• Identified 911 subtype-specific differentially expressed genes associated with cellular senescence and endoplasmic reticulum stress in premature ovarian insufficiency.
• Aurora kinase A and actin binding protein were identified as potential key biomarkers with good diagnostic predictive performance.
• M1 macrophages and resting dendritic cells showed significantly higher infiltration in premature ovarian insufficiency, suggesting immune involvement.
• Animal experiments confirmed decreased expression of aurora kinase A and actin binding protein in ovarian tissue of premature ovarian insufficiency model mice.
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