescents with type 1 diabetes mellitus: relation to obesity. Pediatr Diabetes. 2005 Mar;6(1):5-12. doi: 10.1111/j.1399-543X.2005.00093.x.

    PMID: 15787895BACKGROUND
  • Luczynski W, Szypowska A, Glowinska-Olszewska B, Bossowski A. Overweight, obesity and features of metabolic syndrome in children with diabetes treated with insulin pump therapy. Eur J Pediatr. 2011 Jul;170(7):891-8. doi: 10.1007/s00431-010-1372-7. Epub 2010 Dec 8.

    PMID: 21140273BACKGROUND
  • Luczynski W, Fendler W, Ramatowska A, Szypowska A, Szadkowska A, Mlynarski W, Chumiecki M, Jarosz-Chobot P, Chrzanowska J, Noczynska A, Brandt A, Mysliwiec M, Glowinska-Olszewska B, Bernatowicz P, Kowalczuk O, Bossowski A. Polymorphism of the FTO Gene Influences Body Weight in Children with Type 1 Diabetes without Severe Obesity. Int J Endocrinol. 2014;2014:630712. doi: 10.1155/2014/630712. Epub 2014 Aug 19.

Biospecimen

Retention: SAMPLES WITH DNA

Small amount of peripheral blood for isolation of DNA for assessment of FTO polymorphism.

MeSH Terms

Conditions

Diabetes Mellitus, Type 1OverweightObesityInsulin Resistance

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesAutoimmune DiseasesImmune System DiseasesOvernutritionNutrition DisordersBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsHyperinsulinism

Study Officials

  • Wlodzimierz Luczynski, Ass. Prof.

    Medical University of Bialystok, Poland

    STUDY CHAIR
  • Adam Kretowski, Prof

    Medical University of Bialystok, Poland

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

January 18, 2011

First Posted

January 19, 2011

Study Start

December 1, 2010

Primary Completion

December 1, 2014

Study Completion

December 1, 2014

Last Updated

December 2, 2014

Record last verified: 2014-12

Locations