Cross study transcriptomic investigation of Alzheimer’s brain tissue discoveries and limitations

Developing effective treatments for Alzheimer's disease (AD) likely requires a deep understanding of molecular mechanisms. Integration of transcriptomic datasets and developing innovative computational analyses may yield novel molecular targets with broad applicability. The motivation for this study was conceived from two main observations: (a) most transcriptomic analyses of AD data consider univariate differential expression analysis, and (b) insights are often not transferable across studies. We designed a machine learning-based framework that can elucidate interpretable multivariate relationships from multiple human AD studies to discover robust transcriptomic AD biomarkers transferable across multiple studies. Our analysis of three human hippocampus datasets revealed multiple robust synergistic associations from unrelated pathways along with inconsistencies of gene associations across different studies. Our study underscores the utility of developing AI-assisted next-gen metrics for integration, robustness, and generalization and also highlights the potential benefit of elucidating molecular mechanisms and pathways that are important in targeting a single population.

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Publication Details

Journal
Scientific Reports
Published
2025-05-08
DOI
https://doi.org/10.1038/s41598-025-01017-y
Citations
2
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
1.61

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article

Cross study transcriptomic investigation of Alzheimer’s brain tissue discoveries and limitations

Nimish Khanna, Ranadip Pal, J. Josh Lawrence, Chiquito Crasto et al.
2 citations
Scientific Reports
Bioinformatics and Genomic Networks
1.61
article

Cross study transcriptomic investigation of Alzheimer’s brain tissue discoveries and limitations

Nimish Khanna, Ranadip Pal, J. Josh Lawrence, Chiquito Crasto, Cesar Sanchez-Villalobos, Yixiang Mao, Fernando Koiti Tsurukawa
article en
2 citations

Abstract

Developing effective treatments for Alzheimer's disease (AD) likely requires a deep understanding of molecular mechanisms. Integration of transcriptomic datasets and developing innovative computational analyses may yield novel molecular targets with broad applicability. The motivation for this study was conceived from two main observations: (a) most transcriptomic analyses of AD data consider univariate differential expression analysis, and (b) insights are often not transferable across studies. We designed a machine learning-based framework that can elucidate interpretable multivariate relationships from multiple human AD studies to discover robust transcriptomic AD biomarkers transferable across multiple studies. Our analysis of three human hippocampus datasets revealed multiple robust synergistic associations from unrelated pathways along with inconsistencies of gene associations across different studies. Our study underscores the utility of developing AI-assisted next-gen metrics for integration, robustness, and generalization and also highlights the potential benefit of elucidating molecular mechanisms and pathways that are important in targeting a single population.

Scientific ReportsVol. 15(1)
Texas Tech University (US)
National Institutes of Health
Openalex Percentile: Top 17%
Bioinformatics and Genomic Networks
1.61
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Cross study transcriptomic investigation of Alzheimer’s brain tissue discoveries and limitations — Nimish Khanna, Ranadip Pal, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS