The University of Texas Medical Branch (UTMB) has the required elements to actively participate as a clinical site in the Genomic and Proteomic Network for PrematureBirth Research. The PI, Radoslaw Bukowski, and the co-I, George Saade, bring extensive experience with study design, recruitment, data analysis, and publications from several NIH multisiteclinical trials (First and Second Trimester Evaluation of Risk of Aneuploidy [FASTER], StillbirthCollaborative Research Network [SCRN], Twin-Twin Transfusion Syndrome Trial [TTTS], and Beneficial Effects of AntenatalMagnesiumSulfate Study [BEAM]). We achieve successful patient recruitment/retention by partnering with our Department's broad Regional Maternal & Child Health Program (RMCHP). The RMCHP provides prenatal care to over 11,000 pregnant women a year, with over 6,000 of them delivering at the UTMB hospital in Galveston as high-risk pregnancies. All RMCHP clinics follow protocols set by the Maternal-Fetal Medicine Division.Our clinical infrastructureand population prepare us well to participate in the Network as we deliver over 500 premature pregnancies a year, 89% of then: resulting from spontaneous preterm labor and 97% receiving prenatal care in our system. The Department's Electronic Medical Record System captures antepartum and intrapartum information, entered on-line and readily available for query by authorized investigators.The Department's team of dedicated research nurses and coordinators (Chairman's Research Group) and the Tissue Bank have broadened efficiency inclinical investigations. The excellent and productivecollaborationbetween PI and Co-I offers further benefits to the Network. Jennifer Lee and Aimee Jackson, who will serve as our Research Coordinators, bringconsiderable experience as established coordinators for NIH multisitetrials. Our Department has a productive and well- funded basic science research group, with expertise in many areas of relevance to the RFA such asmolecular mechanisms of uterine contractilityand cervical ripening, animal models of preterm labor, infection, vascular physiology, placental function, and fetal growth. Finally, we have well-established collaborativeties with our University's Division of Neonatology. The PI and co-1, as well as UTMB overall, have particular interest in genomics and proteomics as applied to the uterus in labor and infection/ inflammation. Our concept protocols propose to examine networks of co-expressed genes in the uterus during preterm birth. We accept the RFA's capitation and participatory stipulations and stand ready to contribute as a member of the Network.
| Manuck, Tracy A; Esplin, M Sean; Biggio, Joseph et al. (2016) Predictors of response to 17-alpha hydroxyprogesterone caproate for prevention of recurrent spontaneous preterm birth. Am J Obstet Gynecol 214:376.e1-8 |
| Esplin, M Sean; Manuck, Tracy A; Varner, Michael W et al. (2015) Cluster analysis of spontaneous preterm birth phenotypes identifies potential associations among preterm birth mechanisms. Am J Obstet Gynecol 213:429.e1-9 |
| Manuck, Tracy A; Barbour, Kelli; Janicki, Lindsay et al. (2015) Conversion of Society for Maternal-Fetal Medicine abstract presentations to manuscript publications. Am J Obstet Gynecol 213:405.e1-6 |
| Zhang, Heping; Baldwin, Don A; Bukowski, Radek K et al. (2015) A genome-wide association study of early spontaneous preterm delivery. Genet Epidemiol 39:217-26 |
| Manuck, Tracy A; Esplin, M Sean; Biggio, Joseph et al. (2015) The phenotype of spontaneous preterm birth: application of a clinical phenotyping tool. Am J Obstet Gynecol 212:487.e1-487.e11 |
| Parry, Samuel; Zhang, Heping; Biggio, Joseph et al. (2014) Maternal serum serpin B7 is associated with early spontaneous preterm birth. Am J Obstet Gynecol 211:678.e1-12 |
