Editorial: The early detection of neurodegenerative diseases: an aging perspective

A consistent theme across several contributions is the transition from regional lesion-based models to system-level interpretations of neural dysfunction. Paitel ER et al. systematically reviewed more than 120 electroencephalographic (EEG) studies in AD and mild cognitive impairment (MCI), highlighting reproducible patterns of reduced alpha-band connectivity, revealing that disrupted communication precedes overt neurodegeneration and supporting the view of AD as a disconnection syndrome. Zhao Y et al. demonstrated that peak alpha frequency is a sensitive and robust electrophysiological marker of post-stroke cognitive impairment (PSCI), linking oscillatory slowing to cognitive decline across cortical regions and supporting strong associations with Montreal Cognitive Assessment (MoCA) scores. Together, these studies position EEG as an accessible, temporally precise window into early disconnection processes not visible to conventional structural imaging, as also supported by the leading editor Wang's research group work. This network perspective extends also to PD. Zhao J et al. employed functional near-infrared spectroscopy (fNIRS) to reveal distinct cortical activation patterns during executive tasks. PD patients with MCI displayed enhanced interhemispheric connectivity, suggesting compensatory recruitment, whereas those with dementia showed network hypoactivation, consistent with structural atrophy and network collapse. Hence, electrophysiological and hemodynamic connectivity measures emerge as accessible tools capable of identifying transitional phases between normal and pathological aging, thresholding between adaptive and maladaptive reorganization and offering accessible functional biomarkers for longitudinal monitoring.Vascular mechanisms emerge as another unifying element across this Research Topic. Fu P and Hu M reported that lower plasma von Willebrand Factor (VWF) levels predict faster longitudinal cognitive decline and greater hippocampal and entorhinal cortex atrophy in older adults without dementia , underscoring the prognostic significance of vascular biomarkers in apparently healthy individuals, capturing subclinical vulnerabilities that precede faster deterioration. Xie Q et al. used susceptibilityweighted imaging and artificial intelligence (AI)-based segmentation to quantify superficial cortical veins, revealing correlations between venous morphology, tau levels, and cognitive performance, linking cerebrovascular architecture to neurodegenerative proteinopathy. Together, these contributions suggest neurovascular integrity as both biomarker and mechanistic driver within the neurodegenerative continuum, linking microvascular dysfunction, neuroinflammation and early neurodegenerative cascades.Early biomarkers can also be detected outside the central nervous system. Yuan C et al. identified ferroptosis-related gene signatures as diagnostic and therapeutic targets in hearing loss, an adultonset peripheral disorder with mechanistic parallels to neurodegeneration. Genes such as MEF2C and NEDD4, implicated in age-related auditory nerve deterioration, also appear in deafness associated datasets, suggesting potential cross-organ biomarkers of oxidative stress and cell death. Their multistep approach-combining transcriptomics screening, machine-learning model selection, and experimental validation-highlights how integrated pipelines can accelerate the discovery of peripheral indicators of neural vulnerability. Sensory decline may thus serve as a sentinel of neurodegenerative risk, reflecting broader early neurobiological vulnerability.The identification of sensitive cognitive and behavioral indicators remains essential to early detection. Liu Y et al. validated the modified Face-Name Associative Memory Exam (mFNAME) as a reliable tool for detecting subtle mnemonic deficits, showing robust associations between performance and network efficiency within the default mode and medial temporal systems, even in asymptomatic individuals. Zhào H et al. used actigraphy to analyze fractal dynamics of physical activity in older adults with cerebral small vessel disease, demonstrating that reduced temporal complexity correlates with disease severity. Their findings highlight the value of digital phenotyping into early detection frameworks as a real-world complement to traditional cognitive assessments. Sun H et al. applied network analysis to explore interactions between activities of daily living (ADL) limitations and depressive symptoms in older adults, identifying "toileting" as a bridging node between physical and affective domains. This work illustrates how behavioral interdependencies can reveal early, multidimensional vulnerabilities. Mohamed B et al. showed that baseline cardiorespiratory fitness, but not aerobic capacity, predicts cognitive and motor outcomes in multiple sclerosis (MS), emphasizing disease heterogeneity and suggesting that resilience mechanisms may be domainspecific rather than generalized. Across these behavioral and computational approaches, AI, network modeling, and longitudinal analytics enhance detection sensitivity and help delineate complex patterns across datasets. As these tools grow more sophisticated, maintaining mechanistic interpretability alongside predictive accuracy remains essential.Collectively, these contributions support a multimodal, aging-informed framework for early detection, indicating neurodegeneration not as isolated diseases but as overlapping trajectories shaped by agingrelated biological processes. Across conditions such as AD, PD, VCI, hearing loss, and MS, the early manifestations share overlapping mechanisms like oxidative stress, vascular dysregulation, disrupted connectivity, and impaired compensatory plasticity. Each study captures a different facet of the gradual erosion of neural adaptability. Figure 1 integrates these findings by positioning the aging trajectory against multiple observational levels. Analytical tools such as AI-based modeling, network approaches, and multimodal integration provide the connective framework, while aging-related factors (genetics, lifestyle, vascular health, resilience mechanisms and sensory decline) modulate vulnerability. Future research should build on this integrative model, combining biomarkers across scales to predict the transition from resilience to vulnerability. Ultimately, early detection should not only identify disease risk but also map the biological processes that maintain or erode neural adaptability across the lifespan. From this perspective, aging is not a passive risk factor but an active landscape shaping neurodegenerative trajectories. The challenge ahead is to optimize and operationalize this framework to identify individuals at risk not by the presence of disease, but by the loss of resilience. Five complementary domains-electrophysiological/network (EEG, fNIRS connectivity), vascular/hemodynamic (VWF, cortical vein morphology, cerebrovascular health), molecular/peripheral (ferroptosis-related genes, oxidative stress, hearing loss), cognitive/behavioral (memory performance, executive function, depression networks), and digital/functional (fractal activity patterns, ADL performance, digital biomarkers)-collectively contribute to an integrated earlydetection framework. Individual modifiers such as genetics, lifestyle, comorbidities, resilience mechanisms, and sensory decline modulate biomarker expression and interpretability. The integration of these multimodal signals enhances sensitivity, specificity, and predictive power, enabling transdiagnostic applications across Alzheimer's disease, Parkinson's disease, cerebrovascular disease, hearing loss, and multiple sclerosis (abbreviations: activities of daily living, ADL; electroencephalography, EEG; face-name associative memory exam, FNAME; functional near-infrared spectroscopy, fNIRS; von Willebrand Factor, VWF).