Relaxation techniques may help lower high blood pressure-at least in the short term

Relaxation techniques may help lower high blood pressure-at least in the short term-but the longer term effects are unclear, finds a pooled data analysis of the existing research published in the open access journal BMJ Medicine.

And the risk of bias in the existing body of research means that further, more rigorously designed and longer studies are needed to confirm whether these techniques have a constructive role in the treatment of high blood pressure, conclude the researchers.

High blood pressure affects around a third of 30-79 year olds and is one of the leading attributable causes of deaths in both men and women, note the researchers.

While drugs are available to treat the condition, adherence to them is poor, generating interest in alternative approaches, such as relaxation techniques, to reduce one of the major risk factors for high blood pressure-high stress levels.

But it’s far from clear which of these methods, which can include breath control, mindfulness, yoga, Tai Chi, and biofeedback, among others, might be most effective.

To build on the evidence base, the researchers scoured research databases for studies, published in English up to February 2024 that looked at the potential impact of relaxation techniques on high blood pressure (140/90 mm Hg and above) and elevated blood pressure (120/80 mm Hg and above).

They included 182 studies, 166 of which looked at high blood pressure, and 16 of which looked at elevated blood pressure (pre-hypertension).

Where possible, the researchers deployed network meta analysis, a statistical technique used to simultaneously compare the effects of several different ‘treatments’.

The pooled results of 54 studies showed that most relaxation techniques seemed to lower both systolic and diastolic blood pressure for people with high blood pressure after 3 or fewer months. The most commonly included interventions were breath control (13 studies), yoga/tai chi (11), biofeedback (8), progressive muscle relaxation (7), and music (7).

Compared with no intervention, breath control achieved a reduction of 6.65 mm Hg in systolic blood pressure (the first and higher number in a blood pressure reading), meditation a drop of 7.71 mm Hg, meditative movement, such as tai chi and yoga, a drop of 9.58 mm Hg, and mindfulness a drop of 9.90 mm Hg.

Music was also associated with a fall of 6.61 mm Hg, progressive muscle relaxation with a fall of 7.46 mm Hg, and psychotherapy with a reduction of 9.83 mm Hg. Combined techniques were associated with a drop of 6.78 mm Hg in blood pressure.

There was no statistical evidence of effectiveness for any technique after 3 to 12 months and the certainty of the evidence was very low. The most commonly included techniques at this timepoint were biofeedback (7 studies), yoga/tai chi (4), and progressive muscle relaxation (4).

Very few studies included long term follow up of 12 months or more, and of the 3 included in the network analysis, the results showed that compared with no treatment autogenic (self directed) training might lower both systolic and diastolic blood pressure, but the certainty of the evidence was low.

There was no statistical evidence of effectiveness for other treatments assessed at this time point, including biofeedback, progressive muscle relaxation, and techniques involving a combined approach.

Limited data were available for elevated blood pressure: only two studies compared relaxation techniques with no treatment/usual care and the effects on systolic blood pressure were small.

The researchers note that the descriptions of relaxation interventions were sometimes incomplete or sparse, there were few data on costs and cost effectiveness, and most of the included studies didn’t report information on the risk of cardiovascular disease/events/deaths.

But they suggest: “The results of our systematic review and network meta-analysis indicate that relaxation or stress management techniques might result in meaningful reductions in blood pressure at up to three months of follow-up.”

But they caution: “Uncertainty exists about this effect, however, because of the risk of bias in the primary studies, the potential for publication bias in this area, and imprecision in the effect estimates, meaning that the observed changes in blood pressure might be too small to affect cardiovascular or cerebrovascular outcomes.”

And they add: “Hypertension is a chronic condition, likely to require long term drug treatments or behavioural changes. As such, interventions that are used for a brief period, or provide only short term benefits, are unlikely to be clinically useful.

“Too few studies exist, however, to assess whether the beneficial effects of relaxation are maintained when the techniques are practised for longer than three months. Future studies must clearly report whether participants were still using relaxation methods at the time of the outcome assessment, with details on adherence to the relaxation schedule. These factors might strongly influence the effectiveness of the different relaxation and stress management techniques.” 

Reference:

Katie E Webster, Monika Halicka, Russell J Bowater, Thomas Parkhouse, Effectiveness of stress management and relaxation interventions for management of hypertension and prehypertension: systematic review and network meta-analysis, BMJ Medicine, DOI:10.1136/bmjmed-2024-001098 

Powered by WPeMatico

Antenatal Opioid Exposure tied to smaller brain volumes in Newborn: JAMA

A U.S. prospective study has found that antenatal opioid exposure, particularly during the second or third trimester, was linked to smaller brain volumes in newborns. However the extent of impact varied based on the type and timing of opioid exposure. The study was conducted by Yao Wu and colleagues published in JAMA Pediatrics.

