Evidence map›Paper›PMID 42652249›Full record

ReviewBiomedicines2026

Non-Pharmacological Strategies in Atherosclerotic Cardiovascular Disease: From Molecular Mechanisms to Clinical Integration.

Tatyana I Kovyanova, Maria O Nerush, Vasily P Karagodin, Daria D Borodko, Ulyana V Rozhkova, Stanislav A Antonov, Aleksandra S Utkina

Abstract readReview
In one paragraph

Review in Biomedicines, 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

7 authors.

Tatyana I KovyanovaInstitute for Atherosclerosis Research, 4-1-207 Osennyaya Street, 121609 Moscow, Russia.
Maria O NerushScientific and Educational Center for Molecular and Cellular Technologies, St. Petersburg Chemical Federal University, 21 Rentgen Street, 197101 St. Petersburg, Russia.
Vasily P KaragodinInstitute of General Pathology and Pathophysiology, 8 Baltiiskaya Street, 125315 Moscow, Russia.ORCID 0000-0003-0501-8499
Daria D BorodkoLaboratory of Molecular Genetic Modeling of Inflammaging, Institute of General Pathology and Pathophysiology, 8 Baltiiskaya Street, 125315 Moscow, Russia.ORCID 0000-0003-3596-5470
Ulyana V RozhkovaInstitute for Atherosclerosis Research, 4-1-207 Osennyaya Street, 121609 Moscow, Russia.
Stanislav A AntonovLaboratory of Molecular Genetic Modeling of Inflammaging, Institute of General Pathology and Pathophysiology, 8 Baltiiskaya Street, 125315 Moscow, Russia.ORCID 0000-0002-6866-7077
Aleksandra S UtkinaDepartment of Commodity Expertise and Customs Business, Plekhanov Russian University of Economics, 36 Stremyanny Lane, 115054 Moscow, Russia.

Funding

Russian Science Foundation 26-15-00011
6 · The paper itself

Abstract

Atherosclerotic cardiovascular disease (ASCVD) remains the leading cause of morbidity and mortality worldwide, driven by complex interactions among dyslipidemia, chronic inflammation, insulin resistance, endothelial dysfunction, and gut microbiome-derived metabolites. This review synthesizes mechanistic and clinical evidence on non-pharmacological strategies that modulate these pathways and contribute to ASCVD risk reduction. Dietary patterns such as Mediterranean, DASH, and plant-based diets improve lipid metabolism, attenuate inflammation, and enhance endothelial function. Chrononutrition approaches, including time-restricted feeding and structured fasting protocols, influence circadian regulation of glucose and lipid homeostasis. Circadian misalignment-including irregular sleep timing, shift work, and disrupted feeding-fasting cycles-independently contributes to ASCVD through impaired glucose tolerance, dyslipidemia, endothelial dysfunction, and systemic inflammation. Modulation of the gut microbiome, particularly through increased short-chain fatty acid production and reduced TMAO formation, provides additional cardiometabolic benefits. Key nutraceuticals-phytosterols, omega-3 fatty acids, and berberine-demonstrate clinically meaningful effects through micellar competition, inflammation-resolving lipid mediators, and AMPK activation, respectively. When combined with evidence-based pharmacotherapy, these interventions exert synergistic effects on cardiometabolic risk factors. This integrative biomedical framework highlights the importance of combining lifestyle, metabolic, microbiome-targeted, and nutraceutical strategies for comprehensive ASCVD prevention.

Indexed as

atherosclerotic cardiovascular disease (ASCVD)berberinecardiometabolic riskdietary patternsinflammationlifestyle interventionslipid metabolismnutraceuticalsOmega-3 fatty acids

Identifiers

PMID42652249
PMCPMC13510202

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.