Lorundrostat Significantly Lowers Blood Pressure in Resistant Hypertension: Study

USA: A recent clinical trial has shown that Lorundrostat, a novel aldosterone synthase inhibitor, significantly lowers blood pressure in patients with uncontrolled and treatment-resistant hypertension. The study, which assessed both the efficacy and safety of lorundrostat, presents encouraging prospects for individuals who have struggled to achieve blood pressure control with conventional antihypertensive treatments.

The findings from this double-blind, randomized trial were published online in the New England Journal of Medicine.

Hypertension, often referred to as high blood pressure, is a prevalent condition that can lead to severe cardiovascular events if not adequately controlled. While several medications are available to manage hypertension, some patients, particularly those with treatment-resistant hypertension, remain inadequately controlled, posing a challenge for both healthcare providers and patients.

Aldosterone dysregulation contributes to hypertension by affecting sodium retention and fluid balance. Lorundrostat, an aldosterone synthase inhibitor, offers a potential solution, but its efficacy and safety in hypertensive patients remain underexplored. To fill this gap, Luke J. Laffin, Cleveland Clinic Coordinating Center for Clinical Research, Cleveland, and colleagues focused on evaluating Lorundrostat’s effectiveness and safety, particularly in those with uncontrolled or treatment-resistant hypertension.

For this purpose, the researchers conducted a multicenter, double-blind, randomized, placebo-controlled trial involving patients on two to five antihypertensive medications with office blood pressure readings of 140/90 mm Hg or higher. After a 3-week standardized treatment phase, those with a 24-hour ambulatory blood pressure of 130/80 mm Hg or higher were randomized to receive either a placebo, a stable 50 mg daily dose of lorundrostat, or a dose-adjusted lorundrostat regimen (starting at 50 mg daily and increased to 100 mg if systolic pressure remained ≥130 mm Hg after 4 weeks).

The primary endpoint was the change in 24-hour average systolic blood pressure at 12 weeks, compared to placebo. A key secondary endpoint assessed this change at 4 weeks in the combined lorundrostat groups.

The key findings were as follows:

  • A total of 285 participants were randomized, with 94 assigned to the stable-dose group, 96 to the dose-adjustment group, and 95 to the placebo group. The average age of participants was 60 years, and 53% (150 participants) were Black.
  • After 12 weeks, the least-squares mean change in 24-hour average systolic blood pressure was −15.4 mm Hg in the stable-dose group, −13.9 mm Hg in the dose-adjustment group, and −7.4 mm Hg in the placebo group.
  • The placebo-adjusted change in blood pressure was −7.9 mm Hg for the stable-dose group and −6.5 mm Hg for the dose-adjustment group.
  • From baseline to week 4, the placebo-adjusted change in 24-hour average systolic blood pressure in the combined lorundrostat groups was −5.3 mm Hg.
  • Potassium levels above 6.0 mmol/L were reported in 5 participants (5%) in the stable-dose group, 7 participants (7%) in the dose-adjustment group, and none in the placebo group.

“Lorundrostat demonstrated significantly greater reductions in 24-hour average blood pressure compared to placebo, offering a promising treatment option for patients with uncontrolled and treatment-resistant hypertension,” the authors concluded.

Reference:

Laffin LJ, et al “Lorundrostat efficacy and safety in patients with uncontrolled hypertension.” N Engl J Med 2025; DOI: 10.1056/NEJMoa2501440.

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AIIMS Releases NORCET 8 Stage 2 Admit Cards

New Delhi- All India Institute of Medical Sciences (AIIMS), New Delhi, has made the admit cards for Nursing Officer Recruitment Common Eligibility Test (NORCET) 8 Stage 2 exam available. Therefore, candidates who have qualified for this stage can download their admit cards from the official website of AIIMS, New Delhi.

AIIMS, New Delhi, is going to conduct the NORCET 8 Stage 2 exam tomorrow, ie.e on May 2, 2025. A total of 11,472 candidates have been shortlisted based on their performance in the Stage 1 exam held on April 12, 2025. These candidates were allowed to select their preferred exam city through the MyPage portal between April 20 and April 22, 2025, till 5 pm. However, AIIMS has said that it reserves the right to allot any exam centre regardless of the candidate’s chosen city, and advises all candidates to prepare accordingly.