The prospective cohort study was performed between August 2020 and December 2023 at four U.S. sites and involved a total of 269 term newborns: 173 with antenatal opioid exposure and 96 unexposed controls. MRI scans were performed prior to the infants’ age of 8 weeks, with a mean postmenstrual age of 42.84 weeks at imaging. 3D volumetric MRI was used without sedation, with harmonized protocols on Siemens and Philips 3T scanners. Automated segmentation with DrawEM and 3D U-Net pipelines was followed by manual corrections for accuracy.

Statistical analysis was performed using analysis of covariance (ANCOVA), controlling for important covariates such as postmenstrual age at MRI, sex, birth weight, maternal education, and pregnancy smoking.

Key Findings

The research found that opioid-exposed infants had significantly reduced brain volumes in almost all brain regions compared with unexposed controls.

Total brain volume:

  • Exposed: 387.51 cm³

  • Controls: 407.06 cm³

  • Difference: 19.55 cm³ (95% CI, 8.75–30.35)

Cortical volume:

  • Exposed: 167.07 cm³

  • Controls: 176.35 cm³

  • Difference: 9.28 cm³ (95% CI, 3.86–14.70)

Deep gray matter volume:

  • Exposed: 27.22 cm³

  • Controls: 28.76 cm³

  • Difference: 1.54 cm³ (95% CI, 0.66–2.43)

White matter volume:

  • Exposed: 159.90 cm³

  • Controls: 166.65 cm³

  • Difference: 6.76 cm³ (95% CI, 1.71–11.81)

Cerebellar volume:

  • Exposed: 23.47 cm³

  • Controls: 24.99 cm³

  • Difference: 1.52 cm³ (95% CI, 0.67–2.36)

Brainstem volume:

  • Exposed: 6.80 cm³

  • Controls: 7.18 cm³

  • Difference: 0.38 cm³ (95% CI, 0.19–0.57)

Amygdala volume:

  • Left: 0.48 cm³ vs 0.51 cm³ (difference: 0.03 cm³)

  • Right: 0.51 cm³ vs 0.55 cm³ (difference: 0.04 cm³)

Subgroup analysis demonstrated that:

  • Methadone-exposed infants had significantly reduced white matter volumes compared to controls.

  • Buprenorphine-exposed infants had a reduced right amygdala compared to controls.

  • Infants exposed to opioids alone and polysubstance-exposed infants had significant volume decreases in the cortex, deep gray matter, cerebellum, brainstem, right amygdala, and total brain.

  • Polysubstance-exposed newborns also had reduced white matter and left amygdala volumes compared to controls.

The study authors concluded that antenatal opioid exposure was found to be associated with lower global and regional brain volumes in neonates, as well as lower cortical, white matter, deep gray matter, cerebellar, and amygdala volumes. These observations highlight the susceptibility of the developing brain to in-utero opioid exposure and support proactive measures to counteract long-term neurodevelopmental effects.

Reference:

Wu Y, Merhar SL, Bann CM, et al. Antenatal Opioid Exposure and Global and Regional Brain Volumes in Newborns. JAMA Pediatr. Published online April 07, 2025. doi:10.1001/jamapediatrics.2025.0277

Powered by WPeMatico

Dietary shift after migration increases CV risk by altering composition of individual’s gut microbiome: Study

An Amsterdam UMC-led study has found that migrants, this case from West Africa to Europe, experience a ‘clear change’ in their microbiome composition as compared to their non-migrant peers in West Africa, which expose them to an increase of cardiovascular disease. These peer-reviewed findings are published today in the journal Gut Microbes demonstrating that participants who lost specific groups of microbes or acquired specific new groups of microbes had higher rates of cardiovascular risk factors such as hypertension, diabetes, obesity, and poor kidney function.

“The results clearly demonstrate the importance of our findings in the relation to migration-related health outcomes,” explains postdoctoral researcher at Amsterdam UMC and first author of the study, Barbara Verhaar, who carried out the research together with colleagues at the University of Ghana, and Kwame Nkrumah University of Science & Technology (KNUST).

“It was already thought that migration had an effect on an individual’s microbiome, but previous studies have either lacked in the number of individuals included, didn’t control for variations in diet or only compared first- and second-generation migrants. Our study makes use of our own RODAM study cohort to definitively demonstrate this change,” says Verhaar.

