Evidence map›Paper›PMID 29764331›Full record

ArticleJournal of psychosocial oncology

Psychological impact of von Hippel-Lindau genetic screening in patients with a previous history of hemangioblastoma of the central nervous system.

Claire Rochette, Karine Baumstarck, Hélène Canoni-Zattara, Ahmad Esmaeel Abdullah, Dominique Figarella-Branger, Morgane Pertuit, Anne Barlier, Frédéric Castinetti, Karel Pacak, Philippe Metellus and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of psychosocial oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

11 authors at 5 institutions in 2 countries.

Claire Rochettea Department of Endocrinology , Conception Hospital, Aix-Marseille University , Marseille , France.
Karine Baumstarckb Department of Public Health , EA3279 Self-perceived Health Assessment Research Unit, La Timone University, Aix-Marseille University , Marseille , France.
Hélène Canoni-Zattarac Department of Genetics , La Timone University Hospital, Aix-Marseille University , Marseille , France.
Ahmad Esmaeel Abdullaha Department of Endocrinology , Conception Hospital, Aix-Marseille University , Marseille , France.
Dominique Figarella-Brangerd Department of Neuropathology , La Timone University Hospital, Aix-Marseille University , Marseille , France.
Morgane Pertuite Laboratory of Molecular Biology , Conception Hospital & CNRS, CRN2M UMR 7286, Aix-Marseille University , France.
Anne Barliere Laboratory of Molecular Biology , Conception Hospital & CNRS, CRN2M UMR 7286, Aix-Marseille University , France.
Frédéric Castinettia Department of Endocrinology , Conception Hospital, Aix-Marseille University , Marseille , France.
Karel Pacakf Section on Medical Neuroendocrinology , Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) , National Institutes of Health , Bethesda , Maryland , USA.
Philippe Metellusg Department of Neurosurgery La Timone University Hospital , Aix-Marseille University , Marseille , France.
David Taïebh Department of Nuclear Medicine , La Timone University Hospital & CERIMED & Inserm UMR1068 Marseille Cancerology Research Center, Institut Paoli-Calmettes, Aix-Marseille University , Marseille , France.
Aix-Marseille Université · FRCentre National de la Recherche Scientifique · FRHôpital de la Conception · FREunice Kennedy Shriver National Institute of Child Health and Human Development · USInserm · FR

Funding

Diagnosis, Pathophysiology And Molecular Biology of Pheochromocytoma and ParagangliomaZIAHD008735 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI PACAK, KAREL · 2009 to 2024
$28.4M
Intramural NIH HHS Z99 HD999999
6 · The paper itself

Abstract

Von Hippel-Lindau (VHL) syndrome is a hereditary cancer syndrome characterized by a high risk of developing benign and malignant tumors, including central nervous system hemangioblastomas (CNS HBs). For an early diagnosis of VHL, before the occurrence of cancers (especially renal cell carcinoma), it is of huge importance to initiate VHL genetic testing in at-risk patients. The aim of the study was to assess the psychological impact of VHL genetic testing in patients previously diagnosed with a CNS HB. From 1999 until 2015, 55 patients underwent surgery for CNS HBs. Eleven patients were already screened for VHL mutations and 3 patients deceased before the start of the study. From the remaining 42 patients, 24 were accepted to be enrolled in the study. Assessment of psychological impact of VHL genetic testing was performed by measuring anxiety levels, mood disorders, quality of life, and psychological consequences of genetic screening. Twenty-one of the enrolled 24 patients underwent VHL genetic testing and 12 patients came back for the communication of positive genetic results. The baseline psychological status did not differ between these 2 groups. Patients who attended the visit of communication of genetic results had similar anxiety levels compared to those who had not. Furthermore, they also experienced an improvement in the level of anxiety and two QoL dimension scores compared to their baseline status. In summary, there is no evidence of a negative psychosocial impact of VHL genetic testing in patients with a previous history of CNS HB. We, therefore, recommend the recall of patients who have not been previously screened.

Indexed as

Genetic TestingAdultAgedAnxietyCentral Nervous System NeoplasmsDepressionFemaleHemangioblastomaHumansLongitudinal StudiesMaleMiddle AgedQuality of LifeSurveys and Questionnairesvon Hippel-Lindau Diseaseanxiety/depressiongenetic testinghemangioblastomaquality of lifevon hippel-lindau

Identifiers

PMID29764331
PMCPMC7446124
OpenAlexW2803708342

What OpenQuestion holds

Textmetadata
LicenceTDM
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.