Late-onset neurodegenerative diseases may originate from subtle vulnerabilities established during early development, yet the specific mechanisms linking early-life factors to later pathology remain poorly understood. Emerging evidence suggests that prenatal and postnatal influences, including genetic predispositions, maternal health, and environmental exposures, shape neural circuits in ways that may predispose individuals to neurodegeneration. Subclinical abnormalities in synaptic pruning, neurogenesis, and immune regulation are increasingly recognized as latent risk factors, but their precise contribution to disease onset has not been clearly defined. Advances in biomarker discovery, particularly in proteomic, genetic, and imaging domains, offer promising opportunities to detect such vulnerabilities before clinical symptoms arise. Despite these insights, the field lacks longitudinal and mechanistic studies that connect early developmental disruptions to specific neurodegenerative outcomes. Addressing this gap will require integrative research that combines experimental models with life-course studies to clarify causal pathways. By identifying concrete mechanistic links, future work may inform more targeted preventive strategies, rather than broadly proposing reductions in global disease burden.
Rissardo et al. (Tue,) studied this question.