Assessing Long-Term Test-Retest Reliability of the CPT-IP in Schizophrenia

Background

The Continuous Performance Test-Identical Pairs version (CPT-IP) is a well-established measure of sustained attention, and its more challenging versions are particularly suited to detect subtle processing deficits in patients with schizophrenia. However, while there are few longitudinal samples for the CPT-IP, no study has addressed stability for more than two month in patients with schizophrenia. Assessing long-term test-retest reliability of the CPT-IP would facilitate the ability of clinicians to draw conclusions from studies involving interventions as long term cognitive or pharmacological treatments. The present study assessed 12 month test-retest reliability for the two most challenging versions of CPT-IP (4-digit and shapes) in a matched sample of clinically stable schizophrenia outpatients and healthy controls.

Methods

Fifty clinically stable schizophrenia outpatients and 50 healthy controls were assessed with the CPT-IP for the 4-digit and shape conditions. From these, 40 patients and 47 controls were reassessed with an average interval of 12.3 months between test sessions. Test-retest reliability was analyzed with Pearson correlations and results were compared with previous data involving healthy controls and short-term studies in patients with schizophrenia.

Results

Especially d’ and hit rate discriminated well between patients with schizophrenia and healthy controls for both CPT-IP conditions and at both test sessions. Healthy controls demonstrated sufficient long term test-retest correlations of d’, hit rate and reaction time for both the 4-digit and shape conditions. However, in schizophrenia patients, long-term reliability correlations were at best moderate for d’ and hit rate only.

Conclusions

The current study provides further evidence that d’ and hit rate yield consistent cross-sectional discrimination sensitivity. At best moderate long-term test-retest reliability of d’ in schizophrenia outpatients may be not sufficient for practical use of this measure in long term clinical trials.     

Combining crystallography and molecular dynamics: The case of Schistosoma mansoni phospholipid glutathione peroxidase

Oxidative stress is a widespread challenge for living organisms, and especially so for parasitic ones, given the fact that their hosts can produce reactive oxygen species (ROS) as a mechanism of defense. Thus, long lived parasites, such as the flatworm Schistosomes, have evolved refined enzymatic systems capable of detoxifying ROS. Among these, glutathione peroxidases (Gpx) are a family of sulfur or selenium‐dependent isozymes sharing the ability to reduce peroxides using the reducing equivalents provided by glutathione or possibly small proteins such as thioredoxin. As for other frontline antioxidant enzymatic systems, Gpxs are localized in the tegument of the Schistosomes, the outermost defense layer. In this article, we present the first crystal structure at 1.0 and 1.7 Å resolution of two recombinant SmGpxs, carrying the active site mutations Sec43Cys and Sec43Ser, respectively. The structures confirm that this enzyme belongs to the monomeric class 4 (phospholipid hydroperoxide) Gpx. In the case of the Sec to Cys mutant, the catalytic Cys residue is oxidized to sulfonic acid. By combining static crystallography with molecular dynamics simulations, we obtained insight into the substrate binding sites and the conformational changes relevant to catalysis, proposing a role for the unusual reactivity of the catalytic residue. Proteins 2010. © 2009 Wiley‐Liss, Inc.     

耻垢分枝杆菌感染人脐带间充质干细胞模型的建立及其特征

【背景】结核分枝杆菌(Mycobacterium tuberculosis, Mtb)休眠菌形成被认为是潜伏结核感染(latent tuberculosis infection, LTBI)的主要原因,但目前缺乏体内和体外模型进行机制研究。新近研究表明Mtb可感染间充质干细胞(mesenchymal stem cells, MSC)并以休眠状态在细胞中长期存活。然而Mtb感染细胞模型存在周期长和生物安全要求高等问题,需要探索可用的MSC感染细胞模型用于Mtb休眠机制的研究。【目的】建立快速生长型耻垢分枝杆菌(Mycobacteriumsmegmatis,Ms)感染人脐带间充质干细胞(human umbilical cord MSC, hUCMSC)的细胞模型并研究其特征。【方法】取分离好的hUCMSC,流式细胞术鉴定其表面标志性抗原;以Ms菌株感染hUCMSC,DiI标记细胞膜,荧光显微镜下观察细胞吞噬作用;平板法计数Ms胞内存活率;油红O染色观察细胞脂滴形成;鬼笔环肽荧光染色观察细胞骨架变化;实时荧光定量PCR(realtimequantitativePCR,RT-qPCR)检测Ms...     

COMPARISON OF TETRAPLOID AND SINGLE GENE-INDUCED GIGAS VARIANTS IN CHICKPEA (CICER ARIETINUM). I. ORIGIN AND GENETIC CHARACTERIZATION

Two genetic variants with increased organ size were independently derived from diploid (2n = 2x = 16) chickpea (Cicer arietinum L.) line ICC 640. Radiation-induced mutant PM1101 had greatly enlarged leaves, leaflets, and pods, and an elongated stem with longer internodes but fewer nodes than ICC 640. F₁, F₂, and F₃ data from crosses with ICC 640 showed that the mutant characteristics of PM1101 were the pleiotropic effects of a single, recessive genetic factor. For purposes of comparison, tetraploid derivatives of ICC 640 were produced by colchicine treatment of seed. In the tetraploids, leaflets and pods were enlarged, but less dramatically than in PM1101. Enlarged pollen grains and stomatal guard cells, and increased guard cell chloroplast number were found in tetraploids but not in PM1101, while both variants produced fewer seeds than ICC 640. Mutant PM1101 and the tetraploids represent two very different manifestations of gigantism in chickpea.     

A critical review of permeabilized cell systems for studying mammalian DNA repair

Permeabilized cell systems have proven valuable for studies of the enzymology of mammalian DNA repair and this review will summarize and contrast the different systems used to this end. Results from permeable cell studies will be reviewed which pertain to 3 questions of DNA repair: the role(s) of ATP, DNA polymerase enzymology, and the isolation of repair factors by in vitro correction of repair-defective cells.     

Restriction fragment analysis for differentiation of indistinguishable temperate coliphages

DNA of lambda and seven related phages was digested with restriction endonuclease, EcoRI. Seven different fragment patterns were observed, only two of the eight phages showing identical profiles. Restriction enzyme fragment analysis is thus shown to be a sensitive tool for the differentiation of biologically indistinguishable phages.     

Color pan traps often catch less when there are more flowers around

When assessing changes in populations of species, it is essential that the methods used to collect data have some level of precision and preferably also good accuracy. One commonly used method to collect pollinators is colour pan traps, but this method has been suggested to be biased by the abundance of surrounding flowers. The present study evaluated the relationship between pan trap catches and the frequency of flowers on small (25 m²) and large (2–6 ha) spatial scales. If pan traps work well, one should assume a positive relationship, that is, more insects caught when they have more food. However, in contrast, we found that catches in pan traps were often negatively affected by flower frequency. Among the six taxa evaluated, the negative bias was largest in Vespoidea and Lepturinae, while there was no bias in solitary Apoidea (Cetoniidae, Syrphidae and social Apoidea were intermediate). Furthermore, red flowers seemed to contribute most to the negative bias. There was also a tendency that the negative bias differed within the flight season and that it was higher when considering the large spatial scale compared to the small one. To conclude, pan trap catches may suffer from a negative bias due to surrounding flower frequency and color. The occurrence and magnitude of the negative bias were context and taxon dependent, and therefore difficult to adjust for. Thus, pan traps seem less suited to evaluate differences between sites and the effect of restoration, when gradients in flower density are large. Instead, it seems better suited to monitor population changes within sites, and when gradients are small.