STEPS TO DOWNLOAD THE NORCET 8 STAGE 2 ADMIT CARD

STEP 1- Visit the official AIIMS website.

STEP 2- Navigate to the ‘Recruitment’ section on the homepage.

STEP 3- Click on the ‘NORCET’ link and then select ‘NORCET 8’.

STEP 4- Click on ‘Login’ and enter your registered ID and password.

STEP 5- Submit the details to access your admit card.

STEP 6- Download and print the admit card for future reference.​

AIIMS NORCET 8 Stage 2 exam will consist of 160 multiple-choice questions that need to be completed in a time period of 180 minutes. However, each correct answer will carry one mark, while one-third mark will be deducted for each wrong answer.

Meanwhile, the NORCET 8 Stage 1 exam was conducted on April 12, 2025, and the results were declared on April 19, 2025. Out of 72,462 candidates who applied for the exam, 68,074 appeared. Based on the Stage 1 exam results, 11,472 candidates have been selected to proceed to the Stage 2 exam.

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More than 30 percent of diabetes patients have silent MI which go undetected, reveals research

A new study published in the journal of Cureus showed that more than one-third of people with diabetes have silent myocardial ischemia (SMI), which frequently goes undiagnosed because of its lack of symptoms and restrictions on standard screening.

One of the main causes of elevated cardiovascular morbidity and mortality in individuals with diabetes is silent myocardial ischemia (SMI), a disease that is commonly underdiagnosed. Chronic hyperglycemia, oxidative stress, endothelial dysfunction, and low-grade inflammation further predispose diabetics to SMI, while the lack of common symptoms like angina (especially in diabetics with altered pain perception due to autonomic neuropathy) makes ischemic episodes invisible.

However, because of its lack of symptoms and the limits of routine screening, it frequently goes unnoticed despite its grave effects. This illuminates the critical need for proactive risk stratification and focused diagnostic techniques. Thus, to improve early identification through targeted risk stratification and inform customized screening strategies to lower cardiovascular events in this high-risk group, Hafiz Abdul Manan and team carried out this study to ascertain the prevalence and important risk factors linked to SMI in diabetic adults.

From May 2020 to May 2021, Jinnah Hospital in Lahore hosted this cross-sectional research. Time and budget constraints led to the convenient sampling of 162 diabetic individuals aged ≥40 years, with ≥5 years of diabetes and no history of coronary artery disease. A review of the participants’ medical histories, physical examinations, lab tests (lipid profile, HbA1c), and cardiac evaluations (resting ECG, exercise stress testing, and myocardial perfusion imaging) were all performed.

A total of 61 (37.65%) of the diabetic patients had SMI. A number of independent predictors of SMI were found using multivariate logistic regression analysis, including smoking, high blood pressure, dyslipidemia, diabetes that has been present for more than 10 years, and inadequate glycemic management.

Growing older was also strongly linked to a higher risk of SMI, with a noticeable increase in prevalence seen beyond the age of 55. In order to prevent negative cardiovascular outcomes, our findings emphasize the high prevalence of silent myocardial ischemia in diabetics and the significance of identifying critical indicators to assist early identification, focused screening, and risk-based treatment techniques.

Overall, this study finds a number of important characteristics, such as poor glycemic control, long-standing diabetes, hypertension (HTN), dyslipidemia, smoking, and advanced age, that contribute to the alarming prevalence of SMI in diabetic patients.

Source:

Abdul Manan, H., Chishti, H. R., & Hewlett, F. D. (2025). Prevalence and predictors of silent myocardial ischemia in diabetic patients. Cureus. https://doi.org/10.7759/cureus.82407

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Study reveals emerging role of flavonoids in treatment of type 2 diabetes by regulating enteroendocrine system

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder with a rapidly increasing global prevalence. It is primarily characterized by insulin resistance, β-cell dysfunction, and impaired glucose homeostasis. Emerging research suggests that flavonoids, a diverse group of plant-derived polyphenols, may offer therapeutic potential in managing T2DM. These compounds exert antidiabetic effects through multiple mechanisms, including improving insulin sensitivity, enhancing β-cell function, modulating the gut microbiota, inhibiting gluconeogenesis, and regulating enteroendocrine hormones. This review explores the role of flavonoids in T2DM treatment, with a particular focus on their impact on the enteroendocrine system.

