Study on cardiac sympathetic nerve function in the diagnosis of dementia with Lewy bodies and Alzheimer's disease
- Conditions
- Dementia with Lewy bodies Alzheimer's disease
- Registration Number
- JPRN-UMIN000003419
- Lead Sponsor
- Department of Neurology and Neurobiology of Aging, Kanazawa University School of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 140
Not provided
(1) Exclusion criteria related to I-123 MIBG caridac scintigrphy Excluded are the conditions affecting I-123 MIBG myocardial accumulation as shown below: 1. The patient taking tricyclic antidepressants and/or reserpine. 2. The patient having cardiac failure. 3. The patient having ischemic heart disease within six months to participate in this study. 4. The patient having myocardial blood flow SPECT abnormalities within one year to participate in this study. 5. The patient planning surgeries of major arteries including revascularization within 2 months to participate in this study. 6. The patient having poorly controlled NIDDM [HbA1c >7.0%] or insulin therapy. 7. The patient having severe kidney dysfunction or renal failure [eGFR<15 mL/min/1.73m2]. 8. The patient having hemodialysis. 9. The patient having pheochromocytoma. 10. The patient having amyloid neuropathy or other obvious peripheral neuropathy. 11. The patient having history of neoplasm within five years to participate in this study. 12. The patient having pregnant, nursing or probability of pregnancy. (2) Other exclusion criteria 1. Parkinson's disease, cerebral infarction which affects cognitive function, Huntington disease, normal pressure hydrocephalus, brain tumor, progressive supranuclear palsy, epilepsy, subdural hematoma, multiple sclerosis, head injury with aftereffect. 2. The patient having infection or focal regions revealed by MRI such as cerebral infarction which affects cognitive function. 3. The patient having cardiac pacemaker, aneurysm clip, prosthetic valve, cochlear implant, or other metal implants. 4. The patient having history of alcohol or drug abuse, sever disease or unstable disease, deficiency of vitamin B12 or folic acid, syphilis, or thyroid dysfunction. 5. The case judged by clinical evaluation committee as inappropriate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate usefulness of the each parameter such as heart to mediastinum ratio (early image), heart to mediastinum ratio (delayed image), washout rate(%) and visual rating of 123I-MIBG myocardial scintigraphy in differentiating probable DLB from probable AD.
- Secondary Outcome Measures
Name Time Method To evaluate the usefulness of each parameter of 123I-MIBG myocardial scintigraphy for early diagnosis of DLB after following up of possible DLB cases for 3 years, etc.