Surgical ablation during CABG increased survival in atrial fibrillation patients: Study

A recent study published in The Annals of Thoracic Surgery suggests that despite strong clinical guidelines, the use of surgical ablation during coronary artery bypass grafting (CABG) in patients with atrial fibrillation (AF) remains low and potentially life-shortening.

The study reviewed data from over 87,000 Medicare beneficiaries who had preexisting atrial fibrillation and underwent CABG between 2008 and 2019. This revealed that only 22.2% received concomitant surgical ablation. This technique targets the abnormal electrical signals causing AF and was associated with significantly improved long-term survival.

This study found that patients who received surgical ablation during CABG lived a median of 4.4 months longer than those who did not. Also, risk-adjusted median survival was 7.82 years in the ablation group when compared to 7.46 years in the non-ablation group (P < .001).

The survival benefit was even more pronounced when looked at the surgeon practice patterns. The patients operated on by surgeons who frequently perform ablation (defined as doing so in ≥40% of their CABG cases) had a median survival advantage of nearly 5 months (4.96 months) when compared to the patients treated by infrequent ablation surgeons (<5% of cases). Median survival in this analysis was 7.03 years versus 6.62 years, respectively (P < .001).

While the survival gains may appear modest on paper, the public health impact is substantial, given the high volume of CABG procedures and the prevalence of atrial fibrillation in older adults. This study argues that the findings support current guideline recommendations advocating for surgical ablation in AF patients undergoing CABG and spotlight a significant gap between evidence-based guidance and real-world practice.

In a detail examination, 652 surgeons (frequent ablation) performed the procedure in ≥40% of their CABG patients, 1834 surgeons (occasional ablation) performed it in 5–40% of cases and 1193 surgeons (infrequent ablation) did so in <5% of cases. These numbers suggest that a large proportion of cardiac surgeons either rarely or inconsistently offer this beneficial procedure.

As the study brought out, improving adherence to surgical ablation guidelines could meaningfully enhance long-term outcomes for tens of thousands of cardiac surgery patients every year. Overall, while surgical ablation during CABG clearly offers survival advantages, it remains underutilized, which calls for an urgent need for practice alignment with current evidence and guidelines.

Reference:

Schaffer, J. M., Kluis, A., Squiers, J. J., George, T. J., Shih, E., Banwait, J. K., Mack, M. J., & DiMaio, J. M. (2025). Survival after surgical ablation of atrial fibrillation during coronary artery bypass in Medicare beneficiaries. The Annals of Thoracic Surgery. https://doi.org/10.1016/j.athoracsur.2025.03.044

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Frequent Salt Use Linked to Higher Risk of Liver Diseases: Study

A new study published in the European Journal of Nutrition showed that frequently adding salt to food is associated with a higher risk of developing metabolic dysfunction-associated steatotic liver disease (MASLD), cirrhosis, and hepatocellular carcinoma. This research further highlights stronger associations in nonsmokers, current alcohol consumers, and individuals without diabetes or with lower body weight.

Previously known as non-alcoholic fatty liver disease, MASLD is a rising public health concern that presently affects around 30% of the world’s population. This percentage is expected to increase to 55.7% by 2040, which is concerning. In addition to developing cirrhosis and hepatocellular carcinoma, people with MASLD are especially vulnerable to extrahepatic consequences such type 2 diabetes, cardiovascular disease (CVD), chronic renal disease, and extrahepatic malignancies. However, there is now just one medication licensed for MASLD, resmetirom. Thus, prevention and early identification of cirrhosis, HCC, and modifiable risk factors for MASLD remain top public health priorities.

Adding salt to meals has been positively linked to a number of diseases and death, making it a unique indication for researching habitual sodium consumption. On the other hand, not much is known regarding its connection to liver-related conditions. This study looked at the relationships between the risks of cirrhosis, hepatocellular carcinoma (HCC), and MASLD and the addition of salt to meals.

A total of 4,92,265 people from the UK Biobank who did not have any common liver disorders at baseline were included in this prospective cohort research. Electronic health records were used to identify incident liver-related diseases, and a self-reported query was used to gather the frequency of adding salt to diets. Hazard ratios (HRs) and 95% CIs for the results were estimated using multivariable Cox proportional hazard models.

