ArticleBrain communications2026
Sex-dependent dopaminergic vulnerability may contribute to sex differences in Parkinson's disease risk.
Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
Men are more likely than women to develop Parkinson's disease, yet the biological basis of this sex difference in Parkinson's disease risk remains unresolved. The nigrosome-1 (NG-1), a dopaminergic subregion of the substantia nigra, is selectively vulnerable to degeneration and iron accumulation in Parkinson's disease, therefore representing a plausible locus for sex-linked vulnerability. Using iron-sensitive magnetic resonance imaging from the UK Biobank, we examined sex differences in NG-1 magnetic susceptibility across adulthood. We analysed cross-sectional data from 53 792 individuals aged 45-85 years and longitudinal follow-up in 4068 participants. Across mid-to-late adulthood, men consistently exhibited higher NG-1 magnetic susceptibility than women, suggestive of greater iron-related signal burden. In contrast, age-related trajectories and rates of within-person change were similar between sexes, with no evidence for accelerated nigrostriatal ageing in men. Sensitivity analyses showed that these sex differences were not substantially modified by genetic risk for Parkinson's disease, cardiometabolic disease or major lifestyle factors. Together, these findings suggest that sex differences in NG-1 susceptibility are expressed primarily as a stable baseline offset rather than divergent ageing dynamics. By distinguishing baseline variation from age-related changes in a selectively vulnerable dopaminergic system, this study provides population-scale evidence relevant to understanding sex differences in vulnerability to Parkinson's disease.
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