Amyloidosis causes

Revision as of 20:12, 21 August 2012 by Prashanthsaddala (talk | contribs)
Jump to navigation Jump to search

Amyloidosis Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Primary amyloidosis
Secondary amyloidosis
Familial amyloidosis
Wild-type (senile) amyloidosis
Cardiac amyloidosis
Beta-2 microglobulin related amyloidosis
Gelsolin related amyloidosis
Lysozyme amyloid related amyloidosis
Leucocyte cell-derived chemotaxin 2 related amyloidosis
Fibrinogen A alpha-chain associated amyloidosis

Pathophysiology

Causes

Differentiating Amyloidosis 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

Echocardiography and 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

Case Studies

Case #1

Amyloidosis causes On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Amyloidosis causes

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Amyloidosis causes

CDC on Amyloidosis causes

Amyloidosis causes in the news

Blogs on Amyloidosis causes

Directions to Hospitals Treating Psoriasis

Risk calculators and risk factors for Amyloidosis causes

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

Overview

Amyloid is a pathological extracellular deposit composed predominantly of amyloid fibrils with characteristic morphology and pathognomonic tinctorial properties, specifically the capacity to bind Congo Red dye and then display red-green dichroism when viewed in strong cross polarised light. Amyloid fibrils are formed from normally soluble autologous precursor proteins that have undergone misfolding and aggregated into fibrils with a common cross Beta-sheet core structure.

The deposits are rich in proteoglycans and always contain the non-fibrillar normal plasma glycoprotein, serum amyloid P component (SAP), which binds specifically to all amyloid fibrils.

Amyloidosis is disease caused by amyloid deposits in the tissues. The deposits may be local or systemic in distribution and acquired or hereditary in aetiology. All patients with amyloidosis have amyloid deposits in their tissues when they first present clinically. In each individual, disease is always worse when there is more amyloid present, and arrest or regression of amyloid deposition is associated with clinical benefit. Only organs or tissues in which amyloid deposits are present are directly functionally compromised, even when the amyloid fibril precursor protein is ubiquitous.

In amyloidosis the link between physical presence of amyloid deposits and disease is irrefutably strong. Pre-fibrillar protein aggregates are cytotoxic for cultured cells exposed under artefactual in vitro conditions but there is no evidence that this is pathophysiologically relevant to amyloidosis in vivo. No clinical or pathological effects are detectable in any form of acquired or hereditary systemic amyloidosis until amyloid deposits are demonstrable, regardless of the length of time that the predisposition exists before amyloid develops.

Clinical impairment progresses as amyloid deposits increase in size, and regression of amyloid is associated with clinical improvement and survival. If damaged organs are replaced there is no organ dysfunction, even in the face of unchanged abundance of amyloid fibril precursor proteins fully capable of aggregation and fibril formation, until new amyloid deposits form and accumulate to a critical mass. This usually takes years.

There is usually no histological evidence of inflammation, or cell death or dysfunction, even in massively amyloid laden organs, and the organs continue to function until the amyloid deposits critically compromise structure and/or function. For example, cardiac amyloid deposition impairs diastolic filling by stiffening the ventricle.

There is no evidence of cytotoxicity in the myocardium and the heart muscle continues to contract excellently and propel the progressively reduced stroke volume until the end. Similarly in hereditary transthyretin amyloidosis, amyloid fibrils may accumulate over years in the vitreous humour of the eye until fibril density impairs optical clarity and causes blindness. The amyloidogenic variant transthyretin in the eye is synthesized in the choroid plexus and by the ciliary epithelium directly overlying the retina, and continuously bathes the retina. However replacement of the amyloid laden vitreous with optically clear medium restores perfect vision in every case. The putative toxic pre-fibrillar aggregates evidently have no deleterious effect on retinal neurones, whereas accumulation of amyloid fibrils causes blindness and their removal cures it.

Finally there are many clinical situations in which the local physical presence of substantial amyloid deposits alone is the only possible cause of disease and death, and where reduction or removal of the deposits relieves symptoms and signs and is life saving. [1]

Systemic amyloidosis

Primary/Hereditary amyloidosis

These rare hereditary disorders are usually due to point mutations in precursor proteins, and are also usually autosomal dominantly transmitted.The precursor proteins are;

Secondary amyloidosis

These are far more common than the primary amyloidoses.

Organ-specific amyloidosis

In almost all of the organ-specific pathologies, there is significant debate as to whether the amyloid plaques are the causal agent of the disease or instead a downstream consequence of a common idiopathic agent. The associated proteins are indicated in parentheses.

