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Healthy Aging Program

Head: Roza Adany, MD, PhD

Purpose

The Healthy Aging Program advances translational research aimed at extending healthspan through integrated biological, clinical, and population-level strategies. The program connects geroscience with intervention development, prevention frameworks, and policy-relevant implementation.

Why it matters

• Europe is undergoing rapid demographic aging with escalating burdens of cardiovascular disease, dementia, frailty, and cancer
• Preventable determinants of unhealthy aging remain insufficiently translated into scalable intervention frameworks.
• Bridging geroscience with real-world public health practice is essential to to sustain healthcare systems and preserve functional independence.

What we do

• Preclinical anti-aging research in preclinical models targeting vascular, metabolic, and neurobiological aging pathways
• Advanced transcriptomics and multi-omics pipelines for biomarker discovery and target identification
• Translational clinical studies focused on aging-related risk stratification and intervention testing
• Large-scale epidemiological analyses of determinants of healthy aging
• Cancer survival and aging interaction research
• Retinal epidemiology and vascular aging biomarkers
• Public health genomics and precision prevention
• Integration with the Fodor Center for Prevention and Healthy Aging (Semmelweis University)
• Support for the Semmelweis Study and the Semmelweis-EUniWell Workplace Health Promotion Program
• End-to-end research support: study design, analytics, implementation, and policy translation

Key outputs

• Selected publications (curated list)
• Translational datasets
• Participation in research consortia
• Evidence frameworks for prevention programs

People

• Program Head: Roza Adany, MD, PhD
• Key collaborators: Adam Tabak, MD, PhD,  Stefano Tarantini, PhD, Balazs Gyorffy, MD, PhD, Tamas Csipo, MD, Agnes Lipecz MD, Agnes Szappanos MD, Peter Piko PhD, Monika Fekete MD, PhD, Vince Fazekas-Pongor, MD, PhD, David Major, MD, PhD, Hajnalka Andrikovics, MD, PhD , Tamas Kiss, MD, PhD, Dorina Nagy PhD

Collaborate

• We actively build European research consortia and welcome academic, clinical, and public health partners for Horizon proposals and joint initiatives.

Recent Publications

Life Satisfaction as a Key to Healthy Aging at Work

Healthy aging is about more than preventing disease - it also means supporting mental well-being, resilience, and quality of life throughout the working years. This review explores how life satisfaction can serve as a practical and measurable target for workplace health promotion within the Semmelweis–EUniWell framework. The authors highlight that employees who experience greater well-being are more likely to remain healthy, productive, and engaged as they age. Instead of focusing only on treating illness, the framework promotes preventive strategies that strengthen psychological and social health across the entire workforce.

The publication also emphasizes the importance of interdisciplinary collaboration in developing evidence-based approaches to healthy aging. Researchers from the Translational Research Institute contributed to this international effort, supporting the translation of scientific knowledge into practical solutions that can improve employee health and well-being. By connecting research, prevention, and real-world implementation, the study demonstrates how universities and healthcare institutions can play a leading role in creating healthier workplaces for an aging population.

Journal Reference

  1. Zábó V, Lehoczki A, Buda A, Varga P, Fekete M, Fazekas-Pongor V, et al. Promoting healthy aging in occupational settings: satisfaction with life as a strategic target in the Semmelweis-EUniWell framework. GeroScience. 2026. doi:10.1007/s11357-026-02339-z.

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Transcranial Magnetic Stimulation: Advancing Brain Health from Healthy Aging to Alzheimer’s Disease

As the global population ages, preserving cognitive function has become a major healthcare priority. This review examines the growing role of transcranial magnetic stimulation (TMS), a non-invasive technique that uses magnetic pulses to influence brain activity. The authors summarize current evidence showing that repetitive TMS (rTMS) may improve memory, attention, and executive function by promoting neuroplasticity and supporting communication between brain networks. While further clinical studies are needed, the findings highlight the technology's potential to slow cognitive decline and contribute to healthier brain aging.

