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1.
PLoS One ; 15(8): e0237100, 2020.
Article in English | MEDLINE | ID: mdl-32760159

ABSTRACT

PURPOSE: Cobalt exposure is known to cause adverse effects on health. A major use of cobalt is in the manufacture of hard metal. Exposure can lead to asthma, hard metal lung disease, contact allergy and increased risk of cancer. Cobalt is mainly absorbed from the pulmonary tract, however penetration through skin may occur. The relationships between exposure to inhalable cobalt in air and on skin and the uptake in blood and urine will be investigated, as well as the association between dermal symptoms and dermal exposure. METHODS: Cobalt exposure in 71 workers in hard metal production facilities was measured as inhalable cobalt in the breathing zone and cobalt found on skin with acid wash. Uptake of cobalt was determined with concentrations in blood and urine. Correlations between exposure and uptake were analysed. RESULTS: Inhalable cobalt in air and cobalt in blood and urine showed rank correlations with coefficients 0.40 and 0.25. Cobalt on skin and uptake in blood and urine presented correlation coefficients of 0.36 and 0.17. Multiple linear regression of cobalt in air and on skin with cobalt in blood showed regression coefficients with cobalt in blood (ß = 203 p < 0.0010, and ß = 0.010, p = 0.0040) and with cobalt in urine (ß = 5779, p = 0.0010, and ß = 0.10, p = 0.60). CONCLUSIONS: Our data presents statistically significant correlations between exposure to cobalt in air with uptake of cobalt in blood and urine. Cobalt on skin was statistically significant with cobalt in blood but not with urine.


Subject(s)
Cobalt/blood , Heavy Metal Poisoning/epidemiology , Inhalation Exposure/statistics & numerical data , Metallurgy/statistics & numerical data , Occupational Exposure/statistics & numerical data , Adult , Air Pollutants, Occupational/blood , Air Pollutants, Occupational/urine , Cobalt/urine , Female , Heavy Metal Poisoning/blood , Heavy Metal Poisoning/urine , Humans , Male , Middle Aged , Skin/metabolism , Sweden
2.
Article in English | MEDLINE | ID: mdl-32115369

ABSTRACT

Laboratory testing is an important tool to assist clinicians in evaluation of patients with potential environmentally-related illness, however, it can be challenging to select or interpret the appropriate toxicological tests. Recent advances in analytical techniques and expanded consumer access to environmental laboratories led to a rise in laboratory testing for various environmental toxicants, including metals. However, most environmental tests have scant clinical evidence and are not validated for clinical use. While the tests themselves may not present direct harm to the patients, the results of inappropriately selected tests may lead to significant patient stress and unnecessary follow-up or treatment. Given the lack of environmental health content in medical training, pediatricians may feel ill-equipped to address most environmental issues they encounter in practice, including the interpretation of environmental toxicant lab results. This article provides an overview of how to approach a child and family with environmental health concerns about "toxic metals", select appropriate metal tests if indicated, and enlist the assistance of the Pediatric Environmental Health Specialty Units (PEHSU) for further management guidance.


Subject(s)
Environmental Exposure/analysis , Heavy Metal Poisoning/diagnosis , Child , Environmental Exposure/adverse effects , Fatigue/chemically induced , Female , Heavy Metal Poisoning/blood , Heavy Metal Poisoning/urine , Humans , Laboratories
3.
Eur J Prev Cardiol ; 27(8): 830-839, 2020 05.
Article in English | MEDLINE | ID: mdl-30776917

ABSTRACT

BACKGROUND: Heavy metals were related to increased risk of atherosclerotic cardiovascular disease (ASCVD). However, potential mechanisms under such associations remain unclear. We aimed to investigate the mediating role of mean platelet volume in the associations between heavy metals exposure and 10-year ASCVD risk. METHOD: Urinary heavy metals and mean platelet volume were measured in 3081 adults from the Wuhan-Zhuhai cohort in China. The associations between urinary heavy metals, mean platelet volume and 10-year ASCVD risk were separately analyzed through generalized linear models and logistic regression models. Mediation analyses were conducted to assess the role of mean platelet volume in the associations between urinary heavy metals and 10-year ASCVD risk. RESULTS: After adjusting for potential confounders, 10-year ASCVD risk was positively associated with urinary iron (odds ratio (OR) = 1.142, 95% confidence interval (1.038-1.256)), copper (OR = 1.384 (1.197-1.601)), zinc (OR = 1.520 (1.296-1.783)), cadmium (OR = 1.153 (0.990, 1.342)) and antimony (OR = 1.452 (1.237-1.704)), and negatively related with urinary barium (OR = 0.905 (0.831-0.985)). Also, we found significant dose-response relationships between urinary iron, zinc, antimony and mean platelet volume, as well as between mean platelet volume and 10-year ASCVD risk (all pfor trends < 0.05). Furthermore, mediation analyses indicated that mean platelet volume mediated 17.55%, 6.15% and 7.38% of the associations between urinary iron, zinc, antimony and 10-year ASCVD risk, respectively (all pvalue < 0.05). CONCLUSIONS: Elevated concentrations of urinary iron, copper, zinc, cadmium and antimony were associated with increased risk of 10-year ASCVD. Mean platelet volume partially mediated the associations of urinary iron, zinc and antimony with 10-year ASCVD risk.


