Evidence map›Paper›PMID 36478772›Full record

ArticleIEEE journal of translational engineering in health and medicine2023

Explainable Tensor Multi-Task Ensemble Learning Based on Brain Structure Variation for Alzheimer's Disease Dynamic Prediction.

Yu Zhang, Tong Liu, Vitaveska Lanfranchi, Po Yang

Abstract read
In one paragraph

Article in IEEE journal of translational engineering in health and medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 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

4 authors.

Yu ZhangDepartment of Computer ScienceThe University of Sheffield Sheffield S10 2TN U.K.ORCID 0000-0002-7377-1194
Tong LiuDepartment of Computer ScienceThe University of Sheffield Sheffield S10 2TN U.K.
Vitaveska LanfranchiDepartment of Computer ScienceThe University of Sheffield Sheffield S10 2TN U.K.ORCID 0000-0003-3148-2535
Po YangDepartment of Computer ScienceThe University of Sheffield Sheffield S10 2TN U.K.ORCID 0000-0002-8553-7127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Machine learning approaches for predicting Alzheimer's disease (AD) progression can substantially assist researchers and clinicians in developing effective AD preventive and treatment strategies. This study proposes a novel machine learning algorithm to predict the AD progression utilising a multi-task ensemble learning approach. Specifically, we present a novel tensor multi-task learning (MTL) algorithm based on similarity measurement of spatio-temporal variability of brain biomarkers to model AD progression. In this model, the prediction of each patient sample in the tensor is set as one task, where all tasks share a set of latent factors obtained through tensor decomposition. Furthermore, as subjects have continuous records of brain biomarker testing, the model is extended to ensemble the subjects' temporally continuous prediction results utilising a gradient boosting kernel to find more accurate predictions. We have conducted extensive experiments utilising data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to evaluate the performance of the proposed algorithm and model. Results demonstrate that the proposed model have superior accuracy and stability in predicting AD progression compared to benchmarks and state-of-the-art multi-task regression methods in terms of the Mini Mental State Examination (MMSE) questionnaire and The Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog) cognitive scores. Brain biomarker correlation information can be utilised to identify variations in individual brain structures and the model can be utilised to effectively predict the progression of AD with magnetic resonance imaging (MRI) data and cognitive scores of AD patients at different stages.

Indexed as

Alzheimer DiseaseBrainHumansMachine LearningAlzheimer’s diseasebrain biomarker spatio-temporal correlationgradient boosting ensemble learningmulti-task learningtensor decomposition

Identifiers

PMID36478772
PMCPMC9721355

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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.