Evidence map›Paper›PMID 35080765›Full record

ArticleJournal of molecular neuroscience : MN2022

Detecting Biomarkers of Alzheimer's Disease Based on Multi-constrained Uncertainty-Aware Adaptive Sparse Multi-view Canonical Correlation Analysis.

Wenbo Wang, Wei Kong, Shuaiqun Wang, Kai Wei

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Article in Journal of molecular neuroscience : MN, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 44% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

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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 at 1 institution in 1 country.

Wenbo WangCollege of Information Engineering, Shanghai Maritime University, 1550 Haigang Ave., Shanghai, 201306, People's Republic of China.
Wei KongCollege of Information Engineering, Shanghai Maritime University, 1550 Haigang Ave., Shanghai, 201306, People's Republic of China. weikong@shmtu.edu.cn.ORCID http://orcid.org/0000-0002-6554-4338
Shuaiqun WangCollege of Information Engineering, Shanghai Maritime University, 1550 Haigang Ave., Shanghai, 201306, People's Republic of China.
Kai WeiCollege of Information Engineering, Shanghai Maritime University, 1550 Haigang Ave., Shanghai, 201306, People's Republic of China.
Shanghai Maritime University · CN

Funding

National Natural Science Foundation of China No.61803257Natural Science Foundation of Shanghai No.18ZR1417200
6 · The paper itself

Abstract

Image genetics mainly explores the pathogenesis of Alzheimer's disease (AD) by studying the relationship between genetic data (such as SNP, gene expression data, and DNA methylation) and imaging data (such as structural MRI (sMRI), fMRI, and PET). Most of the existing research on brain imaging genomics uses two-way or three-way bi-multivariate methods to explore the correlation analysis between genes and brain imaging. However, many of these methods are still affected by the gradient domination or cannot take into account the effect of feature redundancy on the results, so that the typical correlation coefficient and program running speed are not significantly improved. In order to solve the above problems, this paper proposes a multi-constrained uncertainty-aware adaptive sparse multi-view canonical correlation analysis method (MC-unAdaSMCCA) to explore associations among SNPs, gene expression data, and sMRI; that is, based on traditional unAdaSMCCA, orthogonal constraints are imposed on the weights of the three data features through linear programming, which can reduce the redundancy of feature weights to improve the correlation between the data and reduce the complexity of the algorithm to significantly speed up the running speed of the program. Three adaptive sparse multi-view canonical correlation analysis methods are used as benchmarks to evaluate the difference between real neuroimaging data and synthetic data. Compared with the other three methods, our proposed method has obtained better or comparable typical correlation coefficients and typical weights. Moreover, the following experimental results show that the MC-unAdaSMCCA method cannot only identify biomarkers related to AD and mild cognitive impairment (MCI), but also has a strong ability to resist noise and process high-dimensional data. Therefore, our proposed method provides a reliable approach to multi-modal imaging genetic researches.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAlgorithmsBiomarkersBrainCanonical Correlation AnalysisHumansMagnetic Resonance ImagingNeuroimagingUncertaintyBiomarkersAdaptive sparse multi-view canonical correlation analysis method (AdaSMCCA)Alzheimer’s disease (AD)Image geneticsMulti-constrained

Identifiers

PMID35080765
OpenAlexW4210327192

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.