Psychological impact of genetic testing for hereditary nonpolyposis colorectal cancer

被引:90
作者
Gritz, ER
Peterson, SK
Vernon, SW
Marani, SK
Baile, WF
Watts, BG
Amos, CL
Frazier, ML
Lynch, PM
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Behav Sci, Houston, TX 77030 USA
[2] Univ Texas, Hlth Sci Ctr, Sch Publ Hlth, Houston, TX USA
关键词
D O I
10.1200/JCO.2005.07.102
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose This study examines the impact of hereditary nonpolyposis colorectal cancer (HNPCC) genetic test results on psychological outcomes among cancer-affected and -unaffected participants up to 1 year after results disclosure. Patients and Methods A total of 155 persons completed study measures before HNPCC genetic testing, and at 2 weeks and 6 and 12 months after disclosure of test results. Results Mean scores on all outcome measures remained stable and within normal limits for cancer-affected participants regardless of mutation status. Among unaffected carriers of, HNPCC-predisposing mutations, mean depression, state anxiety, and cancer worries scores increased from baseline to 2 weeks postdisclosure and decreased from 2 weeks to 6 months postdisclosure. Among unaffected noncarriers, mean depression and anxiety scores did not differ, but cancer worries scores decreased during the same time period. Affected and unaffected carriers had higher mean test-specific distress scores at 2 weeks postdisclosure compared with noncarriers in their respective groups; scores decreased for affected carriers and all unaffected participants from 2 weeks to 12 months postdisclosure. Classification of participants into high- versus low-distress clusters using mean scores on baseline psychological measures predicted significantly higher or lower follow-up scores, respectively, on depression, state anxiety, quality of life, and test-specific distress measures, regardless of mutation status. Conclusion Although HNPCC genetic testing does not result in long-term adverse psychological outcomes, unaffected mutation carriers may experience increased distress during the immediate postdisclosure time period. Furthermore, those with higher levels of baseline mood disturbance, lower quality of life, and lower social support may be at risk for both short- and long-term increased distress. (c) 2005 by American Society of Clinical Oncology.
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页码:1902 / 1910
页数:9
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