4.8 Article

Common variants at 12q14 and 12q24 are associated with hippocampal volume

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NATURE GENETICS
卷 44, 期 5, 页码 545-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ng.2237

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资金

  1. US National Institute on Aging (NIA) [N01-AG-12100]
  2. US NHLBI [HHSN268201100005C, HHSN268201100006C, HHSN268201100007C, HHSN268201100008C, HHSN268201100009C, HHSN268201100010C, HHSN268201100011C, HHSN268201100012C, HL087641, HL59367, HL086694, HL7825, HL087652, HL105756]
  3. National Human Genome Research Institute [U01HG004402]
  4. NIH [HHSN268200625226C]
  5. NIH Roadmap for Medical Research [UL1RR025005]
  6. NHLBI [HL093029]
  7. NIA [AG20098, AG05133, AG08122, AG16495, AG033193, AG013846, AG031287]
  8. Austrian Science Fond (FWF) [P20545-P05, P13180]
  9. Netherlands Organisation for Scientific Research (NWO)
  10. Internationale Stichting Alzheimer Onderzoek (ISAO)
  11. Hersenstichting Nederland (HSN)
  12. Centre for Medical Systems Biology [CMSB1, CMSB2]
  13. US NIA [P30AG10161, AG17917, AG15819]
  14. Illinois Department of Public Health
  15. Rush Clinical Translational Science Consortium
  16. National Heart, Lung and Blood Institute's Framingham Heart Study [N01-HC-25195]
  17. Affymetrix, Inc [N02-HL-6-4278]
  18. Robert Dawson Evans Endowment of the Department of Medicine at the Boston University School of Medicine and Boston Medical Center
  19. NINDS [NS17950]
  20. NWO [175.010.2005.011, 911-03-012, 918-46-615, 904-61-096, 904-61-133, 948-00-010]
  21. Research Institute for Diseases in the Elderly (RIDE) [014-93-015]
  22. NGI-NWO [050-060-810]
  23. Erasmus Medical Center
  24. Erasmus University, Rotterdam
  25. Netherlands Organisation for Health Research and Development (ZonMw)
  26. RIDE2
  27. Dutch Ministry of Education, Culture and Science
  28. Dutch Ministry for Health, Welfare and Sports
  29. European Commission (DG XII)
  30. Municipality of Rotterdam
  31. Nederlandse Hartstichting [2009B102]
  32. Internationaal Parkinson Fonds
  33. National Health and Medical Research Council of Australia (NHMRC) [403000, 491109, 606543, APP1024879]
  34. Wicking Dementia Education and Research Centre, Hobart
  35. NHMRC-National Heart Foundation [606544]
  36. Fondation pour la Recherche Medicale
  37. Caisse Nationale Maladie des Travailleurs Salaries
  38. Direction Generale de la Sante
  39. Mutuelle Generale de l'Education Nationale (MGEN)
  40. Institut de la Longevite
  41. Conseils Regionaux de Aquitaine et Bourgogne
  42. Fondation de France
  43. French Ministry of Research-INSERM
  44. National Foundation for Alzheimer's Disease and Related Disorders
  45. Institut Pasteur de Lille
  46. Centre National de Genotypage
  47. MRC [G0701075, G1100616, G0901254, G1001245, G0700704] Funding Source: UKRI
  48. Austrian Science Fund (FWF) [P13180, P20545] Funding Source: Austrian Science Fund (FWF)
  49. Alzheimers Research UK [ART-PPG2011A-14] Funding Source: researchfish
  50. Austrian Science Fund (FWF) [P 20545] Funding Source: researchfish
  51. Medical Research Council [G0901254, G0700704, G1001245, G0701075, G1100616] Funding Source: researchfish

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Aging is associated with reductions in hippocampal volume that are accelerated by Alzheimer's disease and vascular risk factors. Our genome-wide association study (GWAS) of dementia-free persons (n = 9,232) identified 46 SNPs at four loci with P values of < 4.0 x 10(-7). In two additional samples (n = 2,318), associations were replicated at 12q14 within MSRB3-WIF1 (discovery and replication; rs17178006; P = 5.3 x 10(-11)) and at 12q24 near HRK-FBXW8 (rs7294919; P = 2.9 x 10(-11)). Remaining associations included one SNP at 2q24 within DPP4 (rs6741949; P = 2.9 x 10(-7)) and nine SNPs at 9p33 within ASTN2 (rs7852872; P = 1.0 x 10(-7)); along with the chromosome 12 associations, these loci were also associated with hippocampal volume (P < 0.05) in a third younger, more heterogeneous sample (n = 7,794). The SNP in ASTN2 also showed suggestive association with decline in cognition in a largely independent sample (n = 1,563). These associations implicate genes related to apoptosis (HRK), development (WIF1), oxidative stress (MSR3B), ubiquitination (FBXW8) and neuronal migration (ASTN2), as well as enzymes targeted by new diabetes medications (DPP4), indicating new genetic influences on hippocampal size and possibly the risk of cognitive decline and dementia.

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