Understanding Online Health Information Consumption Through Web Analytics of the Italian Society of Pharmacology Magazine: 3-Year Descriptive Analysis

<strong>Background:</strong> The COVID-19 pandemic underscored that access to reliable and expert-driven scientific information is not only essential but also lifesaving. Since 2020, the Italian Society of Pharmacology has been publishing <i>SIF Magazine</i>, an online magazine dedicated to citizens. This journal was created to make pharmacology accessible to the public, highlighting its impact on health and quality of life while clarifying the truths, theories, and misconceptions surrounding drugs and their use. <strong>Objective:</strong> This work analyzed web interaction data from <i>SIF Magazine</i> to understand how the public reaches and engages with an online scientific journal and gather practical insights for improving digital scientific communication. <strong>Methods:</strong> The data analyzed in this study were obtained from the web analytics of the <i>SIF Magazine</i> website. The analysis covers 3 years (2022-2024). By studying patterns of access, navigation, and engagement, the analysis clarified which types of scientific content connect most with users, how people find and choose trustworthy sources, and what they do after reaching them. <strong>Results:</strong> Average monthly site visits increased from 120,024 in the partial period examined in 2022 to 128,059 in 2023 and 200,379 in 2024, paralleled by higher monthly views (155,785 in 2022, 165,438 in 2023, and 254,297 in 2024). The engagement rate declined modestly (36% in late 2022, 35% in 2023, and 29% in 2024), consistent with scale-related dilution from an expanding top-of-funnel audience. Category-level analyses of top-performing articles indicated disproportionate interest in renal, urogenital, and sexual disorders followed by inflammation and pain and gastrointestinal diseases. Seasonal analyses showed recurrent peaks for season-linked topics (eg, motion sickness, photosensitivity reactions, and influenza vaccination) during expected periods. <strong>Conclusions:</strong> Together, these findings underscore the importance of data-driven content planning and continuous performance monitoring to sustain the effectiveness of digital scientific communication platforms.

Muscle Quality and Fat Distribution Predict Mortality Risk Better than BMI

Researchers at the University Medical Center Freiburg in Germany, say that detailed measures of body composition derived from whole-body MRI scans can predict diabetes, cardiovascular events, and mortality risk better than current methods that rely on body mass index (BMI). Using MRI imaging data from more than 66,000 people, the team has developed age-, sex-, and height-adjusted reference standards that show how fat and muscle are distributed across the body and how these patterns relate to health outcomes. Their findings, published in the journal Radiology, show analysis of both the quantity and quality of skeletal muscle, along with where fat is distributed in the body, can provide a more accurate way to determine risk as opposed to weight-based methods alone.

“Many risk scores and treatment decisions still rely on BMI or waist circumference because they are simple to obtain,” said senior author Jakob Weiss, MD, PhD, an interventional radiologist at University Medical Center Freiburg. “But BMI does not reliably reflect a person’s actual body composition.” This is one of the central findings of the study: that individuals with similar BMI values can have markedly different distributions of fat and muscle, which carry different levels of risk for cardiometabolic disease and mortality.

The team’s retrospective study analyzed whole-body MRI scans from 66,608 people using data from the UK Biobank and the German National Cohort collected between April 2014 and May 2022. The cohort had a mean age of 57.7 years and an average BMI of 26.2. Using a fully automated deep learning framework, the researchers quantified multiple body composition measures, including subcutaneous adipose tissue, visceral adipose tissue, skeletal muscle, skeletal muscle fat fraction, and intramuscular adipose tissue. These measures were normalized for age, sex, and height. A score is developed from these data to show how far individuals deviated from a population-adjusted reference.

“Whole-body MRI–derived BC (body composition) z-scores were used to identify at-risk individuals and predict cardiometabolic outcomes and mortality beyond traditional risk factors.” They then used the z-score categories to assess associations and clinical outcomes.

Their data showed that individuals with high visceral fat had a 2.26-fold increased risk of developing diabetes. High intramuscular fat was associated with a 1.54-fold increased risk of major adverse cardiovascular events, while low skeletal muscle was linked to a 1.44-fold increase in all-cause mortality.

