Related Experiment Video
Updated: Apr 17, 2026

12:28
Abbiategrasso Brain Bank Protocol for Collecting, Processing and Characterizing Aging Brains
Published on: June 3, 2020
18.5K
Prodromal dementia with Lewy bodies
Hiroshige Fujishiro1, Shinichiro Nakamura2, Kiyoshi Sato3
1Department of Sleep Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Geriatrics & Gerontology International
|February 19, 2015
Summary
Prodromal Dementia with Lewy bodies (DLB) symptoms like RBD can predict the disease years before dementia. Identifying these early signs is crucial for potential interventions and understanding DLB progression.
Area of Science:
- Neurodegenerative Disorders
- Neurology
- Geriatrics
Background:
- Dementia with Lewy bodies (DLB) is the second most common neurodegenerative dementia after Alzheimer's disease (AD).
- Limited information exists on the prodromal state of DLB compared to AD.
- Parkinson's disease (PD) and DLB share prodromal symptoms indicative of Lewy body disease (LBD).
Purpose of the Study:
- To review the limited literature on the clinical profiles of prodromal DLB.
- To highlight the importance of identifying prodromal LBD symptoms for early prediction and intervention.
- To discuss the role of Rapid Eye Movement sleep Behavior Disorder (RBD) in DLB progression.
Main Methods:
- Literature review of clinical profiles of prodromal DLB.
- Analysis of shared prodromal symptoms between PD and DLB.
- Discussion of neuroimaging techniques for predicting LBD pathophysiology.
Main Results:
- Prodromal symptoms of DLB include dysautonomia, olfactory dysfunction, RBD, and psychiatric symptoms, often preceding dementia by years.
- Rapid Eye Movement sleep Behavior Disorder (RBD) is a potentially accurate prodromal predictor, though its impact on disease progression may vary.
- Occipital hypoperfusion/hypometabolism and specific neuroimaging findings can aid in predicting LBD pathophysiology in non-demented individuals.
Conclusions:
- Early identification of prodromal DLB symptoms, particularly RBD, is vital for understanding disease progression and enabling timely therapeutic interventions.
- Further large-scale, multi-site studies with pathological verification are needed to clarify the clinical relevance and diversity of DLB progression.
- The long prodromal phase of DLB offers a critical window for disease-modifying therapies, contingent on accurate identification of clinical trajectories.
Related Concept Videos
Dementia
730
Dementia is a collective term for cognitive disorders primarily affecting memory, thinking, and reasoning. It is not a specific disease but a syndrome, with Alzheimer's disease being the most common cause, accounting for approximately 60-80% of cases. Other types include vascular dementia, Lewy body dementia, and frontotemporal dementia. Dementia affects millions worldwide, particularly older adults, though it is not a normal part of aging.
The progression of dementia is generally gradual....
The progression of dementia is generally gradual....
730
Parkinson's Disease: Overview
2.5K
Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is...
2.5K
Alzheimer's Disease: Overview
2.0K
Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
2.0K
Neural Regulation
45.2K
Digestion begins with a cephalic phase that prepares the digestive system to receive food. When our brain processes visual or olfactory information about food, it triggers impulses in the cranial nerves innervating the salivary glands and stomach to prepare for food.
45.2K
Parkinson's Disease: Treatment
1.4K
Neurodegenerative disorders, such as Parkinson's Disease (PD), involve the gradual and irreversible destruction of neurons in particular brain areas. These disorders exhibit standard features like proteinopathies, selective vulnerability of some neurons, and an interaction of intrinsic properties, genetics, and environmental influences in neural injury.
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of...
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of...
1.4K
Alzheimer's Disease: Treatment
1.3K
Alzheimer's Disease (AD), a neurodegenerative disorder, is pathologically identified by amyloid plaques and neurofibrillary tangles composed of tau protein. AD pharmacotherapy aims to manage cognitive symptoms, delay disease progression, and treat behavioral symptoms. The treatment is primarily symptomatic and palliative, with no definitive disease-modifying therapy available. Cholinesterase inhibitors, including donepezil (Aricept), rivastigmine (Exelon), and galantamine (Razadyne), are...
1.3K

