Evidence map›Paper›PMID 41169880›Full record

ReviewFrontiers in cardiovascular medicine2025

Innovative molecular intervention and precision therapy for atherosclerosis.

Zhijie Wang, Wei Peng, Linsheng Huang, Yan Zhang, Jie Yang, Xiaolin Chen, Xiang Liu, Feifeng Li, Qiong Zhang

Abstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Identification of a peptide inhibitor disrupting the PCSK9-LDLR interactionJournal of enzyme inhibition and medicinal chemistry · 2026
    Article
  2. Review
  3. Review
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

9 authors.

Zhijie WangHubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, China.
Wei PengDepartment of Preventive Medicine, School of Public Health, Hubei University of Medicine, Shiyan, China.
Linsheng HuangDepartment of Hepatobiliary Pancreatic Surgery, Taihe Hospital, Hubei University of Medicine, Shiyan, China.
Yan ZhangHealth Management Center, Shiyan Renmin Hospital, Hubei University of Medicine, Shiyan, China.
Jie YangHealth Management Center, Shiyan Renmin Hospital, Hubei University of Medicine, Shiyan, China.
Xiaolin ChenDepartment of Preventive Medicine, School of Public Health, Hubei University of Medicine, Shiyan, China.
Xiang LiuHealth Management Center, Shiyan Renmin Hospital, Hubei University of Medicine, Shiyan, China.
Feifeng LiDepartment of Preventive Medicine, School of Public Health, Hubei University of Medicine, Shiyan, China.
Qiong ZhangHubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Shiyan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerosis is a chronic vascular disorder characterized by the pathological accumulation of lipids, inflammatory cells, and extracellular matrix within arterial walls. With the escalating global incidence of atherosclerosis, the development of more effective therapeutic interventions has emerged as a critical priority in biomedical research. Conventional treatment modalities, encompassing pharmacological agents and, endovascular interventions, have demonstrated partial efficacy in disease management. However, their clinical utility remains constrained by suboptimal therapeutic outcomes, treatment-related adverse effects, and instances of therapeutic failure. In response to these limitations, contemporary research has shifted focus toward novel therapeutic strategies targeting molecular pathways and immunomodulatory mechanisms, aiming to achieve enhanced precision and efficacy. This review synthesizes recent innovations in atherosclerosis therapeutics. Notable advancements include PCSK9 inhibitors and next-generation lipid-modulating agents, which have shown significant promise in clinical trials by achieving substantial reductions in atherogenic lipoprotein levels. Gene-editing technologies, particularly CRISPR-based approaches, exhibit potential for halting disease progression through targeted modulation of pro-atherogenic genes. Furthermore, emerging insights into the regulatory role of microRNAs in atherosclerotic plaque formation and instability have positioned miRNA-based therapeutics as a compelling frontier in precision medicine for cardiovascular diseases.

Indexed as

atherosclerosisMSCsnanoparticlesPCSK9statin

Identifiers

PMID41169880
PMCPMC12570097

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.