Blood Protein May Signal Dementia Risk Decades Before Symptoms Appear

A blood protein long associated with dementia in older adults may also identify people at increased risk decades before symptoms develop, according to a large international study published in Science Advances.

Analyzing data from six large longitudinal cohorts, researchers from the National Institute on Aging found that elevated levels of growth differentiation factor-15 (GDF15)—a circulating cytokine involved in inflammation and cellular stress responses—in adults younger than 55 years were associated with a significantly greater risk of developing dementia later in life, particularly vascular dementia. The findings suggest that molecular changes associated with neurodegeneration may be detectable years before cognitive symptoms emerge.

“Our findings extend existing evidence by demonstrating that elevated GDF15 levels are detectable in midlife—before age 55—in individuals who later develop dementia,’” the authors write.

The study included approximately 500,000 participants from the UK Biobank, more than 15,000 from the Atherosclerosis Risk in Communities (ARIC) study, nearly 5,700 from the AGES-Reykjavik Study, and three additional cohorts. Participants were followed for 15 to 25 years, enabling investigators to determine whether plasma GDF15 levels measured in midlife predicted future dementia.

Across nearly all cohorts, elevated plasma GDF15 was associated with increased risk for all-cause dementia. However, the relationship was strongest for vascular dementia, with effect sizes approximately two to five times greater than those observed for Alzheimer’s disease.

The distinction suggests GDF15 may be particularly useful for identifying individuals at risk for vascular cognitive impairment rather than the amyloid-driven pathology typically associated with Alzheimer’s disease. As the authors note, “the association was particularly pronounced for vascular dementia,” supporting the protein’s potential as an early marker of vascular brain injury.

To investigate whether GDF15 might play a biological role in disease rather than simply reflect ongoing pathology, the researchers performed Mendelian randomization analyses using genetic data. The analyses supported a potential causal relationship between elevated circulating GDF15 and Alzheimer’s disease and related dementias.

Additional analyses linked higher plasma GDF15 concentrations with several established indicators of neurodegeneration, including cerebral small vessel disease, elevated phosphorylated tau (pTau-181) in both plasma and cerebrospinal fluid, and increased neurofilament light, a marker of neuronal injury. In contrast, GDF15 was not associated with amyloid pathology, suggesting that it may reflect alternative disease mechanisms.

Instead, multiple lines of evidence pointed toward inflammation and immune dysregulation. Individuals with elevated GDF15 exhibited cerebrospinal fluid protein signatures consistent with neuroimmune activation, including complement activation, inflammatory signaling pathways, and disease-associated microglial responses.

To better understand these mechanisms, the investigators exposed cultured human macrophages to recombinant GDF15. The protein altered cellular pathways involved in interferon signaling, energy metabolism, and heme scavenging—processes that have all been implicated in dementia risk. Together, the experimental and clinical findings suggest that GDF15 may actively influence neurodegeneration through immune and vascular pathways rather than acting solely as a marker of biological aging.

The authors conclude that “these findings support circulating GDF15’s role as an early biomarker—particularly for vascular dementia and neuroinflammation—and identify the mechanisms by which it may drive dementia risk.”

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Implementing a Commercial AI Fracture Detection Tool in Health Care Using the Non-Adoption, Abandonment, Scale-Up, Spread, and Sustainability Framework: A Formative Evaluation Study

Background: Artificial intelligence (AI) has the potential to enhance resource efficiency, improve patient treatment, and increase safety in health care. Still, there is limited knowledge on how to implement and evaluate AI solutions in real-world clinical settings. To address this gap, we conducted a formative process evaluation of the first large-scale procurement and implementation of a commercial AI solution in Norwegian health care. F The Non-Adoption, Abandonment, Scale-up, Spread, and Sustainability (NASSS) framework, was used for the formative process evaluation throughout the 4-year project to guide data collection, analysis, and real-time feedback. Objective: This study aimed to evaluate the usefulness of the NASSS framework for formative process evaluation of AI implementation in health care. Methods: A formative process evaluation was conducted from 2020 to 2024, covering the procurement, preimplementation, and implementation phases. Data included 65 interviews, observations, and document analysis. Data were analyzed thematically using the 7 NASSS domains, supplemented with subtopics within each domain to capture emerging infrastructural complexities and temporal dynamics. Real-time findings were discussed with the implementation team, decision-makers, and clinicians. Results: Key factors for successful implementation included clinician trust, workflow integration, task distribution, and digital maturity. Major challenges comprised limited documentation of Conformité Européenne–marked solutions, deskilling, and misaligned financial incentives. The NASSS framework enabled the identification of sociotechnical values and complexities, but did not fully capture workflow evolution and changing user perceptions over time. Conclusions: The NASSS framework is useful for evaluating AI implementation but requires adaptation to capture temporal dynamics and workflow changes better. These findings contribute to improving evaluation approaches for AI in health care.
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BIO 2026: AI, federal policy impacts, and general vibes

This was my first year attending BIO. JPM is called the “Super Bowl of biotech,” so with delegations from dozens of countries in attendance, you might say BIO is the World Cup. The big question I had going in, like with any other industry event, was “what are the vibes going to be like?” After witnessing some, frankly, bad overall moods at other major events last year, I was struck by how different things felt at BIO 2026. 

Joining me in San Diego were STAT biotech correspondent Meghana Keshavan, health tech reporter Brittany Trang, and Washington correspondent Daniel Payne. In this week’s STATus Report, you’ll get vibe checks from some industry executives and my three aforementioned colleagues and hear what difference a year can make.

Genome Editing at the Turning Point—Bringing CRISPR to Clinical Reality



Image of Laura Sepp-Lorenzino, PhD

Laura Sepp-Lorenzino, PhD

Former CSO
Intellia Therapeutics

Panelist

Image of Laura Sepp-Lorenzino, PhD

Laura Sepp-Lorenzino, PhD

Laura Sepp-Lorenzino, PhD, is scientific advisor and former chief scientific officer at Intellia Therapeutics, a clinical-stage genome editing company developing potential curative CRISPR-based medicines. Previously, she was vice president and head of Nucleic Acid Therapies at Vertex Pharmaceuticals and part of External Innovation. She also held roles at Alnylam Pharmaceuticals and Merck & Co. In addition, she currently serves as the director of the American Society of Gene and Cell Therapy (ASGCT).



Image of Shengdar Tsai, PhD

Shengdar Tsai, PhD

Associate Member,
Department of Hematology
St. Jude Children’s Research Hospital

Panelist

Image of Shengdar Tsai, PhD

Shengdar Tsai, PhD

Shengdar Tsai, PhD, is an associate member in the Department of Hematology at St. Jude Children’s Research Hospital. His lab’s research focuses on developing genome editing technologies for therapeutics, with a special interest in editing human HSCs for treatment of hemoglobinopathies such as sickle cell disease and T cells for cancer immunotherapy. In 2020, he was chosen as one of the American Society for Gene and Cell Therapy (ASGCT) Outstanding New Investigators.



Broadcast Date: 

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Complex biologics such as bifunctional antibodies are opening new therapeutic possibilities in oncology, but these molecules present CRISPR is now a household term. Stories of genome editing therapies like Casgevy and Baby KJ have been headlines in our inboxes for years. Despite those cases, and the optimism they bring, genome editing has had significant challenges moving into the clinic.

This GEN Live show will bring together a panel of leading experts to break down the latest advances, innovations, and challenges shaping genome editing. The discussion will cover a lot of bases: CRISPR breakthroughs, emerging gene editing platforms, clinical trial milestones, regulatory shifts, access, off-target effects and safety considerations, and the growing role of large-scale population genomics in guiding precision therapies. Please join us to learn more and—because we plan to take questions from the audience—please bring your questions for our panelists, too!

Produced with support from:

seqWell logo

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Intravesical CAR T-Cell Therapy Reduces Bladder Cancer Growth in Preclinical Model

Researchers at Weill Cornell Medicine and Roswell Park Comprehensive Cancer Center have genetically engineered CAR T cells that specifically target and kill bladder cancer (BCa) cells. Through their preclinical study the team, co-led by Taha Merghoub, PhD, a professor at Weill Cornell Medicine, identified the protein MUC16 as a clinically relevant target for bladder cancer, and demonstrated that direct delivery of MUC16-targeting CAR T cells into the bladder via a catheter can control bladder tumors in mice. The investigators say their study raises hopes that a similar approach may be effective in humans.

