Women’s Menstrual Cycles and Ovulation Provide Balanced Estradiol and Progesterone for Fertility and Lifelong Health

In: The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology · 2022 · pp. 196–214 · doi:10.1017/9781108943581.010 · W4283730848
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Menstrual cycles provide balanced estradiol and progesterone for fertility and long-term health, with cycle characteristics reflecting and influencing a woman's overall well-being and susceptibility to disease.

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This review chapter argues that the primary biological purpose of menstrual cycles is to provide balanced estradiol and progesterone for fertility and lifelong health, rather than merely preparing the uterus for implantation. The authors posit that inadequate progesterone relative to estradiol, often indicated by short luteal phases or anovulation, leads to excessive cellular proliferation and increases the risk of conditions such as endometrial cancer, osteoporosis, and heart disease later in life. By framing ovulatory disturbances as predictors of poor future health, the text advocates for clinical approaches that monitor and correct these hormonal imbalances to preserve well-being. Relevance to endometriosis: listed as one indication for GnRH antagonists, though the paper's main focus is uterine fibroids.

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Abstract

Periodic vaginal bleeding occurs in humans (who are henceforth called “women,” a word describing culture as well as biology), old-world apes, and few other mammals. By current concepts, women’s menstrual cycles provide estrogen for thirty to fifty years; following one year of no flow they become menopausal and “estrogen deficient.” By contrast we now know that the purpose of menstrual cycles is to supply all cells and tissues with the balanced essential actions of estradiol (E2) and progesterone (P4) produced in feedback-controlled patterns to facilitate fecundability and preserve younger women’s well-being. We also now know that menopausal women’s health is negatively affected (by increased osteoporosis, heart disease, breast and endometrial cancers) if those past menstrual cycles produced inadequate net P4 to counterbalance and complement E2’s actions. Menstrual periodicity, flow, and ovulatory characteristics in women reflect the integrated actions/interactions of the central nervous system through the hypothalamus and pituitary, ideally leading to each cycle’s stimulation of a dominant egg-containing follicle. That follicle, by central complex feedback loops, produces the cyclic, graded amounts of estradiol (E2) and progesterone (P4) for that three- to five-week period and releases a viable egg. Central reproductive connections allow adult premenopausal women’s menstrual cycle periodicity, ovulation or not, and luteal phase lengths, that can be adapted to the challenges and demands of each woman’s current physiological and sociocultural/emotional environments. These new ideas are based on the differing and complementary cellular and tissue actions of E2 and P4. E2 is essential for cell growth and stimulates cell proliferation. P4 uniquely counterbalances and controls proliferation while stimulating cell differentiation and tissue maturation. Thus, E2–P4 actual and relative productions integrate cycles within each woman’s reproductive lifecycle (adolescent, premenopausal, perimenopausal), and are related to her nutrition, illness, energy expenditure, and social/emotional/spiritual environments. The subtlest indication of a stressed reproductive system is truncated P4 production in the short luteal phase within a normal-length, ovulatory menstrual cycle. This adaptation protects a woman from pregnancy when she has inadequate net energy balance or is under emotional/social/spiritual or physical duress. Thus, a normal luteal phase length within a three- to five-week regular menstrual cycle is a bellwether of women’s well-being. By contrast, regular cycles with ovulatory disturbances (anovulation or short luteal phases; E2>P4) predict current decreased well-being and poor later life health. The purpose of this review is to provide a practical approach to understanding this new women’s menstrual cycle balanced E2–P4 paradigm applied to common clinical situations including subfertility with regular cycles, premenstrual symptoms, and heavy menstrual flow.
