Polygenic hypercholesterolemia: examples of GWAS results and their replication in the Czech-Slavonic population
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
28379035
DOI
10.33549/physiolres.933580
PII: 933580
Knihovny.cz E-resources
- MeSH
- Genome-Wide Association Study methods MeSH
- Adult MeSH
- Hypercholesterolemia blood epidemiology genetics MeSH
- Polymorphism, Single Nucleotide genetics MeSH
- Cholesterol, LDL blood genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Multifactorial Inheritance genetics MeSH
- Population Surveillance * methods MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic epidemiology MeSH
- Slovakia epidemiology MeSH
- Names of Substances
- Cholesterol, LDL MeSH
Since 2007, the year of their first widespread use, genome-wide association studies (GWAS) have become the "gold standard" for the detection of causal genes and polymorphisms in all fields of human medicine. Cardiovascular disease (CVD), one of the major causes of morbidity and mortality, is no exception. The first GWAS focused on hypercholesterolemia and dyslipidemia as the major CVD determinants. GWAS confirm the importance of most of the previously identified genes (e.g. APOE, APOB, LDL-R) and recognize the importance of new genetic determinants (e.g. within the CILP2 or SORT1 gene clusters). Nevertheless, the results of GWAS still require confirmation by independent studies, as interethnic and interpopulation variability of SNP effects have been reported. We analyzed an association between eight variants within seven through GWAs detected loci and plasma lipid values in the Czech post-MONICA population sample (N=2,559). We confirmed an association (all P<0.01) between plasma LDL-cholesterol values and variants within the CILP2 (rs16996148), SORT1 (rs646776), APOB (rs693), APOE (rs4420638) and LDL-R (rs6511720) genes in both males (N=1,194) and females (N=1,368). In contrast, variants within the APOB (rs515135), PCSK9 (rs11206510) and HMGCoAR (rs12654264) genes did not significantly affect plasma lipid values in Czech males or females. Unweighted gene score values were linearly associated with LDL-cholesterol values both in males (P<0.0005) and females (P<0.00005). We confirmed the effects of some, but not all analyzed SNPs on LDL-cholesterol levels, reinforcing the necessity for replication studies of GWA-detected gene variants.
References provided by Crossref.org
Cholesterol associated genetic risk score and acute coronary syndrome in Czech males
Genetics of Familial Hypercholesterolemia: New Insights
Global DNA methylation in rats´ liver is not affected by hypercholesterolemic diet
The Gene Score for Predicting Hypertriglyceridemia: New Insights from a Czech Case-Control Study