The team reported on their results in Journal of Experimental Medicine, in a paper titled “Intravesical mesothelin-based CAR T cells targeting MUC16 effectively control bladder cancer in preclinical models,” concluding that their findings “… not only establish MUC16 as a clinically relevant target for anti-BCa CAR T-cell therapy, but also suggest that intravesical delivery, a commonly used administration route in urological practice, represents a viable, easy-to-implement, and more effective strategy of antitumoral adoptive CAR T-cell transfer.”

Approximately 600,000 new cases of bladder cancer are diagnosed worldwide each year, causing nearly 200,000 deaths, the authors wrote. Treatment generally involves surgical removal of the tumor followed by chemotherapy or immunotherapy. But these approaches are associated with high recurrence and progression rates, often necessitating complete removal of the bladder, a life-altering procedure that can lead to significant complications. “Intravesical therapies are the mainstay of bladder cancer (BCa) management, but their efficacy is limited by toxicities and recurrences,” they continued. “Given these challenges there is a significant unmet clinical need, driving renewed interest in bladder-sparing therapies for patients with high-risk bladder cancer who are unfit or unwilling to have their bladder removed,” Merghoub said.

CAR T cells are immune cells genetically engineered to express an artificial receptor protein capable of specifically targeting cancer cells. This type of immunotherapy has been successfully used to treat many different types of blood cancer. But success against solid tumors has so far been limited due to challenges that include poor tumor infiltration and off-target toxicity. Merghoub and colleagues attempted to overcome these issues by creating CAR T cells with high specificity for bladder cancer cells and then delivering them directly to the bladder via a catheter, known as intravesical delivery.

The team developed an antigen discovery pipeline, through which they identified MUC16 as a promising BCa target. “In this study, we leveraged a computational antigen-identification pipeline, which prioritized high tumor specificity and minimal pan-tissue expression to rationally identify MUC16 as a potential target for BCa-directed CAR T-cell therapy,” they stated. The researchers also noted that MUC16 and its soluble form, CA-125, have previously been identified as prognostic biomarkers for BCa, and MUC16 has been investigated as a CAR T-cell therapy target in other malignancies, and particularly ovarian cancer.

Through their newly reported study the investigators found that MUC16 is highly expressed on the surface of many bladder cancer cells, including types that are resistant to existing therapies, but is largely absent from normal bladder cells and other healthy tissues. “Given its favorable expression profile, absence in normal bladder, and high expression across a broad spectrum of bladder tumors analyzed collectively spanning a total of 1,292 patients, including those recalcitrant to existing therapies, MUC16 was selected as the lead candidate for BCa-specific CAR T-cell therapy development,” they wrote.

The researchers then generated CAR T cells that target MUC16. In initial tests these CAR T cells were able to kill MUC16-positive tumors grown in the lab from patient-derived bladder cancer cells. Merghoub and colleagues then tested the ability of the MUC16-targeting CAR T cells to control the growth of human bladder cancer cells implanted in the bladders of mice. The team found that the CAR T cells were ineffective when administered intravenously, but when delivered intravesically, they reduced tumor growth and extended survival. When administered directly into the bladder, the CAR T cells were unable to spread into the rest of the body, minimizing the risk of any side effects in other tissues. “Intravesical delivery of these CAR T cells reduced the growth of BCa xenografts and prolonged survival in xenograft-bearing mice, showing superior efficacy compared with typical systemic CAR T-cell administration,” the investigators noted.

“Development of engineered T cells for solid tumors has been challenging, in part due to normal tissue expression of potential target antigens,” Wolchok says. “Using a compartmentalized delivery system allows us to overcome this hurdle and hopefully come one step closer to broader use of CAR and transgenic T cells for common solid tumors, like bladder cancer.”

