Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease

被引:7
|
作者
Kuksa, Pavel P. [1 ,2 ]
Liu, Chia-Lun [1 ,2 ]
Fu, Wei [1 ,2 ]
Qu, Liming [1 ,2 ]
Zhao, Yi [1 ,2 ]
Katanic, Zivadin [1 ,2 ]
Clark, Kaylyn [1 ,5 ]
Kuzma, Amanda B. [1 ,2 ]
Ho, Pei-Chuan [1 ,2 ]
Tzeng, Kai-Teh [4 ]
Valladares, Otto [1 ,2 ]
Chou, Shin-Yi [1 ,2 ,4 ]
Naj, Adam C. [1 ,3 ]
Schellenberg, Gerard D. [1 ,2 ]
Wang, Li-San [1 ,2 ]
Leung, Yuk Yee [1 ,2 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Penn Neurodegenerat Genom Ctr, Perelman Sch Med, Philadelphia, PA USA
[2] Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA USA
[3] Univ Penn, Perelman Sch Med, Dept Biostat Epidemiol & Informat, Philadelphia, PA 19104 USA
[4] Lehigh Univ, Dept Econ, Bethlehem, PA 18015 USA
[5] Univ Penn, Perelman Sch Med, Genom & Computat Biol Grad Grp, Philadelphia, PA 19104 USA
关键词
AD GWAS literature curation; Alzheimer's disease; data curation; database; genome-wide association studies; harmonization; GENOME-WIDE ASSOCIATION; IDENTIFIES VARIANTS; COMMON VARIANTS; INNATE IMMUNITY; RISK; LOCI; METAANALYSIS; CLU; DISCOVERY; PATTERNS;
D O I
10.3233/JAD-215055
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Recent Alzheimer's disease (AD) genetics findings from genome-wide association studies (GWAS) span progressively larger and more diverse populations and outcomes. Currently, there is no up-to-date resource providing harmonized and searchable information on all AD genetic associations found by GWAS, nor linking the reported genetic variants and genes with functional and genomic annotations. Objective: Create an integrated/harmonized, and literature-derived collection of population-specific AD genetic associations. Methods: We developed the Alzheimer's Disease Variant Portal (ADVP), an extensive collection of associations curated from >200 GWAS publications from Alzheimer's Disease Genetics Consortium and other consortia. Genetic associations were systematically extracted, harmonized, and annotated from both the genome-wide significant and suggestive loci reported in these publications. To ensure consistent representation of AD genetic findings, all the extracted genetic association information was harmonized across specifically designed publication, variant, and association categories. Results: ADVP V1.0 (February 2021) catalogs 6,990 associations related to disease-risk, expression quantitative traits, endophenotypes, or neuropathology. This extensive harmonization effort led to a catalog containing >900 loci, >1,800 variants, >80 cohorts, and 8 populations. Besides, ADVP provides investigators with a seamless integration of genomic and publicly available functional annotations across multiple databases per harmonized variant and gene records, thus facilitating further understanding and analyses of these genetics findings. Conclusion: ADVP is a valuable resource for investigators to quickly and systematically explore high-confidence AD genetic findings and provides insights into population-specific AD genetic architecture. ADVP is continually maintained and enhanced by NIAGADS and is freely accessible at https://advp.niagads.org.
引用
收藏
页码:461 / 477
页数:17
相关论文
共 50 条
  • [1] Portal to Alzheimer's disease
    Anatoly A Starkov
    Flint M Beal
    Nature Medicine, 2008, 14 : 1020 - 1021
  • [2] Portal to Alzheimer's disease
    Starkov, Anatoly A.
    Beal, Flint M.
    NATURE MEDICINE, 2008, 14 (10) : 1020 - 1021
  • [3] PATHOPHYSIOLOGY OF ALZHEIMER'S DISEASE: EXPERIMENTAL AND GENETIC FINDINGS
    Saka, Esen
    TURKISH JOURNAL OF GERIATRICS-TURK GERIATRI DERGISI, 2010, 13 : 21 - 26
  • [4] Frontal variant of Alzheimer's disease and typical Alzheimer's disease: A comparative study
    Fernandez-Calvo, Bernardino
    Ramos, Francisco
    de Lucena, Virginia Menezes
    ANALES DE PSICOLOGIA, 2013, 29 (01): : 293 - 300
  • [5] Functional ability in executive variant Alzheimer's disease and typical Alzheimer's disease
    Back-Madruga, C
    Boone, KB
    Briere, J
    Cummings, J
    McPherson, S
    Fairbanks, L
    Thompson, E
    CLINICAL NEUROPSYCHOLOGIST, 2002, 16 (03) : 331 - 340
  • [6] Lewy body variant of Alzheimer's disease and Alzheimer's disease: a comparative immunohistochemical study
    Szpak, GM
    Lewandowska, E
    Lechowicz, W
    Bertrand, E
    Wierzba-Bobrowicz, T
    Gwiazda, E
    Pasennik, E
    Kosno-Kruszewska, E
    Lipczynska-Lojkowska, W
    Bochynska, A
    Fiszer, U
    FOLIA NEUROPATHOLOGICA, 2001, 39 (02): : 63 - 71
  • [7] Neuro-ophthalmic findings in the visual variant of Alzheimer's disease
    Lee, AG
    Martin, CO
    OPHTHALMOLOGY, 2004, 111 (02) : 376 - 380
  • [8] Promising findings for Alzheimer's disease
    Laffman-Johnson, Elise
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2013, 93 (03) : 220 - 220
  • [9] Neuroimaging findings in Alzheimer's disease
    Fukuyama, H
    NEUROPATHOLOGY, 1998, 18 (01) : 91 - 97
  • [10] Comparison of Lewy body variant of Alzheimer's disease with pure Alzheimer's disease - Consortium to establish a registry for Alzheimer's disease, part XIX
    Heyman, A
    Fillenbaum, GG
    Gearing, M
    Mirra, SS
    Welsh-Bohmer, KA
    Peterson, B
    Pieper, C
    NEUROLOGY, 1999, 52 (09) : 1839 - 1844