Type 1 Diabetes-Induced Kidney Disease Treated with Phase III Trial Drug

Those living with type 1 diabetes not only face the challenges of living with a chronic illness, but they also contend with the potential of developing secondary conditions, including kidney disease. Nearly a third of patients with type 1 diabetes develop kidney disease, resulting in diabetes as the leading cause of kidney disease worldwide. With such a broad impact, and few approved therapies, research into therapeutic strategies to help patients prevent or recover from diabetes-induced chronic kidney disease is much needed.

Research on type 2 diabetes suggests that inhibitors against the SGLT2 protein improve function and reduce damage to kidneys. Thought the mechanism behind this protective effect remains unclear, an SGLT2 inhibitor, dapagliflozin, has shown success in clinical trials led by Petter Bjornstad, MD, physician-scientist and executive director of the University of Washington Medicine Diabetes Institute.

Bjornstad & colleagues have developed their clinical trial to assess the effects of dapagliflozin in adolescents. Their new paper published in Science Translational Medicine shows the results of a section of their phase III data from the Adolescent Type 1 Diabetes Treatment With SGLT2i for hyperglycEMia & hyPerfilTration (ATTEMPT) trial.

The authors described this analysis of the broader trial as “a multimodal view of how the kidney of a person with T1D responds to SGLT2 inhibition.”

Data from 98 children aged 12 to 21, was analyzed to detail the effects of dapagliflozin in combination with insulin therapy on kidney function and physiology. Participants in both a placebo-control group and the treatment group were treated for 16 weeks, then underwent “sequential kidney biopsies, multiparametric kidney MRI, and plasma/urine proteomics,” though biopsies were only carried out in patients over 18 years of age.

Molecular profiles of the serialized biopsies showed a reversal of molecular hallmarks including transcriptional shifts using single-cell RNA seq, downregulation of glycolysis, gluconeogenesis, and oxidative stress markers, and reduced inflammatory gene expression.

“These molecular changes paralleled clinical improvements, including attenuation of hyperfiltration, improved glycemic control, and normalization of medullary oxygenation,” the authors wrote.

Analysis of proteomics in urine samples showed similar results. The tissue changes included decreased injury markers and increased numbers of protective proteins, suggesting that dapagliflozin has a reversing effect on diabetes-induced kidney damage.

“Cross-cohort comparison against healthy controls showed that over 55% of dapagliflozin-responsive genes shifted toward healthy control expression patterns,” indicated the authors.

Not only were kidney markers improved in treated patients, but these patients also showed overall improvement including improved blood sugar control and more normal kidney function.

“Because adjunctive SGLT2 inhibition is considered for people with T1D in the future, our results offer mechanistic reassurance that the drug engages kidney-protective pathways similar to those in type 2 diabetes,” they wrote.

In addition to determining the mechanistic impacts of dapagliflozin in kidney disease using a subset of data from a clinical trial, the authors point out that this work has a broader impact for other clinical trials with multiple data streams.

“Our study showcases the power of deep phenotyping in clinical trials to elucidate drug mechanisms in vivo,” they point out.

“Ultimately, combining rigorous clinical trials with translational science approaches will accelerate the development of therapies to reduce the burden of DKD in T1D,” concluded the authors.

The post Type 1 Diabetes-Induced Kidney Disease Treated with Phase III Trial Drug appeared first on Inside Precision Medicine.

Turning Solar Power Into Protein

According to projections from the United Nations, global food demand could increase by around 60 percent by 2050, while only about two percent additional agricultural land is expected to become available. Researchers at the Technical University of Munich (TUM) report that they are exploring new approaches to safeguard food security. A team at the TUM Campus Straubing has developed a process for producing crucial amino acids from carbon dioxide, hydrogen, and renewable energy.

Viktoria Lehmann, a doctoral candidate at TUM, describes one potential application for biotechnologically produced amino acids.

“A dairy cow needs far more than the grass growing in its pasture. High milk yields require supplemental protein, which is typically supplied through animal feed. These feeds are enriched with amino acids, the chemical building blocks of proteins,” she explains. “Across livestock production systems worldwide, millions of tons of amino acids are used as feed additives. However, their production consumes large amounts of land, water, and other resources. We wanted to find a more resource-efficient way to meet this protein demand.”