“Our findings establish MUC16 as a clinically relevant target for CAR T-cell therapy in bladder cancer, and highlight that intravesical delivery, a commonly used administration route in urological practice, represents a feasible, effective, and readily easy-to-implement strategy for adoptive CAR T-cell transfer,” Merghoub said. “This approach could be useful for both initial treatment of bladder cancer as well as treatment refractory subsets of tumors, offering an attractive therapeutic option for patients who may have limited therapeutic alternatives besides bladder removal.”

In their paper the team also suggest that their findings “… lay the groundwork for refining CAR T-cell therapies targeting other antigens for BCa.”

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Nipah and Hendra Viruses: Antibody Cocktail Provides Complete Protection in Hamster Model

Nipah virus—and the closely related Hendra virus—are zoonotic pathogens causing severe respiratory and neurological disease with high mortality rates. Outbreaks are rare but often devastating, with mortality rates ranging from 40 to 75 percent. There are no approved human vaccines or therapeutics for people infected with these viruses.

Now, an international research team led by investigators at the Icahn School of Medicine at Mount Sinai has developed the first fully human monoclonal antibody cocktail shown to provide complete protection against Nipah and Hendra virus infection—even when treatment was given after infection had begun. The findings represent an important step toward developing the first antibody-based therapy for Nipah virus and establish a promising strategy for combating emerging infectious diseases.

This work is published in Science Translational Medicine, in the paper, “A cocktail of human mAbs targeting the henipavirus fusion and receptor binding proteins provides cross-species neutralization.”

“One of the biggest challenges in developing treatments for henipaviruses is that human survivor samples are extremely rare,” said Axel Guzman-Solis, a graduate student in the Department of Microbiology at the Icahn School of Medicine. “We wanted to determine whether we could create fully human antibodies that target the virus in multiple ways at once, making it much more difficult for the virus to evolve resistance.”

The researchers used vaccinated humanized mice with the fusion protein (F) and receptor binding protein (RBP) of Nipah virus with the goal of isolating monoclonal antibodies. The investigators discovered two antibodies, 8G3 and 2A1, which targeted the RBP and F proteins, respectively, and together, could neutralize the virus and limit the potential for immune escape. Because the antibodies work through independent mechanisms, they create multiple barriers to infection and make it more difficult for the virus to develop resistance.

Using cryo-EM, the researchers discovered that the 2A1 antibody neutralizes the virus by stabilizing a sugar-containing structure on the viral fusion protein rather than displacing it, as scientists had anticipated. This previously unrecognized strategy may help explain the antibody’s potency and resilience against viral escape.

“We were surprised to find that the antibody essentially embraces a structure on the virus that many antibodies try to move out of the way,” said Benhur Lee, MD, chair in microbiology at the Icahn School of Medicine. “The finding suggests that stabilizing a viral protein can sometimes be just as effective—or even more effective—than disrupting it.”

When administered together, the antibody cocktail completely protected hamsters from lethal Nipah virus infection. The treatment remained effective even after infection was established, an encouraging result for a disease that progresses rapidly and carries a high fatality rate.

The findings may have broader implications for pandemic preparedness. Because many viruses rely on multiple proteins to infect cells, the researchers believe this dual-targeting strategy could be adapted for other high-priority pathogens.

“This work provides a blueprint for developing antibody therapies that are more resistant to viral evolution,” said Lee. “Rather than relying on a single target, we can attack a virus at multiple vulnerable points simultaneously.”

Next steps include studies in nonhuman primates, evaluation of long-term safety, and efforts to optimize the antibodies for clinical use. The team is also exploring next-generation antibody formats, including single molecules capable of targeting multiple viral proteins simultaneously, as well as approaches that could broaden protection against additional members of the henipavirus family.

“As zoonotic outbreaks continue to emerge around the world, there is an urgent need for therapies that can be deployed quickly against high-consequence pathogens,” said Lee. “Our long-term goal is to translate these discoveries into practical tools that help protect people during future outbreaks.”

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Pump You Up: Epigenetic Editor Drives Muscle Growth in FSHD Patients

A first-in-human clinical trial of an experimental epigenetic therapy has produced an outcome long considered elusive in the progressive genetic muscle degeneration disease facioscapulohumeral muscular dystrophy (FSHD): measurable gains in lean muscle volume.