There were 413 HCC cases, 5,546 cirrhosis cases, and 7,005 incident MASLD patients with a median follow-up of 13 years. The HRs (95% CIs) of MASLD throughout the increasing frequency of incorporating salt into foods were 1.00 (reference) for never/rarely, 1.08 (1.02, 1.14) for sometimes, 1.22 (1.13, 1.31) for usually, and 1.40 (1.27, 1.53) for always, with a P for trend < 0.0001, after controlling for sociodemographic characteristics, lifestyle factors, personal history of diseases, and dietary factors.

Adiposity was a contributing factor in this connection. Additionally, the same favorable correlations between HCC and cirrhosis were identified. Overall, higher incidences of cirrhosis, HCC, and MASLD were linked to more frequent salt additions to meals. According to these results, cutting back on salt and sodium consumption may be a good way to avoid liver-related illnesses.

Source:

Zhang, S., Huo, Z., Borné, Y., Sonestedt, E., & Qi, L. (2025). Adding salt to foods and risk of metabolic dysfunction-associated steatotic liver disease and other chronic liver diseases. European Journal of Nutrition, 64(5), 224. https://doi.org/10.1007/s00394-025-03745-3

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DCC Recommends Licensing, Labelling Restrictions on Anti-TB Drugs to Curb Private Market Misuse

New Delhi: In a move to curb potential misuse of critical tuberculosis medications, the Drugs Consultative Committee (DCC) has recommended that licenses for Bedaquiline, Delamanid, Pretomanid, and Rifapentine be issued with strict usage conditions, restricting their use to the National TB Elimination Programme (NTEP) and in accordance with the Standards of TB Care in India (STCI). Additionally, the DCC proposed mandatory red-box warnings on drug labels indicating their restricted use.

The recommendations were made during the 66th DCC meeting, held on June 17, 2025, at CDSCO headquarters, New Delhi, under the chairmanship of Dr Rajeev Singh Raghuvanshi, Drugs Controller General (India).

Unregulated Access in Private Sector Raises Red Flags

The committee was apprised that the Central TB Division, Ministry of Health and Family Welfare, had informed CDSCO that the patents for Bedaquiline and Delamanid expired last year, after which “multiple pharma companies have started manufacturing the molecule and the drug has been made freely available in the private market.”

This open market access, the Division cautioned, “risks indiscriminate use, potentially increasing cases of treatment failure and resistance to these drugs.”

Conditional Licensing and Mandatory Label Warning Proposed

To mitigate this public health risk, the DCC noted, “It has been requested to issue the licenses with condition for use of Bedaquiline, Delamanid, Pretomanid and Rifapentine as per Standards of TB Care in India (STCI) & Conditional access through National TB Elimination Programme (NTEP).”

Further, the DCC recommended that if existing licenses do not mention these usage restrictions, “it then be modified accordingly.”

The committee also proposed specific labelling standards to limit off-label or unregulated use, “The label on the immediate container of the drug as well as the packing in which the container is enclosed should bear the following: ‘WARNING: For the use in National TB Elimination Programme (NTEP)’ which shall be in box with red background.”

Uniform Guidance to State Licensing Authorities (SLAs)

Since these drugs have now crossed four years of market presence and are no longer considered “new drugs”, the DCC noted that State Licensing Authorities (SLAs) are empowered to issue manufacturing licenses, but must do so with the proposed restrictions.

The committee formally recorded, “DCC after detailed deliberation agreed with the proposal to issue suitable guidance to all the SLAs to uniformly address the issue.”

Moreover, in states where such licenses have already been issued without the proposed condition, the DCC advised that, “They can issue separate letter for communicating the above conditions to such manufacturers.”

The DCC’s recommendation comes at a critical juncture for India’s TB elimination mission. While patent expiry and increased production of advanced anti-TB drugs may lower costs and improve availability, unregulated private sector access threatens to erode treatment efficacy.