The Amsterdam UMC led study included more than 1100 individuals from two separate continents and three locations: rural Ghana, urban Ghana or Netherlands. Respondents completed identical dietary questionnaires and provided both fecal and blood samples to determine the composition of their gut microbiomes. Analyses revealed the presence of different microbes across the three groups, in line with the hypothesis that migration would affect microbiome composition. The findings show that some groups of microbes disappear, and new ones emerge along the migration axis.

Health Outcomes

Previous studies, as well as the World Health Organisation, note that migrants frequently experience poorer health outcomes than native residents and research from Amsterdam UMC has found this also to be the case in the Netherlands.

“This research underscores the relevance of gut health and how we look at the adverse health outcomes that are often associated with migration. It is fascinating to learn that when we migrate, we lose some relevant microbes we acquired in our home countries and pick up new microbes in the new countries, and this can influence our health very importantly. We found that macronutrient groups such as protein, fat and salt in food were strongest associated with gut microbiota composition and these were higher in migrants, which might have contributed to the shift in gut microbiota composition. Future longitudinal studies are needed to verify these findings,” adds Charles Agyemang, Professor of Global Migration, Ethnicity & Health at Amsterdam UMC and senior author of the study.

Cardiometabolic risk is a growing concern for researchers across the globe and Agyemang is currently leading a host of projects, both in the Netherlands and several African countries, that aim to develop better interventions to lower the risk of developing cardiometabolic diseases, such as diabetes and hypertension; and to improve management of cardiometabolic diseases.

As part of these efforts, as in this study, he works with the several institutions across the globe especially in the African region to ensure that research in Amsterdam is strengthened with international data and, also, that research findings are translated into concrete policy.

“The findings of this study provide important insights into how migration can reshape our gut microbiota and subsequent health outcomes and emphasizes the needs for north-south collaborations,” adds Ellis Owusu-Dabo, Professor of Epidemiology and Global Health, KNUST.  

Reference:

Barbara J. H. Verhaar, Eva L. van der Linden, Gut microbiota shift in Ghanaian individuals along the migration axis: the RODAM-Pros cohort, Gut Microbes, https://doi.org/10.1080/19490976.2025.2471960.

Powered by WPeMatico

Aspirin Use significantly linked to AKI Risk in Critical Chest Trauma Patients: Study

Researchers have found a significant association between aspirin use and an increased risk of acute kidney injury (AKI) in critically ill patients with chest trauma in a new study.

Non-steroidal anti-inflammatory drugs (NSAIDs) are increasingly utilized in trauma patients, particularly those with critical chest trauma who are susceptible to significant blood loss, leading to renal hypoperfusion. Acute kidney injury (AKI) is known to carry a poor prognosis in chest trauma patients. Therefore, investigating the potential association between NSAID use and acute kidney injury risk in critical patients with chest trauma is crucial. They selected patients admitted to the intensive care unit (ICU) with chest trauma from the Medical Information Mart for Intensive Care III (MIMIC-III) dataset (2001–2012) and the Medical Information Mart for Intensive Care IV (MIMIC-IV) dataset (2013–2019). Propensity score matching (PSM) was used to match patients receiving NSAIDs with those not receiving treatment. Logistic regression was employed to assess the association between different types of NSAIDs and acute kidney injury in these patients. Results: In MIMIC-IV, NSAID use significantly increased the risk of acute kidney injury in critical patients with chest trauma (OR 1.99; 95% CI 1.04 to 3.85). Subgroup analysis revealed that aspirin significantly increased AKI risk in both MIMIC-III (OR 1.81; 95% CI 1.02 to 3.2) and MIMIC-IV (OR 2.47; 95% CI 1.26 to 4.85). However, ibuprofen and ketorolac use were not associated with acute kidney injury in these patients. They observed a significant association between aspirin use and an elevated risk of acute kidney injury in critical patients with chest trauma. These findings suggest that pain management strategies involving ibuprofen and ketorolac may be more appropriate for this patient population.

Reference:

Huang, Y., Xu, H., Xiang, F. et al. Aspirin increases the risk of acute kidney injury in critical patients with chest trauma: a retrospective cohort study. Int J Emerg Med 18, 38 (2025). https://doi.org/10.1186/s12245-025-00835-1

Keywords:

Aspirin, Use, significantly, linked, AKI, Risk, Critical, Chest, Trauma, Patients, Study, Huang, Y., Xu, H., Xiang, F, NSAIDs, Chest trauma, AKI, Aspirin, Ibuprofen, Ketorolac

Powered by WPeMatico

Mindfulness and cognitive behavioral therapy improve chronic low back pain, suggests research

The list of treatments for low back pain is endless, but few offer relief for the one in four Americans who suffer from this persistent pain and leading cause of disability globally. More than 80% of those with chronic low back pain wished there were better treatment options. Yet, without sufficient pain relief, many people need to take opioids, which can be addictive.

