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  1. Article: A novel study evaluation strategy in the systematic review of animal toxicology studies for human health assessments of environmental chemicals

    Dishaw, Laura / Yost, Erin / Arzuaga, Xabier / Luke, April / Kraft, Andrew / Walker, Teneille / Thayer, Kris

    Environment international. 2020 Aug., v. 141

    2020  

    Abstract: A key aspect of the systematic review process is study evaluation to understand the strengths and weaknesses of individual studies included in the review. The present manuscript describes the process currently being used by the Environmental Protection ... ...

    Abstract A key aspect of the systematic review process is study evaluation to understand the strengths and weaknesses of individual studies included in the review. The present manuscript describes the process currently being used by the Environmental Protection Agency’s (EPA) Integrated Risk Information System (IRIS) Program to evaluate animal toxicity studies, illustrated by application to the recent systematic reviews of two phthalates: diisobutyl phthalate (DIBP) and diethyl phthalate (DEP). The IRIS Program uses a domain-based approach that was developed after careful consideration of tools used by others to evaluate experimental animal studies in toxicology and pre-clinical research. Standard practice is to have studies evaluated by at least two independent reviewers for aspects related to reporting quality, risk of bias/internal validity (e.g., randomization, blinding at outcome assessment, methods used to expose animals and assess outcomes, etc.), and sensitivity to identify factors that may limit the ability of a study to detect a true effect. To promote consistency across raters, prompting considerations and example responses are provided to reviewers, and a pilot phase is conducted. The evaluation process is performed separately for each outcome reported in a study, as the utility of a study may vary for different outcomes. Input from subject matter experts is used to identify chemical- and outcome-specific considerations (e.g., lifestage of exposure and outcome assessment when considering reproductive effects) to guide judgments within particular evaluation domains. For each evaluation domain, reviewers reach a consensus on a rating of Good, Adequate, Deficient, or Critically Deficient. These individual domain ratings are then used to determine the overall confidence in the study (High Confidence, Medium Confidence, Low Confidence, or Deficient). Study evaluation results, including the justifications for reviewer judgements, are documented and made publicly available in EPA’s version of Health Assessment Workspace Collaborative (HAWC), a free and open source web-based software application. (The views expressed are those of the authors and do not necessarily represent the views or policies of the US EPA).
    Keywords Internet ; United States Environmental Protection Agency ; computer software ; diethyl phthalate ; environment ; environmental protection ; health effects assessments ; human health ; information systems ; laboratory animals ; risk ; systematic review ; toxicity
    Language English
    Dates of publication 2020-08
    Publishing place Elsevier Ltd
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 554791-x
    ISSN 1873-6750 ; 0160-4120
    ISSN (online) 1873-6750
    ISSN 0160-4120
    DOI 10.1016/j.envint.2020.105736
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: A novel study evaluation strategy in the systematic review of animal toxicology studies for human health assessments of environmental chemicals.

    Dishaw, Laura / Yost, Erin / Arzuaga, Xabier / Luke, April / Kraft, Andrew / Walker, Teneille / Thayer, Kris

    Environment international

    2020  Volume 141, Page(s) 105736

    Abstract: A key aspect of the systematic review process is study evaluation to understand the strengths and weaknesses of individual studies included in the review. The present manuscript describes the process currently being used by the Environmental Protection ... ...

    Abstract A key aspect of the systematic review process is study evaluation to understand the strengths and weaknesses of individual studies included in the review. The present manuscript describes the process currently being used by the Environmental Protection Agency's (EPA) Integrated Risk Information System (IRIS) Program to evaluate animal toxicity studies, illustrated by application to the recent systematic reviews of two phthalates: diisobutyl phthalate (DIBP) and diethyl phthalate (DEP). The IRIS Program uses a domain-based approach that was developed after careful consideration of tools used by others to evaluate experimental animal studies in toxicology and pre-clinical research. Standard practice is to have studies evaluated by at least two independent reviewers for aspects related to reporting quality, risk of bias/internal validity (e.g., randomization, blinding at outcome assessment, methods used to expose animals and assess outcomes, etc.), and sensitivity to identify factors that may limit the ability of a study to detect a true effect. To promote consistency across raters, prompting considerations and example responses are provided to reviewers, and a pilot phase is conducted. The evaluation process is performed separately for each outcome reported in a study, as the utility of a study may vary for different outcomes. Input from subject matter experts is used to identify chemical- and outcome-specific considerations (e.g., lifestage of exposure and outcome assessment when considering reproductive effects) to guide judgments within particular evaluation domains. For each evaluation domain, reviewers reach a consensus on a rating of Good, Adequate, Deficient, or Critically Deficient. These individual domain ratings are then used to determine the overall confidence in the study (High Confidence, Medium Confidence, Low Confidence, or Deficient). Study evaluation results, including the justifications for reviewer judgements, are documented and made publicly available in EPA's version of Health Assessment Workspace Collaborative (HAWC), a free and open source web-based software application. (The views expressed are those of the authors and do not necessarily represent the views or policies of the US EPA).
    MeSH term(s) Animals ; Humans ; Bias ; Ecotoxicology ; Environmental Pollutants/toxicity ; Reproduction ; Systematic Reviews as Topic
    Chemical Substances Environmental Pollutants
    Language English
    Publishing date 2020-05-17
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 554791-x
    ISSN 1873-6750 ; 0160-4120
    ISSN (online) 1873-6750
    ISSN 0160-4120
    DOI 10.1016/j.envint.2020.105736
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Expanded Systematic Evidence Map for Hundreds of Per- and Polyfluoroalkyl Substances (PFAS) and Comprehensive PFAS Human Health Dashboard.

