Alzheimer's disease pathophysiology: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 11: Line 11:


==Pathogenesis==
==Pathogenesis==
Alzheimer disease (AD), is a progressive neurodegenerative disorder. The dysfunction of amyloid precursor protien (APP) metabolism and the resulting build up of of Aβ peptides and their aggregation in the form of senile plaques in the brain parenchyma of individuals have been considered pivotal for neurodegeneration in the disease. There is also an accumulation of intracellular neurofibrillary tangles that consist of hyperphosphorylated tau protein and a profound loss of basal forebrain cholinergic neurons that innervate the hippocampus, and the neocortex.
== Triggers ==
The following factors lead to the development of Alzheimer's dementia:
* Genetic factors
* Environmental factors
=== Genetic Factors ===
Genetic origin of Alzheimer's dementia  (AD) demonstrates an autosomal dominant pattern of inheritance. Alzheimer's dementia arising from genetic alterations may lead to early onset (<60 years) of disease. The following mutations are implicated in the development of AD are:
==== Early onset (Alzheimer's dementia-AD 1, 3 and 4) ====
30-50 percent of early-onset Alzheimer's dementia (AD) is associated with an autosomal dominant inheritance and consists of mutations in the following genes:
* Presenilin1 (''PS1'') gene, also called PSEN1 gene on chromosome 14  (AD3- 20 to 30 percent cases)
* Presenilin 2 (''PS2'') gene, also called PSEN2 gene on chromosome 1 (AD4- rare)
* Point mutations in amyloid beta A4 protein gene, also called amyloid precursor protein (APP) gene on chromosome 21 are associated in some cases of early onset (< 65 yr) familial AD cases
'''Late onset (Alzheimer's dementia -AD2)'''
* Apolipoprotein 4 gene (APOE4) mutation is associated with late onset (>60 years) Alzheimer's dementia (AD)
=== Hypotheses for Alzheimer's dementia ===
Two major hypothese for the development of Alzheimer's dementia (AD) have been proposed:
'''Amyloid cascade hypothesis'''<div style="-webkit-user-select: none;">





Revision as of 17:34, 17 September 2017

https://https://www.youtube.com/watch?v=v5gdH_Hydes%7C350}}

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Alzheimer's disease Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Alzheimer's disease from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic study of choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Alzheimer's disease pathophysiology On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Alzheimer's disease pathophysiology

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Alzheimer's disease pathophysiology

CDC on Alzheimer's disease pathophysiology

Alzheimer's disease pathophysiology in the news

Blogs on Alzheimer's disease pathophysiology

Directions to Hospitals Treating Alzheimer's disease

Risk calculators and risk factors for Alzheimer's disease pathophysiology

Overview

Pathogenesis

Alzheimer disease (AD), is a progressive neurodegenerative disorder. The dysfunction of amyloid precursor protien (APP) metabolism and the resulting build up of of Aβ peptides and their aggregation in the form of senile plaques in the brain parenchyma of individuals have been considered pivotal for neurodegeneration in the disease. There is also an accumulation of intracellular neurofibrillary tangles that consist of hyperphosphorylated tau protein and a profound loss of basal forebrain cholinergic neurons that innervate the hippocampus, and the neocortex.


Triggers

The following factors lead to the development of Alzheimer's dementia:

  • Genetic factors
  • Environmental factors

Genetic Factors

Genetic origin of Alzheimer's dementia (AD) demonstrates an autosomal dominant pattern of inheritance. Alzheimer's dementia arising from genetic alterations may lead to early onset (<60 years) of disease. The following mutations are implicated in the development of AD are:

Early onset (Alzheimer's dementia-AD 1, 3 and 4)

30-50 percent of early-onset Alzheimer's dementia (AD) is associated with an autosomal dominant inheritance and consists of mutations in the following genes:

  • Presenilin1 (PS1) gene, also called PSEN1 gene on chromosome 14 (AD3- 20 to 30 percent cases)
  • Presenilin 2 (PS2) gene, also called PSEN2 gene on chromosome 1 (AD4- rare)
  • Point mutations in amyloid beta A4 protein gene, also called amyloid precursor protein (APP) gene on chromosome 21 are associated in some cases of early onset (< 65 yr) familial AD cases

Late onset (Alzheimer's dementia -AD2)

  • Apolipoprotein 4 gene (APOE4) mutation is associated with late onset (>60 years) Alzheimer's dementia (AD)

Hypotheses for Alzheimer's dementia

Two major hypothese for the development of Alzheimer's dementia (AD) have been proposed:

Amyloid cascade hypothesis


Associated Conditions

References

Template:WH Template:WS