During the previous three cycles of the program project which this application is seeking to renew, we have consolidated strong links with the projects which have led to several publications. As part of the renewal of the program project, we will continue to collaborate with investigators of projects in the program for (i) the design of studies using specimens collected as part of ongoing cohort studies and new trials proposed in the application, (ii) the analysis of data, and (iii) the development of data analytical methods relevant to the scientific aims of the research projects. The design and analysis of the experiments and studies to be conducted under the auspices of the program project will benefit by the inclusion of expertise in biostatistics and epidemiology.
The specific aims of the Biostatistics/Epidemiology Core (BEC) are: 1) To establish methods that promote adherence to standard protocols with particular attention to data collection and management;2) To collaborate with investigators in the projects of the program for the purpose of designing studies and analyzing data. Data from the projects will require nesting case-control studies in the complex cohort studies and the implementation of multivariate (e.g., presence of hepatitis B virus mutations in nucleotides 1762/1764, serum concentrations of the aflatoxin-specific p53 codon 249 mutation, biomarkers for aflatoxins, alkylanilines and polycyclic aromatic hydrocarbons, and treatment arms in a clinical trial) regression methods for the analyses of longitudinal binary and continuous outcome data. Furthermore, we will use methods for the evaluation of treatments administered in clinical trials using changes of biomarkers possibly following a mixture distribution (discrete component due to biomarker being equal to zero in a subgroup and a continuous component for the complement) as the primary outcome measure;3) To develop new statistical methods appropriate for the data generated by the projects of the proposed program. Investigators of the BEC will continue to provide direction on data management, data analysis and methodological research. We have had strong collaborations in the previous cycles of the program project and we will continue to advance the methods for data analysis to characterize how environmental exposures are associated with biomarkers that measure exposure and disease risk and whether interventions can modify such associations to reduce disease in populations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Program Projects (P01)
Project #
5P01ES006052-17
Application #
8078954
Study Section
Special Emphasis Panel (ZES1)
Project Start
Project End
Budget Start
2010-06-01
Budget End
2011-05-31
Support Year
17
Fiscal Year
2010
Total Cost
$105,988
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Chen, Taoyang; Qian, Gengsun; Fan, Chunsun et al. (2018) Qidong hepatitis B virus infection cohort: a 25-year prospective study in high risk area of primary liver cancer. Hepatoma Res 4:
Watson, Sinead; Chen, Gaoyun; Sylla, Abdoulaye et al. (2016) Dietary exposure to aflatoxin and micronutrient status among young children from Guinea. Mol Nutr Food Res 60:511-8
Ravindra, Kodihalli C; Trudel, Laura J; Wishnok, John S et al. (2016) Hydroxyphenylation of Histone Lysines: Post-translational Modification by Quinone Imines. ACS Chem Biol 11:1230-7
Yang, Li; Palliyaguru, Dushani L; Kensler, Thomas W (2016) Frugal chemoprevention: targeting Nrf2 with foods rich in sulforaphane. Semin Oncol 43:146-153
Chao, Ming-Wei; Erkekoglu, P?nar; Tseng, Chia-Yi et al. (2015) Protective effects of ascorbic acid against the genetic and epigenetic alterations induced by 3,5-dimethylaminophenol in AA8 cells. J Appl Toxicol 35:466-77
Techapiesancharoenkij, Nirachara; Fiala, Jeannette L A; Navasumrit, Panida et al. (2015) Sulforaphane, a cancer chemopreventive agent, induces pathways associated with membrane biosynthesis in response to tissue damage by aflatoxin B1. Toxicol Appl Pharmacol 282:52-60
Shirima, Candida P; Kimanya, Martin E; Routledge, Michael N et al. (2015) A prospective study of growth and biomarkers of exposure to aflatoxin and fumonisin during early childhood in Tanzania. Environ Health Perspect 123:173-8
Hernandez-Vargas, Hector; Castelino, Jovita; Silver, Matt J et al. (2015) Exposure to aflatoxin B1 in utero is associated with DNA methylation in white blood cells of infants in The Gambia. Int J Epidemiol 44:1238-48
Chawanthayatham, Supawadee; Thiantanawat, Apinya; Egner, Patricia A et al. (2015) Prenatal exposure of mice to the human liver carcinogen aflatoxin B1 reveals a critical window of susceptibility to genetic change. Int J Cancer 136:1254-62
Castelino, Jovita M; Routledge, Michael N; Wilson, Shona et al. (2015) Aflatoxin exposure is inversely associated with IGF1 and IGFBP3 levels in vitro and in Kenyan schoolchildren. Mol Nutr Food Res 59:574-81

Showing the most recent 10 out of 234 publications