The review also outlines the challenges that must be addressed before TMS can become part of routine clinical care, including optimizing stimulation protocols and identifying the patients most likely to benefit. Researchers from the Institute for Translational Research contributed to this international collaboration, helping bridge fundamental neuroscience with clinical applications. By translating emerging scientific discoveries into evidence-based therapeutic strategies, the Institute supports the development of innovative approaches for preventing and treating age-related cognitive disorders, including Alzheimer's disease.

Schematic representation of transcranial magnetic stimulation (TMS) over the motor cortex. TMS produces a rapidly changing magnetic field that permeates the skull, generates an electric field in the underlying tissue, and, ultimately, leads to the depolarization of cortical neurons. When applied at sufficiently high intensities, this stimulation of motor cortical regions elicits motor-evoked potentials (MEPs) in peripheral muscles associated with these regions. These MEPs can be quantified through electromyography. EMG, electromyography; ICF, intracortical facilitation; ICI, intracortical inhibition. Created with BioRender.com.

Journal Reference

  1. Saleh Velez F, Cedeno-Bruzual M, Zuniga-Gutierrez M, Mercado Pena D, Ballard CL, Kong JS, et al. Transcranial magnetic stimulation from healthy brain aging to Alzheimer's disease: a review on mechanisms, therapeutic potential, and future clinical directions. Frontiers in Aging Neuroscience. 2026;18:1778992. doi:10.3389/fnagi.2026.1778992.

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How the Aging Brain May Accelerate Muscle Loss

Healthy aging depends not only on strong muscles but also on a healthy brain. This study reveals that biological aging processes in the brain may directly contribute to age-related muscle loss, known as sarcopenia. Using an experimental model, the researchers showed that cellular senescence in the brain triggered molecular changes in skeletal muscle that closely resembled those seen during natural aging. The findings suggest that the brain plays a much more active role in regulating muscle health than previously recognized, opening new perspectives on why frailty develops with age.

The study also highlights the importance of targeting aging as a whole-body process rather than treating individual organs in isolation. Researchers from the Institute for Translational Research contributed to this international collaboration, helping uncover the biological links between brain aging and muscle decline. By advancing our understanding of the brain–muscle aging axis, the research may support the development of innovative strategies to prevent frailty, preserve mobility, and promote healthier aging in older adults.

Journal Reference

  1. Ekambaram S, Patai R, Gulej R, Kiss T, Chandragiri SS, Nagy D, et al. Brain senescence drives sarcopenia-like transcriptomic remodeling in skeletal muscle. GeroScience. 2026. doi:10.1007/s11357-026-02205-y.

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Walking Patterns May Reveal the Earliest Signs of Brain Aging

The way we walk can provide valuable insights into how our brain and body age. This study investigated how aging and increased mental effort affect walking patterns by analyzing not only the speed and rhythm of gait but also the natural variability and complexity of each step. The researchers found that older adults show greater changes in walking stability, especially when performing a cognitive task while walking. These subtle alterations may serve as early indicators of declining brain function, long before more obvious symptoms appear, making gait analysis a promising tool for the early detection of age-related cognitive decline. 

Researchers from the Institute for Translational Research contributed to the development of the Semmelweis Study gait assessment framework, which combines digital gait analysis with vascular, metabolic, and cognitive health assessments. This multidisciplinary approach aims to identify early biomarkers of unhealthy aging and support preventive interventions before significant functional decline occurs. By translating advanced research into practical clinical tools, the Institute is helping pave the way for more personalized strategies to promote healthy longevity and preserve independence in older adults.

Journal Reference

  1. Mukli P, Murányi M, Lipecz Á, Szarvas Z, Csípő T, Fekete M, et al. Age- and cognitive load-related variability and entropy of gait: integrating coefficient of variation, median absolute deviation, and permutation entropy of spatiotemporal parameters into the Semmelweis Study gait assessment framework. GeroScience. 2026. doi:10.1007/s11357-026-02256-1.

