Circulating immune/inflammation markers in Chinese workers occupationally exposed to formaldehyde
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Publication date
2015-08
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taverne
Abstract
BACKGROUND: Formaldehyde has been classified as a human myeloid leukemogen. However, the mechanistic basis for this association is still debated. OBJECTIVES: We aimed to evaluate whether circulating immune/inflammation markers were altered in workers occupationally exposed to formaldehyde. METHODS: Using a multiplexed bead-based assay, we measured serum levels of 38 immune/inflammation markers in a cross-sectional study of 43 formaldehyde-exposed and 51 unexposed factory workers in Guangdong, China. Linear regression models adjusting for potential confounders were used to compare marker levels in exposed and unexposed workers. RESULTS: We found significantly lower circulating levels of two markers among exposed factory workers compared with unexposed controls that remained significant after adjusting for potential confounders and multiple comparisons using a false discovery rate of 10%, including chemokine (C-X-C motif) ligand 11 (36.2 pg/ml in exposed versus 48.4 pg/ml in controls, P = 0.0008) and thymus and activation regulated chemokine (52.7 pg/ml in exposed versus 75.0 pg/ml in controls, P = 0.0028), suggesting immunosuppression among formaldehyde-exposed workers. CONCLUSIONS: Our findings are consistent with recently emerging understanding that immunosuppression might be associated with myeloid diseases. These findings, if replicated in a larger study, may provide insights into the mechanisms by which formaldehyde promotes leukemogenesis.
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Taverne, SDG 3 - Good Health and Well-being
Citation
Seow, W J, Zhang, L, Vermeulen, R, Tang, X, Hu, W, Bassig, B A, Ji, Z, Shiels, M S, Kemp, T J, Shen, M, Qiu, C, Reiss, B, Beane Freeman, L E, Blair, A, Kim, C, Guo, W, Wen, C, Li, L, Pinto, L A, Huang, H, Smith, M T, Hildesheim, A, Rothman, N & Lan, Q 2015, 'Circulating immune/inflammation markers in Chinese workers occupationally exposed to formaldehyde', Carcinogenesis, vol. 36, no. 8, pp. 852-857. https://doi.org/10.1093/carcin/bgv055