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Smoking Increases HS Risk in Type 2 Diabetes Patients, suggests study

A new study published in the journal of PloS One found a significant link between smoking and a heightened risk of hidradenitis suppurativa (HS) in individuals with type 2 diabetes mellitus (T2DM). It highlights smoking cessation as a critical strategy to reduce HS risk in this vulnerable group. 

Acne inversa, another name for hidradenitis suppurativa, is a chronic inflammatory skin disorder marked by painful lesions that come again. The axillae, inguinal, and anogenital regions are among the body parts with apocrine glands where these deep-seated, inflammatory lesions are most common.

The exact prevalence of DM in HS patients is still unknown, though, since rates have been found to range from about 4% to 33%. Since HS is more common in people with type 2 diabetes mellitus, it is essential to comprehend modifiable risk factors like smoking in order to improve patient outcomes. Thus, to clarify how smoking contributes to the onset or exacerbation of HS in this high-risk group, this study looked into the relationship between changes in smoking intensity and the risk of HS in patients with type 2 diabetes.

The data from 1,705,427 individuals in the Korean National Health Insurance Service were evaluated in this retrospective cohort research. After controlling for possible confounders such as gender, age, and concomitant diseases, the study looked at smoking status, changes in smoking intensity, and the incidence of HS in people with type 2 diabetes.

According to the study, those who maintained smoking had a 23.6% higher risk of heart disease (HS) than nonsmokers (adjusted hazard ratio (aHR), 1.236; 95% confidence interval (CI), 1.075–1.421). Furthermore, compared to nonsmokers, those who smoked more cigarettes had a 28.5% greater risk of HS (aHR, 1.285; 95% CI, 1.048–1.577). However, when stratified by BMI, no discernible variations were seen in the relationship between changes in smoking intensity and the risk of HS.

Overall, the relevance of quitting smoking as a possible approach for reducing the risk of heart attacks in at-risk DM populations is highlighted by this study, which also shows a correlation between smoking and an elevated risk of heart attacks in people with type 2 diabetes. To further understand how smoking aggravates HS in people with type 2 diabetes and to find efficient treatments for this population, more study is required.

Reference:

Yook, H. J., Kim, E., Kim, Y. H., Lee, G.-N., Han, K., & Lee, J. H. (2025). A link between smoking behaviors and the risk of hidradenitis suppurativa in diabetic patients. PloS One, 20(6), e0325357. https://doi.org/10.1371/journal.pone.0325357

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Depression + inflammation: A bad combo for lung cancer patients, claims research

For the first time, researchers have found that lung cancer patients who have a combination of high levels of depression and inflammation at diagnosis are later found with continuing depressive symptoms in the next several months, even as they receive new, promising therapies.

The study found that having both maladies at diagnosis predicted higher, continuing levels of depression during the next eight months. Those who had only high levels of depression or only high levels of inflammation, or neither of them, showed no changes in depression over time.

In the analyses, the researchers took into account a wide variety of other factors that could affect the results, including age, race, partner status, education, employment status, lifetime smoking, and any cancer treatments the patients received.

“What this suggests is that there may be an additive effect or perhaps a synergy between inflammation and depression that can lead to worse outcomes with depression,” said Barbara L. Andersen, corresponding author of the study and professor of psychology at The Ohio State University.

The results are important because high depression levels have been linked to poorer outcomes in lung cancer patients, suggesting that patients with high inflammation and depression may be at particular risk, Andersen said.

The study was published online recently in the journal Biopsychosocial Science and Medicine.

Andersen and colleagues at Ohio State’s College of Medicine and The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute studied 182 patients who were newly diagnosed with advanced lung cancer (Stage IV). The patients were followed with monthly depression assessments for eight months.

A previous study with the same participants found that depression was linked to higher levels of inflammation in lung cancer patients at diagnosis. This study was designed to see how that combination affected future levels of depression, which had not been studied before, Andersen said.

Participants completed a depression measure. In addition, levels of neutrophils and lymphocytes from patients’ blood samples were used to calculate a measure of systemic inflammation, called the Advanced Lung Cancer Inflammation Index (ALI). A previous study by Andersen showed ALI from these patients predicted their survival. That study also found that overall, 35% of the patients had moderate to severe depressive symptoms. That study was the first to show that, among these patients with higher levels of depression, upwards of 70% also had high inflammation.

