Although puberty is known to influence obesity progression, the molecular
mechanisms underlying the role of sexual maturation in obesity-related complications
remains largely unexplored. Here, we delve into the impact of
puberty on the most relevant pathogenic hallmarks of obesity, namely oxidative
stress and inflammation, and their association with trace element blood
status. To this end, we studied a well-characterized observational cohort comprising
prepubertal (N = 46) and pubertal (N = 48) children with obesity.
From all participants, plasma and erythrocyte samples were collected and subjected
to metallomics analysis and determination of classical biomarkers of
oxidative stress and inflammation. Besides the expected raise of sexual hormones,
pubertal children displayed better inflammatory and oxidative control,
as reflected by lower levels of C-reactive protein and oxidative damage
markers, as well as improved antioxidant defense. This was in turn accompanied
by a healthier multielemental profile, with increased levels of essential
elements involved in the antioxidant system and metabolic control (metalloproteins
containing zinc, molybdenum, selenium, and manganese) and
decreased content of potentially deleterious species (total copper, labile free
iron). Therefore, our findings suggest that children with obesity have an exacerbated
inflammatory and oxidative damage at early ages, which could be ameliorated
during pubertal development by the action of trace element-mediated
buffering mechanisms.