Evidence map›Paper›PMID 31095298›Full record

ArticleBioinformatics (Oxford, England)2019

Incorporating spatial-anatomical similarity into the VGWAS framework for AD biomarker detection.

Meiyan Huang, Yuwei Yu, Wei Yang, Qianjin Feng, Alzheimer’s Disease Neuroimaging Initiative

Open access · greenAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

Meiyan HuangGuangdong Provincial Key Laboratory of Medical Image Processing, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
Yuwei YuGuangdong Provincial Key Laboratory of Medical Image Processing, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
Wei YangGuangdong Provincial Key Laboratory of Medical Image Processing, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
Qianjin FengGuangdong Provincial Key Laboratory of Medical Image Processing, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
Alzheimer’s Disease Neuroimaging Initiative
Southern Medical University · CN

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

motivationThe detection of potential biomarkers of Alzheimer's disease (AD) is crucial for its early prediction, diagnosis and treatment. Voxel-wise genome-wide association study (VGWAS) is a commonly used method in imaging genomics and usually applied to detect AD biomarkers in imaging and genetic data. However, existing VGWAS methods entail large computational cost and disregard spatial correlations within imaging data. A novel method is proposed to solve these issues.

resultsWe introduce a novel method to incorporate spatial correlations into a VGWAS framework for the detection of potential AD biomarkers. To consider the characteristics of AD, we first present a modification of a simple linear iterative clustering method for spatial grouping in an anatomically meaningful manner. Second, we propose a spatial-anatomical similarity matrix to incorporate correlations among voxels. Finally, we detect the potential AD biomarkers from imaging and genetic data by using a fast VGWAS method and test our method on 708 subjects obtained from an Alzheimer's Disease Neuroimaging Initiative dataset. Results show that our method can successfully detect some new risk genes and clusters of AD. The detected imaging and genetic biomarkers are used as predictors to classify AD/normal control subjects, and a high accuracy of AD/normal control classification is achieved. To the best of our knowledge, the association between imaging and genetic data has yet to be systematically investigated while building statistical models for classifying AD subjects to create a link between imaging genetics and AD. Therefore, our method may provide a new way to gain insights into the underlying pathological mechanism of AD. AVAILABILITY AND IMPLEMENTATION: https://github.com/Meiyan88/SASM-VGWAS.

Indexed as

Alzheimer DiseaseBiomarkersBrainGenome-Wide Association StudyHumansMagnetic Resonance ImagingNeuroimagingBiomarkers

Identifiers

PMID31095298
PMCPMC6954655
OpenAlexW2945255879

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.