Here’s why we should be paying special attention to women’s depression treatment.
Depression is the leading cause of disability and a major contributor to the overall global burden of disease.1 As the 2022 Lancet Commission for Depression highlights, despite how common depression is across the life course, critical barriers have prevented depression from receiving sufficient resources and global attention.1 Depression has historically been stigmatized and misunderstood, and it arises due to a combination of biological, social, and psychological factors. Limited access to treatment and lack of cross-disciplinary, collaborative research and care has hindered progress. Additionally, women are disproportionately affected by depression and are twice as likely to have a diagnosis of depression as men, likely due to the combination of health inequities, gender biases, and biological factors.1 Depression is also a risk factor to develop dementia when in older adults, and it might be a reason more women have dementia than men.2 Developing innovative solutions for depression—especially those focused on women that account for sex and gender differences—are critical to improving individual and collective resilience.
To develop women-focused solutions for depression, it is important to understand the various factors that contribute to women’s greater risk for depression. A health equity and public health lens is imperative. The distinction between sex and gender also needs to be clear, with sex referring to biological differences and gender encompassing socially constructed and enacted roles and behaviors shaped by historical and cultural contexts. Additionally, diagnostic tools, symptom screeners, medications, and other health tools must not have sex or gender bias.
Women in their reproductive years undergo cycle changes in steroid hormones (progesterone/estrogen) over the menstrual cycle. The role of these changes as a factor contributing to depression and mood changes is seen in women with premenstrual dysphoric disorder (PMDD) and premenstrual syndrome (PMS). The estimated prevalence in reproductive women is 5% (PMDD) and 20% (PMS). There is growing evidence that the rise in ovarian steroid hormone production and the effect of their metabolites (in particular allopregnanolone) on central brain receptors as progesterone receptor modulators contribute to the mood symptoms in PMDD and PMS.3 More research is needed to understand the long-term neurological impacts of birth control and hormone therapy.4 Treatments are now being developed to target these newer proposed actions of hormones on the central brain systems with either suppressing ovarian function (removing the natural fluctuations in hormones) or “correcting” the neurotransmitter or neurosteroid dysregulation with the use of targeted specific antidepressants.5,6
The female preponderance in depression occurs largely during the reproductive years, is not evident before puberty, and is less marked after menopause. Societal factors may also play an important role; even in developed countries, women still often take a greater responsibility for child rearing and domestic activities while still being expected to progress their careers—known as a “double day.” Women worldwide are also the majority of caregivers for family members needing health care; often this role is unpaid.
Intimate partner violence
Depression is also linked to intimate partner violence (IPV). One in
3 women globally has experienced physical or sexual IPV.7 Since the outbreak of COVID-19, IPV has escalated and been called the shadow pandemic of COVID-19. In numerous countries, there has been a 300% increase in police reports of IPV, likely fueled by effects and mitigation strategies of COVID-19.8 UN Women projected that an additional 15 million women would be affected by IPV for every 3 months of lockdown.9
One particularly devastating yet unaddressed and long neglected impact is the mental and brain health effects—including traumatic brain injury (TBI) and depression—resulting from IPV. Numerous studies have found that women exposed to IPV are more likely to develop depression than women who are not exposed.10 This finding is not surprising, given that mental health issues are common sequelae of brain injury that may emerge and worsen years after injury. However, IPV is too often left out of conversations around prevention and treatment of depression.
Chronic health conditions
It is also important to note the connection between depression and chronic health conditions in women, such as heart disease. Since 1989, heart disease has been the leading cause of death in US women.11 Women are also more likely than men to die after a heart attack.11 Women are more likely to be undiagnosed, misdiagnosed, or poorly treated for their heart disease due to pervasive bias and the male body being the default for biomedical care and research. Additionally, the Guidelines for the Prevention of Cardiovascular Disease in Women by the American Heart Association show the profound impact of hypertension, diabetes, and depression on women’s hearts.12 It is imperative to understand the huge impact of psychosocial risk factors on women’s hearts and address problems including depression and
Understanding the role of depression in dementia for women is also imperative. The WHAM Report (Women’s Health Access Matters) found that women are 66% of the nearly 7 million individuals in the United States with Alzheimer disease, and yet just 12% of 2019 NIH Alzheimer disease fund went to projects focused on women.13
Even more, the report showed the following:
1. Doubling the funds for women’s Alzheimer disease research pays for itself 3 times over.
2. This 224% return on investment adds 15% more to our economy than general Alzheimer disease research.
3. Adding $300 million for research on women generates $930 million in economic gains, adds back 4000 years of life, eliminates 6500 Alzheimer disease and related dementias, and saves 3500 years of nursing home care and costs.
Depression is one of the largest modifiable risk factors for dementia.14 Thus, understanding the link between depression and dementia and accounting for depression in dementia prevention strategies in women is essential.14
Novel, women-focused solutions can reduce the impact of depression and increase global resilience. As a recent Rock Health report finds, women’s health solutions often remain siloed to pregnancy and reproductive-related issues.15 There is a dearth of women-focused solutions for chronic health and behavioral health and an even larger gap for solutions at the intersection of both.15 Women-focused solutions that include technology, drug development, and devices are urgently needed. Additionally, convergence solutions that combine multiple domains and technologies, such as blending platform and frontier technologies, are key.
Developing women-focused solutions is not only a medical and moral imperative, but there is also a significant economic and commercial upside. Emergen Research projects that the global market for women’s health will reach $60 billion in 2027.16 Additionally, women are the chief medical officers of society, controlling 80% of health care decisions in the United States and spending 29% more per capita on health care compared with men.17,18
By developing women-focused solutions for depression that account for various factors, including the relationship between depression with heart disease and dementia in women, we can build a more resilient society and world.
This article was initially published by our sister publication Psychiatric Times.
Ms Smith is an Atlantic Fellow for Equity in Brain Health at Global Brain Health Institute, a Thiel Fellow at Stanford University, and a Steering Committee member for OECD-PRODEO Institute Neuroscience-inspired Policy Initiative.Mr Heinemeyer is CEO of PRODEO and cofounder of the PRODEO Institute. Dr Chapman is founder and chief director of the Center for BrainHealth at UT Dallas. She is a distinguished professor at UT Dallas. Dr Zarutskie is a reproductive endocrinologist at Baylor College of Medicine. He is an active member of the American Society of Reproductive Medicine and the North American Menopause Society, with a special interest in the role of steroid hormones on cognitive function. Dr Wainer is deputy secretary of public health in the Victorian Department of Health and Honorary Melbourne Enterprise Professor with the University of Melbourne. Dr Berk is a NHMRC senior principal research fellow, Alfred Deakin professor of psychiatry at Deakin University, and director of the Institute for Mental and Physical Health and Clinical Translation at Deakin University. Dr Chadha is CEO and cofounder of the Women’s Brain Project. Dr Eyre is colead of the OECD-PRODEO Institute NIPI.He is a senior fellow in brain capital for the Meadows Mental Health Policy Institute. He holds adjunct or advisory roles with IMPACT at Deakin University, the Heka Fund, Brain Health Nexus at Cohen Veterans Bioscience, GBHI, Baylor College of Medicine, Latin American Brain Health (BrainLat), Universidad Adolfo Ibáñez, Chile, University of Texas Health Sciences Center at Houston, the Davos Alzheimer’s Collaborative and the Euro-Mediterranean Economists Association.
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