Meet Cardiovascular Diabetology's Associate Editor of the Year - Dr Francesco Paneni

Coinciding with World Diabetes Day, Dr Francesco Paneni has been awarded with Cardiovascular Diabetology’s annual Associate Editor Award. In this Q&A Dr Paneni shares what it means for him serving as Associate Editor.
Meet Cardiovascular Diabetology's Associate Editor of the Year - Dr Francesco Paneni
Like

Share this post

Choose a social network to share with, or copy the URL to share elsewhere

This is a representation of how your post may appear on social media. The actual post will vary between social networks

Ultimately, the most gratifying aspect [as Associate Editor of Cardiovascular Diabetology] is knowing that by improving how research is communicated and evaluated we accelerate progress that benefits patients with cardiometabolic disease and diabetes.

Congratulations on winning this year’s Cardiovascular Diabetology Associate Editor Award! What were your first thoughts when you learned that you won?

I was genuinely surprised and deeply honored to learn I had received this year’s Cardiovascular Diabetology Associate Editor Award! I have long believed in the journal’s mission as a leading platform for disseminating high quality research at the intersection of diabetes, obesity, and cardiovascular disease. Over the years I have invested considerable effort in launching new initiatives and special issues to highlight important topics within cardiometabolic medicine, diabetology and heart failure. I am very grateful for this recognition; it not only validates those efforts but also motivates me to continue strengthening the journal’s impact and supporting the community of researchers and clinicians it serves.

Please do introduce yourself.

I am Francesco Paneni, Professor of Cardiology at the Medical Faculty of the University of Zurich. I serve as Senior Cardiology Consultant and Head of the Cardiometabolic Division in the Department of Cardiology at Zurich University Hospital. I am also Director of the Center for Translational and Experimental Cardiology (CTEC) at Zurich University Hospital and Group Leader of the Cardiovascular Epigenetics Lab within CTEC.

Why did you choose this research area?

I chose this research area because it sits at the nexus of two of the most urgent health challenges of our time: metabolic disease and cardiovascular disease. Early in my career I became captivated by how metabolic disturbances - driven by lifestyle, environment and aging - reprogramme cells and organs, and by the striking observation that these changes often persist long after the initial trigger. That persistence pointed me toward epigenetic regulation as a fundamental mechanism linking exposures to lasting cardiometabolic risk. What excites me most is the combination of intellectual depth and real-world impact. This field requires mastering molecular biology, systems physiology, clinical science and data analytics, then bringing those disciplines together to understand causal pathways and translate discoveries into better prevention, diagnostics and therapies. We can move from observation to mechanism to intervention: identifying molecular fingerprints of risk, validating biomarkers in human cohorts, testing targets in experimental models and ultimately designing clinical trials that change care in cardiometabolic patients.

What is your vision what you’d like to achieve with your research/work?

My vision is to transform cardiometabolic medicine from symptom management to mechanism driven, precision care by making epigenetic insights actionable. In my clinic and lab we map the epigenetic changes that reprogram the heart, vasculature and immune system under metabolic stress, then validate those signatures in well phenotyped human cohorts to enable early detection and dynamic risk stratification. From these causal insights we pursue targeted interventions (i.e. epigenetic modulators, repurposed drugs, and combined metabolic lifestyle strategies) tested in translational models and early clinical studies. We integrate multi omics, imaging and clinical data with advanced analytics to build individualized treatment algorithms that predict response and guide timely intervention. By partnering across disciplines and with industry, we accelerate discoveries from bench to bedside.

How does a typical working day look like for you?

My days weave clinic and laboratory into a single, purposeful story. I move between patient rooms and microscopes with the same question in mind: how can what I see at the bedside be explained at the molecular level, and how can molecular insight change a life in front of me? Conversations with patients - their histories, worries and responses to therapy - spark hypotheses that I bring back to the lab. There, amid data, assays and animated discussions with students and colleagues, those hypotheses are sharpened into experiments and measurable outcomes. Mentoring and collaboration are constant threads: I learn from trainees’ fresh ideas, coordinate with bioinformaticians to make sense of complex datasets, and align with clinical teams to design studies that can reach patients. Writing grants and papers, designing trials and negotiating partnerships may feel less immediate than a patient consultation, but each is a strategic move to translate discovery into practice. By evening, the day’s threads converge: clinical observations refined by laboratory evidence, experiments oriented toward tangible clinical questions, and plans laid for the next step in moving a finding from bench to bedside. It’s a rhythm that keeps me rooted in patient care while driving the science that can change outcomes - and that balance is what makes the work deeply rewarding.

