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0226 Affection in the auditory brainstem pathway associated with occupational, low-level exposure to ethylbenzene
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  1. Octavio Jiménez-Garza1,
  2. Sergio Márquez-Gamiño1,
  3. Liliana Ruiz-García1,
  4. Giovanni Battista Bartolucci2,
  5. Mariella Carrieri2
  1. 1Universidad de Guanajuato Campus León, Health Sciences Division, Leon, Guanajuato, Mexico
  2. 2University of Padova, Department of Cardiologic, Thoracic and Vascular Science, Padova, Veneto, Italy

Abstract

Introduction Hearing loss in occupational exposure to a solvent mixture has been already reported; however, mixture in those reports did not contain ethylbenzene, a compound showing peripheral ototoxicity in animals exposed to high levels. In this work, we evaluated the auditory brainstem pathway in two samples of workers exposed to different levels of a solvent mixture where ethylbenzene was present, compared to a reference group.

Material and methods Individual exposure levels for up to seven compounds were obtained in two groups: Exposed (n=21 gas station attendants, GS, and leather shoe factory workers, LS) and Non-exposed (n=21, administrative workers) all of them from the city of León Guanajuato, México. The click-evoked auditory brainstem response test was performed in both groups.

Results Toluene, n-hexane, acetone, ethylbenzene, xylene and methyl ethyl ketone exposure levels were higher in LS (p<0.001). Only n-hexane exposure levels were above the permissible levels, while mean ethylbenzene exposure levels ranged 0.4–14.58 mg/m3. Wave V latency at four different points of stimulation for both ears was delayed in the exposed group, as well as the I-V and I-III interwave latencies at 70 dB (p<0.05). LS workers showed a delayed I-III interpeak interval compared to non-exposed group. Also in LS, ethylbenzene exposure levels showed a significant correlation with wave V latency at 40 dB (r=0.8, p=0.008).

Conclusion Our results point out to a central affection in the auditory system caused by ethylbenzene in a dose response manner. Workers exposed to ethylbenzene levels far below the permissible exposure limit should be closely monitored for early ototoxicity effects.

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