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New Research Finds Potential Alternative to Abortion Pill Mifepristone

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New Research Finds Potential Alternative to Abortion Pill Mifepristone

A new study suggests a possible alternative to the abortion pill mifepristone, a drug that continues to be a target of lawsuits and legislation from abortion opponents.

But the potential substitute could further complicate the politics of reproductive health because it is also the key ingredient in a contraceptive morning-after pill.

The new study, published Thursday in the journal NEJM Evidence, involved a drug called ulipristal acetate, the active ingredient in the prescription contraceptive Ella, one of two types of morning-after pills approved in the United States. (The other, Plan B One-Step, which does not require a prescription, contains a different drug and does not work in a way that would terminate a pregnancy, according to scientific evidence.)

In the study, 133 women who were up to nine weeks’ pregnant took twice the dose of the ulipristal acetate contained in Ella, followed by misoprostol, the second drug used in the typical medication abortion regimen. All but four of the women completed the termination of their pregnancies without further intervention, a 97 percent completion rate that is similar to the regimen using mifepristone. (The others finished the process with additional medication or a procedure.)

There were no serious complications, and the study concluded that using ulipristal acetate for abortion was safe.

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Dr. Beverly Winikoff, the lead author of the study and the president of Gynuity Health Projects, a reproductive health research organization, said that after the Supreme Court overturned the national right to abortion in 2022, she began wondering about a possible role for ulipristal acetate, which has a similar chemical structure to mifepristone.

“I was thinking, there’s maybe something else we can do,” she said. “Another option. And this one is already on the market.”

The political implications of the study are complex because of their potential to blur the line between the public perception of emergency contraception and abortion. For years, abortion opponents have opposed morning-after pills by saying they can cause abortions, and reproductive health experts have countered by pointing to scientific evidence that the pills do not terminate pregnancies but instead act to prevent pregnancy after sex.

Some reproductive health experts are concerned that research showing that a morning-after pill ingredient can be used for abortion could stoke attempts to crack down on emergency contraception and sow confusion that could bolster the larger anti-abortion strategy.

Kristi Hamrick, a spokeswoman for Students for Life of America, said her organization would “absolutely” consider litigation over Ella.

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“The pro-life movement should be vindicated,” Ms. Hamrick said. “We’ve been arguing for years that Ella acts as an abortifacient.”

Mary Ziegler, a law professor and abortion expert at the University of California, Davis, said the study could present challenges for both sides of the abortion debate.

“It’s going to put wind in the sails of abortion opponents who have been saying things like contraceptives can be abortifacients,” she said, adding, “This study being released will be difficult, I think, for abortion rights supporters to manage.”

But Ms. Ziegler said the study’s findings could also be “politically risky” for abortion opponents because public support for contraception is high and many voters in conservative states endorsed ballot measures protecting abortion rights. “I think it’s one of those things that’s going to tempt social conservatives to push probably faster than politics would currently permit in the direction of regulating contraception,” she said. “And I think that could backfire.”

Reproductive health experts said the new study did not refute the science showing that morning-after pills don’t induce abortions, because it involved a different dose of the drug.

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Abortion opponents said they were not surprised by the study’s findings.

“After years of denying ulipristal acetate’s potential to end the life of an embryo, abortion advocates are now starting to use it as a substitute for the abortion drug mifepristone,” Dr. Donna Harrison, director of research for the American Association of Pro-Life Obstetricians and Gynecologists, said in a statement. “The reason for this is simple. Ulipristal and mifepristone function in the same way.”

Ella was already a target for some conservatives. Project 2025, a right-wing policy blueprint that has been strongly tied to the new Trump administration, said that Ella should be removed from required insurance coverage of contraception under the Affordable Care Act because it is “a potential abortifacient.”

Mifepristone, the first pill in the standard two-drug medication abortion regimen, is the only drug specifically approved for abortion in the United States. Typically used through 12 weeks’ gestation, mifepristone stops the development of a pregnancy by blocking the hormone progesterone. The second drug, misoprostol, is taken 24 to 48 hours later and causes contractions similar to a miscarriage.

Ulipristal acetate is in the same class of medications as mifepristone and also blocks the activity of progesterone, a hormone that prepares the uterus to receive and hold an embryo, said Dr. Daniel Grossman, a reproductive health physician and researcher at the University of California, San Francisco, who was not involved in the new study.

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In the study, a 60 milligram dose of ulipristal acetate (double the 30 milligrams in Ella) was substituted for mifepristone and followed by misoprostol, which has various medical uses and has not been targeted as much by abortion opponents. (Misoprostol can also facilitate an abortion on its own, but is considered more effective in a combination regimen.)

Reproductive health experts said they welcomed the search for alternatives to mifepristone because abortion opponents have been waging efforts to sharply restrict the medication across the country, most notably with a federal lawsuit against the Food and Drug Administration. The Supreme Court rejected that lawsuit last year, ruling that the initial plaintiffs lacked standing to sue, but the suit has since been revived with three states as plaintiffs.

