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Research reveals link between menstrual cycles, emotions and sleep patterns
Study sheds new light on the intricate relationship between women’s menstrual cycles, emotions and sleep patterns
Women experience disruptions in their sleep patterns and report heightened feelings of anger in the days leading up to their period, new research has shown.
The study, conducted by a group of international researchers, sheds new light on the intricate relationship between women’s menstrual cycles, emotions and sleep patterns.
The research contributes to a growing body of evidence suggesting that menstrual cycles may play a significant role in women’s vulnerability to insomnia and mental health issues.
“Our research provides valuable insights into the complex interplay between menstrual cycles, emotions, and sleep and the impact of hormonal fluctuations on women’s wellbeing,” said co-author Dr Jo Bower, of the University of East Anglia’s School of Psychology.
“By understanding how these factors interact, we can better address the unique needs of women in terms of sleep health and emotional wellbeing.”
The study analysed data from 51 healthy women aged between 18 and 35, who had regular periods and were not taking hormonal contraception.
Utilising ecological momentary assessment (EMA) methodology, reproductive-aged women completed daily self-reports on their sleep and emotion measures and wore actiwatches (a sleep/wake tracking watch) to track sleep across two menstrual months.
The researchers discovered compelling associations between menstrual phases, emotional states, and sleep quality.
They found that women experience disruptions in their sleep patterns in the days leading up to and during their period, spending more time awake at night, with a lower proportion of time spent in bed that is asleep.
Additionally, they discovered that during the peri-menstrual phase, women report heightened feelings of anger compared to other phases of their menstrual cycle.
Sleep disturbances during the peri-menstrual phase, scientists also revealed, correlate with reduced positive emotions such as calmness, happiness, and enthusiasm.
“The findings underscore the importance of considering hormonal fluctuations when addressing sleep disorders and emotional distress in women,” Dr Bower explained.
“The implications of this research reach further than just the controlled setting, providing potential pathways for interventions and treatments aimed at enhancing sleep quality and emotional resilience in women.”
Although the study had unique strengths, such as the use of both objective and subjective prospective data across two menstrual cycles, the researchers said the findings must be interpreted within the context of several limitations.
For example, the data was collected between May 2020 and January 2021, and precisely how the Covid-19 pandemic impacted outcomes can’t be fully known.
Although the researchers did not find strong effects for pandemic stress on outcome variables, they can’t discount the fact that the pandemic likely impacted participants’ emotional experiences and sleep-wake behaviours.
The research was led by Dr Jessica Meers at the Center for Innovations in Quality, Effectiveness and Safety, which is a collaboration between the Michael E. DeBakey VA Medical Center and Baylor College of Medicine, both based in Houston, Texas.
The University of East Anglia and the University of Houston were also partners in the research.
Diagnosis
Lung cancer drug shows breast cancer potential
Ovarian cancer cells quickly activate survival responses after PARP inhibitor treatment, and a lung cancer drug could help block this, research suggests.
PARP inhibitors are a common treatment for ovarian cancer, particularly in tumours with faulty DNA repair. They stop cancer cells fixing DNA damage, which leads to cell death, but many tumours later stop responding.
Researchers identified a way cancer cells may survive PARP inhibitor treatment from the outset, pointing to a potential way to block that response. A Mayo Clinic team found ovarian cancer cells rapidly switch on a pro-survival programme after exposure to PARP inhibitors. A key driver is FRA1, a transcription factor (a protein that turns genes on and off) that helps cancer cells adapt and avoid death.
The team then tested whether brigatinib, a drug approved for certain lung cancers, could block this response and boost the effect of PARP inhibitors. Brigatinib was chosen because it inhibits multiple signalling pathways involved in cancer cell survival.
In laboratory studies, combining brigatinib with a PARP inhibitor was more effective than either treatment alone. Notably, the effect was seen in cancer cells but not normal cells, suggesting a more targeted approach.
Brigatinib also appeared to act in an unexpected way. Rather than working through the usual DNA repair routes, it shut down two signalling molecules, FAK and EPHA2, that aggressive ovarian cancer cells rely on. FAK and EPHA2 are proteins that relay survival signals inside cells. Blocking both at once weakened the cells’ ability to adapt and resist treatment, making them more vulnerable to PARP inhibitors.
Tumours with higher levels of FAK and EPHA2 responded better to the drug combination. Other data link high levels of these molecules to more aggressive disease, pointing to potential benefit in harder-to-treat cases.
Arun Kanakkanthara, an oncology investigator at Mayo Clinic and a senior author of the study, said: “This work shows that drug resistance does not always emerge slowly over time; cancer cells can activate survival programmes very early after treatment begins.”
John Weroha, a medical oncologist at Mayo Clinic and a senior author of the study, said: “From a clinical perspective, resistance remains one of the biggest challenges in treating ovarian cancer. By combining mechanistic insights from Dr Kanakkanthara’s laboratory with my clinical experience, this preclinical work supports the strategy of targeting resistance early, before it has a chance to take hold. This strategy could improve patient outcomes.”
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