Pregnant women with high levels of certain genetic mutations– especially those associated with involuntary muscle contraction – were less likely to respond to preterm treatment. Screening for genetic mutations could allow doctors to tailor effective treatment strategies for preterm birth.
These findings are critical because presently there are no drugs available in the U.S. to treat preterm birth, as FDA removed Makena- a synthetic form of progesterone from market, citing ineffectiveness.
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The study was done in collaboration with Stanford University and published in the journal Science Advances (1✔ ✔Trusted Source
Integrative analysis of noncoding mutations identifies the druggable genome in preterm birth
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Tracking Genetic Variants Offer Personalized Preterm Birth Therapy
“This study calls for a precision framework for future drug development,” said the study’s senior author, Jingjing Li, PhD, associate professor in UCSF’s Department of Neurology and the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research. “In addition to understanding drug effects based on population averages, we also need to take into account the drug response of each patient and ask why some respond and some don’t.”
Preterm birth, or babies born alive before 37 weeks of gestation, is the leading cause of infant mortality and affects some 15 million pregnancies worldwide each year. Preterm birth also leads to a range of long-term health consequences including breathing problems, neurological impairments such as cerebral palsy, developmental disabilities, visual and hearing impairments, heart disease, and other chronic illnesses.
To conduct the study, researchers developed a machine-learning framework to analyze genomes of 43,568 patients who had spontaneous preterm births. The approach uncovered genes that had not previously been known to be associated with preterm birth.
They then examined mutations in the genes among those who had received the progesterone treatment Makena. The FDA had approved the drug in 2011 after a single clinical trial but took it off the market last spring after concluding the drug didn’t work.
The decision left doctors without an approved medication for preterm birth and frustrated those who had found it effective for a subset of their patients. This posed the question: Could there be a genetic reason why progesterone therapy worked for some, but not for others?
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The researchers discovered that the patients in the group with low levels of mutations in the genes associated with muscle contractions were more likely to respond to Makena, but those with higher levels tended not to respond. The finding indicates a personalized medicine approach that involves genetic screening could lead to successful results in patients without a high burden of those mutations.
“Progesterone therapy was the only treatment for recurrent preterm birth over the past decade, and its recent withdrawal by the FDA has left a void in the medication options available for preterm birth patients,” said the study’s first author, Cheng Wang, Ph.D., a postdoctoral scholar at UCSF.
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“In previous clinical practice, we did see that many patients benefited from progesterone therapy,” Wang said. “We probably should reevaluate its efficacy, if we can identify those who respond positively to the treatment.”
Tailoring Effective Treatment for Preterm Birth
The researchers included a cohort of African American patients in the study to determine whether the findings applied broadly across different races. Black women in the U.S. are almost twice as likely to give birth prematurely than white women.
They found the genetic burden did not vary by race. This suggests the high rate of preterm birth among Black mothers may be due primarily to environmental factors such as elevated stress hormones, health care biases, and lack of prenatal care.
The researchers then went beyond that finding to identify new targets and potential therapies to treat preterm birth. They screened more than 4,000 compounds and homed in on 10 that were predicted to interact with the genes associated with preterm birth.
Many of these therapeutic compounds are already being used to treat cancer and other diseases, which means that these drugs could possibly be repurposed to help prevent preterm labor.
A top candidate is the small molecule RKI-1447, a drug that is currently being used to treat cancer, glaucoma, and fatty liver disease. Additional study of the potential of these molecules in treating preterm birth is needed.
Reference:
- Integrative analysis of noncoding mutations identifies the druggable genome in preterm birth – (https://www.science.org/doi/10.1126/sciadv.adk1057)
Source-Eurekalert
