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  1. Article ; Online: Determination of a guidance value for the communication of individual-level biomonitoring data for urinary arsenic.

    Ponce, Gabriela / Valcke, Mathieu / Bourgault, Marie-Hélène / Gagné, Michelle / Laouan-Sidi, Elhadji Anassour / Gagnon, Fabien

    International journal of hygiene and environmental health

    2022  Volume 240, Page(s) 113927

    Abstract: Background: Available guidance values to interpret individual-level biomonitoring data (ILBD) for the sum of urinary inorganic-related arsenic species (SUIAS) are generally based on population statistical descriptors and not on a predetermined exposure ... ...

    Abstract Background: Available guidance values to interpret individual-level biomonitoring data (ILBD) for the sum of urinary inorganic-related arsenic species (SUIAS) are generally based on population statistical descriptors and not on a predetermined exposure level that should not be exceeded. The objective of this study was thus to propose a range of SUIAS concentrations, reflecting an exposure corresponding to WHO's provisional guideline value (PGV) for arsenic in drinking water (10 μg/L), within which an exposure-based biomonitoring guidance value can be identified. METHOD A comprehensive literature review was carried out in order to identify studies that were relevant to the determination of a guidance value. Drinking water arsenic exposure and urinary biomonitoring concentrations obtained from selected studies were used to conduct a structural equation modeling meta-analysis, from which regression coefficients were obtained to derive an interpretative guidance range. RESULTS Individuals exposed to the arsenic background level comparable to North American and European countries and to a water source contaminated at the WHO's PGV, would have, on average, urinary SUIAS between 9 and 20 μg/L, with the most probable value being 15 μg/L. To address the associated uncertainty, the final guidance value selection within this range may be based on a targeted sensitivity and specificity towards detecting overexposed individuals. Indeed, spans of sensitivity of 60-82%, and of specificity of 58-85%, were estimated for the proposed range based on drinking water exposure raw data from the literature. CONCLUSION The range of guidance values obtained appears suitable for interpreting and communicating ILBD in any population biomonitoring studies in which background exposure is comparable to the North American and European context. Before selecting a single value within the proposed range, it will be important for Public Health officials to assess the possible consequences of this selection on the management and communication of the biomonitoring results.
    MeSH term(s) Arsenic/urine ; Biological Monitoring ; Communication ; Environmental Exposure/analysis ; Environmental Monitoring/methods ; Humans
    Chemical Substances Arsenic (N712M78A8G)
    Language English
    Publishing date 2022-01-24
    Publishing country Germany
    Document type Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2009176-X
    ISSN 1618-131X ; 1438-4639
    ISSN (online) 1618-131X
    ISSN 1438-4639
    DOI 10.1016/j.ijheh.2022.113927
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: An assessment of the impact of multi-route co-exposures on human variability in toxicokinetics: A case study with binary and quaternary mixtures of volatile drinking water contaminants.

    Tohon, Honesty / Valcke, Mathieu / Haddad, Sami

    Journal of applied toxicology : JAT

    2019  Volume 39, Issue 7, Page(s) 974–991

    Abstract: This study aimed to assess the impact of multi-route co-exposures to chemicals on interindividual variability in toxicokinetics. Probabilistic physiologically based pharmacokinetic multi-route interaction models were developed for adults and four younger ...

