Literature DB >> 20878544

Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing?

Celine Lewis1, Heather Skirton, Ray Jones.   

Abstract

Receiving the results of genetic carrier testing may have an impact on the psychosocial health of the individual. Numerous studies have been conducted to assess the psychosocial effects of carrier status for a range of conditions. To systematically review research focused on the psychological and social impact of carrier testing on individuals in order to identify factors affecting the impact of carrier testing results, and discern areas where further research is needed. Twenty relevant papers meeting criteria for inclusion in this review were found. The main themes identified across these studies included: anxiety, guilt and stigmatization, effect on family relationships, effect on self image, active coping mechanisms and reproductive issues. Variables related to the psychosocial effect of carrier testing included whether the carrier has an affected child, mode of inheritance, genetic counseling, and life stage. A key finding concerns carriers who already have an affected child; they are more likely to experience guilt and self-blame, and change their reproductive plans compared to carriers without affected children. Additionally, some participants reported clinical features of the disorder for which they were being tested. Genetic counselors may erroneously assume that parents with affected children are aware of their own carrier status in the absence of testing, and they may offer inadequate support. Additionally, counselors should attempt to address patient misconceptions related to their health and carrier status.

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Mesh:

Year:  2010        PMID: 20878544     DOI: 10.1007/s10897-010-9327-8

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


  48 in total

1.  Tay-Sachs screening: social and psychological impact.

Authors:  B Childs; L Gordis; M M Kaback; H H Kazazian
Journal:  Am J Hum Genet       Date:  1976-11       Impact factor: 11.025

2.  A targeted population carrier screening program for severe and frequent genetic diseases in Israel.

Authors:  Joël Zlotogora; Rivka Carmi; Boaz Lev; Stavit A Shalev
Journal:  Eur J Hum Genet       Date:  2008-12-24       Impact factor: 4.246

3.  The impact of population based screening for carriers of cystic fibrosis.

Authors:  H Bekker; G Denniss; M Modell; M Bobrow; T Marteau
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

4.  Longitudinal study of the carrier testing process for fragile X syndrome: perceptions and coping.

Authors:  A McConkie-Rosell; G A Spiridigliozzi; J A Sullivan; D V Dawson; A M Lachiewicz
Journal:  Am J Med Genet       Date:  2001-01-01

5.  Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

Authors:  Jessica Ezzell Hunter; Michael P Epstein; Stuart W Tinker; Krista H Charen; Stephanie L Sherman
Journal:  Genet Epidemiol       Date:  2008-09       Impact factor: 2.135

6.  A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study.

Authors:  Sylvia Metcalfe; Alice Jacques; Alison Archibald; Trent Burgess; Veronica Collins; Anna Henry; Kathleen McNamee; Leslie Sheffield; Howard Slater; Samantha Wake; Jonathan Cohen
Journal:  Genet Med       Date:  2008-07       Impact factor: 8.822

7.  Tay-Sachs disease--carrier screening, prenatal diagnosis, and the molecular era. An international perspective, 1970 to 1993. The International TSD Data Collection Network.

Authors:  M Kaback; J Lim-Steele; D Dabholkar; D Brown; N Levy; K Zeiger
Journal:  JAMA       Date:  1993-11-17       Impact factor: 56.272

8.  Primary care patients' personal illness models for depression: relationship to coping behavior and functional disability.

Authors:  Charlotte Brown; Deena R Battista; Susan M Sereika; Richard D Bruehlman; Jacqueline Dunbar-Jacob; Michael E Thase
Journal:  Gen Hosp Psychiatry       Date:  2007 Nov-Dec       Impact factor: 3.238

9.  Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation.

Authors:  Kami Koldewyn; David Hessl; John Adams; Flora Tassone; Paul J Hagerman; Randi J Hagerman; Susan M Rivera
Journal:  Brain Imaging Behav       Date:  2008-01-18       Impact factor: 3.978

10.  Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines.

Authors:  Kathryn E Kronquist; Stephanie L Sherman; Elaine B Spector
Journal:  Genet Med       Date:  2008-11       Impact factor: 8.822

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  17 in total

Review 1.  Genetics of inherited cardiomyopathy.

Authors:  Daniel Jacoby; William J McKenna
Journal:  Eur Heart J       Date:  2011-08-02       Impact factor: 29.983

2.  Parental Defensiveness about Multifactorial Genomic and Environmental Causes of Children's Obesity Risk.

Authors:  Susan Persky; Megan R Goldring; Sherine El-Toukhy; Rebecca A Ferrer; Brittany Hollister
Journal:  Child Obes       Date:  2019-04-04       Impact factor: 2.992

Review 3.  Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.

Authors:  Jill Fonda Allen; Katie Stoll; Barbara A Bernhardt
Journal:  Semin Perinatol       Date:  2015-12-21       Impact factor: 3.300

4.  Expanded carrier screening in gamete donors of Venezuela.

Authors:  Maria Teresa Urbina; Isaac Benjamin; Randolfo Medina; José Jiménez; Laura Trías; Jorge Lerner
Journal:  JBRA Assist Reprod       Date:  2017-12-01

5.  How people in Benin assess a couple's risk of having a baby with sickle cell disease.

Authors:  Ornheilia Zounon; Paul Clay Sorum; Etienne Mullet
Journal:  J Community Genet       Date:  2014-11-25

6.  "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 7.  Challenging the Current Recommendations for Carrier Testing in Children.

Authors:  Grace E VanNoy; Casie A Genetti; Amy L McGuire; Robert C Green; Alan H Beggs; Ingrid A Holm
Journal:  Pediatrics       Date:  2019-01       Impact factor: 7.124

8.  "There Are Hills and Valleys": Experiences of Parenting a Son With X-Linked Retinoschisis.

Authors:  Amy Turriff; Rosalie Nolen; Celeste D'Amanda; Barbara Biesecker; Catherine Cukras; Paul A Sieving
Journal:  Am J Ophthalmol       Date:  2019-11-23       Impact factor: 5.258

9.  Effect of comprehensive oncogenetics training interventions for general practitioners, evaluated at multiple performance levels.

Authors:  Elisa J F Houwink; Arno M M Muijtjens; Sarah R van Teeffelen; Lidewij Henneman; Jan Joost Rethans; Florijn Jacobi; Liesbeth van der Jagt; Irina Stirbu; Scheltus J van Luijk; Connie T R M Stumpel; Hanne E Meijers-Heijboer; Cees van der Vleuten; Martina C Cornel; Geert Jan Dinant
Journal:  PLoS One       Date:  2015-04-02       Impact factor: 3.240

10.  Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics.

Authors:  S Riedijk; G Oudesluijs; A Tibben
Journal:  J Community Genet       Date:  2012-05-15
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