Quantitative Values (quantitative + value)

Distribution by Scientific Domains


Selected Abstracts


Comparison of the Bayer VERSANT HCV RNA 3.0 and the Roche COBAS Amplicor HCV Monitor, Version 2.0, assays in HCV genotype 4 infection

JOURNAL OF VIRAL HEPATITIS, Issue 11 2007
W. Jessner
summary Prediction of treatment response is clinically important in chronic hepatitis C virus (HCV) genotype 4 infection. Early viral kinetics is useful in this respect for genotype 1 but interpretation is dependent on assay linearity and reproducibility. The VERSANT HCV RNA 3.0 (bDNA-3.0) and the COBAS Amplicor HCV Monitor 2.0 (HCM-2.0) have been widely used quantitative assays. We wanted to comparatively evaluate the two tests in a large genotype 4 sample. Genotyping was performed by NS5b sequencing. Viral load was tested in parallel in 32 patients at least six times on antiviral therapy with interferon , (IFN,). Totally, 198 samples within a quantitative range from undetectable to about 7 × 106 IU/mL (bDNA-3.0) were obtained and compared. Twenty-two samples with viral load above 500 000 IU/mL tested by HCM-2.0 were 1:100 diluted and retested. Quantitative values were fitted to a third order polynomial (M = 0.118303 + 1.07503 × V+ 0.0112128 × V2 , 0.0055504 × V3; M,HCM-2.0, V,bDNA-3.0, both log IU/mL) showing progressive nonlinearity of HCM-2.0 above 100 000 IU/mL but better clinical sensitivity with respect to bDNA-3.0. Dilution lead to a gain of at least a factor of 2.7 and thus, overestimation compared with bDNA-3.0. Deviation from linearity and overestimation upon dilution by HCM-2.0 are similar with HCV genotype 4, compared with other HCV genotypes. Differences in test performance were not detected for subtypes but for individual patients possibly related to specific quasispecies patterns. The interpretation of viral kinetic data becomes difficult due to overestimation upon dilution of baseline values by HCM-2.0. [source]


Summary of contributions to GAW Group 15: family-based samples are useful in identifying common polymorphisms associated with complex traits

GENETIC EPIDEMIOLOGY, Issue S1 2009
Stacey Knight
Abstract Traditionally, family-based samples have been used for genetic analyses of single-gene traits caused by rare but highly penetrant risk variants. The utility of family-based genetic data for analyzing common complex traits is unclear and contains numerous challenges. To assess the utility as well as to address these challenges, members of Genetic Analysis Workshop 16 Group 15 analyzed Framingham Heart Study data using family-based designs ranging from parent,offspring trios to large pedigrees. We investigated different methods including traditional linkage tests, family-based association tests, and population-based tests that correct for relatedness between subjects, and tests to detect parent-of-origin effects. The analyses presented an assortment of positive findings. One contribution found increased power to detect epistatic effects through linkage using ascertainment of sibships based on extreme quantitative values or presence of disease associated with the quantitative value. Another contribution found four single-nucleotide polymorphisms (SNPs) showing a maternal effect, two SNPs with an imprinting effect, and one SNP having both effects on a binary high blood pressure trait. Finally, three contributions illustrated the advantage of using population-based methods to detect association to complex binary or quantitative traits. Our findings highlight the contribution of family-based samples to the genetic dissection of complex traits. Genet. Epidemiol. 33 (Suppl. 1):S99,S104, 2009. © 2009 Wiley-Liss, Inc. [source]


120 Exploration of Morphological Variation Within the Genus Pediastrum Meyen 1829 (Chlorophyceae, Chlorophyta)

JOURNAL OF PHYCOLOGY, Issue 2003
H. A. McManus
Monographic works on the green algal genus, Pediastrum Meyen 1829 (Chlorophyceae, Chlorophyta), have described species, varieties and forms based on such characteristics as the size and shape of the marginal cells, pattern of cell wall sculpturing and extent of cell wall sculpturing. Depending on the author, the number of taxa assigned to the genus Pediastrum varies. Due to the lack of quantitative value to these characteristics, it has been difficult for other researchers to assign appropriate taxonomy to wild isolates. A molecular phylogeny including multiple strains from both culture collections and wild samples confirms relationships found by previous molecular studies on fewer taxa, in which the family Hydrodictyaceae forms a monophyletic group within the Sphaeropleales, and that the genera Hydrodictyon and Sorastrum are derived from Pediastrum. Hydrodicyton forms a monophyletic clade and consists of three species, H. reticulatum, H. africanum, and H. patenaeforme. Multiple isolates of H. reticulatum reveal little genetic variation between different geographic localities. Inclusion of wild isolates permits a more thorough exploration of morphological variation within the genus Pediastrum, and what characters may be taxonomically informative, particularly in the species P. boryanum and P. duplex. Wild isolates sampled from different areas also offers information regarding geographic variation and potential morphological convergence. [source]