“We found that this is a particularly alarming combination. None of the three other groups in our study – those with just high inflammation, those with just high depression, or those with neither – had increasing levels of depression over the eight months,” Andersen said.

Scientists don’t know for sure how inflammation and depression interact to increase depression, she said.

One hypothesis is that inflammation in the body, as seen in this study, can be transmitted to the brain, where it settles into the microglia. During inflammation, the microglia can release harmful substances associated with the development of depression.

These findings are important because of all cancer patients, those with lung cancer are among those with the highest rates of depression, Andersen explained. And the fact that depression is already linked to systemic inflammation suggests the risk is compounded.

“Our findings suggest the need to screen for depression and determine inflammation biomarkers at diagnosis of lung cancer,” she said.

“This can help identify vulnerable patients who need psychological therapies to reduce depressive symptoms with a possibility of impacting inflammation as some studies have found.”

Reference:

Park, Kylie R. MS; Shields, Peter G. MD; Myers, John PhD; Reisinger, Sarah A. PhD; Andersen, Barbara L. PhD. Depression and Inflammation Predict Depression Trajectory of Non-Small Cell Lung Cancer Patients. Biopsychosocial Science and Medicine ():10.1097/PSY.0000000000001379, June 11, 2025. | DOI: 10.1097/PSY.0000000000001379

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Night Shifts Linked to Increased Asthma Risk in Postmenopausal Women: Study

A recent study using data from over 280,000 participants in the UK Biobank revealed a strong link between night shift work and asthma risk in women, particularly in postmenopausal women not using hormone replacement therapy (HRT). The findings published in the ERJ Open Research, highlighted the need to examine how occupational patterns intersect with biological factors to influence respiratory health.

Asthma, already more prevalent in females than males, has also been previously associated with night shift work. With more women joining the shift work labor force, scientists sought to determine whether the asthma risk tied to shift work differs between sexes.

This study employed logistic regression models to assess asthma prevalence across various work schedules, adjusting for factors like age, smoking status, body mass index, and socioeconomic status. The results revealed that women working permanent night shifts had a 50% higher risk of moderate to severe asthma when compared to their counterparts working regular daytime hours. In contrast, no significant association was observed in men.

Also, female night shift workers showed an odds ratio (OR) of 1.50 (95% confidence interval [CI] 1.18–1.91) for moderate to severe asthma when compared to female day workers. Men working night shifts had an OR of 0.95 (CI 0.72–1.26), which suggested no increase in the risk. A statistically significant sex interaction (p=0.01) further highlighted that the relationship between shift work and asthma is indeed stronger in women.

The findings were consistent across broader asthma indicators, including self-reported asthma and symptoms such as wheezing or whistling in the chest. This study explored whether the increased risk in women was related to hormonal changes. Among postmenopausal women not using HRT, the asthma risk was even higher, with an adjusted OR of 1.89 (CI 1.24–2.87) for moderate to severe asthma in permanent night workers versus day workers. However, this elevated risk disappeared among postmenopausal women who were using HRT, suggesting a potential protective effect.

The study also considered chronotype (morning or evening preference), but the observed sex-specific risks remained most clearly aligned with menopause and HRT status rather than sleep timing preference alone. These findings suggest that circadian rhythm disruption, hormonal imbalances, or both may underlie the heightened vulnerability observed in women. Overall, these findings stress the need for proactive health monitoring and tailored workplace policies aimed at minimizing chronic disease risk linked to modern work patterns.

Source:

Maidstone, R. J., Ray, D. W., Liu, J., Bowden, J., Rutter, M. K., & Durrington, H. J. (2025). Increased risk of asthma in female night shift workers. ERJ Open Research, 00137–02025. https://doi.org/10.1183/23120541.00137-2025

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Grip strength gives researchers new handle on psychosis, reveals research

Psychosis often begins not with characteristic disturbances of the mind – delusions like paranoia or hallucinations – but with disturbances in the way we move our body. For researchers like Indiana University Assistant Professor Alexandra Moussa-Tooks in the Department of Psychological and Brain Sciences, these motor disturbances offer critical insights into the condition of psychosis itself.

