Literature DB >> 32616304

The diagnostic challenges of cardiac amyloidosis: A practical approach to the two main types.

Cindy Varga1, Sharmila Dorbala2, Isabelle Lousada3, Michael J Polydefkis4, Ashutosh Wechalekar5, Mathew S Maurer6, Raymond L Comenzo7.   

Abstract

Systemic amyloidosis of the immunoglobulin light-chain (AL) or transthyretin type (ATTR) is a multisystem protein deposition disease that often involves the heart. Delays in diagnosis are very common and can have detrimental consequences on patient outcomes. Because both major types can now be distinguished quickly and treated effectively, clear approaches are required. There have been advances in radioisotope scintigraphy, monoclonal protein testing and mass spectrometry for typing that need coordinated application. We have entered an era in which rapid diagnosis and ready therapy will save lives, therefore we must develop coherent approaches to this multisystem disease. The prognosis for AL has improved significantly with the incorporation of novel agents such as proteasome inhibitors, immunomodulators and monoclonal antibodies against plasma cells. Multiple independent studies have demonstrated the efficacy of these agents in AL, though tolerability can become an issue with dose reductions required in many cases. Median overall survival for patients achieving complete responses after stem cell transplant and consolidation exceeds a decade. The prognosis for ATTR, both age-related wild-type (ATTRwt) and hereditary due to variants of transthyretin (ATTRv), has improved as well due to the availability of the stabilizer tafamidis and the RNA-interference agents patisiran and inotersen. In both AL and ATTR, with elimination or suppression of the pathologic amyloid-forming protein, symptomatic involvement of the heart, kidneys and peripheral nervous system can improve as well. In this review, we present the current state of diagnosing and treating the two major types of systemic amyloidosis, emphasizing the coherent clinical application of the new tools and treatments. Implementation of the approaches we provide will enable rapid identification of amyloid type and rational selection of therapy.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Amyloidosis; Cardiomyopathy; Light chains; Monoclonal gammopathy; Scintigraphy; Transthyretin

Year:  2020        PMID: 32616304     DOI: 10.1016/j.blre.2020.100720

Source DB:  PubMed          Journal:  Blood Rev        ISSN: 0268-960X            Impact factor:   8.250


  4 in total

1.  The use of PYP scan for evaluation of ATTR cardiac amyloidosis at a tertiary medical centre.

Authors:  Joshua Dower; Danai Dima; Mumtu Lalla; Ayan R Patel; Raymond L Comenzo; Cindy Varga
Journal:  Br J Cardiol       Date:  2022-05-31

2.  Accelerated junctional rhythm (AJR) revealing light-chain cardiac amyloidosis: A case report with literature review.

Authors:  Raid Faraj; Zaineb Bourouhou; Sidaty Oussama; Asmaa Bouamoud; Hasna Rami; Amina Samih; Ibtissam Fellat; Jamila Zarzur; Mohamed Cherti
Journal:  Ann Med Surg (Lond)       Date:  2022-03-03

Review 3.  Suspicion, screening, and diagnosis of wild-type transthyretin amyloid cardiomyopathy: a systematic literature review.

Authors:  Katrine Bay; Finn Gustafsson; Michael Maiborg; Anne Bagger-Bahnsen; Anne Mette Strand; Trine Pilgaard; Steen Hvitfeldt Poulsen
Journal:  ESC Heart Fail       Date:  2022-03-27

4.  Pitfalls of the Semi-Quantitative Analyzing 99mTc-Pyrophosphate Planar Images for Diagnosing Transthyretin Cardiac Amyloidosis: A Possible Solution.

Authors:  Yuankai Zhu; Ruping Pan; Dan Peng; Qingjian Dong; Xiaohua Zhu
Journal:  Diagnostics (Basel)       Date:  2022-01-01
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.