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Printable Handouts
Navigable Slide Index
- Introduction
- Lewy body dementia
- DLB underdiagnosis and lack of a systematic approach to management
- Very poor outcomes in DLB
- Prevalence of DLB in the UK
- Clinical diagnostic criteria (1)
- Clinical diagnostic criteria: core clinical features
- Core clinical features: fluctuating cognition
- Core clinical features: Parkinsonism
- Core clinical features: visual hallucinations
- Core clinical features: REM sleep behaviour disorder
- Clinical diagnostic criteria (2)
- Supportive clinical features
- Clinical diagnostic criteria (3)
- Indicative biomarkers
- Clinical diagnostic criteria: supportive biomarkers
- Structural imaging of the medial temporal lobe
- Functional imaging (SPECT/PET)
- EEG as a biomarker
- Problems in diagnosing dementia with Lewy bodies
- The DIAMOND Lewy study
- Diagnostic assessment toolkit for DLB (1)
- Diagnostic assessment toolkit for DLB (2)
- Impact of the diagnostic assessment toolkit
- Prodromal DLB
- Diagnostic criteria for MCI-Lewy body
- Management of dementia with Lewy bodies
- DLB therapeutic challenges
- How do we manage it?
- Taking a holistic perspective
- LBD management guideline
- Cognitive symptoms
- 18–month cluster design pragmatic trial
- Pathways going forward for treatment of DLB
- Targeting alpha-synuclein
- Thank you!
Topics Covered
- Lewy body dementia (LBD)
- Underdiagnosis of Dementia with Lewy Body (DLB)
- DLB Outcomes
- Prevalence of DLB in the UK
- Clinical diagnostic criteria
- Problems in diagnosing dementia with Lewy bodies
- The DIAMOND Lewy study
- The Diagnostic assessment toolkit
- Management of dementia with Lewy bodies
- Targeting alpha-synuclein
Links
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External Links
Talk Citation
Taylor, J. (2021, November 28). Lewy body dementia [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/BWSR8226.Export Citation (RIS)
Publication History
Financial Disclosures
- Professor John-Paul Taylor receives fees from GE Healthcare and Lundbeck Grant funding and consultancy from Sosei-Heptares Consultancy with Kirin-Kyowa.
A selection of talks on Neuroscience
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, my name is John-Paul Taylor.
I am a professor of Translational Dementia Research
at Newcastle University, United Kingdom.
I'm going to be presenting today a summary of "Lewy Body Dementia",
focusing on diagnosis, emerging concepts,
and the management of this condition.
0:18
Before proceeding further, it is important to
address the nomenclature of Lewy body dementia.
Lewy body dementias are part of a spectrum of
Lewy body diseases and include both Parkinson's disease dementia, PDD,
and dementia with Lewy bodies, DLB.
The two conditions are differentiated from each other on the basis of the timing of
motor Parkinsonism symptoms relative to dementia onset.
Typically PDD may manifest where there is established
Parkinson's disease and then there is
a subsequent cognitive decline and functional impairment as a result.
In DLB the dementia occurs before or concurrently
with Parkinsonism or within one year of onset of the motor symptoms.
Splitting DLB from PDD at the moment is still
arbitrary with the one-year rule and sometimes using
the catch-all term of the Lewy body dementia is appropriate where
the onset of either the motor or dementia symptoms is not entirely clear.
For the purposes of the current presentation,
it should be noted that the weight of the discussion is very much on DLB,
although there are very strong overlaps in the management of both DLB and PDD.
1:20
A major problem for DLB is the underdiagnosis of
the condition and a lack of a systematic approach to management.
In people who have died with dementia,
neuropathological interrogation of the brains demonstrates that
15-20 percent have evidence for Lewy body disease.
Indeed some more recent reports suggest that this figure may be higher up to a
quarter of people who have died with dementia may have evidence of Lewy body disease.
In contrast in Parkinson's research studies have suggested
that the diagnostic rates clinically are much lower,
4-7 percent and the rates may be even much lower again in routine clinical services.
We know from several studies,
for example, one here from Galvin and colleagues,
that there is an under-recognition of DLB and many patients receive misdiagnosis,
for example, of Alzheimer's disease.
This is despite the fact that the quality of life for people living with DLB and
their caregivers appears to be a lot lower than comparable dementias.
A management of the condition is fractured between different clinical services.