Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0037116 (silicosis)
 1,822 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Epidemiological data show that chronic diseases of the respiratory apparatus have constantly increased over the last 20 years or so, often involving relatively young age classes. The increased survival rates due to chemotherapy also increase the importance of rehabilitation in such diseases. The officially accepted concept of a "global" rehabilitation is particularly significant in the case of patients of working age. The main rehabilitation procedures include chest physiotherapy, aerosol therapy, oxygen therapy (where selection criteria have been established and where there are new prospects related to long-term oxygen therapy), intermittent positive pressure breathing and physical retraining. Details on the methods of assessment and training and data concerning three groups of patients suffering from respectively chronic obstructive lung disease, silicosis and asbestosis, are given. The data show a general pattern of a decrease in ventilation (for an unchanged level of O2 uptake and CO2 output) and reflect a rise in muscular efficiency (exercising and respiratory) enabling the body to perform the same work load at a lower energy cost. The authors discuss the vocational rehabilitation of the patient with lung disease and illustrate the most useful procedures in the assessment of the subject, the environment and the place of work, including guidelines to achieve this. Rehabilitation treatment is also summarized into a number of stages, with the goals at different therapeutic levels and the ways to reach them.
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PMID:[Rehabilitation of the worker with bronchopneumopathy]. 648 73

Arterial blood gas determinations in patients with chronic obstructive pulmonary disease (COPD) and respiratory chemosensitivity, and arterial blood gas determinations in their sons were compared. Patients with silicosis (n=17) and their sons (n=22) served as control subjects. Arterial blood gases, pH, and HCO-3 concentration in 25 patients with COPD were averaged from at least 3 determinations (mean sample number, 10.1) to compare with the data on their sons (n-34; mean age, 33.9 yr). The Paco2 obtained during stable stages correlated positively between patients with COPD and their sons. The Pao2 of patients with COPD in stable stages correlated with the hypoxic ventilatory response of their sons. The Paco2 and Paco2 obtained during acute exacerbation of COPD correlated with the hypoxic ventilatory response of the sons. Deviations in FEV1 and V25 from predicted values correlated with deviations in Pao2 in the sons of the patients with COPD. In silicosis, significant relationships between patients and sons were not seen with respect to arterial blood gas determinations and ventilatory responses except for Paco2 of patients and hypercapnic ventilatory responses of sons. Smoking habits did not correlate between patients and sons both in COPD and in silicosis. However, the concordance ratio of smokers or nonsmokers between patients and sons was higher in COPD than in silicosis. These results indicate that familial factors are involved in determining the arterial blood gases and ventilatory response to hypoxia in COPD, and blunted chemosensitivity to hypoxia and incipient airway dysfunction antedate clinically manifest COPD.
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PMID:Familial factors affecting arterial blood gas values and respiratory chemosensitivity in chronic obstructive pulmonary disease. 680 34

Ventilatory responses to hypoxia (A) and hypercapnia (S) were measured in 127 healthy men (105 males and 22 females) by a dual control system for regulating Pa O2 and Pa CO2 simultaneously and independently of each other. The subjects were classified into groups according to sex, age, family history, and genetics (twins). Mean values for A were 138 +/- SD 93 liters/min.mmHg in group I (subjects without family history of chronic lung diseases) and 80 +/- 56 liters/min.mmHg in group II (sons of patients with chronic obstructive pulmonary disease or silicosis). The difference was highly significant (P less than 0.001). Mean S were 1.11 +/- 0.39 liters/min.mmHg-1 in group I and 1.16 +/- 0.48 liters/min.mmHg-1 in group H. The difference was not significant. Mean values for A and S in the aged males (mean age = 71.3 years) did not differ from those in 15 adult males (mean age = 29.5 years) and 60 young twins (mean age = 16.4 years). In every respect of age, sex, familial factors, and genetics, A and S were not interrelated. Mouth occlusion pressure (P0.1) was measured during air breathing and it correlated neither with A nor S. These results indicate 1) hypoxic and hypercapnic responses are not strongly related to each other, and 2) the aging process does not alter ventilatory responses to hypoxia and hypercapnia.
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PMID:Relationship between hypoxic and hypercapnic ventilatory responses in man. 730 42

