{"title":"Impact of early adolescent lead exposure on brain function and response: Findings from a Chinese cohort","authors":"Olivia M. Halabicky , Naixue Cui , Jianghong Liu","doi":"10.1016/j.neuro.2025.06.007","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><div>While the detrimental effects of lead exposure on cognition have been well documented, less research has focused on pre-adolescent populations. The purpose of this study was to understand the relationship between adolescent lead exposure and measures of brain functionality.</div></div><div><h3>Methods</h3><div>In a Chinese early adolescent cohort (N = 258 (50.1 % female) mean age 11.51 years) we examined associations between blood lead levels (BLLs) and P300 event-related potential elicited by three types of stimuli during an auditory oddball task.</div></div><div><h3>Results</h3><div>Mean BLLs in adolescence were 3.17 mcg/dl. In ANOVAs comparing BLL groups above and below the mean, those with greater BLLs had significantly prolonged novelty P300 latency (F=4.67; p = 0.032). In linear models adjusted for age, sex, BLLs at 3–5 years, child IQ, residence location, parent's education, and father’s smoking during pregnancy, increasing BLLs were associated with a 20.21 ms increase in target latency (95 % CI 3.73, 36.69). In sex stratified analyses, a 1 mcg/dl increase in BLLs was associated with a 26.64 ms increase in novel latency in males only (95 % CI 3.49, 49.78).</div></div><div><h3>Discussion</h3><div>Our results suggest a modest association between early adolescent lead exposure and detriments in neurophysiology, particularly related to novelty P300 in males and target P300 in the overall sample. Future research can consider how P300 alterations influence child and adolescent developmental trajectories and test ERP measures as a mediator between early life environmental exposures and later health decision making.</div></div>","PeriodicalId":19189,"journal":{"name":"Neurotoxicology","volume":"110 ","pages":"Pages 23-30"},"PeriodicalIF":3.4000,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurotoxicology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0161813X25000798","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose
While the detrimental effects of lead exposure on cognition have been well documented, less research has focused on pre-adolescent populations. The purpose of this study was to understand the relationship between adolescent lead exposure and measures of brain functionality.
Methods
In a Chinese early adolescent cohort (N = 258 (50.1 % female) mean age 11.51 years) we examined associations between blood lead levels (BLLs) and P300 event-related potential elicited by three types of stimuli during an auditory oddball task.
Results
Mean BLLs in adolescence were 3.17 mcg/dl. In ANOVAs comparing BLL groups above and below the mean, those with greater BLLs had significantly prolonged novelty P300 latency (F=4.67; p = 0.032). In linear models adjusted for age, sex, BLLs at 3–5 years, child IQ, residence location, parent's education, and father’s smoking during pregnancy, increasing BLLs were associated with a 20.21 ms increase in target latency (95 % CI 3.73, 36.69). In sex stratified analyses, a 1 mcg/dl increase in BLLs was associated with a 26.64 ms increase in novel latency in males only (95 % CI 3.49, 49.78).
Discussion
Our results suggest a modest association between early adolescent lead exposure and detriments in neurophysiology, particularly related to novelty P300 in males and target P300 in the overall sample. Future research can consider how P300 alterations influence child and adolescent developmental trajectories and test ERP measures as a mediator between early life environmental exposures and later health decision making.
期刊介绍:
NeuroToxicology specializes in publishing the best peer-reviewed original research papers dealing with the effects of toxic substances on the nervous system of humans and experimental animals of all ages. The Journal emphasizes papers dealing with the neurotoxic effects of environmentally significant chemical hazards, manufactured drugs and naturally occurring compounds.