The good news? A multi-institutional team, led by researchers from the Penn State College of Medicine and the University of Wisconsin-Madison, found that eight weeks of either mindfulness or cognitive behavioral therapy (CBT) training led to meaningful improvements among adults with chronic low back pain that’s currently treated with opioids and had not responded to prior treatments. These behavioral therapies helped improve physical function and quality of life and reduce pain and opioid dose in a randomized clinical trial. The benefits persisted for up to 12 months.

The findings were published today (April 7) in JAMA Network Open. This is the largest trial to date comparing mindfulness with CBT as treatments for opioid-treated chronic pain and the research team followed up with participants over a longer time period than many previous trials of mindfulness.

“Both mindfulness and cognitive behavioral therapy were shown to be safe, effective treatments, providing lasting benefits for people with opioid-treated chronic back pain,” said Aleksandra Zgierska, Jeanne L. and Thomas L. Leaman, MD, endowed professor and vice chair of research of family and community medicine and professor of anesthesiology and perioperative medicine and of public health sciences at the Penn State College of Medicine, who led the study. “These evidence-based behavioral therapies should be standard of care available to our patients.”

Pain is multifaceted, especially chronic pain that can last for months or years. Chronic low back pain is the most common form of chronic non-cancer pain that’s treated with opioids. Previous research has shown that adults with chronic pain may benefit from behavioral therapies, which can help people change their thoughts about and relationship to pain, but it’s been understudied, the researchers explained. Studies on behavioral therapies were generally small in size and evaluated benefits over the short-term.

“People think of chronic pain as a physical condition that requires a physical intervention,” said Eric Garland, endowed professor in health sciences and professor of psychology at the University of California, San Diego and senior author of the study.

The research team set out to evaluate the effectiveness of mindfulness compared to CBT as treatments for chronic opioid-treated low back pain and their long-term effects. CBT is considered the standard psychotherapy for chronic pain, but its long-term benefits haven’t been well studied. To date, only 17 studies have evaluated mindfulness for chronic low-back pain and three studies have compared mindfulness and CBT.

This study was planned in partnership with an advisory panel composed of clinicians and representatives of community and advocacy organizations that work with people with chronic pain as well as adults with opioid-treated chronic low back pain and their caregivers. The panel’s feedback, included throughout the study, helped the researchers design and implement the study and better translate the study’s results to be meaningful and useful to patients and clinicians.

The team enrolled 770 adults to participate in a randomized clinical trial conducted in three sites — Madison, Wisconsin; Boston, Massachusetts; and Salt Lake City, Utah. Participants, on average, experienced moderate-to-severe pain, functional limitations, compromised quality of life and numerous prior treatments for their chronic low-back pain and were treated with daily opioid medications for at least three months.

“The people in this study had quite severe back pain that interfered with their life and was bad enough to need opioid medication. Usually, in that condition, people don’t really get better over time on their own,” said Bruce Barrett, professor of family medicine and community health at the University of Wisconsin-Madison and co-lead of the study.

Participants were then assigned to either receive mindfulness-based therapy or CBT, which were conducted in therapist-led, two-hour group sessions for eight weeks. The mindfulness group learned to notice the sensations they experienced, giving them more control over how they related and respond to the pain and other symptoms. The CBT group learned coping skills and strategies to change their negative thought patterns. Participants were instructed to practice on their own for 30 minutes a day, six days a week during the 12-month study and to continue with their routine care. They were not instructed to reduce their opioid dosage. They reported on their pain level, ability to do daily activities, mental and physical health-related quality of life and daily opioid medication use at the start of the study and after three, six, nine and 12 months.

At the end of the study, participants in both groups reported significant and long-lasting benefits including reductions in pain and daily opioid dose. They also reported increased function and health-related quality of life through 12 months. Both mindfulness and CBT tools were shown that they could be effective and used safely over the long-term, the researchers said.

“The goal of pain management is to improve quality of life, increase function and reduce the sense of suffering. The study’s interventions likely helped reduce the participants’ sense of suffering, which probably allowed them to function a whole lot better,” said Penney Cowan, founder of the American Chronic Pain Association and co-author and advisor on the study. “People can live with pain, but they need to know how to do it. This study provides a sense of hope. It says you can do this and help yourself to a better quality of life.”

The research team explained that people living with chronic pain assemble a toolkit filled with different self-coping and self-care methods to manage their pain. They can use these tools at different times and in different ways.

“Mindfulness and CBT are other tools that you can add to your toolbox to increase your capacity to cope and live a meaningful life,” said Christin Veasley, founder of the Chronic Pain Research Alliance and co-author and advisor on the study. “What’s important about the types of therapies, like the ones evaluated in this study, is that they can be used broadly across all pain conditions and all pain severities.”

For example, while participants were told to continue their usual treatment, including pain medication as advised by their usual clinicians, opioid dosage decreased in both groups through 12 months following the intervention. Zgierska explained that participants learned skills, like taking a mindful breath before taking medication. The improvements, the research team said, were the byproduct of people implementing these tools, learning to better cope with pain and deciding to decrease their opioid use on their own.

“These therapies aren’t a total cure, but they teach people how to develop the inner resources they need to cope with chronic pain and to live a better life,” Garland said. “Mindfulness is a self-regulated tool that comes from within, unlike surgery or medication where something is being done to you from the outside. By learning these techniques, patients continue to experience lasting benefit.”

Reference:

Zgierska AE, Edwards RR, Barrett B, et al. Mindfulness vs Cognitive Behavioral Therapy for Chronic Low Back Pain Treated With Opioids: A Randomized Clinical Trial. JAMA Netw Open. 2025;8(4):e253204. doi:10.1001/jamanetworkopen.2025.3204.

Powered by WPeMatico

Does Paxlovid reduce long COVID symptoms? Yale-led trial finds out

Antiviral medications nirmatrelvir/ritonavir (Paxlovid) were not effective in relieving long COVID symptoms, according to a new study published in The Lancet Infectious Diseases on April 3.

The findings came from the Yale Paxlovid for Long COVID (PAX LC) Trial, led by principal investigator Dr. Harlan Krumholz, Harold H. Hines, Jr. Professor of Medicine (Cardiology), and Akiko Iwasaki, Sterling Professor of Immunobiology. The phase 2 investigational new drug clinical trial tested whether a 15-day course of Paxlovid, an FDA-approved antiviral for acute COVID-19, could also help long COVID patients. The PAX LC team pioneered a novel, decentralized design that brought the trial into 100 participants’ homes around the nation. It’s the first fully decentralized phase 2 trial of its scale, the researchers say.

“This is the first time that we’ve been able to execute on a study that enrolled people throughout the entire contiguous United States in a manner that was convenient and easy for them,” said Krumholz. “We got an answer that, though disappointing, at least provides more information for us to continue the effort to try to help relieve suffering among these individuals.”

The trial was based on one of experts’ four hypotheses on what causes long COVID. In a subset of individuals, they speculate, persistent SARS-CoV-2 virus may continue to replicate in the body even after the initial COVID-19 infection. Although there have been case reports that some patients taking longer-term Paxlovid (beyond the standard five-day course for acute infections) experienced symptom relief, at the time of starting the PAX LC Trial, there had been no other clinical trials testing the antiviral’s efficacy in treating the post-acute infection syndrome.

Bringing PAX LC into participants’ homes

Participation in the PAX LC Trial was open to anyone nationwide who experienced any long COVID symptoms — such as fatigue, weakness, and brain fog — within four weeks of having a positive COVID-19 test. All participants shared their medical records through Hugo Health, a platform co-founded by Krumholz that allowed the researchers to access the medical files electronically within a matter of minutes and ensure the individual’s eligibility while protecting their privacy. In total, 100 people joined the study.

Once cleared and enrolled, the participants received by mail their 15-day course of either Paxlovid or a placebo. Each day, they described their symptoms in electronic diaries from their phones or computers to be transmitted to a trial database to be reviewed by the research team. Medical professionals collected blood and saliva samples either at the participants’ homes or at a local laboratory. After 28 days, they reassessed long COVID symptoms.

Krumholz is especially excited about the PAX LC Trial’s novel format, which eased the burden of participating in a clinical trial. “For people who were highly disabled by long COVID we made it so they didn’t have to find transportation or make repetitive site visits,” he said. “We designed the trial with them in mind and, with their input, and we made a strong commitment to ensure that we were attentive to their needs throughout every phase of the trial.”

After publishing the study, the investigators also held a virtual town hall available to all participants. “We wanted them to be among the very first to hear the results and have the opportunity to ask the investigators questions,” he said.

Paxlovid fails to improve long COVID symptoms

The study found that Paxlovid did not cause any significant changes in symptoms across the cohort. Other clinical trials have reported similar results, including the STOP-PASC Trial at Stanford Medicine.

But while the antiviral did not benefit the group as a whole, long COVID is likely caused by several different mechanisms. One recent case study published in Nature involved 13 patients who took an extended course of Paxlovid ranging from 7.5 to 30 days, and showed variable results — five reported lasting improvement [reduction of symptoms lasting months after treatment], four temporary improvement [returned to baseline weeks/months after treatment], and four no improvement.

