Association between PCSK9 and LDLR gene polymorphisms with coronary heart disease: Case-control study and meta-analysis

التفاصيل البيبلوغرافية
العنوان: Association between PCSK9 and LDLR gene polymorphisms with coronary heart disease: Case-control study and meta-analysis
المؤلفون: Lina Zhang, Yanping Le, Jianqing Zhou, Shiwei Duan, Ling-Mei Hao, Meng Ye, Weifeng Xu, Panpan Liu, Yi Huang, Li-Juan Fei, Limin Xu, Fang Yuan, Xi Yang, Xu-Jun Qiu, Jiangfang Lian, Xiaoyan Huang
المصدر: Clinical Biochemistry. 46:727-732
بيانات النشر: Elsevier BV, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Male, Oncology, medicine.medical_specialty, Genotype, Clinical Biochemistry, Coronary Disease, Single-nucleotide polymorphism, Bioinformatics, Polymorphism, Single Nucleotide, Gene Frequency, Risk Factors, Polymorphism (computer science), Internal medicine, medicine, Humans, Genetic Predisposition to Disease, cardiovascular diseases, Allele frequency, Genotyping, Genetic Association Studies, Aged, Genetic association, business.industry, Serine Endopeptidases, Case-control study, Sequence Analysis, DNA, General Medicine, Middle Aged, Receptors, LDL, Case-Control Studies, Meta-analysis, Female, Proprotein Convertases, Proprotein Convertase 9, business
الوصف: To explore the association of rs11206510 (PCSK9 gene) and rs1122608 (LDLR gene) polymorphisms with coronary heart disease (CHD) in Han Chinese.A total of 813 participants (290 CHD cases, 193 non-CHD controls and 330 healthy controls) were recruited in the case-control study. DNA genotyping was performed on the SEQUENOM® Mass-ARRAY iPLEX® platform. χ(2)-test was used to compare the genotype distribution and allele frequencies. Two meta-analyses were performed to establish the association between the two polymorphisms with CHD.No significant associations between the two SNPs and the risk of CHD were observed in the present study. The meta-analysis of rs11206510 of PCSK9 gene comprises 11 case-control studies with a total of 69,054 participants. Significant heterogeneity was observed in Caucasian population in subgroup analysis of the association studies of rs11206510 with CHD (P=0.003, I(2)=67.2%). The meta-analysis of LDLR gene rs1122608 polymorphism comprises 7 case-control studies with a total of 20,456 participants and the heterogeneity of seven studies was minimal (P=0.148, I(2)=36.7%).The results of the meta-analyses indicated that both SNPs were associated with CHD in Caucasians (P0.05) but not in Asians. The results from our case-control study and meta-analyses might be explained by genetic heterogeneity in the susceptibility of CHD and ethnic differences between Asians and Caucasians.
تدمد: 0009-9120
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e2a854139f2bd4f26908a1c93b09a7
https://doi.org/10.1016/j.clinbiochem.2013.01.013
رقم الأكسشن: edsair.doi.dedup.....12e2a854139f2bd4f26908a1c93b09a7
قاعدة البيانات: OpenAIRE