Shared genetic etiology underlying late-onset Alzheimer's disease and posttraumatic stress syndrome

被引:13
|
作者
Lutz, Michael W. [1 ]
Luo, Sheng [2 ]
Williamson, Douglas E. [3 ,4 ,5 ]
Chiba-Falek, Ornit [1 ,6 ]
机构
[1] Duke Univ, Dept Neurol, Div Translat Brain Sci, Med Ctr, Durham, NC USA
[2] Duke Univ, Med Ctr, Dept Biostat & Bioinformat, Durham, NC USA
[3] Duke Univ, Dept Psychiat & Behav Sci, Med Ctr, Durham, NC USA
[4] Durham VA Med Ctr, Res Serv, Durham, NC USA
[5] Duke Univ, Ctr Appl Genom & Precis Med, Med Ctr, 300 North Duke St, Durham, NC 27701 USA
[6] Duke Univ, Ctr Genom & Computat Biol, Med Ctr, Durham, NC USA
基金
美国国家卫生研究院;
关键词
genetic pleiotropy; inflammation and immune-based pathways and Alzheimer's disease; late-onset Alzheimer's disease; MS4A gene family; posttraumatic stress disorder; PTSD; NEUROPSYCHIATRIC SYMPTOMS; FUNCTIONAL ANNOTATION; COMMON VARIANTS; RISK LOCI; DISORDER; PLEIOTROPY; SUSCEPTIBILITY; EXPRESSION; DEMENTIA; IMMUNITY;
D O I
10.1002/alz.12128
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Late-onset Alzheimer's disease (LOAD) manifests comorbid neuropsychiatric symptoms and posttraumatic stress disorder (PTSD) is associated with an increased risk for dementia in late life, suggesting the two disorders may share genetic etiologies. Methods: We performed genetic pleiotropy analysis using LOAD and PTSD genome-wide association study (GWAS) datasets from white and African-American populations, followed by functional-genomic analyses. Results: We found an enrichment for LOAD across increasingly stringent levels of significance with the PTSD GWAS association (LOAD vertical bar PTSD) in the discovery and replication cohorts and a modest enrichment for the reverse conditional association (PTSD vertical bar LOAD). LOAD vertical bar PTSD association analysis identified and replicated the MS4A genes region. These genes showed similar expression pattern in brain regions affected in LOAD, and across-brain-tissue analysis identified a significant association for MS4A6A. The African-American samples showed moderate enrichment; however, no false discovery rate-significant associations. Discussion: We demonstrated common genetic signatures for LOAD and PTSD and suggested immune response as a common pathway for these diseases.
引用
收藏
页码:1280 / 1292
页数:13
相关论文
共 50 条
  • [41] Language Changes in Late-Onset Alzheimer's Disease
    Can, Eda
    Kuruoglu, Gulmira
    PSYCHOLINGUISTICS, 2019, 25 (02): : 50 - 68
  • [42] Plasma Sphingomyelins in Late-Onset Alzheimer's Disease
    Fote, Gianna
    Wu, Jie
    Mapstone, Mark
    Macciardi, Fabio
    Fiandaca, Massimo S.
    Federoff, Howard J.
    JOURNAL OF ALZHEIMERS DISEASE, 2021, 83 (03) : 1161 - 1171
  • [43] LRP gene and late-onset Alzheimer's disease
    Woodward, R
    Singleton, AB
    Gibson, AM
    Edwardson, JA
    Morris, CM
    LANCET, 1998, 352 (9123): : 239 - 240
  • [44] Comparison of the amyloid plaque proteome in Down syndrome, early-onset Alzheimer's disease, and late-onset Alzheimer's disease
    Marta-Ariza, Mitchell
    Leitner, Dominique F.
    Kanshin, Evgeny
    Suazo, Jianina
    Giusti Pedrosa, Ana
    Thierry, Manon
    Lee, Edward B.
    Devinsky, Orrin
    Drummond, Eleanor
    Fortea, Juan
    Lleo, Alberto
    Ueberheide, Beatrix
    Wisniewski, Thomas
    ACTA NEUROPATHOLOGICA, 2025, 149 (01)
  • [45] Genetic association of CTNNA3 with late-onset Alzheimer's disease in females
    Miyashita, Akinori
    Arai, Hiroyuki
    Asada, Takashi
    Imagawa, Masaki
    Matsubara, Etsuro
    Shoji, Mikio
    Higuchi, Susumu
    Urakami, Katsuya
    Kakita, Akiyoshi
    Takahashi, Hitoshi
    Toyabe, Shinichi
    Akazawa, Kohei
    Kanazawa, Ichiro
    Ihara, Yasuo
    Kuwano, Ryozo
    HUMAN MOLECULAR GENETICS, 2007, 16 (23) : 2854 - 2869
  • [46] A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes
    Jimenez-Escrig, A
    Gomez-Tortosa, E
    Baron, M
    Rabano, A
    Arcos-Burgos, M
    Palacios, LG
    Yusta, A
    Anta, P
    Perez, I
    Hierro, M
    Munoz, DG
    Barquero, S
    BRAIN, 2005, 128 : 1707 - 1715
  • [47] Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families
    Barral, Sandra
    Vardarajan, Badri N.
    Reyes-Dumeyer, Dolly
    Faber, Kelley M.
    Bird, Thomas D.
    Tsuang, Debby
    Bennett, David A.
    Rosenberg, Roger
    Boeve, Bradley F.
    Graff-Radford, Neill R.
    Goate, Alison M.
    Farlow, Martin
    Lantigua, Rafael
    Medrano, Martin Z.
    Wang, Xinbing
    Kamboh, M. Ilyas
    Barmada, Mahmud Muhiedine
    Schaid, Daniel J.
    Foroud, TatianaM.
    Weamer, Elise A.
    Ottman, Ruth
    Sweet, Robert A.
    Mayeux, Richard
    NEUROBIOLOGY OF AGING, 2015, 36 (11) : 3116.e9 - 3116.e16
  • [48] Genetic Variation in Imprinted Genes is Associated with Risk of Late-Onset Alzheimer's Disease
    Chaudhry, Mamoonah
    Wang, Xingbin
    Bamne, Mikhil N.
    Hasnain, Shahida
    Demirci, F. Yesim
    Lopez, Oscar L.
    Kamboh, M. Ilyas
    JOURNAL OF ALZHEIMERS DISEASE, 2015, 44 (03) : 989 - 994
  • [49] Genetic variation within endolysosomal system is associated with late-onset Alzheimer's disease
    Gao, Song
    Casey, Aaron E.
    Sargeant, Tim J.
    Makinen, Ville-Petteri
    BRAIN, 2018, 141 : 2711 - 2720
  • [50] The Clinical and Neuropathological Features of Sporadic (Late-Onset) and Genetic Forms of Alzheimer's Disease
    Rujeedawa, Tanzil
    Felez, Eva Carrillo
    Clare, Isabel C. H.
    Fortea, Juan
    Strydom, Andre
    Rebillat, Anne-Sophie
    Coppus, Antonia
    Levin, Johannes
    Zaman, Shahid H.
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (19)