Women’s Hormonal Balance and Adrenal Health
September 19, 2024
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Written by: Kyla Reda
Medically reviewed by: Lara Zakaria PharmD, CNS, IFMCP
The vast network of hormones in women’s bodies plays a crucial role in their overall health and well-being but can lead to a variety of health conditions when imbalanced. Since the adrenal glands are responsible for producing several major regulating hormones for women, adrenal health is a key factor to consider when supporting women’s hormone balance.
When adrenal function is imbalanced, adrenal glands can produce too much or too little of various hormones that are essential for women’s health, leading to a variety of health complications.
One of the main hormones produced by the adrenal gland is cortisol. Cortisol is released in response to stress and helps the body manage its reaction to stress. (Kumar 2022) However, dysregulation of adrenal function can result in insufficient cortisol production, leading to symptoms like extreme fatigue, postural hypotension, depression, unintentional weight loss, low blood sodium levels, and poor immune system regulation. (Adam 2017) (Husebye 2021)
Adrenal dysregulation can also lead to excess cortisol production, causing symptoms such as weight gain, easy bruising, mood changes, memory loss, irregular menstrual periods, and excess hair on the face, neck, chest, abdomen, and thighs for women. (NIDDK 2023)
Dehydroepiandrosterone (DHEA) is a hormone produced by the adrenal glands that helps balance cortisol levels. Chronic stress is associated with reduced DHEA and its sulfated metabolite dehydroepiandrosterone sulfate (DHEA-S). (Lennartsson 2013) DHEA also produces testosterone and estrogen—two hormones vital to women’s hormone health—and therefore has a protective and regenerative role in sex hormone balance. When under chronic stress, DHEA and DHEA-S levels can drop, impacting levels of testosterone and estrogen. (National Library of Medicine n.d.)
Estrogen plays a crucial role in women's health, regulating menstrual cycles, supporting reproductive health, maintaining bone density, and influencing mood and cognitive function throughout the lifecycle. Measuring estrogen levels helps assess hormonal balance and guide treatment for a wide variety of conditions, such as polycystic ovary syndrome (PCOS), irregular cycles, and perimenopause/menopause.
Physiological and emotional stress can significantly impact estrogen, leading to imbalances that can exacerbate hormone-related symptoms. Furthermore, fluctuations in estrogen levels also impact stress resilience, mood, and mental health. (Albert 2019) (Krolick 2022) Understanding these dynamics allows for targeted interventions to support overall health and well-being.
Hot flashes and night sweats may be a sign of estrogen deficiency caused by imbalanced adrenal function.
Produced in both the ovaries and the adrenal glands, testosterone plays an important role in ovarian function, bone strength, and sexual behavior for women. Low testosterone levels can lead to low libido, weakened bone strength, lack of concentration, and depression. (Harvard Health 2023) Stress can cause a reduction in testosterone levels, simultaneously leading to a lower tolerance to stressful situations by increasing anxiety and irritability. (Afrisham 2016)
Progesterone is primarily produced in the ovaries, rising during the luteal phase after ovulation. It’s also formed in smaller amounts by the adrenal glands or the placenta during pregnancy. Progesterone plays a crucial role in regulating the menstrual cycle, supporting sleep, and maintaining overall well-being. During pregnancy, progesterone is essential for preparing the uterine lining for implantation and maintaining a healthy pregnancy.
Low levels of progesterone cause symptoms like irregular periods, mood changes and anxiety, insomnia, and infertility. (Cable 2023) (Haufe 2023) (Standeven 2020)
Integrating lifestyle evaluations and laboratory testing can inform personalized treatment plans for patients to support adrenal health and hormone balance.
Initial patient assessment evaluates any reported symptoms, menstrual and reproductive history, use of contraceptives and other medications, and medical and family history for a comprehensive understanding of the patient’s unique situation.
