Dementia with Lewy Bodies (DLB) is a progressive degenerative disease or syndrome of the brain. It shares symptomsand sometimes
overlapswith several diseases, especially Alzheimer's and Parkinson's.
People who develop DLB have behavioral and memory symptoms of dementia like those of Alzheimer's Disease and, to varying extents, the
physical, motor system symptoms seen in Parkinson's Disease. However, the mental symptoms of a person with DLB might fluctuate frequently,
motor symptoms are milder than for Parkinson's, and DLB patients usually have vivid visual hallucinations.
Dementia with Lewy Body (DLB) is also called "Lewy Body Dementia" (LBD), "Diffuse Lewy Body Disease", "Lewy Body Disease", "Cortical Lewy
Body Disease", "Lewy Body Variant of Alzheimer's Disease" or "Parkinson's Disease Dementia." It is the second most common dementia,
accounting for 20% of those with dementia (Alzheimer's Disease is first). Dementia is a gradual, progressive decline in mental ability
(cognition) that affects memory, thinking processes, behavior and physical activity. In addition to these mental symptoms, persons with DLB
experience physical symptoms of parkinsonism, including mild tremor, muscle stiffness and movement problems. Strong visual hallucinations
DLB is named after smooth round protein lumps (alpha-synuclein) called Lewy bodies, that are found in the nerve cells of the affected
parts of the brain. These "abnormal protein structures" were first described in 1912 by Frederich Heinrich Lewy, M.D., a contemporary of
Alois Alzheimer who first identified the more common form of dementia that bears his name.
Lewy bodies are found throughout the outer layer of the brain (the cerebral cortex) and deep inside the midbrain and brainstem. They are
often found in those diagnosed with Alzheimer's, Parkinson's, Down syndrome and other disorders.
The cause of DLB is unknown and no specific risk factors are identified. Cases have appeared among families but there does not seem to be
a strong tendency for inheriting the disease. Genetic research may reveal more information about causes and risk in the future. It usually
occurs in older adults between 50-85 years old and slightly more men than women have the disease.
Initial symptoms of DLB usually are similar to those of Alzheimer's or Vascular Dementia and are cognitive in nature, such as acute
confusion, loss of memory, and poor judgment. Other patients may first show the neuromuscular symptoms of parkinsonismloss of
spontaneous movement, rigidity (muscles feel stiff and resist movement), and shuffling gait, while still others may have visual
hallucinations as the first symptom. Patients may also suffer from delusions or depression.
Key symptoms are:
- Problems with recent memory such as forgetting recent events.
- Brief episodes of unexplained confusion and other behavioral or cognitive problems. The individual may become disoriented to the time or
location where he or she is, have trouble with speech, have difficulty finding words or following a conversation, experience visuospatial
difficulty (for example, finding one's way), and have problems in thinking such as inattention, mental inflexibility, indecisiveness, lack
of judgment, lack of initiative and loss of insight.
- Fluctuation in the occurrence of cognitive symptoms from moment to moment, hour to hour, day to day or week to week. For example, the
person may converse normally one day and be mute and unable to speak the next day. There are also fluctuations in attention, alertness and
- Well defined, vivid, recurrent visual hallucinations. These hallucinations are well formed and detailed. In DLB's early stage, the
person may even acknowledge and describe the hallucinations. They are generally benign and patients are not scared by them. Hallucinations
may also be auditory (hearing sounds), olfactory (smelling or tasting something) or tactile (feeling or touching something that is not
- Movement problems of parkinsonism, sometimes referred to as "extrapyramidal" signs. These symptoms often seem to start spontaneously and may include flexed posture, shuffling gait, muscle jerks or twitches, reduced arm swing, loss of dexterity, limb stiffness, a tendency to fall, balance problems, bradykinesia (slowness of movement), tremor, shakiness, and lack of facial expression.
- Rapid Eye Movement Sleep Behavior Disorder. This is characterized by vivid dreaming, talking in one's sleep, and excessive movement while asleep, including occasionally hitting a bed partner. The result may be excessive daytime drowsiness and this symptom may appear years before DLB is diagnosed. About 50% of patients have this symptom.
Movement and motor problems occur in later stages for 70% of persons with DLB. But for 30% of DLB patients, and more commonly those that are older, Parkinson's symptoms occur first, before dementia symptoms. In these individuals, cognitive decline tends to start with depression or mild forgetfulness.
Testing and Diagnosis
Dementia with Lewy bodies is difficult to diagnose. Not only does it resemble other dementias, it overlaps with Alzheimer's, Parkinson's
and other disorders which may result in it being difficult to rule out or exclude. Because no single test exists to diagnose DLB, a variety
of medical, neurological and neuropsychological tests are used to pinpoint it and its possible overlap with other illnesses. A definitive
diagnosis can only be made by an autopsy at death. There are no medications currently approved to specifically treat DLB.
Although Lewy bodies are found in brains of patients with other diseases, and because testing will involve several approaches, it is
useful to understand what happens to the brain of a person with DLB. Three significant changes or pathological features are seen in brains
afflicted by DLB:
- The brain's cerebral cortex (outer layers of the brain) degenerates or shrinks. This can affect reasoning and complex thinking,
understanding personality, movement, speech and language, sensory input and visual perceptions of space. Degeneration also occurs in the
limbic cortex at the center of the brain, which plays a major role in emotions and behavior. Lewy bodies form throughout these degenerating
- Nerve cells die in the midbrain, especially in an area that also degenerates in Parkinson's disease, the substantia nigra, located in
the brainstem. These cells are involved in making the neurotransmitter (brain messenger) dopamine. Lewy bodies are found in the nerve cells
that remain. The midbrain is involved in memory formation and learning, attention, and psychomotor (muscular movement) skills.
- Lesions called Lewy neuritis that affect nerve cell function are found in DLB brains, especially in the hippocampus, an area of the
brain essential for forming new memories.
None of the symptoms of Dementia with Lewy Bodies is specific only to DLB. To address this problem, an international group of researchers
and clinicians developed a set of diagnostic criteria in 1995, called the Consensus Guidelines that can reliably point to DLB:
Must be present:
- Progressive cognitive decline (decrease in thinking ability) that interferes with normal social or occupational activities. Memory
problems do not necessarily occur in the early period but will occur as DLB progresses. Attention, language, understanding and reasoning,
ability to do arithmetic, logical thinking and perceptions of space and time will be impaired.
Two of the following are present (one also indicates possibility of DLB):
- Fluctuating cognition and mental problems, vary during the day, especially attention and alertness.
- Visual hallucinations, detailed and well-formed visions occur and recur.
- Parkinsonism: motor related and movement problems appear.
A DLB diagnosis is even more likely if the patient also experiences repeated falls, fainting, brief loss of consciousness, delusions, or
is sensitive to neuroleptic medications that are given to control hallucinations and other psychiatric symptoms.
Finally, the timing of symptoms is a reliable clue: if both mental and motor symptoms appear within one year of each other, DLB is
more likely the cause. Signs of stroke or vascular dementia usually negate the likelihood of DLB.
Testing is usually done to rule out other possible causes of dementia. Brain imaging (CT scan or MR imaging) can detect brain shrinkage
and help rule out stroke, fluid on the brain (normal pressure hydrocephalus), or subdural hematoma. Blood and other tests might show vitamin
B 12 deficiency, thyroid problems, syphilis, HIV, or vascular disease. Depression is also a common cause of dementia-like symptoms.
Additional tests can include an electroencephalogram (EEG) or spinal tap. Scans using SPECT or PET technology have shown promise in
detecting differences between DLB and Alzheimer's disease.
Alzheimer's and Parkinson's: Differences and Overlap with DLB
DLB's similarity to Alzheimer's and Parkinson's diseases and the fact that Lewy bodies are often found in the brains of patients with
these diseases means that clinicians must pay close attention to the factors that distinguish DLB:
- Memory and other cognitive problems occur in both DLB and Alzheimer's. However, in DLB they fluctuate frequently.
- DLB patients experience more depression than do Alzheimer's patients.
- Hallucinations are experienced by Alzheimer's patients in late stages, and by Parkinson's patients who take medications to improve
movement and tremor. In DLB, hallucinations occur in early stages, and they are frequent, vivid and detailed.
- Neuroleptic drugs (sometimes called psychotropic drugs) prescribed to lessen the so-called psychiatric symptoms of dementia, such as
hallucinations, agitation or restlessness will induce Parkinson's in some DLB patients.
- Life expectancy is slightly shorter for DLB than for Alzheimer's patients.
- At autopsy the brains of DLB patients have senile plaques, a hallmark of Alzheimer's. Another Alzheimer's feature, neurofibrillary
tangles, are absent or found in fewer numbers and are concentrated in the neocortex. Other Alzheimer's features—regional neuronal loss,
spongiform change and synapse loss, neurochemical abnormalities and neurotransmitter deficits—are also seen. However, DLB-afflicted brains
are less damaged than are Alzheimer's brains.
- In DLB movement problems are spontaneous; the symptoms begin suddenly.
- Tremor is less pronounced in DLB than in Parkinson's. Also, DLB patients respond less dramatically to drugs such as Levodopa that are
used to treat Parkinson's. Nerve cell loss in the subtantia nigra is not as severe in DLB.
Both DLB and Parkinson's patients may sometimes experience fainting and wide alterations in blood pressure.
Some Parkinson's patients develop dementia in later stages. Dementia is usually the presenting symptom in DLB.
- Parkinson's patients lose the neurotransmitter dopamine; Alzheimer's patients lose the neurotransmitter acetylcholine. DLB patients lose
- In DLB, Alzheimer-like and Parkinson-like symptoms appear within one year of each other.
Despite these differences, a diagnosis of Dementia with Lewy Bodies does not preclude a positive diagnosis of Alzheimer's, Parkinson's or
other diseases common in older age.
Duration and Treatment
With an average lifespan after onset of 5 to 7 years, the progress of Dementia with Lewy Bodies is relentless; however, the rate of
decline varies with each person. DLB does not follow a pattern of stages as is seen in some other dementias. Death usually occurs from
pneumonia or other illness. There is neither cure nor specific treatment to arrest the course of the disease.
Caution must be used in treating a person with DLB. Medications must be monitored closely for proper balance because some patients are
adversely affected by some drugs. Neuroleptic (tranquilizing) anti-psychotic medications such as haloperidol (Haldol) or thioridazine
(Mellaril), as well as benzodiazepines (Valium, Ativan) and anti-histamines can cause extreme adverse reactions in DLB patients. Side
effects include motor related symptoms, catatonia (non-responsiveness), loss of cognitive function and/or development of muscle rigidity.
These medications are sometimes used in Alzheimer's patients to help with hallucinations and behavioral symptoms, but should not be used in
patients with DLB. Levodopa may be given to treat the parkinsonism, however, it may increase the hallucinations of DLB patients and
aggravate other symptoms, such as cognitive functioning. It is less effective in treating tremor in DLB patients than in Parkinson's
patients. Aricept or other cholinesterase inhibitors are given to treat the hallucinations. Some anti-depressants have shown positive
results, while others are counter indicated.
When considering surgery, families should meet with the anesthesiologist to discuss possible side effects of anesthesia, as DLB patients
are prone to delusions and a decline in motor functioning after anesthesia.
Caregiving and DLB
DLB patients can live at home with frequent reassessment and careful monitoring and supervision. Caregivers must watch the patient
closely because of the tendency for them to fall or lose consciousness. Particular care should be taken when a patient is standing up from a
chair or getting out of bed, as blood pressure can drop, causing the patient to lose his or her balance. Dementia prevents patients from
learning new actions that might help them overcome movement problems, such as learning to use a walker. They may need more assistance some
days than others, and can be reassured by a caregiver's help in turning attention away from the hallucinations.
Caregivers must learn to navigate both skills in dealing with cognitive, behavioral and motor disabilities. Attending support groups and
learning skills in how to communicate with someone with dementia as well as learning skills in helping someone with a motor disorder will
reduce caregiver stress and frustration.
Caregivers can turn to a California Caregiver Resource Center for assistance and to a qualified diagnostic center for initial diagnosis
and follow up. In other states, resources can be found through local and state offices on aging and health such as your Area Agency on Aging
or the Alzheimer's Association in your area.
Credits and References
Lewy Body Dementia Association. P.O. Box 451429. Atlanta, GA 31145. (404) 422-5434. www.lbda.org
Riding the Roller Coaster with Lewy Body Dementia by Helen Whitworth, available at
[email protected], or (480) 981-1117.
LewyNet, The University of Nottingham, Division of Pathology, University Park, Nottingham, England NG7 2RD. Telephone +44 115 9515151.
Web site: http://www.ccc.nottingham.ac.uk/~mpzjlowe/lewy/lewyhome.html.
"Dementia with Lewy Bodies: A Distinct Non-Alzheimer Dementia Syndrome?" by Paul G. Ince, Elaine K. Perry, and Chris M. Morris, Brain
Pathology, April, 1998. (Available with extensive bibliographies at LewyNet web site.)
"Similarities to Alzheimer's and Parkinson's Make Lewy Body Dementia Difficult to Recognize and Challenging to Treat," John Douglas
French Center for Alzheimer's Disease Journal, 1998/1999.
Parkinson's Disease UPDATE, a monthly newsletter, Medical Publishing Company, P. O. Box 450, Huntingdon Valley, PA 19006. Issue #10,
"Dementia with Lewy Bodies" by Ian G. McKeith, M.D., FRCPsych., High Notes, News from the John Douglas French Alzheimer's Foundation,
"Consensus guidelines for the clinical and pathological diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB
International Workshop," by I. G. McKeith, D. Galasko, K. Kosaka, E. K. Perry, et al, 1996. Neurology, 47:1113-24.
Dementia with Lewy Bodies by Robert H. Perry, Ian G. McKeith, and Elaine K. Perry (editors), Forward by Jeffrey L. Cummings, 1996.
