149 research outputs found

    The Grizzly, November 3, 1978

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    Task Force Proposes Curricular Revisions: Faculty Discusses Broad Academic Changes • Computer Programs To Be Studied • Reed This Message • Liberal Education for a Modern World • Letters to the Editor • Campus Committees Graded • Springsteen Revisited • Halloween Horrors! • Annual Messiah Rehearsal • French Club Wined and Dined • GM: Looking Good For \u2779 • Soccer Trounces Widener • Founders\u27 Convocation • Harriers Cap 12-1 Season • Mermaids Anticipate Slick Season • Hockey J. V.s With No Losses • Zetans Take Intramural Football Championship • News in Brief: Egdon Heath to Rock T. G.; Forum Presents Workshop, Performance; Ursinus Appoints Band Directorhttps://digitalcommons.ursinus.edu/grizzlynews/1005/thumbnail.jp

    Alterations in vascular function in primary aldosteronism - a cardiovascular magnetic resonance imaging study

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    Introduction: Excess aldosterone is associated with increased cardiovascular risk. Aldosterone has a permissive effect on vascular fibrosis. Cardiovascular magnetic resonance imaging (CMR) allows study of vascular function by measuring aortic distensibility. We compared aortic distensibility in primary aldosteronism (PA), essential hypertension (EH) and normal controls and explored the relationship between aortic distensibility and pulse wave velocity (PWV).<p></p> Methods: We studied PA (n=14) and EH (n=33) subjects and age-matched healthy controls (n=17) with CMR, including measurement of aortic distensibility, and measured PWV using applanation tonometry. At recruitment, PA and EH patients had similar blood pressure and left ventricular mass.<p></p> Results: Subjects with PA had significantly lower aortic distensibilty and higher PWV compared to EH and healthy controls. These changes were independent of other factors associated with reduced aortic distensibility, including aging. There was a significant relationship between increasing aortic stiffness and age in keeping with physical and vascular aging. As expected, aortic distensibility and PWV were closely correlated.<p></p> Conclusion: These results demonstrate that PA patients display increased arterial stiffness compared to EH, independent of vascular aging. The implication is that aldosterone invokes functional impairment of arterial function. The long-term implications of arterial stiffening in aldosterone excess require further study.<p></p&gt

    The Grizzly, November 10, 1978

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    Physical Education Program To Change • Task Force Continues Recommendations • No Funds For Bomberger • Forum: High Strung • Hockey Not Safe • Staffer Clears Misinterpretation • Dining Service Transitions • Letters to the Editor • Portrait of the Professor: Gayle A. Byerly • For Whom The Walls Toil • Egdon Heath - A New Look For Monday Night • The Good Doctor Makes House Call To Protheatre • Eighteen Named to Who\u27s Who • Free V. D. Clinic • GM: Looking Good For \u2779 • Sports Profile: Keith Kemper • Thinclads Nab Third At MAC\u27s • Soccer Kicks Moravian • Bears Blast Dickinson • Gymnastics Get New Coach • Hockey Ends • Women\u27s B-Ball Preview • News in Brief: Senior Symposium Cancelled; Deans Attend State Conventionhttps://digitalcommons.ursinus.edu/grizzlynews/1006/thumbnail.jp

    The Grizzly, October 27, 1978

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    Bomberger Tower Razed • Homecoming Brings Crowning, Presentations • Self Study Continues • Hockey Ties Nation\u27s Best • No Tickets at Door • Campus Sunshine to Set? • Ravine Paradise Revisited • Portrait of the Professor: Randy Davidson • Letters to the Editor • Springsteen & Dylan: Poet Laureates or Veritable Zeroes? • Art is a Math is an Art is a Math... • Escher Takes On New Dimension • Commencement Speaker Announced • Plea From the Press • GM: Looking Good For \u2779 • Soccer Splits: 2-2 • Sports Profile: Don Paolicelli • Thin Clads Receive Treat • Swarthmore Superior In Homecoming Game • J.V.s Romp to Win • Hockey Returns Home • News in Brief: Fire Alarm Installations Near Completion; ProTheatre to Present The Good Doctor ; Art Exhibit to Open Soonhttps://digitalcommons.ursinus.edu/grizzlynews/1004/thumbnail.jp

