Disruption of Sleep Continuity During the Perimenopause: Associations with Female Reproductive Hormone Profiles

Author:

Coborn Jamie12,de Wit Anouk13,Crawford Sybil4,Nathan Margo12,Rahman Shadab256ORCID,Finkelstein Lauren1,Wiley Aleta12,Joffe Hadine12ORCID

Affiliation:

1. Department of Psychiatry, Brigham and Women’s Hospital, Harvard Medical School , Boston, MA, 02115 , United States

2. Connors Center for Women’s Health and Gender Biology, Brigham and Women’s Hospital, Harvard Medical School , Boston, MA, 02115 , United States

3. Department of Psychiatry, University of Groningen/ University Medical Center Groningen , Groningen , Netherlands

4. Tan Chingfen Graduate School of Nursing at UMass Chan Medical School , Worcester, MA, 01605 , United States

5. Division of Sleep and Circadian Disorders, Departments of Medicine and Neurology, Brigham and Women’s Hospital, Boston , MA, 02115, United States

6. Division of Sleep Medicine, Harvard Medical School, Boston , MA, 02115, United States

Abstract

Abstract Context 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. Objective We aimed to determine the association between female reproductive hormones and perimenopausal sleep discontinuity independent of nVMS and DepSx. Methods 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. Results 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. Conclusion 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.

Funder

National Institute of Mental Health

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference53 articles.

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