Epicrispr Biotechnologies announced updated interim results from its ongoing Phase I/II study of EPI-321, reporting that all three FSHD patients who reached the six-month evaluation point experienced increases in lean muscle mass following a single intravenous (IV) infusion of the therapy. The findings represent what the company says is the first clinical evidence that a treatment may be capable of increasing muscle volume in FSHD, which affects an estimated 870,000 people worldwide and is one of the most common forms of muscular dystrophy. 

Although the study remains in its early stages with only nine total patients across two dosing cohorts, the promising findings were supported by imaging data, functional measurements, and biomarker changes that together suggest the therapy may be altering the biological drivers of the disease.

FSHD lacks disease-modifying treatments to intervene in the characteristic loss of skeletal muscle function, starting in the face, shoulders, and upper arms and spreading throughout the body. “We were pretty blown away,” Epicrispr CEO Amber Salzman told Inside Precision Medicine. “Every single patient gained lean muscle volume. No one has seen that.”

A silencing GEM

FSHD is caused by hypomethylation of the D4Z4 region, which is a polymorphic variable number tandem repeat (VNTR) array made up of 3.3 kilobase units, with each unit encoding the DUX4 gene. This hypomethylation leads to abnormal activation of the DUX4 gene, triggering muscle cell death and tissue degeneration, resulting in progressive muscle weakness, asymmetry, and fat infiltration.

Unlike conventional gene-editing therapies that permanently alter DNA sequences, Epicrispr’s therapy uses their Gene Expression Modulation System (GEMS). Epicrispr’s EPI-321 is an adeno-associated virus (AAV)-delivered epigenetic gene therapy that restores D4Z4 methylation and suppresses DUX4 expression, and preclinical studies show improved muscle function and reduced muscle cell death. “We don’t cut DNA,” Salzman said. “We’re not using Cas9 in the traditional editing sense. We use a dead Cas protein and an epigenetic mechanism to silence the gene.”

According to Epicrispr, preclinical studies demonstrated that the epigenetic modifications persist through many rounds of cell division, suggesting long-term suppression may be possible after a single treatment.

In addition to the therapeutic innovation, Epicrispr has also made headway into the long-standing challenge of identifying reliable molecular biomarkers for FSHD to evaluate activity downstream of DUX4. Traditional muscle biopsies provide information from only a small tissue sample and can be difficult to interpret when substantial fat replacement has already occurred.

Instead, Epicrispr collaborated with researchers at the University of Colorado investigating circulating cell-free DNA signatures associated with DUX4-driven disease activity. The biomarker, known as CBT17, emerged from studies comparing blood samples from approximately 50 healthy individuals and 50 FSHD patients. The biomarker may provide a whole-body readout of disease activity, offering evidence that DUX4 suppression is occurring beyond individual muscles examined through biopsy.

As of the May 12, 2026 data cutoff, EPI-321 has demonstrated a manageable safety profile, with nine patients treated across two dose cohorts. One IV infusion was administered to six patients in the first cohort at a target dose of 2×10¹³ vg/kg and to three patients in the second cohort at a target dose of 4×10¹³ vg/kg.

The company reported a “manageable” safety profile, with no severe dose-limiting toxicities disclosed to date. Salzman was careful not to overstate the findings. “I never want to be hubristic when it comes to AAV,” she said. “You’re giving people a lot of virus.”

She described the treatment experience as somewhat analogous to vaccine-related immune responses, noting that prophylactic immunosuppression is used as part of the protocol. “It’s manageable,” she said. “I’m not going to say it’s favorable. It’s manageable.” No serious grade 3 or grade 4 treatment-related safety concerns have been reported so far.

Baseline levels of CBT17 in treated patients fell substantially after therapy. “When we looked at baseline and three months, our patients’ levels came down so that it was just about in the healthy range,” she said.

Functional measures match MRI

The headline result comes from whole-body MRI analyses conducted six months after treatment. Among the first three evaluable patients, lean muscle volume increased in every individual compared with baseline measurements. On average, patients gained approximately 370 milliliters of lean muscle tissue, equivalent to roughly 0.8 pounds of muscle mass. Individual gains ranged from about 0.5 to 1.3 pounds. For a disease characterized by chronic muscle loss, even stabilizing muscle mass would be considered a meaningful achievement. Actual gains are potentially more significant.