In a new study published on June 25 in the American Journal of Psychiatry, senior-author Moussa-Tooks and first-author Heather Burrell Ward, assistant professor of psychiatry and behavioral sciences at Vanderbilt University Medical Center, explore one such motor ability – grip strength – to uncover the mechanisms linking motor disturbances to psychosis.

As Moussa-Tooks explains: “Poor grip strength has been associated with many negative outcomes in a variety of people: lower well-being, higher risk of mortality, poor day-to-day functioning, poor quality of life. Grip strength seems to capture that things are not going well. But it hasn’t been well studied in relation to brain function or early psychosis. Our study looks at how grip strength may be an important sign of brain and psychological health in early psychosis.”

The study is the first to suggest that grip strength and overall well-being share common patterns of brain connectivity. It shows that impairment in grip strength and well-being may reflect alterations in what researchers call “resting-state functional connectivity,” a measure of brain network function that may be key to understanding psychosis.

Through a novel neuroimaging analysis, Moussa-Tooks and her collaborators demonstrate that brain networks with important roles in both motor and cognitive function play key roles in gripping ability and mental well-being. Their findings lay the groundwork for interventions aimed at improving functioning and wellness in early psychosis.

A unifying brain circuit explanation

The study’s data came from the Human Connectome Project for Early Psychosis, a large initiative conducted from 2016 to 2020 across multiple sites, among them the IU School of Medicine. It included 89 individuals in the first five years of psychotic illness and 51 healthy controls for whom age- or medication-related motor decline could be ruled out.

The analysis confirmed that participants with early psychosis had lower grip strength and well-being scores than healthy controls. These metrics related to three key brain regions -the anterior cingulate cortex, sensorimotor cortex, and cerebellum-each of which were shown to be connected to the default mode network. Higher grip strength and greater well-being correlated with greater connectivity between these regions and the default mode network.

Identifying brain targets for new treatments

“Our findings are particularly exciting because they identify potential brain targets for new treatments for psychosis,” Ward said. For example, both researchers see enormous potential in transcranial magnetic stimulation. If in psychosis there is poor communication within the default mode network, TMS is a non-invasive tool that can be used to directly increase that connectivity. Motor training, like exercise, to strengthen brain networks indirectly can offer another promising strategy.

“Grip strength and other motor functions,” Moussa-Tooks explains, “are easily assessed and more readily interpretable than complex tasks often used to study psychosis. Our work is showing that these seemingly simple metrics can help us understanding disturbances not only in the motor system, but across complex brain systems that give rise to the complex symptoms we see in psychosis.”

Consider the following analogy, she suggests: “If psychosis is a house on fire, symptoms such as delusions and hallucinations are the smoke. In a fire you don’t target the smoke, you target the fire and its source. And yet, currently that’s not how we approach treatment for psychosis. Motor disturbances help us get closer to identifying where the fire may have started and spread. They are more fundamental in the sense that they’re easier to link to different disturbances in the brain.”

With this new study researchers are getting closer to the fire. By drawing a line between motor function and mental health – from grip strength and well-being to patterns of brain connectivity with a key role in psychosis – they are mapping out new paths for understanding and treating an elusive disorder. 

Reference:

Heather Burrell Ward, Adam Beermann, Karlos Manzanarez Felix, Grip Strength as a Marker of Resting-State Network Integrity and Well-Being in Early Psychosis, American Journal of Psychiatry, https://doi.org/10.1176/appi.ajp.20240780

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Roxadustat Linked to Hemoglobin Overshoot in Non-Dialyzed CKD Patients: Study

Japan: Researchers have found in a new study that Roxadustat therapy in non-dialyzed chronic kidney disease (CKD) patients may lead to hemoglobin (Hb) overshoot, particularly when switching from erythropoiesis-stimulating agents (ESAs). Researchers further highlighted the need for careful Hb monitoring before and after initiating treatment to avoid potential adverse outcomes.

