An exploratory cross-sectional study of serum biomarkers as related to respiratory outcomes and workplace silica exposure levels in UK brick-manufacturing and stone workers

肺表面活性物质 肺活量测定 医学 单核细胞 免疫学 内科学 矽肺 趋化性 呼吸系统 喘息 支气管肺泡灌洗 生理学 呼吸道疾病 脂质运载蛋白 脂褐素 肺 病理 内分泌学 炎症 生物标志物 哮喘 肺容积 化学 尿检 表面活性蛋白A 胃肠病学 肺活量
作者
Howard J. Mason,Nick Warren,Kate Jones,Jade Sumner,Edward Robinson,Christopher Michael Barber,David Fishwick
出处
期刊:Annals of Work Exposures and Health [Oxford University Press]
卷期号:70 (6)
标识
DOI:10.1093/annweh/wxag058
摘要

In a cross-sectional study of UK brick and stone workers exposed to respirable crystalline silica, Club cell protein (CC16), neutrophil gelatinase-associated lipocalin, platelet-derived growth factor (PDGFββ), C-reactive protein, rheumatoid factor, antinuclear antibodies, lung surfactant proteins A & D, and monocyte chemoattractant protein 1 were measured in serum samples from 261 workers. Questionnaire data on health outcomes were also recorded, along with spirometry and a chest X-ray. Individual cumulative respirable crystalline silica exposures were calculated. Four subjects (1.5%) had silicosis, and these were characterised by evidence of small airways obstruction, reduced predicted forced expiratory volume in 1 s and noticeable increases in monocyte chemoattractant protein 1 and surfactant protein A. CC16 and surfactant protein D significantly increased with cumulative respirable crystalline silica exposure, but CC16 also independently decreased with evidence of airflow obstruction or small airways obstruction. Therefore, the interpretation of serum CC16 levels in silica-exposed populations may be complex. There was some evidence of down-regulation of the PDGFββ pathway with increasing exposure. Surfactant protein D levels were also associated with several chronic respiratory symptoms reported by workers. Serum surfactant protein A, monocyte chemoattractant protein 1, and neutrophil gelatinase-associated lipocalin showed little or no relationship to cumulative respirable crystalline silica levels. These data raise the possibility that surfactant protein D, CC16, surfactant protein A, and monocyte chemoattractant protein 1 may have a role in defining the natural history of silicosis, with the latter 2 biomarkers possibly reflecting where pathology is evidenced on imaging techniques.

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