Flavonoids: Classification, Absorption, and Metabolism

Flavonoids are categorized into several subclasses based on their chemical structure, including flavonols, flavanones, flavones, flavan-3-ols, isoflavones, and anthocyanins. These compounds are abundant in fruits, vegetables, tea, and medicinal plants. Upon ingestion, flavonoids undergo extensive metabolism, involving hydrolysis, microbial degradation, and biotransformation in the liver. The bioavailability of flavonoids is influenced by their glycosylation, food matrix composition, and interaction with gut microbiota. Studies indicate that specific flavonoids, such as quercetin, anthocyanins, and epigallocatechin gallate (EGCG), are efficiently absorbed and exert beneficial metabolic effects.

Mechanisms of Flavonoid Action in T2DM

Improving Insulin Sensitivity and Secretion

Flavonoids enhance insulin signaling pathways by increasing phosphorylation of insulin receptor substrate-1 (IRS-1) and activating AMP-activated protein kinase (AMPK). Certain flavonoids, such as cyanidin-3-O-glucoside, have been shown to improve glucose uptake in adipocytes and skeletal muscle cells. Additionally, flavonoids stimulate insulin secretion by promoting pancreatic β-cell function and reducing oxidative stress-induced β-cell apoptosis.

Modulating Glucose Metabolism and Gluconeogenesis

Flavonoids inhibit key enzymes involved in hepatic glucose production, such as glucose-6-phosphatase and phosphoenolpyruvate carboxykinase (PEPCK). Baicalin and epicatechin suppress gluconeogenesis via the PI3K/Akt and AMPK pathways, thereby reducing hepatic glucose output. Additionally, flavonoids regulate glucose transporter expression, facilitating glucose uptake in peripheral tissues.

Regulating Gut Microbiota

The gut microbiota plays a critical role in glucose metabolism and T2DM pathophysiology. Flavonoids promote gut microbiome diversity and enhance the growth of beneficial bacteria while suppressing pathogenic microbes. They influence microbial-derived metabolites, such as short-chain fatty acids (SCFAs), which improve insulin sensitivity and modulate gut hormone secretion.

Flavonoids and the Enteroendocrine System

The enteroendocrine system, composed of hormone-secreting intestinal cells, regulates glucose homeostasis through various peptides, including glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), peptide YY (PYY), and cholecystokinin (CCK). Flavonoids have been found to influence the secretion and activity of these hormones, contributing to improved glycemic control.

GLP-1 and GIP Regulation

GLP-1 and GIP are incretin hormones that stimulate insulin secretion and inhibit glucagon release. Several flavonoids, such as quercetin and hesperidin, enhance GLP-1 secretion from L-cells, thereby prolonging incretin action. Furthermore, flavonoids inhibit dipeptidyl peptidase-4 (DPP-4), the enzyme responsible for incretin degradation, leading to sustained incretin activity and improved insulinotropic effects.

Influence on PYY and CCK

Flavonoids regulate satiety-related gut hormones, such as PYY and CCK, which contribute to appetite control and weight management in T2DM. Procyanidins and epicatechins have been shown to enhance PYY secretion, leading to reduced food intake and improved metabolic outcomes. Additionally, flavonoids like catechin and resveratrol modulate CCK secretion, which plays a role in slowing gastric emptying and improving postprandial glucose levels.

Therapeutic Potential and Future Directions

The therapeutic application of flavonoids in T2DM management is promising, yet challenges remain regarding their bioavailability, dosage optimization, and long-term efficacy. Future research should focus on clinical trials evaluating the effectiveness of specific flavonoids in T2DM treatment. Additionally, the development of novel flavonoid-based formulations, including nanoparticles and encapsulated supplements, may enhance their stability and absorption. Investigating the synergistic effects of flavonoids with existing antidiabetic medications could further expand their clinical utility.

Conclusion

Flavonoids represent a promising class of natural compounds with potential benefits in T2DM treatment through their effects on insulin sensitivity, glucose metabolism, gut microbiota, and enteroendocrine hormone regulation. Their ability to modulate GLP-1, GIP, PYY, and CCK secretion highlights their relevance in metabolic health. While further studies are needed to elucidate optimal dosages and clinical applications, flavonoids offer a promising adjunctive strategy for managing T2DM and improving overall metabolic health.

