Dementia pathophysiology: Difference between revisions

Jump to navigation Jump to search
No edit summary
Line 3: Line 3:
{{CMG}};{{AE}},{{SAI}}
{{CMG}};{{AE}},{{SAI}}


== Overview ==
==Overview==


== Pathophysiology ==
==Pathophysiology==
<br />__NOTOC__
While the pathogenesis of AD remains unclear, It is thought that Dementia  is the result of
 
* overproduction and/or decreased clearance of amyloid beta peptides
* accumulation of tau proteins
* accumulation of neurofibrillary tangles
* production of oxygen radicals and nitric oxide, and inflammatory processes
* decreased levels of cholinergic neurotransmission.
* Over-excitation of the glutamate neurotransmitter system via N-methyl-D-aspartate receptors 
 
These changes are usually present in the hippocampus, amygdala, cortex, and nucleus basalis
 
<br />
__NOTOC__
{{Template:Dementia}}
{{Template:Dementia}}


== References ==
==References==
{{reflist|2}}
{{reflist|2}}
{{WH}}
{{WH}}

Revision as of 23:15, 28 September 2020

Dementia Microchapters

Patient Information

Overview

Classification

Causes

Differential Diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: ,Sabeeh Islam, MBBS[2]

Overview

Pathophysiology

While the pathogenesis of AD remains unclear, It is thought that Dementia is the result of

  • overproduction and/or decreased clearance of amyloid beta peptides
  • accumulation of tau proteins
  • accumulation of neurofibrillary tangles
  • production of oxygen radicals and nitric oxide, and inflammatory processes
  • decreased levels of cholinergic neurotransmission.
  • Over-excitation of the glutamate neurotransmitter system via N-methyl-D-aspartate receptors

These changes are usually present in the hippocampus, amygdala, cortex, and nucleus basalis


Dementia Microchapters

Patient Information

Overview

Classification

Causes

Differential Diagnosis

References

Template:WH Template:WS