Attitudes and distress levels in women at risk to carry a BRCA1/BRCA2 gene mutation who decline genetic testing

被引:25
|
作者
Lodder, L
Frets, PG
Trijsburg, RW
Klijn, JGM
Seynaeve, C
Tilanus, MMA
Bartels, CCM
Meijers-Heijboer, EJ
Verhoog, LC
Niermeijer, MF
机构
[1] Erasmus Univ, Dept Med Psychol & Psychotherapy, Netherlands Inst Hlth Sci, Rotterdam, Netherlands
[2] Erasmus Univ, Univ Hosp Dijkzigt, Dept Clin Genet, Rotterdam, Netherlands
[3] Univ Rotterdam Hosp, David den Hoed Canc Inst, Rotterdam, Netherlands
来源
关键词
genetic testing; non-participants; breast and ovarian cancer; attitudes;
D O I
10.1002/ajmg.a.10168
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic testing enables women at risk for hereditary breast and/or ovarian cancer to find out whether they have inherited the gene mutation, and if so, to opt for undergoing frequent surveillance and/or prophylactic surgery. However, the option to know about one's genetic status is not always seen as a benefit by women at risk. Motives for declining genetic testing were explored in 13 women at 25% or 50% risk to be a BRCA1/ BRCA2 mutation carrier, who participated in a surveillance program for breast/ovarian cancer (the non-tested group). We hypothesized that high anxiety might be an important motive to decline testing. In addition, we investigated whether the non-tested group differed from a reference group of women who did undergo the test (tested group; n = 85) with regard to biographical factors, experience with cancer in relatives, and personality traits. Most non-tested women (10/13) were satisfied with participating in the surveillance program. Four reported to feel emotionally unprepared to cope with the consequences of testing. Compared with the tested group, the non-tested women had similar mean distress levels (which were not high), but a higher education level, they were more often childless, showed more reluctance towards prophylactic surgery, were younger when first confronted with a relative affected with breast/ovarian cancer, and were longer aware of the genetic nature of the disease. This study showed that women were more likely to have thoroughly reflected on their decision not to undergo genetic testing, than to deny the whole issue due to high anxiety. Being confronted at a relatively young age with breast/ovarian cancer in a relative, and being aware of the genetic risk for a many years, may have resulted in the risk for cancer becoming an integrated part of their lives. However, generalization of these results to women who neither underwent the test nor participated in a surveillance program should be considered with caution. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:266 / 272
页数:7
相关论文
共 50 条
  • [21] Management updates for women with a BRCA1 or BRCA2 mutation
    Nusbaum, Rachel
    Isaacs, Claudine
    MOLECULAR DIAGNOSIS & THERAPY, 2007, 11 (03) : 133 - 144
  • [22] BRCA1 and BRCA2: The genetic testing and the current management options for mutation carriers
    Palma, M
    Ristori, E
    Ricevuto, E
    Giannini, G
    Gulino, A
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2006, 57 (01) : 1 - 23
  • [23] Genetic testing and prophylactic surgery in familiar clusters of BRCA1 or BRCA2 mutation
    Meijers-Heijboer, EJ
    Verhoog, LC
    Brekelmans, CTM
    Seynaeve, C
    Tilanus-Linthorst, MMA
    Wagner, A
    Dukel, L
    Devilee, P
    van den Ouweland, AMW
    van Geel, AN
    Klijn, JGM
    GYNAKOLOGE, 2000, 33 (10): : 768 - 769
  • [24] Development and Testing of a Decision Aid for Unaffected Women with a BRCA1 or BRCA2 Mutation
    Jabaley, Terri
    Underhill-Blazey, Meghan L.
    Berry, Donna L.
    JOURNAL OF CANCER EDUCATION, 2020, 35 (02) : 339 - 344
  • [25] Development and Testing of a Decision Aid for Unaffected Women with a BRCA1 or BRCA2 Mutation
    Terri Jabaley
    Meghan L. Underhill-Blazey
    Donna L. Berry
    Journal of Cancer Education, 2020, 35 : 339 - 344
  • [26] Genetic testing for BRCA1 and BRCA2 in the Province of Ontario
    Finch, A.
    Wang, M.
    Fine, A.
    Atri, L.
    Khalouei, S.
    Pupavac, M.
    Rosen, B.
    Eisen, A.
    Elser, C.
    Charames, G.
    Metcalfe, K.
    Chang, M. C.
    Narod, S. A.
    Lerner-Ellis, J.
    CLINICAL GENETICS, 2016, 89 (03) : 304 - 311
  • [27] Modeling the probability that Ashkenazi Jewish women carry a founder mutation in BRCA1 or BRCA2 - Response
    Wacholder, S
    Hartge, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (06) : 1775 - 1776
  • [28] Why not to screen high-risk women anticipating BRCA1/BRCA2 testing for psychological distress
    Benazon, NR
    Coyne, JC
    Calzone, KA
    Weber, BL
    JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 2002, 70 (01) : 258 - 258
  • [29] Retesting of women who are negative for a BRCA1 and BRCA2 mutation using a 20-gene panel
    Lerner-Ellis, Jordan
    Sopik, Victoria
    Wong, Andrew
    Lazaro, Conxi
    Narod, Steven A.
    Charames, George S.
    JOURNAL OF MEDICAL GENETICS, 2020, 57 (06) : 380 - 384
  • [30] Clinical testing for gene rearrangements in BRCA1 AND BRCA2
    Hendrickson, B. C.
    Judkins, T.
    Eliason, K.
    Schoenberger, J.
    Rajamani, S.
    McCulloch, J.
    Potekhin, V.
    Deffenbaugh, A. M.
    Ward, B. E.
    Scholl, T.
    Roa, B. B.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (05): : 629 - 629