Reference:

Daifen Wen and Mingrui Li, The Emerging Role of Flavonoids in the Treatment of Type 2 Diabetes Mellitus: Regulating the Enteroendocrine System, Exploratory Research and Hypothesis in Medicine, doi: 10.14218/ERHM.2024.00055

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Nasal spray shows preclinical promise for treating traumatic brain injury, reveals study

A new study led by researchers at Mass General Brigham suggests a nasal spray developed to target neuroinflammation could one day be an effective treatment for traumatic brain injury (TBI). By studying the effects of the nasal anti-CD3 in a mouse model of TBI, researchers found the spray could reduce damage to the central nervous system and behavioral deficits, suggesting a potential therapeutic approach for TBI and other acute forms of brain injury. The results are published in Nature Neuroscience.

“Traumatic brain injury is a leading cause of death and disability-including cognitive decline-and chronic inflammation is one of the key reasons,” said lead author Saef Izzy, MD, FNCS, FAAN, a neurologist and head of the Immunology of Brain Injury Program at Brigham and Women’s Hospital (BWH), a founding member of the Mass General Brigham healthcare system. “Currently, there is no treatment to prevent the long-term effects of traumatic brain injury.”

The study examines the monoclonal antibody Foralumab, made by Tiziana, which has been tested in clinical trials for patients with multiple sclerosis, Alzheimer’s disease, and other conditions.

“This opens up a whole new area of research and treatment in traumatic brain injury, something that’s almost impossible to treat,” said senior author Howard Weiner, MD, co-director of the Ann Romney Center for Neurologic Diseases at BWH. “It also means this could work in intracerebral hemorrhage and other stroke patients with brain injury.”

Multiple experiments were done in mouse models with moderate-to-severe traumatic brain injury to explore the communication between regulatory cells induced by the nasal treatment and the microglial immune cells in the brain. Over time, researchers were able to identify how they modulate immune response.

“Modulating the neuroinflammatory response correlated with improved neurological outcomes, including less anxiety, cognitive decline, and improved motor skills,” Izzy said.

In addition to assessing the effects of the treatment, the research team was able to learn about immune response over time and compare the immune responses and effects of TBI in the mice.

The next step in the research is to translate the findings from preclinical models to human patients.

“Our patients with traumatic brain injury still don’t have an effective therapeutic to improve their outcomes, so this is a very promising and exciting time to move forward with something that’s backed up with solid science and get it to patients’ bedsides,” said Izzy.

Once in the clinical setting, Weiner said the hope is this treatment could be used on a variety of traumatic brain injury patients, including football players with repetitive concussions.

“We envision giving a nasal spray right there on the sidelines,” said Weiner. “It isn’t something we can do yet, but we see the potential.”

Reference:

Izzy, S., Yahya, T., Albastaki, O. et al. Nasal anti-CD3 monoclonal antibody ameliorates traumatic brain injury, enhances microglial phagocytosis and reduces neuroinflammation via IL-10-dependent Treg–microglia crosstalk. Nat Neurosci (2025). https://doi.org/10.1038/s41593-025-01877-7

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Obesity and Hypothyroxinemia Together Heighten Risk of LGA Births in Pregnant Women: Study Finds

China: A recent Chinese cohort study published in Reproductive Biology and Endocrinology has found that maternal obesity and isolated maternal hypothyroxinemia (IMH) in late pregnancy significantly increase the risk of large-for-gestational-age (LGA) births. IMH, defined by low free thyroxine (FT4) with normal thyroid-stimulating hormone (TSH) levels, independently raised LGA risk by 1.3 times.

Obesity alone was linked to a nearly sixfold higher LGA risk and a sevenfold increase in IMH. Notably, women with both conditions had a 7.6-fold greater risk of delivering LGA newborns, indicating a strong synergistic effect. The findings highlight the importance of monitoring BMI and thyroid function during pregnancy.

The combined impact of isolated maternal hypothyroxinemia and other contributing factors on fetal growth outcomes has not been well established. To address this gap, Bin Zhang, Nanjing Medical University, Changzhou, China, and colleagues aimed to investigate whether the presence of IMH in the third trimester—characterized by free thyroxine (FT4) levels below the 5th percentile and TSH levels within the normal range—along with elevated prenatal body mass index (BMI), jointly increases the risk of delivering large-for-gestational-age newborns.

