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ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable.
Brannagan, Thomas H; Auer-Grumbach, Michaela; Berk, John L; Briani, Chiara; Bril, Vera; Coelho, Teresa; Damy, Thibaud; Dispenzieri, Angela; Drachman, Brian M; Fine, Nowell; Gaggin, Hanna K; Gertz, Morie; Gillmore, Julian D; Gonzalez, Esther; Hanna, Mazen; Hurwitz, David R; Khella, Sami L; Maurer, Mathew S; Nativi-Nicolau, Jose; Olugemo, Kemi; Quintana, Luis F; Rosen, Andrew M; Schmidt, Hartmut H; Shehata, Jacqueline; Waddington-Cruz, Marcia; Whelan, Carol; Ruberg, Frederick L.
  • Brannagan TH; Department of Neurology, Columbia University, New York, NY, USA.
  • Auer-Grumbach M; Vienna General Hospital, Vienna, Austria.
  • Berk JL; Boston University, Boston, MA, USA.
  • Briani C; University of Padova, Padova, Italy.
  • Bril V; University Health Network, Toronto, ON, Canada.
  • Coelho T; Centro Hospitalar Universitário do Porto, Porto, Portugal.
  • Damy T; Referral Center for Cardiac Amyloidosis, Cardiology Department, APHP-Henri Mondor Hospital, Creteil, France.
  • Dispenzieri A; Mayo Clinic, Rochester, MN, USA.
  • Drachman BM; Penn Presbyterian Medical Center, Philadelphia, PA, USA.
  • Fine N; University of Calgary, Calgary, AB, Canada.
  • Gaggin HK; Massachusetts General Hospital, Boston, MA, USA.
  • Gertz M; Mayo Clinic, Rochester, MN, USA.
  • Gillmore JD; National Amyloidosis Centre, Royal Free Hospital, London, UK.
  • Gonzalez E; Hospital Puerta de Hierro of Madrid, Madrid, Spain.
  • Hanna M; Cleveland Clinic, Cleveland, OH, USA.
  • Hurwitz DR; Akcea Therapeutics, Boston, MA, USA.
  • Khella SL; University of Pennsylvania, Philadelphia, PA, USA.
  • Maurer MS; Columbia University, New York, NY, USA.
  • Nativi-Nicolau J; University of Utah, Salt Lake City, UT, USA.
  • Olugemo K; Akcea Therapeutics, Boston, MA, USA.
  • Quintana LF; Hospital Clinic, University of Barcelona, Barcelona, Spain.
  • Rosen AM; Akcea Therapeutics, Boston, MA, USA.
  • Schmidt HH; University Hospital of Münster, Münster, Germany.
  • Shehata J; Akcea Therapeutics, Boston, MA, USA.
  • Waddington-Cruz M; Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Whelan C; National Amyloidosis Centre, Royal Free Hospital, London, UK.
  • Ruberg FL; Section of Cardiovascular Medicine, Department of Medicine and Amyloidosis Center, Boston University School of Medicine, Boston Medical Center, Boston, MA, USA. Frederick.Ruberg@bmc.org.
Orphanet J Rare Dis ; 16(1): 204, 2021 05 06.
Article in English | MEDLINE | ID: covidwho-1219017
ABSTRACT

BACKGROUND:

The global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causing the ongoing coronavirus disease 2019 (COVID-19) pandemic has raised serious concern for patients with chronic disease. A correlation has been identified between the severity of COVID-19 and a patient's preexisting comorbidities. Although COVID-19 primarily involves the respiratory system, dysfunction in multiple organ systems is common, particularly in the cardiovascular, gastrointestinal, immune, renal, and nervous systems. Patients with amyloid transthyretin (ATTR) amyloidosis represent a population particularly vulnerable to COVID-19 morbidity due to the multisystem nature of ATTR amyloidosis. MAIN BODY ATTR amyloidosis is a clinically heterogeneous progressive disease, resulting from the accumulation of amyloid fibrils in various organs and tissues. Amyloid deposition causes multisystem clinical manifestations, including cardiomyopathy and polyneuropathy, along with gastrointestinal symptoms and renal dysfunction. Given the potential for exacerbation of organ dysfunction, physicians note possible unique challenges in the management of patients with ATTR amyloidosis who develop multiorgan complications from COVID-19. While the interplay between COVID-19 and ATTR amyloidosis is still being evaluated, physicians should consider that the heightened susceptibility of patients with ATTR amyloidosis to multiorgan complications might increase their risk for poor outcomes with COVID-19.

CONCLUSION:

Patients with ATTR amyloidosis are suspected to have a higher risk of morbidity and mortality due to age and underlying ATTR amyloidosis-related organ dysfunction. While further research is needed to characterize this risk and management implications, ATTR amyloidosis patients might require specialized management if they develop COVID-19. The risks of delaying diagnosis or interrupting treatment for patients with ATTR amyloidosis should be balanced with the risk of exposure in the health care setting. Both physicians and patients must adapt to a new construct for care during and possibly after the pandemic to ensure optimal health for patients with ATTR amyloidosis, minimizing treatment interruptions.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Amyloid Neuropathies, Familial / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Orphanet J Rare Dis Journal subject: Medicine Year: 2021 Document Type: Article Affiliation country: S13023-021-01834-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Amyloid Neuropathies, Familial / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Orphanet J Rare Dis Journal subject: Medicine Year: 2021 Document Type: Article Affiliation country: S13023-021-01834-0