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4795 citation(s) found for "Yu, Jennifer".

Genetic Variants That Confer Resistance to Malaria Are Associated with Red Blood Cell Traits in African-Americans: An Electronic Medical Record-based Genome-Wide Association Study
Ding, Keyue , Manolio, Teri A. , Crawford, Dana C. , Rasmussen‐Torvik, Laura J. , Ritchie, Marylyn D. , Denny, Joshua C. , Masys, Daniel R., Jouni, Hayan, Pachecho, Jennifer A, Roden, Dan M. , Chisholm, Rex L. , Andrade, Mariza de , Kho, Abel , Roden, Dan M. , Kullo, Iftikhar J. , Denny, Joshua C , Rasmussen-Torvik, Laura J

G3 Genes|Genomes|Genetics | May 29, 2013 | Volume: 3 | Issue: 7 | Pages: 1061-1068

10.1534/g3.113.006452 | PMID 23696099 Get It

Abstract To identify novel genetic loci influencing interindividual variation in red blood cell (RBC) traits in African-Americans, we conducted a genome-wide association study (GWAS) in 2315 individuals, divided into discovery (n = 1904) and replication (n = 411) cohorts. The traits included hemoglobin concentration (HGB), hematocrit (HCT), RBC count, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC). Patients were participants in the electronic MEdical Records and GEnomics (eMERGE) network and underwent genotyping of ~1.2 million single-nucleotide polymorphisms on the Illumina Human1M-Duo array. Association analyses were performed adjusting for age, sex, site, and population stratification. Three loci previously associated with resistance to malaria—HBB (11p15.4), HBA1/HBA2 (16p13.3), and G6PD (Xq28)—were associated (P ≤ 1 × 10−6) with RBC traits in the discovery cohort. The loci replicated in the replication cohort (P ≤ 0.02), and were significant at a genome-wide significance level (P < 5 × 10−8) in the combined cohort. The proportions of variance in RBC traits explained by significant variants at these loci were as follows: rs7120391 (near HBB) 1.3% of MCHC, rs9924561 (near HBA1/A2) 5.5% of MCV, 6.9% of MCH and 2.9% of MCHC, and rs1050828 (in G6PD) 2.4% of RBC count, 2.9% of MCV, and 1.4% of MCH, respectively. We were not able to replicate loci identified by a previous GWAS of RBC traits in a European ancestry cohort of similar sample size, suggesting that the genetic architecture of RBC traits differs by race. In conclusion, genetic variants that confer resistance to malaria are associated with RBC traits in African-Americans.
TROY (TNFRSF19) Promotes Glioblastoma Survival Signaling and Therapeutic Resistance
Loftus, Joseph C. , Tuncali, Serdar, Kloss, Jean , Schumacher, Cassie, Cao, Brian, Williams, Bart O. , Eschbacher, Jennifer , Ross, Julianna T.D., Tran, Nhan L. , Dhruv, Harshil , Yang, Zhongbo , Tran, Nhan L

Molecular Cancer Research | May 23, 2013 | Volume: 11 | Issue: 8 | Pages: 865-874

10.1158/1541-7786.mcr-13-0008 | PMID 23699535 Get It

Abstract Of the features that characterize glioblastoma, arguably none is more clinically relevant than the propensity of malignant glioma cells to aggressively invade into the surrounding normal brain tissue. These invasive cells render complete resection impossible, confer significant resistance to chemo- and radiation-therapy, and virtually assure tumor recurrence. Expression of TROY (TNFRSF19), a member of the TNF receptor superfamily, inversely correlates with patient survival and stimulates glioblastoma cell migration and invasion in vitro. In this study, we report that TROY is overexpressed in glioblastoma tumor specimens and TROY mRNA expression is increased in the invasive cell population in vivo. In addition, inappropriate expression of TROY in mouse astrocytes in vivo using glial-specific gene transfer in transgenic mice induces astrocyte migration within the brain, validating the importance of the TROY signaling cascade in glioblastoma cell migration and invasion. Knockdown of TROY expression in primary glioblastoma xenografts significantly prolonged survival in vivo. Moreover, TROY expression significantly increased resistance of glioblastoma cells to both IR- and TMZ-induced apoptosis via activation of Akt and NF-κB. Inhibition of either Akt or NF-κB activity suppressed the survival benefits of TROY signaling in response to TMZ treatment. These findings position aberrant expression and/or signaling by TROY as a contributor to the dispersion of glioblastoma cells and therapeutic resistance. Implications: Targeting of TROY may increase tumor vulnerability and improve therapeutic response in glioblastoma. Mol Cancer Res; 11(8); 865–74. ©2013 AACR.
Physical Activity Among Somali Men in Minnesota
Mohamed, Ahmed A. , Hassan, Abdullahi, Weis, Jennifer A., Sia, Irene G. , Wieland, Mark L. , Sia, Irene G

American Journal of Men's Health | May 22, 2013 | Volume: 8 | Issue: 1 | Pages: 35-44

