Abstract

Despite the toxicity and health risk characteristics of formaldehyde (FA), it is currently used as a cytological fixative and the definition of safe exposure levels is still a matter of debate. Our aim was to investigate the alterations in both oxidative and inflammatory status in a hospital working population. The 68 workers recruited wore a personal air-FA passive sampler, provided a urine sample to measure 15-F2t-Isoprostane (15-F2t-IsoP) and malondialdehyde (MDA) and a blood specimen to measure tumour necrosis factor α (TNFα). Subjects were also genotyped for GSTT1 (Presence/Absence), GSTM1 (Presence/Absence), CYP1A1 exon 7 (A > G), and IL6 (−174, G > C). Workers were ex post split into formalin-employers (57.3 μg/m3) and non-employers (13.5 μg/m3). In the formalin-employers group we assessed significantly higher levels of 15-F2t-IsoP, MDA and TNFα (<0.001) in comparison to the non-employers group. The air-FA levels turned out to be positively correlated with 15-F2t-IsoP (p = 0.027) and MDA (p < 0.001). In the formalin-employers group the MDA level was significantly higher in GSTT1 Null (p = 0.038), GSTM1 Null (p = 0.031), and CYP1A1 exon 7 mutation carrier (p = 0.008) workers, compared to the wild type subjects. This study confirms the role of FA in biomolecular profiles alterations, highlighting how low occupational exposure can also result in measurable biological outcomes.

Highlights

  • Several studies have focused on hospital workers and their occupational risks [1,2,3,4,5], e.g., operating theatre nurses and pathologists, including those who are chronically exposed to formaldehyde (FA) [6,7,8]

  • The main aim of this study was to investigate wide range of outcomes in terms of alteration of the oxidative and inflammatory status related to occupational exposure to FA, considering the possible role of genetic polymorphisms in modulating the individual response

  • We found a significant difference in TNF-α level, with the higher concentration in the formalinemployers group

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Summary

Introduction

FA inhalation has been associated with several toxic effects: low exposure levels (0.1 ppm) can irritate the eyes, nose and upper respiratory airways, while high concentrations may result in pulmonary function impairment and asthma [9,10]. Prolonged exposure to FA has been associated with nasopharyngeal cancer [11,12] and leukaemia [12,13], and there is limited evidence of a possible association of this compound with sinonasal cancer [14]. In this context, the International Agency for Research on Cancer (IARC) classifies

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