Using Genetic Admixture to Study the Biology of Obesity Traits and to Map Genes in Admixed Populations

NUTRITION REVIEWS, Issue 2004
José R. Fernández Ph.D.
Differences among ethnic and racial groups in obesity-related traits have been clearly established in the scientific literature. To explore the genetic component underlying these differences, the genetic admixture approach has been used. In this approach, ancestry informative genetic markers are used to estimate a quantitative value representing the degree of ancestral background in individuals of admixed genetic background. Genetic admixture has been successfully used to explain racial and ethnic variation in obesity related traits; however, the understanding and measure of cultural and environmental components that also influence these phenotypes still requires further exploration [source]


Incorporating multiple criteria into the design of conservation area networks: a minireview with recommendations

DIVERSITY AND DISTRIBUTIONS, Issue 2 2006
Alexander Moffett
ABSTRACT We provide a review of multicriteria decision-making (MCDM) methods that may potentially be used during systematic conservation planning for the design of conservation area networks (CANs). We review 26 methods and present the core ideas of 19 of them. We suggest that the computation of the non-dominated set (NDS) be the first stage of any such analysis. This process requires only that alternatives be qualitatively ordered by each criterion. If the criteria can also be similarly ordered, at the next stage, Regime is the most appropriate method to refine the NDS. If the alternatives can also be given quantitative values by the criteria, Goal Programming will prove useful in many contexts. If both the alternatives and the criteria can be quantitatively evaluated, and the criteria are independent of each other but may be compounded, then multi-attribute value theory (MAVT) should be used (with preferences conveniently elicited by a modified Analytic Hierarchy Process (mAHP) provided that the number of criteria is not large). [source]


Fatigue damage analysis in a duplex stainless steel by digital image correlation technique

FATIGUE & FRACTURE OF ENGINEERING MATERIALS AND STRUCTURES, Issue 2 2008
A. EL BARTALI
ABSTRACT Strain field measurements by digital image correlation today offer new possibilities for analysing the mechanical behaviour of materials in situ during mechanical tests. The originality of the present study is to use this technique on the micro-structural scale, in order to understand and to obtain quantitative values of the fatigue surface damage in a two-phased alloy. In this paper, low-cycle fatigue damage micromechanisms in an austenitic-ferritic stainless steel are studied. Surface damage is observed in real time, with an in situ microscopic device, during a low-cycle fatigue test performed at room temperature. Surface displacement and strain fields are calculated using digital image correlation from images taken during cycling. A detailed analysis of optical images and strain fields measured enables us to follow precisely the evolution of surface strain fields and the damage micromechanisms. Firstly, strain heterogeneities are observed in austenitic grains. Initially, the austenitic phase accommodates the cyclic plastic strain and is then followed by the ferritic phase. Microcrack initiation takes place at the ferrite/ferrite grain boundaries. Microcracks propagate to the neighbouring austenitic grains following the slip markings. Displacement and strain gradients indicate probable microcrack initiation sites. [source]


Summary of contributions to GAW Group 15: family-based samples are useful in identifying common polymorphisms associated with complex traits

GENETIC EPIDEMIOLOGY, Issue S1 2009
Stacey Knight
Abstract Traditionally, family-based samples have been used for genetic analyses of single-gene traits caused by rare but highly penetrant risk variants. The utility of family-based genetic data for analyzing common complex traits is unclear and contains numerous challenges. To assess the utility as well as to address these challenges, members of Genetic Analysis Workshop 16 Group 15 analyzed Framingham Heart Study data using family-based designs ranging from parent,offspring trios to large pedigrees. We investigated different methods including traditional linkage tests, family-based association tests, and population-based tests that correct for relatedness between subjects, and tests to detect parent-of-origin effects. The analyses presented an assortment of positive findings. One contribution found increased power to detect epistatic effects through linkage using ascertainment of sibships based on extreme quantitative values or presence of disease associated with the quantitative value. Another contribution found four single-nucleotide polymorphisms (SNPs) showing a maternal effect, two SNPs with an imprinting effect, and one SNP having both effects on a binary high blood pressure trait. Finally, three contributions illustrated the advantage of using population-based methods to detect association to complex binary or quantitative traits. Our findings highlight the contribution of family-based samples to the genetic dissection of complex traits. Genet. Epidemiol. 33 (Suppl. 1):S99,S104, 2009. © 2009 Wiley-Liss, Inc. [source]