10.1177/1557988313489132 | PMID 23697961 Get It

Immigrants and refugees arrive to the United States healthier than the general population, but this advantage declines with increasing duration of residence. One factor contributing to this decline is suboptimal physical activity, but reasons for this are poorly understood. Persons from Somalia represent the largest African refugee population to the United States, yet little is known about perceptions of physical activity among Somali men. Somali members of a community-based participatory research partnership implemented three age-stratified focus groups and three semistructured interviews among 20 Somali men in Rochester, Minnesota. Team-based inductive analysis generated themes for barriers and facilitators to physical activity. Barriers to physical activity included less walking opportunities in the United States, embarrassment about exercise clothing and lack of familiarity with exercise equipment/modalities, fear of harassment, competing priorities, facility costs, transportation, and winter weather. Facilitators to physical activity included high knowledge about how to be active, success stories from others in their community as inspiration, and community cohesion. Findings may be used to derive interventions aimed to promote physical activity among Somali men in the United States.
Cognitive outcomes of patients undergoing therapeutic hypothermia after cardiac arrest
Fugate, Jennifer E. , Moore, Samuel A., White, Roger D., Knopman, David S. , Claassen, Daniel O. , Wijdicks, Eelco F. M. , Rabinstein, Alejandro A.

Neurology | May 18, 2013 | Volume: 81 | Issue: 1 | Pages: 40-45

10.1212/wnl.0b013e318297ee7e | PMID 23685933 Get It

Hb Grove City [β38(C4)Thr→Ser, A C C>A G C; HBB : c.116C>G]: A New Low Oxygen Affinity β Chain Variant
Taliercio, Rachel M., Ashton, Rendell W. , Horwitz, Leonard, Swanson, Kenneth C., Wendt, Patricia, Hoyer, James D., Oliveira, Jennifer L. , Herrick, Jennifer L.

Hemoglobin | May 7, 2013 | Volume: 37 | Issue: 4 | Pages: 396-403

10.3109/03630269.2013.789794 | PMID 23651408 Get It

Causal attributions and attitudes toward lung cancer
Hamann, Heidi , Howell, Lisa , McDonald, Jennifer

Journal of Applied Social Psychology | May 3, 2013 | Volume: 43 | Issue: S1 | Pages: No page available

10.1111/jasp.12053 Get It

AbstractThis study investigated causal attributions and attitudes toward a hypothetical lung cancer patient. Participants included 147 undergraduate students who read 1 of 3 vignettes about a man recently diagnosed with lung cancer. The vignettes were identical except for the causal description of the patient's lung cancer (genetic, smoking, or combined). Compared with the other 2 conditions, participants in the genetic condition believed the hypothetical patient had less control and less responsibility for his illness; they also noted more pity and less anger. There were no significant differences in these variables between the smoking and combined conditions. Information about genetic information appears to trigger more positive perceptions of lung cancer patients, but only in the absence of smoking histories.
Improving the accuracy of pancreatobiliary tract cytology with fluorescence in situ hybridization
Kipp, Benjamin R. , Pettengill, Jennifer, Halling, Kevin C. , Clayton, Amy C., Fritcher, Emily G. Barr

Cancer Cytopathology | April 30, 2013 | Volume: 121 | Issue: 11 | Pages: 610-619

10.1002/cncy.21303 | PMID 23633236 Get It

The detection of aneuploidy by fluorescence in situ hybridization (FISH) has revolutionized how laboratories diagnose cholangiocarcinoma and pancreatic adenocarcinoma using cytology specimens. Numerous clinical studies have demonstrated that FISH increases the diagnostic sensitivity of routine cytology for detecting pancreatobiliary tract malignancy with minimal decreases in clinical specificity. FISH also provides useful information in difficult clinical scenarios, including the assessment of patients with biliary strictures who have equivocal cytology results and the assessment of patients with primary sclerosing cholangitis who have clinical features suggestive of malignancy. The improved ability to detect pancreatobiliary tract cancers offers the possibility of earlier detection when patients are amenable to surgical intervention and can decrease health care costs by reducing the amount of clinical evaluation required to arrive at a cancer diagnosis. Cytopathology personnel should maintain familiarity with molecular cytology testing methodologies, because morphologic and aneuploidy assessment of tumors will continue to be an integral part of large‐scale genome analyses of individual tumors. Cancer (Cancer Cytopathol) 2013;121:610‐9. © 2013 American Cancer Society.
Training Mid-level Providers on Palliative Care
Lesperance, Mary, Shannon, Robert P. , Pumphrey, Phyllis K., Dunbar, Erin, Genther, Renee, Coleman, C. Lynn, Tabano, Margaret, Maurer, Jennifer, Vazquez, Adrienne Marie, Capp, Elizabeth, McMillan, Jessica , Wilkerson, Katie, Robbins, Gerald, Phillips, Dorothy Green, Howick, Priscilla H., Solaun, Catherine, Sloan, Jeff A. , Colón‐Otero, Gerardo