For this purpose, the researchers conducted a retrospective analysis of 11,478 Chinese pregnant women, utilizing laboratory data, including thyroid hormone levels, routine biochemical tests, and hospitalization records from a specialized hospital.

The study led to the following findings:

  • The prevalence of obesity (BMI ≥ 30 kg/m²) and isolated maternal hypothyroxinemia (IMH) among the study population was 20.1% and 4.5%, respectively.
  • Obese women had a 6.96-fold higher risk of developing IMH compared to women with normal weight (BMI < 25 kg/m²).
  • The risk of delivering large-for-gestational-age (LGA) newborns was 5.88 times higher in obese women than in those with normal weight.
  • Women with IMH had a 1.32-fold increased risk of LGA births compared to euthyroid women.
  • These associations remained consistent in sensitivity analyses conducted among women under 35, first-time mothers, and those without pregnancy complications.
  • Women with both obesity and IMH had a 7.60-fold greater risk of delivering LGA newborns compared to euthyroid women with normal weight.
  • There was a statistically significant interaction between BMI categories and IMH on the risk of LGA births.
  • Subgroup analyses confirmed this interaction among younger women, those with multiple pregnancies, and those without pregnancy-related complications.

The researchers found that in the large cohort of Chinese pregnant women, both obesity and isolated maternal hypothyroxinemia (IMH) in late pregnancy were independently associated with an increased risk of delivering large-for-gestational-age newborns. Notably, the coexistence of these two conditions further amplified this risk.

“The findings emphasize the potential value of combining prenatal BMI assessment with thyroid hormone profiling to identify women at elevated risk for LGA births,” the authors stated. They further noted, “If confirmed in future studies, this approach could have significant clinical and public health implications, particularly given the growing concern surrounding LGA-related health outcomes.”

Reference:

Zhang, B., Xi, S., Zhan, Z. et al. Maternal obesity and the incidence of large-for-gestational-age newborns in isolated hypothyroxinemia pregnancies: a comparative cohort study. Reprod Biol Endocrinol 23, 60 (2025). https://doi.org/10.1186/s12958-025-01394-z

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Early-life exposure to air and light pollution linked to increased risk of pediatric thyroid cancer: Study

 A new study led by researchers at Yale University suggests that early-life exposure to two widespread environmental pollutants-small particle air pollution and outdoor artificial light at night-could increase the risk of pediatric thyroid cancer.

The study-a collaborative effort involving multiple Yale departments and institutions across the U.S.-found a “significant association” between exposure to ambient fine particulate matter air pollution (PM2.5) and outdoor artificial light at night (O-ALAN) and increased risk of papillary thyroid cancer in children and young adults up to 19 years old. The exposures occurred during the perinatal stage of life, typically defined as the time from when pregnancy occurs up to a year after birth.

“These results are concerning, especially given how widespread both of these exposures are,” said Dr. Nicole Deziel, PhD, MHS, an environmental epidemiologist with the Yale School of Public Health (YSPH) and the study’s lead author. “Fine particulate matter is found in urban air pollution due to automobile traffic and industrial activity, and artificial light at night is common, particularly in densely populated urban areas.”

The research team analyzed data from 736 individuals diagnosed with papillary thyroid cancer before age 20 and 36,800 matched control participants based on birth year. Using advanced geospatial and satellite modeling, the team assessed individual-level exposure to PM2.5 and O-ALAN based on residential location at birth. All of the study participants were from California.

The findings showed that for every 10 micrograms per cubic meter increase in PM2.5 exposure, the odds of developing thyroid cancer rose by 7% overall. The strongest association between exposure and thyroid cancer was found among teenagers (15–19 years of age) and Hispanic children. Similarly, children born in areas with high levels of exposure to outdoor light at night were 23–25% more likely to develop thyroid cancer, according to the study.

“Thyroid cancer is among the fastest growing cancers among children and adolescents, yet we know very little about what causes it in this population,” said Deziel, an associate professor of epidemiology (environmental health sciences) and co-director of the Yale Center for Perinatal, Pediatric, and Environmental Epidemiology. “Our study is the first large-scale investigation to suggest that these exposures early in life-specifically to PM2.5 and outdoor light at night-may play a role in this concerning trend.”

