Evidence mapPaperPMID 40427496Full record

ReviewAntioxidants (Basel, Switzerland)2025

Sex-Specific Antioxidant and Anti-Inflammatory Protective Effects of AMPK in Cardiovascular Diseases.

Lea Strohm, Dominika Mihalikova, Alexander Czarnowski, Zita Schwaibold, Andreas Daiber, Paul Stamm

Abstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Integrative phytochemical profiling andFrontiers in nutrition · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Lea StrohmDepartment of Cardiology, Cardiology I, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.
Dominika MihalikovaDepartment of Cardiology, Cardiology I, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.
Alexander CzarnowskiDepartment of Cardiology, Cardiology I, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.
Zita SchwaiboldDepartment of Cardiology, Cardiology I, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.
Andreas DaiberDepartment of Cardiology, Cardiology I, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.ORCID 0000-0002-2769-0094
Paul StammDepartment of Cardiology, Cardiology I, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.

Funding

Else Kröner-Fresenius-Stiftung 2022_EKEA.15 to Paul StammGerman Center for Cardiovascular Research (DZHK) continuous structural funding for Partnersite Rhine-Mainz, Mainz, Germany to Andreas Daiber
6 · The paper itself

Abstract

Cardiovascular diseases such as coronary heart disease, heart failure, or stroke are the most common cause of death worldwide and are regularly based on risk factors like diabetes mellitus, hypertension, or obesity. At the same time, both diseases and risk factors are significantly influenced by sex hormones. In order to better understand this influence and also specifically improve the therapy of female patients, medical research has recently focused increasingly on gender-specific differences. The goal is to develop personalized, gender-specific therapy concepts for these diseases to further enhance health outcomes. The enzyme adenosine monophosphate-activated protein kinase (AMPK) is a central regulator of energy metabolism, protecting the cardiovascular system from energy depletion, thereby promoting vascular health and preventing cellular damage. AMPK confers cardioprotective effects by preventing endothelial and vascular dysfunction, and by controlling or regulating oxidative stress and inflammatory processes. For AMPK, sex-specific effects were reported, influencing metabolic and cardiovascular responses. Exercise and metabolic stress generally cause higher AMPK activity in males. At the same time, females exhibit protective mechanisms against insulin resistance or oxidative stress, particularly in conditions like obesity. Additionally, males subject to AMPK deficiency seem to experience greater cardiac and mitochondrial dysfunction. In contrast, females show improvement in cardiovascular function after pharmacological AMPK activation. These differences, influenced by hormones, body composition, and gene expression, highlight the potential to develop personalized, sex-specific AMPK-targeted therapeutic strategies for cardiovascular diseases in the future. Here, we discuss the most actual scientific background, focusing on the protective, gender-specific effects of AMPK, and highlight potential clinical applications.

Indexed as

AMPKantioxidantcardiovascular diseasesoxidative stresssex-specific differences

Identifiers

PMID40427496
PMCPMC12108612

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.