Genome-wide association studies identify novel loci in rapidly progressive Alzheimer's disease

被引:0
作者
Wang, Ping [1 ,9 ]
Lynn, Audrey [1 ,2 ]
Miskimen, Kristy [1 ]
Song, Yeunjoo E. [1 ]
Wisniewski, Thomas [3 ]
Cohen, Mark [4 ,5 ]
Appleby, Brian S. [4 ,5 ,6 ,7 ]
Safar, Jiri G. [4 ,6 ,8 ]
Haines, Jonathan L. [1 ,2 ,10 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Populat & Quantitat Hlth Sci, Cleveland, OH USA
[2] Cleveland Inst Computat Biol, Cleveland, OH USA
[3] NYU, Ctr Cognit Neurol, Grossman Sch Med, Dept Neurol Pathol & Psychiat, New York, NY USA
[4] Case Western Reserve Univ, Dept Pathol, Cleveland, OH USA
[5] Case Western Reserve Univ, Natl Pr Dis Pathol Surveillance Ctr, Cleveland, OH USA
[6] Case Western Reserve Univ, Dept Neurol, Cleveland, OH USA
[7] Case Western Reserve Univ, Dept Psychiat, Cleveland, OH USA
[8] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH USA
[9] Case Western Reserve Univ, Sch Med, Dept Populat & Quantitat Hlth Sci, 1-326 Wolstein Res Bldg,2103 Cornell Rd, Cleveland, OH 44106 USA
[10] Case Western Reserve Univ, Sch Med, Dept Populat & Quantitat Hlth Sci, 2-529 Wolstein Res Bldg,2103 Cornell Rd, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; genetic risk; rapid progression; APOLIPOPROTEIN-E; NATIONAL INSTITUTE; COGNITIVE DECLINE; BETA; METAANALYSIS; GUIDELINES; HISPANICS; GENOTYPE; INSIGHTS; FEATURES;
D O I
10.1002/alz.13655
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
INTRODUCTION: Recent data suggest that distinct prion-like amyloid beta and tau strains are associated with rapidly progressive Alzheimer's disease (rpAD). The role of genetic factors in rpAD is largely unknown.METHODS: Previously known AD risk loci were examined in rpAD cases. Genomewide association studies (GWAS) were performed to identify variants that influence rpAD. RESULTS: We identified 115 pathology-confirmed rpAD cases and 193 clinical rpAD cases, 80% and 69% were of non-Hispanic European ancestry. Compared to the clinical cohort, pathology-confirmed rpAD had higher frequencies of apolipoprotein E (APOE) epsilon 4 and rare missense variants in AD risk genes. A novel genome-wide significant locus (P < 5x10(-8)) was observed for clinical rpAD on chromosome 21 (rs2832546); 102 loci showed suggestive associations with pathology-confirmed rpAD (P < 1x10(-5)).DISCUSSION: rpAD constitutes an extreme subtype of AD with distinct features. GWAS found previously known and novel loci associated with rpAD.
引用
收藏
页码:2034 / 2046
页数:13
相关论文
共 66 条
  • [41] Apolipoprotein E - Structure, function, and possible roles in Alzheimer's disease
    Mahley, RW
    Nathan, BP
    Pitas, RE
    [J]. NEUROBIOLOGY OF ALZHEIMER'S DISEASE, 1996, 777 : 139 - 145
  • [42] The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
    McKhann, Guy M.
    Knopman, David S.
    Chertkow, Howard
    Hyman, Bradley T.
    Jack, Clifford R., Jr.
    Kawas, Claudia H.
    Klunk, William E.
    Koroshetz, Walter J.
    Manly, Jennifer J.
    Mayeux, Richard
    Mohs, Richard C.
    Morris, John C.
    Rossor, Martin N.
    Scheltens, Philip
    Carrillo, Maria C.
    Thies, Bill
    Weintraub, Sandra
    Phelps, Creighton H.
    [J]. ALZHEIMERS & DEMENTIA, 2011, 7 (03) : 263 - 269
  • [43] National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease: a practical approach
    Montine, Thomas J.
    Phelps, Creighton H.
    Beach, Thomas G.
    Bigio, Eileen H.
    Cairns, Nigel J.
    Dickson, Dennis W.
    Duyckaerts, Charles
    Frosch, Matthew P.
    Masliah, Eliezer
    Mirra, Suzanne S.
    Nelson, Peter T.