You have been working as Associate Editor for Cardiovascular Diabetology since 2022, what do you like about your work as Associate Editor for the journal?

Serving as Associate Editor for Cardiovascular Diabetology has been deeply rewarding. I value the opportunity to shape the scientific conversation at the interface of metabolism and cardiovascular disease by promoting rigorous, clinically relevant research. The role lets me support high quality science - identifying innovative studies, guiding authors to strengthen their work, and ensuring sound peer review - so findings reach clinicians and researchers who can apply them. I also appreciate the intellectual breadth: I read across basic, translational and clinical disciplines, which sharpens my own thinking and inspires new research directions. Mentoring authors and reviewers, fostering special issues and new initiatives, and helping the journal highlight emerging topics are all ways I contribute to advancing the field. Ultimately, the most gratifying aspect is knowing that by improving how research is communicated and evaluated we accelerate progress that benefits patients with cardiometabolic disease and diabetes.

Now that you’ve worked for 3 years on the journal, what was the most rewarding or challenging interaction/situation you had? 

After three years with the journal, the most rewarding moments have been when editorial work directly improved a paper’s clarity and impact - turning a promising but rather confusing manuscript into a crisp, clinically relevant contribution that advances the field. Those transformations, often achieved through constructive reviewer feedback and hands on guidance to authors, feel like true scholarship in service of patients. The most challenging situations involve balancing fairness and speed: handling borderline manuscripts where reviewers disagree, or urgent submissions with important clinical implications that require rapid yet rigorous assessment. Navigating these tensions - protecting scientific quality while minimizing delay - has taught me a lot about transparent communication and editorial judgment.

Has the journal work had any impact on your research or views?

Yes, my editorial work has meaningfully influenced both my research and my perspective. Reading broadly across submissions exposes me to emerging methods, novel hypotheses and diverse patient centered study designs that I might not encounter otherwise, which has directly inspired new experiments and collaborative projects. Evaluating manuscripts and peer reviews has sharpened my critical appraisal skills, improved how I frame research questions and strengthened study designs and reporting in my own group. The role also reinforced the value of rigorous, transparent science and clear communication: reproducibility, robust statistics, and translational relevance are non negotiable if findings are to change clinical practice. Finally, engaging with authors, reviewers and editors worldwide has broadened my view of priorities in cardiometabolic medicine and motivated me to align our work more closely with real world needs and implementation pathways.

Please sign in or register for FREE

If you are a registered user on Research Communities by Springer Nature, please sign in

Follow the Topic

Diabetes
Life Sciences > Health Sciences > Clinical Medicine > Diseases > Diabetes
Cardiovascular Diseases
Life Sciences > Health Sciences > Clinical Medicine > Diseases > Cardiovascular Diseases

Related Collections

With Collections, you can get published faster and increase your visibility.

Organoids as emerging models in diabetes and cardiovascular research

Organoids—three-dimensional structures derived from stem cells—are transforming biomedical research by modeling key aspects of human physiology and disease. By replicating native tissue architecture, cellular heterogeneity, and functional behavior, they provide human-relevant systems that address limitations inherent to conventional in-vitro and animal models.

Diabetes and cardiovascular disease are deeply interconnected conditions, characterized by shared, multi-organ pathophysiology. Organoid technologies offer unique opportunities to dissect disease mechanisms, evaluate therapeutic strategies, and develop personalized, physiologically relevant models. These systems enable the investigation of cardiometabolic processes in platforms that better reflect the complexity and progression of human disease.

Cardiovascular Diabetology welcomes original research articles, reviews, and meta-analyses for this Collection, which aims to highlight the use of organoid technologies in advancing our understanding of cardiovascular complications associated with diabetes.

