Evidence map›Paper›PMID 33957949›Full record

ArticleOrphanet journal of rare diseases2021

ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable.

Thomas H Brannagan, Michaela Auer-Grumbach, John L Berk, Chiara Briani, Vera Bril, Teresa Coelho, Thibaud Damy, Angela Dispenzieri, Brian M Drachman, Nowell Fine and 17 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. COVID-19-Associated cardiac pathology at the postmortem evaluation: a collaborative systematic review.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 19 institutions in 9 countries.

Thomas H BrannaganDepartment of Neurology, Columbia University, New York, NY, USA.
Michaela Auer-GrumbachVienna General Hospital, Vienna, Austria.
John L BerkBoston University, Boston, MA, USA.
Chiara BrianiUniversity of Padova, Padova, Italy.
Vera BrilUniversity Health Network, Toronto, ON, Canada.
Teresa CoelhoCentro Hospitalar Universitário do Porto, Porto, Portugal.
Thibaud DamyReferral Center for Cardiac Amyloidosis, Cardiology Department, APHP-Henri Mondor Hospital, Creteil, France.
Angela DispenzieriMayo Clinic, Rochester, MN, USA.
Brian M DrachmanPenn Presbyterian Medical Center, Philadelphia, PA, USA.
Nowell FineUniversity of Calgary, Calgary, AB, Canada.
Hanna K GagginMassachusetts General Hospital, Boston, MA, USA.
Morie GertzMayo Clinic, Rochester, MN, USA.
Julian D GillmoreNational Amyloidosis Centre, Royal Free Hospital, London, UK.
Esther GonzalezHospital Puerta de Hierro of Madrid, Madrid, Spain.
Mazen HannaCleveland Clinic, Cleveland, OH, USA.
David R HurwitzAkcea Therapeutics, Boston, MA, USA.
Sami L KhellaUniversity of Pennsylvania, Philadelphia, PA, USA.
Mathew S MaurerColumbia University, New York, NY, USA.
Jose Nativi-NicolauUniversity of Utah, Salt Lake City, UT, USA.
Kemi OlugemoAkcea Therapeutics, Boston, MA, USA.
Luis F QuintanaHospital Clinic, University of Barcelona, Barcelona, Spain.
Andrew M RosenAkcea Therapeutics, Boston, MA, USA.
Hartmut H SchmidtUniversity Hospital of Münster, Münster, Germany.
Jacqueline ShehataAkcea Therapeutics, Boston, MA, USA.
Marcia Waddington-CruzFederal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Carol WhelanNational Amyloidosis Centre, Royal Free Hospital, London, UK.
Frederick L RubergSection of Cardiovascular Medicine, Department of Medicine and Amyloidosis Center, Boston University School of Medicine, Boston Medical Center, Boston, MA, USA. Frederick.Ruberg@bmc.org.ORCID 0000-0002-6424-4413
Akebia Therapeutics (United States) · USColumbia University · USMayo Clinic in Arizona · USThe Royal Free Hospital · GBBoston University · USCentro Hospitalar do Porto · PTCleveland Clinic · USHospital Universitario Puerta de Hierro Majadahonda · ESMassachusetts General Hospital · USPenn Presbyterian Medical Center · USUniversidade Federal do Rio de Janeiro · BRUniversitat de Barcelona · ESUniversity Health Network · CAUniversity Hospital Münster · DEUniversity of Calgary · CAUniversity of Padua · ITUniversity of Pennsylvania · USUniversity of Utah · USVienna General Hospital · AT

Funding

Austrian Science Fund FWF I 4699
6 · The paper itself

Abstract

backgroundThe 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.

conclusionPatients 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.

Indexed as

Amyloid Neuropathies, FamilialCOVID-19AmyloidHumansPandemicsPrealbuminSARS-CoV-2AmyloidPrealbuminAmyloidosisATTRCOVID-19Rare diseaseSARS-CoV-2

Identifiers

PMID33957949
PMCPMC8100737
OpenAlexW3159685312

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.