Abstract
Recent research has linked exposure to chronic stress to altered acute stress responses and suggests a sensitizing effect of chronic stress leading to a stronger endocrine and cardiovascular response to acute stressors. Substantial evidence indicates that familial breast cancer risk is a chronic life stressor with higher levels of self reported distress. In this study, we investigated whether the endocrine response to a brief psychological stressor was stronger for women at familial risk for breast cancer. Thirty-six women at normal risk of breast cancer (FR- Stress Group) and 17 women at familial risk (FR+ Stress Group) underwent a brief psychological laboratory stress test (speech task and mental arithmetic) over a 15 min period. Thirty women at normal risk not subjected to the stressful task served as controls (FR- Control Group). Plasma epinephrine, norepinephrine and cortisol were measured at baseline, directly after the stress test (15 min) and at 30 min and 45 min post baseline. Heart rate data confirmed the effectiveness of the stress regimen. While there were no significant baseline group differences in the endocrine parameters, the response curves for the familial risk group revealed stronger epinephrine and cortisol reactivity to the stress test, as confirmed by significant group by time interactions. Norepinephrine levels showed a similar pattern, but results did not reach significance. These findings are in line with previous research documenting the facilitating effects of chronic stressors on acute stress response in animals and humans and provide the first evidence in the literature of a heightened endocrine reactivity to acute psychological stress in women at familial risk of breast cancer. The heightened endocrine reactivity to the experimental tasks seen here suggests that these women may experience stronger responses to stressors in their daily lives. According to the recently proposed concept of allostatic load, repeated overly strong stress responses may cumulatively have negative health implications.
Original language | English |
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Pages (from-to) | 584-593 |
Number of pages | 10 |
Journal | Psychoneuroendocrinology |
Volume | 28 |
Issue number | 4 |
DOIs | |
Publication status | Published - May 2003 |
Bibliographical note
Funding Information:This investigation was supported in part by Grant M01RR00047 from the General Clinical Research Centers Program of the Division of Research Resources, National Institutes of Health. The study was also sponsored in part by grants from the Department of Defense (#DAMD J-4139 and J-4164) and the National Cancer Institute (#R01 CA72457). We are required to indicate that the content of the information contained in this report does not necessarily reflect the position or policy of the United States Government. We would also like to acknowledge the helpful comments of the anonymous reviewers.
Other keywords
- Allostatic load
- Catecholamines
- Cortisol
- Experimental stress
- Familial breast cancer risk
- Recovery