Non Alzheimer Dementias

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Non Alzheimer Dementias Randolph B Schiffer Department of Neuropsychiatry and Behavioral Science Texas Tech University Health Sciences Center 9/11/2007

Statement of Financial Disclosure Randolph B Schiffer,, MD Dr. Schiffer is on no industry speakers bureaus Dr. Schiffer also acknowledges that he has not received other compensation including honoraria, consultant fees and educational program development funds from industry sources Dr. Schiffer is not a major stockholder in any of the pharmaceutical companies

Objectives To familiarize the audience with the clinical features and diagnostic criteria for the most common non-alzheimer dementias To review available treatment information for these non-ad dementias

Factual Statement Number 1 EVERYBODY WITH A MEMORY DISORDER DOES NOT HAVE ALZHEIMER DISEASE (AD)

Types of Non-AD Memory Disorders Non-AD Neurodegenerative Syndromes Vascular Syndromes Non-Neurodegenerative, Non- Vascular

Non-AD Neurodegenerative Disorders Fronto-Temporal Disorders Parkinson s Disease (PD) Spectrum Disorders

The Frontotemporal Lobar Dementia Syndromes (FTLD) Frontotemporal Dementia syndromes Progressive Semantic Dementia Progressive Non-Fluent aphasia Motor Neuron Syndromes Persistent Psychotic Syndromes

FTLD Clinical Features Personality change of frontal lobe type; apathy, disinhibition, fronto-executive type cognitive loss Affective symptoms; depression, emotional dysregulation Speech/language disorder; mutism, aphasia Motor neuron loss

FTLD Clinical Course and Treatment May be younger than AD patients May be older than AD patients May progress faster than AD patients May progress slower than Ad patients Cholinesterase inhibitors contraindicated SSRI psychiatry drugs may help

PD Spectrum Disorders Idiopathic PD Multi-System Atrophy Lewy Body Dementia Essential Tremor Cortico-basal ganglionic Degeneration Progressive Supranuclear Palsy

Dementia with Lewy Bodies (DLB) Clinical Features Cortical dementia Atypical parkinsonism Hallucinations and delusions Depression Psychotropic drug sensitivity Fluctuations in consciousness Falls

DLB Diagnostic Criteria A. Cortical dementia B. Two of the following; fluctuating cognition, recurrent visual hallucinations, parkinsonism C. Supportive features D. Warning features; stroke, other neuromedical illness

DLB Clinical Course and Treatment Clinical progression probably faster than AD Positive response to cholinesterase inhibitors (most of them have Ad neuropathology, too) L-DOPA Lazarus responses

Vascular Dementia What is it? Cognitive Loss Syndrome attributable to some combination of; thromboembolic stroke(s), small vessel lacunar strokes, chronic ischemia with neuronal loss (Binswanger s disease), hemorrhages

Problems with Vascular Dementia Syndrome We have competing sets of diagnostic criteria for Vascular dementia At autopsy, most people with Vascular Dementia have AD MRI scans are not very reliable in sorting vascular dementia from AD The most powerful disease modulators for AD may be vascular risk factors

Vascular Dementia It Must be Out There

Vascular Dementia Criteria at Texas Tech Cognitive decline in two domains Neurovascular disease, indicated by focal exam findings, imaging Relationship between vascular disease and dementia Exclusion criteria

Vascular Dementia Clinical Course and Treatment Median survival from onset 3.3 years Positive response to cholinesterase inhibitors Risk factor management

Non-Degenerative Non-Vascular Syndromes Psychodementias Trauma Infection Autoimmune Brain Syndromes Toxin exposure Metabolic syndromes

Psychodementia Cognitive loss syndrome in association with a general psychiatric disorder, sufficient to cause impairment of psychosocial or vocational function

Psychodementia Clinical Criteria Subjective complaint of memory loss, with or without other cognitive domain affected Demonstrated cognitive dysfunction on standardized test(s) Causal association of intercurrent general psychiatric disorder, in judgment of clinician

Frequency Rates of Psychodementia in Texas Tech Memory Disorders Program N=13; Depression=4; Psychosocial stress=2; Subjective cognitive loss=2; GAD=1; Bereavement=1; Conversion=1Sensory deprivation=1; Sleep disorder=1 Non AD psych syndromes=11% of total; Psychodementia

Summary Non-Alzheimer syndromes account for about 20% of subjects in University Memory Disorder programs They are a heterogeneous group Their treatments are substantially different from AD