    Shirke, Avanti V / Radke, Elizabeth G / Lin, Cynthia / Blain, Robyn / Vetter, Nicole / Lemeris, Courtney / Hartman, Pamela / Hubbard, Heidi / Angrish, Michelle / Arzuaga, Xabier / Congleton, Johanna / Davis, Allen / Dishaw, Laura V / Jones, Ryan / Judson, Richard / Kaiser, J Phillip / Kraft, Andrew / Lizarraga, Lucina / Noyes, Pamela D /
    Patlewicz, Grace / Taylor, Michele / Williams, Antony J / Thayer, Kristina A / Carlson, Laura M

    Environmental health perspectives

    2024  Volume 132, Issue 2, Page(s) 26001

    Abstract: Background: Per- and polyfluoroalkyl substances (PFAS) encompass a class of chemically and structurally diverse compounds that are extensively used in industry and detected in the environment. The US Environmental Protection Agency (US EPA) 2021 PFAS ... ...

    Abstract Background: Per- and polyfluoroalkyl substances (PFAS) encompass a class of chemically and structurally diverse compounds that are extensively used in industry and detected in the environment. The US Environmental Protection Agency (US EPA) 2021 PFAS Strategic Roadmap describes national research plans to address the challenge of PFAS.
    Objectives: Systematic Evidence Map (SEM) methods were used to survey and summarize available epidemiological and mammalian bioassay evidence that could inform human health hazard identification for a set of 345 PFAS that were identified by the US EPA's Center for Computational Toxicology and Exposure (CCTE) for
    Methods: SEM methods were used to search, screen, and inventory mammalian bioassay and epidemiological literature from peer-reviewed and gray literature sources using manual review and machine-learning software. For each included study, study design details and health end points examined were summarized in interactive web-based literature inventories. Some included studies also underwent study evaluation and detailed extraction of health end point data. All underlying data is publicly available online as interactive visuals with downloadable metadata.
    Results: More than 13,000 studies were identified from scientific databases. Screening processes identified 121 mammalian bioassay and 111 epidemiological studies that met screening criteria. Epidemiological evidence (available for 12 PFAS) mostly assessed the reproductive, endocrine, developmental, metabolic, cardiovascular, and immune systems. Mammalian bioassay evidence (available for 30 PFAS) commonly assessed effects in the reproductive, whole-body, nervous, and hepatic systems. Overall, 41 PFAS had evidence across mammalian bioassay and epidemiology data streams (roughly 11% of searched chemicals).
    Discussion: No epidemiological and/or mammalian bioassay evidence were identified for most of the PFAS included in our search. Results from this SEM, our 2022 SEM on
    MeSH term(s) Animals ; United States ; Humans ; Dashboard Systems ; United States Environmental Protection Agency ; Reproduction ; Risk Assessment ; Fluorocarbons/toxicity ; Mammals
    Chemical Substances Fluorocarbons
    Language English
    Publishing date 2024-02-06
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 195189-0
    ISSN 1552-9924 ; 0091-6765 ; 1078-0475
    ISSN (online) 1552-9924
    ISSN 0091-6765 ; 1078-0475
    DOI 10.1289/EHP13423
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Use of the Adverse Outcome Pathway (AOP) framework to evaluate species concordance and human relevance of Dibutyl phthalate (DBP)-induced male reproductive toxicity.

