510 research outputs found

    Active Material Properties of the Myocardium: Correlation With Left Ventricular Function in Man

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    Author Institution: Department of Engineering and Physiology, Wright State UniversityThe effects of anisotrophy and nonhomogeneity of the ventricular myocardium as represented by a linear increase in the midwall effective modulus of elasticity were investigated in the present study, specifically as they effect the circumferential stress distribution. Various studies are presented suggesting a linear increase in the effective modulus of elasticity from endocardium to epicardium. In our study, this increase in the effective modulus was constrained by the approximation that stress per unit sarcomere length is constant. We evaluated 12 functionally normal cases and 9 functionally abnormal cases. The stress distribution for the 9 functionally abnormal cases was calculated, first with the normal and secondly with the abnormal variation in the modulus of elasticity. Assuming the myocardium has constant material properties that do not change with functional decomposition, the stress distributions in the first calculations indicated higher stresses through the inner half of the myocardium and lower stresses through the outer half of the myocardium as compared to the second. This finding suggests that the inner fibers are overloaded and the outer fibers are underloaded in left ventricular decompensation. The difference between the first and second stress distributions averaged 26% (range: 11% to 48%). A useful, clinical, and quantitative measure of stress loading of the sarcomeres in functionally normal and abnormal left ventricles is proposed

    Prospectus, April 26, 1977

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    VOTE TODAY-TOMORROW: FOUR VIE FOR PRES. IN STU-GO ELECTION; Remus, Mayeda run for V.P.; Albert Dodson unopposed; Activities Day May 3; Letters to the editor: Pres. Praises carnival, Mayeda warns of lies, Cartoon good…but, Stu-Go made many contributions: Onley; Editorial: Trouble for athletics; Hackett vs. Slack for convo., Cox opposes Stoeber for IOC; Unopposed: Propeck runs alone for secretary; Thursday set for wheel chair awareness; State provides funding for food sanitation course; Law Enforcement Club sponsors Mk\u27t Place fair; Markland: bigger not better for Twin City police force; Energy saving tips: Ripple effect causes waste; Police Chief Dye: \u27Recruitment-lifeline of police dep\u27t.\u27; Bike race today; Blooming Idiots come out of woodwork for IOC Carnival; Workshop set for Saturday: Puppetmaster Schmidt displays at PC; Afro American Theatre Workshop starts at PC; \u27Alcohol, sophisticated, sexy?\u27; Bike tour Sunday, May 1; Classifieds; Bat girls provide needed help for baseball team; Cobras expand record with 3rd no-hitter; Lincolnland doubleheader tomorrow: Women\u27s softball season nears end; June 7-10: Mudrock headed to JC golf nationalshttps://spark.parkland.edu/prospectus_1977/1018/thumbnail.jp

    Increasing dominance of large lianas in Amazonian forests

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    Ecological orthodoxy suggests that old-growth forests should be close to dynamic equilibrium, but this view has been challenged by recent findings that neotropical forests are accumulating carbon and biomass, possibly in response to the increasing atmospheric concentrations of carbon dioxide. However, it is unclear whether the recent increase in tree biomass has been accompanied by a shift in community composition. Such changes could reduce or enhance the carbon storage potential of old-growth forests in the long term. Here we show that non-fragmented Amazon forests are experiencing a concerted increase in the density, basal area and mean size of woody climbing plants (lianas). Over the last two decades of the twentieth century the dominance of large lianas relative to trees has increased by 1.7–4.6% a year. Lianas enhance tree mortality and suppress tree growth, so their rapid increase implies that the tropical terrestrial carbon sink may shut down sooner than current models suggest. Predictions of future tropical carbon fluxes will need to account for the changing composition and dynamics of supposedly undisturbed forests