Document any of the symptoms listed below, making note of onset and duration. Inquire about menstrual regularity, including any missed periods, changes in flow, or premenstrual symptoms. Make sure to discuss libido levels and fertility if applicable.
Given the number of bodily functions affected by hormones and adrenal glands, several related conditions can develop as a result of imbalances. Note any autoimmune diseases or thyroid disorders, along with any known family history of endocrine or adrenal disorders. Make sure to document any medications or dietary supplements that the patient is using.
There are many common symptoms of both hormonal imbalances and adrenal dysfunction to assess. If a patient displays some of the following symptoms, it may indicate that their hormones are imbalanced due to poor adrenal health:
Assess blood pressure levels for signs of orthostatic hypotension during physical examinations.
Adrenal imbalances present themselves through a variety of hormonal symptoms. The following lab tests may be helpful for further assessment of a patient’s adrenal health status.
Measure morning cortisol levels to assess adrenal function. Consider an adrenocorticotropic hormone (ACTH) stimulation test if adrenal insufficiency is suspected. (Bornstein 2016) Cortisol levels can be measured through saliva, serum, and urine.
A morning saliva cortisol test involves collecting a single saliva sample immediately upon waking to measure peak cortisol levels. Alternatively, with a diurnal cortisol rhythm test, saliva samples are collected at multiple times throughout the day (usually upon waking, mid-morning, afternoon, and evening) to evaluate the cortisol curve. This may also include cortisol awakening response (CAR) collected 30 minutes after waking. (Kobayashi 2017)
Morning serum cortisol measures a single blood sample taken typically between 8–9 a.m. when cortisol levels are at their peak. Additional blood sample(s) can be drawn later in the day to compare with morning levels. This is generally inconvenient and less common. (National Library of Medicine n.d.)
A spot urine test takes a single urine sample at a specific time (often in the morning) to measure cortisol levels. (Reynolds 2007) A 24-hour urinary free cortisol (UFC) test collects all urine produced over a 24-hour period to measure total free (unbound) cortisol. (HealthLink BC n.d.)
Alternatively, a dried urine spot test collects urine samples on filter paper at different times of the day before they’re dried and sent to a lab for cortisol level assessment. This method is convenient and allows for multiple collections over a period without the need for refrigeration. (Newman 2021)
Test DHEA and DHEA-S to evaluate their levels, extent of sulfation, and overall adrenal androgen production. (Kassem 2012) Assessment methods include serum, saliva, urine, and dried-spot urine testing.
A dried urine test measures DHEA and DHEA-S using dried urine samples. This method relies on collection of urine on filter paper. The test is non-invasive and can be done at home, making it convenient and allowing for urine samples over the course of the day to provide a comprehensive view of DHEA and DHEA-S. (Newman 2021)
Salivary testing measures the free, bioavailable form of DHEA and its metabolite DHEA-S in saliva. The main advantage is that this is reliable, sensitive, and non-invasive and reflects bioactive hormone levels. (Meshari 2022)
Serum DHEA-S testing involves a blood draw, typically done in the morning. This provides a direct measurement of DHEA-S, which has a longer half-life and more stable levels than DHEA. Serum levels are a reflection of the immediate levels of DHEA. (National Library of Medicine n.d.)
Assessing levels of estrogen, progesterone, testosterone, and other relevant hormones can help clinicians identify the impact of stress on sex hormone balance. (National Library of Medicine n.d.) (Sharma 2021)
Serum, saliva, and dried urine estrogen tests measure estradiol (E2), estrone (E1), and estriol (E3). Estradiol is most commonly measured as it’s the predominant form of estrogen in premenopausal women. This test is crucial for evaluating estrogen levels in various phases of the menstrual cycle or in postmenopausal women. (National Library of Medicine n.d.)