    Arzuaga, Xabier / Walker, Teneille / Yost, Erin E / Radke, Elizabeth G / Hotchkiss, Andrew K

    Reproductive toxicology (Elmsford, N.Y.)

    2019  Volume 96, Page(s) 445–458

    Abstract: Dibutyl phthalate (DBP) is a phthalate ester used as a plasticizer, and solvent. Studies using rats consistently report that DBP exposure disrupts normal development of the male reproductive system in part via inhibition of androgen synthesis. However, ... ...

    Abstract Dibutyl phthalate (DBP) is a phthalate ester used as a plasticizer, and solvent. Studies using rats consistently report that DBP exposure disrupts normal development of the male reproductive system in part via inhibition of androgen synthesis. However, studies using xenograft models report that in human fetal testis DBP exposure is unlikely to impair testosterone synthesis. These results question the validity of the rat model for assessment of male reproductive effects caused by DBP. The Adverse Outcome Pathway (AOP) framework was used to evaluate the available evidence for DBP-induced toxicity to the male reproductive system. Three relevant biological elements were identified: 1) fetal rats are more sensitive than other rodents and human fetal xenografts to DBP-induced anti-androgenic effects, 2) DBP-induced androgen-independent adverse outcomes are conserved amongst different mammalian models and human fetal testis xenografts, and 3) DBP-induced anti-androgenic effects are conserved in different mammalian species when exposure occurs during postnatal life stages.
    MeSH term(s) Adverse Outcome Pathways ; Animals ; Dibutyl Phthalate/toxicity ; Endocrine Disruptors/toxicity ; Genitalia, Male/drug effects ; Humans ; Male
    Chemical Substances Endocrine Disruptors ; Dibutyl Phthalate (2286E5R2KE)
    Language English
    Publishing date 2019-06-28
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 639342-1
    ISSN 1873-1708 ; 0890-6238
    ISSN (online) 1873-1708
    ISSN 0890-6238
    DOI 10.1016/j.reprotox.2019.06.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Modes of action associated with uranium induced adverse effects in bone function and development.

    Arzuaga, Xabier / Gehlhaus, Martin / Strong, Jamie

    Toxicology letters

    2015  Volume 236, Issue 2, Page(s) 123–130

    Abstract: Uranium, a naturally occurring element used in military and industrial applications, accumulates in the skeletal system of animals and humans. Evidence from animal and in-vitro studies demonstrates that uranium exposure is associated with alterations in ... ...

    Abstract Uranium, a naturally occurring element used in military and industrial applications, accumulates in the skeletal system of animals and humans. Evidence from animal and in-vitro studies demonstrates that uranium exposure is associated with alterations in normal bone functions. The available studies suggest that upon absorption uranium directly affects bone development and maintenance by inhibiting osteoblast differentiation and normal functions, and indirectly by disrupting renal production of Vitamin D. Animal studies also provide evidence for increased susceptibility to uranium-induced bone toxicity during early life stages. The objective of this review is to provide a summary of uranium-induced bone toxicity and the potential mechanisms by which uranium can interfere with bone development and promote fragility. Since normal Vitamin D production and osteoblast functions are essential for bone growth and maintenance, young individuals and the elderly may represent potentially susceptible populations to uranium-induced bone damage.
    MeSH term(s) Alpha Particles/adverse effects ; Biomechanical Phenomena/radiation effects ; Bone Development/radiation effects ; Bone Diseases/etiology ; Humans ; Uranium/adverse effects
    Chemical Substances Uranium (4OC371KSTK)
    Language English
    Publishing date 2015-07-16
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 433788-8
    ISSN 1879-3169 ; 0378-4274
    ISSN (online) 1879-3169
    ISSN 0378-4274
    DOI 10.1016/j.toxlet.2015.05.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Polluted-site killifish (Fundulus heteroclitus) embryos are resistant to organic pollutant-mediated induction of CYP1A activity, reactive oxygen species, and heart deformities.

    Arzuaga, Xabier / Elskus, Adria

    Environmental toxicology and chemistry

    2010  Volume 29, Issue 3, Page(s) 676–682

    Abstract: Exposure to coplanar polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) can adversely affect fish embryonic development, induce expression of cytochrome P4501A (CYP1A), and increase reactive oxygen species (ROS) production, ... ...

