Evidence map›Paper›PMID 38252350›Full record

ArticleMolecular biology reports2024

Cholesterol associated genetic risk score and acute coronary syndrome in Czech males.

Jaroslav A Hubacek, Vera Adamkova, Vera Lanska, Vladimir Staněk, Jolana Mrázková, Marie Gebauerová, Jiri Kettner, Josef Kautzner, Jan Pitha

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 2 institutions in 1 country.

Jaroslav A HubacekExperimental Medicine Centre, Institute for Clinical and Experimental Medicine, IKEM-CEM-LMG, Videnska 1958/9, 140 21, Prague 4, Czech Republic. jahb@ikem.cz.ORCID http://orcid.org/0000-0001-6537-1353
Vera AdamkovaPreventive Cardiology Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Vera LanskaInformation Technology Division, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Vladimir StaněkCardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Jolana MrázkováExperimental Medicine Centre, Institute for Clinical and Experimental Medicine, IKEM-CEM-LMG, Videnska 1958/9, 140 21, Prague 4, Czech Republic.
Marie GebauerováCardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Jiri KettnerCardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Josef KautznerCardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Jan PithaExperimental Medicine Centre, Institute for Clinical and Experimental Medicine, IKEM-CEM-LMG, Videnska 1958/9, 140 21, Prague 4, Czech Republic.
Institute of Clinical and Experimental Medicine · CZCharles University · CZ

Funding

Ministerstvo Zdravotnictví Ceské Republiky 00023001next generation EU LX22NPO5104
6 · The paper itself

Abstract

backgroundDespite a general decline in mean levels across populations, LDL-cholesterol levels remain a major risk factor for acute coronary syndrome (ACS). The APOB, LDL-R, CILP, and SORT-1 genes have been shown to contain variants that have significant effects on plasma cholesterol levels. METHODS AND

resultsWe examined polymorphisms within these genes in 1191 controls and 929 patients with ACS. Only rs646776 within SORT-1 was significantly associated with a risk of ACS (P < 0.05, AA vs. + G comparison; OR 1.21; 95% CI 1.01-1.45). With regard to genetic risk score (GRS), the presence of at least 7 alleles associated with elevated cholesterol levels was connected with increased risk (P < 0.01) of ACS (OR 1.26; 95% CI 1.06-1.52). Neither total mortality nor CVD mortality in ACS subjects (follow up-9.84 ± 3.82 years) was associated with the SNPs analysed or cholesterol-associated GRS.

conclusionsWe conclude that, based on only a few potent SNPs known to affect plasma cholesterol, GRS has the potential to predict ACS risk, but not ACS associated mortality.

Indexed as

Acute Coronary SyndromeGenetic Risk ScoreCholesterolCzech RepublicHumansMalePolymorphism, Single NucleotideCholesterolAcute coronary syndromeCholesterolPolymorphismRisk estimation

Identifiers

PMID38252350
PMCPMC10803395
OpenAlexW4391103258

What OpenQuestion 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 OpenQuestion graph.