Urine testing can also evaluate estrogen metabolites, providing a picture of how well estrogen is metabolized, which is particularly important in assessing estrogen dominance. (Coburn 2018)
Testing for progesterone is typically conducted during the luteal phase of the menstrual cycle to assess ovulation and luteal phase adequacy. It provides a clear picture of progesterone production by the ovaries. Testing progesterone levels can be done by measuring serum, saliva, and dried urine. (Konishi 2012) (Mesen 2015) (Newman 2019)
Serum testosterone tests measure both total and free testosterone levels. Total testosterone includes both bound and unbound testosterone, while free testosterone reflects the bioavailable fraction. This test is vital for assessing androgen levels, which can impact libido, mood, and metabolic function. (Krakowsky 2015) (National Library of Medicine n.d.)
Saliva testing for testosterone measures the bioavailable fraction and is particularly useful for evaluating diurnal fluctuations. It’s often used in conjunction with cortisol testing to assess adrenal and androgen function. (Crewther 2017)
Urine testing allows the opportunity to measure testosterone metabolites, such as androsterone and etiocholanolone, providing a detailed view of androgen production and metabolism. (Scott 2024)
Include thyroid-stimulating hormone (TSH), free triiodothyronine (T3), and free thyroxine (T4) to rule out thyroid dysfunctions that can mimic or exacerbate adrenal issues. (Garber 2012)
This test measures the pituitary gland’s signal to the thyroid to produce hormones. Elevated TSH typically indicates hypothyroidism, while low levels may suggest hyperthyroidism. TSH is the first-line screening test for both hypothyroidism and hyperthyroidism. (American Thyroid Association 2020)
T4 is the dominant form of thyroid hormone produced by the thyroid gland. Total T4 measures all T4, bound and unbound to transport proteins. Free T4 specifically measures the unbound portion of thyroxine available to tissues. Both are a useful addition to TSH in assessing thyroid function, and low levels often indicate hypothyroidism. (American Thyroid Association 2020)
T4 has to be converted to T3, the biologically active form of thyroid hormones. This test measures the total amount of T3, including both bound and free T3. It helps evaluate the overall level of active thyroid hormone in the body and can be useful in assessing hyperthyroidism or the severity of hypothyroidism. (American Thyroid Association 2020)
Free T3 is the measure of the most biologically active form of thyroid hormone, free and unbound to carrier proteins. Low free T3 levels can suggest impaired conversion, often seen in chronic stress or illness. Often this is accompanied with elevated reverse T3 (rT3) levels. (DeGroot 2015) (Yamazaki 2021)
Under conditions of elevated physiological, psychological, or environmental stress, the production of rT3 instead of active T3 helps the body adapt and preserve energy by slowing down metabolism. Evaluating levels of rT3 with other thyroid function tests can help clinicians connect the impacts of stress on thyroid dysfunction. (Fröhlich 2021)
To prevent potential adrenal and hormonal imbalances in the future, it’s essential to identify risk factors and implement early interventions as needed. Assess the patient's lifestyle and occupational stressors that could contribute to adrenal dysfunction. Take a detailed family history to identify genetic predispositions to adrenal or hormonal disorders.
Educate patients on a balanced diet rich in essential nutrients that support adrenal health, such as magnesium and vitamins B and C. (Moritz 2020) (Noah 2021) Encourage regular exercise tailored to the patient's fitness level, emphasizing stress-reducing activities like yoga and walking. (Stubbs 2017)
If stress management is needed, introduce techniques like mindfulness, meditation, and deep-breathing exercises to help mitigate the impact of chronic stress on adrenal function. (Pascoe 2020) Consider referring patients experiencing significant stress, anxiety, or depression to mental health professionals.
If any risk factors are identified, schedule regular physical examinations to assess and monitor health status and detect any early symptoms.
Overall, women’s hormones play a vital role in their health and well-being, and maintaining adrenal health is part of a whole person care strategy for ensuring healthy hormone balance. If adrenal imbalance is suspected due to presenting symptoms, risk factors, or genetic predisposition, following this whole person approach to assessment and treatment can help optimize patient outcomes.