    Abstract This study aimed to assess the impact of multi-route co-exposures to chemicals on interindividual variability in toxicokinetics. Probabilistic physiologically based pharmacokinetic multi-route interaction models were developed for adults and four younger subpopulations. Drinking water-mediated multi-route exposures were simulated for benzene alone or in co-exposure with toluene, ethylbenzene and m-xylene, for trichloroethylene or vinyl chloride (VC), alone and in mixture. These simulations were performed for "low" and "high" exposure scenarios, involving respectively the US EPA's short-term drinking water health advisories, and 10 times these advisory values. Distributions of relevant internal dose metrics for benzene, trichloroethylene and VC were obtained using Monte Carlo simulations. Intergroup variability indexes (VI) were computed for the "low" (VI
    MeSH term(s) Adolescent ; Adult ; Age Factors ; Dietary Exposure/adverse effects ; Dietary Exposure/analysis ; Drinking Water/chemistry ; Drinking Water/standards ; Environmental Exposure/adverse effects ; Environmental Exposure/analysis ; Humans ; Infant ; Inhalation Exposure/adverse effects ; Inhalation Exposure/analysis ; Models, Biological ; Organ Specificity ; Skin Absorption/drug effects ; Toxicokinetics ; Volatile Organic Compounds/pharmacokinetics ; Volatile Organic Compounds/toxicity ; Water Pollutants, Chemical/pharmacokinetics ; Water Pollutants, Chemical/toxicity
    Chemical Substances Drinking Water ; Volatile Organic Compounds ; Water Pollutants, Chemical
    Language English
    Publishing date 2019-03-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 604625-3
    ISSN 1099-1263 ; 0260-437X
    ISSN (online) 1099-1263
    ISSN 0260-437X
    DOI 10.1002/jat.3787
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  3. Article: A probabilistic toxicokinetic modeling approach to the assessment of the impact of daily variations of lead concentrations in tap water from schools and daycares on blood lead levels in children

    Valcke, Mathieu / Bourgault, Marie-Hélène / Gagné, Michelle / Levallois, Patrick

    Science of the total environment. 2021 June 25, v. 775

    2021  

    Abstract: The aim of this study was to assess the impact of exposure to tap water lead concentration ([Pb]TW) occurring in schools or daycares on blood lead level (BLL) of attending children. Given the potentially wide variations in space and time of ([Pb]TW) ... ...

    Abstract The aim of this study was to assess the impact of exposure to tap water lead concentration ([Pb]TW) occurring in schools or daycares on blood lead level (BLL) of attending children. Given the potentially wide variations in space and time of ([Pb]TW) documented in the literature, a simple probabilistic toxicokinetic (STK) model that allows the simulation of the time-varying evolution of BLL in response to these variations was developed. Thus, basic toxicokinetic equations were assembled to simulate BLL in a typical infant, toddler and pupil. The STK model's steady-state BLL predictions showed good correspondence when validated against Integrated Exposure and Uptake BioKinetic model predictions for comparable [Pb]TW values. Exposures to three distributions of [Pb]TW in specific sets of Canadian schools and daycares documented in the scientific literature were simulated probabilistically with Monte Carlo simulations. For the highest distribution of [Pb]TW simulated (median, 90th percentile = 24, 412 μg/L), average annual BLL (median, 97.5th percentile) varies between 1.5 and 6.4 μg/dL in infant and 1.1 and 3 μg/dL in pupils. Toddler's results were midway between those from the infants and pupils. Under this exposure scenario, the infant may present BLL > 5 μg/dL for a significant number of days over the course of the academic year (median; 97.5th: 17; 227 days). However, peak exposure may remain unnoticed if rare and drowned out by the background BLL. In conclusion, even if they may be sparse, peak exposure episodes to [Pb]TW in schools and daycares may suffice to increased BLL in attending individuals. This finding emphasizes the need for further characterization of [Pb]TW in schools and daycares in order to identify potentially problematic institutions and therefore avoid undesirable exposures for the children attending them.
    Keywords blood ; environment ; evolution ; exposure scenario ; lead ; models ; tap water
    Language English
    Dates of publication 2021-0625
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 121506-1
    ISSN 1879-1026 ; 0048-9697
    ISSN (online) 1879-1026
    ISSN 0048-9697
    DOI 10.1016/j.scitotenv.2021.145866
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  4. Article ; Online: Estimation of toluene exposure in air from BMA (S-benzylmercapturic acid) urinary measures using a reverse dosimetry approach based on physiologically pharmacokinetic modeling.

