Your browser doesn't support javascript.
loading
INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis.
Jing, Hua; Zhu, Jun-Xia; Wang, Hui-Fu; Zhang, Wei; Zheng, Zhan-Jie; Kong, Ling-Li; Tan, Chen-Chen; Wang, Zi-Xuan; Tan, Lin; Tan, Lan.
Affiliation
  • Jing H; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
  • Zhu JX; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
  • Wang HF; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
  • Zhang W; Department of Emergency, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
  • Zheng ZJ; Department of Geriatric, Qingdao Mental Health Center, Qingdao, PR China.
  • Kong LL; Department of Geriatric, Qingdao Mental Health Center, Qingdao, PR China.
  • Tan CC; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
  • Wang ZX; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
  • Tan L; College of Medicine and Pharmaceutics, Ocean University of China, Qingdao, PR China.
  • Tan L; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.
Oncotarget ; 7(43): 69225-69230, 2016 Oct 25.
Article in En | MEDLINE | ID: mdl-27750211
ABSTRACT
Inositol polyphosphate-5-phosphatase (INPP5D) was reported to be associated with Alzheimer's disease (AD) through modulating the inflammatory process and immune response. A recent genome-wide association study discovered a new locus single nucleotide polymorphism (SNP, rs35349669) of INPP5D which was significantly associated with susceptibility to late-onset Alzheimer's disease (LOAD) in Caucasians. In this study, we investigated the relations between the INPP5D polymorphism rs35349669 and LOAD in Han Chinese population comprising 984 LOAD cases and 1352 healthy controls being matched for age and gender. Our results showed no obvious differences in the genotypic or allelic distributions of rs35349669 polymorphism between LOAD cases and healthy controls (genotype p = 0.167; allele p = 0.094). Additionally, when these data were stratified by APOEε4 status, there are still no evident differences in the genotypic or allelic distributions in APOEε4 carriers (p > 0.05). Furthermore, meta-analysis of 81964 individuals confirmed that rs35349669 was significantly associated with the risk for LOAD (OR=1.08, 95%CI=1.06-1.11), but the results remained negative in Chinese subgroup (OR=0.77, 95%CI=0.53-1.13). Overall, the current evidence did not indicate that INPP5D rs35349669 polymorphism play a role in the genetic predisposition to LOAD in Chinese population.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Predisposition to Disease / Alzheimer Disease / Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases Type of study: Systematic_reviews Limits: Aged / Aged80 / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Oncotarget Year: 2016 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Predisposition to Disease / Alzheimer Disease / Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases Type of study: Systematic_reviews Limits: Aged / Aged80 / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Oncotarget Year: 2016 Type: Article