Skip to content
Open access

Comparative evaluation of reference-free transcriptomic deconvolution highlights the importance of biological validation in astrocytes across Alzheimer’s disease

Jul 2026 · Frontiers in Bioinformatics · Vol 6 · 0 citations · 48 references
Medicine

TL;DR

A comparative framework evaluating two complementary unsupervised approaches, CDSeq and DECODER, to reconstruct astrocyte-associated transcriptomic profiles from human hippocampal samples spanning control, mild cognitive impairment, and AD stages establishes a reproducible strategy for evaluating deconvolution methods and their functional consequences.

Abstract

Introduction Astrocytes are central regulators of neuronal energy metabolism and redox homeostasis—processes that become progressively disrupted across the Alzheimer’s disease (AD) continuum. However, bulk transcriptomic data obscure cell-type–specific signals, and existing reference-free deconvolution methods often prioritize either statistical robustness or quantitative accuracy without fully integrating both dimensions. Methods Here, we present a comparative framework evaluating two complementary unsupervised approaches, CDSeq and DECODER, to reconstruct astrocyte-associated transcriptomic profiles from human hippocampal samples spanning control, mild cognitive impairment (incipient and moderate), and AD (severe) stages (GSE28146; n = 30). The inferred profiles were functionally contextualized through integration into a genome-scale metabolic model of human astrocytes, enabling the assessment of system-level metabolic alterations associated with disease progression. Results Our results reveal consistent dysregulation of key astrocytic pathways, including impairment of the astrocyte–neuron lactate shuttle, disruption of glutamine metabolism, and reduced glutathione-mediated an oxidant capacity. Methodological benchmarking showed distinct yet complementary performance profiles: DECODER achieved higher accuracy in reconstructing global expression magnitudes, whereas CDSeq exhibited greater stability and preservation of gene–gene relationships. Crucially, external validation using independent single-nucleus RNA-seq astrocyte data demonstrated that CDSeq-derived profiles achieve moderate but robust concordance with reference signatures (r ≈ 0.43–0.44), substantially exceeding DECODER-derived concordance (r ≈ 0.19–0.23), with higher concordance with astrocyte-associated signatures, alongside preservation of canonical astrocyte markers and enrichment of astrocyte-specific pathways, indicating superior biological coherence. Discussion Together, these findings demonstrate that technical accuracy does not necessarily translate into biological validity and highlight CDSeq as the method that more reliably captures astrocyte-specific transcriptional programs in this context. While DECODER remains valuable for detecting absolute expression changes, CDSeq provides a more consistent recovery of astrocyte-associated transcriptional patterns. More broadly, our results support the incorporation of biological validation alongside statistical benchmarking when selecting deconvolution methods for downstream systems biology and metabolic modeling applications. This framework establishes a reproducible strategy for evaluating deconvolution methods and their functional consequences, advancing the interpretation of bulk transcriptomic data in neurodegenerative disease.

Read PDF

Similar papers

Open access Sep 2026

Integrative genome-scale metabolic model of GABAergic neurons reveals metabolic signatures across the mild cognitive impairment – Alzheimer disease continuum

This work provides a systems-level computational framework linking transcriptomic alterations with predicted metabolic remodeling in GABAergic neurons and generates experimentally testable hypotheses regarding metabolic dysfunction during progression from MCI to AD.

Andrea Angarita-Rodríguez, Johan H. Largo-González, Julián Pérez-Mejía et al. · 0 citations
Open access Aug 2026

Systematic assessment of the biological impact of cellular deconvolution on downstream analyses of disease transcriptomes

Parallel evaluation of uncorrected and CTC analyses distinguishes composition-driven from cell-intrinsic transcriptional effects and highlights robust disease signatures in heterogeneous tissues such as the brain.

Sanga Mitra, Maziya Ibrahim, Manikandan Narayanan · 0 citations
Open access Aug 2026

In silico analysis of transcriptomic datasets reveals nonlinear gene expression trajectories in aging microglia and Alzheimer's disease.

It is suggested that middle age may represent a critical transition stage preceding neuroinflammation and neurodegeneration, making it an attractive window to identify preventive or therapeutic targets in early AD.

Andrés Muedano-Sosa, Magalli Trujillo-Pineda, Samuel Ruiz-Pérez et al. · 0 citations
Open access Aug 2026

Glial-adjusted residual transcriptomics with leave-one-out transcriptome-wide association study influence analysis prioritizes GALNT6 and other high-impact genes in Alzheimer's disease

Findings support glial-adjusted residual transcriptomics with leave-one-out TWAS influence analysis as a computational prioritization strategy for Alzheimer's disease, rather than as evidence of broad pathway-level genetic enrichment.

Cheung Ngo · 0 citations
Open access Sep 2026

An Integrated Single-Nucleus Atlas Resolves Cell-Type-Specific Programs and Molecular Subtypes in Alzheimer’s Disease

Interindividual heterogeneity in Alzheimer’s disease (AD) remains poorly understood, as disparate single-cell studies leave it unclear whether findings reflect shared architecture or dataset-specific idiosyncrasies. Here, we present panAD, a transcriptomic atlas of >3 million nuclei from 791 individuals across 13 studi...

Negin Rahimzadeh, S. Morabito, S. Khullar et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.