In a recently published study “Plug and Play – Enzymatic Amino Acid Production from Methanol and Carbon Dioxide” in Nature Communications, the team demonstrated its approach. The concept behind it: solar energy is converted into electricity using photovoltaic systems. This electricity is used to generate hydrogen, which, together with carbon dioxide, is converted into methanol—an alcohol widely used in industry as a chemical precursor. Specialized enzymes then convert the methanol step by step into amino acids. Which amino acid is produced depends on the specific enzymes used.

“Plants use sunlight to build biomass, but they are relatively inefficient at doing so. We are investigating an alternative pathway in which renewable energy is first converted into chemical energy carriers and then into valuable protein building blocks,” notes Volker Sieber, PhD, professor of chemistry of Biogenic Resources and Rector of the TUM Campus Straubing. “In the long term, this approach could help make more productive use of available land and enable a more sustainable production of amino acids.”

A modular platform technology

In 2023, the researchers demonstrated the production of the amino acid L-alanine from green methanol. Their latest work expands the approach to a total of seven amino acids. “Our modular plug-and-play concept can be compared to a construction kit,” says Vivian Willers, PhD, whose doctoral research laid the foundation for the study. “What started with a single amino acid is increasingly evolving into a platform technology for producing protein building blocks from renewable energy.”

The team successfully produced the amino acids glycine, serine, L-aspartic acid, L-valine, L-glutamic acid, and L-proline. In the future, this technology could help reduce dependence on protein-rich feed ingredients such as soy, which are not always produced sustainably. These amino acids are also key components of nutrient media used in cultured meat production. As a result, the researchers see applications extending well beyond conventional agriculture.

While the team was able to demonstrate the entire process chain—from carbon dioxide via methanol ultimately to amino acids—the current production volumes are still too low for commercial use. The researchers are working to further improve the performance of the enzymes involved.

“Our work is primarily a proof of technological feasibility,” points out Sieber. “We have shown that a broad range of biologically relevant amino acids can be produced from CO₂-based methanol. This opens up new possibilities for the sustainable production of protein building blocks.”

 

The post Turning Solar Power Into Protein appeared first on GEN – Genetic Engineering and Biotechnology News.

Designing an mHealth App for Stroke Rehabilitation in Indonesia: Mixed Methods Design Science Research Study

Background: Indonesia has the second-highest prevalence of stroke in Southeast Asia, with 4,918,487 people (1.7% of the population) living with this condition as of 2025. This is attributable to the living conditions in Indonesia, where limited health care workers and facilities are available to assist with stroke rehabilitation via mobile health (mHealth) interventions. Objective: This study designed an mHealth app to facilitate stroke rehabilitation in Indonesia. Methods: In this mixed methods study, interviews were conducted with 10 experts (doctors, therapists, and medical students) and 8 patients who have experienced a stroke to explore the need for stroke rehabilitation management apps. Using a design science research approach, we conducted 3 iterative design cycles, each comprising design, development, and evaluation, to construct an mHealth app for stroke rehabilitation. The first iteration produced a low-fidelity app prototype informed by intervention theory. The prototype, which comprised 13 features for patients and 12 for medical personnel, was evaluated through interviews with medical personnel. The second iteration produced a design for a high-fidelity app prototype based on feedback from the first iteration. The third iteration yielded an improved app based on feedback from the second iteration. Results: This study identified app features that support patient rehabilitation, including patient training programs with progress monitoring in functional, speech, and occupational therapy, along with consultations and home visits to connect rehabilitating patients with medical personnel. Other features of the app include onboarding, gamification, users’ authentication, user profile management, schedule reminders, activity targets, therapeutic progress reports, and educational materials and videos. The prototypes received a System Usability Scale score of 71.83 (“good”) and average scores of 2.32 (system usefulness), 2.39 (information quality), 2.42 (interface quality), and 2.35 (overall). Conclusions: This study provides guidance for health care facilities and regulators to improve the quality of rehabilitation services for patients with stroke in Indonesia.
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AI Software Among Commercially Insured Populations: Cross-Sectional Study of Patient and Plan Characteristics

We describe the adoption of AI software among commercially insured adults from 2018 to 2023 and find rapid growth but variable use across patients, plans, and regional characteristics, highlighting the need for research and policy to support equitable and beneficial adoption.
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Medical Students’ Perceptions and Attitudes Toward English as a Medium of Instruction at the Faculty of Medicine and Pharmacy of Rabat: Cross-Sectional Study

Background: The global adoption of English-medium instruction (EMI) in higher education has introduced complex implementation challenges, the severity of which often depends on the resources available within specific educational contexts. Evidence remains limited in public medical schools in under-resourced, non-Anglophone countries, which serve a socioeconomically and educationally diverse student population. In such settings, the direct transfer of existing EMI integration models presents significant practical challenges. Objective: This exploratory, observational, monocentric study aimed to investigate medical students’ perceptions and attitudes toward EMI implementation at the Faculty of Medicine and Pharmacy of Rabat (FMPR) in Morocco and to evaluate their readiness for EMI adoption. Methods: A cross-sectional survey was administered to 102 second-cycle medical students at FMPR. The 23-item questionnaire included Likert-type scales and multiple-choice questions across 4 domains: demographic data, self-reported English language proficiency, language perceptions and attitudes, and EMI needs. Bivariate, univariate, and multivariate logistic regression analyses were conducted to determine the effects of the explanatory variables on EMI choice. Results: The sample comprised 65 female and 37 male participants. Most reported using English speaking and listening skills “often” on a daily basis, while writing skills were reported as being used “rarely.” Participants rated their general English proficiency and their academic listening and reading skills as “good.” Overall, 82.4% (84/102) of students were strongly in favor of implementing EMI at FMPR. Bivariate analysis showed significant positive associations between EMI choice and age (=.04), course year (<.001), interest in learning English (=.006), and the belief that English should be the language of higher education (=.02). Preference for EMI increased alongside course year, peaking at 96.4% (27/28) among students in the third and fourth years. Multivariate logistic regression confirmed that being in the fourth vs third course year (adjusted odds ratio 22.12, 95% CI 2.56‐190.84; =.005) and having an interest in learning English (adjusted odds ratio 5.12, 95% CI 1.05‐25.03; =.04) were significant positive predictors of EMI choice. Conclusions: Medical students at FMPR exhibit highly positive perceptions and attitudes toward the potential implementation of EMI, despite variations in their self-reported English readiness. These findings provide actionable insights for the successful integration of EMI that extend beyond the Moroccan context, offering a valuable framework for medical institutions in other under-resourced, low- and middle-income, non-Anglophone settings across the Global South.

Why Young People Fail to Report Harmful Online Experiences

Research shows that 80% of youth who experience negative online interactions never report them. Here’s what parents can do to help.

Most parents assume that if something bad happened to their child online, they’d hear about it. But new research suggests that may not be the case.

In a study of over 1,000 youth ages 9–15 with mental health or neurodevelopmental concerns, researchers from the Child Mind Institute found that one in four experienced a negative online interaction — including cyberbullying, sexual harassment, or doxxing — in the past year. Among those who experienced an incident, nearly 69% said it happened more than once. Yet only 20% reported it.

The problem isn’t that young people don’t care or don’t know something is wrong. There are real, identifiable barriers getting in the way.

Why youth stay silent

The study identified three major barriers preventing young people from reporting harmful online experiences:

  • They don’t know how. Many find the reporting process confusing and don’t understand how to use the tools on the platforms they frequent.
  • They’re unsure if their experience qualifies. Young people often struggle to determine whether the incident is serious enough to report. When intent and severity are unclear, many default to staying quiet.
  • They’re worried about the consequences. Embarrassment, fear of retaliation or escalation, and worries about anonymity are commonly reported. These emotional barriers were especially pronounced in young participants with anxiety or mood challenges.

What parents and caregivers can do

The study found that family dynamics can play an important role in both a child’s likelihood of experiencing online harm and how they respond to it.

Inconsistent discipline and poor supervision were linked with higher rates of negative online encounters. On the other hand, youth from families with open and supportive communication were more comfortable seeking help when something went wrong online. And when given the choice, most preferred telling a trusted adult rather than using platform reporting tools.

Here’s what parents can do:

  • Keep communication open. Don’t wait for something to go wrong. Create space for low-pressure conversations about both positive and negative online experiences.
  • Make it safe to speak up. To be able to talk openly about their issues with you, youth need to believe that it won’t result in punishment, judgment, or loss of their devices.
  • Help them know what counts. When researchers presented hypothetical scenarios, youth were clear about what should be reported. But with their own real experiences, they hesitated. Talk through real and imagined scenarios to help them build confidence recognizing situations in which they should speak up.
  • Learn the tools together. Sit down together and get familiar with the blocking, privacy, and reporting features on the platforms they regularly use.

Creating safer digital spaces

The responsibility for online safety shouldn’t fall entirely on children or their families.