The study, published in Internal Medicine and led by Dr. Masanori Tamaki and colleagues from the Department of Nephrology, Tokushima University Hospital, Japan, examined the short-term effects of switching from ESA therapy to roxadustat in CKD patients with anemia who were not on dialysis. Roxadustat, an oral hypoxia-inducible factor-prolyl hydroxylase inhibitor, is known to boost hemoglobin production, but little data exists on how rapidly Hb levels could rise following a treatment change.

The retrospective, 8-week pilot study involved 86 adult patients with advanced CKD. Of these, 23 patients transitioned from ESA therapy (either darbepoetin or epoetin beta pegol) to roxadustat, while 63 continued on ESAs. The primary outcome was the occurrence of hemoglobin overshoot, defined as an Hb level exceeding 12.5 g/dL during the study period.

The key findings were as follows:

  • Hemoglobin (Hb) overshoot occurred in 34.8% of patients (8 out of 23) who received roxadustat.
  • In contrast, only 3.2% of patients (2 out of 63) in the ESA group experienced Hb overshoot.
  • The likelihood of Hb overshoot was significantly higher in the roxadustat group, with an odds ratio of 20.2 after adjusting for patient background factors.
  • In patients who stopped taking roxadustat the following overshoot, hemoglobin levels returned close to baseline within four weeks.
  • Risk factors for Hb overshoot included younger age and higher baseline levels of hemoglobin and hematocrit.

The authors emphasized that while roxadustat is effective in managing anemia in non-dialyzed CKD patients, the risk of rapid Hb elevation must be considered. Early and regular monitoring of hemoglobin levels after initiating treatment is critical to avoid potential complications, such as cardiovascular events that may be associated with elevated Hb.

The authors concluded, “The study sheds light on the need for individualized anemia management strategies when using roxadustat in CKD care. Clinicians are advised to remain cautious and adopt proactive monitoring protocols when switching patients from ESAs to roxadustat therapy.”

Reference:

Tamaki M, Inagaki T, Minato M, Shibata E, Nishioka R, Nishioka S, Matsubara Y, Sasaki M, Tamaki M, Tamaki M, Hasegawa K, Nagai K, Wakino S. Roxadustat for Treating Anemia in Patients with Advanced Chronic Kidney Disease Not Undergoing Dialysis: A Retrospective Study. Intern Med. 2025 May 1;64(9):1303-1314. doi: 10.2169/internalmedicine.3773-24. Epub 2024 Oct 17. PMID: 39370259; PMCID: PMC12120232.

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AAN issues position statement on possible therapies for neurological conditions

The American Academy of Neurology (AAN) has issued a position statement on therapies for neurological conditions that have limited evidence or no approved use by the Food and Drug Administration (FDA). The statement is published June 25, 2025, in Neurology®, the medical journal of the American Academy of Neurology. The statement includes guiding principles for discussions with patients and policymakers about these therapies. Although the statement includes illustrative examples, it does not provide clinical recommendations regarding the use of specific therapies.

“As the experts in brain health, neurologists and neuroscience professionals are continually working toward achieving scientific breakthroughs through rigorous research,” said American Academy of Neurology President Natalia S. Rost, MD, MPH, FAAN, FAHA. “Still, people often ask about emerging therapies not yet supported by science. In our efforts to provide brain health resources for all, the American Academy of Neurology has issued this position statement to help facilitate conversations between patients and their doctors about emerging therapies.”

The position statement says the AAN recommends that a patient and their neurologist carefully review all available evidence and discuss the potential risks and benefits of the therapy, including when patients are considering using their “Right to Try.” The Right to Try Act allows people with life-threatening diseases who have tried all other approved treatments, and who cannot participate in a clinical trial, to try an experimental treatment.

“There is a growing and unmet need for effective treatments for a variety of neurological disorders,” said author Larry B. Goldstein, MD, FAAN, FAHA, of the University of Kentucky, and who serves on the AAN Board of Directors. “Whenever considering a potential treatment that has not been thoroughly researched, a person and their neurologist need to have a discussion about the available data supporting effectiveness and what is known about any risks to their health.”

The statement says the AAN supports the “off-label” use of FDA-approved therapies when high-quality evidence indicates that the benefit of the therapy outweighs the risks, with shared decision making between the patient and physician.

