Evidence map›Paper›PMID 35699189›Full record

ArticleJournal of the American Heart Association2022

Low-Density Lipoprotein Cholesterol Attributable Cardiovascular Disease Risk Is Sex Specific.

Arjen J Cupido, Folkert W Asselbergs, A Floriaan Schmidt, G Kees Hovingh

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
8.7field-weighted citation impact, top 1% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  6. Cardiovascular contributions to dementia: Examining sex differences and female-specific factors.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Review
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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

4 authors at 3 institutions in 3 countries.

Arjen J CupidoDepartment of Vascular Medicine Amsterdam University Medical Centerslocation AMCUniversity of Amsterdam Netherlands.ORCID 0000-0003-3300-8124
Folkert W AsselbergsDepartment of Cardiology Division of Heart & Lungs University Medical Center UtrechtUtrecht University Utrecht the Netherlands.ORCID 0000-0002-1692-8669
A Floriaan SchmidtDepartment of Cardiology Division of Heart & Lungs University Medical Center UtrechtUtrecht University Utrecht the Netherlands.ORCID 0000-0003-1327-0424
G Kees HovinghDepartment of Vascular Medicine Amsterdam University Medical Centerslocation AMCUniversity of Amsterdam Netherlands.ORCID 0000-0002-8145-1676
Utrecht University · NLAmsterdam University Medical Centers · NLUniversity of California, Los Angeles · US

Funding

Bioinformatics Strategies for Genome-Wide Association StudiesR01LM010098 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H., WILLIAMS, SCOTT MATTHEW · 2009 to 2023
$5.1M
British Heart Foundation AA/18/6/34223British Heart Foundation PG/18/50/33837British Heart Foundation PG/18/5033837Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NLM NIH HHS R01 LM010098
6 · The paper itself

Abstract

Background Epidemiological studies show that women are generally at lower risk for cardiovascular disease than men. Here, we investigated the sex-specific differential effect of genetically increased low-density lipoprotein cholesterol (LDL-C) on cardiovascular disease (CVD) and other lipid-associated diseases. Methods and Results This is a 2-sample Mendelian randomization study that uses individual participant data from 425 043 participants from the UK Biobank, including 229 279 female participants. An 80-variant LDL-C weighted genetic score was generated. Linear and logistic regression models with interactions were used to identify differences between sex-specific LDL-C effects on lipids, carotid-intima media thickness, and multiple cardiovascular outcomes such as CVD, ischemic heart disease, peripheral artery disease, heart failure, aortic valve disease, type 2 diabetes, atrial fibrillation, and aortic aneurysm and dissection. After correction for multiple testing, we observed that the genetically increased LDL-C effect on CVD events was sex specific: per SD genetically increased LDL-C, female participants had a higher LDL-C increase but an attenuated CVD risk increase compared with male participants (LDL-C: female participants 0.71 mmol/L, 95% CI, 0.70-0.72 and male participants 0.57 mmol/L, 95% CI, 0.56-0.59.

Indexed as

Aortic Valve StenosisCardiovascular DiseasesDiabetes Mellitus, Type 2Heart FailureMyocardial IschemiaCarotid Intima-Media ThicknessCholesterol, HDLCholesterol, LDLFemaleHumansMaleRisk FactorsCholesterol, HDLCholesterol, LDLcardiovascular diseasegeneticsrisk factorsex‐differences

Identifiers

PMID35699189
PMCPMC9238661
OpenAlexW4282838906

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.