References
Adam, E. K., Quinn, M. E., Tavernier, R., McQuillan, M. T., Dahlke, K. A., & Gilbert, K. E. (2017). Diurnal cortisol slopes and mental and physical health outcomes: A systematic review and meta-analysis. Psychoneuroendocrinology, 83, 25–41. https://doi.org/10.1016/j.psyneuen.2017.05.018
Afrisham, R., Sadegh-Nejadi, S., SoliemaniFar, O., Kooti, W., Ashtary-Larky, D., Alamiri, F., Aberomand, M., Najjar-Asl, S., & Khaneh-Keshi, A. (2016). Salivary Testosterone Levels Under Psychological Stress and Its Relationship with Rumination and Five Personality Traits in Medical Students. Psychiatry Investigation, 13(6), 637. https://doi.org/10.4306/pi.2016.13.6.637
Albert, K. M., & Newhouse, P. A. (2019). Estrogen, stress, and depression: cognitive and biological interactions. Annual Review of Clinical Psychology, 15(1), 399–423. https://doi.org/10.1146/annurev-clinpsy-050718-095557
American Thyroid Association. (2020, June 8). Thyroid function Tests. American Thyroid Association. https://www.thyroid.org/thyroid-function-tests/#:~:text=A%20high%20TSH%20level%20indicates,much%20thyroid%20hormone%20(hyperthyroidism)
Bornstein, S. R., Allolio, B., Arlt, W., Barthel, A., Don-Wauchope, A., Hammer, G. D., Husebye, E. S., Merke, D. P., Murad, M. H., Stratakis, C. A., & Torpy, D. J. (2016). Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology and Metabolism, 101(2), 364–389. https://doi.org/10.1210/jc.2015-1710
Cable, J.K., & Grider, M.H. (2023) Physiology, Progesterone. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK558960/
Coburn, S. B., Stanczyk, F. Z., Falk, R. T., McGlynn, K. A., Brinton, L. A., Sampson, J., Bradwin, G., Xu, X., & Trabert, B. (2018). Comparability of serum, plasma, and urinary estrogen and estrogen metabolite measurements by sex and menopausal status. Cancer Causes & Control, 30(1), 75–86. https://doi.org/10.1007/s10552-018-1105-1
Crewther, B. T., Obmiński, Z., Orysiak, J., & Al‐Dujaili, E. a. S. (2017). The utility of salivary testosterone and cortisol concentration measures for assessing the stress responses of junior athletes during a sporting competition. Journal of Clinical Laboratory Analysis, 32(1). https://doi.org/10.1002/jcla.22197
DeGroot, L.J. (2015). The Non-Thyroidal Illness Syndrome. In: Feingold KR, Anawalt B, Blackman MR, et al., editors. Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK285570/
Fröhlich, E., & Wahl, R. (2021). Physiological role and use of thyroid hormone metabolites - Potential utility in COVID-19 patients. Frontiers in Endocrinology, 12. https://doi.org/10.3389/fendo.2021.587518
Garber, J. R., Cobin, R. H., Gharib, H., Hennessey, J. V., Klein, I., Mechanick, J. I., Pessah-Pollack, R., Singer, P. A., & Woeber, K. A. (2012). Clinical Practice Guidelines for Hypothyroidism in Adults: cosponsored by the American Association of Clinical Endocrinologists and the American Thyroid Association. Endocrine Practice, 18(6), 988–1028. https://doi.org/10.4158/ep12280.gl
Harvard Health. (2023, June 22). Testosterone: What it is and how it affects your health. https://www.health.harvard.edu/staying-healthy/testosterone--what-it-does-and-doesnt-do
Haufe, A., & Leeners, B. (2023). Sleep disturbances across a woman’s lifespan: What is the role of reproductive hormones? Journal of the Endocrine Society, 7(5). https://doi.org/10.1210/jendso/bvad036
