Exploring the genetic basis of AD progression
Exploring the genetic basis of AD progression
批准号:
10322097
负责人:
Tian Ge
金额:
$24.41万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-15 至 2022-11-30
关键词:
Alzheimer&aposs DiseaseAlzheimer’s disease biomarkerAwardCognitiveCognitive agingComplexDataDementiaDependenceDiagnosisDiseaseDisease MarkerDisease ProgressionDropsElderlyExhibitsFundingGeneticGenetic MarkersGenetic RiskGenetic VariationGenetic studyGenomicsHeritabilityImageImpaired cognitionIndividualInterdisciplinary StudyKnowledgeLate Onset Alzheimer DiseaseLongitudinal StudiesMRI ScansMagnetic Resonance ImagingMeasurementMemoryMethodsModelingNamesNeuropsychologyPhasePhenotypeProcessPublishingResearchResearch PersonnelScienceSpeedStatistical MethodsTestingTimeTrainingVariantaging brainbasebrain magnetic resonance imagingcase controlcognitive changecohortcomputerized toolsdata modelingexecutive functionexperiencegenome wide association studygenome-widegenomic datagenomic locushigh dimensionalityimage processingimaging biomarkerimaging geneticsinnovationinsightlongitudinal analysislongitudinal datasetmultiple datasetsneuroimagingneuroimaging markernovelpre-clinicalprogramsrate of changerisk variantserial imagingstatisticstooluser friendly software
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY / ABSTRACT
Late-onset Alzheimer's disease (AD) is known to have a variable temporal course and a complex genetic basis
that likely involves hundreds of loci. However, due to the lack of computational tools that can relate longitudinal
markers of AD to genetic variation, our current knowledge about the genetic underpinnings of AD progression
is very limited. To date, most genetic studies of AD are cross-sectional, which treat diagnosis, cognitive meas-
urements, or neuroimaging biomarkers of AD as stationary. Yet, the pathophysiological process of AD is dy-
namic and progressive, and individuals advance through disease stages at variable speeds. Existing genetic
studies of longitudinal AD markers often involve only a smaller number of data points spanning a short period
of time, which do not fully characterize the disease trajectory, or employ suboptimal statistical methods when
handling serial measurements, which produces biased estimates and reduces statistical power. This project
aims to systematically investigate the genetic basis of AD progression by analyzing longitudinal structural brain
magnetic resonance imaging (MRI) scans, neuropsychological assessments and genomic data from two large-
scale independently funded studies: the Alzheimer's Disease Neuroimaging Initiative (ADNI) and the Harvard
Aging Brain Study (HABS). Innovative statistical methods will be developed and implemented to integrate high-
dimensional genomic data and longitudinal markers of AD (on average ~5 time points per subject spanning 3+
years) that exhibit serial dependence within subjects, missing data points, drop-outs and irregularly spaced
measurements across subjects. This project will offer critical analysis tools to model the trajectories of cogni-
tive decline and change in AD biomarkers over time, and dissect the genetic basis of AD progression. The pro-
ject will build on Dr. Ge's strong quantitative background and prior experience in neuroimaging statistics and
imaging genetics. During the award period, Dr. Ge will receive formal training in statistical genetics and ge-
nomics, and cognitive aging and AD, which will help him develop into an independent investigator and launch a
multidisciplinary research program at the intersection of imaging sciences, genomics, statistics and Alzheimer's
research.
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DOI:
10.1038/s41588-022-01054-7
发表时间:
2022-05
期刊:
NATURE GENETICS
影响因子:
30.8
作者:
[Ruan, Yunfeng, Lin, Yen-Feng, Feng, Yen-Chen Anne, Chen, Chia-Yen, Lam, Max, Guo, Zhenglin, He, Lin, Sawa, Akira, Martin, Alicia R., Qin, Shengying, Huang, Hailiang, Ge, Tian]
通讯作者:
Ge, Tian
DOI:
10.1038/s41467-022-34418-y
发表时间:
2022-11-11
期刊:
NATURE COMMUNICATIONS
影响因子:
16.6
作者:
[Lam, Max, Chen, Chia-Yen, Hill, W. David, Xia, Charley, Tian, Ruoyu, Levey, Daniel F., Gelernter, Joel, Stein, Murray B., Hatoum, Alexander S., Huang, Hailiang, Malhotra, Anil K., Runz, Heiko, Ge, Tian, Lencz, Todd]
通讯作者:
Lencz, Todd
DOI:
10.1176/appi.ajp.2020.19111158
发表时间:
2020-10-01
期刊:
AMERICAN JOURNAL OF PSYCHIATRY
影响因子:
17.7
作者:
[Choi, Karmel W., Stein, Murray B., Nishimi, Kristen M., Ge, Tian, Coleman, Jonathan R., I, Chen, Chia-Yen, Ratanatharathorn, Andrew, Zheutlin, Amanda B., Dunn, Erin C., Breen, Gerome, Koenen, Karestan C., Smoller, Jordan W.]
通讯作者:
Smoller, Jordan W.
DOI:
10.1093/cercor/bhac056
发表时间:
2022
期刊:
Cerebral cortex (New York, N.Y. : 1991)
影响因子:
--
作者:
[Setton,Roni, Mwilambwe-Tshilobo,Laetitia, Girn,Manesh, Lockrow,AmberW, Baracchini,Giulia, Hughes,Colleen, Lowe,AlexanderJ, Cassidy,BenjaminN, Li,Jian, Luh,Wen-Ming, Bzdok,Danilo, Leahy,RichardM, Ge,Tian, Margulies,DanielS, Misic,Bratis]
通讯作者:
Misic,Bratis
DOI:
10.1002/ajmg.b.32868
发表时间:
2021-12
期刊:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
影响因子:
--
作者:
[Stein MB, Jain S, Campbell-Sills L, Ware EB, Choi KW, He F, Ge T, Gelernter J, Smoller JW, Kessler RC, Ursano RJ]
通讯作者:
Ursano RJ
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Exploring the genetic basis of AD progression
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财政年份:2017
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Exploring the genetic basis of AD progression
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批准号:10058453
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资助金额:$24.41万
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财政年份:2017
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负责人:Tian Ge
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