Τρίτη 3 Ιουλίου 2018
Reply to “Clinical Practice Guidelines or Clinical Research Guidelines?”
Source:Clinical Neurophysiology
Author(s): Riitta Hari, Sylvain Baillet, Gareth Barnes, Nina Forss, Joachim Gross, Matti Hämäläinen, Ole Jensen, Ryusuke Kakigi, François Mauguière, Nobukazu Nakasato, Aina Puce, Gian-Luca Romani, Alfons Schnitzler, Samu Taulu
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Association between Mismatch Negativity and Voxel-Based Brain Volume in Schizophrenia
Source:Clinical Neurophysiology
Author(s): Wei-Lieh Huang, Chao-Yu Liu, Chih-Min Liu, Hon-Man Liu, Chung-Yi Yang, Tzung-Jeng Hwang, Ming H. Hsieh, Hai-Gwo Hwu
ObjectiveThis study aimed to investigate the association between mismatch negativity (MMN) and volumes of several brain regions measured using a semi-automated method in patients with schizophrenia and healthy controls.MethodsMMN in response to duration deviants and magnetic resonance imaging were acquired from 36 schizophrenia patients and 14 healthy controls. FreeSurfer was used for volumetric analysis. MMN amplitudes, brain volumes and their association were compared between schizophrenia and controls. Correlation analysis and multiple linear regression analysis were used to examine the correlated variables of MMN.ResultsMMN amplitude was significantly lower in the schizophrenia group. In schizophrenia, MMN was positively correlated with age and negatively correlated with left hippocampal and right pars opercularis volumes. The association between left hippocampal volume and MMN in schizophrenia remained significant after controlling for potential confounders.ConclusionsSmaller hippocampal volume may play a role in the abnormal manifestation of MMN in schizophrenia.SignificanceThe significant association between MMN and left hippocampal volume may suggest unique neurobiological contribution of hippocampus in auditory processing in schizophrenia.
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Clinical Practice Guidelines or Clinical Research Guidelines?
Source:Clinical Neurophysiology
Author(s): Anto I. Bagić, Gregory L. Barkley, Chun Kee Chung, Xavier De Tiege, John S. Ebersole, Michael E Funke, Kyousuke Kamada, Stefan Rampp, Douglas F. Rose, William W. Sutherling
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Optimising Genomic Selection in Wheat: Effect of Marker Density, Population Size and Population Structure on Prediction Accuracy
Genomic selection applied to plant breeding enables earlier estimates of a line's performance and significant reductions in generation interval. Several factors affecting prediction accuracy should be well understood if breeders are to harness genomic selection to its full potential. We used a panel of 10,375 bread wheat (Triticum aestivum) lines genotyped with 18,101 SNP markers to investigate the effect and interaction of training set size, population structure and marker density on genomic prediction accuracy. Through assessing the effect of training set size we showed the rate at which prediction accuracy increases is slower beyond approximately 2,000 lines. The structure of the panel was assessed via principal component analysis and K-means clustering, and its effect on prediction accuracy was examined through a novel cross-validation analysis according to the K-means clusters and breeding cohorts. Here we showed that accuracy can be improved by increasing the diversity within the training set, particularly when relatedness between training and validation sets is low. The breeding cohort analysis revealed that traits with higher selection pressure (lower allelic diversity) can be more accurately predicted by including several previous cohorts in the training set. The effect of marker density and its interaction with population structure was assessed for marker subsets containing between 100 and 17,181 markers. This analysis showed that response to increased marker density is largest when using a diverse training set to predict between poorly related material. These findings represent a significant resource for plant breeders and contribute to the collective knowledge on the optimal structure of calibration panels for genomic prediction.
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Editorial Board
Publication date: August 2018
Source:International Journal of Psychophysiology, Volume 130
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International Organization of Psychophysiology
Publication date: August 2018
Source:International Journal of Psychophysiology, Volume 130
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Gliadin effect on the oxidative balance and DNA damage: An in-vitro, ex-vivo study
Gliadins are involved in gluten-related disorders and are responsible for the alteration of the cellular redox balance. It is not clear if the gliadin-related oxidative stress can induce DNA damage in enterocytes.
