The investigation of lipoprotein-related phospholipase A2 (LP-PLA2) V279F mutation in coronary artery disease
dc.contributor.author | Yıldırım Yaroğlu, Hatice | |
dc.contributor.author | Akciğer, Nazli | |
dc.contributor.author | Sungur, Mehmet Ali | |
dc.contributor.author | Yılmaz, Dilek Cicek | |
dc.contributor.author | Tamer, Lulufer | |
dc.date.accessioned | 2024-08-23T16:07:45Z | |
dc.date.available | 2024-08-23T16:07:45Z | |
dc.date.issued | 2023 | en_US |
dc.department | Düzce Üniversitesi | en_US |
dc.description.abstract | Aim: Despite advances in the treatment of cardiovascular diseases, coronary artery disease (CAD) is the leading cause of death worldwide. The media layer of normal and diseased arteries contains lipoprotein-associated phospholipase A2 (Lp-PLA2), which is mostly made by mast cells, T lymphocytes, and monocytes. Our research aimed to define how the Lp-PLA2 and V279F gene polymorphisms are related to CAD. Materials and Methods: This study included 109 CAD patients and 71 controls. Fasting blood glucose (FBG) and lipid profiles were measured via the enzymatic colorimetric technique. Lp-PLA2 levels were detected with ELISA. The genomic DNAs were isolated from whole blood. Real-time polymerase chain reaction (RT-PCR) with the V279F mutation detection kit was used to identify the Lp-PLA2 V279F mutation. Results: In the CAD group compared to controls, serum Lp-PLA2 levels were higher (p=0.001). While FF (mutant) genotypes and VF (heterozygous) genotypes were absent in both groups, the Lp-PLA2 V279F mutation was discovered as the VV (wild) genotype in both the CAD group and controls. Conclusion: As a result, we determined that the Lp-PLA2 V279F mutation cannot be considered a genetic risk factor for CAD, but that Lp-PLA2 elevation may be an important parameter for CAD. Keywords: Lp-PLA2, Coronary artery disease, V279F. | en_US |
dc.identifier.doi | 10.5455/annalsmedres.2023.08.182 | |
dc.identifier.endpage | 1222 | en_US |
dc.identifier.issn | 2636-7688 | |
dc.identifier.issue | 10 | en_US |
dc.identifier.startpage | 1217 | en_US |
dc.identifier.trdizinid | 1204271 | en_US |
dc.identifier.uri | https://doi.org/10.5455/annalsmedres.2023.08.182 | |
dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/1204271 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/14830 | |
dc.identifier.volume | 30 | en_US |
dc.indekslendigikaynak | TR-Dizin | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Annals of Medical Research | en_US |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | The investigation of lipoprotein-related phospholipase A2 (LP-PLA2) V279F mutation in coronary artery disease | en_US |
dc.type | Article | en_US |
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