Evidence map›Paper›PMID 42719277›Full record

ArticleCardiovascular diagnosis and therapy2026

Long-term high-sensitivity C-reactive protein trajectories and risk of major adverse cardiovascular events in statin-treated patients: a retrospective cohort.

Qin Ma, Shaoping Wang, Hua Chen

Abstract read
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Article in Cardiovascular diagnosis and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Qin MaDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0009-0000-2329-4732
Shaoping WangDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-2902-7376
Hua ChenDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0009-0001-1635-5469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: High-sensitivity C-reactive protein (hs-CRP) is a key inflammatory marker in atherosclerosis; however, the association between its long-term patterns and cardiovascular prognosis under statin therapy remains incompletely understood. This study characterized hs-CRP trajectories and their prognostic value for MACE in statin users, aiming to refine risk assessment and tailored therapy. Methods: We conducted a retrospective cohort study at the Center for Coronary Artery Disease, Beijing Anzhen Hospital, Capital Medical University (Beijing, China), using data from patients who received statin therapy for at least 12 months between January 2023 and December 2024. Eligible participants had three or more hs-CRP measurements and were free from major adverse cardiovascular events (MACEs) six months before enrollment. Latent class growth modeling was applied to categorize hs-CRP trajectories. The primary composite outcome included cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or rehospitalization for unstable angina. Event-free survival was compared across trajectory groups using Kaplan-Meier curves with log-rank testing. Multivariable Cox proportional hazards regression evaluated the association between hs-CRP trajectories and MACE, with adjustments for age, sex, hypertension, diabetes, baseline lipids, and statin intensity. Results: This study included 210 patients with a median follow-up of 11.9 months. Latent class growth modeling identified three distinct hs-CRP trajectories: persistently low (45.2%, <2 mg/L), moderately fluctuating (40.0%, 2-5 mg/L), and persistently high (14.8%, ≥5 mg/L). Over follow-up, 38 patients (18.1%) experienced a MACE. Kaplan-Meier analysis revealed significantly higher cumulative MACE incidence in persistently high compared to persistently low (38.7% Conclusions: Statin-treated patients with rising hs-CRP levels face elevated MACE risk. Longitudinal patterns show prognostic promise but need validation in future trials.

Indexed as

high-sensitivity C-reactive protein (hs-CRP)major adverse cardiovascular events (MACEs)retrospective cohort studyStatinstrajectory

Identifiers

PMID42719277
PMCPMC13554320

What Socratic 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 Socratic graph.