Functional MRI Biomarkers of Cognitive Decrements in Diabetes
NCT ID: NCT01705210
Last Updated: 2015-04-10
Study Results
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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COMPLETED
106 participants
OBSERVATIONAL
2012-05-31
2015-04-30
Brief Summary
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Detailed Description
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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 DM2 and MetS; ii) to investigate which cerebral biomarkers are shared and differ between DM2 and MetS; iii) to assess whether these cerebral biomarkers are associated with cognitive decrements.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Diabetes mellitus type 2 (DM2)
No interventions assigned to this group
metabolic syndrome (MetS)
No interventions assigned to this group
healthy controls
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Subjects enrolled in the existing 'Maastricht Study' (M-Study)
* Subjects gave written consent to be approached for additional research
* Subjects belongs to the 20% of the worst and 20% of the best performing (as based on neuropsychological cognitive testing (Stroop color-word test, 15 word learning test, and Delayed recall and recognition 15 word learning test)
Individuals Diabetes type 2:
\- Fasting blood glucose ≥ 7.0 mmol/l, after an oral glucose tolerance test (OGTT)blood glucose ≥ 11.1 mmol/l or used oral glucose-lowering medication or insulin
Metabolic syndrome:
* Participants should meet three out of 5 of the following criteria \[8\]:
1. Waist circumference \> 88 cm (women), \> 102 cm (men)
2. Triglycerides ≥ 1.7 mmol/l
3. HDL cholesterol \< 1.3 mmol/l (women), \< 1.0 mmol/l (men)
4. Blood pressure ≥ 130/85 mmHg (or medication)
5. Fasting blood glucose ≥ 6.1 mmol/l, after an OGTT blood glucose ≥ 7.8 mmol/l
Control participants:
* Those who fulfilled no more than 1 criterium of the metabolic syndrome, no DM2.
Exclusion Criteria
* Psychiatric co-morbidity and inability to perform the functional MRI tests.
* Incomplete cognitive assessment data
* Diabetes mellitus type 1 (DM1)
* Subjects who are not belonging to the 20% of the worst and 20% of the best performing individuals (as based on neuropsychological cognitive testing (Stroop color-word test, 15 word learning test, and Delayed recall and recognition 15 word learning test).
* Last visit of the subjects to the M-Study should be less than one year
40 Years
75 Years
ALL
Yes
Sponsors
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ZonMw: The Netherlands Organisation for Health Research and Development
OTHER
Netherlands Organisation for Scientific Research
OTHER_GOV
Maastricht University Medical Center
OTHER
Responsible Party
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Principal Investigators
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Jacobus FA Jansen, PhD
Role: PRINCIPAL_INVESTIGATOR
Maastricht University Medical Center
Locations
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Maastricht University Medical Center
Maastricht, , Netherlands
Countries
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References
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van Bussel FC, Backes WH, Hofman PA, van Oostenbrugge RJ, Kessels AG, van Boxtel MP, Schram MT, Stehouwer CD, Wildberger JE, Jansen JF. On the interplay of microvasculature, parenchyma, and memory in type 2 diabetes. Diabetes Care. 2015 May;38(5):876-82. doi: 10.2337/dc14-2043. Epub 2015 Feb 17.
Other Identifiers
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916.11.059
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
NL34329.068.10 / METC 10-2-023
Identifier Type: -
Identifier Source: org_study_id
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