Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia
Gespeichert in:
Verfasser / Beitragende:
[Abhilasha Surampalli, Manaswitha Khare, Georgette Kubrussi, Marie Wencel, Jasmin Tanaja, Sandra Donkervoort, Kathryn Osann, Mariella Simon, Douglas Wallace, Charles Smith, Aideen M.McInerney-Leo, Virginia Kimonis]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Genetic Counseling, 24/5(2015-10-01), 842-850
Format:
Artikel (online)
Online Zugang:
| LEADER | caa a22 4500 | ||
|---|---|---|---|
| 001 | 605544808 | ||
| 003 | CHVBK | ||
| 005 | 20210128100933.0 | ||
| 007 | cr unu---uuuuu | ||
| 008 | 210128e20151001xx s 000 0 eng | ||
| 024 | 7 | 0 | |a 10.1007/s10897-015-9819-7 |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1007/s10897-015-9819-7 | ||
| 245 | 0 | 0 | |a Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia |h [Elektronische Daten] |c [Abhilasha Surampalli, Manaswitha Khare, Georgette Kubrussi, Marie Wencel, Jasmin Tanaja, Sandra Donkervoort, Kathryn Osann, Mariella Simon, Douglas Wallace, Charles Smith, Aideen M.McInerney-Leo, Virginia Kimonis] |
| 520 | 3 | |a 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. | |
| 540 | |a National Society of Genetic Counselors, Inc., 2015 | ||
| 690 | 7 | |a Presymptomatic genetic testing |2 nationallicence | |
| 690 | 7 | |a Huntington's disease |2 nationallicence | |
| 690 | 7 | |a Neurodegenerative |2 nationallicence | |
| 690 | 7 | |a Paget's disease |2 nationallicence | |
| 690 | 7 | |a Hospital anxiety and depression scale |2 nationallicence | |
| 700 | 1 | |a Surampalli |D Abhilasha |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Khare |D Manaswitha |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Kubrussi |D Georgette |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Wencel |D Marie |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Tanaja |D Jasmin |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Donkervoort |D Sandra |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Osann |D Kathryn |u Division of Hematology/Oncology, Department of Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Simon |D Mariella |u Developmental and Cell Biology, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Wallace |D Douglas |u Developmental and Cell Biology, University of California, 92697, Irvine, CA, USA |4 aut | |
| 700 | 1 | |a Smith |D Charles |u Department of Neurology and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA |4 aut | |
| 700 | 1 | |a M.McInerney-Leo |D Aideen |u The University of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Brisbane, Australia |4 aut | |
| 700 | 1 | |a Kimonis |D Virginia |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | |
| 773 | 0 | |t Journal of Genetic Counseling |d Springer US; http://www.springer-ny.com |g 24/5(2015-10-01), 842-850 |x 1059-7700 |q 24:5<842 |1 2015 |2 24 |o 10897 | |
| 856 | 4 | 0 | |u https://doi.org/10.1007/s10897-015-9819-7 |q text/html |z Onlinezugriff via DOI |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 900 | 7 | |a Metadata rights reserved |b Springer special CC-BY-NC licence |2 nationallicence | |
| 908 | |D 1 |a research-article |2 jats | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-springer | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1007/s10897-015-9819-7 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Surampalli |D Abhilasha |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Khare |D Manaswitha |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Kubrussi |D Georgette |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Wencel |D Marie |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Tanaja |D Jasmin |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Donkervoort |D Sandra |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Osann |D Kathryn |u Division of Hematology/Oncology, Department of Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Simon |D Mariella |u Developmental and Cell Biology, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Wallace |D Douglas |u Developmental and Cell Biology, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Smith |D Charles |u Department of Neurology and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a M.McInerney-Leo |D Aideen |u The University of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Brisbane, Australia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Kimonis |D Virginia |u Department of Pediatrics, Division of Genetics and Genomic Medicine, University of California, 92697, Irvine, CA, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Journal of Genetic Counseling |d Springer US; http://www.springer-ny.com |g 24/5(2015-10-01), 842-850 |x 1059-7700 |q 24:5<842 |1 2015 |2 24 |o 10897 | ||