PMID- 38393211 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240227 IS - 2305-6304 (Electronic) IS - 2305-6304 (Linking) VI - 12 IP - 2 DP - 2024 Jan 30 TI - The Associations between Exposure to Multiple Heavy Metals and Total Immunoglobulin E in U.S. Adults. LID - 10.3390/toxics12020116 [doi] LID - 116 AB - Immunoglobulin E (IgE) is a type of immunoglobulin, and elevated serum total IgE is often present in allergic diseases. Exposure to environmental heavy metals has been markedly linked to allergic diseases, leading to elevated total IgE levels. However, studies concerning the effects of multiple metal exposures on total IgE levels are limited. Therefore, the current study seeks to explore the correlation between heavy-metal co-exposure and total IgE levels based on the National Health and Nutrition Examination Survey (NHANES, 2005-2006). Participants possessed complete data on total IgE levels, 11 urinary metal concentrations and other covariates. The correlations between 11 metals and total IgE levels were analyzed using multiple linear regression, and total IgE levels were a continuous variable. Total IgE levels exceeding 150 kU/L were considered sensitized. Binary logistic regression analyses were employed to assess the correlation between metal exposure and the occurrence of an allergic state. Then, the association between co-exposure to the 11 metals and total IgE levels or the occurrence of sensitization status was further analyzed by Bayesian kernel machine regression (BKMR), a multi-contaminant model. There were 1429 adults with complete data included. Based on the median concentration, molybdenum (Mo) had the highest concentration (46.60 mug/L), followed by cesium (Cs), barium (Ba), lead (Pb), and mercury (Hg). And the median (interquartile range) for total IgE levels was 43.7 (17.3, 126.0) kU/L. Multiple linear regression results showed that Pb was significantly and positively associated with total IgE levels (beta = 0.165; 95% CI: 0.046, 0.284). Binary logistic regression showed a significant positive correlation between urinary Pb (OR: 1.258; 95% CI: 1.052, 1.510) and tungsten (W) (OR: 1.251; 95% CI: 1.082, 1.447). Importantly, the BKMR model found a positive correlation between combined-metal exposure and total IgE levels and the occurrence of sensitization status. The mixed heavy-metal exposure was associated with increased total IgE levels, and this association may be driven primarily by the exposure of Pb and W. This study provides new insights into the relationship between heavy-metal exposure and allergic diseases. More research is needed to confirm these findings. FAU - Song, Xin AU - Song X AD - Department of Occupational Health and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China. AD - Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, China. FAU - Ding, Xiaowen AU - Ding X AD - Beijing Institute of Occupational Disease Prevention and Treatment, Beijing 100093, China. FAU - Niu, Piye AU - Niu P AUID- ORCID: 0000-0002-0155-3438 AD - Department of Occupational Health and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China. AD - Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, China. FAU - Chen, Tian AU - Chen T AD - Department of Occupational Health and Environmental Health, School of Public Health, Capital Medical University, Beijing 100069, China. AD - Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, China. FAU - Yan, Tenglong AU - Yan T AUID- ORCID: 0000-0002-2424-0223 AD - Beijing Institute of Occupational Disease Prevention and Treatment, Beijing 100093, China. LA - eng GR - 7234402/Beijing Natural Science Foundation/ PT - Journal Article DEP - 20240130 PL - Switzerland TA - Toxics JT - Toxics JID - 101639637 PMC - PMC10891582 OTO - NOTNLM OT - BKMR OT - heavy metals OT - mixture OT - total immunoglobulin E (total IgE) COIS- The authors declare no conflicts of interest. EDAT- 2024/02/23 12:42 MHDA- 2024/02/23 12:43 PMCR- 2024/01/30 CRDT- 2024/02/23 10:34 PHST- 2023/12/28 00:00 [received] PHST- 2024/01/25 00:00 [revised] PHST- 2024/01/27 00:00 [accepted] PHST- 2024/02/23 12:43 [medline] PHST- 2024/02/23 12:42 [pubmed] PHST- 2024/02/23 10:34 [entrez] PHST- 2024/01/30 00:00 [pmc-release] AID - toxics12020116 [pii] AID - toxics-12-00116 [pii] AID - 10.3390/toxics12020116 [doi] PST - epublish SO - Toxics. 2024 Jan 30;12(2):116. doi: 10.3390/toxics12020116.