This Program Project Grant (PPG) is designed to explore the causal pathway from pet exposure to bacteria in the home and infant gastrointestinal tract, to immune development, to pediatric allergic asthma. The Biostatistics and Data Management Core (Core B) is critical to support the development and conduct of the four Projects in this PPG. Specifically, this Core will ensure the timely and accurate acquisition of data and its dispersion to the various Projects. The Core will provide a centralized database comprised of data collected for all Projects and Cores. A centralized database is an advantage when dealing with multiple sites, assuring the accurate linkage and confidentiality of all data types, along with ease of reporting on study progress. In addition, automated reports will be generated to enable the strict and regular monitoring of data activities by the PPG investigators. All data will undergo rigorous and regular data quality review. Further, secure and automated data transfer protocols will be developed and disseminated when necessary and where needed. This Core will also provide the resources to provide all investigators with data analyses needed to address their Specific Aims. The biostatistical expertise will ensure that all four Projects are efficiently and rigorously designed, conducted, monitored, and analyzed. The biostatisticians have a long history of collaboration with each other and with the investigators, resulting in funded grants and numerous publications. The Core will provide statistical methodological development and expertise to provide up-to-date statistical methods to design and analyze the various studies in the PPG. Biostatisticians will work regularly and directly with all investigators in the preparation of manuscripts and abstracts, ensuring rigorous analysis and interpretation of study data.
Allergic diseases are a massive public health burden. This project will study the role of pet exposure, bacterial exposures and risk of allergy and atopic asthma. This Core will support the conduct of the proposed investigations and maintain a centralized, secure database, as well as provide statistical analyses of the data to support the conclusions of the studies.
|Cassidy-Bushrow, Andrea E; Wegienka, Ganesa; Havstad, Suzanne et al. (2016) Race-specific Association of Caesarean-Section Delivery with Body Size at Age 2 Years. Ethn Dis 26:61-8|
|Cassidy-Bushrow, Andrea E; Havstad, Suzanne; Basu, Niladri et al. (2016) Detectable Blood Lead Level and Body Size in Early Childhood. Biol Trace Elem Res 171:41-7|
|Mar, Jordan S; LaMere, Brandon J; Lin, Din L et al. (2016) Disease Severity and Immune Activity Relate to Distinct Interkingdom Gut Microbiome States in Ethnically Distinct Ulcerative Colitis Patients. MBio 7:|
|Johnson, Christine C; Ownby, Dennis R (2016) Allergies and Asthma: Do Atopic Disorders Result from Inadequate Immune Homeostasis arising from Infant Gut Dysbiosis? Expert Rev Clin Immunol 12:379-88|
|Ownby, Dennis; Johnson, Christine Cole (2016) Recent Understandings of Pet Allergies. F1000Res 5:|
|Cassidy-Bushrow, A E; Sitarik, A; Levin, A M et al. (2016) Maternal group B Streptococcus and the infant gut microbiota. J Dev Orig Health Dis 7:45-53|
|Levin, Albert M; Sitarik, Alexandra R; Havstad, Suzanne L et al. (2016) Joint effects of pregnancy, sociocultural, and environmental factors on early life gut microbiome structure and diversity. Sci Rep 6:31775|
|Lynch, Susan V; Boushey, Homer A (2016) The microbiome and development of allergic disease. Curr Opin Allergy Clin Immunol 16:165-71|
|Joseph, Christine L M; Zoratti, Edward M; Ownby, Dennis R et al. (2016) Exploring racial differences in IgE-mediated food allergy in the WHEALS birth cohort. Ann Allergy Asthma Immunol 116:219-224.e1|
|Fujimura, Kei E; Sitarik, Alexandra R; Havstad, Suzanne et al. (2016) Neonatal gut microbiota associates with childhood multisensitized atopy and T cell differentiation. Nat Med 22:1187-1191|
Showing the most recent 10 out of 34 publications