Evidence map›Paper›PMID 32442237›Full record

ArticlePloS one2020

Cornea verticillata and acroparesthesia efficiently discriminate clusters of severity in Fabry disease.

Wladimir Mauhin, Olivier Benveniste, Damien Amelin, Clémence Montagner, Foudil Lamari, Catherine Caillaud, Claire Douillard, Bertrand Dussol, Vanessa Leguy-Seguin, Pauline D'Halluin and 13 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% 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, 15 citations in OpenAlex.

  1. Observational
  2. Article
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  8. Review
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  10. Interstitial lung disease in lysosomal storage disorders.European respiratory review : an official journal of the European Respiratory Society · 2021
    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

23 authors at 17 institutions in 1 country.

Wladimir MauhinInternal Medicine Department, Reference Center for Lysosomal Storage Disorders, Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France.ORCID 0000-0003-4463-9757
Olivier BenvenisteUMRS 974, INSERM, Sorbonne Université, Paris, France.
Damien AmelinUMRS 974, INSERM, Sorbonne Université, Paris, France.
Clémence MontagnerInternal Medicine Department, Reference Center for Lysosomal Storage Disorders, Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France.
Foudil LamariMetabolic Biochemistry Department, Pitié Salpêtrière University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
Catherine CaillaudBiochemistry, Metabolomic and Proteomic Department, Necker Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
Claire DouillardReference Center for Inborn Metabolic Diseases, Jeanne de Flandres Hospital, Lille, France.
Bertrand DussolNephrology Department, Assistance Publique Hôpitaux de Marseille, Marseille, France.
Vanessa Leguy-SeguinInternal Medicine and Clinical Immunology Department, Francois Mitterrand Hospital, Dijon, France.
Pauline D'HalluinNephrology and Haemodialysis Department, Centre Hospitalier Côte Basque, Bayonne, France.
Esther NoelInternal Medicine Department, Strasbourg University Hospital, Strasbourg, France.
Thierry ZenoneInternal Medicine Department, Valence Hospital, Valence, France.
Marie MatignonNephrology and Renal Transplantation Department, Institut Francilien de Recherche en Néphrologie et Transplantation (IFRNT), Henri-Mondor/Albert-Chenevier University Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France.
François MaillotInternal Medicine Department, Tours University Hospital, Tours, France.
Kim-Heang LyInternal Medicine Department, Dupuytren University Hospital, Limoges, France.
Gérard BessonNeurology Department, Grenoble University Hospital, Grenoble, France.
Marjolaine WillemsMedical Genetics and Rare Diseases Department, Montpellier University Hospital, Montpellier, France.
Fabien LabombardaCardiology Department, Caen University Hospital, Caen, France.
Agathe MasseauInternal Medicine Department, Hôtel-Dieu University Hospital, Nantes, France.
Christian LavigneInternal Medicine and Vascular Diseases Department, Angers University Hospital, Angers, France.
Didier LacombeMedical Genetics Department, Bordeaux University Hospital, Bordeaux, France.
Hélène MaillardInternal Medicine Department, Huriez Hospital, University of Lille, Lille, France.
Olivier LidoveInternal Medicine Department, Reference Center for Lysosomal Storage Disorders, Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France.
Inserm · FRCentre d'Investigation Clinique de Nantes · FRCentre Hospitalier de la Côte Basque · FRCentre Hospitalier de Valence · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Grenoble · FRCHU Dijon Bourgogne · FRGroupe Hospitalier Diaconesses Croix Saint-Simon · FRHôpital Dupuytren · FRHôpital Jeanne de Flandre · FRHôpital Necker-Enfants Malades · FRHôpitaux Universitaires de Strasbourg · FRSorbonne Université · FRUniversité de Lille · FRUniversité de Montpellier · FRUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroudFabry disease (OMIM #301 500), the most prevalent lysosomal storage disease, is caused by enzymatic defects in alpha-galactosidase A (GLA gene; Xq22.1). Fabry disease has historically been characterized by progressive renal failure, early stroke and hypertrophic cardiomyopathy, with a diminished life expectancy. A nonclassical phenotype has been described with an almost exclusive cardiac involvement. Specific therapies with enzyme substitution or chaperone molecules are now available depending on the mutation carried. Numerous clinical and fundamental studies have been conducted without stratifying patients by phenotype or severity, despite different prognoses and possible different pathophysiologies. We aimed to identify a simple and clinically relevant way to classify and stratify patients according to their disease severity.

methodsBased on data from the French Fabry Biobank and Registry (FFABRY; n = 104; 54 males), we applied unsupervised multivariate statistics to determine clusters of patients and identify clinical criteria that would allow an effective classification of adult patients. Thanks to these criteria and empirical clinical considerations we secondly elaborate a new score that allow the severity stratification of patients.

resultsWe observed that the absence of acroparesthesia or cornea verticillata is sufficient to classify males as having the nonclassical phenotype. We did not identify criteria that significantly cluster female patients. The classical phenotype was associated with a higher risk of severe renal (HR = 35.1; p <10-3) and cardiac events (HR = 4.8; p = 0.008) and a trend toward a higher risk of severe neurological events (HR = 7.7; p = 0.08) compared to nonclassical males. Our simple, rapid and clinically-relevant FFABRY score gave concordant results with the validated MSSI.

conclusionAcroparesthesia and cornea verticillata are simple clinical criteria that efficiently stratify Fabry patients, defining 3 different groups: females and males with nonclassical and classical phenotypes of significantly different severity. The FFABRY score allows severity stratification of Fabry patients.

Indexed as

AdultCohort StudiesCorneaFabry DiseaseFemaleFranceHumansMiddle AgedParesthesiaPhenotypeProspective StudiesRegistriesYoung Adult

Identifiers

PMID32442237
PMCPMC7244174
OpenAlexW3028561505

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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.