Conserved neuroectodermal aging encodes primate health and longevity

Abstract

Neuroectoderm-derived tissues are highly metabolically active and exhibit minimal regenerative turnover, rendering them uniquely vulnerable to age-related stress while preserving undiluted degenerative signals. Yet aging dynamics in these tissues remain elusive in living primates. Here, we introduce an in vivo neuroectodermal aging clock and trace its trajectory in 66,602 human adults and six rhesus macaques across nine health and disease cohorts using an in situ optical biopsy. Through a digital histology atlas integrated with artificial intelligence, we resolve tissue representations of neuroectodermal aging within the human retina, predominantly localized to the metabolically active ganglion and bipolar cell populations and the photoreceptor complex, while demonstrating their evolutionary conservation across primate species. Neuroectodermal aging predicts health and longevity, scales across space and time, and captures preclinical aging signals within and beyond the neuroectodermal compartment. This framework is further validated in a diabetic population, where robust prognostic and dynamic sensitivity are preserved across physiological and perturbed states. Our work establishes a scalable framework for resolving neuroectodermal aging in living primates and linking tissue-level vulnerability to systemic health trajectories.