Movement disorders experts from Rush answer frequently asked questions about Lewy body dementia.
What is Lewy Body Dementia?
LBD is a disease associated with abnormal deposits of a protein called alpha-synuclein in the brain. These deposits, called Lewy bodies, affect chemicals in the brain whose changes, in turn, can lead to problems with thinking, movement, behavior, and mood. LBD is one of the most common causes of dementia, after Alzheimer’s disease and vascular disease.
Dementia is a severe loss of thinking abilities that interferes with a person’s capacity to perform daily activities such as household tasks, personal care, and handling finances. Dementia has many possible causes, including stroke, brain tumor, depression, and vitamin deficiency, as well as disorders such as LBD, Parkinson’s, and Alzheimer’s.
Diagnosing LBD can be challenging for a number of reasons. Early LBD symptoms are often confused with similar symptoms found in other brain diseases like Alzheimer’s. Also, LBD can occur alone or along with Alzheimer’s or Parkinson’s disease.
What Are Lewy Bodies?
Lewy bodies are named for Dr. Friederich Lewy, a German neurologist. In 1912, he discovered abnormal protein deposits that disrupt the brain’s normal functioning in people with Parkinson’s disease. These abnormal deposits are now called “Lewy bodies.”
Lewy bodies are made of a protein called alpha-synuclein. In the healthy brain, alpha-synuclein plays a number of important roles in neurons (nerve cells) in the brain, especially at synapses, where brain cells communicate with each other. In LBD, alpha-synuclein forms into clumps inside neurons, starting in particular regions of the brain. This process causes neurons to work less effectively and, eventually, to die. The activities of brain chemicals important to brain function are also affected. The result is widespread damage to certain parts of the brain and a decline in abilities affected by those brain regions.
Which areas of the brain are affected?
Lewy bodies affect several different brain regions in LBD:
- The cerebral cortex, which controls many functions, including information processing, perception, thought, and language
- The limbic cortex, which plays a major role in emotions and behavior
- The hippocampus, which is essential to forming new memories
- The midbrain, including the substantia nigra, which is involved in movement
- The brain stem, which is important in regulating sleep and maintaining alertness
- Brain regions important in recognizing smells (olfactory pathways)
Who is affected by LBD?
Although less known than its “cousins” Alzheimer’s disease and Parkinson’s disease, LBD is not a rare disorder. More than 1 million Americans, most of them older adults, are affected by its disabling changes in the ability to think and move. LBD typically begins at age 50 or older, although sometimes younger people have it. LBD appears to affect slightly more men than women.
What are the stages of LBD?
LBD is a progressive disease, meaning symptoms start slowly and worsen over time. The disease lasts an average of 5 to 7 years from the time of diagnosis to death, but the time span can range from 2 to 20 years. How quickly symptoms develop and change varies greatly from person to person, depending on overall health, age, and severity of symptoms.
In the early stages of LBD, usually before a diagnosis is made, symptoms can be mild, and people can function fairly normally. As the disease advances, people with LBD require more and more help due to a decline in thinking and movement abilities. In the later stages of the disease, they may depend entirely on others for assistance and care.
Are there any effective treatments for LBD? Is there a cure?
Some LBD symptoms may respond to treatment for a period of time. Currently, however, there is no cure for the disease. Research is improving our understanding of this challenging condition, and advances in science may one day lead to better diagnosis, improved care and new treatments.
For instance, Rush is part of the , which is taking a deep dive into studying the biological changes of Lewy body dementias. Families struggle to get an early and accurate diagnosis, so your participation could help improve the early diagnosis of Lewy body dementia. Study participation involves imaging and neurological testing every six to 12 months to help us understand how these conditions progress. We are currently recruiting participants and their caregivers for this program. If you are interested, please contact clinical research coordinator Alice Negron at (312) 942-6686 or firstname.lastname@example.org.