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The Bridging Integrator 1 Gene Polymorphism rs744373 and the Risk of Alzheimer’s Disease in Caucasian and Asian Populations: An Updated Meta-Analysis

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Abstract

Recent genome-wide association studies have identified an association between the bridging integrator 1 gene (BIN1) rs744373 polymorphism and late-onset Alzheimer’s disease (LOAD) in individuals of European ancestry. Additionally, a number of studies have focused on the association between rs744373 and Alzheimer’s disease in Caucasian and East Asian populations. However, these results remain inconclusive because of the relatively small sample sizes investigated. Here, we reevaluated this association using samples from seven articles including 22 independent studies comprising 11,832 LOAD patients and 18,133 controls identified by searching PubMed, MEDLINE, and AlzGene databases up to December 2015. We observed no significant heterogeneity between Asian and Caucasian populations. Additive, dominant, and recessive models revealed a significant association between rs744373 and LOAD in the pooled population, while subgroup analysis also identified significant findings in the East Asian population under the additive model (odds ratio (OR) = 1.10, 95 % confidence interval (CI) 1.02–1.19, P = 0.01) and dominant model (OR = 1.13, 95 % CI 1.03–1.25, P = 0.01), but not under the recessive model. The current meta-analysis further supports previous findings that the rs744373 polymorphism may be associated with LOAD risk in Caucasian and Asian populations. To our knowledge, this is the first large meta-analysis to investigate the association between the rs744373 polymorphism and LOAD in East Asian, American, and European populations.

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References

  1. Dye RV, Miller KJ, Singer EJ, Levine AJ (2012) Hormone replacement therapy and risk for neurodegenerative diseases. Int J Alzheimers Dis 2012:258454

    PubMed  PubMed Central  Google Scholar 

  2. Liu G, Yao L, Liu J, Jiang Y, Ma G, Chen Z et al (2014) Cardiovascular disease contributes to Alzheimer’s disease: evidence from large-scale genome-wide association studies. Neurobiol Aging 35(4):786–79

    Article  PubMed  Google Scholar 

  3. Lambert JC, Zelenika D, Hiltunen M, Chouraki V, Combarros O, Bullido MJ et al (2011) Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations. Neurobiol Aging 32:756

    Article  PubMed  Google Scholar 

  4. Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM et al (2011) Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease. Nat Genet 43(5):429–435

  5. Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J et al (2011) Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer’s disease. Nat Genet 43(5):436–441

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M et al (2010) Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA 303(18):1832–1840

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Chapuis J, Hansmannel F, Gistelinck M, Mounier A, Cauwenberghe V, Di Paolo G et al (2013) Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Mol Psychiatry 18(11):1225–1234

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Tan MS, Yu JT, Tan L (2013) Bridging integrator 1 (BIN1): form, function, and Alzheimer’s disease. Trends Mol Med 19:594e603

    Article  Google Scholar 

  9. Di Paolo G, Sankaranarayanan S, Wenk MR, Daniell L, Perucco E, Caldarone BJ et al (2002) Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice. Neuron 33:789–804

    Article  PubMed  Google Scholar 

  10. Sun L, Tan MS, Hu N, Yu JT, Tan L (2013) Exploring the value of plasma BIN1 as a potential biomarker for Alzheimer’s disease. J Alzheimers Dis 37:291e295

    Google Scholar 

  11. Tan L, Yu JT, Zhang W, Wu ZC, Zhang Q, Liu QY et al (2013) Association of GWAS-linked loci with late-onset Alzheimer’s disease in a northern Han Chinese population. Alzheimers Dement 9(5):546–553

  12. Ohara T, Ninomiya T, Hirakawa Y, Ashikawa K, Monji A, Kiyohara Y et al (2012) Association study of susceptibility genes for late-onset Alzheimer’s disease in the Japanese population. Psychiatr Genet 22(6):290–293

    Article  CAS  PubMed  Google Scholar 

  13. Wang HZ, Bi R, Hu QX, Xiang Q, Zhang C, Zhang DF (2014) Validating GWAS-identified risk loci for Alzheimer’s disease in Han Chinese populations. Mol Neurobiol Dec 3. [Epub ahead of print].

  14. Li HL, Yang P, Liu ZJ, Sun YM, Lu SJ, Tao QQ et al (2015) Common variants at Bin1 are associated with sporadic Alzheimer’s disease in the Han Chinese population. Psychiatr Genet 25(1):21–25

    Article  PubMed  Google Scholar 

  15. Clark MF, Baudouin SV (2006) A systematic review of the quality of genetic association studies in human sepsis. Intensive Care Med 32:1706–1712

  16. Tan MS, Yu JT, Jiang T, Zhu XC, Guan HS, Tan L (2014) Genetic variation in BIN1 gene and Alzheimer’s disease risk in Han Chinese individuals. Neurobiol Aging 35:1781

    Article  PubMed  Google Scholar 

  17. Hu X, Pickering E, Liu YC, Hall S, Fournier H, Katz E et al (2011) Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer’s disease. PLoS One 6(2), e16616

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Gharesouran J, Rezazadeh M, Khorrami A, Ghojazadeh M, Talebi M (2014) Genetic evidence for the involvement of variants at APOE, BIN1, CR1, and PICALM loci in risk of late-onset Alzheimer's disease and evaluation for interactions with APOE genotypes. J Mol Neurosci 54(4):780–786

    Article  CAS  PubMed  Google Scholar 

  19. Liu G, Zhang S, Cai Z, Li Y, Cui L, Ma G (2013) BIN1 gene rs744373 polymorphism contributes to Alzheimer’s disease in East Asian population. Neurosci Lett 7(544):47–51

    Article  CAS  Google Scholar 

  20. Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML et al (2009) Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer’s disease. Nat Genet 41(10):1088–1093

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Carrasquillo MM, Belbin O, Hunter TA, Ma L, Bisceglio GD, Zou F (2011) Replication of BIN1 association with Alzheimer’s disease and evaluation of genetic interactions. J Alzheimers Dis 24:751–758

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Meunier B, Quaranta M, Daviet L, Hatzoglou A, Leprince C (2009) The membrane-tubulating potential of amphiphysin 2/BIN1 is dependent on the microtubule-binding cytoplasmic linker protein 170 (CLIP-170). Eur J Cell Biol 88:91–102

    Article  CAS  PubMed  Google Scholar 

  23. Anekonda TS, Quinn JF (2011) Calcium channel blocking as a therapeutic strategy for Alzheimer’s disease: the case for isradipine. Biochim Biophys Acta 1812:1584–159

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

This work was supported by the National Natural Science Foundation of China (81400950, 81501006). We are deeply grateful to all participants of this study.

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Correspondence to Zhiyi He.

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Zhu, R., Liu, X. & He, Z. The Bridging Integrator 1 Gene Polymorphism rs744373 and the Risk of Alzheimer’s Disease in Caucasian and Asian Populations: An Updated Meta-Analysis. Mol Neurobiol 54, 1419–1428 (2017). https://doi.org/10.1007/s12035-016-9760-2

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  • DOI: https://doi.org/10.1007/s12035-016-9760-2

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