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Temporary Disruption We have implemented additional assurance measures to protect our systems. As a result, we have suspended some of our systems and services. We apologise for any temporary disruption some customers may experience. - The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology - The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology - Copyright page - Contents - Contributors - Preface - Part I Controversies and Unresolved Issues - Part II Applications to Health, Law, and Pornography - 6 Male Reproductive Health - 7 Women’s Menstrual Cycles and Ovulation Provide Balanced Estradiol and Progesterone for Fertility and Lifelong Health - 8 Female Genital Cutting - 9 Costs of Polygyny - 10 Male Sexual Disorders - 11 An Evolutionary Perspective on Female Sexual Concerns and Dysfunctions - 12 Evolutionary Perspectives on Male Sexual Offending - 13 Pornography and Male Sexual Psychology - Part III Nonhuman Primate Sexual Behavior - Index - References from Part II - Applications to Health, Law, and Pornography Published online by Cambridge University Press: 30 June 2022 Edited by Book contents - The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology - The Cambridge Handbook of Evolutionary Perspectives on Sexual Psychology - Copyright page - Contents - Contributors - Preface - Part I Controversies and Unresolved Issues - Part II Applications to Health, Law, and Pornography - 6 Male Reproductive Health - 7 Women’s Menstrual Cycles and Ovulation Provide Balanced Estradiol and Progesterone for Fertility and Lifelong Health - 8 Female Genital Cutting - 9 Costs of Polygyny - 10 Male Sexual Disorders - 11 An Evolutionary Perspective on Female Sexual Concerns and Dysfunctions - 12 Evolutionary Perspectives on Male Sexual Offending - 13 Pornography and Male Sexual Psychology - Part III Nonhuman Primate Sexual Behavior - Index - References Periodic vaginal bleeding occurs in humans (who are henceforth called “women,” a word describing culture as well as biology), old-world apes, and few other mammals. By current concepts, women’s menstrual cycles provide estrogen for thirty to fifty years; following one year of no flow they become menopausal and “estrogen deficient.” By contrast we now know that the purpose of menstrual cycles is to supply all cells and tissues with the balanced essential actions of estradiol (E2) and progesterone (P4) produced in feedback-controlled patterns to facilitate fecundability and preserve younger women’s well-being. We also now know that menopausal women’s health is negatively affected (by increased osteoporosis, heart disease, breast and endometrial cancers) if those past menstrual cycles produced inadequate net P4 to counterbalance and complement E2’s actions. Menstrual periodicity, flow, and ovulatory characteristics in women reflect the integrated actions/interactions of the central nervous system through the hypothalamus and pituitary, ideally leading to each cycle’s stimulation of a dominant egg-containing follicle. That follicle, by central complex feedback loops, produces the cyclic, graded amounts of estradiol (E2) and progesterone (P4) for that three- to five-week period and releases a viable egg. Central reproductive connections allow adult premenopausal women’s menstrual cycle periodicity, ovulation or not, and luteal phase lengths, that can be adapted to the challenges and demands of each woman’s current physiological and sociocultural/emotional environments. These new ideas are based on the differing and complementary cellular and tissue actions of E2 and P4. E2 is essential for cell growth and stimulates cell proliferation. P4 uniquely counterbalances and controls proliferation while stimulating cell differentiation and