Proteine che "fibrillano"

L'amiloidosi. Nuove speranze per una malattia che il cardiologo deve conoscere

Translated title of the contribution: Fibril-forming proteins: The amyloidosis. New hopes for a disease that cardiologists must know

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Several proteins share the property of conforming as antiparallel β-sheets, and forming insoluble amyloid fibrils that deposit in the interstitium of organs/tissues and cause systemic amyloidosis. Cardiac involvement is frequent and constitutes a major predictor of poor outcome. Its typical phenotype is that of restrictive cardiomyopathy. The biochemical classification of the amyloidogenic proteins provides the bases for innovative therapeutic approaches. Primary systemic amyloidosis (AL) is a protein conformation disorder in which monoclonal immunoglobulin light chains (κ or λ) produced by clonal plasma cells, are deposited as amyloid in kidneys, heart, liver, and other organs. The recent evidence that chemotherapy reduces or even eradicates the amyloidogenic clone with consequent functional improvement of the affected organs raises new hopes for a treatment, whose key of success is early diagnosis. Heart transplantation can be proposed in patients <years of age in association with autologous stem cell transplantation. In serum amyloid A amyloidosis, fibrils are constituted of the acute phase serum amyloid A protein that is produced in excess in chronic inflammatory diseases such as familial mediterranean fever, autoimmune disorders and chronic infections. The strategy is to treat the underlying inflammatory disease, but new molecules inhibiting amyloid formation and promoting amyloid resorption are facing the clinical scenario and trials are in progress. In transthyretin (TTR) amyloidosis, the non-senile forms are autosomal dominant diseases caused by defective proteins synthesized by mutated TTR genes (more than 70 known mutations with different genotype-phenotype correlations). The treatment is based on transplantation of the TTR-producing liver; exceptionally, liver plus heart or kidney are transplanted. Apolipoprotein A1 amyloidosis is an inherited autosomal dominant disease that benefits from the transplantation of the most impaired organs, usually heart, liver or kidney, either single or combined. The diagnosis of apolipoprotein A1 and TTR amyloidosis relies on positive family history, immunocharacterization of the amyloid fibrils in a tissue biopsy, gene defect detection and absence of light chains in serum and urines. Vice versa, non-familial primary amyloidoses are diagnosed when κ or λ light chains are identified with immunofixation in serum or urines. Tissue studies provide the gold standard for the diagnosis and immunocharacterization of amyloid protein. Heart involvement is diagnosed with a multiparametric approach that includes clinical, electrocardiographic and echocardiographic evaluation. The fine-needle biopsy of the periumbilical fat is the preferral procedure for amyloid detection and immunocharacterization of amyloid protein. This approach excludes, with a few exceptions, the need of endomyocardial biopsy.

Original languageItalian
Pages (from-to)590-597
Number of pages8
JournalItalian Heart Journal Supplement
Volume3
Issue number6
Publication statusPublished - 2002

Fingerprint

Amyloidosis
Amyloid
Amyloidogenic Proteins
Serum Amyloid A Protein
Proteins
Prealbumin
Liver
Apolipoprotein A-I
Kidney
Hope
Transplantation
Restrictive Cardiomyopathy
Urine
Immunoglobulin Light Chains
Familial Mediterranean Fever
Biopsy
Light
Protein Conformation
Amyloid Plaques
Genetic Association Studies

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

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