If we want young people to report unwanted experiences, the tools and systems around them need to be clearer, safer, and easier to use. Platforms need reporting tools designed with young users in mind. Policies and safety guidance should be written in clear, developmentally appropriate language. This way, children will have a better understanding of what kinds of experiences should be reported and what happens after a report is submitted.

Based on research published in JAACAP Open.
Read the full study

The post Why Young People Fail to Report Harmful Online Experiences appeared first on Child Mind Institute.

Gene Regulation Map Uncovers Heart Failure Targets

Scientists have created the most detailed map to date of single-cell gene regulation in heart failure. Published today in Science, the study integrates multiple layers of genomics data to identify new therapeutic targets for the world’s leading cause of death.

“Our goal is to use this atlas to discover targets that we can act on therapeutically,” said Neil C. Chi, MD, PhD, professor of medicine at UC San Diego School of Medicine. “Right now, one of the biggest limitations in cardiology is not the lack of tools, but the lack of targets. This kind of data changes that.”

While previous genetic studies have uncovered many genetic changes linked to heart failure, more than 85% of them were found in noncoding DNA regions, making it difficult to understand how they contribute to the condition and develop targeted therapeutics. Because of this, treatment options for heart failure remain limited.

“What makes this study unique is the ability to integrate multiple layers of genome regulation in the same cells,” said Bing Ren, PhD, professor emeritus of cellular and molecular medicine at UC San Diego School of Medicine and scientific director and CEO of the New York Genome Center. “These technologies allow us to look beyond which genes are active to understand how the genome is organized and controlled, revealing regulatory elements and interactions that were previously inaccessible.”

The researchers analyzed more than 750,000 individual heart cells from 36 participants with and without heart failure. Results revealed that heart failure is associated with major shifts in cell composition, with a reduction in the number of cardiomyocytes and an increase of fibroblasts and immune cells. In failing hearts, over 10,000 genes showed altered expression patterns and more than 50,000 DNA regions showed changes in chromatin states that altered the ability of proteins to interact with them. 

Compared to other cell types, fibroblasts and cardiomyocytes showed the most extensive remodeling of their gene regulation networks. These cells also showed several distinct cell states as they progressed from healthy to diseased—in the case of fibroblasts, transforming into activated fibroblasts and myofibroblasts that contribute to scarring and fibrosis. 

“These intermediate states are where the disease is actively unfolding,” said Chi. “If we can understand and target those transitions, we may be able to intervene earlier and more effectively.”

Integrating the single-cell atlas with genome-wide association data, the team showed that genetic changes are concentrated in specific regulatory regions active in certain cell types, particularly in cardiomyocytes. These findings suggest that targeting cardiomyocyte genes may be more effective than targeting genes found on other cell types when treating heart disease. 

“This is a higher-order view of disease biology,” said Chi. “Instead of just asking which genes are turned on or off, we’re now understanding how their regulation is controlled across the genome—and that’s where most disease risk actually resides. By connecting genetic risk, gene regulation and cell-specific disease processes, this study provides a blueprint for precision therapies in heart failure. It opens the door to targeting the right mechanisms in the right cells at the right time.”

The post Gene Regulation Map Uncovers Heart Failure Targets appeared first on Inside Precision Medicine.

Autism-Like Traits in Mice Improved After Single Rapamycin Dose

The results of a preclinical study led by UCLA Health researchers suggest that inflammation during pregnancy in mice can trigger autism-like brain and behavior changes in offspring, and that the effects may be rapidly but temporarily reversible in adulthood with a short-term dose of the immunosuppressive drug rapamycin.

The study showed that a single dose of rapamycin rapidly improved changes including brain overactivity, seizure risk, sensory sensitivity, repetitive behaviors, and abnormal brain functional network organization. Rapamycin itself is not considered a viable candidate for human therapy, as the effects of the drug were found to be temporary, with repeated dosing losing efficacy, and repeated use also having the potential for toxicity. However, the researchers said the study findings indicate that some autism-related brain changes may still be treatable in adulthood, and point to possible therapeutic approaches that target the underlying pathway rather than only symptoms.

“These results reframe how autism-associated symptoms might be treated,” said Janel Le Belle, PhD, an associate professor in the UCLA Department of Neurosurgery. “If the adult brain remains capable of functional normalization, then some features of autism may be successfully addressed without needing to correct underlying structural differences.” Le Belle is first author of the researchers’ published paper in Nature Communications, titled “Acute rapamycin treatment reveals distinct mechanisms of dysfunction in a maternal inflammation mouse model.”