tissue maturation. Thus, E2–P4 actual and relative productions integrate cycles within each woman’s reproductive lifecycle (adolescent, premenopausal, perimenopausal), and are related to her nutrition, illness, energy expenditure, and social/emotional/spiritual environments. The subtlest indication of a stressed reproductive system is truncated P4 production in the short luteal phase within a normal-length, ovulatory menstrual cycle. This adaptation protects a woman from pregnancy when she has inadequate net energy balance or is under emotional/social/spiritual or physical duress. Thus, a normal luteal phase length within a three- to five-week regular menstrual cycle is a bellwether of women’s well-being. By contrast, regular cycles with ovulatory disturbances (anovulation or short luteal phases; E2>P4) predict current decreased well-being and poor later life health. The purpose of this review is to provide a practical approach to understanding this new women’s menstrual cycle balanced E2–P4 paradigm applied to common clinical situations including subfertility with regular cycles, premenstrual symptoms, and heavy menstrual flow. - Type - Chapter - Information - Publisher: Cambridge University PressPrint publication year: 2022 Anderson, G., Cummings, S., Freedman, L. S., Furberg, C., Henderson, M., Johnson, S. R., … & Clark, A. (1998). Design of the Women’s Health Initiative clinical trial and observational study. The Women’s Health Initiative Study Group. Controlled Clinical Trials; 19(1), 61–109.Google Scholar Anderson, G. L., Limacher, M., Assaf, A. R., Bassford, T., Beresford, S. A., Black, H., … & Women’s Health Initiative Steering Committee (2004). Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women’s Health Initiative randomized controlled trial. JAMA, 291(14), 1701–1712.Google Scholar Barr, S. I., Janelle, K. C., & Prior, J. C. (1995). Energy intakes are higher during the luteal-phase of ovulatory menstrual cycles. American Journal of Clinical Nutrition, 61(1), 39–43.CrossRefGoogle ScholarPubMed Barr, S. I., Prior, J. C., & Vigna, Y. M. (1994). Restrained eating and ovulatory disturbances: Possible implications for bone health. American Journal Clinical Nutrition, 59, 92–97.Google Scholar Barry, J. A., Azizia, M. M., & Hardiman, P. J. (2014). Risk of endometrial, ovarian and breast cancer in women with polycystic ovary syndrome: A systematic review and meta-analysis. Human Reproduction Update, 20(5), 748–758.CrossRefGoogle ScholarPubMed Barth, C., Steele, C. J., Mueller, K., Rekkas, V. P., Arélin, K., Pampel, A., … & Sacher, J. (2016). In-vivo dynamics of the human hippocampus across the menstrual cycle. Scientific Reports, 6, 32833.Google Scholar Bedford, J. L., Prior, J. C., & Barr, S. I. (2010). A prospective exploration of cognitive dietary restraint, subclinical ovulatory disturbances, cortisol and change in bone density over two years in healthy young women. JCEM, 95(7), 3291–3299.Google Scholar Bedford, J. L., Prior, J. C., Hitchcock, C. L., & Barr, S. (2009). Detecting evidence of luteal activity by least-squares quantitative basal temperature analysis against urinary progesterone metabolites and the effect of wake-time variability. European Journal of Obstetrics and Gynecology Reproductive Biology, 146(1), 76–80.CrossRefGoogle ScholarPubMed Beral, V. (2003). Breast cancer and hormone-replacement therapy in the Million Women Study. Lancet, 362(9382), 419–427.CrossRefGoogle ScholarPubMed Bhattacharya, S., Porter, M., Amalraj, E., Templeton, A., Hamilton, M., Lee, A. J., & Kurinczuk, J. J. (2009). The epidemiology of infertility in the North East of Scotland. Human Reproduction, 24(12), 3096–3107.Google Scholar Briden, L., Shirin, S., & Prior, J. C. (2020). The central role of ovulatory disturbances in the etiology