Study Overview
The primary aim of this study is to test whether the rate of
cognitive decline and structural brain change in people with diabetes
treated with standard care guidelines is different than in people
with diabetes treated with intensive care guidelines. This comparison
will be made in a sub-sample of 2800 people with diabetes participating
in the already funded National Heart Lung and Blood Institute (NHLBI)
randomized factorial clinical trial Action to Control Cardiovascular
Risk in Diabetes (ACCORD).
Background
Type 2 diabetes and cognitive impairment are two of the most
common chronic conditions found in persons 60 years and older.
Approximately 18%-20% of older persons suffer from diabetes. And,
in the general population, the prevalence of cognitive impairment,
measured with the simple Mini-Mental State Exam, increases steadily
from 5% at 65 years to 15% percent at 80 years of age. Many persons
with cognitive impairment go on to develop dementia, which doubles
in incidence and prevalence every additional 5 years of age. Studies
suggest diabetes is one risk factor for cognitive impairment and
dementia.
Further, the brains of people with diabetes are at risk for adverse
sequelae following repeated hypoglycemic events. Magnetic Resonance
Imaging (MRI) provides a measure of the structural changes in the
brain that form the anatomical substrate for cognitive decline
and dementia. At present there are a few MRI studies showing people
with diabetes have increased risk for brain atrophy and (mainly
silent) lacunae.
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ACCORD-MIND Study Overview >>
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