Neurodevelopmental disorders result from the disruption of brain development in utero or in early life, with genetic, environmental, epigenetic, and immunological factors all potential contributors to complex pathogenesis, the authors wrote. Previous studies have shown that offspring of mothers who experience inflammation while pregnant have a higher likelihood of developing autism-associated traits such as repetitive behaviors and difficulty with social interaction, as well as brain overgrowth and disrupted sensory processing that continue into adulthood. “Maternal inflammatory response (MIR) during early mouse gestation induces a cascade of physiological and behavioral changes associated with autism spectrum disorder (ASD),” they stated.

Rapamycin has been shown in previous mouse autism studies to improve symptoms by suppressing an overactive mTOR pathway that signals cell growth and proliferation. What has been less clear is whether these brain changes could still be modifiable in adulthood, and whether rapamycin’s benefits came from long-term structural repair or faster functional changes. “We wanted to understand the mechanisms that underlie the effects of adult mTOR inhibition, where treatment isn’t aimed at preventing or reversing structural brain abnormalities,” the team stated.

For their newly reported study the scientists exposed pregnant mice to a mild inflammatory trigger early in gestation at a dose that was too low to make the mothers significantly ill. The resulting offspring went on to develop chronic brain and body-wide inflammation, mild brain overgrowth, overactive cell-signaling in the mTOR pathway, disorganized brain functional network connectivity and behaviors associated with autism.

When researchers gave adult offspring a single dose of rapamycin they found rapid improvement across nearly every measure. Neurons that had been firing abnormally calmed down, susceptibility to seizures dropped, brain regions that had been miscommunicating reorganized into more typical patterns and repetitive behaviors and sensory over-responsivity eased. These changes occurred within roughly two hours of drug administration, which was too rapid to be explained by the kind of physical rewiring of brain synapses that typically takes longer.

“The level of functional normalization achieved over this short time suggests new mechanisms by which possible treatments may act,” said the study’s senior author Harley Kornblum, MD, PhD, director of the UCLA Intellectual and Developmental Disabilities Research Center in the Semel Institute for Neuroscience and Human Behavior. “It suggests the adult brain may be more adaptable than we assumed, even when the underlying structural changes from early development are still there. This points us toward the brain’s functional circuitry, not just its physical structure, as a target for future treatment approaches.”

To understand the mechanisms of rapid rapamycin effects, researchers examined gene activity in brain cells before and after treatment. They found that rapamycin reversed abnormal expression of genes tied to autism, epilepsy and ion channel function, particularly in excitatory neurons, suggesting the drug works by quickly rebalancing brain cell excitability rather than by repairing structural brain differences.

The findings suggest that mTOR pathway activity, brain network organization and neuronal excitation levels as potential targets for future therapies aimed at specific autism symptoms such as sensory over-responsivity, a common but difficult-to-treat symptom of autism. “Our findings demonstrate that mTOR dysregulation drives dysfunctional brain development in MIR offspring but the adult brain remains amenable to rapid functional normalization, rescuing core and comorbid ASD associated brain and behavior phenotypes,” the authors stated.

Co-senior author and professor in the UCLA Department of Neurosurgery, Neil Harris, PhD, cautioned that the results showed the treatment effects to be temporary and that daily dosing produced tolerance over several weeks. This, along with rapamycin’s high potential for toxicity and the fact that these studies were performed in mice, makes it unsuitable for broad use in humans. “This points toward new therapeutic targets like sensory circuit neuromodulation or balancing neuronal inhibition and excitation, rather than toward rapamycin itself as a treatment,” Harris said. As the authors further commented in their paper, “Restoring excitatory/inhibitory imbalance and sensory functional network modularity may be important targets for therapeutically addressing multiple ASD phenotypes.”

The post Autism-Like Traits in Mice Improved After Single Rapamycin Dose appeared first on GEN – Genetic Engineering and Biotechnology News.

Jagged Little Pill: With Merck’s Oral PCSK9 Inhibitor, Does LDL-C Care Change?

