CR1 rs3818361 Polymorphism Contributes to Alzheimer's Disease Susceptibility in Chinese Population.

Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China. Department of Neurology, The Second Hospital of Harbin, Harbin, China. College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China. Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, Harbin, China. Department of Statistics, Rice University, Houston, TX, USA. Department of Oncology, The First Hospital of Harbin, Harbin, China. Department of Human Genetics, University of California at Los Angeles, Los Angeles, CA, USA. Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China. wangrz@126.com. School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150001, China. qhjiang@hit.edu.cn. College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China. liuguiyou1981@163.com.

Molecular neurobiology. 2016;(6):4054-4059
Full text from:

Abstract

Recent genome-wide association studies (GWAS) reported CR1 rs3818361 polymorphism to be an Alzheimer's disease (AD) susceptibility variant in European ancestry. Three independent studies investigated this association in Chinese population. However, these studies reported weak or no significant association. Here, we reinvestigated the association using all the samples from three independent studies in Chinese population (N = 4047, 1244 AD cases and 2803 controls). We also selected three independent studies in European ancestry population (N = 11787, 3939 AD cases and 7848 controls) to evaluate the effect of rs3818361 polymorphism on AD risk in different ethnic backgrounds. In Chinese population, we did not identified significant heterogeneity using additive, recessive, and dominant genetic models. Meta-analysis showed significant association between rs3818361 and AD with P = 6.00E-03 and P = 5.00E-03. We further identified no heterogeneity of rs3818361 polymorphism between Chinese and European populations. We found that rs3818361 polymorphism contributed to AD with similar genetic risk in Chinese and European populations. In summary, this is the first study to show significant association between rs3818361 polymorphism and AD in Chinese population by a meta-analysis method. Our findings indicate that the effect of CR1 rs3818361 polymorphism on AD risk in Chinese cohorts is consistent with the increased risk observed in European AD cohorts.

Methodological quality

Publication Type : Meta-Analysis

Metadata