While there were no significant differences in the symptoms reported by the Paxlovid versus placebo arms, individual participants experienced varying outcomes. In future research, Iwasaki hopes to better understand this variation. Her lab team is continuing to conduct detailed analyses of participants’ immune systems based on the collected blood samples and plans to publish the results later in the year. “Even if there are only one or two people who truly experienced benefit, we want to understand what the biological mechanisms might be by looking at the immune signatures,” she said.

Furthermore, there might be ways to tweak the PAX LC Trial protocol so that more people may benefit. “The case study goes on to show that maybe the duration of the drug wasn’t long enough, or maybe our selection criteria should be different,” she said. “There are lots of reasons why a clinical trial fails, but it’s still important for us to be able to say that this particular regimen wasn’t effective when compared to a placebo.”

To evaluate the impact of the decentralized trial design, the researchers also asked participants to rate their experiences on a scale of one to 10. The average overall satisfaction rating was 7.9, the study’s team friendliness was rated at 8.1, and the likelihood of referring others to PAX LC or a similar study was 8.3.

Benefits of decentralized clinical trials

The researchers are disappointed that Paxlovid did not provide relief to the participants. However, they are optimistic that the PAX LC Trial is proof that decentralized trials are not only immensely beneficial to the participants but can also be conducted in an efficient and cost-effective way. “We hope to use this platform for any future studies that don’t require a doctor’s visit for drug treatment,” Iwasaki said.

The participant satisfaction also emphasizes the importance of making clinical trials accessible, Krumholz adds. Noting that it is unusual to report on the experiences of people within a clinical trial, he explained, “I insisted with the journal we published in that we include a metric that showed how satisfied people were with the trial.

“This is a group that’s frustrated because they’re very sick. Many of them have been dismissed by the medical care system — so it’s understandable that they’re not optimistic. But their ratings of their experience in this trial were exceptionally high.”

Reference:

Sawano, Mitsuaki et al., Nirmatrelvir–ritonavir versus placebo–ritonavir in individuals with long COVID in the USA (PAX LC): a double-blind, randomised, placebo-controlled, phase 2, decentralised trial, The Lancet Infectious Diseases.

Powered by WPeMatico

Sugary Drinks Linked to Higher Oral Cancer Risk in Women: JAMA study

A study published in JAMA Otolaryngology-Head & Neck Surgery has revealed that women who consumed sugary drinks daily had a 4 to 5 times higher risk of oral cavity cancer (OCC). However, the overall risk remained low, with three cases per 100,000 people.

The incidence of oral cavity cancer (OCC) is increasing among nonsmokers and young individuals without traditional risk factors worldwide. High sugar-sweetened beverage (SSB) intake is associated with various gastrointestinal cancers, but its association with OCC has not been explored. A study was done to evaluate the association between SSB intake and the risk of OCC among smoking and nonsmoking women participating in the Nurses’ Health Study (NHS) and Nurses’ Health Study II (NHSII). This longitudinal cohort study analyzed data from women in the NHS (follow-up, 1986-2016) and NHSII (follow-up, 1991-2017) after excluding those with a history of cancer, implausible caloric intake, or missing SSB intake data. Participants were followed up until the diagnosis of OCC. Data analysis was performed from July 2023 to June 2024. Cox proportional hazards regression models with age and questionnaire period as the time scale were used to estimate hazard ratios (HRs) and 95% CIs associated with the development of OCC for each category of SSB intake, with less than 1 SSB per month as the reference group. Results A total of 162 602 women (mean [SD] age, 43.0 [9.9] years) were evaluated. During 30 years of follow-up, 124 invasive OCC cases were documented. In multivariable-adjusted models, participants consuming 1 or more SSB daily (5 people per 100 000 population) had a 4.87 times (95% CI, 2.47-9.60 times) higher risk of OCC compared with those consuming less than 1 SSB monthly (2 people per 100 000 population), increasing the rate of OCC to 3 more people per 100 000 population. When restricted to both nonsmokers or light smokers and nondrinkers or light drinkers, the risk of OCC was 5.46 times (95% CI, 1.75-17.07 times) higher, increasing the rate of OCC to 3 more people per 100 000 population. In this study, high SSB intake was associated with a significantly increased risk of OCC in women, regardless of smoking or drinking habits, yet with low baseline risk. Additional studies are needed in larger cohorts, including males, to validate the impact of these findings.

