Evidence map›Paper›PMID 41473015›Full record

ArticleAmerican journal of preventive cardiology2025

Time in LDL cholesterol target range and major adverse cardiovascular events risk: A pooled analysis of two cohorts.

Yezhou Liu, Zhe Lv, Hong Yan, Yamei Liu, Jiaheng Zhang, Wenming Bian, Yetong Liu, Zhaojie Song, Peng Han, Tao Chen and 1 more

Abstract read
In one paragraph

Article in American journal of preventive cardiology, 2025. 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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0citing papers in PubMed
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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

11 authors.

Yezhou LiuDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Zhe LvDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Hong YanDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Yamei LiuDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Jiaheng ZhangDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Wenming BianDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Yetong LiuDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Zhaojie SongDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Peng HanDepartment of Otolaryngology-Head and Neck Surgery, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Tao ChenDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Chao LiDepartment of Epidemiology and Health Statistics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Traditional management of low-density lipoprotein cholesterol (LDL-C) relies on single-point measurements, neglecting long-term magnitude and the duration of exposure to elevated LDL-C over time. This study aimed to evaluate the association between LDL-C time in target range (TTR) and the risk of major adverse cardiovascular events (MACE) in two US cohorts. Methods: This study was a secondary analysis of the Atherosclerosis Risk in Communities (ARIC) study and the Multi-Ethnic Study of Atherosclerosis (MESA) cohorts. LDL-C TTR was defined as the percentage of the area under curve for LDL-C values below 100 mg/dL relative to the total area over the first 4 visits. Association between LDL-C TTR and MACE was estimated using adjusted Cox models and Fine-Gray competing risk models. Results: Over a mean follow-up of 21.2 ± 8.1 years, 3306 MACE occurred among 16,310 participants. The highest LDL-C TTR quartile was associated with a 25 % reduction in MACE (HR: 0.75, 95 % CI: 0.68 to 0.83), 42 % reduction in myocardial infarction (HR: 0.58, 95 % CI: 0.49 to 0.68), 24 % reduction in stroke (HR: 0.76, 95 % CI: 0.64 to 0.91), and 13 % reduction in CVD death (HR: 0.87, 95 % CI: 0.76 to 1.00; borderline significance). TTR remained significantly associated with MACE after adjusting for mean LDL-C or LDL-C variability, and were robust in competing risk analyses. TTR also outperformed mean LDL-C and LDL-C variability in prognostic value (Akaike information criterion, C-statistics). Conclusions: LDL-C TTR independently predicts MACE and may offer a more comprehensive assessment of long-term LDL-C control than mean levels or variability, supporting its potential clinical utility.

Indexed as

Cardiovascular deathLow-density lipoproteinMajor adverse cardiovascular eventsMyocardial infarctionStrokeTime in target range

Identifiers

PMID41473015
PMCPMC12746287

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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 OpenQuestion graph.