Evidence map›Paper›PMID 37119078›Full record

ArticleJournal of the American Heart Association2023

Association of Multitrajectories of Lipid Indices With Premature Cardiovascular Disease: A Cohort Study.

Xue Tian, Shuohua Chen, Penglian Wang, Yijun Zhang, Xiaoli Zhang, Qin Xu, Shouling Wu, Anxin Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

8 authors at 2 institutions in 1 country.

Xue TianDepartment of Neurology Beijing Tiantan Hospital, Capital Medical University Beijing China.
Shuohua ChenDepartment of Cardiology, Kailuan Hospital North China University of Science and Technology Tangshan China.ORCID 0000-0002-6274-7471
Penglian WangDepartment of Neurology Beijing Tiantan Hospital, Capital Medical University Beijing China.
Yijun ZhangDepartment of Neurology Beijing Tiantan Hospital, Capital Medical University Beijing China.
Xiaoli ZhangDepartment of Neurology Beijing Tiantan Hospital, Capital Medical University Beijing China.
Qin XuDepartment of Neurology Beijing Tiantan Hospital, Capital Medical University Beijing China.ORCID 0000-0002-8039-709X
Shouling WuDepartment of Cardiology, Kailuan Hospital North China University of Science and Technology Tangshan China.ORCID 0000-0001-7095-6022
Anxin WangDepartment of Neurology Beijing Tiantan Hospital, Capital Medical University Beijing China.ORCID 0000-0003-4351-2877
Capital Medical University · CNNorth China University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background The multitrajectory model can identify joint longitudinal patterns of different lipids simultaneously, which might help better understand the heterogeneous risk of premature cardiovascular disease (CVD) and facilitate targeted prevention programs. This study aimed to investigate the associations between multitrajectories of lipids with premature CVD. Methods and Results The study enrolled 78 526 participants from the Kailuan study, a prospective cohort study in Tangshan, China. Five distinct multitrajectories of triglyceride, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol over 6-year exposure were identified on the basis of Nagin's criteria, using group-based multitrajectory modeling. During a median follow-up of 6.75 years (507 645.94 person-years), 665 (0.85%) premature CVDs occurred. After adjustment for confounders, the highest risk of premature CVD was observed in group 4 (the highest and increasing triglyceride, optimal and decreasing LDL-C, low and decreasing high-density lipoprotein cholesterol) (hazard ratio [HR], 2.13 [95% CI, 1.36-3.32]), followed by group 5 (high and decreasing triglyceride, optimal and increasing LDL-C, low and decreasing high-density lipoprotein cholesterol) (HR, 2.07 [95% CI, 1.45-2.98]), and group 3 (optimal and increasing triglyceride, borderline high and increasing LDL-C, optimal and decreasing high-density lipoprotein cholesterol) (HR, 1.90 [95% CI, 1.32-2.73]). Conclusions Our results showed that the residual risk of premature CVD caused by increasing triglyceride levels remained high despite the fact that LDL-C levels were optimal or declining over time. These findings emphasized the importance of assessing the joint longitudinal patterns of lipids and undertaking potential interventions on triglyceride lowering to reduce the residual risk of premature CVD, even among individuals with optimal LDL-C levels.

Indexed as

Cardiovascular DiseasesHydroxymethylglutaryl-CoA Reductase InhibitorsCholesterol, HDLCholesterol, LDLCohort StudiesHumansProspective StudiesRisk FactorsTriglyceridesCholesterol, HDLCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorsTriglyceridescohort studylipidsmultitrajectorypremature cardiovascular diseaseresidual risk

Identifiers

PMID37119078
PMCPMC10227234
OpenAlexW4367368294

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC
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 OpenQuestion graph.