期刊
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 97, 期 9, 页码 3207-3215出版社
ENDOCRINE SOC
DOI: 10.1210/jc.2012-1413
关键词
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资金
- Harvard Medical School Fund for Women's Health, Friends of Dana-Farber Cancer Institute
- Massachusetts General Hospital Claflin Distinguished Scholar Award
- NIMH
- NIH
- Cephalon
- Tufts University
- Janssen Pharmaceuticals
- Forest Research Institute
- Shire Development Inc.
- Medtronic
- Cyberonics
- Northstar
- MGH Psychiatry Academy
- BrainCells Inc.
- Systems Research and Applications Corporation
- Boston University
- National Association of Social Workers Massachusetts
- Massachusetts Medical Society
- Oxford University Press
Context: Hot flashes are a common side effect of adjuvant endocrine therapies (AET; leuprolide, tamoxifen, aromatase inhibitors) that reduce quality of life and treatment adherence in breast cancer patients. Because hot flashes affect only some women, preexisting neurobiological traits might predispose to their development. Previous studies have implicated the insula during the perception of hot flashes and the hypothalamus in thermoregulatory dysfunction. Objective: The aim of the study was to understand whether neurobiological factors predict hot flashes. Design: [18F]-Fluorodeoxyglucose (FDG) positron emission tomography (PET) brain scans coregistered with structural magnetic resonance imaging were used to determine whether metabolic activity in the insula and hypothalamic thermoregulatory and estrogen-feedback regions measured before and in response to AET predict hot flashes. Findings were correlated with CYP2D6 genotype because of CYP2D6 polymorphism associations with tamoxifen-induced hot flashes. Outcome Measures: We measured regional cerebral metabolic rate of glucose uptake (rCMRglu) in the insula and hypothalamus on FDG-PET. Results: Of 18 women without hot flashes who began AET, new-onset hot flashes were reported by 10 (55.6%) and were detected objectively in nine (50%) participants. Prior to the use of all AET, rCMRglu in the insula (P <= 0.01) and hypothalamic thermoregulatory (P = 0.045) and estrogen-feedback (P = 0.007) regions was lower in women who reported developing hot flashes. In response to AET, rCMRglu was further reduced in the insula in women developing hot flashes (P <= 0.02). Insular and hypothalamic rCMRglu levels were lower in intermediate than extensive CYP2D6 metabolizers. Conclusions: Trait neurobiological characteristics predict hot flashes. Genetic variability in CYP2D6 may underlie the neurobiological predisposition to hot flashes induced by AET. (J Clin Endocrinol Metab 97: 3207-3215, 2012)
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