Evidence mapPaperPMID 41758439Full record

ReviewCurrent atherosclerosis reports2026

Upfront Combination or Stepwise Escalation: Personalising LDL-C Reduction in Clinical Practice.

Angela Pirillo, Alberico L Catapano

Abstract readReview
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In one paragraph

Review in Current atherosclerosis reports, 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

2 authors.

Angela PirilloCenter for the Study of Atherosclerosis, E. Bassini Hospital, Via Gorki 50, Cinisello Balsamo, Milan, 20092, Italy.ORCID http://orcid.org/0000-0002-2948-6257
Alberico L CatapanoCenter for the Study of Atherosclerosis, IRCCS MultiMedica, Via Milanese 300, Sesto S. Giovanni, Milan, 20099, Italy. alberico.catapano@unimi.it.ORCID http://orcid.org/0000-0002-7593-2094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewLow-density lipoprotein cholesterol (LDL-C) reduction is central to the prevention of atherosclerotic cardiovascular disease. This review examines the evolving shift from goal-oriented lipid management toward an approach that prioritises the magnitude and timing of LDL-C reduction, focusing on the comparative roles of stepwise escalation and upfront combination therapy. RECENT

findingsEvidence from randomised clinical trials confirms that incremental LDL-C reductions lead to proportional reductions in cardiovascular events, supporting the principles that “lower is better” and “earlier is better.” The concept of cumulative LDL-C burden further highlights the importance of early and sustained LDL-C lowering. Upfront combination therapy, typically combining statins with ezetimibe, bempedoic acid, and, when indicated, proprotein convertase subtilisin/kexin type 9 inhibitors, achieves faster and greater LDL-C reductions than statin monotherapy and improves attainment of guideline-recommended goals, particularly in very high-risk patients. Conversely, while guideline-endorsed, the traditional stepwise approach may delay optimal LDL-C reduction due to reassessment intervals and therapeutic inertia, prolonging exposure to atherogenic lipoproteins in high-risk patients. Stepwise escalation remains appropriate for patients at low to moderate cardiovascular risk, those with modest LDL-C elevations, concerns about tolerability, or where cost and access limit early use of non-statin agents. Upfront combination therapy is an effective strategy for rapid LDL-C reduction in patients at high or very high cardiovascular risk, whereas a stepwise approach remains suitable for lower-risk individuals. Optimal lipid management requires an individualised strategy that integrates cardiovascular risk, baseline LDL-C, safety, adherence, and health system considerations, rather than rigid adherence to a single therapeutic goal.

Indexed as

Anticholesteremic AgentsAtherosclerosisCardiovascular DiseasesCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorsPrecision MedicineDicarboxylic AcidsDrug Therapy, CombinationEzetimibeFatty AcidsHumansPCSK9 Inhibitors8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acidAnticholesteremic AgentsCholesterol, LDLDicarboxylic AcidsEzetimibeFatty AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsPCSK9 InhibitorsAtherosclerotic cardiovascular disease preventionCumulative LDL-C burdenLDL-C reductionStepwise lipid-lowering escalationUpfront combination lipid therapy

Identifiers

What Socratic holds

Texttitle and abstract
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.