    The Grizzly, October 27, 1978

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    Bomberger Tower Razed • Homecoming Brings Crowning, Presentations • Self Study Continues • Hockey Ties Nation\u27s Best • No Tickets at Door • Campus Sunshine to Set? • Ravine Paradise Revisited • Portrait of the Professor: Randy Davidson • Letters to the Editor • Springsteen & Dylan: Poet Laureates or Veritable Zeroes? • Art is a Math is an Art is a Math... • Escher Takes On New Dimension • Commencement Speaker Announced • Plea From the Press • GM: Looking Good For \u2779 • Soccer Splits: 2-2 • Sports Profile: Don Paolicelli • Thin Clads Receive Treat • Swarthmore Superior In Homecoming Game • J.V.s Romp to Win • Hockey Returns Home • News in Brief: Fire Alarm Installations Near Completion; ProTheatre to Present The Good Doctor ; Art Exhibit to Open Soonhttps://digitalcommons.ursinus.edu/grizzlynews/1004/thumbnail.jp

    The Grizzly, November 17, 1978

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    Tuition, Room And Board Fees Raised • GreaseBand Slated For January • Snow Precautions Outlined • Forum Highlights • Mail Theft In New Men\u27s • Hockey Violence Must Stop • Should Ursinus Teach Moral Values? • Acapulco: Gold • Rock\u27s Lesser-Knowns Provide Fresh Sound • Audio Corner: Purchasing audio equipment • Forum Committee • GM: Looking Good For \u2779 • A History Of Accomplishment • Bear Pack Bombs At Districts • Equestrians Riding High • Letters to the Editor: Public Apology; Grading Disputedhttps://digitalcommons.ursinus.edu/grizzlynews/1007/thumbnail.jp

    Localized rest and stress human cardiac creatine kinase reaction kinetics at 3 T.

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    Changes in the kinetics of the creatine kinase (CK) shuttle are sensitive markers of cardiac energetics but are typically measured at rest and in the prone position. This study aims to measure CK kinetics during pharmacological stress at 3 T, with measurement in the supine position. A shorter "stressed saturation transfer" (StreST) extension to the triple repetition time saturation transfer (TRiST) method is proposed. We assess scanning in a supine position and validate the MR measurement against biopsy assay of CK activity. We report normal ranges of stress CK forward rate (kfCK ) for healthy volunteers and obese patients. TRiST measures kfCK in 40 min at 3 T. StreST extends the previously developed TRiST to also make a further kfCK measurement during <20 min of dobutamine stress. We test our TRiST implementation in skeletal muscle and myocardium in both prone and supine positions. We evaluate StreST in the myocardium of six healthy volunteers and 34 obese subjects. We validated MR-measured kfCK against biopsy assays of CK activity. TRiST kfCK values matched literature values in skeletal muscle (kfCK  = 0.25 ± 0.03 s-1 vs 0.27 ± 0.03 s-1 ) and myocardium when measured in the prone position (0.32 ± 0.15 s-1 ), but a significant difference was found for TRiST kfCK measured supine (0.24 ± 0.12 s-1 ). This difference was because of different respiratory- and cardiac-motion-induced B0 changes in the two positions. Using supine TRiST, cardiac kfCK values for normal-weight subjects were 0.15 ± 0.09 s-1 at rest and 0.17 ± 0.15 s-1 during stress. For obese subjects, kfCK was 0.16 ± 0.07 s-1 at rest and 0.17 ± 0.10 s-1 during stress. Rest myocardial kfCK and CK activity from LV biopsies of the same subjects correlated (R = 0.43, p = 0.03). We present an independent implementation of TRiST on the Siemens platform using a commercially available coil. Our extended StreST protocol enables cardiac kfCK to be measured during dobutamine-induced stress in the supine position.Funded by: a Sir Henry Dale Fellowship from the Wellcome Trust and the Royal Society [098436/Z/12/B] to CTR, the BHF Centre of Research Excellence (OJR), a BHF clinical research training fellowship [FS/15/80/31803] to MAP, a BHF fellowship [FS/14/54/30946] to JJR, an NIHR OBRC fellowship to BR, a BHF programme grant [RG/13/8/30266] to CAL and SN, and a DPhil studentship from the Medical Research Council to WTC. We acknowledge support from the Oxford NIHR Biomedical Research Centre

    Cardiac Energetics in Patients With Aortic Stenosis and Preserved Versus Reduced Ejection Fraction.