American Journal of Hospice and Palliative Medicine® | April 24, 2013 | Volume: 31 | Issue: 3 | Pages: 237-243

10.1177/1049909113486335 | PMID 23616274 Get It

Palliative care services are not available in most outpatient oncology practices. A program training 11 mid-level providers from oncology practices on advanced directive discussions and supportive symptom assessment and management performed by palliative care specialists was completed. A follow-up session 9 months later identified barriers to implementation. Of the 11 mid-level providers, 8 participated in the follow-up session, and 9 of the 11 providers implemented advanced directive’s discussions and symptom assessment and management for patients with metastatic cancer. Main barriers included uncertainties about reimbursement, patients’ lack of knowledge about palliative care, and lack of access to supportive services. This program successfully promoted advanced directive discussions and supportive/palliative care symptom assessment and management to community oncology practices, which will hopefully translate into improved quality of life for patients with metastatic cancer.
Can New-Onset Diabetes After Kidney Transplant Be Prevented?
Chakkera, Harini A. , Weil, E. Jennifer , Pham, Phuong-Thu, Pomeroy, Jeremy , Knowler, William C. , Pham, Phuong‐Thu T., Chakkera, Harini A

Diabetes Care | April 23, 2013 | Volume: 36 | Issue: 5 | Pages: 1406-1412

10.2337/dc12-2067 | PMID 23613600 Get It

Because the negative consequences of new-onset diabetes mellitus after transplantation (NODAT) diminish the significant gains of kidney transplantation, it is imperative to develop clinical interventions to reduce the incidence of NODAT. In this review, we discuss whether intensive lifestyle interventions that delay or prevent type 2 diabetes mellitus may decrease the incidence of NODAT. We examine the literature pertaining to incidence and timing of onset of NODAT, as well as the risk factors and pathophysiology that NODAT shares with type 2 diabetes mellitus, namely pathways related to increased insulin resistance and decreased insulin secretion. Our central hypothesis is that NODAT results from the same metabolic risk factors that underlie type 2 diabetes mellitus. These risk factors are altered and enhanced by transplantation, “tipping” some transplant recipients with seemingly normal glucose homeostasis before transplant toward the development of NODAT. We describe the diabetogenic properties of transplant immunosuppressive drugs. We describe novel methods of prevention that are being explored, including resting the pancreatic β-cells by administration of basal insulin during the period immediately after transplant. On the basis of the current evidence, we propose that intensive lifestyle modification, adapted for individuals with chronic kidney disease or end-stage renal disease, as well as resting pancreatic β-cells during the immediate postoperative period, may lower the incidence of NODAT.
Rescue Treatment of Thromboembolic Complications During Endovascular Treatment of Cerebral Aneurysms
Brinjikji, Waleed , Kallmes, David F. , Cloft, Harry J. , McDonald, Jennifer S.

Stroke | April 19, 2013 | Volume: 44 | Issue: 5 | Pages: 1343-1347

10.1161/strokeaha.111.000628 | PMID 23598522 Get It

Background and Purpose— Acute intraprocedural thrombus formation complicating endovascular cerebral aneurysm treatment is often treated with intra-arterial or intravenous administration of thrombolytic agents or glycoprotein IIb/IIIa (GpIIb/IIIa) inhibitors. We sought to evaluate the morbidity and mortality associated with such treatments using a large multihospital database. Methods— Using the Premier Perspective Database, we examined outcomes for patients receiving endovascular coiling for ruptured and unruptured aneurysms requiring rescue therapy, defined as treatment with GpIIb/IIIa inhibitors and fibrinolytic therapy. We compared discharge status, length of stay, and complication rates across 3 groups: (1) patients receiving GpIIb/IIIa inhibitors only, (2) patients receiving fibrinolytic therapy only, and (3) patients receiving both GpIIb/IIIa inhibitors and fibrinolytics. Student t test was used to compare continuous variables, and Fisher exact test was used to compare categorical variables. Results— Seven-percent (254/3627) of patients treated for unruptured aneurysms received rescue therapy. When compared with patients receiving GpIIb/IIIa inhibitors alone, patients receiving only fibrinolytics had significantly higher rates of discharge to institutions other than home (37.5% [9/24] versus 7.4% [15/201]; P <0.0001). Eight-percent of patients (338/4204) treated for ruptured aneurysms received rescue therapy. When compared with patients receiving GpIIb/IIIa inhibitors alone, patients receiving only fibrinolytics had significantly higher rates of mortality (26.0% [18/69] versus 14.5% [35/241]; P =0.02) and discharge to institutions other than home (59.4% [41/69] versus 36.5% [88/241]; P <0.0001). Conclusions— Pharmacological rescue therapy occurred in 7% to 8% of endovascular coiling patients with unruptured and ruptured intracranial aneurysms. Rescue therapy with thrombolytic agents resulted in significantly more morbidity and mortality than rescue therapy with GpIIb/IIIa inhibitors.