Evidence map›Paper›PMID 36394351›Full record

ArticleHuman brain mapping2023

Generative adversarial network constrained multiple loss autoencoder: A deep learning-based individual atrophy detection for Alzheimer's disease and mild cognitive impairment.

Rong Shi, Can Sheng, Shichen Jin, Qi Zhang, Shuoyan Zhang, Liang Zhang, Changchang Ding, Luyao Wang, Lei Wang, Ying Han and 1 more

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 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

11 authors at 3 institutions in 2 countries.

Rong ShiSchool of Information and Communication Engineering, Shanghai University, Shanghai, China.ORCID 0000-0002-6440-1263
Can ShengDepartment of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.
Shichen JinSchool of Information and Communication Engineering, Shanghai University, Shanghai, China.
Qi ZhangSchool of Information and Communication Engineering, Shanghai University, Shanghai, China.
Shuoyan ZhangSchool of Information and Communication Engineering, Shanghai University, Shanghai, China.
Liang ZhangKey Laboratory of Biomedical Engineering of Hainan Province, School of Biomedical Engineering, Hainan University, Haikou, China.
Changchang DingSchool of Information and Communication Engineering, Shanghai University, Shanghai, China.ORCID 0000-0002-3051-7479
Luyao WangSchool of Information and Communication Engineering, Shanghai University, Shanghai, China.
Lei WangCollege of Computing and Informatics, Drexel University, Philadelphia, Pennsylvania, USA.
Ying HanDepartment of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.ORCID 0000-0003-0377-7424
Jiehui JiangInstitute of Biomedical Engineering, School of Life Science, Shanghai University, Shanghai, China.ORCID 0000-0003-4948-3683
Shanghai University · CNCapital Medical University · CNHainan University · CN

Funding

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

Abstract

Exploring individual brain atrophy patterns is of great value in precision medicine for Alzheimer's disease (AD) and mild cognitive impairment (MCI). However, the current individual brain atrophy detection models are deficient. Here, we proposed a framework called generative adversarial network constrained multiple loss autoencoder (GANCMLAE) for precisely depicting individual atrophy patterns. The GANCMLAE model was trained using normal controls (NCs) from the Alzheimer's Disease Neuroimaging Initiative cohort, and the Xuanwu cohort was employed to validate the robustness of the model. The potential of the model for identifying different atrophy patterns of MCI subtypes was also assessed. Furthermore, the clinical application potential of the GANCMLAE model was investigated. The results showed that the model can achieve good image reconstruction performance on the structural similarity index measure (0.929 ± 0.003), peak signal-to-noise ratio (31.04 ± 0.09), and mean squared error (0.0014 ± 0.0001) with less latent loss in the Xuanwu cohort. The individual atrophy patterns extracted from this model are more precise in reflecting the clinical symptoms of MCI subtypes. The individual atrophy patterns exhibit a better discriminative power in identifying patients with AD and MCI from NCs than those of the t-test model, with areas under the receiver operating characteristic curve of 0.867 (95%: 0.837-0.897) and 0.752 (95%: 0.71-0.790), respectively. Similar findings are also reported in the AD and MCI subgroups. In conclusion, the GANCMLAE model can serve as an effective tool for individualised atrophy detection.

Indexed as

Alzheimer DiseaseCognitive DysfunctionDeep LearningAtrophyBrainHumansMagnetic Resonance ImagingAlzheimer's diseaseGANmagnetic resonance imagingprecision medicine

Identifiers

PMID36394351
PMCPMC9875916
OpenAlexW4309246358

What OpenQuestion holds

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LicenceCC BY
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.