The Early Warning System for the Diabetic Encephalopathy

Sponsor
Tang-Du Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT02420470
Collaborator
(none)
300
1
140
2.1

Study Details

Study Description

Brief Summary

Diabetes( mainly type II diabetes )lead to the central nervous system (CNS) function impairment, especially the mild cognitive impairment that increased the risk of progression to dementia.The primary objectives are defined according to a hierarchical design: i) to tailor and apply multi-parametric, functional MRI techniques to identify cerebral abnormalities (cerebral biomarkers) in type 2 diabetes mellitus and prodromal diabetes mellitus ; ii) to assess whether these cerebral biomarkers are associated with cognitive decrements;iii) to follow up with the putative prediabetic condition patients to verify whether they can transform into diabetes.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Diabetes ( mainly type II diabetes ) lead to the central nervous system (CNS) function impairment, especially the mild cognitive impairment (MCI) that increased the risk of progression to dementia. It was regarded that neurodegeneration contributes to the diabetic MCI, however, recent research suggested that CNS microvascular alterations are the mechanism for early diabetic MCI. But there still lacks an early warning system for the CNS micro-structure alterations during early diabetes. Latest neuroimaging techniques enable the measurement of brain blood flow, local neural activity,and the nuclei deposition of iron to reflect CNS micro-structure alterations. But these techniques are complicated and can not fully reflect the alterations with one single technique.We previous observed that 44.4% of diabetic patients demonstrate MCI and established the comprehensive protocols of measuring brain blood flow, local neural activity and the nuclei deposition of iron simultaneously based on the multimodal MRI technique so as to reflect the microstructure alterations reliably and validly. Therefore, we intend to integrate psychological measurement and clinical biochemical examination, and to establish the early warning system for the central nervous system micro-structure alterations during early diabetes based on the multi-modal MRI technique. The reliability and validity of this system will be tested in the diabetic rat model. The early warning system will likely assist in screening patients with diabetic microstructure alterations, to perform early intervention so as to prevent or delay the progression from diabetic MCI to dementia.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Early Warning System for the Central Nervous System Micro-structure Alterations During Early Diabetes Based on the Multi-mode MRIs
    Study Start Date :
    Apr 1, 2015
    Anticipated Primary Completion Date :
    Nov 1, 2025
    Anticipated Study Completion Date :
    Dec 1, 2026

    Arms and Interventions

    Arm Intervention/Treatment
    healthy control group

    fasting plasma glucose(FPG)<6.11mmol/L,and 2-h plasma glucose(2hPG)<7.77mmol/L;

    prodromal diabetes group

    IFG:fasting plasma glucose(FPG) ≥5.6mmol/L (100mg/dl),and<7.0mmol/L (126mg/dl),oral glucose tolerance test(OGTT) 2-h plasma glucose(2hPG) <7.8 mmol/L ;IGT:oral glucose tolerance test(OGTT) 2-h plasma glucose(2hPG) ≥7.8mmol/L (140mg/dl),and<11.1mmol/L (200mg/dl),fasting plasma glucose(FPG)< 5.6mmol/L

    diabetes group

    fasting plasma glucose(FPG)>7.0mmol/L, or 2-h plasma glucose(2hPG)>11.1mmol/L

    Outcome Measures

    Primary Outcome Measures

    1. Functional and structural connectivity relationships of multiple brain regions and biomarkers of brain alterations, and the changes in relationships and biomarkers at 2.5 years. [subjects will be assessed six times (once half a year, up to 2.5 years )]

      Differences in macro-structural and micro-structural between patients,prodromal group and healthy controls will be evaluated. These MRI measures include volumetric characteristics (e.g. hyper-intensities, white matter lesions, atrophy, cerebral microbleeds), quantitative measures (e.g. T2 relaxation times, mean diffusivity, fractional anisotropy, mean kurtosis), functional characteristics (e.g. activated regions, cerebral blood flow), network properties (e.g. functional and structural connectivity, graph-theoretical measures).

    Secondary Outcome Measures

    1. evaluation of obesity and the changes in the state of obesity at 2.5 years [subjects will be assessed six times (once half a year, up to 2.5 years)]

      Simple evaluation of obesity will include: Body mass index will be calculated as the weight (kg) divided by the square of the height (m). Waist circumference (WC) will be taken as the minimum circumference between the umbilicus and xiphoid process and measured to the nearest 0.5 cm.

    2. metabolic characteristics and their changes at 2.5 years [subjects will be assessed six times (once half a year, up to 2.5 years)]

      Simple metabolic characteristics will include: oral glucose tolerance test, C peptide releasing test and insulin releasing test will be assessed;homeostasis model assessment of insulin resistance,insulin secretion of homeostasis model assessment and homeostasis model assessment-β will be calculated. what's more, cardiovascular risk factors(e.g. albumin, creatinin, total cholesterol, LDL- and HDL-cholesterol, triglycerides, HbA1c) will be assessed.

    3. Mental health and the changes in the scores of the scales at 2.5 years [subjects will be assessed six times (once half a year, up to 2.5 years)]

      To evaluate the mental health, a series of psychiatric evaluation scale(e.g. mini-mental state examination, Montreal Cognitive Assessment,Hamilton anxiety scale, self-rating depression scale, frontal assessment battery) will be assessed.

    4. Lifestyle and its changes at 2.5 years [subjects will be assessed six times (once half a year, up to 2.5 years)]

      Lifestyle specifics, including alcohol consumption, smoking behavior and mobility and exercise habit will be obtained. At the same time, quality of life will be obtained through a questionnaire.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • without dementia

    • Inform Consent Form

    • Education time more than 6 years

    • blood glucose matches the group standard

    Exclusion Criteria:
    • Pregnant woman

    • suffer from serious brain disease

    • Magnetic resonance contraindications

    • lack of compliance

    • image quality is too poor to deal with

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tangdu Hospital Xi'an Shaanxi China 710032

    Sponsors and Collaborators

    • Tang-Du Hospital

    Investigators

    • Study Chair: Guangbin Cui, professor, Tang-Du Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tang-Du Hospital
    ClinicalTrials.gov Identifier:
    NCT02420470
    Other Study ID Numbers:
    • TDLL-2014086
    First Posted:
    Apr 17, 2015
    Last Update Posted:
    Jul 13, 2022
    Last Verified:
    Jul 1, 2022
    Keywords provided by Tang-Du Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 13, 2022