Evidence map›Paper›PMID 25716352›Full record

ArticleJournal of genetic counseling2015

Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia.

Abhilasha Surampalli, Manaswitha Khare, Georgette Kubrussi, Marie Wencel, Jasmin Tanaja, Sandra Donkervoort, Kathryn Osann, Mariella Simon, Douglas Wallace, Charles Smith and 2 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of genetic counseling, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01353430 (Characterization of Familial Myopathy and Paget Disease of Bone), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 32% 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.

NCT01353430 recruitingnot on this map

Characterization of Familial Myopathy and Paget Disease of Bone

TypeobservationalSponsorUniversity of California, IrvineRan2007 to 2030Enrolled50ConditionsInclusion Body Myopathy With Early-onset Paget Disease and Frontotemporal Dementia, Paget Disease of Bone, Frontotemporal Dementia, Myopathy
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. 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

12 authors at 4 institutions in 2 countries.

Abhilasha SurampalliDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA.
Manaswitha KhareDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA.
Georgette KubrussiDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA.
Marie WencelDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA.
Jasmin TanajaDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA.
Sandra DonkervoortDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA.
Kathryn OsannDivision of Hematology/Oncology, Department of Medicine, University of California, Irvine, CA, 92697, USA.
Mariella SimonDevelopmental and Cell Biology, University of California, Irvine, CA, 92697, USA.
Douglas WallaceDevelopmental and Cell Biology, University of California, Irvine, CA, 92697, USA.
Charles SmithDepartment of Neurology and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA.
Aideen M McInerney-LeoThe University of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Brisbane, Australia.
Virginia KimonisDepartment of Pediatrics, Division of Genetics and Genomic Medicine, University of California, Irvine, CA, 92697, USA. vkimonis@uci.edu.
University of California, Irvine · USChildren's Hospital of Philadelphia · USTranslational Research Institute · AUUniversity of Kentucky · US

Funding

Genetic basis of myopathy with Paget disease of boneR01AR050236 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI KIMONIS, VIRGINIA EUNICE · 2004 to 2008
$1.3M
Characterizing the Role of VCP in Paget's Disease of the BoneK01AR056002 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI WATTS, GILES D · 2009 to 2009
$5k
NIAMS NIH HHS 1K01AR056002-01A2NIAMS NIH HHS K01 AR056002NIAMS NIH HHS R01 AR050236
6 · The paper itself

Abstract

Inclusion Body Myopathy associated with Paget's disease of bone and Fronto-temporal Dementia, also known as multisystem proteinopathy is an autosomal dominant, late onset neurodegenerative disorder caused by mutations in Valosin containing protein (VCP) gene. This study aimed to assess uptake and decision making for predictive genetic testing and the impact on psychological well-being. Individuals who had participated in the gene discovery study with a 50 % a priori risk of inheriting VCP disease were sent a letter of invitation offering genetic counseling and testing and were also invited to participate in this psychosocial study. A total of 102 individuals received an invitation and 33 individuals participated in genetic counseling and testing (32.3 %) with 29 completing baseline questionnaires. Twenty completed the follow-up post-test Hospital Anxiety and Depression Scale questionnaire including 13 of the 18 who had tested positive. Mean risk perception at baseline was 50.1 %. Reasons for testing included planning for the future, relieving uncertainty, informing children and satisfying curiosity. At baseline, one quarter of the participants had high levels of anxiety. However, scores were normal one year following testing. In this small cohort, one third of individuals at 50 % risk chose pre-symptomatic testing. Although one quarter of those choosing testing had high anxiety at baseline, this was not evident at follow-up.

Indexed as

AdultAnxietyCohort StudiesFemaleFrontotemporal DementiaGenetic CounselingGenetic Predisposition to DiseaseGenetic TestingHumansMaleMiddle AgedMyositis, Inclusion BodyOsteitis DeformansHospital anxiety and depression scaleHuntington’s diseaseNeurodegenerativePaget’s diseasePresymptomatic genetic testing

Identifiers

PMID25716352
PMCPMC5565393
OpenAlexW2005964913

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.