The story of PCSK9 is an archetypal chapter from the precision medicine book of successes. It opens with the discovery of rare genetic variants that naturally lower PCSK9 activity, showing how well lowering low-density lipoprotein cholesterol (LDL-C) protects against cardiovascular disease. That discovery leads to a renaissance in lipid management, with monoclonal antibodies, RNA-based therapies, and experimental gene-editing methods to permanently silence the gene. The latest advance in delivering PCSK9-inhibiting therapies is perhaps also the simplest: a pill. 

Last week, the FDA approved Merck’s once-daily oral PCSK9 inhibitor LIPFENDRA (enlicitide), making it the first pill to target one of cardiovascular medicine’s most validated therapeutic pathways. In two pivotal Phase III studies, enlicitide reduced placebo-adjusted LDL-C by as much as 60% in adults with hypercholesterolemia, including those with heterozygous familial hypercholesterolemia (HeFH), when added to diet and exercise.  

Seth S. Martin, MD, professor and preventive cardiologist at Johns Hopkins, believes cheaper, oral PCSK9 inhibition—a 30-day supply of LIPFENDRA costs $315 compared to injectable PCSK9 inhibitors that cost $500-$600 per month—could help expand the use of one of cardiology’s most effective therapeutic strategies.  

“I see oral PCSK9 inhibition as a meaningful advance that can help build on momentum in this regard by expanding the options available to patients and clinicians,” Martin told Inside Precision Medicine. “Having a once-daily oral medication as an option can significantly broaden the use of PCSK9-targeted therapy. The more options we have, the better positioned we are to collaborate with our patients in finding treatment approaches that work and close gaps in care.” 

The approval could solve one of preventive cardiology’s biggest problems: implementing highly effective LDL-lowering therapies. “Atherosclerotic cardiovascular disease (ASCVD) remains the leading cause of death, and elevated LDL-C is one of its most important modifiable drivers,” Martin said. “If we’re going to knock ASCVD off the top of that list, we’ll need to scale up the use of effective LDL-C-lowering therapies to consistently hit LDL-C goals that we set in our 2026 ACC/AHA/Multisociety Dyslipidemia Guideline.” 

Molecular innovation meets medicinal chemistry 

Enlicitide is a macrocyclic peptide that binds PCSK9 with high affinity while remaining orally bioavailable—a feat many researchers once considered unattainable.   

“For years, many medicinal chemists believed it simply wasn’t possible to develop an oral molecule that could inhibit the PCSK9–LDL receptor interaction the way monoclonal antibodies do,” Christie Mitchell Ballantyne, MD, chief of cardiology at Baylor College of Medicine and an investigator in the enlicitide clinical development program, told Inside Precision Medicine. “This isn’t a conventional small molecule. It’s a macrocyclic peptide, and developing it required extraordinary chemistry.”  

The challenge went beyond finding a PCSK9-binding molecule. Ballantyne said it took multiple rounds of innovation to optimize the lead compound for oral absorption, metabolic stability, and scalable manufacturing after screening massive macrocyclic libraries. With these manufacturing advances, which may be as important as molecular design, Merck was able to introduce enlicitide at a lower price than injectable PCSK9 inhibitors and even some oral LDL-lowering therapies by simplifying chemical synthesis, potentially overcoming one of the main barriers to the drug class’s use.  

Two Phase III CORALreef studies supported FDA approval. In the 2,904-patient CORALreef Lipids trial, adults with hypercholesterolemia at high cardiovascular risk had a placebo-adjusted 56% LDL reduction at 24 weeks, increasing to 60% with revised post hoc data handling that excluded biologically implausible baseline LDL-C values. Enlicitide also reduced non-high-density lipoprotein (HDL) cholesterol by 54% and apolipoprotein B by 50%. The 303-patient CORALreef HeFH study produced similarly robust findings, with placebo-adjusted LDL reductions of 59% alongside significant decreases in non-HDL cholesterol and ApoB. 

Overall, Ballantyne said, the Phase III program largely confirmed what decades of PCSK9 biology had led researchers to expect, lining up remarkably well with what has been seen from monoclonal antibodies. 

Karol Watson, MD, PhD, professor of medicine/cardiology at the David Geffen School of Medicine at UCLA and co-director of the UCLA Program in Preventive Cardiology, expects the trial to validate what decades of LDL biology have consistently suggested, while emphasizing that definitive evidence still matters. “Based on everything we’ve learned over the last several decades, I think it’s very reasonable to expect that those LDL reductions will translate into fewer cardiovascular events,” Watson told Inside Precision Medicine. “But we’ll let the outcomes trial give us the definitive answer.” 

