Trial Search Results
Effects of Liraglutide on Hippocampal Structure and Function in Aging Adults With Prediabetes
The purpose of this study is to evaluate the effects of liraglutide on the memory and attention of people with insulin resistance. Liraglutide is a medication that makes the body more sensitive to insulin, and therefore may allow it to manage sugar more effectively.
The investigators are looking specifically at a region of the brain that is associated with memory and attention, called the hippocampus, in order to see whether treatment this treatment will change performance on memory and attention tasks. The investigators are also taking an MRI of the brain to see whether there are changes to the size and shape of the hippocampus after treatment.
All subjects in this study will be 50-70 years old and have pre- diabetes. Half of all subjects will have a family history of dementia, while the other half will not.
Stanford is currently not accepting patients for this trial.
Collaborator: American Diabetes Association
- Drug: Liraglutide
- Drug: Placebo
- Subjects will be men and women between the ages of 50 and 70 yrs of age, with a BMI of
27 to 37 kg/m2 and at least 12 yrs of education.
- All subjects will be medically stable (i.e. no uncontrolled or poorly controlled
medical illnesses), cognitively-intact as defined by Mini Mental Status Exam (MMSE)
score of > 27, and will have adequate visual and auditory acuity to allow for
- Metabolic function will be determined as impaired fasting glucose 100-125 mg/dL and/or
impaired 2-hr glucose concentration 140-199 and <200mg/dL on 75-g oral glucose
- Also, half of all subjects will have a family history of dementia.
- Diagnosis of possible or probable AD, MCI, or any other dementia; evidence of
cognitive decline by MMSE score of <27 or self-reported significant decline in memory
within the past year (per the Memory Function Questionnaire) (MFQ)
- History of Type I or Type II diabetes, or fasting plasma glucose > 126 mg/dL
- History of significant CVD or myocardial infarction; unstable cerebrovascular or
pulmonary disease, gallstones, pancreatitis or cancer, multiple endocrine neoplasia
(MEN) untreated hypothyroidism, unstable or untreated hypertension, anemia as
determined by hematocrit < 30%
- Abnormal renal clearance as determined by the serum creatinine ³ 1.5 mg/d, hepatic
dysfunction as determined by ALT > 2 times the upper limit of normal
- Presence of medications known to affect insulin action or insulin secretion
- Premature birth (which may affect MRI findings), history of neurological disorder
(ischemic attacks, carotid bruits, or lacunes upon MRI scan), or evidence of
neurologic or other physical illness that could produce cognitive deterioration; use
of any drug that may significantly affect the OGTT results or cognitive testing
results (specifically: cs)
- Drug or alcohol abuse or dependence within the past 6 months, positive urine
toxicology screen for illicit substances at eligibility screening, history of mental
illness, with the exception of past mood disorder, or evidence of acute depression as
determined by a 17-item Hamilton Depression Rating Scale (HDRS-17) score of 8 or more.
- Participants with history of mood disorder must be in remission for at least 6 months
prior to study entry.
Ages Eligible for Study
50 Years - 70 Years
Genders Eligible for Study