of androgenic polycystic ovary syndrome (PCOS) – Evidence for treatment with cyclic progesterone. Drug Discovery Today: Disease Models, 32, 71–82.Google Scholar Bullen, B. A., Skrinar, G. S., Beitins, I. Z., von Mering, G., Turnbull, B. A., & McArthur, J. W. (1985). Induction of menstrual disorders by strenuous exercise in untrained women. New England Journal of Medicine, 312, 1349–1353.Google Scholar Clarke, C. L., & Sutherland, R. L. (1990). Progestin regulation of cellular proliferation. Endocrine Reviews, 11, 266–301.Google Scholar Cole, L. A., Ladner, D. G., & Byrn, F. W. (2009). The normal variabilities of the menstrual cycle. Fertility and Sterility, 91(2), 522–527.Google Scholar Courtin, A., Communal, L., Vilasco, M., Cimino, D., Mourra, N., de Bortoli, M., … & Gompel, A. (2012). Glucocorticoid receptor activity discriminates between progesterone and medroxyprogesterone acetate effects in breast cells. Breast Cancer Research and Treatment, 131(1), 49–63.Google Scholar Crawford, N. M., Pritchard, D. A., Herring, A. H., & Steiner, A. Z. (2017). Prospective evaluation of luteal phase length and natural fertility. Fertility and Sterility, 107(3), 749–755.Google Scholar Davis, S. R., Lambrinoudaki, I., Lumsden, M., Mishra, G. D., Pal, L., Rees, M., Santoro, N., & Simoncini, T. (2015). Menopause. Nature Reviews Disease Primers, 23(1), 15004.Google Scholar Finegood, D., Johnston, L., Steinberg, M., & Matteson, C. L. (2014). Complexity, systems thinking, and health behavior change. In Johnson, L., Steinberg, M., Matteson, C. L., & Deck, P. B. (Eds.), Health behavior change in populations (pp. 435–539). Baltimore, MD: Johns Hopkins University Press.Google Scholar Fournier, A., Berrino, F., & Clavel-Chapelon, F. (2008). Unequal risks for breast cancer associated with different hormone replacement therapies: Results from the E3N cohort study. Breast Cancer Research and Treatment, 107(1), 103–111.Google Scholar Gordon, J. L., Rubinow, D. R., Eisenlohr-Moul, T. A., Leserman, J., & Girdler, S. S. (2016). Estradiol variability, stressful life events, and the emergence of depressive symptomatology during the menopausal transition. Menopause, 23(3), 257–266.Google Scholar Gorgels, W. J., Graaf, Y., Blankenstein, M. A., Collette, H. J., Erkelens, D. W., & Banga, J. D. (1997). Urinary sex hormone excretions in premenopausal women and coronary heart disease risk: A nested case-referent study in the DOM-cohort. Journal of Clinical Epidemiology, 50(3), 275–281.CrossRefGoogle Scholar Gracia, C. R., & Freeman, E. W. (2018). Onset of the menopause transition: The earliest signs and symptoms. Obstetrics and Gynecology Clinics of North America, 45(4), 585–597.Google Scholar Hale, G. E., Hitchcock, C. L., Williams, L. A., Vigna, Y. M., & Prior, J. C. ( 2003). Cyclicity of breast tenderness and night-time vasomotor symptoms in mid-life women: Information collected using the Daily Perimenopause Diary. Climacteric, 6(2), 128–139.Google Scholar Hallberg, L., Hogdahl, A. M., Nillson, L., & Rybo, G. (1966). Menstrual blood loss – a population study. Variation at different ages and attempts to define normality. Acta Obstetrics and Gynecology Scandinavia, 45, 320–351.Google Scholar Hitchcock, C. L., & Prior, J. C. (2012). Oral micronized progesterone for vasomotor symptoms in healthy postmenopausal women – a placebo-controlled randomized trial. Menopause, 19, 886–893.CrossRefGoogle ScholarPubMed Kaplan, J. R., & Manuck, S. B. (2008). Ovarian dysfunction and the premenopausal origins of coronary heart disease. Menopause, 15(4 Pt 1), 768–776.CrossRefGoogle ScholarPubMed Kaufert, P. A. (1980). The perimenopausal woman and her use of health services. Maturitas, 2, 191–205.CrossRefGoogle ScholarPubMed Landgren, B. H., Unden, A. L., & Diczfalusy, E. (1980). Hormonal