    HPV testing in primary screening of older women

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    Certain types of the human papilloma virus (HPV) are well established as the primary cause of cervical cancer. Several studies have shown that HPV testing can improve the detection rate of high-grade cervical intraepithelial neoplasia (CIN), but these have been carried out primarily in younger women. In this study we evaluated the role of HPV testing as an adjunct to cytology in women aged 35 or over. An additional aim was to evaluate commercially available kits for HPV testing. A total of 2988 eligible women aged 34 or more attending for a routine smear in 40 general practitioner practices received HPV testing in addition to routine cytology, after having given written informed consent. Samples were assayed by polymerase chain reaction (PCR) and two versions of the Hybrid Capture test for HPV, and women were invited for colposcopy if there was any cytological abnormality (including borderline smears) or the PCR test was positive. Any apparent abnormality was biopsied and loop-excision was performed as necessary. CIN was judged by histology; 42 women had high-grade CIN, of which six were cytology negative (86% sensitivity for borderline or worse) and three had a borderline smear (79% sensitivity for mild dyskaryosis or worse). The positive predictive value of a borderline smear was only 3.1%. Eleven high-grade lesions were negative by the PCR HPV test (sensitivity 74%). The first generation Hybrid Capture II test had a similar sensitivity but an unacceptably high false positive rate (18.3%), while the newer Hybrid Capture II microtitre kit had a 95% sensitivity and a 2.3% positivity rate in normal women when used at a 2 pg ml−1 cut-off (positive predictive value 27%). Cytology performed very well in this older cohort of women. The newer Hybrid Capture II microtitre test may be a useful adjunct, especially if the results reported here are reproducible in other studies. A combined screening test offers the possibility of greater protection and/or longer screening intervals, which could reduce the overall cost of the screening programme. © 1999 Cancer Research Campaig

    Effects of acute nutritional ketosis during exercise in adults with glycogen storage disease typeIIIaare phenotype-specific:An investigator-initiated, randomized, crossover study

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    Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by a debranching enzyme deficiency. A subgroup of GSDIIIa patients develops severe myopathy. The purpose of this study was to investigate whether acute nutritional ketosis (ANK) in response to ketone-ester (KE) ingestion is effective to deliver oxidative substrate to exercising muscle in GSDIIIa patients. This was an investigator-initiated, researcher-blinded, randomized, crossover study in six adult GSDIIIa patients. Prior to exercise subjects ingested a carbohydrate drink (~66 g, CHO) or a ketone-ester (395 mg/kg, KE) + carbohydrate drink (30 g, KE + CHO). Subjects performed 15-minute cycling exercise on an upright ergometer followed by 10-minute supine cycling in a magnetic resonance (MR) scanner at two submaximal workloads (30% and 60% of individual maximum, respectively). Blood metabolites, indirect calorimetry data, and in vivo 31P-MR spectra from quadriceps muscle were collected during exercise. KE + CHO induced ANK in all six subjects with median peak βHB concentration of 2.6 mmol/L (range: 1.6-3.1). Subjects remained normoglycemic in both study arms, but delta glucose concentration was 2-fold lower in the KE + CHO arm. The respiratory exchange ratio did not increase in the KE + CHO arm when workload was doubled in subjects with overt myopathy. In vivo 31P MR spectra showed a favorable change in quadriceps energetic state during exercise in the KE + CHO arm compared to CHO in subjects with overt myopathy. Effects of ANK during exercise are phenotype-specific in adult GSDIIIa patients. ANK presents a promising therapy in GSDIIIa patients with a severe myopathic phenotype. Trial registration number: ClinicalTrials.gov identifier: NCT03011203

    The Unusual Temporal and Spectral Evolution of SN2011ht. II. Peculiar Type IIn or Impostor?

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    SN2011ht has been described both as a true supernova and as an impostor. In this paper, we conclude that it does not match some basic expectations for a core-collapse event. We discuss SN2011ht's spectral evolution from a hot dense wind to a cool dense wind, followed by the post-plateau appearance of a faster low density wind during a rapid decline in luminosity. We identify a slow dense wind expanding at only 500--600 km/s, present throughout the eruption. A faster wind speed V ~ 900 km/s may be identified with a second phase of the outburst. There is no direct or significant evidence for any flow speed above 1000 km/s; the broad asymmetric wings of Balmer emission lines in the hot wind phase were due to Thomson scattering, not bulk motion. We estimate a mass loss rate of order 0.04 Msun/yr during the hot dense wind phase of the event. There is no evidence that the kinetic energy substantially exceeded the luminous energy, roughly 2 X 10^49 ergs; so the total energy was far less than a true SN. We suggest that SN2011ht was a giant eruption driven by super-Eddington radiation pressure, perhaps beginning about 6 months before the discovery. A strongly non-spherical SN might also account for the data, at the cost of more free parameters.Comment: To appear in the Astrophysical Journal, Nov. 20 issue. Expanded discussion re SN impostors and Type IIn SNe plus two new figure

    Cigarettes and alcohol in relation to colorectal cancer: the Singapore Chinese Health Study