The deep learning system used to develop the risk profiles was trained and evaluated against radiologist-defined reference standards, allowing it to extract volumetric measurements across the entire body rather than relying on single cross-sectional slices. This method allowed the researchers to capture meaningful variations in muscle quality and fat distribution that are not visible through other techniques.

“Manual BC measurement in large-scale imaging datasets is prohibitively time-consuming,” the researchers wrote. “However, recent advances in deep learning have enabled fully automated, accurate, and efficient quantification from cross-sectional imaging.” This capability allowed the team to construct reference curves reflective of how body composition changes with age and differs between men and women.

Importantly, the research shines a light on the limitations of using BMI to determine future risk. Because BMI is calculated using only two metrics, height and weight, it does not distinguish between fat and muscle or account for where fat is stored. Because of this, two people with the same BMI may have very different levels of visceral fat or muscle mass, factors that can lead to different to different health risks. The researchers showed that deviations in these specific components, captured via their MRI-based z-scores, were predictive of outcomes even after accounting for traditional risk factors.

“It’s not only how much muscle you have, but also it’s the quality of that muscle,” said first author Matthias Jung, MD, a radiologist at University Medical Center Freiburg. “Knowing the volume of intramuscular fat gives us a window into muscle quality that other methods like BMI, bioelectrical impedance analysis, or DEXA can’t easily provide.” This distinction is relevant because intramuscular fat is linked to metabolic dysfunction and cardiovascular risk.

The study also produced a web-based calculator that allows clinicians and researchers to compare individual patient data with population-based reference values. According to Weiss, this tool could be applied to existing imaging studies. “A dedicated whole-body MRI is not necessarily required. If a routine CT or MRI body scan already exists, the information can be extracted for benchmarking against the reference values,” he said.

The study has limitations, including a cohort of primarily White Western European adults, which may impact the generalizability of the findings. The researchers also pointed out that whole-body MRI is not routinely performed in clinical practice, although they provided reference values for commonly imaged regions such as the chest, abdomen, and pelvis to address this.

The team will continue their work by seeking to validate the reference curves in clinical populations and exploring their use in predicting treatment outcomes, including toxicity, survival, and recurrence in cancer patients. The team also plans to develop disease-specific reference values for broader patient groups to broaden the use of body composition analysis into clinical care.

The post Muscle Quality and Fat Distribution Predict Mortality Risk Better than BMI appeared first on Inside Precision Medicine.

Statement on Mental Health and Access to Evidence-Based Care

The IOCDF is proud to be a member of the Mental Health Liaison Group, which distributed the below statement. To learn more about appropriate treatment for OCD, including the use of medication and SSRIs, visit IOCDF’s Treatment Guide.

Following the MAHA Institute May 4, 2026, Summit entitled, “Mental Health and Overmedicalization,” and HHS’ MAHA Action Plan to Curb Psychiatric Overprescribing, the Mental Health Liaison Group (MHLG)— a nonprofit coalition of national organizations representing people with mental health and substance use conditions, family members and caregivers, providers of mental health and substance use treatment and support, advocates, and other stakeholders— reaffirms that improving mental health outcomes requires expanding access to comprehensive, evidence-based care.

MHLG recognizes that mental health care should be appropriate, individualized, and guided by clinical expertise and informed patient decision-making. The goal is the right care, delivered at the right time and tailored to each person’s unique needs.

A strong body of evidence supports a range of effective, individualized treatments, including psychotherapy and, when clinically appropriate, medications such as Selective Serotonin Reuptake Inhibitors (SSRIs). These treatments are effective for many individuals when appropriately prescribed, monitored, and supported as part of a comprehensive care plan. Individuals should be supported in working with their health care providers to determine and refine over time the care plan, including the benefits and risks, that best meets their needs, and engage in medical professional recommendation-based treatment, which for many may include psychotherapy and medication as part of a comprehensive approach to care.

Public discussion of mental health treatment should be informed by scientific evidence to support informed decision-making and patient-centered care. Misinformation or claims not supported by evidence may discourage individuals from seeking or continuing treatment, particularly at a time when many already face significant barriers to care.