Reference:

Gomez-Castillo L, Cushing-Haugen KL, Useche M, et al. High Sugar-Sweetened Beverage Intake and Oral Cavity Cancer in Smoking and Nonsmoking Women. JAMA Otolaryngol Head Neck Surg. Published online March 13, 2025. doi:10.1001/jamaoto.2024.5252

Keywords:

Gomez-Castillo L, Cushing-Haugen KL, Useche M, High, Sugar-Sweetened, Beverage Intake

Powered by WPeMatico

Research unravels Improvement of melanoma treatment by blocking an enzyme

About 65% of melanoma patients do not respond to immunotherapy. New work by the team of Prof. Max Mazzone (VIB-KU Leuven Center for Cancer Biology) discovered that an enzyme called HPGDS (expressed in a specific subset of macrophages), plays a key role in immunotherapy resistance. Blocking HPGDS may be a new way to overcome immunotherapy resistance in melanoma patients and potentially in other tumors facing similar challenges. The results of this study were published in Cancer Discovery, a journal of the American Association for Cancer Research.

Immune suppression

The field of cancer immunotherapy has witnessed exciting therapeutic advances in the last decade, particularly in the treatment of melanoma, a highly aggressive form of skin cancer. However, approximately 65% of melanoma patients still do not respond to immune checkpoint blockade (ICB) therapies. The immunosuppression induced by tumor-associated macrophages (TAMs) may be pivotal in this process. TAMs have been shown to impede immune system function, thereby fostering tumor growth and metastasis dissemination. Thus, reprogramming TAM phenotype away from their immunosuppressive state might boost cancer treatments.

New work by the team of Prof. Max Mazzone (VIB-KU Leuven) and colleagues zooms in on a specific enzyme known as hematopoietic prostaglandin D2 synthase (HPGDS), which is produced by TAMs. HPGDS promotes the formation of a metabolite called prostaglandin D2 (PGD2), which, in turn, helps cancer cells to resist treatment by blocking the activity of T-cells, which are vital for attacking tumors.

Reprogramming TAMs

“By analyzing the expression of genes related to the immune response in patients who responded to immune checkpoint blockade therapies compared to those who did not, we found that HPGDS levels were high in non-responding patients during treatment, whereas were downregulated if the treatment was working and T-cells were then activated against the tumor” says Dr. Rosa Trotta, first author of the study.

By employing genetic deletion of HPGDS in macrophages and using pharmacological inhibitors in mouse and humanized models, the researchers proved a remarkable shift in the macrophages’ behavior from promoting tumor growth to supporting a more robust and anti-tumoral immune response.

“Targeting HPGDS not only enhanced the recruitment and activation of T-cells per se,” says Prof. Max Mazzone, “but also showed promise in overcoming resistance to existing therapies. Our findings suggest that blocking HPGDS or the two downstream receptors may be a new potential strategy for improving treatment options for melanoma patients and perhaps others facing similar challenges.”

This study suggests that HPGDS inhibitors or PGD2 receptor blockers could serve as new therapeutic agents, either alone or in combination with existing treatments for melanoma and other cancers (i.e., pancreatic ductal adenocarcinoma) that show similar resistance mechanisms. As the research progresses, the team emphasizes the need for further studies to validate these findings in clinical settings.

Reference:

Trotta, R., et al. (2025). Activated T cells break tumor immunosuppression by macrophage re-education. Cancer Discovery. doi.org/10.1158/2159-8290.cd-24-0415.

