Evidence map›Paper›PMID 42980097›Full record

ReviewClinical science (London, England : 1979)2026

Tick tock: how the body's circadian clock keeps cardiometabolic rhythm in check.

Masaaki Sato, Abdulaziz M A Alammar, Frédéric Gachon, Daniel Mauvoisin, Denuja Karunakaran

Abstract readReview
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In one paragraph

Review in Clinical science (London, England : 1979), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Masaaki Sato *Cardiometabolic Immunity Laboratory, Department of Physiology, Cardiovascular Disease and Metabolism, Diabetes & Obesity Programs, Biomedicine Discovery Institute (BDI) and Victorian Heart Institute (VHI), Monash University, Level 2, Victorian Heart Hospital, 631 Blackburn Road, Clayton, Victoria 3168, Australia.
Abdulaziz M A Alammar *Cardiometabolic Immunity Laboratory, Department of Physiology, Cardiovascular Disease and Metabolism, Diabetes & Obesity Programs, Biomedicine Discovery Institute (BDI) and Victorian Heart Institute (VHI), Monash University, Level 2, Victorian Heart Hospital, 631 Blackburn Road, Clayton, Victoria 3168, Australia.ORCID 0009-0009-6960-5896
Frédéric GachonDepartment of Biomedicine, Aarhus University, Høegh-Guldbergs Gade 10, 8000 Aarhus C, Denmark.ORCID 0000-0002-9279-9707
Daniel MauvoisinNantes Université, CNRS, Inserm, l'institut du thorax, F-44000 Nantes, France.ORCID 0000-0003-0571-0741
Denuja KarunakaranCardiometabolic Immunity Laboratory, Department of Physiology, Cardiovascular Disease and Metabolism, Diabetes & Obesity Programs, Biomedicine Discovery Institute (BDI) and Victorian Heart Institute (VHI), Monash University, Level 2, Victorian Heart Hospital, 631 Blackburn Road, Clayton, Victoria 3168, Australia.ORCID 0000-0002-4789-8634

Funding

DHAC | National Health and Medical Research Council (NHMRC) 2012772French National Research Agency ANR-16-IDEX-0007Novo Nordisk Foundation Center for Basic Metabolic Research (NovoNordisk Foundation Center for Basic Metabolic Research) 0087882
6 · The paper itself

Abstract

The circadian clock orchestrates the internal timing of numerous physiological processes through an approximately 24-h cycle. It comprises a hypothalamic central clock, which responds to light cues and entrains peripheral clocks within individual cells and organs that, depending on the tissue, regulate gene expression across diverse biological functions in a tissue-specific manner. Peripheral clocks are also entrained by feeding and exercise-related cues, enabling their synchronization with feeding rhythm and physiology. Together, these clocks maintain a complex molecular network essential for metabolic homeostasis. Disruption of circadian rhythms, driven by genetic, environmental, or behavioral factors, is increasingly recognized as a major contributor to cardiometabolic disorders. Modern lifestyles, including shift work, irregular sleep, prolonged exposure to artificial light at night, jet lag, and erratic eating schedules, misalign circadian clocks with environmental cues, contributing to disruption of circadian rhythms or chronodisruption. This misalignment alters hormonal regulation, promotes systemic inflammation, and impairs metabolic balance, thereby increasing the risk of cardiovascular disease, obesity, type 2 diabetes, and related complications. The present review examines the mechanistic roles of core circadian clock genes in cardiometabolic health, highlighting their regulation of physiological processes in peripheral organs such as the heart, liver, and adipose tissue. We further discuss how circadian clock disruption accelerates disease onset and progression and explore emerging therapeutic strategies, including pharmacological modulation of the molecular circadian clock components and personalized chronotherapy. These approaches offer promising avenues to restore circadian alignment and mitigate cardiometabolic risk.

Indexed as

Cardiovascular DiseasesCircadian ClocksCircadian RhythmAnimalsHumanscardiometabolic diseaseschronobiologychronodisruptionchronotherapeuticscircadian rhythmsclock genes

Identifiers

PMID42980097

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.