MHLG supports policies that support ongoing research to expand access to comprehensive, evidence-based mental health services, reduce stigma, and strengthen the ability of individuals to initiate and remain engaged in appropriate care across the continuum of prevention, treatment, crisis and recovery. These priorities are consistent with MHLG’s principles, available at https://www.mhlg.org/about-us/

MHLG stands ready to engage with the Administration and policymakers as they consider and advance approaches impacting mental health care.


The Mental Health Liaison Group (MHLG) is a nonprofit coalition of national organizations representing people with mental health and substance use conditions, family members and caregivers, providers of mental health and substance use treatment and support, advocates, and other stakeholders committed to strengthening Americans’ access to mental health and substance use care. As trusted leaders in the field, our 100+ member organizations are dedicated to elevating the national conversation around mental health and substance use. Together, we work to advance federal policies that support prevention, early intervention, treatment, crisis response, and recovery services and supports.

The post Statement on Mental Health and Access to Evidence-Based Care appeared first on International OCD Foundation.

Genotype-Guided Antidepressants Could Have Long-Term Benefits

Prescribing antidepressants according to a patient’s genetic makeup could help manage depressive symptoms in the long-term, a clinical trial suggests.

The findings, in JAMA Network Open, suggest pharmacogenetic guidance could have extended benefits, which may not be apparent early on.

Primary results did not indicate that genotype-guided SSRI treatment was better than usual care at three months in A Depression and Opioid Pragmatic Trial in Pharmacogenetics (ADOPT PGx).

However, significantly more patients receiving genotype-guided therapy achieved the secondary endpoint of depression remission at six months.

“Although outcomes were similar early in treatment, differences emerged over time,” noted Kathryn Blake, PharmD, from Nemours Center for Pharmacogenomics and Translational Research in Jacksonville, Florida, and colleagues.

“These findings suggest a possible longer-term clinical benefit and indicate that future studies should focus on evaluating the durability and long-term impact of genotype-guided prescribing in the management of depressive symptoms.”

SSRIs are the most common pharmacotherapy for depression and variants in cytochrome P450 enzymes CYP2D6 and CYP2C19 can affect their metabolism, influencing exposure to this medication.

Indeed, guidelines from the Clinical Pharmacogenetics Implementation Consortium (CPIC) provide recommendations for SSRI prescribing when genotype information is available.

However, most psychiatry experts and practice guidelines for treating depression have not yet endorsed pharmacogenetic-informed therapy, citing insufficient evidence.

ADOPT PGx was a set of three randomized clinical trials, designed to test whether routine use of pharmacogenetic testing improves medication response among patients with depression, acute pain, or chronic pain.

The ADOPT PGx Depression trial included 221 children and 1239 adults, aged eight years or older who had experienced depression for three months or longer.

A total of 692 patients (47.4%) had an actionable phenotype, of whom 351 (50.7%) were assigned to the intervention, and 341 (49.3%) to usual care.

Among this group, two-thirds reported having depressive symptoms for more than two years, and three quarters were female. The vast majority were on pharmacologic treatment, at 87.1%, with just over half receiving nonpharmacologic treatment.

Participants were randomly assigned to genotype-guided SSRI prescribing or usual care to examine whether pharmacogenetic guidance improves depression over six months.

At three months, there were no significant differences between the intervention and usual care groups in the primary endpoint of change in Patient-Reported Outcomes Measurement Information System (PROMIS) depression T scores among patients with an actionable phenotype.

At this timepoint, there were also no differences in the secondary outcome of adverse effect severity.

However, another secondary endpoint of depression remission according to a PROMIS depression T-score of 16 or less was more likely with the intervention than usual care, at 48.3% (153 of 317 patients) versus 39.4%. (122 of 310 patients).

Based on this, the authors proposed: “These findings suggest that pharmacogenetic testing, including evaluation for CYP2D6 enzyme inhibition (phenoconversion), may offer meaningful benefit with longer follow-up.”

The post Genotype-Guided Antidepressants Could Have Long-Term Benefits appeared first on Inside Precision Medicine.

STAT+: A new attack on AMA’s billing codes

You’re reading the web edition of D.C. Diagnosis, STAT’s twice-weekly newsletter about the politics and policy of health and medicine. Sign up here to receive it in your inbox on Tuesdays and Thursdays.

