Evidence map›Paper›PMID 40600033›Full record

ArticleFrontiers in medicine2025

GAN-enhanced deep learning for improved Alzheimer's disease classification and longitudinal brain change analysis.

Purushottam Pandey, Surbhi Bhatia Khan, Jyoti Pruthi, Eid Albalawi, Ali Algarni, Ahlam Almusharraf

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Frontiers in artificial intelligence · 2026
    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

6 authors.

Purushottam PandeyManav Rachna University (MRU), Faridabad, Haryana, India.
Surbhi Bhatia KhanSchool of Science, Engineering and Environment, University of Salford, Salford, United Kingdom.
Jyoti PruthiManav Rachna University (MRU), Faridabad, Haryana, India.
Eid AlbalawiDepartment of Computer Science, College of Computer Sciences and Information Technology, King Faisal University, Al Ahsa, Saudi Arabia.
Ali AlgarniDepartment of Informatics and Computer Systems, College of Computer Science, King Khalid University, Abha, Saudi Arabia.
Ahlam AlmusharrafDepartment of Management, College of Business Administration, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is commonly defined by a progressive decline in cognitive functions and memory. Early detection is crucial to mitigate the devastating impacts of AD, which can significantly impair a person's quality of life. Traditional methods for diagnosing AD, while still in use, often involve time-consuming processes that are prone to errors and inefficiencies. These manual techniques are limited in their ability to handle the vast amount of data associated with the disease, leading to slower diagnosis and potential misclassification. Advancements in artificial intelligence (AI), specifically machine learning (ML) and deep learning (DL), offer promising solutions to these challenges. AI techniques can process large datasets with high accuracy, significantly improving the speed and precision of AD detection. However, despite these advancements, issues such as limited accuracy, computational complexity, and the risk of overfitting still pose challenges in the field of AD classification. To address these challenges, the proposed study integrates deep learning architectures, particularly ResNet101 and long short-term memory (LSTM) networks, to enhance both feature extraction and classification of AD. The ResNet101 model is augmented with innovative layers such as the pattern descriptor parsing operation (PDPO) and the detection convolutional kernel layer (DCK), which are designed to extract the most relevant features from datasets such as ADNI and OASIS. These features are then processed through the LSTM model, which classifies individuals into categories such as cognitively normal (CN), mild cognitive impairment (MCI), and Alzheimer's disease (AD). Another key aspect of the research is the use of generative adversarial networks (GANs) to identify the progressive or non-progressive nature of AD. By employing both a generator and a discriminator, the GAN model detects whether the AD state is advancing. If the original and predicted classes align, AD is deemed non-progressive; if they differ, the disease is progressing. This innovative approach provides a nuanced view of AD, which could lead to more precise and personalized treatment plans. The numerical outcome obtained by the proposed model for ADNI dataset is 0.9931, and for OASIS dataset, the accuracy gained by the model is 0.9985. Ultimately, this research aims to offer significant contributions to the medical field, helping healthcare professionals diagnose AD more accurately and efficiently, thus improving patient outcomes. Furthermore, brain simulation models are integrated into this framework to provide deeper insights into the underlying neural mechanisms of AD. These brain simulation models help visualize and predict how AD may evolve in different regions of the brain, enhancing both diagnosis and treatment planning.

Indexed as

ADNIAlzheimer's diseasegenerative adversarial networklong short term memoryOASIS datasetResNet101

Identifiers

PMID40600033
PMCPMC12209275

What OpenQuestion holds

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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.