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A harmonized longitudinal biomarkers and cognition database for assessing the natural history of preclinical Alzheimer's disease from young adulthood and for designing prevention trials
Author(s) -
Xiong Chengjie,
Luo Jingqin,
Agboola Folasade,
Li Yan,
Albert Marilyn,
Johnson Sterling C.,
Koscik Rebecca L.,
Masters Colin L.,
Soldan Anja,
Villemagne Victor L.,
Li QiaoXin,
McDade Eric M.,
Fagan Anne M.,
Massoumzadeh Parinaz,
Benzinger Tammie,
Hassenstab Jason,
Bateman Randall J.,
Morris John C.
Publication year - 2019
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2019.06.4955
Subject(s) - positron emission tomography , biomarker , magnetic resonance imaging , longitudinal study , neuroimaging , clinical trial , alzheimer's disease neuroimaging initiative , cognition , medicine , cognitive decline , disease , longitudinal data , cerebrospinal fluid , alzheimer's disease , database , oncology , psychology , pathology , nuclear medicine , dementia , radiology , psychiatry , data mining , computer science , chemistry , biochemistry
Large longitudinal biomarkers database focusing on middle age is needed for Alzheimer's disease (AD) prevention. Methods Data for cerebrospinal fluid analytes, molecular imaging of cerebral fibrillar β‐amyloid with positron emission tomography, magnetic resonance imaging–based brain structures, and clinical/cognitive outcomes were harmonized across eight AD biomarker studies. Statistical power was estimated. Results The harmonized database included 7779 participants with clinical/cognitive data: 3542 were 18∼65 years at the baseline, 5865 had longitudinal cognitive data for a median of 4.7 years, 2473 participated in the cerebrospinal fluid studies (906 had longitudinal data), 2496 participated in the magnetic resonance imaging studies (1283 had longitudinal data), and 1498 participated in the positron emission tomography amyloid studies (849 had longitudinal data). The database provides adequate power for detecting early biomarker changes, and demonstrates the feasibility of AD prevention trials on middle‐aged individuals. Discussion The harmonized database is an optimum resource to design AD prevention trials decades before symptomatic onset.