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    BACKGROUND: Why some but not all patients with severe aortic stenosis (SevAS) develop otherwise unexplained reduced systolic function is unclear. We investigate the hypothesis that reduced creatine kinase (CK) capacity and flux is associated with this transition. METHODS: We recruited 102 participants to 5 groups: moderate aortic stenosis (ModAS) (n=13), SevAS, left ventricular (LV) ejection fraction ≥55% (SevAS-preserved ejection fraction, n=37), SevAS, LV ejection fraction 0.99). Accompanying the fall in CK flux, total CK and citrate synthase activities and the absolute activities of mitochondrial-type CK and CK-MM isoforms were also lower (P<0.02, all analyses). Median mitochondria-sarcomere diffusion distances correlated well with CK total activity (r=0.86, P=0.003). CONCLUSIONS: Total CK capacity is reduced in SevAS, with median values lowest in those with systolic failure, consistent with reduced energy supply reserve. Despite this, in vivo magnetic resonance spectroscopy measures of resting CK flux suggest that ATP delivery is reduced earlier, at the moderate AS stage, where LV function remains preserved. These findings show that significant energetic impairment is already established in moderate AS and suggest that a fall in CK flux is not by itself a necessary cause of transition to systolic failure. However, because ATP demands increase with AS severity, this could increase susceptibility to systolic failure. As such, targeting CK capacity and flux may be a therapeutic strategy to prevent and treat systolic failure in AS.This study was principally funded by a British Heart Foundation Clinical Training Research Fellowship FS/15/80/31803 (to Dr Peterzan) with support from a British Heart Foundation Program Grant (RG/18/12/34040). Drs Neubauer and Rider acknowledge support from British Heart Foundation Center of Research Excellence. Dr Neubauer acknowledges support from the National Institute of Health Research Oxford Biomedical Research Center. Dr Rodgers receives funding from the Wellcome Trust and the Royal Society (grant no. 098436/Z/12/B) and supported by the National Institute of Health Research Cambridge Biomedical Research Center. Dr Rider is funded by the British Heart Foundation FS/16/70/32157. Dr Miller was supported by a Novo Nordisk Postdoctoral Fellowship run in conjunction with the University of Oxford. The Biotechnology and Biological Sciences Research Council provided Advanced Life Sciences Research Technology Initiative 13 funding for serial block-face scanning electron microscopy through grant BB/C014122/1 (to Prof Chris Hawes, Oxford Brookes University)

    Risk of Ovarian Cancer and Inherited Variants in Relapse-Associated Genes

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    Background: We previously identified a panel of genes associated with outcome of ovarian cancer. The purpose of the current study was to assess whether variants in these genes correlated with ovarian cancer risk. Methods and Findings: Women with and without invasive ovarian cancer (749 cases, 1,041 controls) were genotyped at 136 single nucleotide polymorphisms (SNPs) within 13 candidate genes. Risk was estimated for each SNP and for overall variation within each gene. At the gene-level, variation within MSL1 (male-specific lethal-1 homolog) was associated with risk of serous cancer (p = 0.03); haplotypes within PRPF31 (PRP31 pre-mRNA processing factor 31 homolog) were associated with risk of invasive disease (p = 0.03). MSL1 rs7211770 was associated with decreased risk of serous disease (OR 0.81, 95 % CI 0.66–0.98; p = 0.03). SNPs in MFSD7, BTN3A3, ZNF200, PTPRS, and CCND1A were inversely associated with risk (p,0.05), and there was increased risk at HEXIM1 rs1053578 (p = 0.04, OR 1.40, 95 % CI 1.02–1.91). Conclusions: Tumor studies can reveal novel genes worthy of follow-up for cancer susceptibility. Here, we found that inherited markers in the gene encoding MSL1, part of a complex that modifies the histone H4, may decrease risk of invasiv
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