    Tohon, Honesty / Valcke, Mathieu / Aranda-Rodriguez, Rocio / Nong, Andy / Haddad, Sami

    Regulatory toxicology and pharmacology : RTP

    2021  Volume 120, Page(s) 104860

    Abstract: This study aimed to use a reverse dosimetry PBPK modeling approach to estimate toluene atmospheric exposure from urinary measurements of S-benzylmercapturic acid (BMA) in a small group of individuals and to evaluate the uncertainty associated to urinary ... ...

    Abstract This study aimed to use a reverse dosimetry PBPK modeling approach to estimate toluene atmospheric exposure from urinary measurements of S-benzylmercapturic acid (BMA) in a small group of individuals and to evaluate the uncertainty associated to urinary spot-sampling compared to 24-h collected urine samples. Each exposure assessment technique was developed namely to estimate toluene air exposure from BMA measurements in 24-h urine samples (24-h-BMA) and from distributions of daily urinary BMA spot measurements (DUBSM). Model physiological parameters were described based upon age, weight, size and sex. Monte Carlo simulations with the PBPK model allowed converting DUBSM distribution (and 24-h-BMA) into toluene air levels. For the approach relying on DUBSM distribution, the ratio between the 95% probability of predicted toluene concentration and its 50% probability in each individual varied between 1.2 and 1.4, while that based on 24-h-BMA varied between 1.0 and 1.1. This suggests more variability in estimated exposure from spot measurements. Thus, estimating toluene exposure based on DUBSM distribution generated about 20% more uncertainty. Toluene levels estimated (0.0078-0.0138 ppm) are well below Health Canada's maximum chronic air guidelines. PBPK modeling and reverse dosimetry may be combined to interpret urinary metabolites data of VOCs and assess related uncertainties.
    MeSH term(s) Acetylcysteine/analogs & derivatives ; Acetylcysteine/urine ; Adult ; Air Pollutants/toxicity ; Environmental Biomarkers/drug effects ; Environmental Biomarkers/physiology ; Environmental Monitoring/methods ; Humans ; Models, Biological ; Monte Carlo Method ; Toluene/toxicity
    Chemical Substances Air Pollutants ; Environmental Biomarkers ; Toluene (3FPU23BG52) ; Acetylcysteine (WYQ7N0BPYC) ; S-benzyl-N-acetyl-L-cysteine (X3H719RFPT)
    Language English
    Publishing date 2021-01-03
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 604672-1
    ISSN 1096-0295 ; 0273-2300
    ISSN (online) 1096-0295
    ISSN 0273-2300
    DOI 10.1016/j.yrtph.2020.104860
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  5. Article: Assessing human variability in kinetics for exposures to multiple environmental chemicals: a physiologically based pharmacokinetic modeling case study with dichloromethane, benzene, toluene, ethylbenzene, and m-xylene.

    Valcke, Mathieu / Haddad, Sami

    Journal of toxicology and environmental health. Part A

    2015  Volume 78, Issue 7, Page(s) 409–431

    Abstract: The objective of this study was to compare the magnitude of interindividual variability in internal dose for inhalation exposure to single versus multiple chemicals. Physiologically based pharmacokinetic models for adults (AD), neonates (NEO), toddlers ( ... ...