Twenty-six coal miners, without associated functional chronic obstructive lung disease (COLD), assessed by normal airway resistance, were divided into three groups: (1) Group C, normal X-ray; (2) Group S1, micronodular silicosis; and (3) Group S2, complicated silicosis. All subjects were evaluated while at rest and during exercise. Significant lung volume reduction was observed in the S2 Group only. Blood gases, pulmonary pressure, and cardiac output were found to be within the normal range for all three groups when at rest. The pulmonary pressure and pulmonary vascular resistance were higher, however, for the S1 and S2 Groups when compared to the C Group. During exercise, pulmonary hypertension was observed in 50% of teh patients with complicated silicosis. When all data (N = 26) were included, the high values for pulmonary pressure and pulmonary vascular resistance correlated well with the loss in vital capacity (VC) and the decrease in forced expiratory volume in 1 sec (FEV 1.0). From the initial 26 patients, 19 were selected on the basis of their normal airway resistance and FEV 1.0/VC ratio. This selection did not alter the differences noted for the pulmonary pressure and total pulmonary vascular resistance, which previously existed between the groups, even though the correlations were not statistically significant. We conclude that silicosis without associated COLD leads to mineral hemodynamic impairment at rest and during exercise, and that airway resistance does not detect impairment of flow as effectively as FEV 1.0 reduction. The increased pulmonary vascular resistance observed, especially in complicated silicosis, may be best explained by the loss of lung parenchyma and possible impairment of small airways.
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PMID:Cardiopulmonary adaptation to exercise in coal miners. 745 18

Angiotensin-converting enzyme (ACE) activity in serum is used as an aid to the diagnosis and follow-up of patients with sarcoidosis. A theoretical limitation of measurements of activity is that these may be affected by the presence of pharmacologic or endogenous inhibitors of ACE. Immunoassays of ACE concentration avoid this problem and, when combined with tests of ACE activity, permit calculation of specific activity of ACE. In this study, we set out to develop a sensitive radioimmunoassay for ACE to compare results obtained with this method with results of ACE activity and calculated ACE specific activity in patients suffering from a variety of lung diseases. In a group of control subjects (n = 32), the ACE concentration was 453.7 +/- 159.8 (SD) ng/mL; 95% confidence interval (CI), 398.34 to 509.06, but levels were significantly elevated in sarcoidosis (979.3 +/- 558.6 ng/mL; 95% CI, 827.5 to 1,131.1; n = 51; p < 0.001 vs control subjects), silicosis (646.5 +/- 239.1 ng/mL; 95% CI, 544.2 to 748.8; n = 21; p < 0.01), and miliary tuberculosis (647.0 +/- 217.1 ng/mL; 95% CI, 551.9 to 742.1; n = 29; p < 0.01). The levels were normal in COPD, interstitial pulmonary fibrosis, and active cavitary pulmonary tuberculosis. The overall correlation between ACE activity and concentration measurements was strong (r = 0.93). No evidence of endogenous ACE inhibition was observed in any of the disease categories studied except in COPD where an elevation of ACE specific activity was observed, raising the possibility that in this condition different isozymes of ACE with higher specific activity might be released.
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PMID:Serum angiotensin-converting enzyme activity, concentration, and specific activity in granulomatous interstitial lung disease, tuberculosis, and COPD. 787 41

We describe silicosis in a patient with chronic obstructive pulmonary disease who worked as a maintenance mechanic for less than 5 years in a plant in South Carolina that manufactures silica flour and industrial sand. An open lung biopsy showed an early stage of silicosis manifested by perivascular and peribronchial collections of macrophages as well as early granuloma formation. An antinuclear antibody profile compatible with Sjogren's syndrome or systemic lupus erythematosus occurred with no symptoms of either disease. Excessive occupational exposure levels of respirable free silica were documented.
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PMID:Silicosis following employment in the manufacture of silica flour and industrial sand. 836 96

We used noninvasive positive-pressure ventilation to treat hypercapnea due to acute exacerbations of chronic respiratory failure (21 episodes in 19 patients; COPD, 4; pulmonary tuberculosis sequelae, 4; silicosis, 3; silicotuberculosis, 3; bronchiectasis, 3; others, 2). All patients had acute onsets of severe hypercapnea (PaCO2 > 45 Torr), acute decreases in pH (< 7.35), and tachypnea, paradoxical breathing or both. During the first 2 to 4 hours of bi-level positive airway pressure, PaCO2 decreased from 72 to 61 Torr (p < 0.0005), pH increased from 7.26 to 7.31 (p < 0.001), and respiratory rate decreased from 30 to 25 breaths/min (p < 0.005). In three cases leakage of air through the mouth prevented improvement in the patients' conditions, but in two of those a face mask was then used successfully. In 17 of the 21 episodes (81%) gas exchange improved and intubation was not necessary. In those 17, the mean duration of noninvasive positive-pressure ventilation was 6.3 days. We conclude that noninvasive positive-pressure ventilation can improve gas exchange in patients with acute hypercapnea complicating chronic respiratory failure.
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PMID:[Outcomes of noninvasive positive-pressure ventilation in patients with acute hypercapnia complicating chronic respiratory failure]. 939 53