profile of the cycle in 68 normally menstruating women. Acta Endocrinologica Copenhagen, 94, 89–98.Google Scholar Li, D., Hitchcock, C. L., Barr, S. I., Yu, T., & Prior, J. C. (2014). Negative spinal bone mineral density changes and subclinical ovulatory disturbances – prospective data in healthy premenopausal women with regular menstrual cycles. Epidemiologic Reviews, 36(137), 147.CrossRefGoogle ScholarPubMed Liu, A. Y., Petit, M. A., & Prior, J. C. (2020). Exercise and the hypothalamus: Ovulatory adaptations. In Hackney, A. C. & Constantini, N. W. (Eds.), Endocrinology of physical activity and sport (pp. 123–151). Cham: Humana Press.CrossRefGoogle Scholar Macbeth, A. B., Goshtasebi, A., Mercer, G. W., & Prior, J. C. (2020). Does interest in sex peak at mid-cycle in ovulatory menstrual cycles of healthy, community-dwelling women? An 11-month prospective observational study. Women’s Reproductive Health, 8(2), 79–91.Google Scholar Malcolm, C. E., & Cumming, D. C. (2003). Does anovulation exist in eumenorrheic women? Obstetrics & Gynecology, 102(2), 317–318.Google Scholar Marjoribanks, J., Lethaby, A., & Farquhar, C. (2003). Surgery versus medical therapy for heavy menstrual bleeding. The Cochrane Database of Systemic Reviews, 3, 1–65.Google Scholar Mather, K. J., Norman, E. G., Prior, J. C., & Elliott, T. G. (2000). Preserved forearm endothelial responses with acute exposure to progesterone: A randomized cross-over trial of 17-b estradiol, progesterone, and 17-b estradiol with progesterone in healthy menopausal women. Journal of Clinical Endocrinology and Metabolism, 85, 4644–4649.Google Scholar McCrohon, J. A., Adams, M. R., McCredie, R. J., Robinson, J., Pike, A., Abbey, M., … & Celermajer, D. S. (1996). Hormone replacement therapy is associated with improved arterial physiology in healthy post-menopausal women. Clin Endocrinol (Oxf), 45(4), 435–441.Google Scholar McLean, J. A., Barr, S. I., & Prior, J. C. (2001). Cognitive dietary restraint is associated with higher urinary cortisol excretion in healthy premenopausal women. American Journal Clinical Nutrition, 73, 7–12.Google Scholar Moen, M. H., Kahn, H., Bjerve, K. S., & Halvorsen, T. B. (2004). Menometrorrhagia in the perimenopause is associated with increased serum estradiol. Maturitas, 47(2), 151–155.Google Scholar Mohammed, H., Russell, I. A., Stark, R., Rueda, O. M., Hickey, T. E., Tarulli, G. A., … & Carroll, J. S. (2015). Progesterone receptor modulates ERα action in breast cancer. Nature, 523(7560), 313–317.Google Scholar Mountjoy, M., Sundgot-Borgen, J., Burke, L., Carter, S., Constantini, N., Lebrun, C., … & Ljungqvist, A. (2014). The IOC consensus statement: beyond the female athlete triad – relative energy deficiency in sport (RED-S). British Journal of Sports Medicine, 48(7), 491–497.Google Scholar Munster, K., Helm, P., & Schmidt, L. (1992). Secondary amenorrhoea: Prevalence and medical contact – a cross-sectional study from a Danish county. British Journal Obstetrics Gynaecology, 99(5), 430–433.CrossRefGoogle ScholarPubMed Munster, K., Schmidt, L., & Helm, P. (1992). Length and variation in the menstrual cycle – a cross-sectional study from a Danish county. British Journal Obstetrics Gynaecology, 99(5), 422–429.Google Scholar Nagata, I., Kato, K., Seki, K., & Furuya, K. (1986). Ovulatory disturbances: Causative factors among Japanese student nurses in a dormitory. Journal of Adolescent Health Care, 7, 1–5.CrossRefGoogle Scholar Nielsen, H. K., Brixen, K., Bouillon, R., & Mosekilde, L. (1990). Changes in biochemical markers of osteoblastic activity during the menstrual cycle. Journal of Clinical Endocrinology and Metabolism, 70, 1431–1437.Google Scholar Odening, K. E., Choi, B. R., Liu, G. X., Hartmann, K., Ziv, O., Chaves, L., … & Koren, G. (2012). Estradiol