    Abstract The objective of this study was to compare the magnitude of interindividual variability in internal dose for inhalation exposure to single versus multiple chemicals. Physiologically based pharmacokinetic models for adults (AD), neonates (NEO), toddlers (TODD), and pregnant women (PW) were used to simulate inhalation exposure to "low" (RfC-like) or "high" (AEGL-like) air concentrations of benzene (Bz) or dichloromethane (DCM), along with various levels of toluene alone or toluene with ethylbenzene and xylene. Monte Carlo simulations were performed and distributions of relevant internal dose metrics of either Bz or DCM were computed. Area under the blood concentration of parent compound versus time curve (AUC)-based variability in AD, TODD, and PW rose for Bz when concomitant "low" exposure to mixtures of increasing complexities occurred (coefficient of variation (CV) = 16-24%, vs. 12-15% for Bz alone), but remained unchanged considering DCM. Conversely, AUC-based CV in NEO fell (15 to 5% for Bz; 12 to 6% for DCM). Comparable trends were observed considering production of metabolites (AMET), except for NEO's CYP2E1-mediated metabolites of Bz, where an increased CV was observed (20 to 71%). For "high" exposure scenarios, Cmax-based variability of Bz and DCM remained unchanged in AD and PW, but decreased in NEO (CV= 11-16% to 2-6%) and TODD (CV= 12-13% to 7-9%). Conversely, AMET-based variability for both substrates rose in every subpopulation. This study analyzed for the first time the impact of multiple exposures on interindividual variability in toxicokinetics. Evidence indicates that this impact depends upon chemical concentrations and biochemical properties, as well as the subpopulation and internal dose metrics considered.
    MeSH term(s) Adolescent ; Adult ; Aged ; Benzene/pharmacokinetics ; Benzene/toxicity ; Benzene Derivatives/pharmacokinetics ; Benzene Derivatives/toxicity ; Child, Preschool ; Computer Simulation ; Female ; Humans ; Infant ; Infant, Newborn ; Inhalation Exposure/adverse effects ; Methylene Chloride/pharmacokinetics ; Methylene Chloride/toxicity ; Middle Aged ; Models, Theoretical ; Monte Carlo Method ; Pregnancy ; Sensitivity and Specificity ; Toluene/pharmacokinetics ; Toluene/toxicity ; Xylenes/pharmacokinetics ; Xylenes/toxicity ; Young Adult
    Chemical Substances Benzene Derivatives ; Xylenes ; Toluene (3FPU23BG52) ; Methylene Chloride (588X2YUY0A) ; Benzene (J64922108F) ; ethylbenzene (L5I45M5G0O) ; 3-xylene (O9XS864HTE)
    Language English
    Publishing date 2015
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1413345-3
    ISSN 1528-7394 ; 0098-4108 ; 1087-2620
    ISSN 1528-7394 ; 0098-4108 ; 1087-2620
    DOI 10.1080/15287394.2014.971477
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  6. Article ; Online: Regional variations in human chemical exposures in Canada: A case study using biomonitoring data from the Canadian Health Measures Survey for the provinces of Quebec and Ontario.

    Valcke, Mathieu / Karthikeyan, Subramanian / Walker, Mike / Gagné, Michelle / Copes, Ray / St-Amand, Annie

    International journal of hygiene and environmental health

    2020  Volume 225, Page(s) 113451

    Abstract: The Canadian Health Measures Survey (CHMS), an ongoing national health survey conducted in two-year cycles, collects extensive biomonitoring data that is used to assess the exposure of Canadians to environmental chemicals of concern. Combining data from ... ...

