Evidence map›Paper›PMID 35887731›Full record

ArticleJournal of clinical medicine2022

Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series.

Maria do Carmo Vilas-Boas, Pedro Filipe Pereira Fonseca, Inês Martins Sousa, Márcio Neves Cardoso, João Paulo Silva Cunha, Teresa Coelho

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. Gait abnormalities in older adults with transthyretin cardiac amyloidosis.Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis · 2024
    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

6 authors at 2 institutions in 1 country.

Maria do Carmo Vilas-BoasCentro Hospitalar Universitário do Porto, Hospital Santo António, Unidade Corino de Andrade, E.P.E., Largo do Prof. Abel Salazar, 4099-001 Porto, Portugal.ORCID 0000-0002-5012-789X
Pedro Filipe Pereira FonsecaLABIOMEP: Porto Biomechanics Laboratory, University of Porto, R. Dr. Plácido de Costa, 91, 4200-450 Porto, Portugal.ORCID 0000-0002-4885-4924
Inês Martins SousaLABIOMEP: Porto Biomechanics Laboratory, University of Porto, R. Dr. Plácido de Costa, 91, 4200-450 Porto, Portugal.
Márcio Neves CardosoCentro Hospitalar Universitário do Porto, Hospital Santo António, Unidade Corino de Andrade, E.P.E., Largo do Prof. Abel Salazar, 4099-001 Porto, Portugal.
João Paulo Silva CunhaINESC TEC (Instituto de Engenharia de Sistemas e Computadores, Tecnologia e Ciência), FEUP (Faculdade de Engenharia da Universidade do Porto), University of Porto, R. Dr. Roberto Frias, 4200-465 Porto, Portugal.
Teresa CoelhoCentro Hospitalar Universitário do Porto, Hospital Santo António, Unidade Corino de Andrade, E.P.E., Largo do Prof. Abel Salazar, 4099-001 Porto, Portugal.
Universidade do Porto · PTHospital de Santo António · PT

Funding

CHUP BI.02/2018/UCA/CHP ScholarshipFCT UIDB/50014/2020
6 · The paper itself

Abstract

Hereditary amyloidosis associated with transthyretin (ATTRv), is a rare autosomal dominant disease characterized by length-dependent symmetric polyneuropathy that has gait impairment as one of its consequences. The gait pattern of V30M ATTRv amyloidosis patients has been described as similar to that of diabetic neuropathy, associated with steppage, but has never been quantitatively characterized. In this study we aim to characterize the gait pattern of patients with V30M ATTRv amyloidosis, thus providing information for a better understanding and potential for supporting diagnosis and disease progression evaluation. We present a case series in which we conducted two gait analyses, 18 months apart, of five V30M ATTRv amyloidosis patients using a 12-camera, marker based, optical system as well as six force platforms. Linear kinematics, ground reaction forces, and angular kinematics results are analyzed for all patients. All patients, except one, showed a delayed toe-off in the second assessment, as well as excessive pelvic rotation, hip extension and external transverse rotation and knee flexion (in stance and swing phases), along with reduced vertical and mediolateral ground reaction forces. The described gait anomalies are not clinically quantified; thus, gait analysis may contribute to the assessment of possible disease progression along with the clinical evaluation.

Indexed as

ATTRv amyloidosisclinical neurologyFamilial Amyloid Polyneuropathygait analysismovement quantificationperipheral neuropathy

Identifiers

PMID35887731
PMCPMC9320786
OpenAlexW4284879082

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.