Literature DB >> 33788978

Men with an FMR1 premutation and their health education needs.

Matthew B Walsh1, Krista Charen1, Lisa Shubeck1, Allyn McConkie-Rosell2, Nadia Ali1, Cecelia Bellcross1, Stephanie L Sherman1.   

Abstract

Men who carry an FMR1 premutation are at-risk to develop a late-onset neurodegenerative disorder called fragile X-Associated Ataxia/Tremor syndrome (FXTAS). However, little is known about their health informational needs. This qualitative study is the first to describe diagnostic experiences and identify specific health information needs of male premutation carriers. In-depth qualitative interviews were conducted by phone with ten men who carry an FMR1 premutation. Interviews were analyzed using direct content analysis. Saturation was assessed through use of the Comparative Method for Themes Saturation in qualitative interviews (CoMeTS). Five themes were identified: diagnosis experience, sources of health information, desired health information, barriers to obtaining health information, and facilitators to desired health information. Participants desired information about inheritance, symptoms, expectations for disease, and actions available to slow progression. Facilitators to obtaining health information included healthcare provider knowledge, positive experiences with providers, beneficial family dynamics, participating in research, and access to experts. Barriers to obtaining health information included lack of personal knowledge, lack of healthcare provider knowledge, negative experiences with providers, and uncertainty. Addressing the educational needs of men with/at-risk for FXTAS could improve the quality of life of men who carry a fragile X premutation.
© 2021 National Society of Genetic Counselors.

Entities:  

Keywords:  FMR1 premutation; FXTAS; communication; education; genetic counseling; qualitative analysis

Mesh:

Substances:

Year:  2021        PMID: 33788978      PMCID: PMC8363520          DOI: 10.1002/jgc4.1399

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.717


  28 in total

1.  Three approaches to qualitative content analysis.

Authors:  Hsiu-Fang Hsieh; Sarah E Shannon
Journal:  Qual Health Res       Date:  2005-11

2.  Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective.

Authors:  Allyn McConkie-Rosell; Jacqueline Del Giorno; Elizabeth Melvin Heise
Journal:  J Genet Couns       Date:  2010-09-28       Impact factor: 2.537

3.  Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).

Authors:  Heather S Hipp; Krista H Charen; Jessica B Spencer; Emily G Allen; Stephanie L Sherman
Journal:  Menopause       Date:  2016-09       Impact factor: 2.953

Review 4.  Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.

Authors:  Luis R Hoyos; Mili Thakur
Journal:  J Assist Reprod Genet       Date:  2016-12-19       Impact factor: 3.412

5.  "It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.

Authors:  Charlotte von der Lippe; Jan C Frich; Anna Harris; Kari Nyheim Solbrække
Journal:  J Genet Couns       Date:  2017-05-26       Impact factor: 2.537

Review 6.  Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management.

Authors:  Randi J Hagerman; Paul Hagerman
Journal:  Nat Rev Neurol       Date:  2016-06-24       Impact factor: 42.937

Review 7.  Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines.

Authors:  Elizabeth Berry-Kravis; Liane Abrams; Sarah M Coffey; Deborah A Hall; Claudia Greco; Louise W Gane; Jim Grigsby; James A Bourgeois; Brenda Finucane; Sebastien Jacquemont; James A Brunberg; Lin Zhang; Janet Lin; Flora Tassone; Paul J Hagerman; Randi J Hagerman; Maureen A Leehey
Journal:  Mov Disord       Date:  2007-10-31       Impact factor: 10.338

8.  Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.

Authors:  Sébastien Jacquemont; Randi J Hagerman; Maureen A Leehey; Deborah A Hall; Richard A Levine; James A Brunberg; Lin Zhang; Tristan Jardini; Louise W Gane; Susan W Harris; Kristin Herman; James Grigsby; Claudia M Greco; Elizabeth Berry-Kravis; Flora Tassone; Paul J Hagerman
Journal:  JAMA       Date:  2004-01-28       Impact factor: 56.272

9.  How does the mode of inheritance of a genetic condition influence families? A study of guilt, blame, stigma, and understanding of inheritance and reproductive risks in families with X-linked and autosomal recessive diseases.

Authors:  Cynthia A James; Donald W Hadley; Neil A Holtzman; Jerry A Winkelstein
Journal:  Genet Med       Date:  2006-04       Impact factor: 8.822

10.  "It's got to be on this page": age and cognitive style in a study of online health information seeking.

Authors:  Emily M Agree; Abby C King; Cynthia M Castro; Adrienne Wiley; Dina L G Borzekowski
Journal:  J Med Internet Res       Date:  2015-03-24       Impact factor: 5.428

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