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A prospective study of estrogen replacement therapy and the risk of developing Alzheimer's disease

965

Citations

44

References

1997

Year

TLDR

Previous reports suggest estrogen replacement therapy may protect women against Alzheimer’s disease, but randomized trials are needed to confirm this potentially significant public health association. The study examined the association between estrogen replacement therapy and Alzheimer’s disease risk in the Baltimore Longitudinal Study of Aging. The study followed 472 post‑ or perimenopausal women for up to 16 years, prospectively recorded ERT use, and used time‑dependent Cox proportional hazards models to compare Alzheimer’s disease risk between users and non‑users. Among 472 women, 45% used ERT and 34 developed Alzheimer’s disease, with ERT users showing a 54% lower risk (RR = 0.46, 95% CI 0.21–0.997) and no dose–response effect, supporting a protective role of estrogen.

Abstract

Previous reports have suggested that estrogen replacement therapy (ERT) in women may exert a protective effect on their risk of developing Alzheimer9s disease (AD). We investigated this relationship in the Baltimore Longitudinal Study of Aging (BLSA), a prospective multidisciplinary study of normal aging conducted by the National Institute on Aging. The sample consisted of 472 post- or perimenopausal women followed for up to 16 years in the BLSA. We documented ERT prospectively at each BLSA visit, and we categorized women who had used oral or transdermal estrogens at anytime as ERT users. We used Cox proportional hazards models with time-dependent covariates to estimate the relative risk of developing AD after ERT as compared with women who had not used estrogen replacement. Approximately 45% of the women in the cohort had used ERT, and we diagnosed 34 incident cases of AD (NINCD/ADRDA criteria) during follow-up, including nine estrogen users. After adjusting for education, the relative risk for AD in ERT users as compared with nonusers was 0.46 (95% CI, 0.209–0.997), indicating a reduced risk of AD for women who had reported the use of estrogen. Our data did not show an effect for duration of ERT usage. Our finding offers additional support for a protective influence of estrogen in AD. Randomized clinical trials are necessary to confirm this association, which could have significant public health impact.

References

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