For example, although LDL-C is one of medicine’s most extensively validated surrogate biomarkers, regulators appropriately distinguish between lowering cholesterol and demonstrating reductions in heart attacks, strokes, and cardiovascular death. 

 Merck’s ongoing CORALreef Outcomes trial aims to answer that question directly. The study has enrolled more than 14,500 high-risk patients and is evaluating whether enlicitide reduces major cardiovascular events in addition to lowering LDL-C. Ballantyne noted that investigators continue collecting long-term safety and efficacy data through both the outcomes trial and extension studies. 

Making prevention practical 

PCSK9 inhibitors have reduced LDL-C by roughly 60% and lowered cardiovascular events for nearly a decade. Yet despite strong clinical evidence, they remain substantially underused in routine practice. The reasons have been familiar: high initial prices, burdensome insurance requirements, physician inertia, and patient reluctance to begin lifelong injectable therapy for a condition that causes no immediate symptoms.  

“The challenge has never really been whether PCSK9 inhibition works,” Ballantyne said. “These have been excellent drugs. But they’ve had an access problem.” 

For Ballantyne, the promise of enlicitide came through while taking a look at the CORALreef safety data, where findings closely mirrored the placebo. Adverse event-related discontinuation rates were similar across treatment groups, while diarrhea and dizziness occurred infrequently. 

“When I review a placebo-controlled trial, one of the first things I examine is whether patients discontinue therapy more often than placebo,” Ballantyne said. “If discontinuation rates are similar, that’s generally very good news because it tells you patients can tolerate the medication.”  

Watson believes oral therapy addresses one of those barriers by giving physicians another option for patients who hesitate when injections enter the conversation. “Having an oral PCSK9 inhibitor is a really important step forward because it gives us another option for patients who just don’t want an injectable medication,” she said. “Many patients do perfectly well with injections, but for others it’s a real barrier. Sometimes they put off starting treatment, and sometimes they never start it at all. If we can offer a pill instead, I think we’ll be able to get more patients on effective therapy sooner.” 

That flexibility may be especially valuable for patients with established cardiovascular disease or HeFH who remain above guideline-recommended LDL targets despite maximally tolerated statins and ezetimibe. “We now have another way to lower LDL cholesterol without asking patients to make the jump to an injectable if they’re reluctant,” Watson said. 

Still, Watson cautions against assuming an oral formulation will automatically solve the adherence problem. “An oral medication has the potential to improve adherence for some patients because many people would rather take a pill than give themselves an injection,” she said. “But we have to remember another group of patients hates taking daily medications, so they will prefer an every 2-week injectable.” 

 Keith C. Ferdinand, MD, professor of medicine at the Tulane University School of Medicine and the Tulane Heart & Vascular Institute, shares that assessment. “Undertreatment is widespread and common,” Ferdinand told Inside Precision Medicine. “PCSK9 inhibitor uptake has been poor, but probably due to early access barriers and costs. But generic high-intensity statins, costing much less, are underutilized, and most ASCVD patients do not obtain a [cholesterol target of <70 mg/dL]. If an oral PCSK9 inhibitor has cost barriers, uptake will be poor and may not increase goal attainment.” 

For Ferdinand, introducing another effective drug is only part of the solution. Measuring whether clinicians actually achieve LDL targets may be equally important. “Oral PCSK9 inhibitors may be costly and underutilized,” he said. “A performance measure of goal attainment would have to overcome therapeutic inertia. Clinicians need a report card on their care and outcomes and respond to high LDL-C. Widespread coverage with easy prior authorization is key.” 

A new chapter for PCSK9—and precision medicine  

The arrival of the first oral PCSK9 inhibitor also comes as cardiovascular medicine enters another transformative era. Several investigational gene-editing therapies are designed to permanently disable PCSK9 after a single treatment, raising the possibility that lifelong cholesterol management could eventually become a one-time intervention. 

At first glance, the technologies appear to compete. Ballantyne sees them as addressing different clinical needs. “The numbers you’re seeing are on top of statin therapy,” he said. “Patients didn’t stop their statins—they received gene editing in addition to their daily medication.” That context changes the comparison. “If you’re still taking a pill every day,” Ballantyne said, “and you could instead take a pill that combines a statin with an oral PCSK9 inhibitor, that’s another way of thinking about the problem.” 