Dr. Grossman, who wrote an editorial about the study, said the prospect of a substitute for mifepristone was “certainly a promising finding.” But, he added, “if because of this new evidence that at higher doses, ulipristal acetate could cause an abortion, that were to lead to ulipristal acetate being taken off the market for emergency contraception, that would be really, really bad.”

The company that manufactures Ella, Perrigo, issued a statement saying that Ella “was not tested in this study.” It added, “Ella is an F.D.A.-approved emergency contraception pill that acts before pregnancy can occur,” she continued. “There continues to be no evidence to show that, on its own, Ella causes an abortion.”

The study was conducted in Mexico City and was co-led by researchers there.

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Several experts said that because it was a relatively small first study with no comparison group of patients, more research was needed before ulipristal acetate should be used for abortion. “We can’t change clinical practice based on this study,” said Kelly Cleland, a researcher who is the executive director of the American Society for Emergency Contraception.

Scientists have long understood that hormone-based drugs may be able to play different functions at different doses along the spectrum of a woman’s reproductive health cycle.

In Europe, researchers including Dr. Rebecca Gomperts, a Dutch physician and founder of telemedicine organizations that provide abortion pills globally, are studying low doses of mifepristone as a weekly birth control pill. Dr. Gomperts said she considered the new ulipristal acetate study sufficient to prescribe the drug off-label for medication abortion.

“The more uses we have for these medications, the harder it will be for people to take them away,” said Dr. Paul Blumenthal, an emeritus professor of obstetrics and gynecology at Stanford University who was in an advisory group for the study.

Plan B is a much more widely used morning-after pill in the United States, but Ella is considered more effective for some women, including people who are overweight. Plan B is intended to be taken within three days after unprotected sex, while Ella can be taken within five days.

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Both pills prevent pregnancy by blocking ovulation, the release of eggs from the ovaries that occurs before eggs can be fertilized, scientific studies have shown.

The claim by some abortion opponents that morning-after pills are abortion drugs is based on a theory that they might also prevent a fertilized egg from implanting in the womb. Most scientific research has not found that to be the case.

For years, despite scientific evidence to the contrary detailed in an investigation by The New York Times, the F.D.A.-approved label and packaging for Plan B One-Step said that while the pill worked by blocking ovulation, there was a possibility it might prevent implantation. In 2022, the agency changed the language to make it clear that Plan B acts only before fertilization, “will not work if you’re already pregnant, and will not affect an existing pregnancy.”

The F.D.A. label for Ella says that its “likely primary mechanism of action” is to stop or delay ovulation. The label adds that the medication may also affect implantation. Studies in recent years, however, suggest that Ella does not operate by blocking a fertilized egg from implanting in the womb.

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Quitting smoking could offer a major benefit beyond heart and lung health, study finds

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Quitting smoking could offer a major benefit beyond heart and lung health, study finds

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People who quit smoking may reduce their risk of developing dementia later in life, according to new research.

A team of researchers at a university in China analyzed data from more than 32,000 adults over a 25-year period and found that former smokers had a lower risk of dementia compared to people who continued smoking.

The findings were published in the journal Neurology.

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During the study period, researchers documented 5,868 cases of dementia.

Participants who quit smoking during the study had a significantly lower risk of developing dementia than current smokers. Their risk was similar to people who had quit smoking before the study began and those who had never smoked.

New research suggests that quitting smoking may lower the chance of developing dementia later in life. (iStock)

The researchers also found that dementia risk continued to decline the longer a person remained smoke-free, approaching that of never-smokers after about seven years.

The benefits appeared strongest among people who gained little or no weight after quitting.

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“Our findings suggest that quitting smoking may support long-term brain health, but they also highlight that what happens after quitting matters,” lead researcher Hui Chen said in a statement.

The reduction in dementia risk was most pronounced among people who experienced little or no weight gain after they stopped smoking. (iStock)

Zaid Fadul, a Harvard-trained physician and chief medical officer of Bespoke Concierge MD who was not involved in the research, said the findings add to growing evidence that quitting smoking can help protect long-term brain health.

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“The key takeaway is that the brain appears to benefit from smoking cessation at virtually any stage,” Fadul told Fox News Digital.

“Smoking contributes to chronic inflammation, oxidative stress, and damage to blood vessels that supply the brain, all of which are associated with cognitive decline and dementia risk.”

Fadul said the findings should encourage smokers who may feel it is too late to quit.

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“Importantly, it is rarely ‘too late’ to quit,” he said.

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“While earlier cessation offers the greatest benefit, the body and brain begin recovering soon after smoking stops.”

