Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, United States.
Connors Center for Women's Health and Gender Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, United States.
J Clin Endocrinol Metab. 2022 Sep 28;107(10):e4144-e4153. doi: 10.1210/clinem/dgac447.
Nocturnal vasomotor symptoms (nVMS), depressive symptoms (DepSx), and female reproductive hormone changes contribute to perimenopause-associated disruption in sleep continuity. Hormonal changes underlie both nVMS and DepSx. However, their association with sleep continuity parameters resulting in perimenopause-associated sleep disruption remains unclear.
We aimed to determine the association between female reproductive hormones and perimenopausal sleep discontinuity independent of nVMS and DepSx.
Daily sleep and VMS diaries, and weekly serum assays of female reproductive hormones were obtained for 8 consecutive weeks in 45 perimenopausal women with mild DepSx but no primary sleep disorder. Generalized estimating equations were used to examine associations of estradiol, progesterone, and follicle stimulating hormone (FSH) with mean number of nightly awakenings, wakefulness after sleep onset (WASO) and sleep-onset latency (SOL) adjusting for nVMS and DepSx.
Sleep disruption was common (median 1.5 awakenings/night, WASO 24.3 and SOL 20.0 minutes). More awakenings were associated with estradiol levels in the postmenopausal range (β = 0.14; 95% CI, 0.04 to 0.24; P = 0.007), and higher FSH levels (β [1-unit increase] = 0.12; 95% CI, 0.02 to 0.22; P = 0.02), but not with progesterone (β [1-unit increase] = -0.02; 95% CI, -0.06 to 0.01; P = 0.20) in adjusted models. Female reproductive hormones were not associated with WASO or SOL.
Associations of more awakenings with lower estradiol and higher FSH levels provide support for a perimenopause-associated sleep discontinuity condition that is linked with female reproductive hormone changes, independent of nVMS and DepSx.
夜间血管舒缩症状(nVMS)、抑郁症状(DepSx)和女性生殖激素变化导致围绝经期睡眠连续性中断。nVMS 和 DepSx 都与激素变化有关。然而,它们与导致围绝经期睡眠障碍的睡眠连续性参数之间的关联尚不清楚。
我们旨在确定女性生殖激素与围绝经期睡眠中断之间的关联,而不考虑 nVMS 和 DepSx。
在 45 名患有轻度 DepSx 但无原发性睡眠障碍的围绝经期妇女中,连续 8 周每天记录睡眠和 VMS 日记,并每周进行女性生殖激素的血清检测。使用广义估计方程来检查雌二醇、孕酮和卵泡刺激素(FSH)与每晚觉醒次数、睡眠起始后觉醒(WASO)和睡眠起始潜伏期(SOL)的平均值之间的关联,同时调整 nVMS 和 DepSx。
睡眠中断很常见(中位数为 1.5 次夜间觉醒,WASO 为 24.3 分钟,SOL 为 20.0 分钟)。更多的觉醒与绝经后范围内的雌二醇水平相关(β=0.14;95%置信区间,0.04 至 0.24;P=0.007),与较高的 FSH 水平相关(β[1 个单位增加]=0.12;95%置信区间,0.02 至 0.22;P=0.02),但与孕酮无关(β[1 个单位增加]=-0.02;95%置信区间,-0.06 至 0.01;P=0.20)。在调整后的模型中,女性生殖激素与 WASO 或 SOL 无关。
更多觉醒与较低雌二醇和较高 FSH 水平相关,为围绝经期相关睡眠中断状态提供支持,该状态与女性生殖激素变化有关,而与 nVMS 和 DepSx 无关。