Improving Renal Complications in Adolescents With Type 2 Diabetes Through REsearch Cohort Study (National iCARE Study)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Type 2 Diabetes, Proteinuria, Stress, Nephropathy. Basic parameters: 10 years — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
The overall aim of the project is to elucidate the primary bio-psycho-social (BPS) risk factors for albuminuria in youth with type 2 diabetes (T2D) and the mechanisms by which they cause renal injury. The Study aims include: 1. Characterize the primary BPS risk factors associated with prevalent and progressive albuminuria in youth with T2D. 2. Determine individual, family and community level factors that influence biological and psychological risk factors and behaviors (adherence) that could be modified to protect against prevalent and progressive albuminuria. 3. Determine if systemic and renal inflammation is the common pathway through which BPS risk factors lead to albuminuria in youth with T2D. Study Hypotheses include: 1. Biological factors (poor glycemic control and systolic ambulatory hypertension), and psychological and social adversity (stress, mental distress and poverty) are significant predictors of prevalent and progressive albuminuria in youth with T2D. 2. Community and family support will be negatively associated with stress, and a lower risk of both prevalent and progressive albuminuria. 3. Systemic and renal inflammation is the common pathway through which BPS risk factors lead to albuminuria in youth with T2D.
Detailed description
The investigators will conduct a case-control study within a two-year, prospective observational cohort study of 500 prevalent cases of T2D diagnosed \<18 years of age. The investigators will evaluate the primary BPS risk factors associated with prevalent albuminuria using a principal component analysis (PCA) of associations between primary exposure variables at enrollment. After confirming the relevant BPS factors in the PCA analysis, the investigators will utilize a structural equation modeling approach to confirm the developed model.
Primary outcome measures
- Persistent Albuminuria [Time frame: 2 years]
- Change in albumin excretion over time. [Time frame: 2 years]
Secondary outcome measures (1)
- Change in estimated glomerular filtration rate (eGFR) over time. [Time frame: 2 years]
Eligibility criteria
Inclusion criteria
- All youth with T2D that do not meet exclusion criteria are eligible for the study.
Criteria for Diagnosis of T2D:
- Diagnosis of diabetes will be made according to the Canadian Diabetes Association criteria. There must be 2 abnormal blood glucose tests on different days OR 1 abnormal blood glucose test + symptoms of diabetes:
- Fasting plasma glucose of > 7.0 mmol/L or
- Random glucose > 11.1mmol/L or
- 2 hour glucose > 11.1 mmol/L after a standard oral glucose tolerance test (75g) or
- Hemoglobin A1c value ≥ 6.5%
- Distinguishing T2D from type 1 diabetes (T1D) will be based on clinical risk factors including:
- Presence of overweight/obesity,
- Other evidence of insulin resistance (acanthosis nigricans)
- Family history of type 2 diabetes (1st degree relative)
- Intrauterine exposure to hyperglycemia,
- Family heritage from a high-risk ethnic group (Indigenous, Hispanic, South Asian, Asian or African descent)
- Absence of diabetes associated auto-antibodies
- HNF-1 alpha heterozygote or homozygote
Exclusion criteria
- Diabetes secondary to medication use or surgery
- Antibodies suggestive of type 1 diabetes
- Current treatment with oral steroids or immunosuppressive agents as they may interfere with cortisol assessment and inflammatory markers
- Ever cancer
- Other chronic illness associated with systemic inflammation (ex. Juvenile rheumatoid arthritis, Crohns disease)
- Patient and or caregiver unable or unwilling to provide voluntary informed assent/consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Canada · 1 center
- Children's Hospital Research Institute of Manitoba/University of Manitoba — Winnipeg
Publications
- Dart AB, Wicklow BA, Sellers EA, Dean HJ, Malik S, Walker J, Chateau D, Blydt-Hansen TD, McGavock JM; iCARE investigators. The Improving Renal Complications in Adolescents With Type 2 Diabetes Through the REsearch (iCARE) Cohort Study: rationale and Protocol. Can J Diabetes. 2014 Oct;38(5):349-55. doi: 10.1016/j.jcjd.2014.07.224. PMID 25284698
Identifiers
NCT: NCT02818192 · B2011:024