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Utility of Repeat Magnetic Resonance Imaging in Surgical Patients with Lumbar Stenosis without Disc Herniation
Routine use of magnetic resonance imaging (MRI) as a diagnostic tool in lumbar stenosis is becoming more prevalent due to the aging population. Currently there is no clinical guideline to clarify the utility of repeat MRI in patients with lumbar stenosis, without instability, neurological deficits, or disc herniation.
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Association between Mismatch Negativity and Voxel-Based Brain Volume in Schizophrenia
Mismatch negativity (MMN), a type of event-related potential (ERP), is generated when a discernable change occurs in a series of repetitive standard stimuli (Naatanen et al., 1978). MMN represents the pre-attentive process of auditory discrimination and is associated with the function of auditory memory and involuntary attention shifting (Naatanen et al., 1979, Javitt et al., 1995, Naatanen et al., 2007). MMN deficit is extensively observed in schizophrenia patients (Shelley et al., 1991, Javitt et al., 1993, Umbricht et al., 2005).
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Reply to “Clinical Practice Guidelines or Clinical Research Guidelines?”
We thank our esteemed clinical colleagues Bagić et al. (2018) for their interest in our paper "IFCN-endorsed practical guidelines for clinical magnetoencephalography (MEG)" (Hari et al. 2018). We hereby respectfully respond to the criticism that our paper has (1) a confusing title and (2) poorly-weighted contents.
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Clinical Practice Guidelines or Clinical Research Guidelines?
We write in regard to the recent publication, "IFCN-endorsed practical guidelines for clinical magnetoencephalography (MEG)", by Hari et al. (2018) We find the title misleading and the content, though extensive, inadequate for guidelines in "clinical magnetoencephalography", as practiced. Our concerns follow:
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Effect of noisy galvanic vestibular stimulation in community-dwelling elderly people: a randomised controlled trial
Balance disorders are a risk factor for falls in the elderly. Although noisy galvanic vestibular stimulation (nGVS) has been reported to improve balance in young people, randomised control trials targeting com...
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Increased active phase atrial contraction is related to marathon runner performance
Abstract
Purpose
Left atrial (LA) contraction is essential for left ventricular (LV) filling during exertion. We sought to evaluate the relationship of LA contraction and exercise capacity in trained athletes.
Methods
Sixteen male marathon runners were recruited and allocated into two groups according to their previous training status (≥ or < 100 km peer week). All subjects underwent a baseline cardiopulmonary test to evaluate maximal aerobic capacity and a transthoracic echocardiography previous and immediate post-marathon. LA contractile function evaluation was accomplished by measuring the negative deformation of the post P wave strain curve (LASa). LASa change was defined as LASa pre-marathon minus LASa immediate post-marathon.
Results
Mean age was 39 ± 6 years. LA volume index (39 ± 13 vs. 31 ± 5 mL/m2, p = 0.04), LV mass index (91 ± 21 vs. 73 ± 12 g/m2, p = 0.04), VO2 max (59 ± 3 vs. 50 ± 8 mL/kg/min, p = 0.036) were higher in more intensive trained group and marathon time was lower (185 ± 14 vs. 219 ± 24 min, p = 0.017). An increase in LASa after immediate post-marathon was observed in both groups, which was significantly greater in the highly trained group (18.9 ± 5.8 vs. 6.3 ± 3.5%, p < 0.003). Maximum VO2 measured previous to the marathon was inversely related to marathon time and directly correlated to LASa change (rho = 0.744, p = 0.001, rho = 0.546, p = 0.028, respectively).
Conclusions
Athletes with more intensive training load have larger LV mass and LA size. An increase in LA contraction was seen post-marathon, which was significantly greater in the highly trained group. This increase in the LA contraction was related to the maximum VO2 measured previous to the marathon and to performance in a highly demanding test.