In addition to Deziel, the research team included experts from Yale’s Departments of Biostatistics, Chronic Disease Epidemiology, and Pediatrics, as well as researchers from the University of Southern California, UC Berkeley, and the American Cancer Society. Deziel and several of the study’s authors are affiliated with the Yale Cancer Center. The team’s collective expertise ranged from environmental exposure modeling and biostatistics to pediatric endocrinology and cancer epidemiology.

The impact of papillary thyroid cancer on children can be extensive.

Compared to adults, children are often diagnosed with thyroid cancer at more advanced stages with larger tumor sizes. Pediatric survivors of thyroid cancer can suffer aftereffects ranging from temperature dysregulation and headaches to physical disabilities and mental fatigue. The disease can interfere with important life milestones such as education, employment, and raising a family and it can contribute to feelings of anxiety and depression.

Both PM2.5 and O-ALAN are considered environmental carcinogens that have been shown to disrupt the body’s endocrine system, including thyroid function, in animals and adults. The particles associated with PM2.5 pose a threat because they are small enough to enter the bloodstream and can interfere with hormone signaling, including those involved in regulating cancer pathways. Outdoor artificial light at night has been shown to suppress melatonin and alter circadian rhythms, which can also influence hormone-regulated cancer pathways.

The current research raises important environmental justice concerns. Communities of color and lower-income populations are often disproportionately exposed to both air pollution and light pollution-inequities that may contribute to the higher thyroid cancer burden observed in Hispanic children.

The researchers emphasized that more work is needed to replicate and expand on their findings, ideally using improved exposure metrics and longitudinal designs.

“In the meantime,” Deziel noted, “our results point to the critical importance of addressing environmental factors in childhood cancer research. Reducing exposures to air pollution and managing light pollution could be important steps in protecting children’s health.”

Reference:

 Nicole C. Deziel, Rong Wang, Joshua L. Warren, Catherine Dinauer, Perinatal Exposures to Ambient Fine Particulate Matter and Outdoor Artificial Light at Night and Risk of Pediatric Papillary Thyroid Cancer, Environmental Health Perspectives, https://doi.org/10.1289/EHP14849.

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Menopause Age Key to Unlocking Type 2 Diabetes Risk, suggests study

Recent research indicates a potential association between age at menopause and the incidence of type 2 diabetes (T2D), yet comprehensive evidence remains limited, especially among Asian populations. A cohort study involving over 1.1 million postmenopausal Korean women aimed to clarify whether age at menopause and instances of premature menopause are linked to the onset of T2D.

Significance of Type 2 Diabetes

Type 2 diabetes represents a chronic health issue significantly contributing to cardiovascular diseases, microvascular complications, and elevated mortality rates. Despite advances in medical treatments, T2D prevalence continues to rise, emphasizing the need for effective preventative measures and the identification of at-risk populations. While men are generally at a higher risk at younger ages, the risk for women escalates post-menopause. Female-specific risk factors and their implications on health, particularly links to cardiovascular disease and T2D, are under-explored.

Data Collection Methodology

The study utilized data from the Korean National Health Insurance Service, which covers nearly the entire South Korean population, providing robust health examination records including self-reported data and clinical health assessments. A total of 3,181,150 women aged 30 and above were initially screened, with exclusions for pre-existing T2D, premenopausal status, and data inconsistencies, resulting in a final cohort of 1,125,378 participants. Age at menopause was self-reported, categorized into four groups: <40 years, 40-44 years, 45-49 years, and ≥50 years, with premature menopause defined as menopause before age 40. Identified T2D cases were defined as fasting blood glucose levels of 126 mg/dL or higher or records of antidiabetic medication claims.

Follow-Up Results

Throughout a median follow-up of 8.4 years, 113,864 new T2D cases emerged, indicating a cumulative incidence of approximately 10.1%. The results indicated that women with premature menopause had a higher incidence of T2D compared to their peers, with a hazard ratio (HR) of 1.13 after accounting for various confounders. Women experiencing menopause at an earlier age (particularly <40 years) faced a significantly increased risk for developing T2D, corresponding with the hypothesis that lower estrogen levels, due to shorter exposure periods, may contribute significantly to insulin resistance and metabolic dysregulation.

