Evidence map›Paper›PMID 38756750›Full record

ReviewFrontiers in cardiovascular medicine2024

Cardiopulmonary determinants of reduced exercise tolerance in Fabry disease.

Oriana De Marco, Jessica Gambardella, Antonio Bianco, Antonella Fiordelisi, Federica Andrea Cerasuolo, Antonietta Buonaiuto, Roberta Avvisato, Ivana Capuano, Maria Amicone, Teodolinda Di Risi and 5 more

Abstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Observational
  6. 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

15 authors.

Oriana De MarcoDepartment of Public Health, Federico II University, Naples, Italy.
Jessica GambardellaCentro Interdipartimentale di Ricerca in Ipertensione Arteriosa e Patologie Associate, Federico II University of Naples, Naples, Italy.
Antonio BiancoDepartment of Public Health, Federico II University, Naples, Italy.
Antonella FiordelisiDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Federica Andrea CerasuoloDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Antonietta BuonaiutoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Roberta AvvisatoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Ivana CapuanoDepartment of Public Health, Federico II University, Naples, Italy.
Maria AmiconeDepartment of Public Health, Federico II University, Naples, Italy.
Teodolinda Di RisiDepartment of Public Health, Federico II University, Naples, Italy.
Eleonora RiccioDepartment of Public Health, Federico II University, Naples, Italy.
Letizia SpinelliCentro Interdipartimentale di Ricerca in Ipertensione Arteriosa e Patologie Associate, Federico II University of Naples, Naples, Italy.
Antonio PisaniDepartment of Public Health, Federico II University, Naples, Italy.
Guido IaccarinoCentro Interdipartimentale di Ricerca in Ipertensione Arteriosa e Patologie Associate, Federico II University of Naples, Naples, Italy.
Daniela SorrientoCentro Interdipartimentale di Ricerca in Ipertensione Arteriosa e Patologie Associate, Federico II University of Naples, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease (FD), also known as Anderson-Fabry disease, is a hereditary disorder of glycosphingolipid metabolism, caused by a deficiency of the lysosomal alpha-galactosidase A enzyme. This causes a progressive accumulation of glycosphingolipids in tissues and organs which represents the main pathogenetic mechanism of FD. The disease is progressive and multisystemic and is characterized by early symptoms and late complications (renal, cardiac and neurological dysfunction). Fatigue and exercise intolerance are early common symptoms in FD patients but the specific causes are still to be defined. In this narrative review, we deal with the contribution of cardiac and pulmonary dysfunctions in determining fatigue and exercise intolerance in FD patients.

Indexed as

cardiac dysfunctionexercise intoleranceFabry diseasefatiguepulmonary dysfunction

Identifiers

PMID38756750
PMCPMC11096481

What OpenQuestion holds

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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.