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    The relations were examined between colorectal cancer and cigarette smoking and alcohol consumption within the Singapore Chinese Health Study, a population-based, prospective cohort of 63 257 middle-aged and older Chinese men and women enrolled between 1993 and 1998, from whom baseline data on cigarette smoking and alcohol consumption were collected through in-person interviews. By 31 December 2004, 845 cohort participants had developed colorectal cancer (516 colon cancer, 329 rectal cancer). Compared with nondrinkers, subjects who drank seven or more alcoholic drinks per week had a statistically significant, 72% increase in risk of colorectal cancer hazard ratio (HR)=1.72; 95% confidence interval (CI)=1.33–2.22). Cigarette smoking was associated with an increased risk of rectal cancer only. Compared with nonsmokers, HRs (95% CIs) for rectal cancer were 1.43 (1.10–1.87) for light smokers and 2.64 (1.77–3.96) for heavy smokers. Our data indicate that cigarette smoking and alcohol use interact in the Chinese population in an additive manner in affecting risk of rectal cancer, thus suggesting that these two exposures may share a common etiologic pathway in rectal carcinogenesis

    BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers

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    Background: The K3326X variant in BRCA2 (BRCA2*c.9976A>T; p.Lys3326*; rs11571833) has been found to be associated with small increased risks of breast cancer. However, it is not clear to what extent linkage disequilibrium with fully pathogenic mutations might account for this association. There is scant information about the effect of K3326X in other hormone-related cancers. Methods: Using weighted logistic regression, we analyzed data from the large iCOGS study including 76 637 cancer case patients and 83 796 control patients to estimate odds ratios (ORw) and 95% confidence intervals (CIs) for K3326X variant carriers in relation to breast, ovarian, and prostate cancer risks, with weights defined as probability of not having a pathogenic BRCA2 variant. Using Cox proportional hazards modeling, we also examined the associations of K3326X with breast and ovarian cancer risks among 7183 BRCA1 variant carriers. All statistical tests were two-sided. Results: The K3326X variant was associated with breast (ORw = 1.28, 95% CI = 1.17 to 1.40, P = 5.9x10- 6) and invasive ovarian cancer (ORw = 1.26, 95% CI = 1.10 to 1.43, P = 3.8x10-3). These associations were stronger for serous ovarian cancer and for estrogen receptor–negative breast cancer (ORw = 1.46, 95% CI = 1.2 to 1.70, P = 3.4x10-5 and ORw = 1.50, 95% CI = 1.28 to 1.76, P = 4.1x10-5, respectively). For BRCA1 mutation carriers, there was a statistically significant inverse association of the K3326X variant with risk of ovarian cancer (HR = 0.43, 95% CI = 0.22 to 0.84, P = .013) but no association with breast cancer. No association with prostate cancer was observed. Conclusions: Our study provides evidence that the K3326X variant is associated with risk of developing breast and ovarian cancers independent of other pathogenic variants in BRCA2. Further studies are needed to determine the biological mechanism of action responsible for these associations

    Genetic polymorphisms in the cyclooxygenase-2 gene, use of nonsteroidal anti-inflammatory drugs, and breast cancer risk

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    INTRODUCTION: The association between use of nonsteroidal anti-inflammatory drugs (NSAIDs) and breast cancer risk remains unclear. Inconsistencies in previously reported findings may be partly due to differences in expression of cyclooxygenase (COX)-2. We hypothesized that genetic polymorphisms (COX-2 .926, COX-2 .5209, and COX-2 .8473) may reduce overall breast cancer risk or risk for subtypes of breast cancer by modulating the inflammatory response and may interact with aspirin or any NSAID use. METHODS: We conducted a population-based, case-control study in which we genotyped 1,067 breast cancer cases and 1,110 control individuals included in the Long Island Breast Cancer Study Project. RESULTS: No major effects of the three COX-2 variant alleles on breast cancer risk were found. A total of eight distinct haplotypes and 18 diplotypes were observed in the population. Overall, no significant associations between COX-2 haplotypes/diplotypes and breast cancer risk were observed. Among women who used aspirin or any NSAID there was little evidence for an interaction with the at-risk COX-2 genotypes, with one exception. Among women with hormone receptor positive breast cancer, the reduced risk for any NSAID use was only evident among those who had at least one variant C allele of COX-2 .8473 (odds ratio = 0.7, 95% confidence interval = 0.5 to 1.0; P for the interaction = 0.02). There was no corresponding interaction for aspirin use, possibly because of limited power. CONCLUSION: These data provide modest evidence that the C allele of COX-2 .8473 may interact with NSAIDs to reduce risk for hormone receptor positive breast cancer
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