    Abstract Exposure to coplanar polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) can adversely affect fish embryonic development, induce expression of cytochrome P4501A (CYP1A), and increase reactive oxygen species (ROS) production, effects believed to be mediated by the aryl hydrocarbon receptor (AHR). Killifish (Fundulus heteroclitus) populations in New Bedford Harbor, Massachusetts, USA (NBH) and Newark Bay, New Jersey, USA (NB) are generationally exposed to coplanar PCBs and PAHs and have developed resistance to PCB mediated induction of CYP1A. We hypothesized that fish resistant to CYP1A induction would also exhibit resistance to PCB and PAH induced ROS production and teratogenesis. Killifish embryos from two contaminated (NB, NBH) and two reference-site populations were exposed to vehicle or 3,3'4,4'5-pentachlorobiphenyl (PCB126) or 3-methylcholanthrene (3-MC) and evaluated for in ovo CYP1A activity, heart deformities, and ROS production. Both chemicals significantly increased in ovo ethoxyresorufin-O-deethylase (EROD) and ROS production in reference-site embryos. These chemicals provoked only moderate induction of in ovo EROD in NBH and NB embryos, and neither PCB126 nor 3-MC induced ROS production in these populations. Similarly, heart deformities were significantly induced by PCB126 in reference-site embryos, but had no significant effects on NB and NBH animals. These results indicate that fish resistant to CYP1A induction also exhibit decreased sensitivity to PCB126 and 3-MC-induced ROS production and teratogenesis. These findings further our understanding of toxicant resistance by demonstrating that reduced response to coplanar PCBs and PAHs extends beyond resistance to CYP1A induction to resistance to the physiological and teratogenic effects of these toxicants, responses that undoubtedly contribute to the increased survival of killifish inhabiting contaminated sites.
    MeSH term(s) Abnormalities, Drug-Induced ; Animals ; Cytochrome P-450 CYP1A1/biosynthesis ; Cytochrome P-450 CYP1A1/metabolism ; Embryo, Nonmammalian/drug effects ; Enzyme Induction/drug effects ; Female ; Fundulidae/embryology ; Heart Defects, Congenital/chemically induced ; Methylcholanthrene/toxicity ; Organic Chemicals/toxicity ; Polychlorinated Biphenyls/toxicity ; Reactive Oxygen Species/metabolism ; Receptors, Aryl Hydrocarbon/drug effects ; Water Pollutants, Chemical/toxicity
    Chemical Substances Organic Chemicals ; Reactive Oxygen Species ; Receptors, Aryl Hydrocarbon ; Water Pollutants, Chemical ; Methylcholanthrene (56-49-5) ; Polychlorinated Biphenyls (DFC2HB4I0K) ; Cytochrome P-450 CYP1A1 (EC 1.14.14.1) ; 3,4,5,3',4'-pentachlorobiphenyl (TSH69IA9XF)
    Language English
    Publishing date 2010-03
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 46234-2
    ISSN 1552-8618 ; 0730-7268
    ISSN (online) 1552-8618
    ISSN 0730-7268
    DOI 10.1002/etc.68
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Hazards of diethyl phthalate (DEP) exposure: A systematic review of animal toxicology studies

    Weaver, James A / Beverly, Brandiese E.J / Keshava, Nagalakshmi / Mudipalli, Anuradha / Arzuaga, Xabier / Cai, Christine / Hotchkiss, Andrew K / Makris, Susan L / Yost, Erin E

    Environment international. 2020 Dec., v. 145

    2020  

    Abstract: Diethyl phthalate (DEP) is widely used in many commercially available products including plastics and personal care products. DEP has generally not been found to share the antiandrogenic mode of action that is common among other types of phthalates, but ... ...

