medRxiv : the preprint server for health sciences · 2026
Cell composition, transcriptomic, and functional pathway changes in the hippocampus in Alzheimer's disease and overlap with lead (Pb) exposure signatures.
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Wang Herong, Matei Evelyn, Dou John, Morgan Rachel K, Colacino Justin, Bakulski Kelly M
Аннотация
BACKGROUND: Lead (Pb) is associated with Alzheimer's disease (AD); however, the relationships between Pb and AD hippocampal transcription remains unclear. We evaluated overlap between Pb-response signatures and cell-type-independent AD transcriptomic signatures.
METHOD: Three toxicology studies (two neuronal cell lines, one mouse hippocampus) provided Pb-response genes. Five human postmortem hippocampal AD case-control transcriptional datasets (n=90 AD, n=106 normal cognition) were cell type deconvoluted and tested with beta regression. Differential gene expression, adjusted for age, sex, and estimated cell-types, were meta-analyzed. Overlapping Pb and AD genes and biological pathways were identified (padj<0.05).
RESULTS: Consistent Pb response was observed at 25 genes (INPP5F, KIF20B, KIFC1) and 47 pathways (ensheathment of neurons, glial cell differentiation, regulation of nervous system processes). Relative to controls, AD samples had fewer neurons (-2.46%), greater microglia (0.42%), astrocytes (0.31%), oligodendrocytes (0.46%), and endothelial cells (0.95%), and 1,455 differentially expressed genes, which were enriched for cellular energy production and metabolism pathways. Six genes (EHD3, LAP3, NRXN3, PPP1R16B, RPL29, THRA) and four pathways (synaptic vesicle maturation, vesicle docking) overlapped between Pb and AD.
CONCLUSION: We identified overlapping Pb and AD transcriptomic signatures and pathways, providing molecular context for epidemiologic associations.
METHOD: Three toxicology studies (two neuronal cell lines, one mouse hippocampus) provided Pb-response genes. Five human postmortem hippocampal AD case-control transcriptional datasets (n=90 AD, n=106 normal cognition) were cell type deconvoluted and tested with beta regression. Differential gene expression, adjusted for age, sex, and estimated cell-types, were meta-analyzed. Overlapping Pb and AD genes and biological pathways were identified (padj<0.05).
RESULTS: Consistent Pb response was observed at 25 genes (INPP5F, KIF20B, KIFC1) and 47 pathways (ensheathment of neurons, glial cell differentiation, regulation of nervous system processes). Relative to controls, AD samples had fewer neurons (-2.46%), greater microglia (0.42%), astrocytes (0.31%), oligodendrocytes (0.46%), and endothelial cells (0.95%), and 1,455 differentially expressed genes, which were enriched for cellular energy production and metabolism pathways. Six genes (EHD3, LAP3, NRXN3, PPP1R16B, RPL29, THRA) and four pathways (synaptic vesicle maturation, vesicle docking) overlapped between Pb and AD.
CONCLUSION: We identified overlapping Pb and AD transcriptomic signatures and pathways, providing molecular context for epidemiologic associations.