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      Some pleural effusions labeled as idiopathic could be produced by the inhalation of silica

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          Abstract

          Objectives

          Exposure to silica nanoparticles has been associated with pleural effusions (PEs) in animal models and case series. We hypothesized that some PEs labelled as “idiopathic” could, in fact, be secondary to inhalation of silica.

          Methods

          A retrospective case control study was designed utilizing a prospectively maintained pleural database. Cases, represented by idiopathic PEs, were matched by age and gender to control patients who had been diagnosed with malignant, cardiac, or infectious PEs. A survey consisting of questions about occupational life and possibility of silica inhalation was conducted. In a subgroup of patients, pleural fluid concentrations of silica were quantified by plasma atomic emission spectrometry analysis. Also, the pleural biopsy of a silica-exposed case was subjected to an energy dispersive X-ray spectroscopy (EDX) to identify the mineral, the size of which was determined by electron microscopy.

          Results

          A total of 118 patients (59 cases and 59 controls) completed the survey. There were 25 (42%, 95% CI 31–55%) and 13 (22%, 95% CI 13–34%) silica-exposed workers in case and control groups, respectively. The exposure attributable fraction was 0.62 (95% CI 0.14–0.83). Four of eight exposed cases showed detectable levels of silica in the pleural fluid (mean 2.37 mg/L), as compared to none of 16 tested controls. Silica nanoparticles of 6–7 nm were identified in the pleural biopsy of an exposed case patient.

          Conclusions

          It is plausible that some idiopathic PEs could actually be caused by occupational silica inhalation.

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          Most cited references22

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          The nanosilica hazard: another variable entity

          Silica nanoparticles (SNPs) are produced on an industrial scale and are an addition to a growing number of commercial products. SNPs also have great potential for a variety of diagnostic and therapeutic applications in medicine. Contrary to the well-studied crystalline micron-sized silica, relatively little information exists on the toxicity of its amorphous and nano-size forms. Because nanoparticles possess novel properties, kinetics and unusual bioactivity, their potential biological effects may differ greatly from those of micron-size bulk materials. In this review, we summarize the physico-chemical properties of the different nano-sized silica materials that can affect their interaction with biological systems, with a specific emphasis on inhalation exposure. We discuss recent in vitro and in vivo investigations into the toxicity of nanosilica, both crystalline and amorphous. Most of the in vitro studies of SNPs report results of cellular uptake, size- and dose-dependent cytotoxicity, increased reactive oxygen species levels and pro-inflammatory stimulation. Evidence from a limited number of in vivo studies demonstrates largely reversible lung inflammation, granuloma formation and focal emphysema, with no progressive lung fibrosis. Clearly, more research with standardized materials is needed to enable comparison of experimental data for the different forms of nanosilicas and to establish which physico-chemical properties are responsible for the observed toxicity of SNPs.
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            Observational research methods. Research design II: cohort, cross sectional, and case-control studies

            C Mann (2003)
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              Exposure to nanoparticles is related to pleural effusion, pulmonary fibrosis and granuloma.

              Nano materials generate great benefits as well as new potential risks. Animal studies and in vitro experiments show that nanoparticles can result in lung damage and other toxicity, but no reports on the clinical toxicity in humans due to nanoparticles have yet been made. The present study aimed to examine the relationship between a group of workers' presenting with mysterious symptomatic findings and their nanoparticle exposure. Seven young female workers (aged 18-47 yrs), exposed to nanoparticles for 5-13 months, all with shortness of breath and pleural effusions were admitted to hospital. Immunological tests, examinations of bacteriology, virology and tumour markers, bronchoscopy, internal thoracoscopy and video-assisted thoracic surgery were performed. Surveys of the workplace, clinical observations and examinations of the patients were conducted. Polyacrylate, consisting of nanoparticles, was confirmed in the workplace. Pathological examinations of patients' lung tissue displayed nonspecific pulmonary inflammation, pulmonary fibrosis and foreign-body granulomas of pleura. Using transmission electron microscopy, nanoparticles were observed to lodge in the cytoplasm and caryoplasm of pulmonary epithelial and mesothelial cells, but are also located in the chest fluid. These cases arouse concern that long-term exposure to some nanoparticles without protective measures may be related to serious damage to human lungs.
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                Author and article information

                Contributors
                Journal
                Pleura Peritoneum
                Pleura Peritoneum
                pp
                pp
                Pleura and Peritoneum
                De Gruyter
                2364-7671
                2364-768X
                3 January 2022
                1 March 2022
                : 7
                : 1
                : 27-33
                Affiliations
                deptDepartment of Internal Medicine , universityPleural Medicine Unit, Arnau de Vilanova University Hospital, Biomedical Research Institute of Lleida (IRBLleida), University of Lleida , Lleida, Spain
                deptChemical Analysis Service , universityScience Faculty, Zaragoza University, Zaragoza, Spain
                deptDepartment of Laboratory Medicine , universityArnau de Vilanova University Hospital, IRBLleida , Lleida, Spain
                deptAragon Nanoscience Institute , universityAdvanced Microscopy Laboratory, Zaragoza University , Zaragoza, Spain
                Author notes
                Corresponding author: Prof. José M. Porcel, deptDepartment of Internal Medicine , universityPleural Medicine Unit, Arnau de Vilanova University Hospital, Biomedical Research Institute of Lleida (IRBLleida) , Avda Alcalde Rovira Roure 80, 265198 Lleida, Spain, E-mail: jporcelp@ 123456yahoo.es
                Article
                pp-2021-0135
                10.1515/pp-2021-0135
                9069498
                2958a16d-5536-4edc-91a3-425be7d6f963
                © 2021 Silvia Bielsa et al., published by De Gruyter, Berlin/Boston

                This work is licensed under the Creative Commons Attribution 4.0 International License.

                History
                : 14 July 2021
                : 15 December 2021
                Page count
                Figures: 02, Tables: 04, References: 22, Pages: 07
                Categories
                Article

                idiopathic pleural effusion,occupational disease,pleural effusion,silica nanoparticles

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