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Presence of artificial radionuclides in samples from potable water and wastewater treatment plants
Publication date: December 2018
Source:Journal of Environmental Radioactivity, Volume 192
Author(s): J. Martínez, A. Peñalver, T. Baciu, M. Artigues, M. Danús, C. Aguilar, F. Borrull
Human activity, such as the operation of nuclear power plants (NPPs) and the use of radionuclides in nuclear medicine, results in the presence of artificial radionuclides in surface waters, which may even reach potable water treatment plants (PWTPs) and wastewater treatment plants (WWTPs).In this study, water and sludge samples from a PWTP are radiologically monitored. The incoming water of the plant is influenced by the presence of an NPP upstream. Two WWTPs receiving wastewater from medical centres and other origins are also studied. As a result, 131I, 60Co and 137Cs have been determined in the dewatered sludge samples from the PWTP, while 131I, 99mTc, 67Ga and 111In were detected in the sludge samples from the WWTPs. The radionuclide activities in the influent water from the WWTPs studied were lower than the minimum detectable activity values. Therefore, on the basis of our results, the analysis of sludge samples is very useful as it enables the concentration of any radionuclides that may be present in the incoming water.Lastly, as higher activity of 131I was detected in the samples studied, the total effective dose was assessed for WWTP workers, as they handle dewatered sludge containing this radionuclide. It can be concluded that there is no risk in terms of total exposure.
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A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment
Abstract
Hereditary hearing impairment is a common sensory disorder that is genetically and phenotypically heterogeneous. In this study, we used a homozygosity mapping and exome sequencing strategy to study a consanguineous Pakistani family with autosomal recessive severe-to-profound hearing impairment. This led to the identification of a missense variant (p.Ile369Thr) in the LMX1A gene affecting a conserved residue in the C-terminus of the protein, which was predicted damaging by an in silico bioinformatics analysis. The p.Ile369Thr variant disrupts several C-terminal and homeodomain residue interactions, including an interaction with homeodomain residue p.Val241 that was previously found to be involved in autosomal dominant progressive HI. LIM-homeodomain factor Lmx1a is expressed in the inner ear through development, shows a progressive restriction to non-sensory epithelia, and is important in the separation of the sensory and non-sensory domains in the inner ear. Homozygous Lmx1a mutant mice (Dreher) are deaf with dysmorphic ears with an abnormal morphogenesis and fused and misshapen sensory organs; however, computed tomography performed on a hearing-impaired family member did not reveal any cochleovestibular malformations. Our results suggest that LMX1A is involved in both human autosomal recessive and dominant sensorineural hearing impairment.
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Craig Emery Tenke, 1950–2017
Craig Emery Tenke, born October 19, 1950, passed away unexpectedly on December 19, 2017, at the age of 67. Craig, having worked as a senior neuroscientist and dedicated electrophysiologist at New York State Psychiatric Institute (NYSPI) and Columbia University for many years, was at the prime of his career and in keen pursuit of new challenges. He served as an Associate Editor for Clinical Neurophysiology from 2008 to 2016, and as a member of the Editorial Board from 2003 to 2008.
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Population analysis of Magnaporthe oryzae by using endogenous repetitive DNA sequences and mating-type alleles in different districts of Karnataka, India
Abstract
Rice is the staple food crop of more than 60% of the population of the world. This crop suffers from blast disease caused by Magnaporthe oryzae. Information on the mating-type allele distribution and diversity of the pathogen population for the state of Karnataka, India is scanty. With this background, a total of 72 isolates of M. oryzae from rice in different districts of Karnataka were examined for identifying sexual mating alleles MAT1, MAT2 and understanding the genetic diversity based on DNA fingerprint of pot2, an inverted repeat transposon. Among 72 isolates, 44 isolates belonged to MAT1 type (male fertile) and 28 isolates were of MAT2 (female fertile) and there were no hermaphrodite isolates. In a given geographical location, only one mating type was identified. Results revealed that the isolates obtained from these regions are not sexually fertile showing predominant asexual reproduction. Hence, genetic variation observed in the pathogen may be mainly because of high copy number of transposons. A high copy number transposon, namely Pot2, was selected in our study to detect genetic diversity of the pathogen. Pot2 rep-PCR DNA fingerprinting profile showed 27 polymorphic bands with bands ranging in size from 0.65 to 4.0 kb and an average of 10 to 14 bands per isolate. Five distinct clusters were formed with two major, two minor, and one outlier. Clusters 4 and 5 are further subdivided into three sub-clusters. Some of the isolates belonging to clusters 3, 4, and 5 are interlinked as these locations are close to one another sharing common geographical parameters and boundaries. This knowledge on the sexual behavior and genetic diversity of M. oryzae is important with respect to breeding for disease resistance.
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