Age-related plasma reference ranges for two heparin-binding proteins , vitronectin and platelet factor 4

INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, Issue 6 2009
F. NEWALL
Summary This study was conducted to establish age-related reference ranges for two heparin-binding proteins , vitronectin and platelet factor 4 (PF4) , and to determine if the quantitative values of these proteins may contribute to the reported age-dependent effect of unfractionated heparin (UFH). Plasma samples were obtained from healthy children aged between 1 month and 16 years and from healthy adult volunteers. Two commercial kits were used to measure plasma vitronectin and PF4 levels. Results were reported as mean and boundaries including 95% of the population. Plasma vitronectin levels for children aged 1,5 years were significantly higher compared with adults. Plasma PF4 levels for infants <1 year of age were significantly lower compared with adults. The differences between reference values for both proteins in all other age-groups were not statistically significant. This study for the first time has established age-related reference ranges for vitronectin and PF4. In establishing these ranges, the quantitative values of these proteins do not appear to be the major contributory cause for the age-dependent variation in UFH effect. Future studies are required to evaluate the possible impact of age-dependent differences in binding between heparin-binding proteins and UFH. [source]


Quantitation of cytological parameters of malignant lymphocytes using computerized image analysis

INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, Issue 4 2008
S. A. HAMID JAHANMEHR
Summary Computerized image analysis may add to morphological evaluation by turning qualitative data into quantitative values. In this study, image analysis program was used to quantitate cytological parameters of lymphocytes in B-cell lymphoproliferative disorders. Chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL) and B-cell prolymphocytic leukemia (B-PLL) were selected to represent typically small, medium, and large-sized lymphocytes, respectively. Image analysis was performed to determine the morphological parameters. A set of measurements was generated for quantitation of total cell area, cell diameter, cytoplasm area, nuclear area, nuclear/cell ratio, and nuclear density. The quantitated parameters substantiated morphological characteristics of the tumor cells. Comparative assessments demonstrated that CLL, MCL, and PLL can be differentiated by the quantitative descriptors. The results from image analysis may assist in defining morphological criteria and in developing quantitative cell morphology. [source]


Ethyl Glucuronide in Hair Compared With Traditional Alcohol Biomarkers,A Pilot Study of Heavy Drinkers Referred to an Alcohol Detoxification Unit

ALCOHOLISM, Issue 5 2009
Gudrun Hřiseth
Background:, Traditional biomarkers for heavy alcohol use include serum carbohydrate-deficient transferrin (CDT), the enzymes aspartate aminotranserase (AST), and alanine aminotransferase (ALT) as well as gamma-glutamyl transferase (GGT). Measurement of the nonoxidative ethanol metabolite, ethyl glucuronide (EtG) in hair, has been proposed as a new marker with superior qualities. The aim of this study was to investigate the sensitivity of EtG in hair to detect heavy alcohol use compared with CDT, AST, ALT, and GGT. We also wanted to study the quantitative relation between alcohol intake and the different biomarkers. Methods:, Sixteen patients with a history of heavy alcohol use over the previous 3 months were recruited directly after admission to a withdrawal clinic. They were thoroughly interviewed about their drinking pattern as well as relevant diseases and use of medicines or drugs. Serum was sampled and analyzed for %CDT, AST, ALT, and GGT. Hair samples were collected and analyzed for EtG. Results:, The mean estimated daily intake (EDI) over the previous 3 months was 206 ± 136 g pure alcohol. All patients fulfilled the criteria for heavy alcohol use. The sensitivity to detect heavy alcohol use was 64% for %CDT, 67% for AST, 67% for ALT, 93% for GGT, and 94% for EtG. There was no correlation between the quantitative values of EDI and %CDT, AST, ALT, and GGT. There was a positive, statistically significant correlation between EDI and the level of EtG in hair. Conclusions:, In this study, EtG in hair and GGT showed the best sensitivity to detect heavy alcohol use and there was a positive correlation between EDI and the concentrations of EtG in hair. Before giving recommendations for clinical practice, further studies should be carried out on larger materials and populations with a wider range of alcohol intake. [source]