promotes sudden cardiac death in transgenic long QT type 2 rabbits while progesterone is protective. Heart Rhythm, 9(5), 823–832.Google Scholar Parfitt, A. M. (1982). The coupling of bone formation to bone resorption: A critical analysis of the concept and of its relevance to the pathogenesis of osteoporosis. Metabolic Bone Disease Related Research, 4, 1–6.Google Scholar Pletzer, B., Harris, T., & Hidalgo-Lopez, E. (2018). Subcortical structural changes along the menstrual cycle: Beyond the hippocampus. Scientific Reports, 8(1), 16042.Google Scholar Prior, J. C. (1987). Physical exercise and the neuroendocrine control of reproduction. Baillieres Clinical Endocrinology and Metabolism, 1, 299–317.Google Scholar Prior, J. C. (1989). The cultural causes of osteoporosis for women. In Kahn, S. E. (Ed.), Women, stress and coping: An interdisciplinary research workshop (pp. 13–22). Vancouver, BC: University of British Columbia.Google Scholar Prior, J. C. (1990). Progesterone as a bone-trophic hormone. Endocrine Reviews, 11, 386–398.Google Scholar Prior, J. C. (1996) Exercise-associated menstrual disturbances. In Adashi, E. Y., Rock, J. A., & Rosenwaks, Z. (Eds.), Reproductive endocrinology, surgery and technology (pp. 1077–1091). New York: Raven Press.Google Scholar Prior, J. C. (1998). Perimenopause: The complex endocrinology of the menopausal transition. Endocrine Reviews, 19, 397–428.Google Scholar Prior, J. C. (2002). Premenstrual symptoms and signs. In Rabel, R. E. & Bope, E. T. (Eds.), Conn’s current therapy 2002. (pp. 1078–1080). New York: W. B. Saunders Company.Google Scholar Prior, J. C. (2005). Clearing confusion about perimenopause. British Columbia Medical Journal, 47(10), 534–538.Google Scholar Prior, J. C. (2006). Perimenopause lost – reframing the end of menstruation. Journal of Reproductive and Infant Psychology, 24 (4), 323–335.Google Scholar Prior, J. C. (2011). Progesterone for symptomatic perimenopause treatment – progesterone politics, physiology and potential for perimenopause. Facts, Views and Visions on Obstetrics and Gynecology, 3, 109–120.Google Scholar Prior, J. C. (2014). Progesterone within ovulatory menstrual cycles needed for cardiovascular protection – an evidence-based hypothesis. Journal of Restorative Medicine, 3, 85–103.Google Scholar Prior, J. C. (2018a). Estrogen’s storm season – stories of perimenopause (e-book), 2nd ed. Vancouver, BC: CEMCOR.Google Scholar Prior, J. C. (2018b). Progesterone for the prevention and treatment of osteoporosis in women. Climacteric, 21, 366–374.Google Scholar Prior, J. C. (2020a). The menstrual cycle. Its biology in the context of silent ovulatory disturbances. In Ussher, J. M., Chrisler, J., & Perz, J. (Eds.), Routledge international handbook of women’s sexual and reproductive health (pp. 39–54). London: Routledge.Google Scholar Prior, J. C. (2020b). Women’s reproductive system as balanced estradiol and progesterone actions – a revolutionary, paradigm-shifting concept in women’s health. Drug Discovery Today: Disease Models, 32, 31–40.Google Scholar Prior, J. C., Cameron, A., & Hitchcock, C. L. (2018a). Oral micronized progesterone beneficial for perimenopausal hot flushes/flashes and night sweats. Endocrine Reviews, 39(2).Google Scholar Prior, J. C., Cameron, K., Ho Yeun, B., & Thomas, J. (1982a). Menstrual cycle changes with marathon training: Anovulation and short luteal phase. Canadian Journal of Applied Sport Science, 7, 173–177.Google Scholar Prior, J. C., Elliott, T. G., Norman, E., Stajic, V., & Hitchcock, C. L. (2014). Progesterone therapy, endothelial function and cardiovascular risk factors: A 3-month randomized, placebo-controlled trial in healthy early postmenopausal women. PLOS ONE, 9, e84698.CrossRefGoogle ScholarPubMed Prior, J. C., Ho