What happens after menopause? (WHAM): Impact of risk-reducing salpingo-oophorectomy on depressive and anxiety symptoms at 24 months.

Gynecol Oncol

Connors Center for Women's Health and Gender Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Published: November 2024

AI Article Synopsis

  • Women with BRCA1 and BRCA2 pathogenic variants may experience surgical menopause after RRSO, with previous studies showing increased depressive and anxiety symptoms at 6 and 12 months post-surgery.
  • A controlled study tracking 59 women undergoing RRSO and 91 comparison women found that, at 24 months, depressive and anxiety symptoms were not significantly elevated and did not differ between the two groups. However, symptoms at 12 months strongly predicted outcomes at 24 months.
  • The study concluded that while symptoms don't seem to escalate after 24 months, persistent symptoms observed at 12 months can indicate ongoing issues, with no significant impact from Menopausal Hormone Therapy on mental health.

Article Abstract

Objective: For women with pathogenic variants in BRCA1 and BRCA2, risk-reducing salpingo-oophorectomy (RRSO) at the recommended age causes surgical menopause. We previously reported elevated depressive symptoms at 6 and 12 months and elevated anxiety symptoms at 6 months after RRSO. We now report these outcomes at 24 months, their baseline and 12-month predictors and the effect of Menopausal Hormone Therapy (MHT).

Methods: Prospective controlled study of 59 premenopausal women planning RRSO and 91 comparisons who retained their ovaries. Depressive (CESD) and anxiety symptoms (GAD-7) were measured at baseline (before RRSO) and at 12 and 24 months. We used ordinary and logistic multivariable regression to estimate differences between and within groups at 24 months, before and after conditioning on baseline and 12 month measures.

Results: Overall, depressive and anxiety symptoms were not elevated above baseline at 24 months and did not differ between RRSO and comparisons, before or after adjusting for previous measures (P > 0.05). Elevated depressive symptoms at 12 months (OR = 24, P < 0.001), and elevated anxiety symptoms at 12 months (OR = 13, P < 0.001), strongly predicted 24 month measures. Elevated depressive symptoms at baseline no longer predicted 24 month symptoms once 12 month symptoms were considered, but elevated baseline anxiety still predicted anxiety at 24 months, even when 12 month anxiety was considered. No association between MHT use and depressive or anxiety symptoms was observed.

Conclusions: Depressive and anxiety symptoms are not elevated 24 months after RRSO. However, depressive symptoms at 12 months after RRSO are likely to persist at 24 months.

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Source
http://dx.doi.org/10.1016/j.ygyno.2024.10.031DOI Listing

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