HealthLink BC. (n.d.). Cortisol in urine test. HealthLink BC. https://www.healthlinkbc.ca/tests-treatments-medications/medical-tests/cortisol-urine
Husebye, E. S., Pearce, S. H., Krone, N. P., & Kämpe, O. (2021). Adrenal insufficiency. Lancet, 397(10274), 613–629. https://doi.org/10.1016/s0140-6736(21)00136-7
Kassem, L. S., Sibai, K. E., Chaiban, J., Abdelmannan, D., & Arafah, B. M. (2012). Measurements of serum DHEA and DHEA sulphate levels improve the accuracy of the Low-Dose cosyntropin test in the diagnosis of central adrenal insufficiency. The Journal of Clinical Endocrinology and Metabolism, 97(10), 3655–3662. https://doi.org/10.1210/jc.2012-1806
Kobayashi, H., Song, C., Ikei, H., Park, B., Kagawa, T., & Miyazaki, Y. (2017). Diurnal changes in distribution characteristics of salivary cortisol and immunoglobulin A concentrations. International Journal of Environmental Research and Public Health, 14(9), 987. https://doi.org/10.3390/ijerph14090987
Konishi, S., Brindle, E., Guyton, A., & O’Connor, K. A. (2012). Salivary concentration of progesterone and cortisol significantly differs across individuals after correcting for blood hormone values. American Journal of Physical Anthropology, 149(2), 231–241. https://doi.org/10.1002/ajpa.22114
Krakowsky, Y., & Grober, E. D. (2015). Testosterone deficiency - Establishing a biochemical diagnosis. The Journal of the International Federation of Clinical Chemistry and Laboratory Medicine, 26(2), 105–113. https://pubmed.ncbi.nlm.nih.gov/27683486
Krolick, K. N., & Shi, H. (2022). Estrogenic action in Stress-Induced neuroendocrine regulation of energy homeostasis. Cells, 11(5), 879. https://doi.org/10.3390/cells11050879
Kumar, R., & Wassif, W. S. (2022). Adrenal insufficiency. Journal of Clinical Pathology, 75(7), 435–442. https://doi.org/10.1136/jclinpath-2021-207895
Lennartsson, A., Theorell, T., Rockwood, A. L., Kushnir, M. M., & Jonsdottir, I. H. (2013). Perceived Stress at Work Is Associated with Lower Levels of DHEA-S. PLoS ONE, 8(8), e72460. https://doi.org/10.1371/journal.pone.0072460
Mesen, T. B., & Young, S. L. (2015). Progesterone and the luteal phase. Obstetrics and Gynecology Clinics of North America, 42(1), 135–151. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436586/
Meshari, S. Z. A., & Aldweesh, A. H. (2022). Correlation between salivary dehydroepiandrosterone sulfate (DHEA-S) levels and cervical vertebral maturation in Saudi individuals. The Saudi Dental Journal, 34(5), 355–361. https://doi.org/10.1016/j.sdentj.2022.05.001
Moritz, B., Schmitz, A. E., Rodrigues, A. L. S., Dafre, A. L., & Cunha, M. P. (2020). The role of vitamin C in stress-related disorders. The Journal of Nutritional Biochemistry, 85, 108459. https://doi.org/10.1016/j.jnutbio.2020.108459
National Institute of Diabetes and Digestive and Kidney Diseases. (2023). Cushing’s Syndrome. NIDDK. https://www.niddk.nih.gov/health-information/endocrine-diseases/cushings-syndrome#:~:text=Clinical%20Trials-,What%20is%20Cushing's%20syndrome%3F,maintain%20blood%20pressure
NIDDK. (2022). Symptoms & Causes of Adrenal Insufficiency & Addison’s Disease. National Institute of Diabetes and Digestive and Kidney Diseases. https://www.niddk.nih.gov/health-information/endocrine-diseases/adrenal-insufficiency-addisons-disease/symptoms-causes