Yeun, B., Clement, P., Bowie, L., & Thomas, J. (1982b). Reversible luteal phase changes and infertility associated with marathon training. Lancet, 1, 269–270.Google Scholar Prior, J. C., Konishi, C., Hitchcock, C. L., Kingwell, E., Janssen, P., Cheung, A. P., … & Goshtasebi, A. (2018b). Does molimina indicate ovulation? Prospective data in a hormonally documented single-cycle in spontaneously menstruating women. International Journal of Environmental Research and Public Health, 15(5), 1016.Google Scholar Prior, J. C., Naess, M., Langhammer, A., & Forsmo, S. (2015). Ovulation prevalence in women with spontaneous normal-length menstrual cycles – a population-based cohort from HUNT3, Norway. PLOS ONE, 10(8), e0134473.Google Scholar Prior, J. C., Seifert-Klauss, V. R., Giustini, D., Adachi, J. D., Kalyan, S., & Goshtasebi, A. (2017). Estrogen-progestin therapy causes a greater increase in spinal bone mineral density than estrogen therapy – a systematic review and meta-analysis of controlled trials with direct randomization. Journal of Musculoskeletal and Neuronal Interacts, 17(3), 146–154.Google Scholar Prior, J. C., Vigna, Y. M., & Alojado, N. (1986). Conditioning exercise decreases premenstrual symptoms – a prospective controlled three month trial. European Journal of Applied Physiology, 55, 349–355.Google Scholar Prior, J. C., Vigna, Y. M., Barr, S. I., Rexworthy, C., & Lentle, B. C. (1994). Cyclic medroxyprogesterone treatment increases bone density: a controlled trial in active women with menstrual cycle disturbances. American Journal Medicine, 96, 521–530.Google Scholar Prior, J. C., Vigna, Y. M., Schulzer, M., Hall, J. E., & Bonen, A. (1990a). Determination of luteal phase length by quantitative basal temperature methods: validation against the midcycle LH peak. Clinical & Investigative Medicine, 13, 123–131.Google ScholarPubMed Prior, J. C., Vigna, Y. M., Schechter, M. T., & Burgess, A. E. (1990b). Spinal bone loss and ovulatory disturbances. New England Journal of Medicine, 323, 1221–1227.Google Scholar Prior, J. C., Vigna, Y. M., Sciarretta, D., Alojado, N., & Schulzer, M. (1987). Conditioning exercise decreases premenstrual symptoms: A prospective controlled six month trial. Fertility and Sterility, 47, 402–408.Google Scholar Ronkainen, H. R., Pakarinen, A. J., Kirkinen, P., & Kauppila, A. (1985). Physical exercise-induced changes and season-associated differences in the pituitary-ovarian function of runners and joggers. Journal of Clinical Endocrinology and Metabolism, 60, 416–422.Google Scholar Santoro, N., Rosenberg, J., Adel, T., & Skurnick, J. H. (1996). Characterization of reproductive hormonal dynamics in the perimenopause. Journal of Clinical Endocrinology and Metabolism, 81(4), 1495–1501.Google Scholar Schliep, K. C., Mumford, S. L., Vladutiu, C. J., Ahrens, K. A., Perkins, N. J., Sjaarda, L. A., … & Schisterman, E. F. (2015). Perceived stress, reproductive hormones, and ovulatory function: A prospective cohort study. Epidemiology, 26, 177–184.Google Scholar Schmidt, P. J., Ben, D. R., Martinez, P. E., Guerrieri, G. M., Harsh, V. L., Thompson, K., … & Rubinow, D. R. (2015). Effects of estradiol withdrawal on mood in women with past perimenopausal depression: A randomized clinical trial. JAMA Psychiatry, 72(7), 714–726.Google Scholar Schummers, L., Hutcheon, J. A., Hacker, M. R., VanderWeele, T. J., Williams, P. L., McElrath, T. F., & Hernandez-Diaz, S. (2018). Absolute risks of obstetric outcomes by maternal age at first birth: a population-based cohort. Epidemiology, 29(3), 379–387.Google Scholar Sedlak, T., Shufelt, C., Iribarren, C., & Merz, C. N. (2012). Sex hormones and the QT interval: a review. Journal of Women’s Health (Larchmt), 21(9), 933–941.CrossRefGoogle Scholar Seltzer, V. I., Benjamin, F., & Deutsch, S. (1990). Perimenopausal