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Can Plasma-Based Therapies Help Slow the Aging Process?

Scientists have long been fascinated by the possibility that factors circulating in the blood could influence how our bodies age. This review examines the scientific evidence behind plasma-based rejuvenation strategies, including plasma transfer and therapeutic plasma exchange, which have shown promising results in experimental models. While these approaches have improved brain, vascular, and immune function in preclinical studies, the authors emphasize that there is currently insufficient evidence to support their widespread use as anti-aging therapies in humans. Instead, they argue that understanding the specific biological mechanisms behind these effects is essential before such treatments can become part of routine clinical practice.

Researchers from the Institute for Translational Research contributed to this international review, highlighting the importance of translating discoveries in aging biology into safe, evidence-based medical interventions. Rather than promoting unproven rejuvenation therapies, the authors advocate for precision medicine approaches that identify the molecular drivers of aging and develop targeted treatments. This work provides a realistic roadmap for future research while reinforcing the need for rigorous clinical validation before plasma-based interventions can be safely introduced into healthcare.

Journal Reference

  1. Ungvari Z, Tarantini S, Csipo T, Yabluchanskiy A, Kiss T, Gulej R, et al. Plasma-based strategies for systemic rejuvenation: critical perspectives on clinical translation. GeroScience. 2026. doi:10.1007/s11357-026-02136-8.

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How “Young Blood” May Help Protect the Aging Brain

As we age, the brain gradually becomes less efficient at matching blood flow to the activity of nerve cells - a process known as neurovascular coupling. This decline contributes to memory problems and increases the risk of cognitive impairment. In this study, researchers investigated why exposure to a young circulatory system can restore healthy brain blood flow in older animals. They found that a key role is played by IGF-1 (insulin-like growth factor-1) and its receptor in the cells lining blood vessels. Although these molecules do not fully explain the rejuvenating effects of young blood, they appear to be essential components of the biological pathways that help maintain healthy brain function during aging.

Researchers from the Institute for Translational Research contributed to this international collaboration, advancing our understanding of the molecular mechanisms that underlie healthy brain aging. By identifying how IGF-1 signaling supports vascular function in the aging brain, the study provides valuable insights for the development of future therapies aimed at preserving cognitive health and preventing age-related neurovascular disorders. This work represents another important step toward translating discoveries in aging biology into innovative strategies for healthy longevity.

IGF-1/IGF-1R signaling contributes to young blood–mediated rejuvenation of cerebrovascular endothelial function and neurovascular coupling. A Experimental groups included wild-type aged isochronic parabionts (A–(A)), wild-type heterochronic aged parabionts (A–(Y)), aged parabionts paired with young IGF-1–deficient mice (A–(YIGF1-KD)), and endothelial IGF-1R–deficient heterochronic aged parabionts (AIGF1R-KD–(Y)). Parentheses denote the non-measured parabiont in each pair. B Experimental timeline. C Schematic of whisker stimulation–induced NVC assessment using laser speckle contrast imaging in parabionts. D Representative differential maps showing changes in cerebral blood flow within the contralateral somatosensory cortex during whisker stimulation. Warmer colors indicate greater increases in CBF relative to baseline. E Quantification and statistical comparison of NVC responses across experimental groups. NVC data for wild-type parabionts (A–(A) and A–(Y)) were reported previously [36]. Data are shown as mean ± SD; N = 7–8 per group. Statistical analysis was performed using one-way ANOVA with Sidak’s post hoc test; *p < 0.05, ***p < 0.001, ****p < 0.0001

Journal Reference

  1. Gulej R, Kiss T, Tarantini S, Csipo T, Chandragiri SS, Yabluchanskiy A, et al. Young blood-induced rejuvenation of neurovascular coupling involves endothelial IGF-1/IGF-1R signaling: evidence from heterochronic parabiosis using endothelial IGF-1R deficient and systemic IGF-1 knockdown mice. GeroScience. 2026. doi:10.1007/s11357-026-02118-w.