    Abstract Diethyl phthalate (DEP) is widely used in many commercially available products including plastics and personal care products. DEP has generally not been found to share the antiandrogenic mode of action that is common among other types of phthalates, but there is emerging evidence that DEP may be associated with other types of health effects.To inform chemical risk assessment, we performed a systematic review to identify and characterize outcomes within six broad hazard categories (male reproductive, female reproductive, developmental, liver, kidney, and cancer) following exposure of nonhuman mammalian animals to DEP or its primary metabolite, monoethyl phthalate (MEP).A literature search was conducted in online scientific databases (PubMed, Web of Science, Toxline, Toxcenter) and Toxic Substances Control Act Submissions, augmented by review of online regulatory sources as well as forward and backward searches. Studies were selected for inclusion using PECO (Population, Exposure, Comparator, Outcome) criteria. Studies were evaluated using criteria defined a priori for reporting quality, risk of bias, and sensitivity using a domain-based approach. Evidence was synthesized by outcome and life stage of exposure, and strength of evidence was summarized into categories of robust, moderate, slight, indeterminate, or compelling evidence of no effect, using a structured framework.Thirty-four experimental studies in animals were included in this analysis. Although no effects on androgen-dependent male reproductive development were observed following gestational exposure to DEP, there was evidence including effects on sperm following peripubertal and adult exposures, and the overall evidence for male reproductive effects was considered moderate. There was moderate evidence that DEP exposure can lead to developmental effects, with the major effect being reduced postnatal growth following gestational or early postnatal exposure; this generally occurred at doses associated with maternal effects, consistent with the observation that DEP is not a potent developmental toxicant. The evidence for liver effects was considered moderate based on consistent changes in relative liver weight at higher dose levels; histopathological and biochemical changes indicative of hepatic effects were also observed, but primarily in studies that had significant concerns for risk of bias and sensitivity. The evidence for female reproductive effects was considered slight based on few reports of statistically significant effects on maternal body weight gain, organ weight changes, and pregnancy outcomes. Evidence for cancer and effects on kidney were judged to be indeterminate based on limited evidence (i.e., a single two-year cancer bioassay) and inconsistent findings, respectively.These results suggest that DEP exposure may induce androgen-independent male reproductive toxicity (i.e., sperm effects) as well as developmental toxicity and hepatic effects, with some evidence of female reproductive toxicity. More research is warranted to fully evaluate these outcomes and strengthen confidence in this database.
    Keywords adults ; bioassays ; body weight changes ; chemical risk assessment ; databases ; developmental toxicity ; diethyl phthalate ; environment ; females ; histopathology ; kidneys ; liver ; males ; mammals ; maternal exposure ; mechanism of action ; metabolites ; reproductive toxicology ; risk ; spermatozoa ; systematic review ; tissue weight
    Language English
    Dates of publication 2020-12
    Publishing place Elsevier Ltd
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 554791-x
    ISSN 1873-6750 ; 0160-4120
    ISSN (online) 1873-6750
    ISSN 0160-4120
    DOI 10.1016/j.envint.2020.105848
    Database NAL-Catalogue (AGRICOLA)

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  8. Article ; Online: Erratum: "Systematic Evidence Map for over One Hundred and Fifty Per- and Polyfluoroalkyl Substances (PFAS)".

    Carlson, Laura M / Angrish, Michelle / Shirke, Avanti V / Radke, Elizabeth G / Schulz, Brittany / Kraft, Andrew / Judson, Richard / Patlewicz, Grace / Blain, Robyn / Lin, Cynthia / Vetter, Nicole / Lemeris, Courtney / Hartman, Pamela / Hubbard, Heidi / Arzuaga, Xabier / Davis, Allen / Dishaw, Laura V / Druwe, Ingrid L / Hollinger, Hillary /
    Jones, Ryan / Kaiser, J Phillip / Lizarraga, Lucina / Noyes, Pamela D / Taylor, Michele / Shapiro, Andrew J / Williams, Antony J / Thayer, Kristina A

    Environmental health perspectives

    2024  Volume 132, Issue 1, Page(s) 19001

    Language English
    Publishing date 2024-01-10
    Publishing country United States
    Document type Journal Article ; Published Erratum
    ZDB-ID 195189-0
    ISSN 1552-9924 ; 0091-6765 ; 1078-0475
    ISSN (online) 1552-9924
    ISSN 0091-6765 ; 1078-0475
    DOI 10.1289/EHP14191
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Key Characteristics of Human Hepatotoxicants as a Basis for Identification and Characterization of the Causes of Liver Toxicity.

    Rusyn, Ivan / Arzuaga, Xabier / Cattley, Russell C / Corton, J Christopher / Ferguson, Stephen S / Godoy, Patricio / Guyton, Kathryn Z / Kaplowitz, Neil / Khetani, Salman R / Roberts, Ruth A / Roth, Robert A / Smith, Martyn T

    Hepatology (Baltimore, Md.)

    2021  Volume 74, Issue 6, Page(s) 3486–3496

    Abstract: Hazard identification regarding adverse effects on the liver is a critical step in safety evaluations of drugs and other chemicals. Current testing paradigms for hepatotoxicity rely heavily on preclinical studies in animals and human data (epidemiology ... ...

