Environmental health research, whether involving experiments at the cellular level, investigations using laboratory animals, or studies of human populations, is becoming increasingly complex. There are several reasons for this added complexity. The valid quantification of human exposures to environmental hazards requires consideration of complicated time-dependent individual-specific multiple exposure profiles. Assessment of early biologic effects (e.g., biomarkers) requires elucidation of how these exposure profiles relate to multiple, intermediate, and often correlated endpoints. Assessment of exposure-disease relationships requires knowledge of the connections between exposure, early biological effects, and multiple correlated health outcomes. The further necessity of simultaneously considering the impact of gene-environment interactions and molecular-level mechanisms argues strongly for the use of innovative, well-designed, and appropriately analyzed environmental health research studies to insure the validity and precision of scientific conclusions. Such validity and precision requirements mandate that biostatisticians and bioinformaticians be involved as active research collaborators from the planning stages of environmental health studies through final analyses and dissemination of research conclusions via presentations and publications. Without state-of-the-art input from biostatisticians on study design and data analysis, there is no question that environmental health research studies can be severely biased and can suffer from a lack of sufficient precision to detect important exposure-response relationships. The Biostatistics and Bioinformatics Facility Core (BBFC) provides the CEHS with the needed expertise to apply state-of-the-art statistical methods to the design and analysis of all types of environmental health research studies, ranging from laboratory study design, analysis of multidimensional gene by environment interactions, and quantification of complex time-dependent exposures. BBFC personnel have expertise in essentially all state-of-the-art statistical methods required to address the most complex of study design and data analysis issues. It is fair to say that the CEHS cannot function effectively without making continued use of the BBFC, from study planning through data analysis and interpretation. It is an efficient and cost-effective allocation of resources to assign these important statistical design and data analysis activities to the BBFC. In the sections to follow, detailed descriptions of BBFC (formerly the Biostatitics and Epidemiological Methods Facility Core, or BEMFC) activities since April 2006 will be given. In particular, important functional changes will be highlighted, BBFC members and their unique expertise will be detailed, involvements of BBFC members in CEHS pilot and research projects will be described, and BBFC enrichment activities will be mentioned.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES010126-12
Application #
8376570
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2012-04-01
Budget End
2013-03-31
Support Year
12
Fiscal Year
2012
Total Cost
$126,255
Indirect Cost
$40,948
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
van Bömmel, Alena; Love, Michael I; Chung, Ho-Ryun et al. (2018) coTRaCTE predicts co-occurring transcription factors within cell-type specific enhancers. PLoS Comput Biol 14:e1006372
McNeill, Robert S; Stroobant, Emily E; Smithberger, Erin et al. (2018) PIK3CA missense mutations promote glioblastoma pathogenesis, but do not enhance targeted PI3K inhibition. PLoS One 13:e0200014
Daniels, Julie L (2018) Considerations for Studying Folate Beyond the Typical Range of Exposure. Paediatr Perinat Epidemiol 32:112-113
Reidel, Boris; Radicioni, Giorgia; Clapp, Phillip W et al. (2018) E-Cigarette Use Causes a Unique Innate Immune Response in the Lung, Involving Increased Neutrophilic Activation and Altered Mucin Secretion. Am J Respir Crit Care Med 197:492-501
Tennyson, Robert L; Gettler, Lee T; Kuzawa, Christopher W et al. (2018) Lifetime socioeconomic status and early life microbial environments predict adult blood telomere length in the Philippines. Am J Hum Biol 30:e23145
Thomas, Nancy E; Edmiston, Sharon N; Orlow, Irene et al. (2018) Inherited Genetic Variants Associated with Melanoma BRAF/NRAS Subtypes. J Invest Dermatol 138:2398-2404
Porrello, Alessandro; Leslie, Patrick L; Harrison, Emily B et al. (2018) Factor XIIIA-expressing inflammatory monocytes promote lung squamous cancer through fibrin cross-linking. Nat Commun 9:1988
Manuck, Tracy A; Smeester, Lisa; Martin, Elizabeth M et al. (2018) Epigenetic Regulation of the Nitric Oxide Pathway, 17-? Hydroxyprogesterone Caproate, and Recurrent Preterm Birth. Am J Perinatol 35:721-728
Barrington, William T; Wulfridge, Phillip; Wells, Ann E et al. (2018) Improving Metabolic Health Through Precision Dietetics in Mice. Genetics 208:399-417
Cui, Tianqu; Zeng, Zhexi; Dos Santos, Erickson O et al. (2018) Development of a hydrophilic interaction liquid chromatography (HILIC) method for the chemical characterization of water-soluble isoprene epoxydiol (IEPOX)-derived secondary organic aerosol. Environ Sci Process Impacts 20:1524-1536

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