Occupational exposure to crystalline silica dust is associated with an increased risk for pulmonary diseases such as silicosis, tuberculosis, chronic bronchitis, chronic obstructive pulmonary disease (COPD) and lung cancer. This review summarizes the current knowledge about the health effects of amorphous (non-crystalline) forms of silica. The major problem in the assessment of health effects of amorphous silica is its contamination with crystalline silica. This applies particularly to well-documented pneumoconiosis among diatomaceous earth workers. Intentionally manufactured synthetic amorphous silicas are without contamination of crystalline silica. These synthetic forms may be classified as (1) wet process silica, (2) pyrogenic ("thermal" or "fumed") silica, and (3) chemically or physically modified silica. According to the different physicochemical properties, the major classes of synthetic amorphous silica are used in a variety of products, e.g. as fillers in the rubber industry, in tyre compounds, as free-flow and anti-caking agents in powder materials, and as liquid carriers, particularly in the manufacture of animal feed and agrochemicals; other uses are found in toothpaste additives, paints, silicon rubber, insulation material, liquid systems in coatings, adhesives, printing inks, plastisol car undercoats, and cosmetics. Animal inhalation studies with intentionally manufactured synthetic amorphous silica showed at least partially reversible inflammation, granuloma formation and emphysema, but no progressive fibrosis of the lungs. Epidemiological studies do not support the hypothesis that amorphous silicas have any relevant potential to induce fibrosis in workers with high occupational exposure to these substances, although one study disclosed four cases with silicosis among subjects exposed to apparently non-contaminated amorphous silica. Since the data have been limited, a risk of chronic bronchitis, COPD or emphysema cannot be excluded. There is no study that allows the classification of amorphous silica with regard to its carcinogenicity in humans. Further work is necessary in order to define the effects of amorphous silica on morbidity and mortality of workers with exposure to these substances.
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PMID:Health hazards due to the inhalation of amorphous silica. 1187 95

The Transkei is one of two regions from which a majority of South African mine workers used to be recruited, and the destination to which many return. The study was done to determine the prevalences of lung diseases in these ex-workers, links between these diseases and age, links between diseases and duration of mining, and the association between silicosis and tuberculosis. It was done in Umtata General Hospital. Participants' (n = 300) ages ranged from 35 to 66+ years (mean 51.6). Durations of mining ranged from < 1 to 31+ years. 29/300 X-rays (9.6%) were unreadable; 59 (21.8%) were disease-free; and 212 (78.2%) showed lung abnormalities. Pulmonary tuberculosis (PTB) with or without silicosis was evident in 64.2% of the x-rays, silicosis with or without PTB in 34%, COPD in 7%, and asbestosis in 1.5%. The relative risk for tuberculosis was 5.08 (2.58-9.88) for men with silicosis compared with others, p < 0.01. The extremely high burden of lung disease in ex-mine workers places enormous challenges on health service delivery systems and compensation authorities.
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PMID:Patterns of lung diseases in former mine workers of the former Republic of the Transkei: an X-ray-based study. 1201 76

The cases of 6 patients (4 men, 2 women) with antisynthetase syndrome are reported. The mean age was 60 years and the most frequent symptom was increasing dyspnea (4 patients). One of the remaining 2 patients had hemoptysis and the last was asymptomatic. Systemic symptoms included Raynaud's phenomenon (2 patients), arthritis in hands (3) and muscle impairment (4). Chest films showed linear interstitial infiltrates of varying severity in 5 patients; the patient without such infiltrates also suffered silicosis. Functional assessment showed restrictive impairment in 4 patients; of the remaining 2 patients, 1 had chronic obstructive pulmonary disease and 1 had normal function. The antisynthetase antibody (ASAB) detected was anti-Jo-1 in 4 cases, anti-PL-12 in 1 case, and unidentified in 1 case. The course of disease was satisfactory for 5 patients. ASAB analysis is useful for studying idiopathic interstitial lung disease.
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PMID:[Antisynthetase syndrome and interstitial lung involvement. Report of 6 cases]. 1237 2


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