Literature DB >> 35082397

Outcomes of support groups for carriers of BRCA 1/2 pathogenic variants and their relatives: a systematic review.

Benedetta Bertonazzi1, Daniela Turchetti2,3, Lea Godino1,4.   

Abstract

People tested positive for BRCA1/2 face an increased risk of cancer; to help them cope with the genetic information received, support to BRCA1/2 families should be continued after testing. Nonetheless how such support should be provided has not been established yet. As a potentially valuable option is represented by support groups, the aim of this systematic review was to assess studies exploring the outcomes of support groups for BRCA1/2 carriers. This study adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and was registered in the International Prospective Register of Systematic Reviews (PROSPERO) database (CRD42021238416). Peer-reviewed papers published between January 1995 and February 2021 were searched for, using four databases. Among 1586 records identified, 34 papers were reviewed in full-text and eleven were included in the qualitative synthesis of the results. Three themes emerged as major focuses of support groups: risk management decisions, family dynamics and risk communication, and psychosocial functioning. Our findings show that support groups proved helpful in supporting women's decision-making on risk-reducing options. Moreover, during those interventions, BRCA1/2 carriers had the opportunity to share thoughts and feelings, and felt that mutual support through interacting with other mutation carriers help them release the emotional pressure. However, no significant impact was reported in improving family communication. Overall, a high level of satisfaction and perceived helpfulness was reported for support group. The findings suggest that support groups represent a valuable tool for improving BRCA1/2 families care.
© 2022. The Author(s), under exclusive licence to European Society of Human Genetics.

Entities:  

Mesh:

Year:  2022        PMID: 35082397      PMCID: PMC8989997          DOI: 10.1038/s41431-022-01044-7

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  47 in total

1.  Psychological distress in women at risk for hereditary breast cancer: the role of family communication and perceived social support.

Authors:  Mariska den Heijer; Caroline Seynaeve; Kathleen Vanheusden; Hugo J Duivenvoorden; Carina C M Bartels; Marian B E Menke-Pluymers; Aad Tibben
Journal:  Psychooncology       Date:  2010-10-05       Impact factor: 3.894

2.  Ambiguous loss and disenfranchised grief: the impact of DNA predictive testing on the family as a system.

Authors:  Susan Sobel; C Brookes Cowan
Journal:  Fam Process       Date:  2003

3.  "Social separation" among women under 40 years of age diagnosed with breast cancer and carrying a BRCA1 or BRCA2 mutation.

Authors:  Regina Kenen; Audrey Ardern-Jones; Rosalind Eeles
Journal:  J Genet Couns       Date:  2006-06       Impact factor: 2.537

4.  Presymptomatic genetic testing for hereditary cancer in young adults: a survey of young adults and parents.

Authors:  Lea Godino; Daniela Turchetti; Leigh Jackson; Catherine Hennessy; Heather Skirton
Journal:  Eur J Hum Genet       Date:  2018-10-04       Impact factor: 4.246

5.  Impact of genetic testing for Huntington disease on the family system.

Authors:  S K Sobel; D B Cowan
Journal:  Am J Med Genet       Date:  2000-01-03

6.  Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 years.

Authors:  Karin M Landsbergen; Judith B Prins; Yvonne J L Kamm; Han G Brunner; Nicoline Hoogerbrugge
Journal:  Fam Cancer       Date:  2010-06       Impact factor: 2.375

7.  Family issues in a psychoeducation group for women with a BRCA mutation.

Authors:  J Speice; S H McDaniel; P T Rowley; S Loader
Journal:  Clin Genet       Date:  2002-08       Impact factor: 4.438

8.  A multicenter study of supportive-expressive group therapy for women with BRCA1/BRCA2 mutations.

Authors:  Mary Jane Esplen; Jon Hunter; Molyn Leszcz; Ellen Warner; Steven Narod; Kelly Metcalfe; Gord Glendon; Kate Butler; Alexander Liede; Mary Anne Young; Stephanie Kieffer; Lisa DiProspero; Ellen Irwin; Jiahui Wong
Journal:  Cancer       Date:  2004-11-15       Impact factor: 6.860

9.  Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research.

Authors:  Alison Metcalfe; Jane Coad; Gill M Plumridge; Paramjit Gill; Peter Farndon
Journal:  Eur J Hum Genet       Date:  2008-04-23       Impact factor: 4.246

10.  Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach.

Authors:  Maria Luisa Di Pietro; Drieda Zaçe; Alessia Orfino; Francesca Romana Di Raimo; Andrea Poscia; Elisabetta de Matteis; Daniela Turchetti; Lea Godino; Benedetta Bertonazzi; Marzena Franiuk; Carla Bruzzone; Liliana Varesco; Emanuela Lucci-Cordisco; Maurizio Genuardi
Journal:  Eur J Hum Genet       Date:  2020-09-14       Impact factor: 4.246

View more
  1 in total

1.  No April fools in clinical genomics.

Authors:  Alisdair McNeill
Journal:  Eur J Hum Genet       Date:  2022-04       Impact factor: 4.246

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.