    Abstract The Canadian Health Measures Survey (CHMS), an ongoing national health survey conducted in two-year cycles, collects extensive biomonitoring data that is used to assess the exposure of Canadians to environmental chemicals of concern. Combining data from multiple cycles of the CHMS allows for the calculation of robust regional estimates of chemical concentrations in blood and urine. The objective of this work was to compare biomarkers of exposure to several environmental chemicals for the provinces of Quebec and Ontario, two major CHMS regions, as well as the entire CHMS (representing Canada) minus Quebec (CMQ), and the entire CHMS minus Ontario (CMO), and to interpret differences between regions. Geometric means and 95th percentiles of blood and/or urinary concentrations of 45 environmental chemicals or their metabolites for Ontario, Quebec, CMQ, and CMO were calculated by combining the two most recent cycles of data available for a chemical (cycles 1 and 2, or cycles 2 and 3) from the first three cycles of the CHMS (2007-2013). Weighted one-way ANOVA was used to test the differences between regional estimates. After applying a Bonferonni-Holm adjustment for multiple comparisons, the following measures were significantly higher in Quebec as compared to Ontario and CMQ: blood lead, urinary lead and the urinary polyaromatic hydrocarbon (PAH) metabolites, 9-hydroxyfluorene, 1-hydroxyphenanthrene, 2- hydroxyphenanthrene and 3-hydroxyphenanthrene. In Quebec compared to CMQ only, urinary 2-hydroxfluorene, 3-hydroxyfluorene, 2-hydroxynaphthalene, and 4-hydroxyphenanthrene were higher. The concentration of urinary fluoride was significantly higher in Ontario as compared to Quebec and CMO. Blood manganese and urinary fluoride were significantly lower in Quebec compared to CMQ, and blood and urinary selenium were significantly lower in Ontario compared to CMO. Regional differences in tobacco use, age of dwellings and drinking water fluoridation are among the possible contributing factors to some of the observed differences. In conclusion, this is the first study where biomonitoring data from multiple cycles of CHMS were combined in order to generate robust estimates for subsets of the Canadian population. Such assessments can contribute to a regional-level prioritization of control measures to reduce the exposure of Canadians to chemicals in their environment.
    MeSH term(s) Adolescent ; Adult ; Aged ; Biological Monitoring ; Child ; Child, Preschool ; Environmental Pollutants/blood ; Environmental Pollutants/urine ; Health Surveys ; Humans ; Metals/blood ; Metals/urine ; Middle Aged ; Ontario ; Organic Chemicals/blood ; Organic Chemicals/urine ; Quebec ; Young Adult
    Chemical Substances Environmental Pollutants ; Metals ; Organic Chemicals
    Language English
    Publishing date 2020-01-20
    Publishing country Germany
    Document type Comparative Study ; Journal Article
    ZDB-ID 2009176-X
    ISSN 1618-131X ; 1438-4639
    ISSN (online) 1618-131X
    ISSN 1438-4639
    DOI 10.1016/j.ijheh.2020.113451
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  7. Article ; Online: Characterization of the human kinetic adjustment factor for the health risk assessment of environmental contaminants.

    Valcke, Mathieu / Krishnan, Kannan

    Journal of applied toxicology : JAT

    2014  Volume 34, Issue 3, Page(s) 227–240

    Abstract: A default uncertainty factor of 3.16 (√10) is applied to account for interindividual variability in toxicokinetics when performing non-cancer risk assessments. Using relevant human data for specific chemicals, as WHO/IPCS suggests, it is possible to ... ...

    Abstract A default uncertainty factor of 3.16 (√10) is applied to account for interindividual variability in toxicokinetics when performing non-cancer risk assessments. Using relevant human data for specific chemicals, as WHO/IPCS suggests, it is possible to evaluate, and replace when appropriate, this default factor by quantifying chemical-specific adjustment factors for interindividual variability in toxicokinetics (also referred to as the human kinetic adjustment factor, HKAF). The HKAF has been determined based on the distributions of pharmacokinetic parameters (e.g., half-life, area under the curve, maximum blood concentration) in relevant populations. This article focuses on the current state of knowledge of the use of physiologically based algorithms and models in characterizing the HKAF for environmental contaminants. The recent modeling efforts on the computation of HKAF as a function of the characteristics of the population, chemical and its mode of action (dose metrics), as well as exposure scenario of relevance to the assessment are reviewed here. The results of these studies, taken together, suggest the HKAF varies as a function of the sensitive subpopulation and dose metrics of interest, exposure conditions considered (route, duration, and intensity), metabolic pathways involved and theoretical model underlying its computation. The HKAF seldom exceeded the default value of 3.16, except in very young children (i.e., <≈ 3 months) and when the parent compound is the toxic moiety. Overall, from a public health perspective, the current state of knowledge generally suggest that the default uncertainty factor is sufficient to account for human variability in non-cancer risk assessments of environmental contaminants.
    MeSH term(s) Age Factors ; Animals ; Environmental Exposure/analysis ; Environmental Exposure/statistics & numerical data ; Environmental Pollutants/pharmacokinetics ; Environmental Pollutants/toxicity ; Humans ; Metabolic Detoxication, Phase I ; Metabolic Detoxication, Phase II ; Models, Biological ; Public Health/statistics & numerical data ; Risk Assessment ; Uncertainty
    Chemical Substances Environmental Pollutants
    Language English
    Publishing date 2014-03
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 604625-3
    ISSN 1099-1263 ; 0260-437X
    ISSN (online) 1099-1263
    ISSN 0260-437X
    DOI 10.1002/jat.2919
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  8. Article: Reverse dosimetry modeling of toluene exposure concentrations based on biomonitoring levels from the Canadian health measures survey.

