Assessing program effects in the presence of treatment—baseline interactions: A latent curve approach.

Methods for assessing treatment effects of longitudinal randomized intervention are considered. The focus is on modeling the nonlinear relationship between treatment effects and baseline often observed in prevention programs designed for at-risk populations. Piecewise linear growth modeling was used to study treatment effects during the different periods of development. A multistep multiple-group analysis procedure is proposed for assessing treatment effects in the presence of nonlinear treatment-baseline interactions. Standard errors of the estimates from this multistep procedure were obtained using a bootstrap approach. The methods are illustrated using data from the Johns Hopkins Prevention Research Center involving an intervention aimed at improving classroom behavior. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Probe beam amplification via degenerate optical wave mixing in a Kerr medium

The theory of probe beam amplification via degenerate optical wave mixing in a Kerr medium is presented. This theory includes consideration of the self-phase modulation, two-wave mixing, and multiwave mixing terms in the coupled-wave equations. Both analytical solutions, under the assumptions of a nondepleted pump beam and a transparent Kerr medium, and numerical solutions with these assumptions removed are presented. Our solutions show that under certain conditions, phase matching can be satisfied and a high probe beam gain is possible, even for a zero phase shift between the refractive index and the intensity gratings.     

Attenuation of neutrophil and endothelial activation by intravenous morphine in patients with acute myocardial infarction

To investigate the effects of morphine on neutrophil and endothelial activation, we measured serum levels of intercellular adhesion molecule-1 (ICAM-1), L-selectin, and neutrophil endopeptidase 24.11 (NEP) in 38 patients with acute myocardial infarction (group 1) and 16 control subjects (group 2). In group 1, all the patients underwent blood sampling at initial presentation and 10 minutes later. Twenty of them had 3 mg of morphine administered intravenously immediately after the first sampling (group 1A) and the other 18 after a second sampling (group 1B). The serum levels of ICAM-1 and L-selectin were both significantly higher in groups 1A and 1B than in group 2. In group 1A, the ICAM-1 decreased significantly at second blood samplings (310 +/- 28 vs 368 +/- 30 ng/ml; p <0.001), whereas in group 1B there was no significant change in ICAM-1 (357 +/- 33 vs 359 +/- 26 ng/ml; p = NS). In group 1A, the L-selectin decreased significantly at second blood samplings (2.3 +/- 1.2 mg/L, p <0.001 vs baseline), whereas in group 1B there was no significant change in L-selectin (3.9 +/- 1.0 mg/L, p = NS vs baseline). There was no significant difference in baseline NEP activities between groups 1A and 1B (4.89 +/- 1.22 vs 5.14 +/- 1.57 nmol/mg protein; p = NS). However, the NEP activities at second blood samplings decreased significantly in group 1A (9.88 +/- 1.86 nmol/mg protein, p <0.001 vs baseline), whereas no significant changes were observed in group 1B (5.09 +/- 1.62 nmol/mg protein, p = NS vs baseline). In conclusion, morphine increased NEP activities and thus attenuated shedding of L-selectin and ICAM-1.     

Transduction of envelope stress in Escherichia coli by the Cpx two-component system

Disruption of normal protein trafficking in the Escherichia coli cell envelope (inner membrane, periplasm, outer membrane) can activate two parallel, but distinct, signal transduction pathways. This activation stimulates the expression of a number of genes whose products function to fold or degrade the mislocalized proteins. One of these signal transduction pathways is a two-component regulatory system comprised of the histidine kinase CpxA and the response regulator, CpxR. In this study we characterized gain-of-function Cpx* mutants in order to learn more about Cpx signal transduction. Sequencing demonstrated that the cpx* mutations cluster in either the periplasmic, the transmembrane, or the H-box domain of CpxA. Intriguingly, most of the periplasmic cpx* gain-of-function mutations cluster in the central region of this domain, and one encodes a deletion of 32 amino acids. Strains harboring these mutations are rendered insensitive to a normally activating signal. In vivo and in vitro characterization of maltose-binding-protein fusions between the wild-type CpxA and a representative cpx* mutant, CpxA101, showed that the mutant CpxA is altered in phosphotransfer reactions with CpxR. Specifically, while both CpxA and CpxA101 function as autokinases and CpxR kinases, CpxA101 is devoid of a CpxR-P phosphatase activity normally present in the wild-type protein. Taken together, the data support a model for Cpx-mediated signal transduction in which the kinase/phosphatase ratio is elevated by stress. Further, the sequence and phenotypes of periplasmic cpx* mutations suggest that interactions with a periplasmic signaling molecule may normally dictate a decreased kinase/phosphatase ratio under nonstress conditions.     

High-level genetic diversity in the vapD chromosomal region of Helicobacter pylori

Helicobacter pylori isolates from different patients are characterized by diversity in the nucleotide sequences of individual genes, variation in genome size, and variation in gene order. Genetic diversity is particularly striking in vacuolating cytotoxin (vacA) alleles. In this study, five open reading frames (ORFs) were identified within a 4.2-kb region downstream from vacA in H. pylori 60190. One of these ORFs was closely related to the virulence-associated protein D (vapD) gene of Dichelobacter nodosus (64.9% nucleotide identity). A probe derived from vapD of H. pylori 60190 hybridized with only 19 (61.3%) of 31 H. pylori strains tested. Sequence analysis of the vapD region in vapD-negative H. pylori strains revealed that there were two different families of approximately 0.5-kb DNA segments, which were both unrelated to vapD. The presence of vapD was not associated with any specific family of vacA alleles. These findings are consistent with a recombinational population structure for H. pylori.     

Computing the Percentage Points of the Run-Length Distributions of Multivariate CUSUM Control Charts

Multivariate CUSUM control charts are often used instead of the standard Hotelling's control charts in many practical problems when detection of small shifts in the process mean is important. However, design of multivariate CUSUM control charts are usually based on the average run length (ARL). In this work, we will compute the percentage points of the run-length distributions of two multivariate CUSUM control charts. It will be shown that interpretations based on ARL can be misleading since the in-control run-length distribution of a multivariate CUSUM is highly skewed. On the other hand, the percentage points of the run-length distribution provide additional information such as the median run length, early false out-of-control signals, and the skewness of the run-length distribution for a particular scheme. These extra information might provide quality control engineers further knowledge of a particular multivariate CUSUM control chart scheme.