Evidence map›Paper›PMID 40999979›Full record

ReviewMolecular medicine reports2025

Small dense LDL: An underestimated driver of atherosclerosis (Review).

Makhabbat Bekbossynova, Timur Saliev, Tatyana Ivanova-Razumova, Saltanat Andossova, Aknur Kali, Gulzhan Myrzakhmetova

Abstract readReview
In one paragraph

Review in Molecular medicine reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. NLRP3 Inflammasome Activation and Atherogenic Lipid Profile in Hemodialysis Patients.Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy · 2026
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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.

Makhabbat BekbossynovaHeart Center, University Medical Center, Nazarbayev University, Astana 010000, Kazakhstan.
Timur SalievInstitute of Fundamental and Applied Medical Research, S.D. Asfendiyarov Kazakh National Medical University, Almaty 050000, Kazakhstan.
Tatyana Ivanova-RazumovaHeart Center, University Medical Center, Nazarbayev University, Astana 010000, Kazakhstan.
Saltanat AndossovaHeart Center, University Medical Center, Nazarbayev University, Astana 010000, Kazakhstan.
Aknur KaliHeart Center, University Medical Center, Nazarbayev University, Astana 010000, Kazakhstan.
Gulzhan MyrzakhmetovaHeart Center, University Medical Center, Nazarbayev University, Astana 010000, Kazakhstan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular disease remains the leading cause of death globally, despite advances in lipid‑lowering strategies. A distinct subfraction of low‑density lipoprotein (LDL) particles, known as small LDL (sdLDL; particle size, 15‑20 nm), has been found to play a disproportionately large role in atherogenesis and residual cardiovascular risk when present at elevated concentrations, particularly in individuals with normocholesterolemia but underlying metabolic disorders. The present review critically examines the pathophysiological characteristics that render sdLDL highly atherogenic. These include increased permeability, prolonged circulation and heightened susceptibility to oxidative modification. The review also explores how sdLDL promotes endothelial dysfunction, foam cell formation, inflammation and plaque instability. Furthermore, it emphasizes the diagnostic challenges of sdLDL measurement, its clinical relevance in high‑risk populations and the limitations of current lipid panels in capturing its contribution to disease progression. Elevated sdLDL levels are commonly observed among individuals with metabolic syndrome, insulin resistance, type 2 diabetes and obesity. Multiple epidemiological studies indicate that elevated sdLDL levels are an independent predictor of cardiovascular events. Targeted lifestyle and pharmacological strategies to reduce sdLDL levels are also reviewed, including statins, fibrates, niacin, w‑3 fatty acids, proprotein convertase subtilisin/kexin type 9 inhibitors and RNA‑targeting agents. The greater incorporation of sdLDL testing into risk assessment tools and clinical guidelines is recommended, and strategies for advancing diagnostics, including artificial intelligence‑driven prediction models and advanced lipid profiling are proposed.

Indexed as

AtherosclerosisLipoproteins, LDLAnimalsBiomarkersHumansBiomarkersLipoproteins, LDLatherogenesiscardiovascular riskdiabetesinflammationoxidative stresssmall dense low‑density lipoprotein

Identifiers

PMID40999979
PMCPMC12512508

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.