The MRI analyses were performed in collaboration with Springbok Analytics, a company specializing in AI-powered muscle imaging. In addition to being widely used in professional sports to monitor injury recovery and rehabilitation, as well as a growing number of clinical settings, FSHD is one of Springbok’s primary clinical focus areas, along with disorders such as Charcot-Marie-Tooth disease and Duchenne muscular dystrophy. Using a specialized MRI protocol that runs on standard scanners, the company can quantify changes across as many as 140 individual muscles throughout the body, measuring muscle volume, muscle composition, and fat infiltration, producing objective data on muscle health.

According to Salzman, Springbok compared patients’ baseline scans against machine-learning models trained on longitudinal imaging datasets from more than 100 FSHD patients. “They can predict what it’s going to look like in six months—how much muscle patients will lose and where,” she said. “Then we sent them the six-month scans, and every patient gained lean muscle volume.”

The gains were not evenly distributed throughout the body. Patients appeared to benefit most in muscles that still retained substantial healthy tissue before treatment. “If you have too much fat in that muscle, there’s not that much we can do,” Salzman explained. “But if you have some residual muscle, it can not only stop getting worse because we’re cutting off the poison, but you can also regenerate muscle.” 

One participant, a post-menopausal woman, gained approximately 1.3 pounds of lean muscle mass according to the MRI analysis. The increase was particularly notable because age-related muscle loss would normally be expected in that population. Earlier data released by Epicrispr showed favorable trends across several functional and strength assessments at the three-month mark. These measures included tests commonly used in neuromuscular disease studies, such as the Timed Up and Go test, 10-meter walk/run assessments, and quantitative muscle testing.

Because many functional endpoints depend on patient effort, interpreting changes in small open-label studies can be challenging. Investigators and investors alike often question whether participants simply perform better because they know they received treatment. Salzman acknowledged those concerns. “You could say maybe they had a good day, and that’s why the functional measures were better,” she said.

MRI measurements, however, are not subject to effort-dependent variability. “You can’t fake MRI,” she added. Importantly, the regions showing muscle growth on imaging appeared to correspond with areas where patients demonstrated improved performance.

One participant who gained substantial upper-body muscle volume showed corresponding gains on upper-body strength assessments, while lower-body improvements were more limited in areas where muscle loss had already become severe. “The whole story is holding together,” Salzman said. “Their functional measures are getting better; their lean muscle is increasing.”

Taken together, the MRI, biomarker, and functional data provide multiple independent signals supporting biological activity. “You can’t fake blood; you can’t fake MRIs,” Salzman said. “Those are totally supportive.”

Epitome of epigenetic editing?

Beyond FSHD, researchers are closely watching EPI-321 because it represents one of the first clinical tests of an epigenetic CRISPR-based therapeutic strategy. “This is an important milestone not just for FSHD but for epigenetic medicine,” Salzman said. The approach could potentially be adapted to other diseases caused by harmful gene activation or insufficient gene silencing.

Still, significant hurdles remain before EPI-321 can be considered a proven therapy. The current dataset includes only three patients with six months of follow-up. Epicrispr plans to present additional data from six patients at the World Muscle Society Annual Congress in September 2026.

The company expects the initial Phase I/II study to complete enrollment and generate a full readout in mid-2027. Yet, larger studies will be needed to determine whether muscle gains persist, whether they translate into meaningful long-term functional benefits, and whether safety remains acceptable over time.

Regulators will also require evidence linking increases in lean muscle volume to tangible improvements in patient function and quality of life. To that end, Epicrispr is preparing discussions with the U.S. Food and Drug Administration regarding potential future endpoints and whether MRI-based muscle measurements could eventually serve as surrogate markers of clinical benefit.

Whether those early signals hold up in larger populations remains to be seen. But for a disease in which muscle loss has long been viewed as inevitable, the possibility of reversing that trend, even modestly, marks a notable moment for the FSHD field.

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