    Tohon, Honesty / Nong, Andy / Moreau, Marjory / Valcke, Mathieu / Haddad, Sami

    Journal of toxicology and environmental health. Part A

    2018  Volume 81, Issue 20, Page(s) 1066–1082

    Abstract: Biomonitoring might provide useful estimates of population exposure to environmental chemicals. However, data uncertainties stemming from interindividual variability are common in large population biomonitoring surveys. Physiologically based ... ...

    Abstract Biomonitoring might provide useful estimates of population exposure to environmental chemicals. However, data uncertainties stemming from interindividual variability are common in large population biomonitoring surveys. Physiologically based pharmacokinetic (PBPK) models might be used to account for age- and gender-related variability in internal dose. The objective of this study was to reconstruct air concentrations consistent with blood toluene measures reported in the third Canadian Health Measures Survey using reverse dosimetry PBPK modeling techniques. Population distributions of model's physiological parameters were described based upon age, weight, and size for four subpopulations (12-19, 20-39, 40-59, and 60-79 years old). Monte Carlo simulations applied to PBPK modeling allowed converting the distributions of venous blood measures of toluene obtained from CHMS into related air levels. Based upon blood levels observed at the 50
    MeSH term(s) Adolescent ; Adult ; Aged ; Canada ; Environmental Monitoring/methods ; Environmental Pollutants/pharmacokinetics ; Health Surveys ; Humans ; Middle Aged ; Models, Biological ; Monte Carlo Method ; Toluene/pharmacokinetics ; Young Adult
    Chemical Substances Environmental Pollutants ; Toluene (3FPU23BG52)
    Language English
    Publishing date 2018-10-26
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1413345-3
    ISSN 1528-7394 ; 0098-4108 ; 1087-2620
    ISSN 1528-7394 ; 0098-4108 ; 1087-2620
    DOI 10.1080/15287394.2018.1534174
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  9. Article: Biological monitoring of exposure to rare earth elements and selected metals in the Inuit population of Nunavik, Canada

    Cirtiu, Ciprian Mihai / Valcke, Mathieu / Gagné, Michelle / Bourgault, Marie-Hélène / Narame, Céline / Gadio, Souleymane / Poulin, Patrick / Ayotte, Pierre

    Chemosphere. 2022 Feb., v. 289

    2022  

    Abstract: In Nunavik (Northern Quebec, Canada), some mining projects are envisioned, that could increase the contamination of the environment by various chemicals, including rare earth elements (REEs), and implicitly Inuit population exposure. The objective of ... ...