Subject(s)
Atherosclerosis/epidemiology , Blood Platelets , Heart Disease Risk Factors , Heavy Metal Poisoning/epidemiology , Mean Platelet Volume , Metals, Heavy/adverse effects , Aged , Atherosclerosis/blood , Atherosclerosis/diagnosis , Atherosclerosis/urine , Cardiotoxicity , China/epidemiology , Cross-Sectional Studies , Female , Heavy Metal Poisoning/blood , Heavy Metal Poisoning/diagnosis , Heavy Metal Poisoning/urine , Humans , Male , Mediation Analysis , Metals, Heavy/urine , Middle Aged , Predictive Value of Tests , Prognosis , Risk Assessment , Time Factors
4.
Medicine (Baltimore) ; 98(29): e16471, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31335706

ABSTRACT

Thallium is highly toxic and its effects are cumulative. The clinical symptoms of thallium poisoning are non-specific, thereby delaying admission and treatment. This study aimed to summarize the clinical features and treatment experience of patients with delayed admission who experience thallium poisoning.We conducted a retrospective descriptive analysis of patients in our hospital from 2008 to 2018 who had thallium poisoning and experienced a delay in hospital admission. The time from symptom onset to admission was assessed. The patients were divided into 3 groups and descriptive analyses of their clinical characteristics, including basic patient information, symptoms, laboratory test results, examination findings, treatment methods, outcomes, and follow-up information, were conducted.A total of 34 patients with thallium poisoning were included: 8 were admitted to the hospital early or with mild delay, 9 had a moderate delay, and 17 had a severely delayed admission. The time from illness onset to admission was 13 (interquartile range, 7.5-26) days. Some patients with delayed admission had significant symptoms associated with central nervous system damage, and changes in magnetic resonance images and electroencephalograms were also noted. After admission, all patients received Prussian blue treatment, and some patients with relatively high blood concentration received blood purification treatments. Following treatment, the blood and urine thallium concentrations of all patients decreased significantly, and their symptoms were alleviated.Our results show that delayed patient admission in cases of thallium poisoning is associated with greater risk of central nervous system damage. Use of Prussian blue combined with blood purification treatments might improve patients' conditions.


Subject(s)
Delayed Diagnosis , Heavy Metal Poisoning/diagnosis , Heavy Metal Poisoning/therapy , Hospitalization , Thallium/poisoning , Time-to-Treatment , Adolescent , Adult , Antidotes/therapeutic use , Female , Ferrocyanides/therapeutic use , Heavy Metal Poisoning/blood , Heavy Metal Poisoning/urine , Hemoperfusion , Humans , Male , Middle Aged , Retrospective Studies , Thallium/blood , Thallium/urine
6.
Chemosphere ; 202: 48-55, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29554507

ABSTRACT

Lead (Pb) and cadmium (Cd) are toxic metals that exist ubiquitously in the environment. Children in polluted areas are particularly vulnerable to metal exposure, where clinical signs and symptoms could be nonspecific. Absorbed metals are excreted primarily in urine and reflect exposure from all sources. We analyzed Pb and Cd concentrations in blood, feces and urine of children from polluted townships near a lead-zinc mine in Kabwe, Zambia, to determine concurrent childhood exposure to the metals. Moreover, the study determined the Pb and Cd relationships among urine, feces and blood as well as accessed the potential of urine and fecal analysis for biomonitoring of Pb and Cd exposure in children. Fecal Pb (up to 2252 mg/kg, dry weight) and urine Pb (up to 2914 µg/L) were extremely high. Concentrations of Cd in blood (Cd-B) of up to 7.7 µg/L, fecal (up to 4.49 mg/kg, dry weight) and urine (up to 18.1 µg/L) samples were elevated. metal levels were higher in younger children (0-3 years old) than older children (4-7). Positive correlations were recorded for Pb and Cd among blood, urine and fecal samples whereas negative correlations were recorded with age. These findings indicate children are exposed to both metals at their current home environment. Moreover, urine and feces could be useful for biomonitoring of metals due to their strong relationships with blood levels. There is need to conduct a clinical evaluation of the affected children to fully appreciate the health impact of these metal exposure.


Subject(s)
Cadmium/analysis , Environmental Monitoring/methods , Environmental Pollutants/analysis , Feces/chemistry , Heavy Metal Poisoning/urine , Lead/analysis , Urinalysis/methods , Body Weight , Child , Child, Preschool , Female , Humans , Infant , Male , Zambia
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