Subgroup Analysis Insights

Subgroup analyses revealed nuances in the relationship, with factors like body mass index (BMI) and depressive disorders influencing the risk association. Notably, the risk was exacerbated among individuals without obesity and those struggling with depressive disorders, suggesting a potential interaction between mental health and metabolic outcomes.

Implications of Findings

The findings support the hypothesis that both premature and early menopause can act as significant risk factors for the development of T2D. Given these associations, there is a strong argument for including menopause history in T2D screening protocols. Recommendations suggest recognizing premature menopause as a noteworthy risk factor within diabetes management guidelines, emphasizing preventive care strategies and early detection initiatives.

Conclusions and Future Directions

Overall, the study elucidates important links between menopausal age and T2D incidence, advocating for greater awareness and proactive measures in managing women’s health, particularly concerning metabolic disorders in postmenopausal populations. Further research is essential to explore these relationships across diverse demographic groups and establish effective interventions to mitigate T2D risk.

Key Points

– A cohort study involving over 1.1 million postmenopausal Korean women was conducted to investigate the association between age at menopause, instances of premature menopause, and the incidence of type 2 diabetes (T2D), particularly as evidence is lacking in Asian populations.

– Type 2 diabetes is a chronic health concern linked to cardiovascular diseases and increased mortality rates, with rising prevalence emphasizing the necessity for effective preventive strategies. The risk for women increases significantly post-menopause, making female-specific health factors critical for understanding T2D risk.

– The study analyzed comprehensive health data from the Korean National Health Insurance Service, screening 3,181,150 women aged 30 and above and narrowing the final cohort to 1,125,378. Age at menopause was categorized, and T2D was defined through specific blood glucose levels and medication records.

– Over a median follow-up of 8.4 years, 113,864 new T2D cases emerged, indicating a cumulative incidence of approximately 10.1%. Women experiencing premature menopause exhibited a higher incidence of T2D (hazard ratio of 1.13), particularly those with menopause before age 40, indicating potential metabolic dysregulation linked to lower estrogen levels.

– Subgroup analyses indicated that body mass index (BMI) and depressive disorders significantly influenced the risk association. Increased T2D risk was noted in individuals without obesity and those with depressive issues, suggesting a complex interplay between mental health and metabolic conditions.

– The study underscores the necessity of incorporating menopause history into T2D screening protocols, advocating for recognizing premature menopause as a critical risk factor in diabetes management. Recommendations emphasize the importance of preventive strategies and early detection among postmenopausal women to mitigate T2D risk.

Reference –

B. Ko et al. (2025). Age At Menopause And Development Of Type 2 Diabetes In Korea. *JAMA Network Open*, 8. https://doi.org/10.1001/jamanetworkopen.2024.55388.

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Weekly Home BP Monitoring Enhances Hypertension Detection in Hemodialysis Patients: Study Finds

Greece: Accurate blood pressure (BP) monitoring is essential for managing hypertension in patients undergoing hemodialysis. A recent study found that in hemodialysis patients, home blood pressure monitoring (HBPM) over a week was more accurate in detecting hypertension than routine BP measurements taken at dialysis centers.

“HBPM demonstrated greater diagnostic accuracy than 44-hour ambulatory BP monitoring (AUC: 0.934). With a threshold of 141.0 mmHg, HBPM achieved optimal sensitivity (85.7%) and specificity (92.9%), reinforcing its value as a reliable screening tool for this patient population,” the researchers reported in the Journal of Human Hypertension.

The best approach for diagnosing hypertension in hemodialysis patients remains a subject of debate. To address this, Panagiotis I. Georgianos, 2nd Department of Nephrology, AHEPA Hospital, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece, and colleagues evaluated the accuracy of home blood pressure monitoring and routine dialysis-unit BP recordings, using 44-hour ambulatory BP monitoring (ABPM) as the reference standard.

For this purpose, the researchers assessed hypertension over two weeks using three methods: (i) routine predialysis and post dialysis BP recordings averaged over six consecutive dialysis sessions, (ii) home BP monitoring (HBPM) for seven days with duplicate morning and evening measurements (Microlife WatchBP Home N), and (iii) 44-hour ambulatory BP monitoring (ABPM) with 20-minute intervals over an entire interdialytic period (Microlife WatchBPO3). The study included 70 patients (mean age: 65.3 ± 13.2 years), 87.1% receiving hypertension treatment, and an average 44-hour ambulatory systolic/diastolic BP of 120.6 ± 15.2/66.3 ± 10.1 mmHg.