Brain Reid, who writes a newsletter on drug pricing policies, wrote “health care [sic]” in his Friday edition. I feel like a huge dork for laughing at that “sic” notation. Share your thoughts on the AP’s new compound noun dictum here, and send news tips to John.Wilkerson@statnews.com or John_Wilkerson.07 on Signal.

CPT codes are the new front in fraud allegations

House oversight committee Chair James Comer (R-Ky.) is taking aim at the American Medical Association, linking the biggest doctor lobby’s billing codes to potential fraud, waste, and abuse.

Continue to STAT+ to read the full story…

Real-world use of brexpiprazole during inpatient treatment for schizophrenia: continuation, discontinuation, and concomitant psychotropics

IntroductionIn the treatment of schizophrenia, antipsychotics used during acute inpatient care must control acute symptoms while remaining sufficiently tolerable to support treatment beyond the acute phase. Brexpiprazole, a serotonin-dopamine activity modulator may be one such option; however, its real-world use and short-term continuation in acute inpatient settings remain insufficiently characterized.MethodsWe conducted a retrospective observational study of inpatients with DSM-5 schizophrenia treated with brexpiprazole at a university hospital in Japan between June 2018 and July 2024. The index date (week 0) was defined as the date of brexpiprazole initiation during the index hospitalization. The primary outcome was brexpiprazole continuation at week 8. We compared baseline demographic and treatment-related variables between the continuation and discontinuation groups and summarized reasons for discontinuation from electronic medical records. As a secondary exploratory analysis, we examined longitudinal changes in Clinical Global Impressions–Severity scale (CGI-S) and Brief Psychiatric Rating Scale (BPRS) total scores (weeks 0/4/8) in the continuation group using a linear mixed-effects model including time, concomitant psychotropic medication status, and their interaction.ResultsSixty-seven patients were included. Baseline illness severity was substantial (median CGI-S 5.0 [IQR 5.0–6.0]; mean BPRS total 58.5 ± 9.6). Concomitant psychotropic medications were common. Thirty-six patients continued brexpiprazole to week 8 (53.7%). In unadjusted exploratory comparisons, continuation was associated with the female sex (p = 0.036), lower prior chlorpromazine-equivalent dose (p = 0.015), and shorter duration of untreated psychosis (p = 0.003), with a trend toward shorter duration since onset (p = 0.073). The most frequent reason for discontinuation was adverse events (n = 10, 32.3%), most commonly akathisia (n = 6), followed by insufficient efficacy (n = 9, 29.0%) and patient preference/refusal (n = 7, 22.6%). In exploratory mixed-effects analyses within the continuation group, CGI-S and BPRS total scores decreased over time, with significant group-by-time interactions by concomitant medication status. However, between-group differences should be interpreted cautiously.DiscussionThis study describes 8-week continuation and reasons for discontinuation of brexpiprazole in acute inpatient schizophrenia care. Given the retrospective single-center design and potential selection/information bias and unmeasured confounding, further studies are warranted to clarify its clinical positioning in real-world practice.

Multinational validation of the PREVENT and SCORE2 cardiovascular risk equations across 6.4 million individuals

Nature Medicine, Published online: 05 May 2026; doi:10.1038/s41591-026-04437-z

Comprehensive, multinational validation of the PREVENT and SCORE2 cardiovascular risk scores, used in the United States and Europe, respectively, in 44 observational studies and 18 randomized trials, shows similar performance for the two risk scores and generally good performance across geographical regions.

What you need to know about hantavirus (don’t panic)

Good morning. Yesterday, the writer Yiyun Li won a Pulitzer Prize for her heartbreaking memoir, “Things in Nature Merely Grow.” Lately, I’ve been reading her short stories. Here’s one for after you’ve read the news, about a health care worker of sorts: “A Sheltered Woman.” 

The latest on the abortion pill

A Monday order from the Supreme Court, signed by Justice Samuel Alito, temporarily restored broad access to mifepristone after a federal appeals court ruling on Friday jeopardized access to the abortion medication at pharmacies or through the mail. The Supreme Court order will remain in effect until the end of the day next Monday, giving both sides time to respond while the court considers the issue. The AP has more details.

Read the rest…