News
US foundation awards $1.6m to improve maternal and child health outcomes
Rates of premature births in the US have steadily increased since 2014
The US non-profit organisation Elevance Health Foundation has expanded its maternal and child health grants with an additional US$1.6m in awards.
Each grant will address maternal and child health, focusing on issues, including mental health, access to care, support, and health-related social needs.
The foundation says this second phase of maternal and child health grants are a part of the US$30m it plans to invest through 2024 to make significant progress on improving maternal and child health outcomes, bringing the total awarded thus far to more than US$18m.
Despite being one of the wealthiest developed countries, the US maternal mortality rate is double that of most other high-income countries, with black women three to four times more likely to die from pregnancy and birth-related causes than white women.
Additionally, rates of premature births have steadily increased since 2014 – the US preterm birthrate increased to 10.5 per cent in 2021, a four per cent increase from 2020.
Of those births, black and native American women are 62 per cent more likely to have a preterm birth and their babies are twice as likely to die compared to white women.
“With a purpose of improving the health of humanity, the Elevance Health Foundation is a key pillar in helping us advance health equity, especially when it comes to maternal and child health,” said Dr Shantanu Agrawal, chief health officer of Elevance Health.
“We’re beginning to see early results from our first phase of maternal health grantees, which further fuels our mission to eliminate health inequities.
“Our foundation’s grants are addressing key social drivers of health – such as where someone lives, economic stability, ethnic background, and more – to ensure that every pregnant woman and child has a fair and just opportunity to be as healthy as possible.”
According to its website, the Elevance Health Foundation uses innovative social-mapping technology and analyses public health data to “gain a snapshot” of the major health issues affecting each state and address health disparities.
The new maternal and child health grantees join 18 organisations awarded last year who have already begun seeing early clinical outcomes.
As of December 2022, 474 babies have been born as part of the foundation’s grant programmes, of which 445 were born full term – this is a 6.1 per cent preterm birth rate, which is lower than the national 10.5 per cent average.
“This funding has allowed us to approach our work in new ways,” said Mandolin Restivo, executive director of Postpartum Support Virginia, an organisation the foundation awarded funding to last year.
“Heading into year two of this grant, we have already been able to triple the number of healthcare providers we have trained and have developed new strategies for providing services to those affected by maternal mental health issues.”
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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