    Abstract Hazard identification regarding adverse effects on the liver is a critical step in safety evaluations of drugs and other chemicals. Current testing paradigms for hepatotoxicity rely heavily on preclinical studies in animals and human data (epidemiology and clinical trials). Mechanistic understanding of the molecular and cellular pathways that may cause or exacerbate hepatotoxicity is well advanced and holds promise for identification of hepatotoxicants. One of the challenges in translating mechanistic evidence into robust decisions about potential hepatotoxicity is the lack of a systematic approach to integrate these data to help identify liver toxicity hazards. Recently, marked improvements were achieved in the practice of hazard identification of carcinogens, female and male reproductive toxicants, and endocrine disrupting chemicals using the key characteristics approach. Here, we describe the methods by which key characteristics of human hepatotoxicants were identified and provide examples for how they could be used to systematically identify, organize, and use mechanistic data when identifying hepatotoxicants.
    MeSH term(s) Animals ; Chemical and Drug Induced Liver Injury/diagnosis ; Chemical and Drug Induced Liver Injury/pathology ; Humans ; Liver/drug effects ; Liver/pathology
    Language English
    Publishing date 2021-07-13
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 604603-4
    ISSN 1527-3350 ; 0270-9139
    ISSN (online) 1527-3350
    ISSN 0270-9139
    DOI 10.1002/hep.31999
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A systematic evidence map for the evaluation of noncancer health effects and exposures to polychlorinated biphenyl mixtures

    Carlson, Laura M. / Christensen, Krista / Sagiv, Sharon K. / Rajan, Pradeep / Klocke, Carolyn R. / Lein, Pamela J. / Coffman, Evan / Shaffer, Rachel M. / Yost, Erin E. / Arzuaga, Xabier / Factor-Litvak, Pam / Sergeev, A. P. / Toborek, Michal / Bloom, Michael S. / Trgovcich, Joanne / Jusko, Todd A. / Robertson, Larry / Meeker, John D. / Keating, Aileen F. /
    Blain, Robyn / Silva, Raquel A. / Snow, Samantha / Lin, Cynthia / Shipkowski, Kelly / Ingle, Brandall / Lehmann, Geniece M.

    Environmental Research. 2023 Mar., v. 220 p.115148-

    2023  

    Abstract: Assessing health outcomes associated with exposure to polychlorinated biphenyls (PCBs) is important given their persistent and ubiquitous nature. PCBs are classified as a Group 1 carcinogen, but the full range of potential noncancer health effects from ... ...

    Abstract Assessing health outcomes associated with exposure to polychlorinated biphenyls (PCBs) is important given their persistent and ubiquitous nature. PCBs are classified as a Group 1 carcinogen, but the full range of potential noncancer health effects from exposure to PCBs has not been systematically summarized and evaluated. We used systematic review methods to identify and screen the literature using combined manual review and machine learning approaches. A protocol was developed that describes the literature search strategy and Populations, Exposures, Comparators, and Outcomes (PECO) criteria used to facilitate subsequent screening and categorization of literature into a systematic evidence map of PCB exposure and noncancer health endpoints across 15 organs/systems. A comprehensive literature search yielded 62,599 records. After electronic prioritization steps, 17,037 studies were manually screened at the title and abstract level. An additional 900 studies identified by experts or supplemental searches were also included. After full-text screening of 3889 references, 1586 studies met the PECO criteria. Relevant study details such as the endpoints assessed, exposure duration, and species were extracted into literature summary tables. This review compiles and organizes the human and mammalian studies from these tables into an evidence map for noncancer health endpoints and PCB mixture exposure to identify areas of robust research as well as areas of uncertainty that would benefit from future investigation. Summary data are available online as interactive visuals with downloadable metadata. Sufficient research is available to inform PCB hazard assessments for most organs/systems, but the amount of data to inform associations with specific endpoints differs. Furthermore, despite many years of research, sparse data exist for inhalation and dermal exposures, which are highly relevant human exposure routes. This evidence map provides a foundation for future systematic reviews and noncancer hazard assessments of PCB mixtures and for strategic planning of research to inform areas of greater uncertainty.
    Keywords carcinogens ; exposure duration ; humans ; metadata ; polychlorinated biphenyls ; prioritization ; research ; systematic review ; uncertainty ; Evidence map ; Polychlorinated biphenyl ; Risk assessment ; Hazard identification ; PCB ; SR ; SEM ; HHRA
    Language English
    Dates of publication 2023-03
    Publishing place Elsevier Inc.
    Document type Article ; Online
    Note Use and reproduction
    ZDB-ID 205699-9
    ISSN 1096-0953 ; 0013-9351
    ISSN (online) 1096-0953
    ISSN 0013-9351
    DOI 10.1016/j.envres.2022.115148
    Database NAL-Catalogue (AGRICOLA)

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