Evidence map›Paper›PMID 34410494›Full record

ArticleJournal of neurology2022

Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis.

Alessandro Salvalaggio, Daniele Coraci, Laura Obici, Mario Cacciavillani, Marco Luigetti, Anna Mazzeo, Francesca Pastorelli, Marina Grandis, Tiziana Cavallaro, Giulia Bisogni and 19 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Quantitative muscle ultrasound as a disease biomarker in hereditary transthyretin amyloidosis with polyneuropathy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  4. Early detection of nerve involvement in presymptomatic TTR mutation carriers: exploring potential markers of disease onset.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. High-resolution ultrasound of peripheral nerves in late-onset hereditary transthyretin amyloidosis with polyneuropathy: similarities and differences with CIDP.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  9. Can we identify hereditary TTR amyloidosis by the screening of carpal tunnel syndrome patients?Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  10. Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  11. Article
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

29 authors at 13 institutions in 1 country.

Alessandro SalvalaggioDepartment of Neurosciences, University of Padova, Via Giustiniani 5, 35128, Padova, Italy.
Daniele CoraciNeuroriabilitazione Ad Alta Intensità, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Laura ObiciAmyloidosis Research and Treatment Centre, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Mario CacciavillaniCEMES-EMG Lab, Synlab Group, Padova, Italy.
Marco LuigettiNeurology Unit, Fondazione Policlinico Universitario Gemelli IRCCS, Rome, Italy.
Anna MazzeoUnit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Francesca PastorelliDivision of Neurology, IRCCS Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.
Marina GrandisDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genova, Genova, Italy.
Tiziana CavallaroNeurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Giulia BisogniCentro Clinico NEMO Adulti, Rome, Italy.
Alessandro LozzaAmyloidosis Research and Treatment Centre, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Chiara GemelliDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genova, Genova, Italy.
Luca GentileUnit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Massimo RussoUnit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Mario ErmaniDepartment of Neurosciences, University of Padova, Via Giustiniani 5, 35128, Padova, Italy.
Gian Maria FabriziNeurology Unit, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Rosaria PlasmatiDivision of Neurology, IRCCS Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.
Federica De NapoliDepartment of Neurosciences, University of Padova, Via Giustiniani 5, 35128, Padova, Italy.
Marta CampagnoloDepartment of Neurosciences, University of Padova, Via Giustiniani 5, 35128, Padova, Italy.
Francesca CastellaniDepartment of Neurosciences, University of Padova, Via Giustiniani 5, 35128, Padova, Italy.
Fabrizio SalviDivision of Neurology, IRCCS Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.
Silvia FenuRare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Grazia DevigiliNeurological Unit I, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Davide PareysonRare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Roberto GasparottiDepartment of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.
Claudio RapezziCardiological Center, University of Ferrara, Ferrara, Italy.
Carlo MartinoliOspedale Policlinico San Martino IRCCS, Genova, Italy.
Luca PaduaNeuroriabilitazione Ad Alta Intensità, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Chiara BrianiDepartment of Neurosciences, University of Padova, Via Giustiniani 5, 35128, Padova, Italy. chiara.briani@unipd.it.ORCID http://orcid.org/0000-0001-8035-0200
University of Padua · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITInstitute of Neurological Sciences · ITUniversity of Messina · ITOspedale Policlinico San Martino · ITPoliclinico San Matteo Fondazione · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Verona · ITAgostino Gemelli University Polyclinic · ITCentro Clinico Nemo · ITUniversity of Brescia · ITUniversity of Ferrara · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axonal polyneuropathy is the main feature of hereditary transthyretin amyloidosis (ATTRv). Nerve morphological abnormalities have been reported, but longitudinal changes have never been assessed. We performed a prospective widespread nerve ultrasound evaluation and nerve cross-sectional area (CSA) was compared with baseline data in both ATTRv patients and pre-symptomatic carriers. Thirty-eight subjects were evaluated (mean follow-up 17.1 months), among them 21 had polyneuropathy while 17 were pre-symptomatic carriers. CSA significantly increased at brachial plexus in both groups (p = 0.008 and p = 0.012) pointing to progressive brachial plexus enlargement as a longitudinal biomarker of both disease progression and disease occurrence in pre-symptomatic carriers.

Indexed as

Amyloid Neuropathies, FamilialBrachial PlexusBiomarkersDisease ProgressionHumansNeuronsPolyneuropathiesProspective StudiesBiomarkersAmyloidosisBrachial plexusPeripheral nervesTransthyretinUltrasound

Identifiers

PMID34410494
PMCPMC8940842
OpenAlexW3194674752

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.