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Lombardi Cancer Center, Georgetown University Medical Center, Washington, D.C. 20007
| Abstract |
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| Introduction |
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A novel goal of this study was to explore the role of spirituality in testing decisions. Although spirituality has been linked to the avoidance of health risk behaviors (7) and decreased mortality for a variety of diseases (8) , little is known about its effects on medical decision making or on genetic testing, in particular. However, research and theory on coping with illness suggests that spirituality may actually deter participation in genetic testing for cancer risk. For example, research has shown that highly spiritual individuals are more optimistic (7) , have greater acceptance of their cancer diagnoses (9) , and are more likely to attribute health threats to external forces than to factors such as heredity (10) . Thus, a woman with breast cancer who is highly spiritual may question the need for genetic testing because she accepts her condition and believes that whether she becomes ill or not is out of her hands. This is consistent with a previous study showing an inverse relationship between spirituality and interest in prenatal testing (11) . Therefore, we hypothesized that highly spiritual individuals would be less likely than less spiritual individuals to receive BRCA1/2 testing.
The present study also focused on cancer-specific distress and perceived risk, two psychological variables that have been implicated in BRCA1/2 testing decisions. Perceived risk and cancer-specific distress have predicted intentions to obtain BRCA1/2 testing (12) . For example, among women from HBC families, we found that cancer-specific distress predicted BRCA1/2 test use (13) . Similarly, in a recent study, both perceived risk and cancer worries were associated with genetic testing for colorectal cancer susceptibility (14) . Therefore, in the present study, we predicted that perceived risk and cancer-specific distress would increase the likelihood of BRCA1/2 testing, whereas spirituality would reduce test use.
| Materials and Methods |
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Procedures.
Probands who contacted the CARE program were screened by telephone to
determine eligibility. Eligible probands completed a structured
telephone interview that assessed sociodemographics, cancer family
history, spirituality, perceived risk, and psychological distress.
Following this interview, participants were invited to a pretest
education session with a genetic counselor. Information provided to
probands during this 1.52-h session included qualitative risk
assessments based on their personal and family history, details about
the process of testing for BRCA1/2 mutations and
interpretation of test results, cancer risks associated with
BRCA1/2 mutations, options for cancer prevention and
surveillance (based on published guidelines; Ref. 16
), details about
the benefits and risks/limitations of testing, and details about the
possible psychosocial impact of testing.
Following the educational session, participants were offered the opportunity to provide a blood sample for BRCA1/2 mutation testing after providing written consent. When a participants test result became available, the participant was invited to a disclosure/counseling session. Participants could decline to continue at any point in the process (i.e., before education, after education, or before the receipt of test results). Thus, uptake was defined as the actual receipt of BRCA1/2 test results.
| Measures |
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Sociodemographics.
We assessed age, race, religion, education, and marital status.
Family History of Cancer.
We assessed the number of first-degree relatives (i.e.,
parents, siblings, children) who were affected with breast and/or
ovarian cancer. We dichotomized family history as one to two affected
relatives versus three or more affected relatives.
Spirituality.
Spirituality was assessed with the following item adopted by the NIH
Cancer Genetics Studies Consortium: "How strong would you say your
religious or spiritual faith is?" Participants responded using a
four-point Likert scale ranging from not very strong to very strong. To
create groups of as close to equal in size as possible, we dichotomized
this item into very strong (n = 123) versus
not very strong/a little strong/moderately strong (n =
167).
Cancer-specific Distress.
We used The Intrusion Subscale of the Impact of Events Scale
(17)
to measure the frequency and severity of intrusive
thoughts, worries, and feelings about being at increased risk for
breast and ovarian cancer. Responses were on a Likert scale ranging
from not at all to often. The seven-item Intrusion subscale had good
internal consistency (Cronbachs
, 0.84) and has been used in
previous studies to measure cancer-specific distress (13
, 18)
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Breast Cancer Perceived Risk.
We measured perceived risk for breast cancer with the following
Likert-style item (19)
: "In your opinion, compared to
other women your age, what are your chances of developing breast cancer
again?" (1 = much lower to 5 = much higher). Because
responses to this item were not normally distributed, we dichotomized
the item as close to the median as possible [much higher
(n = 151) versus somewhat higher/the
same/lower (n = 139)].
Ovarian Cancer Perceived Risk.
We measured perceived risk for ovarian cancer with the following
Likert-style item: "In your opinion, compared to other women your
age, what are your chances of developing ovarian cancer?" (1 =
much lower to 5 = much higher). We dichotomized this item as close
to the median as possible [much higher/somewhat higher
(n = 148) versus the same/lower
(n = 142).
Dependent Variable.
