Literature DB >> 20878217

More appreciation of life or regretting the test? Experiences of living as a mutation carrier of Huntington's disease.

Anette Hagberg1, The-Hung Bui, Elisabeth Winnberg.   

Abstract

Little is known about how the knowledge of being a mutation carrier for Huntington's disease (HD) influences lives, emotionally and socially. In this qualitative study 10 interviews were conducted to explore the long term (>5 years) experiences of being a mutation carrier. The results showed a broad variety of both positive and negative impact on the carriers' lives. The most prominent positive changes reported were a greater appreciation of life and a tendency to bring the family closer together. On the other hand, some participants expressed decisional regrets and discussed the negative impact this knowledge had on their psychological well-being. The knowledge variously served as either a motivator or an obstacle in pursuing further education, career or investment in personal health. Deeper understanding of people's reactions to the certainty of knowing they will become affected with HD is essential for the genetic counseling team in order to provide appropriate support.

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Year:  2010        PMID: 20878217     DOI: 10.1007/s10897-010-9329-6

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  30 in total

1.  Psychological studies in Huntington's disease: making up the balance.

Authors:  M Duisterhof; R W Trijsburg; M F Niermeijer; R A Roos; A Tibben
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

Review 2.  Content analysis: review of methods and their applications in nutrition education.

Authors:  Nancy L Kondracki; Nancy S Wellman; Daniel R Amundson
Journal:  J Nutr Educ Behav       Date:  2002 Jul-Aug       Impact factor: 3.045

3.  Adverse effects of predictive testing for Huntington disease underestimated: long-term effects 7-10 years after the test.

Authors:  Reinier Timman; Raymund Roos; Anneke Maat-Kievit; Aad Tibben
Journal:  Health Psychol       Date:  2004-03       Impact factor: 4.267

4.  Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic status.

Authors:  T B Wahlin; A Lundin; L Bäckman; E Almqvist; A Haegermark; B Winblad; M Anvret
Journal:  Am J Med Genet       Date:  1997-12-19

5.  A polymorphic DNA marker genetically linked to Huntington's disease.

Authors:  J F Gusella; N S Wexler; P M Conneally; S L Naylor; M A Anderson; R E Tanzi; P C Watkins; K Ottina; M R Wallace; A Y Sakaguchi
Journal:  Nature       Date:  1983 Nov 17-23       Impact factor: 49.962

Review 6.  The qualitative research interview.

Authors:  Barbara Dicicco-Bloom; Benjamin F Crabtree
Journal:  Med Educ       Date:  2006-04       Impact factor: 6.251

7.  Risk reversals in predictive testing for Huntington disease.

Authors:  E Almqvist; S Adam; M Bloch; A Fuller; P Welch; D Eisenberg; D Whelan; D Macgregor; W Meschino; M R Hayden
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

8.  On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program.

Authors:  A Tibben; P G Frets; J J van de Kamp; M F Niermeijer; M Vegtervan der Vlis; R A Roos; H G Rooymans; G J van Ommen; F Verhage
Journal:  Am J Med Genet       Date:  1993-07-15

9.  Impact on couple relationships of predictive testing for Huntington disease: a longitudinal study.

Authors:  Fiona Richards; Katrina Williams
Journal:  Am J Med Genet A       Date:  2004-04-15       Impact factor: 2.802

10.  Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk.

Authors:  M Huggins; M Bloch; S Wiggins; S Adam; O Suchowersky; M Trew; M Klimek; C R Greenberg; M Eleff; L P Thompson
Journal:  Am J Med Genet       Date:  1992-02-15
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  7 in total

1.  What to Do with a Second Chance in Life? Long-Term Experiences of Non-carriers of Huntington's Disease.

Authors:  Elisabeth Winnberg; Ulrika Winnberg; Lilian Pohlkamp; Anette Hagberg
Journal:  J Genet Couns       Date:  2018-04-07       Impact factor: 2.537

Review 2.  The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature.

Authors:  S Crozier; N Robertson; M Dale
Journal:  J Genet Couns       Date:  2014-09-20       Impact factor: 2.537

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

Authors:  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
Journal:  J Genet Couns       Date:  2015-02-26       Impact factor: 2.537

4.  Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease.

Authors:  K M Stuttgen; J M Bollinger; R L Dvoskin; A McCague; B Shpritz; J Brandt; Debra J H Mathews
Journal:  J Genet Couns       Date:  2018-07-02       Impact factor: 2.537

5.  'A sword of Damocles': patient and caregiver beliefs, attitudes and perspectives on presymptomatic testing for autosomal dominant polycystic kidney disease: a focus group study.

Authors:  Charlotte Logeman; Yeoungjee Cho; Benedicte Sautenet; Gopala K Rangan; Talia Gutman; Jonathan Craig; Albert Ong; Arlene Chapman; Curie Ahn; Helen Coolican; Juliana Tze-Wah Kao; Ron T Gansevoort; Ronald Perrone; Tess Harris; Vincent Torres; Kevin Fowler; York Pei; Peter Kerr; Jessica Ryan; David Johnson; Andrea Viecelli; Clair Geneste; Hyunsuk Kim; Yaerim Kim; Martin Howell; Angela Ju; Karine E Manera; Armando Teixeira-Pinto; Gayathri Parasivam; Allison Tong
Journal:  BMJ Open       Date:  2020-10-10       Impact factor: 2.692

6.  Understanding the physical and emotional impact of early-stage ADPKD: experiences and perspectives of patients and physicians.

Authors:  Anna Baker; Dominic King; James Marsh; Andrew Makin; Alison Carr; Catherine Davis; Cara Kirby
Journal:  Clin Kidney J       Date:  2015-07-28

7.  More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington's Disease.

Authors:  Nicolò Zarotti; Maria Dale; Fiona J R Eccles; Jane Simpson
Journal:  J Pers Med       Date:  2022-01-07
  7 in total

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