    Schneider, Julie A.
    Thal, Dietmar Rudolf
    Trojanowski, John Q.
    Vinters, Harry V.
    Hyman, Bradley T.
    [J]. ACTA NEUROPATHOLOGICA, 2012, 123 (01) : 1 - 11
  • [44] Murphy MP, 2010, J ALZHEIMERS DIS, V19, P311, DOI [10.3233/JAD-2009-1221, 10.3233/JAD-2010-1221]
  • [45] Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project
    Naj, Adam C.
    Lin, Honghuang
    Vardarajan, Badri N.
    White, Simon
    Lancour, Daniel
    Ma, Yiyi
    Schmidt, Michael
    Sun, Fangui
    Butkiewicz, Mariusz
    Bush, William S.
    Kunkle, Brian W.
    Malamon, John
    Amin, Najaf
    Choi, Seung Hoan
    Hamilton-Nelson, Kara L.
    van der Lee, Sven J.
    Gupta, Namrata
    Koboldt, Daniel C.
    Saad, Mohamad
    Wang, Bowen
    Nato, Alejandro Q., Jr.
    Sohi, Harkirat K.
    Kuzma, Amanda
    Wang, Li-San
    Cupples, L. Adrienne
    van Duijn, Cornelia
    Seshadri, Sudha
    Schellenberg, Gerard D.
    Boerwinkle, Eric
    Bis, Joshua C.
    Dupuis, Josee
    Salerno, William J.
    Wijsman, Ellen M.
    Martin, Eden R.
    DeStefano, Anita L.
    [J]. GENOMICS, 2019, 111 (04) : 808 - 818
  • [46] Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation
    Neumann, Alexander
    Kucukali, Fahri
    Bos, Isabelle
    Vos, Stephanie J. B.
    Engelborghs, Sebastiaan
    De Pooter, Tim
    Joris, Geert
    De Rijk, Peter
    De Roeck, Ellen
    Tsolaki, Magda
    Verhey, Frans
    Martinez-Lage, Pablo
    Tainta, Mikel
    Frisoni, Giovanni
    Blin, Oliver
    Richardson, Jill
    Bordet, Regis
    Scheltens, Philip
    Popp, Julius
    Peyratout, Gwendoline
    Johannsen, Peter
    Froelich, Lutz
    Vandenberghe, Rik
    Freund-Levi, Yvonne
    Streffer, Johannes
    Lovestone, Simon
    Legido-Quigley, Cristina
    ten Kate, Mara
    Barkhof, Frederik
    Strazisar, Mojca
    Zetterberg, Henrik
    Bertram, Lars
    Visser, Pieter Jelle
    van Broeckhoven, Christine
    Sleegers, Kristel
    [J]. MOLECULAR PSYCHIATRY, 2022, 27 (04) : 1990 - 1999
  • [47] Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease
    Nho, Kwangsik
    Horgusluoglu, Emrin
    Kim, Sungeun
    Risacher, Shannon L.
    Kim, Dokyoon
    Foroud, Tatiana
    Aisen, Paul S.
    Petersen, Ronald C.
    Jack, Clifford R., Jr.
    Shaw, Leslie M.
    Trojanowski, John Q.
    Weiner, Michael W.
    Green, Robert C.
    Toga, Arthur W.
    Saykin, Andrew J.
    [J]. BMC MEDICAL GENOMICS, 2016, 9
  • [48] EYS is a major gene involved in retinitis pigmentosa in Japan: genetic landscapes revealed by stepwise genetic screening
    Numa, Shogo
    Oishi, Akio
    Higasa, Koichiro
    Oishi, Maho
    Miyata, Manabu
    Hasegawa, Tomoko
    Ikeda, Hanako Ohashi
    Otsuka, Yuki
    Matsuda, Fumihiko
    Tsujikawa, Akitaka
    [J]. SCIENTIFIC REPORTS, 2020, 10 (01)
  • [49] Rapidly Progressive Alzheimer's Disease in Two Distinct Autopsy Cohorts
    Pillai, Jagan A.
    Appleby, Brian S.
    Safar, Jiri
    Leverenz, James B.
    [J]. JOURNAL OF ALZHEIMERS DISEASE, 2018, 64 (03) : 973 - 980
  • [50] Missing lnc(RNAs) in Alzheimer's Disease?
    Policarpo, Rafaela
    d'Ydewalle, Constantin
    [J]. GENES, 2022, 13 (01)