We classified test uptake based on whether or not participants
underwent testing and received their result versus declined
testing or test results (i.e., declined to attend the
pretest education session, declined to provide a DNA sample, or
declined to learn their test result).
| Results |
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Predictors of Test Use.
As shown in Table 2
, spiritual faith [
2 (1, n =
290) = 6.01, P = 0.01] and perceived risk for
ovarian cancer [
2 (1, n =
290) = 8.53, P < 0.01] were significantly
associated with uptake. The association between breast cancer perceived
risk and uptake approached significance [
2 (1,
n = 290) = 3.47, P = 0.06] and
was included in the multivariate modeling.
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2 change (1, n = 290) = 0.14,
P > 0.20]. None of the remaining variables could be
removed from the model. Thus, the final model (see Table 3
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| Discussion |
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Women who perceived their risk for ovarian cancer to be high, were most likely to be tested. This is not surprising because none of these women had previously been diagnosed with ovarian cancer. For this group, the results of a BRCA1/2 test could have important implications for decision-making regarding ovarian cancer prevention and surveillance. Thus, women who believe that they are at high risk for ovarian cancer may be particularly motivated to learn their BRCA1/2 status.
Although the role of spirituality in health and well-being has have received extensive attention (20, 21, 22) , the present study is the first to evaluate its influence on genetic testing for cancer susceptibility. The influence of spirituality on testing decisions may be attributable, in part, to the fact that this sample was comprised of individuals who had been previously affected with breast cancer. Previous research has found that spiritual and religious beliefs are used by cancer patients to find meaning in and to facilitate acceptance of their cancer experience (9) . Whereas finding meaning may involve attempts to understand the cause of the disease, acceptance involves coming to terms with the fact that it has happened (23 , 24) . Breast cancer patients with higher levels of spiritual faith may be less likely to receive BRCA1/2 testing because they are less motivated to understand the cause of their cancer and have greater acceptance.
This effect of spiritual faith on testing decisions was dependent on a womans perceived risk of developing cancer again. Among women with low levels of perceived risk, those who were highly spiritual were five times less likely to receive test results compared with women with lower levels of spiritual faith. Importantly, spiritual faith did not predict uptake of testing among women who perceived their cancer risk to be high. The modifying influence of perceived cancer risk is consistent with previous research showing that low levels of perceived cancer risk are associated with decreased readiness and interest in genetic testing (25 , 26) . Thus, women with high spiritual faith and low perceived risk would be least likely to obtain BRCA1/2 test results. However, as perceived cancer risk increases, motivation to reduce uncertainty may also increase, so that even highly spiritual women overcome their reluctance to obtain test results.
There are a few caveats about these findings. First, this sample was limited to women who self-referred for genetic counseling and agreed to complete a baseline telephone interview. Thus, the 83% uptake rate may be higher than rates of test use in population-based or clinic-based samples in which the denominator includes all eligible women. Second, all study participants were affected with breast cancer and members of high-risk families. Thus, we cannot assume that rates of test use or predictors of use would apply to low risk or unaffected individuals. Third, all testing and counseling was offered free of charge and, therefore, may overestimate levels of uptake in fee-for-service settings. Finally, our measure of spirituality was based on a single item. The use of more sophisticated measures of spirituality could yield a better understanding of the association between spirituality and BRCA1/2 test use. Nonetheless, the primary finding regarding the role of spirituality in testing decisions is not likely to be influenced by factors such as the cost of testing; however, this may vary among members of different ethnic groups.
Despite these limitations, this study is the first to show that high levels of spiritual faith may deter genetic testing among some women with familial breast cancer. Future research should extend these findings by evaluating the role of spirituality in the testing decisions of unaffected individuals and members of different ethnic groups. Also, additional studies are needed to elucidate the cognitive and emotional correlates of spirituality that may deter genetic testing. Such research is important to better inform clinicians about how and when to incorporate discussions of spirituality into genetic counseling.
| Acknowledgments |
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| Footnotes |
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1 Supported by Department of Defense Grant DAMB
17-96-C-6069 (to C. L.), Grant RO1 CA/HG74861 (to C. L.) from
the National Cancer Institute and Institute for Human Genome Research,
and National Cancer Institute Grant KO7 CA65597 (to M. D. S.). ![]()
2 To whom requests for reprints should be
addressed, at Lombardi Cancer Center, Cancer Control, 2233 Wisconsin
Avenue, Suite 317, Washington, D.C. 20007. Phone: (202) 687-0185; Fax:
(202) 687-8444; E-mail: Schwartm{at}gunet.georgetown.edu ![]()
3 The abbreviations used are: HBC, hereditary
breast cancer; CARE, Cancer Assessment and Risk Evaluation; OR, odds
ratio; CI, confidence interval. ![]()
Received 10/ 7/99; revised 1/10/00; accepted 1/28/00.
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