Based on the study, the researchers reported the following findings:

  • The mean difference between ambulatory daytime systolic BP (SBP) and routine BP measurements was:
    • Predialysis SBP: -11.4 ± 13.4 mmHg
    • Postdialysis SBP: -4.0 ± 15.1 mmHg
    • Home SBP: -8.6 ± 10.7 mmHg
  • Home BP monitoring (HBPM) showed superior diagnostic performance for detecting ambulatory daytime SBP ≥135 mmHg:
    • Home SBP: AUC 0.934
    • Predialysis SBP: AUC 0.778
    • Postdialysis SBP: AUC 0.766
    • HBPM was significantly more accurate than both predialysis and postdialysis SBP (P = 0.02).
  • At a cut-off of 141.0 mmHg, home SBP provided the best balance of sensitivity (85.7%) and specificity (92.9%) for diagnosing hypertension.

The study findings highlight that in hemodialysis patients, home blood pressure monitoring conducted over a week is more reliable than routine dialysis-unit BP recordings averaged over two weeks in detecting ambulatory hypertension. HBPM demonstrated greater accuracy in identifying elevated blood pressure levels, making it a valuable tool for improving hypertension diagnosis in this population.

“These results suggest that integrating HBPM into routine clinical practice could enhance blood pressure management, leading to better cardiovascular outcomes for hemodialysis patients,” the authors concluded.

Reference:

Leonidou, K., Georgianos, P. I., Kollias, A., Kontogiorgos, I., Vaios, V., Leivaditis, K., Karligkiotis, A., Stamellou, E., Balaskas, E. V., Stergiou, G. S., & Liakopoulos, V. (2025). Home versus routine dialysis-unit blood pressure recordings among patients on hemodialysis. Journal of Human Hypertension, 1-7. https://doi.org/10.1038/s41371-025-01007-7

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Statins Reduce Liver Cancer and Hepatic Decompensation Risk among patients with chronic liver disease: JAMA

Researchers have found in a new cohort study that the use of statins in patients with chronic liver disease was associated with a lower risk of liver cancer and hepatic decompensation. Patients who used statins experienced a significant reduction in these risks compared to those who did not, with lipophilic statins and longer treatment duration providing even greater protective effects. Statins may help prevent hepatocellular carcinoma by slowing the progression of liver fibrosis, which is a key factor in the severity of liver disease. This study examined the relationship between the use of statins and the risk of hepatocellular carcinoma and hepatic decompensation, with a focus on how statins influence the progression of liver fibrosis. Researchers analyzed patient data from the year 2000 to the year 2023, selecting adults who were 40 years or older with chronic liver disease and an elevated baseline Fibrosis-4 score, which is a measure of liver fibrosis. Participants were categorized into those who used statins and those who did not, and their health outcomes were tracked over a ten-year period. Findings indicated that patients who used statins had a significantly lower incidence of hepatocellular carcinoma and hepatic decompensation than those who did not use statins. The protective effects were particularly pronounced among individuals who used lipophilic statins and those who had prolonged statin therapy. In addition to reducing the risks of liver cancer and hepatic decompensation, patients who used statins showed a slower progression of liver fibrosis and were more likely to improve their fibrosis risk category over time. Among patients with intermediate or high Fibrosis-4 scores at baseline, those who used statins were more likely to experience a regression in their fibrosis severity compared to those who did not use statins. This suggests that statins may not only help prevent severe liver complications but also contribute to improved liver health over time. Overall, the study supports the potential role of statins in reducing the risk of hepatocellular carcinoma and slowing the progression of liver disease. These findings highlight the need for further research on incorporating statins into treatment strategies for patients with chronic liver disease.

Reference:

Choi J, Nguyen VH, Przybyszewski E, et al. Statin Use and Risk of Hepatocellular Carcinoma and Liver Fibrosis in Chronic Liver Disease. JAMA Intern Med. Published online March 17, 2025. doi:10.1001/jamainternmed.2025.0115

Keywords:

Statins, Reduce, Liver Cancer, Hepatic, Decompensation Risk, among, patients, chronic liver disease, JAMA, Choi J, Nguyen VH, Przybyszewski E, JAMA Intern Med

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