Areas of interest include, but are not limited to:

- Organoid models of diabetic cardiomyopathy and heart failure

- Matrigel alternatives for organoid development

- Cell-cell and extracellular matrix interactions in organoids

- Organoid-based drug testing for cardiovascular diseases

- Organoid-on-chip systems for tissue crosstalk and perfusion3D bioprinting and tissue engineering for cardiovascular organoids

- Artificial intelligence–driven analysis of organoid function and phenotypes

- Organoid models of gestational diabetes–induced congenital heart disease

- Functional genomics using CRISPR in cardiovascular organoids

- Single-cell and spatial omics to map disease states in organoids

- Co-culture systems of vascular and pancreatic organoids to study metabolic-vascular crosstalk

- Organoid-based screening platforms for anti-diabetic and cardioprotective drugs

Submissions that contribute to conceptual clarity (e.g., distinctions between organoids and spheroids), incorporate multi-organ or metabolic system perspectives, or connect technological development with clinical or translational insights are especially welcome.

This Collection supports and amplifies research related to SDG 3, Good Health and Well-Being.

All submissions in this collection undergo the journal’s standard peer review process. Similarly, all manuscripts authored by a Guest Editor(s) will be handled by the Editor-in-Chief. As an open access publication, this journal levies an article processing fee (details here). We recognize that many key stakeholders may not have access to such resources and are committed to supporting participation in this issue wherever resources are a barrier. For more information about what support may be available, please visit OA funding and support, or email OAfundingpolicy@springernature.com or the Editor-in-Chief.

Publishing Model: Open Access

Deadline: Apr 07, 2026

Cardiometabolic and Hepatic Interconnections: From Mechanisms to Clinical Implications

Cardiometabolic and liver diseases are no longer viewed as isolated entities. Growing evidence shows that hepatic and cardiovascular dysfunctions are tightly interconnected through shared metabolic, inflammatory, hemodynamic, and hormonal pathways. This crosstalk shapes disease trajectories and opens opportunities for integrated diagnostics and therapies.

Key interconnections include:

- Insulin resistance. The liver is pivotal for glucose and lipid homeostasis. Hepatic insulin resistance drives excess glucose production and dyslipidemia, contributing to the cardiovascular–kidney–metabolic (CKM) syndrome.

- Metabolic dysfunction–associated steatotic liver disease (MASLD). Highly prevalent in obesity and metabolic syndrome, and especially common in type 2 diabetes (T2D), which bears the highest MASLD burden. Progression to steatohepatitis or fibrosis markedly increases atherosclerotic risk.

- Liver-derived factors. Hepatokines (e.g., FGF21) and extracellular vesicles influence cardiac tissue, vascular tone, and systemic metabolism, potentially amplifying inflammation, oxidative stress, and lipotoxicity across organs.

- Systemic inflammation and lipotoxicity. Visceral adipose tissue and the liver release inflammatory cytokines and triglyceride-rich lipids, promoting endothelial dysfunction and perpetuating metabolic disturbances.

- Dyslipidemia. Elevated triglycerides and LDL, with reduced HDL, accelerate atherogenesis and cardiovascular risk.

- Hemodynamic and metabolic stress. Heart failure can cause hepatic congestion and hypoperfusion, while advanced liver disease can precipitate cirrhotic cardiomyopathy and arrhythmias, even in the absence of prior heart failure.

In summary, hepatic and cardiometabolic systems are functionally and pathologically intertwined: liver dysfunction worsens cardiovascular and metabolic health, and cardiometabolic disturbances accelerate hepatic pathology.

This Collection welcomes original research articles, reviews, and meta-analyses focused on this reciprocal relationship. Given the high prevalence of MASLD in T2D, we especially encourage submissions at the T2D–MASLD–cardiovascular interface. Addressing hepatic and cardiometabolic health in parallel is essential for effective risk reduction and patient care.

This Collection supports and amplifies research related to SDG 3, Good Health and Well-Being.

All submissions in this Collection undergo the journal’s standard peer review process. Similarly, all manuscripts authored by a Guest Editor(s) will be handled by the Editor-in-Chief. As an open access publication, this journal levies an article processing fee (details here). We recognize that many key stakeholders may not have access to such resources and are committed to supporting participation in this issue wherever resources are a barrier. For more information about what support may be available, please visit OA funding and support, or email OAfundingpolicy@springernature.com or the Editor-in-Chief.

Publishing Model: Open Access

Deadline: Jul 15, 2026