APOL1 polymorphisms are not influencing acute coronary syndrome risk in Czech males
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
Grantová podpora
00023001
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
39171649
PubMed Central
PMC11339648
DOI
10.1002/mgg3.2449
Knihovny.cz E-zdroje
- Klíčová slova
- Caucasians, apolipoprotein L1, cardiovascular disease, mortality, polymorphism,
- MeSH
- akutní koronární syndrom * genetika MeSH
- apolipoprotein L1 * genetika MeSH
- apolipoproteiny genetika MeSH
- běloši genetika MeSH
- genetická predispozice k nemoci MeSH
- haplotypy MeSH
- jednonukleotidový polymorfismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipoproteiny HDL genetika MeSH
- rizikové faktory MeSH
- senioři MeSH
- studie případů a kontrol MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- APOL1 protein, human MeSH Prohlížeč
- apolipoprotein L1 * MeSH
- apolipoproteiny MeSH
- lipoproteiny HDL MeSH
BACKGROUND: The highest mortality and morbidity worldwide is associated with atherosclerotic cardiovascular disease (ASCVD), which has in background both environmental and genetic risk factors. Apolipoprotein L1 (APOL1) variability influences the risk of ASCVD in Africans, but little is known about the APOL1 and ASCVD in other ethnic groups. METHODS: To investigate the role of APOL1 and ASCVD, we have genotyped four (rs13056427, rs136147, rs10854688 and rs9610473) APOL1 polymorphisms in a group of 1541 male patients with acute coronary syndrome (ACS) and 1338 male controls. RESULTS: Individual APOL1 polymorphisms were not associated with traditional CVD risk factors such as smoking, hypertension or diabetes prevalence, with BMI values or plasma lipid levels. Neither individual polymorphisms nor haplotypes were associated with an increased risk of ACS nor did they predict total or cardiovascular mortality over the 10.2 ± 3.9 years of follow-up. CONCLUSIONS: We conclude that APOL1 genetic variability has no major effect on risk of ACS in Caucasians.
3rd Department of Internal Medicine 1st Faculty of Medicine Charles University Prague Czech Republic
Cardiology Department Institute for Clinical and Experimental Medicine Prague Czech Republic
Department of Informatics Institute for Clinical and Experimental Medicine Prague Czech Republic
Experimental Medicine Centre Institute for Clinical and Experimental Medicine Prague Czech Republic
Preventive Cardiology Centre Institute for Clinical and Experimental Medicine Prague Czech Republic
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