Despite evidence for sex differences in age-related changes in functional connectivity (FC), extant age-prediction studies have relied on mixed-sex samples. We applied connectome-based predictive modeling (CPM) on whole-brain resting-state FCs (parcellated into 100/16-cortical/subcortical regions) from the Human Connectome Project-Aging (age 36–100 years) dataset, separately for males (M; n = 263) and females (F; n = 339). Model performance and cross-sex generalizability were evaluated using Pearson’s r and externally validated with the Aging Adult Brain Connectome dataset (age 36–89 years; M/F: n = 143/201). Predictive edges were mapped to functional networks to characterize sex-shared and different networks. Within sex-different networks, we tested whether cognitive/emotional factors moderated age-related FC changes. CPM robustly predicted age within sex (M/F: r = 0.66–0.68/0.58–0.60; all p ’s < 0.001), across sexes (M → F/F → M r = 0.66/0.60), and in validation dataset (M/F: r = 0.70/0.57). Default mode network (DMN) contributed strongly to age-prediction across sexes, but network composition differed, with affective-control networks more significantly involved in females and sensory-perceptual networks in males. DMN-limbic connectivity change with age was negatively moderated by diminished fluid cognition in males and positively by enhanced negative emotion in females. These findings reveal sex-shared and different network mechanisms of brain aging and identify DMN-limbic connectivity as a convergent, age-sensitive circuit, influenced by individual differences in cognition and emotion across sexes.
No takes yet. Share an insight, caveat, or question.
Chaudhary et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: