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Featured researches published by Brian N. Griffith.


BMC Public Health | 2011

Self-rated health in rural Appalachia: health perceptions are incongruent with health status and health behaviors

Brian N. Griffith; Gretchen D Lovett; Donald N Pyle; Wayne C. Miller

BackgroundAppalachia is characterized by poor health behaviors, poor health status, and health disparities. Recent interventions have not demonstrated much success in improving health status or reducing health disparities in the Appalachian region. Since ones perception of personal health precedes his or her health behaviors, the purpose of this project was to evaluate the self-rated health of Appalachian adults in relation to objective health status and current health behaviors.MethodsAppalachian adults (n = 1,576) were surveyed regarding health behaviors - soda consumer (drink ≥ 355 ml/d), or non-consumer (drink < 355 ml/d), fast food consumer (eating fast food ≥ 3 times/wk) or healthy food consumer (eating fast food < 3 times/wk), smoking (smoker or non-smoker), exercise (exerciser > 30 min > 1 d/wk) and sedentary (exercise < 30 min 1 d/wk), blood pressure medication (yes, no), and self-rated health. Blood pressure was measured through auscultation and serum cholesterol measured via needle prick. Weight status was based on BMI: normal weight (NW ≥ 18.5 and < 25.0), overweight (OW ≥ 25.0 and < 30.0), and obese (OB ≥ 30.0). Jaccard Binary Similarity coefficients, odds ratios, chi-square, and prevalence ratios were calculated to evaluate the relationships among self-rated health, objective health status, and health behaviors. Significance was set at p < 0.05.ResultsRespondents reported being healthy, while being sedentary (65%), hypertensive (76%), overweight (73%), or hyperlipidemic (79%). Between 57% and 66% of the respondents who considered themselves healthy had at least two disease conditions or poor health behaviors. Jaccard Binary Similarity coefficients and odds ratios showed the probability of reporting being healthy when having a disease condition or poor health behavior was high.ConclusionsThe association between self-rated health and poor health indicators in Appalachian adults is distorted. The public health challenge is to formulate messages and programs about health and health needs which take into account the current distortion about health in Appalachia and the cultural context in which this distortion was shaped.


Journal of Biological Chemistry | 2006

An Exonic Splicing Silencer Is Involved in the Regulated Splicing of Glucose 6-Phosphate Dehydrogenase mRNA

Wioletta Szeszel-Fedorowicz; Indrani Talukdar; Brian N. Griffith; Callee M. Walsh; Lisa M. Salati

The inhibition of glucose-6-phosphate dehydrogenase (G6PD) expression by arachidonic acid occurs by changes in the rate of pre-mRNA splicing. Here, we have identified a cis-acting RNA element required for regulated splicing of G6PD mRNA. Using transfection of G6PD RNA reporter constructs into rat hepatocytes, the cis-acting RNA element involved in this regulation was localized to nucleotides 43-72 of exon 12 in the G6PD mRNA. In in vitro splicing assays, RNA substrates containing exon 12 were not spliced. In contrast, RNA substrates containing other regions (exons 8 and 9 or exons 10 and 11) of the G6PD mRNA were efficiently spliced. Furthermore, exon 12 can inhibit splicing when substituted for other exons in RNA substrates that are readily spliced. This activity of the exon 12 regulatory element suggests that it is an exonic splicing silencer. Consistent with its activity as a splicing silencer, spliceosome assembly was inhibited on RNA substrates containing exon 12 compared with RNAs representing other regions of the G6PD transcript. Elimination of nucleotides 43-72 of exon 12 did not restore splicing of exon 12-containing RNA; thus, the 30-nucleotide element may not be exclusively a silencer. The binding of heterogeneous nuclear ribonucleoproteins K, L, and A2/B1 from both HeLa and hepatocyte nuclear extracts to the element further supports its activity as a silencer. In addition, SR proteins bind to the element, consistent with the presence of enhancer activity within this sequence. Thus, an exonic splicing silencer is involved in the inhibition of splicing of a constitutively spliced exon in the G6PD mRNA.


Biochimica et Biophysica Acta | 2013

Starvation actively inhibits splicing of glucose-6-phosphate dehydrogenase mRNA via a bifunctional ESE/ESS element bound by hnRNP K.

T.J. Cyphert; Amanda L. Suchanek; Brian N. Griffith; Lisa M. Salati

Regulated expression of glucose-6-phosphate dehydrogenase (G6PD) is due to changes in the rate of pre-mRNA splicing and not changes in its transcription. Starvation alters pre-mRNA splicing by decreasing the rate of intron removal, leading to intron retention and a decrease in the accumulation of mature mRNA. A regulatory element within exon 12 of G6PD pre-mRNA controls splicing efficiency. Starvation caused an increase in the expression of heterogeneous nuclear ribonucleoprotein (hnRNP) K protein and this increase coincided with the increase in the binding of hnRNP K to the regulatory element and a decrease in the expression of G6PD mRNA. HnRNP K bound to two C-rich motifs forming an ESS within exon 12. Overexpression of hnRNP K decreased the splicing and expression of G6PD mRNA, while siRNA-mediated depletion of hnRNP K caused an increase in the splicing and expression of G6PD mRNA. Binding of hnRNP K to the regulatory element was enhanced in vivo by starvation coinciding with a decrease in G6PD mRNA. HnRNP K binding to the C-rich motifs blocked binding of serine-arginine rich, splicing factor 3 (SRSF3), a splicing enhancer. Thus hnRNP K is a nutrient regulated splicing factor responsible for the inhibition of the splicing of G6PD during starvation.


The Journal of the American Osteopathic Association | 2013

Tobacco Dependence Curricula in US Osteopathic Medical Schools: A Follow-up Study

Brian N. Griffith; Norman J. Montalto; Lance Ridpath; Kendra Sullivan

CONTEXT Tobacco use is the leading preventable cause of illness and death in the United States. A 1998 survey of US osteopathic medical schools identified deficiencies in tobacco dependence curricula. OBJECTIVE To assess the current content and extent of tobacco dependence education and intervention skills in US osteopathic medical school curricula. DESIGN An electronic survey. SETTING Osteopathic medical schools with students enrolled for the 2009-2010 academic year. PARTICIPANTS Twenty-seven osteopathic medical school deans or their designated administrators. MAIN OUTCOME MEASURES Reported instruction in 7 basic science and 6 clinical science content areas (elective or required) and hours of tobacco dependence education were assessed and compared with the 1998 data. RESULTS The mean (standard deviation) number of content areas reported as covered in 2010 was 10.6 (2.3) (6.1 [1.2] basic science areas, 4.6 [1.3] clinical science areas). Seventeen of 27 respondents (63%) reported that smokeless tobacco content was covered at their school, and 9 of 27 (33%) reported that the stages of change counseling technique was covered. Compared with 1998, a significant increase was noted in the percentage of schools covering tobacco dependence (92.6% in 2010 compared with 57.9% in 1998, P=.0002). Reported hours of tobacco dependence instruction were also significantly higher in 2010 compared with those in 1998 (Fisher exact test, P<.05). No statistically significant changes were found in the proportion of schools covering all 13 content areas (15.7% vs 22.2%), the proportion covering motivational interviewing in detail (26.3% vs 33.3%), or the proportion requiring curricula on smokeless tobacco (57.9% vs 59.3%). CONCLUSION Osteopathic medical school respondents reported more instruction on tobacco dependence in 2010 compared with those in 1998. However, some important basic science and clinical science content areas are not being adequately taught in US osteopathic medical schools.


Life Sciences | 2007

Gossypol induces apoptosis in human PC-3 prostate cancer cells by modulating caspase-dependent and caspase-independent cell death pathways.

Manchao Zhang; Hongpeng Liu; Zhenkun Tian; Brian N. Griffith; Min Ji; Q. Quentin Li


Biochimica et Biophysica Acta | 2006

Identification of hnRNPs K, L and A2/B1 as candidate proteins involved in the nutritional regulation of mRNA splicing

Brian N. Griffith; Callee M. Walsh; Wioletta Szeszel-Fedorowicz; Aaron T. Timperman; Lisa M. Salati


Annals of Hematology | 2007

A novel Bcl-2 small molecule inhibitor 4-(3-methoxy-phenylsulfannyl)-7-nitro-benzofurazan-3-oxide (MNB)-induced apoptosis in leukemia cells.

Manchao Zhang; Yan Ling; Chao Yie Yang; Hongpeng Liu; Renxiao Wang; Xihan Wu; Ke Ding; Feng Zhu; Brian N. Griffith; Ramzi M. Mohammad; Shaomeng Wang; Dajun Yang


Protein Expression and Purification | 2004

Improved expression and characterization of Ca2+-ATPase and phospholamban in High-Five cells.

Jason R. Waggoner; Jamie Huffman; Brian N. Griffith; Larry R. Jones; James E. Mahaney


Cancer Letters | 2007

Bioinformatics-based discovery and characterization of an AKT-selective inhibitor 9-chloro-2-methylellipticinium acetate (CMEP) in breast cancer cells

Manchao Zhang; Xueliang Fang; Hongpeng Liu; Ribo Guo; Xiaojin Wu; Bihua Li; Feng Zhu; Yan Ling; Brian N. Griffith; Shaomeng Wang; Dajun Yang


International Journal of Mathematics | 2014

Misconceptions about health and disease prevention behaviors of rural Appalachian Americans

Wayne C. Miller; Brian N. Griffith; Timothy J. Bikman; Cameron Meyer

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Wayne C. Miller

George Washington University

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Lisa M. Salati

West Virginia University

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Cameron Meyer

West Virginia School of Osteopathic Medicine

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Dajun Yang

University of Michigan

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Feng Zhu

Georgetown University

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Timothy J. Bikman

West Virginia School of Osteopathic Medicine

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