Cambridge University Press, Cambridge.
Ala, T. A., Yang, K. H., Sung, J. H., Frey, W. H., 1997. Hallucinations and signs of parkinsonism help distinguish patients with dementia
and cortical Lewy bodies from patients with Alzheimer's disease at presentation: a clinicopathological study. Journal of Neurology,
Neurosurgery and Psychiatry, 62:16-21.
Dickson, D. W., Ruan, D., Crystal, H., Mark, M. H., et al, 1991. Hippocampal degeneration differentiates diffuse Lewy body disease (DLBD)
from Alzheimer's disease. Neurology, 41:1402-9.
Galasko, D., Katzman, R., Salmon, D. P., Hansen, L., 1996. Clinical features and neuropathological findings in Lewy body dementias. Brain
Graham, C., Ballard, C., Saad, K., 1997. Variables which distinguish patients fulfilling clinical criteria for dementia with Lewy bodies
from those with dementia, Alzheimer's disease. International Journal of Geriatric Psychiatry, 12:314-8.
Hansen, L. A., Samuel, W. 1997. Criteria for Alzheimer's disease and the nosology of dementia with Lewy bodies. Neurology, 48:126-32.
Ince, P., Irving, D., MacArther, F., Perry, R.H., 1991. Quantitative neuropathology of the hippocampus: comparison of senile dementia of
Alzheimer type, senile dementia of Lewy body type, Parkinson's disease and non-demented elderly control patients. J Neurol Sci,
Ince, P. G., McArthur, F. K., Bjertness, E., Torvik, A., et al, 1995. Neuropathological diagnoses in elderly patients in Oslo:
Alzheimer's disease, Lewy body disease and vascular lesions. Dementia, 6:162-8.
Klatka, L. A., Louis, E. D., Schiffer, R. B., 1996. Psychiatric features in diffuse Lewy body disease: a clinicopathological study using
Alzheimer's disease and Parkinson's disease. Neurology, 47:1148-52.
Kosaka, K., Iseki, E., Odawara, T., et al, 1996. Cerebral type of Lewy body disease. Neuropathology, 16:32-5.
Louis, E. D., Klatka, L. A., Lui, Y., Fahn, S., 1997. Comparison of extrapyramidal features in 31 pathologically confirmed cases of
diffuse Lewy body disease and 34 pathologically confirmed cases of Parkinson's disease. Neurology, 48:376-80.
McKeith, I. G., Fairbairn, A., Perry, R. H., Thompson, P., Perry, E. K., 1992. Neuroleptic sensitivity in patients with senile dementia
of Lewy body type. British Medical Journal, 305:673-8.
Mega, M. S., Masterman, D. L., Benson, D. F., Vinters, H. V., et al, 1996. Dementia with Lewy bodies: reliability and validity of
clinical and pathological criteria. Neurology, 47:1403-9.
Perry, E. K., Haroutunian, V., Davis, K. L., Levy, R., et al, 1994. Neocortical cholinergic activities differentiate Lewy body dementia
from classical Alzheimer's disease. Neuroreport, 5:747-9.
Salmon, D. P., Glasko, D., Hansen, L. A., Masliah, E. et al, 1996. Neuropsychological deficits associated with diffuse Lewy body disease.
Brain Cognition, 31:148-65.
Samuel, W., Alford, M., Hofstter, C. R., Hansen, L., 1997. Dementia with Lewy bodies versus pure Alzheimer's disease: differences in
cognition, neuropathology, cholinergic dysfunction, and synaptic density. Journal of Neuropathology and Experimental Neurology,
Family Caregiver Alliance
785 Market Street, Suite 750
San Francisco, CA 94103
(415) 434-3388 or
(415) 434-3408 (Fax)
E-mail: [email protected]
Web Site: www.caregiver.org
Family Care Navigator: http://caregiver.org/caregiver/jsp/fcn_content_node.jsp?nodeid=2083
Family Caregiver Alliance (FCA) seeks to improve the quality of life for caregivers through education, services, research and
FCA's National Center on Caregiving offers information on current social, public policy and caregiving issues; provides assistance in the
development of public and private programs for caregivers; publishes timely reports, newsletters and fact sheets; and assists caregivers
nationwide in locating resources in their communities.
For residents of the greater San Francisco Bay Area, FCA provides direct family support services for caregivers of those with Alzheimer's
disease, stroke, ALS, head injury, Parkinson's and other debilitating health conditions that occurs most often in adults.
Reviewed by William Jagust, MD and prepared by Family Caregiver Alliance. February 2001. Updated June, 2010. Funded by the Alameda County
Area Agency on Aging and the California Department of Mental Health. ©2010 All rights reserved.
E-mail to a Friend