Evidence map›Paper›PMID 32384747›Full record

ArticleJournal of clinical medicine2020

Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT Study.

Céline Bordet, Sandrine Brice, Carole Maupain, Estelle Gandjbakhch, Bertrand Isidor, Aurélien Palmyre, Alexandre Moerman, Annick Toutain, Linda Akloul, Anne-Claire Brehin and 28 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. The Role of Genetics in the Management of Heart Failure Patients.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
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

38 authors at 18 institutions in 2 countries.

Céline BordetAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Sandrine BriceSorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, F75013 Paris, France.
Carole MaupainAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Estelle GandjbakhchAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Bertrand IsidorDepartment of Genetics, Nantes University Hospital, 44000 Nantes, France.
Aurélien PalmyreAPHP, department of Genetics, Ambroise Paré University Hospital, 92100 Boulogne-Billancourt, France.
Alexandre MoermanDepartment of Genetics, Lille University Hospital, Jeanne de Flandre Hospital, 59000 Lille, France.
Annick ToutainDepartment of Medical Genetics, Tours University Hospital, 37044 Tours, France.
Linda AkloulDepartment of Medical Genetics, Rennes University Hospital, 35000 Rennes, France.
Anne-Claire BrehinNormandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F 76000, Rouen, France.
Caroline SawkaMedical Genetics Unit, FHU TRANSLAD and GIMI Institute, Dijon University Hospital, 21000 Dijon, France.
Caroline Rooryck-ThamboDepartment of Medical Genetics, CHU Bordeaux, Bordeaux, France, F-33000 Bordeaux, France.
Elise SchaeferDepartment of Genetics, Strasbourg University Hospital, Institut de Génétique Médicale d'Alsace, 67200 Strasbourg, France.
Karine NguyenDepartment of Medical Genetics, APHM, Timone Hospital, Marseille Medical Genetics, Aix Marseille University, 13000 Marseille, France.
Delphine Dupin DeguineDepartment of Medical Genetics, Toulouse University Hospital, 31300 Toulouse, France.
Cécile RouzierDepartment of Medical Genetics, Université Côte d'Azur, CHU, Inserm, CNRS, IRCAN, 06000 Nice, France.
Gipsy BillyDepartment of Medical Genetics, Centre Hospitalo-Universitaire Grenoble Alpes, 38700 Grenoble, France.
Krystelle SénéClinical Genetics Unit, University Hospital, Guadeloupe University Hospital, 97159 Guadalupe Island, France.
Isabelle DenjoyAPHP, Department of cardiology, Referral Center for hereditary heart disease, Bichat Hospital, 75018 Paris, France.
Bruno LeheupDepartment of Medical Genetics, University Hospital, 54042 Nancy, France.
Marc PlanesDepartment of Medical Genetics, University Hospital Morvan, 29200 Brest, France.
Jean-Michael MazzellaAPHP, Department of Medical Genetics, Hôpital Européen Georges Pompidou,75015 Paris, France.
Stéphanie StaraciAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Mélanie HebertAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Elsa Le BoetteDepartment of Genetics, Saint Brieuc Hospital, 22000 Saint-Brieuc, France.
Claire-Cécile MichonFilière nationale de santé CARDIOGEN, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Marie-Lise BabonneauFilière nationale de santé CARDIOGEN, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Angélique CurjolAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Amine BekhechiAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Rafik MansouriAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Ibticem RajiAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Jean-François PrunyAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Véronique FressartAPHP, UF Molecular Cardiogenetics and Myogenetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Flavie AderAPHP, UF Molecular Cardiogenetics and Myogenetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Pascale RichardAPHP, UF Molecular Cardiogenetics and Myogenetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Sophie Tezenas du MontcelSorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière-Charles Foix, F75013, Paris, France.
Marcela GargiuloSorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière-Charles Foix, F75013, Paris, France.
Philippe CharronAPHP, Referral Center for hereditary heart disease, Department of Genetics, Pitié-Salpêtrière University Hospital, 75013 Paris, France.
Sorbonne Université · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FRAix-Marseille Université · FRCentre Hospitalier de Saint-Brieuc · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Rennes · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRGenomic and Immunotherapy Medical Institute · FRHôpital Ambroise-Paré · FRHôpital Jeanne de Flandre · FRInstitut Pasteur de la Guadeloupe · GPNantes Université · FRUniversité de Strasbourg · FRUniversité de Tours · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FR

Funding

Fondation maladies rares FMR R14196DD
6 · The paper itself

Abstract

Predictive genetic testing (PGT) is offered to asymptomatic relatives at risk of hereditary heart disease, but the impact of result disclosure has been little studied. We evaluated the psychosocial impacts of PGT in hereditary heart disease, using self-report questionnaires (including the State-Trait Anxiety Inventory) in 517 adults, administered three times to the prospective cohort (PCo:

Indexed as

anxietycardiomyopathiesdistresshereditary heart diseasespredictive genetic testingpsychologicalsocial

Identifiers

PMID32384747
PMCPMC7290753
OpenAlexW3023425682

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.