Evidence map›Paper›PMID 32218482›Full record

ArticleScientific reports2020

Multimodal Phenotyping of Alzheimer's Disease with Longitudinal Magnetic Resonance Imaging and Cognitive Function Data.

Yejin Kim, Xiaoqian Jiang, Luca Giancardo, Danilo Pena, Avram S Bukhbinder, Albert Y Amran, Paul E Schulz, Alzheimer’s Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yejin KimSchool of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA. yejin.kim@uth.tmc.edu.
Xiaoqian JiangSchool of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Luca GiancardoSchool of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Danilo PenaSchool of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Avram S BukhbinderDepartment of Neurology, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Albert Y AmranDepartment of Neurology, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Paul E SchulzDepartment of Neurology, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Alzheimer’s Disease Neuroimaging Initiative

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Convalescent Plasma to Limit Coronavirus Associated ComplicationsUL1TR003167 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARP, DANIEL D, MCPHERSON, DAVID D · 2019 to 2023
$45.3M
Privacy-preserving methods and tools for handling missing data in distributed health data networksR01GM124111 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LONG, QI · 2017 to 2020
$2.3M
NCATS NIH HHS UL1 TR003167NIA NIH HHS U01 AG024904NIGMS NIH HHS R01 GM124111
6 · The paper itself

Abstract

Alzheimer's disease (AD) varies a great deal cognitively regarding symptoms, test findings, the rate of progression, and neuroradiologically in terms of atrophy on magnetic resonance imaging (MRI). We hypothesized that an unbiased analysis of the progression of AD, regarding clinical and MRI features, will reveal a number of AD phenotypes. Our objective is to develop and use a computational method for multi-modal analysis of changes in cognitive scores and MRI volumes to test for there being multiple AD phenotypes. In this retrospective cohort study with a total of 857 subjects from the AD (n = 213), MCI (n = 322), and control (CN, n = 322) groups, we used structural MRI data and neuropsychological assessments to develop a novel computational phenotyping method that groups brain regions from MRI and subsets of neuropsychological assessments in a non-biased fashion. The phenotyping method was built based on coupled nonnegative matrix factorization (C-NMF). As a result, the computational phenotyping method found four phenotypes with different combination and progression of neuropsychologic and neuroradiologic features. Identifying distinct AD phenotypes here could help explain why only a subset of AD patients typically respond to any single treatment. This, in turn, will help us target treatments more specifically to certain responsive phenotypes.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAtrophyBrainDisease ProgressionFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleModels, TheoreticalNeuropsychological TestsPhenotypeRetrospective Studies

Identifiers

PMID32218482
PMCPMC7099007

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.