When discussing such therapies more broadly, including with policymakers, the statement says for those that have FDA approval but a high risk or incomplete data on side effects, or newly recognized and potentially serious side effects, the AAN supports waiting to take a definitive position until after further FDA review. If a suspended therapy is reintroduced, or as the data otherwise warrants, the AAN supports FDA required post-approval monitoring. The AAN supports neurologists and patients incorporating data about side effects in their shared decision making about the relative risks and benefits of a possible therapy.

The statement notes the proliferation of unproven treatments for neurological diseases that people may want to use to self-treat their conditions, yet those treatments may have limited or no supporting data and can have the potential to cause harm. These may be of interest especially to people with rare neurologic conditions with no approved therapies.

The statement says that rigorous investigation of any treatment is necessary to determine its efficacy and ensure safety and recommends patients discuss any potential treatment with their neurologist.

Reference:

Larry B. Goldstein, Principles for Novel Neurologic Therapeutics An AAN Position Statement, Neurology, https://doi.org/10.1212/WNL.0000000000213850

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Poor Prepregnancy Cardiovascular Health tied to Midlife Heart Risk, Independent of Gestational Diabetes: JAMA

Researchers have discovered in a new cohort study that less favorable prepregnancy cardiovascular health (CVH) is associated with subclinical cardiovascular disease (CVD) in midlife. While gestational diabetes (GD) played a minor mediating role, the findings suggest that GD is more a marker of poor prepregnancy CVH than a direct cause. The study published in JAMA highlights the importance of improving cardiovascular health early in life, well before pregnancy. The study was conducted by Natalie A. and fellow researchers.

The study aimed to examine whether gestational diabetes acts as a mediator (a causal link) or a marker (a signal) of the relationship between prepregnancy CVH and later cardiovascular risks. It was performed in the context of the CARDIA (Coronary Artery Risk Development in Young Adults) study, a long-term, multi-center, population-based cohort study that has followed a diverse cohort of young adults in four US cities since 1985. The researchers identified a cohort of 1,052 Black and White women with at least one singleton birth between baseline and 15-year follow-up, complete data on their CVH prior to pregnancy, and data on coronary artery calcium (CAC) assessed between 15 and 25 years later. All patients had no history of diabetes before pregnancy.

The exposure of interest was cardiovascular health pre-pregnancy, which was quantified using the American Heart Association’s Life’s Simple 7 scoring system, which incorporates aspects such as diet, physical activity, blood pressure, and cholesterol. The scores range from 0 to 14, with higher scores reflecting improved heart health. Researchers segregated participants into two categories: low to moderate CVH (scores 0–10) and high CVH (scores 11–14). The primary outcome was the presence of coronary artery calcium (CAC), a subclinical atherosclerosis marker, identified by CT scans between the 15–25-year follow-up period. The analysis controlled for age, race, education, and parity, and was supplemented with mediation modeling to calculate the proportion of the CVH-CAC relationship that was explained by gestational diabetes.

Results

  • Participants’ average age was 28.6 years, and almost half (47.6%) were Black and 52.4% were White.

  • Women with a lower CVH prior to pregnancy had higher rates of GD (8.8%) than those with high CVH (6.3%).

  • They were also at greater odds of exhibiting CAC in midlife: 28.2% with low/moderate CVH exhibited CAC compared with 19.2% with high CVH.

  • The adjusted odds ratio for the development of GD in women with poor CVH was 1.8 (95% CI: 1.1–3.0), and for the development of CAC, 1.7 (95% CI: 1.2–2.5).

  • Nonetheless, GD accounted for only 6% of the augmented risk of CAC (95% CI: 0%–22%), indicating that it is not the principal cause of midlife CVD in this population.

Overall, this large, long-term study demonstrates that poor prepregnancy cardiovascular health is highly predictive of the presence of subclinical heart disease in later life, though not substantially mediated through gestational diabetes.

Reference:

Cameron NA, Petito LC, Colangelo LA, et al. Prepregnancy Cardiovascular Health, Gestational Diabetes, and Coronary Artery Calcium. JAMA Cardiol. Published online June 25, 2025. doi:10.1001/jamacardio.2025.1887

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