bleeding patterns and pathological findings. Journal American Medical Women’s Association, 45, 132–134.Google Scholar Shea, A., & Vitzthum, V. J. (2020). The extent and causes of natural variation in menstrual cycles: Integrating empirically-based models of ovarian cycling into research on women’s health. Drug Discovery Today: Disease Models, 32, 41–49.Google Scholar Simon, J. A., Robinson, D. E., Andrews, M. C., Hildebrand, J. R. 3rd, Rocci, M. L. Jr., Blake, R. E., & Hodgen, G. D. (1993). The absorption of oral micronized progesterone: the effect of food, dose proportionality, and comparison with intramuscular progesterone. Fertility and Sterility, 60(1), 26–33.Google Scholar van Hooff, M. H., Voorhorst, F. J., Kaptein, M. B., Hirasing, R. A., Koppenaal, C., & Schoemaker, J. (1998). Relationship of the menstrual cycle pattern in 14–17 year old adolescents with gynaecological age, body mass index and historical parameters. Human Reproduction, 13(8), 2252–2260.Google Scholar Vitzthum, V. J., Bentley, G. R., Spielvogel, H., Caceres, E., Thornburg, J., Jones, L., … & Chatterton, R. T. (2002). Salivary progesterone levels and rate of ovulation are significantly lower in poorer than in better-off urban-dwelling Bolivian women. Human Reproduction, 17(7), 1906–1913.Google Scholar Vitzthum, V. J., Spielvogel, H., Caceres, E., & Gaines, J. (2000). Menstrual patterns and fecundity among non-lactating and lactating cycling women in rural highland Bolivia: implications for contraceptive choice. Contraception, 62(4), 181–187.Google Scholar Vitzthum, V. J., Spielvogel, H., & Thornburg, J. (2004). Interpopulational differences in progesterone levels during conception and implantation in humans. Proceedings of the National Academy of Science of the USA, 101(6), 1443–1448.Google Scholar Vitzthum, V. J., Thornburg, J., & Spielvogel, H. (2009). Seasonal modulation of reproductive effort during early pregnancy in humans. American Journal of Human Biology, 21(4), 548–558.Google Scholar Waugh, E. J., Polivy, J., Ridout, R., & Hawker, G. A. (2007). A prospective investigation of the relations among cognitive dietary restraint, subclinical ovulatory disturbances, physical activity, and bone mass in healthy young women. American Journal of Clinical Nutrition, 86(6), 1791–1801.Google Scholar Wei, S., Schmidt, M. D., Dwyer, T., Norman, R. J., & Venn, A. J. (2009). Obesity and menstrual irregularity: Associations with SHBG, testosterone, and insulin. Obesity (SilverSpring), 17(5), 1070–1076.Google Scholar Weiss, N. S., Szekely, D. R., & Austin, D. F. (1976). Increasing incidence of endometrial cancer in the United States. New England Journal of Medicine, 294(23), 1259–1262.Google Scholar Williams, N. I., Berga, S. L., & Cameron, J. L. (2007). Synergism between psychosocial and metabolic stressors: Impact on reproductive function in cynomolgus monkeys. American Journal of Physiology-Endocrinology and Metabolism, 293(1), E270–E276.Google Scholar Williams, N. I., Leidy, H. J., Hill, B. R., Lieberman, J. L., Legro, R. S., & De Souza, M. J. (2015). Magnitude of daily energy deficit predicts frequency but not severity of menstrual disturbances associated with exercise and caloric restriction. American Journal of Physiology-Endocrinology and Metabolism, 308(1), E29–39.Google Scholar Writing Group for the Women’s Health Initiative I. (2002). Risks and benefits of estrogen plus progestin in health postmenopausal women: Principal results from the Women’s Health Initiative Randomized Control trial. JAMA, 288, 32–33.Google Scholar Accessibility compliance for the HTML of this chapter is currently unknown and may be updated in the future. - 1 - Cited by To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. 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