Evidence map›Paper›PMID 42214234›Full record

ArticleEnvironment international2026

GRADE concept article: Evaluating risk of bias in a body of evidence from studies of environmental and other exposures.

Elizabeth G Radke, Suril S Mehta, Krista Y Christensen, Barbara Glenn, Andrew A Rooney, Paul Whaley, Rebecca L Morgan, Brandiese E J Beverly, Kris Thayer, Kyla W Taylor and 4 more

Abstract read
In one paragraph

Article in Environment international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Elizabeth G RadkeU.S. Environmental Protection Agency, Washington, DC, USA. Electronic address: radke-farabaugh.elizabeth@epa.gov.
Suril S MehtaDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Durham, NC, USA.
Krista Y ChristensenU.S. Environmental Protection Agency, Washington, DC, USA.
Barbara GlennU.S. Environmental Protection Agency, Washington, DC, USA.
Andrew A RooneyDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Durham, NC, USA.
Paul WhaleyLancaster Environment Centre, Lancaster University, UK; Evidence-Based Toxicology Collaboration, Johns Hopkins University, Bloomberg School of Public Health, Baltimore, MD, USA.
Rebecca L MorganDepartment of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, ON, Canada; School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Brandiese E J BeverlyDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Durham, NC, USA.
Kris ThayerOffice of Environmental Health Hazard Assessment, Sacramento, CA, USA.
Kyla W TaylorDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Durham, NC, USA.
Franca BarbicClinical Epidemiology and Research Center (CERC), Humanitas University, Milan, Italy; IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Elie A AklAmerican University of Beirut, Lebanon.
Holger J SchünemannClinical Epidemiology and Research Center (CERC), Humanitas University, Milan, Italy; Allergology and Immunology, Charité, Universitätsmedizin-Berlin, Germany.
GRADE Working Group

Funding

Intramural EPA EPA999999
6 · The paper itself

Abstract

introductionEvaluating the impact of bias in observational epidemiology studies is critical to systematic reviews in public health (as is the case with any study type). However, researchers have expressed concern that useful epidemiological data may not receive full consideration in some reviews due to overemphasizing potential for bias without critical assessment of its impact. This concern should be balanced against the need to appropriately assess the degree of bias in observational studies to accurately characterize their validity and reach appropriate conclusions.

objectiveIn this paper, we describe how examining bias across studies may alleviate or solidify concerns identified in individual studies. We describe how to assess the likelihood that specific sources of bias explain and/or meaningfully distort an observed association.

methodsWe followed the methods for development of Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) workgroup guidance. Various sensitivity analyses are proposed to probe risk of bias in the body of evidence. Two illustrative case studies were conducted: the associations between trichloroethylene (TCE) exposure and kidney cancer occurrence and between two individual per-and polyfluoroalkyl substances (PFAS) and changes of alanine aminotransferase (ALT) levels.

resultsSensitivity analyses can inform the potential for bias to influence the results of a body of evidence, including consideration of direction of bias, subsets/stratification, counterbalancing biases, use of positive/negative controls, and others. To incorporate these into a synthesis, consideration is needed throughout the planning and execution process: (1) Planning the systematic review; (2) Assessing risk of bias in individual studies; (3) Performing sensitivity analyses, including exploration of heterogeneity and bias impact; and (4) Determining final rating. DISCUSSION: These nuanced concepts and approaches for more accurately characterizing the magnitude and impact of bias in a body of evidence can be applied within GRADE and more broadly to systematic reviews outside that framework.

Indexed as

Environmental ExposureBiasHumansTrichloroethyleneTrichloroethylene

Identifiers

PMID42214234
PMCPMC13501407

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.