Nutritional Diseases of the Nervous System Flashcards
Acute effects of ethanol
Severe cerebral edema
Large quantities of alcohol can lead to death from central cardiorespiratory paralysis
Chronic effects of ethanol
- Meningeal fibrosis
- Cerebral cortex white matter volume loss, neuronal loss and dendritic reduction;
- Cerebellar vermis: crests of folia most affected, granule cell neurons> Purkinje cell neurons lost
Fetal alcohol syndrome
- Hyperactivity, poor motor skills, learning difficulties; severely affected kids have mental retardation
- No single laboratory test to make diagnosis
- Brain damage due to liver disease/cirrhosis
Hepatic encephalopathy
- Asterixis, stupor, coma
- Putative toxins: ammonia, mercaptans, short-chain fatty acids, benzodiazepine-like substances, GABA-like substances, impaired glutamatergic neurotransmission
- Grey matter astrocytes transform to “Alzheimer II” (metabolically active) astrocytes, especially in deep cerebral cortex and subcortical structures
Wilson’s disease
Autosomal recessive disorder of copper metabolism, gene localized to chromosome 13
Hepatic failure most common presentation in young children (heptatic encephalopathy)
Choreoathetosis and dementia may be present in young adults
The putamen is the major site of damage followed by the globus pallidus
Thiamine deficiency
(vitamin B1): associated with chronic alcoholism
Wernicke’s encephalopathy - full triad of ataxia, nystagmus (or ophthalmoplegia) and confusion may be absent
Selective vulnerability: mammillary bodies, walls of third ventricle, medial thalamus, inferior colliculi, brainstem tegmentum
Peripheral neuropathy
Cobalamin deficiency (vitamin B12)
Vegans
Can cause megaloblastic anemia
Subacute combined degeneration - paresthesias, ataxia, diminished vibration sense or proprioception
Dementia - psychoses, mood disturbances
Selective vulnerability: posterior and lateral spinal cord white matter, especially in lower cervical and thoracic cord; cerebral white matter
Central pontine myelinolysis (CPM)
- Disease first appeared in 1950’s following “plastic revolution” with advent of intravenous tubing and fluid administration
- Mostly occurs in patients with chronic medical conditions including cancer, liver disease, liver transplantation, sepsis, burns
- Patients have fluid and electrolyte imbalances
- Many cases clinically silent; quadraparesis and “locked in syndrome” with severe lesions
- Ventral pons and extrapontine sites
- Excessive, rapid correction and/or overcorrection of hyponatremia is causative
- Slower correction of hyponatremia and possibly administration of organic osmoles such as myoinositol are preventative/therapeutic
Korsakoff Syndrome
Memory loss found in thiamine deficiency
Involvement of the dorsomedial nucleus of the thalamus