    Abstract In Nunavik (Northern Quebec, Canada), some mining projects are envisioned, that could increase the contamination of the environment by various chemicals, including rare earth elements (REEs), and implicitly Inuit population exposure. The objective of this study was to determine the baseline biological exposure of the population to these elements, before the potential mining development occurs. In the framework of the 2017 Qanuilirpitaa? Inuit health survey, urine samples were obtained from a representative sample of the adult Nunavik population, which were used to constitute 30 pooled samples according to age, sex and Nunavik subregions. Pooled samples were analyzed using sensitive and accurate methods involving ICP-MS platforms to quantify urinary concentrations of 17 REEs and 7 elements of interest in Nunavik (arsenic, antimony, chromium, cobalt, nickel, thallium and uranium). REEs were mostly not detected in pooled samples from this population. Detectable concentrations were found in some samples for cerium (range: 0.5–0.7 nmol/L; 27% > method detection limit (MDL) and lanthanum (range: 0.2–0.4 nmol/L; 33% > MDL). As for the other elements of interest, antimony, arsenic, cobalt and thallium were detected in 100% of the samples, whereas chromium and nickel were detected in 83% and 80% of the samples, respectively. Concentrations of arsenic (geometric mean (GM) = 0.5 μmol/L) and cobalt (GM = 5.2 nmol/L) were greater than in the general Canadian population; the opposite was observed for nickel (GM = 8.9 nmol/L). Arsenic concentrations increased significantly with age, whereas the opposite trend was observed for nickel and thallium. In this first biomonitoring study focusing on REEs and carried out in a representative sample of the Nunavik population, we found no evidence of significant exposure from pooled samples analysis. These results could eventually be used as baseline values in future studies aiming to assess temporal trends of exposure to REEs.
    Keywords Inuit ; adults ; antimony ; arsenic ; cerium ; chromium ; cobalt ; detection limit ; environmental monitoring ; health surveys ; lanthanum ; nickel ; thallium ; uranium ; urine ; Quebec
    Language English
    Dates of publication 2022-02
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 120089-6
    ISSN 1879-1298 ; 0045-6535 ; 0366-7111
    ISSN (online) 1879-1298
    ISSN 0045-6535 ; 0366-7111
    DOI 10.1016/j.chemosphere.2021.133142
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  10. Article ; Online: Public Health Consequences of Lead in Drinking Water.

    Levallois, Patrick / Barn, Prabjit / Valcke, Mathieu / Gauvin, Denis / Kosatsky, Tom

    Current environmental health reports

    2018  Volume 5, Issue 2, Page(s) 255–262

    Abstract: Purpose of review: Lead can enter drinking water from lead service lines and lead-containing plumbing, particularly in the presence of corrosive water. We review the current evidence on the role of drinking water as a source of lead exposure and its ... ...

    Abstract Purpose of review: Lead can enter drinking water from lead service lines and lead-containing plumbing, particularly in the presence of corrosive water. We review the current evidence on the role of drinking water as a source of lead exposure and its potential impacts on health, with an emphasis on children. Drinking water guidelines and mitigation strategies are also presented.
    Recent findings: The impact of lead on neurodevelopmental effects in children even at low levels of exposure is well established. Population and toxicokinetic modeling studies have found a clear relationship between water lead levels and blood lead levels in children at low levels of lead in drinking water. Various mitigation strategies can lower lead levels in water. The importance of drinking water as a contributor to total lead exposure depends on water lead levels and the amount consumed, as well as the relative contribution of other sources. Efforts should be made to reduce lead exposure for all sources, including drinking water, considering that no threshold level of exposure exists for the neurodevelopmental effects of lead in children.
    MeSH term(s) Child ; Drinking Water/chemistry ; Environmental Exposure/adverse effects ; Humans ; Lead/analysis ; Lead Poisoning/etiology ; Public Health/standards ; Water Pollutants, Chemical/analysis ; Water Supply/standards
    Chemical Substances Drinking Water ; Water Pollutants, Chemical ; Lead (2P299V784P)
    Language English
    Publishing date 2018-03-19
    Publishing country Switzerland
    Document type Journal Article ; Review
    ISSN 2196-5412
    ISSN (online) 2196-5412
    DOI 10.1007/s40572-018-0193-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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