Experts say it is almost never too late to quit smoking, as the body and brain start to recover soon after a person stops, although quitting earlier provides the greatest health benefits. (iStock)

Improvements in circulation, reduced inflammation and better cardiovascular health can help preserve cognitive function later in life, according to Fadul.

“Every year without tobacco is a step toward lowering future dementia risk and improving overall health,” he said.

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While the findings were encouraging, the study does have limitations.

Researchers identified an association between quitting smoking and a lower risk of dementia, but the study was not designed to prove that ending smoking directly prevents the condition.

Other health, lifestyle and environmental factors may have also influenced participants’ outcomes.

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Fox News Digital reached out to the researchers for further comment.

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How 3 Women Reversed Fatty Liver Disease and Lost Nearly 300 Lbs. Combined

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How 3 Women Reversed Fatty Liver Disease and Lost Nearly 300 Lbs. Combined


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Just 5 minutes of prayer could have surprising health benefits, study finds

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Just 5 minutes of prayer could have surprising health benefits, study finds

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Adult patients experienced significant relief from pain and anxiety after just five minutes of in-person prayer, as found in a randomized controlled trial.

The study, led by researchers at the University of Maryland School of Medicine’s Department of Family and Community Medicine, compared the effects of direct prayer to the effects of listening to music, revealing that prayer provided greater and more sustained relief for both symptoms.

“Prayer is powerful and beneficial on many levels,” Jesse Bradley, pastor of Grace Community Church in Washington, told Fox News Digital.

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According to statistics cited in the study, prayer is the most used form of complementary medicine in the United States, relied on by 43% of Americans.

The researchers focused on a practice known as proximal intercessory prayer (PIP), which is defined as in-person, face-to-face prayer directed toward another individual’s well-being.

The researchers tracked changes in the participants’ self-reported pain and anxiety levels at multiple intervals: immediately after the five-minute session, at two weeks and at six weeks. (iStock)

The research team recruited 180 adult patients from a family medicine waiting room, according to a press release. All participants had previously reported experiencing moderate to severe pain, anxiety or both.

Following their standard medical appointments, the patients were randomly assigned to one of two groups: the prayer group, in which participants received five minutes of in-person Christian prayer delivered by a trained volunteer, and the music group, where they spent five minutes listening to music.

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The researchers then tracked changes in the participants’ self-reported pain and anxiety levels at multiple intervals: immediately after the five-minute session, at two weeks and at six weeks.

“It was very well-received,” Katherine Jacobson, MD, assistant professor of family and community medicine at the University of Maryland School of Medicine, told Fox News Digital. She noted that 97% of participants said they were “neutral or supportive” when asked about having this kind of prayer available as part of their medical visits.

An expert described the transformative power of prayer through “healing and comfort,” and shared that he himself once went through a long, painful recovery process. (iStock)

The study, which was published in The Annals of Family Medicine, revealed that while patients in both groups showed improvements, those in the prayer group reported substantially greater relief.

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Bradley, who was not involved in the study, described the transformative power of prayer through “healing and comfort,” and shared that he himself once went through a long, painful recovery process.

“Daily prayer was essential in my healing journey,” he shared.

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For pain reduction, the individuals who received in-person prayer experienced greater drops in pain intensity immediately following the session. This superior level of relief remained evident during the two-week follow-up compared to the music group, the researchers found.

For anxiety reduction, the benefits of prayer were even longer-lasting. The prayer recipients reported significantly greater reductions in anxiety immediately after the session, and these positive effects remained statistically significant at both the two-week and six-week checkpoints.

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The prayer recipients reported significantly greater reductions in anxiety immediately after the session, and these positive effects remained statistically significant at both the two-week and six-week checkpoints. (iStock)

“We expected that patients who expected prayer to work would benefit more, but that wasn’t what we found,” Jacobson said.

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“Religious affiliation, religious intensity and expectancy of healing did not predict who improved,” he went on. “Benefits appeared across a wide range of patients, including those not of the Christian faith and those who did not expect the intervention to help them.”

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The study had some limitations, the researchers acknowledged, primarily that it could not prove that prayer itself caused the improvements.

The team also noted that patients receiving prayer had human contact, while the music control group did not. The eye contact and gentle laying of hands from the prayer volunteers may have had an impact, as that type of contact is known to reduce pain.

The researchers suggested that PIP could serve as a low-cost, non-pharmacologic and effective complement to standard medical care. (iStock)

The authors hope to conduct future studies with a control group that receives interpersonal contact but no prayer.

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“For physicians and health systems, the study supports continuing to ask patients about spiritual care preferences as part of whole-person care, and considering whether trained Christian volunteer prayer practitioners could be integrated into outpatient settings for interested patients,” Jacobson said.

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The researchers suggest that PIP could serve as a low-cost, non-pharmacologic and effective complement to standard medical care.

Rather than replacing traditional treatments, the authors indicate that this type of brief, faith-based intervention could be integrated into primary care settings to help manage pain and anxiety.

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