Rather than viewing oral therapy and gene editing as mutually exclusive, he expects cardiovascular prevention to evolve into a spectrum of treatment options. Most patients may continue using inexpensive oral medications, while one-time genetic interventions could eventually serve carefully selected populations for whom lifelong adherence is particularly challenging or extraordinarily high LDL levels warrant more aggressive intervention. Ballantyne believes the field will ultimately determine which patients benefit most from each approach based on durability, safety, cost, practicality, and patient preference rather than assuming a single technology will replace all others. 

After all, PCSK9 remains the target that human genetics first illuminated more than two decades ago. What is changing is how clinicians and patients may choose to intervene. “The more options we have, the better positioned we are to collaborate with our patients in finding treatment approaches that work and close gaps in care,” Ballantyne said. “If oral PCSK9 inhibitors help more patients initiate treatment, stay on therapy, and achieve guideline-recommended LDL-C levels, they can meaningfully improve cardiovascular disease prevention over the next several years and beyond.” 

Whether enlicitide ultimately becomes transformative will depend on factors extending well beyond medicinal chemistry. “This has the potential to be more than just another cholesterol-lowering drug,” Watson said. “Whether it becomes truly practice-changing will depend on several things: cost, access, and whether clinicians are comfortable incorporating it into routine care.” 

Watson expects the cardiovascular outcomes data to determine just how broadly clinicians embrace the therapy. “Given what we know about LDL-C as a causal driver of atherosclerotic cardiovascular disease and given the amount of LDL lowering this drug produces, I’d be surprised if we didn’t see cardiovascular benefit,” she said. “If those outcome data are positive, I think this could become another really valuable tool in our toolbox. I don’t see it replacing statins or ezetimibe, but I do see it helping many more high-risk patients actually reach their LDL goals.” 

For Ballantyne, however, the approval represents something even larger than another effective lipid-lowering therapy. “It’s a remarkable science story,” he said. “You start with human genetics, then monoclonal antibodies, then RNA therapies, now macrocyclic peptides. It’s another example of how understanding biology can lead to entirely new therapeutic approaches.” 

For patients who continue to struggle to reach recommended LDL targets despite existing therapies, that story has now produced something both novel and reassuringly familiar: a once-daily pill. 

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Midlife Brain Aging Linked to Immune Cell Remodeling, Blood-Brain Barrier Decline

New data from a National Institutes of Health-funded study shows that midlife, the immune cell landscape of the hippocampus, undergoes substantial remodeling. It points to a potential mechanism by which aging may contribute to the chronic neuroinflammation commonly seen in neurodegenerative disease. Details are published in a new Science paper titled “Epigenetic and 3D genome reprogramming during the aging of human hippocampus.”

The work was done by a collaborative team of scientists from the University of California, San Diego, the New York Genome Center, and the University of California, Irvine. According to the paper, the scientists analyzed postmortem hippocampal tissue from 40 neurologically healthy adults aged 20 to 95 years old. 

Digging into the details, the scientists used traditional measures of gene expression alongside more advanced techniques to analyze the genome’s 3D architecture and epigenome. “Gene expression tells us what a cell is doing today, but epigenetic signatures preserve information about where a cell came from,” said Nathan Zemke, PhD, director of single-cell genomics at the UC San Diego Center for Epigenomics and first author on the study. “By combining these approaches, we uncovered a major shift in the identity and lineage of immune cells in the aging human brain’s immune cells that gene expression data alone would not have revealed.”

They found that the brain’s primary immune cells progressively decline from age 50 to 75 years of age, and are replaced by cells with elevated inflammatory signatures and other features that resemble the characteristics of peripheral blood-derived immune cells. It raises questions as to whether microglia, which emerge during embryonic development, may not renew throughout the human lifespan as previously thought. The data also showed that cells that typically maintain the protective blood-brain barrier deteriorated with age. And across many brain cell types, aging accompanied a widespread and coordinated disruption of genome architecture.

“The progressive structural disruptions were closely linked to shifts in gene regulation and cell identity, potentially revealing a fundamental feature of aging in the human brain,” said Bing Ren, PhD, scientific director and CEO of the New York Genome Center, and professor of genetics and development at Columbia University. Ren is also a corresponding author on the study, 

Future studies will investigate the mechanisms driving the loss of resident microglia and determine whether the newly identified immune-cell transition contributes directly to Alzheimer’s disease and other age-related neurological disorders. Insights from the current study as well as others could provide new opportunities to develop therapies that help to preserve brain function and reduce vulnerability to neurodegenerative disease.

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