dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Casares-Marfil, Desiré |
dc.contributor.author | Kerick, Martin |
dc.contributor.author | Andrés-León, Eduardo |
dc.contributor.author | Bosch Nicolau, Pau |
dc.contributor.author | Chagas Genetics CYTED Network |
dc.contributor.author | Molina Romero, Israel |
dc.date.accessioned | 2022-05-12T11:14:23Z |
dc.date.available | 2022-05-12T11:14:23Z |
dc.date.issued | 2021-10-29 |
dc.identifier.citation | Casares-Marfil D, Kerick M, Andrés-León E, Bosch-Nicolau P, Molina I, Chagas Genetics CYTED Network, et al. GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels. PLoS Negl Trop Dis. 2021 Oct 29;15(10):e0009874. |
dc.identifier.issn | 1935-2735 |
dc.identifier.uri | https://hdl.handle.net/11351/7517 |
dc.description | Cardiomyopathies; Genomics; Chagas disease |
dc.description | Cardiomiopatías; Genómica; Enfermedad de Chagas |
dc.description.abstract | A recent genome-wide association study (GWAS) identified a locus in chromosome 11 associated with the chronic cardiac form of Chagas disease. Here we aimed to elucidate the potential functional mechanism underlying this genetic association by analyzing the correlation among single nucleotide polymorphisms (SNPs) and DNA methylation (DNAm) levels as cis methylation quantitative trait loci (cis-mQTL) within this region. A total of 2,611 SNPs were tested against 2,647 DNAm sites, in a subset of 37 chronic Chagas cardiomyopathy patients and 20 asymptomatic individuals from the GWAS. We identified 6,958 significant cis-mQTLs (False Discovery Rate [FDR]<0.05) at 1 Mb each side of the GWAS leading variant, where six of them potentially modulate the expression of the SAC3D1 gene, the reported gene in the previous GWAS. In addition, a total of 268 cis-mQTLs showed differential methylation between chronic Chagas cardiomyopathy patients and asymptomatic individuals. The most significant cis-mQTLs mapped in the gene bodies of POLA2 (FDR = 1.04x10-11), PLAAT3 (FDR = 7.22x10-03), and CCDC88B (FDR = 1.89x10-02) that have been associated with cardiovascular and hematological traits in previous studies. One of the most relevant interactions correlated with hypermethylation of CCDC88B. This gene is involved in the inflammatory response, and its methylation and expression levels have been previously reported in Chagas cardiomyopathy. Our findings support the functional relevance of the previously associated genomic region, highlighting the regulation of novel genes that could play a role in the chronic cardiac form of the disease. |
dc.language.iso | eng |
dc.publisher | Public Library of Science |
dc.relation.ispartofseries | PLOS Neglected Tropical Diseases;15(10) |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Chagas, Malaltia de |
dc.subject | Miocardi - Malalties |
dc.subject | ADN - Metilació |
dc.subject.mesh | Chagas Cardiomyopathy |
dc.subject.mesh | DNA Methylation |
dc.subject.mesh | Genome-Wide Association Study |
dc.title | GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.1371/journal.pntd.0009874 |
dc.subject.decs | miocardiopatía chagásica |
dc.subject.decs | metilación del ADN |
dc.subject.decs | estudio de asociación genómica completa |
dc.relation.publishversion | https://doi.org/10.1371/journal.pntd.0009874 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [Casares-Marfil D, Kerick M, Andrés-León E, Chagas Genetics CYTED Network] Institute of Parasitology and Biomedicine López-Neyra, CSIC, Granada, Spain. [Bosch-Nicolau P, Molina I] Unitat de Medicina Tropical i Salud Internacional, Vall d’Hebron Hospital Universitari, Barcelona, Spain. PROSICS, Barcelona, Spain |
dc.identifier.pmid | 34714828 |
dc.identifier.wos | 000715222100004 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |