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Xiao-Yan Wu

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Sep 2026

Association between prenatal trace element and toxic metal exposures and autism spectrum disorder symptoms in children: Potential mediating role of cord serum metabolites.

Prenatal element exposure has been linked to autism spectrum disorder (ASD) symptoms; however, the mediating role of metabolites remains unclear. Based on the Ma'anshan Birth Cohort, 18 elements were quantified in maternal serum during the first, second, and third trimesters, and averaged concentrations of three trimesters represented the whole pregnancy exposure. Untargeted metabolomics characterized the metabolomic profiles in umbilical cord serum. ASD symptoms at ages 3, 5, and 6 years were evaluated by the Chinese version of the Clancy Autism Behavior Scale and analyzed independently across developmental stages. Analytical strategies encompassed exposure-wide associations, quantile-based g-computation, meet-in-the-middle approach, pathway enrichment, and causal mediation model. At age 3, each log10-unit increase in cadmium and magnesium concentrations was associated with 1.29-point (95%CI: 0.09, 2.50) and 4.59-point (95%CI: 0.97, 8.22) increases in ASD symptom scores, respectively, whereas selenium was associated with a 3.41-point decrease (95%CI: -6.00, -0.83). Vanadium and copper were inversely associated with ASD symptom scores at age 5; cadmium was positively associated at age 6; and mercury was inversely associated at ages 3 and 6. Overlapping exposure- and outcome-associated metabolites were identified only at age 5. Alpha-Furyl Methyl Diketone mediated an inverse indirect association between cobalt exposure and ASD symptom scores (indirect effect = -0.24, 95%CI: -0.46, -0.08), whereas 3-Methoxypropylamine showed a positive indirect association between barium exposure and ASD symptom scores (indirect effect = 0.13, 95%CI: 0.03, 0.28). Neither cobalt nor barium exhibited a significant total association; thus, these indirect associations were considered exploratory. These findings indicate element- and age-specific patterns rather than a uniform direction of association, while the indirect associations involving cord serum metabolites require confirmation in independent studies.

Ying-Ying Zuo, C. Geng, Chun-Mei Liang et al. · 0 citations
Sep 2026

Differences in circadian rhythm changes between myopic and non-myopic college students over 2 years.

This study aimed to characterize and compare the differences in circadian rhythm changes during 2 years between college students with myopia and non-myopia based on a longitudinal cohort study. Wake-up time and bedtime were obtained through a self-administered questionnaire. Chronotype was assessed using the reduced Morningness-Eveningness Questionnaire (rMEQ). Circadian rhythm timing was determined by dim-light melatonin onset (DLMO), measured through hourly saliva collection from 21:00 to 01:00. A total of 450 college students (146 [32.4%] males) with a mean age of 18.65 ± 1.05 years were included, of whom 353 (78.4%) students had myopia. Compared with non-myopic individuals, myopic students slept later, woke up earlier, and exhibited lower rMEQ scores at baseline. Over the 2-year follow-up, both groups showed significantly earlier bedtimes, later wake-up times, and higher rMEQ scores. Only myopic students demonstrated a 45-minute delay in DLMO after the 2-year follow-up. After adjusting for potential confounders, linear mixed-effects models showed that myopic individuals had later bedtimes and earlier wake-up times. These findings indicate significant circadian rhythm changes in individuals with myopia, suggesting the potential of targeted sleep rhythm interventions on preventing myopia.

Zhong Guan, Tingting Li, L. Zou et al. · 0 citations
Jul 2026

Sex- and Trimester-Specific Associations of Prenatal Co-Exposure to Organophosphate Esters and Phthalates with Preschoolers' Trajectories of Co-Occurring ADHD and ASD Symptoms: Cord Blood Metabolomic Study in the Ma'anshan Birth Cohort.

Cord blood metabolomics identified pyrimidine, biotin, lysine, cysteine, and methionine metabolism as key mediators of OPE-induced cotrajectories, and purine metabolism mediated PAEs' effects (p < 0.05), which highlights OPE/PAE neurotoxicity and reveals novel cord metabolomic insights.

Xing Wang, J. Tong, Meng-Juan Lu et al. · 2 citations

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