Neurological amyloid

Cardiovascular amyloid

Other

Gross Pathology

Amyloidosis Lesion In Left Atrium: Gross natural color view of a diagnostic lesion
Amyloidosis Lesion In Left Atrium: Gross natural color close-up
Amyloidosis, left atrium, endocardial nodules
Amyloidosis, left atrium, endocardial nodules
Amyloidosis and left ventricular hypertrophy
URINARY SYSTEM: Kidney, amyloidosis
SKIN: AMYLOIDOSIS, PRIMARY; YELLOW LESIONS
TONGUE: PRIMARY AMYLOIDOSIS
THYROID GLAND: AMYLOIDOSIS OF THE THYROID This illustration shows the outer aspect and cut surface of localized amyloidosis of the thyroid gland (amyloid tumor). The gland is enlarged and bosselated and exhibits a salmon color on cross section.
LOWER RESPIRATORY TRACT: NODULAR PARENCHYMAL AMYLOIDOSIS This nodule of amyloid shells taken out from the lung as an irregular, tan, waxy mass.
LIVER: Amyloidosis
LIVER-BILIARY TRACT: Liver, amyloidosis
KIDNEY-BLADDER-URINARY: AMYLOIDOSIS OF URINARY BLADDER (Courtesy of Dr. George M. Farrow, Rochester, MN.)

Microscopic Pathology

Amyloid can be diagnosed on histological examination of affected tissue.

Images shown below are courtesy of Professor Peter Anderson and published with permission. © PEIR, University of Alabama at Birmingham, Department of Pathology

Heart: Amyloidosis, aldehyde fuchsin stain
Heart: Perivascular amyloid, amyloidosis, congo red showing birefringence
Heart: Perivascular amyloid, amyloidosis (Hematoxylin and eosin staining)
Congo red stain, which, combined with polarized light, makes the amyloid proteins appear apple-green on microscopy

What is not Amyloidosis?

Several important diseases are associated with amyloid deposits but are not amyloidosis.

The neuropathology of Alzheimer’s disease by definition includes intra-cerebral ABeta amyloid deposits, but it is not known whether these deposits are responsible for the neuronal cell death that causes cognitive decline; non-fibrillar ABeta aggregates may be more directly involved. In contrast, by analogy with the notable friability of systemic blood vessels containing AL amyloid deposits, it seems likely that the cerebrovascular ABeta amyloid deposits in cerebral amyloid angiopathy are responsible for cerebral hemorrhage.

Most patients with type 2 diabetes have amyloid deposits in the islets of Langerhans, which may exacerbate islet dysfunction, but amyloid is not the original cause of their diabetes. Cerebral amyloid deposits of the prion protein are present in many forms of transmissible spongiform encephalopathy but are absent in others, including bovine spongiform encephalopathy in cows and fatal familial insomnia in humans, and amyloid is thus not essential for pathogenesis of TSE.

Many other diseases are associated with, and possibly caused by, protein misfolding and aggregation. Some of these aggregates share the amyloid cross Beta-sheet fold, for example in Huntington’s disease and related poly-glutamine repeat hereditary neurodegenerative diseases, and in Parkinson’s disease.

However intracellular and intranuclear protein aggregates have very different pathogenetic effects than extracellular amyloid deposits, and are in radically different locations for drug intervention. They are also not associated with the non-fibrillar components of amyloid deposits, the proteoglycans and SAP. These intracellular protein aggregates are thus not amyloid and the diseases with which they are associated are not amyloidosis. Although there may be informative similarities and parallels, especially in protein misfolding and aggregation studied in vitro, to conflate such widely different processes is misleading and potentially dangerous when extrapolated to development of therapeutic interventions.

Other protein misfolding diseases, such as the serpinopathies, are even more remote from amyloidosis, with intracellular deposition of protein aggregates that do not share the typical amyloid cross-Beta fold and where much of the pathogenesis of disease is related to loss of normal serpin function rather than adverse effects of the aggregates.

What is SAP?

SAP is a highly conserved constitutive normal trace plasma protein with specific avid calcium dependent binding to all amyloid fibrils that causes its remarkable selective concentration and persistence in amyloid deposits of all types.

SAP is intrinsically resistant to proteolysis and is further stabilised by its tight binding to amyloid fibrils, which in turn stabilises the fibrils and protects them from proteolysis.

SAP knockout mice show delayed and reduced deposition of experimentally induced reactive systemic amyloid. SAP is therefore a valid therapeutic target, and in vivo inhibition of SAP binding and/or depletion of circulating SAP should reduce amyloid burden.

References

  1. Amyloid and amyloidosis. Gilles Grateau, Robert A. Kyle, Martha Skinner, 2005 ISBN 0-8493-3534-5

Template:WH Template:WS