National Library of Medicine. (n.d.). Cortisol test. MedlinePlus. https://medlineplus.gov/lab-tests/cortisol-test/
National Library of Medicine. (n.d.). DHEA sulfate test. MedlinePlus. https://medlineplus.gov/lab-tests/dhea-sulfate-test/
National Library of Medicine. (n.d.). Estrogen levels test. MedlinePlus. https://medlineplus.gov/lab-tests/estrogen-levels-test/
National Library of Medicine. (n.d.). Testosterone levels test. MedlinePlus. https://medlineplus.gov/lab-tests/testosterone-levels-test/
Newman, M., & Curran, D. A. (2021). Reliability of a dried urine test for comprehensive assessment of urine hormones and metabolites. BMC Chemistry, 15(1). https://doi.org/10.1186/s13065-021-00744-3
Newman, M., Pratt, S. M., Curran, D. A., & Stanczyk, F. Z. (2019). Evaluating urinary estrogen and progesterone metabolites using dried filter paper samples and gas chromatography with tandem mass spectrometry (GC–MS/MS). BMC Chemistry, 13(1). https://doi.org/10.1186/s13065-019-0539-1
Noah, L., Dye, L., De Fer, B. B., Mazur, A., Pickering, G., & Pouteau, E. (2021). Effect of magnesium and vitamin B6 supplementation on mental health and quality of life in stressed healthy adults: Post‐hoc analysis of a randomised controlled trial. Stress and Health, 37(5), 1000–1009. https://doi.org/10.1002/smi.3051
Pascoe, M. C., Thompson, D. R., & Ski, C. F. (2020). Meditation and endocrine health and wellbeing. Trends in Endocrinology and Metabolism, 31(7), 469–477. https://doi.org/10.1016/j.tem.2020.01.012
Reynolds, R., Ho, C., Sawyers, L., Gough, K., & Shearing, C. (2007, March 1). Establishing a reference range for urine cortisol:creatinine ratio. SFEBES2007 | Society for Endocrinology BES | Endocrine Abstracts. https://www.endocrine-abstracts.org/ea/0013/ea0013p270
Scott, S. N., Siguencia, M., Stanczyk, F. Z., Hartmann, M. F., Wudy, S. A., White, M., Chung, W. K., Santella, R. M., Terry, M. B., & Houghton, L. C. (2024). Urinary androgens provide additional evidence related to metabolism and are correlated with serum androgens in girls. Journal of the Endocrine Society, 8(3). https://doi.org/10.1210/jendso/bvad161
Shah, S. (2012). Hormonal link to autoimmune allergies. ISRN Allergy, 2012, 1–5. https://doi.org/10.5402/2012/910437
Sharma, A., & Welt, C. K. (2021). Practical approach to hyperandrogenism in women. Medical Clinics of North America, 105(6), 1099–1116. https://doi.org/10.1016/j.mcna.2021.06.008
Standeven, L. R., McEvoy, K. O., & Osborne, L. M. (2020). Progesterone, reproduction, and psychiatric illness. Best Practice & Research Clinical Obstetrics & Gynaecology, 69, 108–126. https://doi.org/10.1016/j.bpobgyn.2020.06.001
Stubbs, B., Vancampfort, D., Rosenbaum, S., Firth, J., Cosco, T., Veronese, N., Salum, G. A., & Schuch, F. B. (2017). An examination of the anxiolytic effects of exercise for people with anxiety and stress-related disorders: A meta-analysis. Psychiatry Research, 249, 102–108. https://doi.org/10.1016/j.psychres.2016.12.020
Yamazaki, Y., Shoji, T., Miyashima, M., Nagata, Y., Kakutani, Y., Ochi, A., Morioka, T., Nakatani, S., Mori, K., Tsujimoto, Y., & Emoto, M. (2021). Low free triiodothyronine level as a Predictor of Cardiovascular Events and All-Cause Mortality in patients undergoing hemodialysis: The DREAM Cohort. Journal of Atherosclerosis and Thrombosis, 28(10), 1071–1082. https://doi.org/10.5551/jat.60624