Powered by WPeMatico

Postpartum Hormonal Contraceptives use tied to Depression Risk: JAMA

Researchers have found in a new cohort study that initiating hormonal contraceptives postpartum is linked to an increased immediate risk of developing depression. The risk was higher when contraceptives, particularly combined oral contraceptives, were started earlier postpartum. Hormonal contraceptive (HC) use is associated with depression. It is, however, unknown whether this is also true in the postpartum period when women have a heightened depression risk and are routinely offered HC treatment. A study was done to examine whether HC initiation post partum is associated with the development of depression within 12 months post partum. A population-based cohort study based on nationwide Danish register data was conducted including all primiparous women who gave birth from January 1, 1997, through December 31, 2022. Women were excluded if they had depression within 24 months before delivery, multiple births or stillbirth, or a diagnosis of breast cancer or liver tumor. Data analysis was conducted between March 20, 2023, and January 17, 2025. Hormonal contraceptive initiation within 12 months post partum was treated as a time-varying exposure. Hormonal contraceptive types were categorized as combined oral contraceptives (COCs), combined nonoral contraceptives (CNOCs), progestogen-only pills (POPs), and progestogen-only nonoral contraceptives (PNOCs). Depression within 12 months post partum, defined as filling an antidepressant prescription or receiving a hospital diagnosis of depression, was the main outcome. Adjusted hazard ratios (AHRs) and average absolute risks of depression within 12 months post partum were estimated using Cox proportional hazards regression and a G-formula estimator. Results Of 610 038 first-time mothers, 248 274 (40.7%) initiated HCs within 12 months post partum (mean [SD] age, 27.6 [4.3] years for HC users vs 29.6 [4.8] years for nonusers). Hormonal contraceptive initiation was associated with subsequent depression, with an AHR of 1.49 (95% CI, 1.42-1.56) compared with no use, resulting in an increase in the 12-month absolute risk from 1.36% (95% CI, 1.32%-1.39%) to 1.54% (95% CI, 1.50%-1.57%). The AHR for COC was 1.72 (95% CI, 1.63-1.82); CNOC, 1.97 (95% CI, 1.64-2.36); and PNOC, 1.40 (95% CI, 1.25-1.56). Progestogen-only pill exposure was associated with an instantaneously reduced risk in the early study period, but it was increased late post partum. The earlier COCs were initiated post partum the higher the associated rate ratio of depression. In this cohort study, HC initiation post partum was associated with an instantaneous increased risk of developing depression. The associated risk was higher the earlier it was initiated post partum, at least for COC. This finding raises the issue of whether the incidence of depression post partum is increased by routine HC initiation after childbirth.

Reference:

Larsen SV, Ozenne B, Mikkelsen AP, et al. Postpartum Hormonal Contraceptive Use and Risk of Depression. JAMA Netw Open. 2025;8(3):e252474. doi:10.1001/jamanetworkopen.2025.2474

Keywords:

Postpartum, Hormonal, Contraceptives, use, tied, Depression Risk, JAMA, Larsen SV, Ozenne B, Mikkelsen AP

Powered by WPeMatico

Upfront combination therapy of statin and ezitamide may transform cardiac care, suggests research

Ochsner Health Medical Director for Cardiac Rehabilitation and Preventive Cardiology, Carl J. “Chip” Lavie, Jr., MD, recently co-authored a groundbreaking research study featured in the prestigious Mayo Clinic Proceedings highlighting the comparative efficacy of lipid-lowering therapies for reducing cardiovascular risks and led by Maciej Banach, MD,PhD from Poland and leader of the International Lipid Expert Panel ( ILEP). Impact of Lipid-Lowering Combination Therapy With Statins and Ezetimibe vs Statin Monotherapy on the Reduction of Cardiovascular Outcomes: A Meta-analysis explores the outcomes of combination lipid-lowering therapy (LLT) using statins and ezetimibe relative to statin monotherapy and could prevent thousands of deaths due to heart disease and stroke.

With a comprehensive evaluation of 14 studies encompassing over 108,000 high-risk individuals, the analysis reveals that the combination of statins with ezetimibe markedly lowers LDL cholesterol levels, achieving a mean reduction difference of -12.96 mg/dL and significantly diminishing the risk of all-cause mortality by 19%, major adverse cardiovascular events by 18%, and stroke incidence by 17%. The research underscores the comparable safety profile of combination LLT to statin monotherapy, with both approaches presenting similar risks of adverse effects and therapy discontinuation.

This pivotal study advocates for the integration of combination therapy early in treatment protocols, particularly for high and very high-risk groups. It highlights the potential for this integrative approach to not only meet LDL-C targets more effectively but also to substantially curtail mortality and CVD events.

Dr. Lavie stated, “The findings underscore the importance of a proactive, combination-based strategy in lipid-lowering therapy. By optimizing LDL-C reductions early, we can dramatically improve patient outcomes and reduce the global burden of cardiovascular disease.”

The study authors encourage early intervention with combinations therapy in very high-risk patients, even before they suffer a cardiac event or stroke. By adopting a framework that includes upfront combination therapy, clinicians can enhance patient outcomes in the management of cardiovascular risks and diseases. This research represents significant progress toward optimizing prevention strategies and improving patient outcomes. 

Reference:

Maciej Banach, Vikash Jaiswal, Song Peng Ang, Aanchal Sawhney, Novonil Deb, Pierre Amarenco, Dan Gaita, Zeljko Reiner, Ivan Pećin, Carl J. Lavie, Peter E. Penson, Peter P. Toth, Impact of Lipid-Lowering Combination Therapy With Statins and Ezetimibe vs Statin Monotherapy on the Reduction of Cardiovascular Outcomes: A Meta-analysis, Mayo Clinic Proceedings, https://doi.org/10.1016/j.mayocp.2025.01.018.

Powered by WPeMatico