Ingramnissen3697

In visual search, the internal representation of the target feature is referred to as the attentional template. The attentional template can be broad or precise depending on the task requirements. In singleton search, the attentional template is broad because the target is the only colored element in the display. In feature search, a precise attentional template is required because the target is in a specific color in an array of varied colors. To measure the precision of the attentional template, we used a cue-target paradigm where cueing benefits decrease when the cue color differs from the target color. Consistent with broad and precise attentional templates, the decrease of cueing effects was stronger in feature than in singleton search. Measurements of ERPs showed that the N2pc elicited by the cue decreased with increasing color difference, suggesting that attention was more strongly captured by cues that were similar to the target. However, the cue-elicited N2pc did not differ between feature and singleton search, making it unlikely to reflect the mechanism underlying attentional template precision. Furthermore, there was no evidence for attentional suppression as there was no cue-elicited PD, even in conditions where the cueing benefit turned into a same-location cost. However, an index of signal enhancement, the contralateral positivity, reflected attention template precision. In general, there was sensory enhancement of the stimulus appearing at the cued location in the search display. With broad attentional templates, any stimulus at the cued location was enhanced, whereas enhancement was restricted to target-matching colors with precise attentional templates.

The long-term effect of low and moderate doses of ionizing radiation on the lens is still a matter of debate and needs to be evaluated in more detail.

We conducted a detailed histological analysis of eyes from B6C3F1 mice cohorts after acute gamma irradiation (

Co source; 0.063 Gy/min) at young adult age of 10 weeks with doses of 0.063, 0.125, and 0.5 Gy. Sham irradiated (0 Gy) mice were used as controls. To test for genetic susceptibility heterozygous

mutant mice were used and compared to wild-type mice of the same strain background. Mice of both sexes were included in all cohorts. Eyes were collected 4 h, 12, 18 and 24 months after irradiation. For a better understanding of the underlying mechanisms, metabolomics analyses were performed in lenses and plasma samples of the same mouse cohorts at 4 and 12 h as well as 12, 18 and 24 months after irradiation. For this purpose, a targeted analysis was chosen.

This analysis revealed histological changes particularly in the posterior part of the lens that rarely can be observed by using Scheimpflug imaging, as we reported previously. We detected a significant increase of posterior subcapsular cataracts (PSCs) 18 and 24 months after irradiation with 0.5 Gy (odds ratio 9.3; 95% confidence interval 2.1-41.3) independent of sex and genotype. Doses below 0.5 Gy (i.e. 0.063 and 0.125 Gy) did not significantly increase the frequency of PSCs at any time point. In lenses, we observed a clear effect of sex and aging but not of irradiation or genotype. While metabolomics analyses of plasma from the same mice showed only a sex effect.

This article demonstrates a significant radiation-induced increase in the incidence of PSCs, which could not be identified using Scheimpflug imaging as the only diagnostic tool.

This article demonstrates a significant radiation-induced increase in the incidence of PSCs, which could not be identified using Scheimpflug imaging as the only diagnostic tool.Background Quality of life in adenomyosis (AD) patients has been poorly investigated. BAY-1895344 Previous data suggest that AD has negative impact on the quality of life in these women. Materials and Methods From September 2018 to December 2019, all consecutive female premenopausal patients aged ≥18 years diagnosed with AD by transvaginal ultrasound (TVU) were invited to participate in a comparative cross-sectional study. The Short Form-36-item (SF-36) health questionnaire and the Hospital Anxiety and Depression Scale (HADS) were administered. Work productivity and activity impairment were assessed using the Work Productivity and Activity Impairment Questionnaire General Health version (WPAIGH). Data obtained from these patients were compared with women with normal-appearing myometrium in the TVU recruited during routine gynecological visits. The study was approved by the Clinical Research Ethics Committee of the Hospital Clinic (reference HCB/2018/0919). Results One hundred three patients with AD and 214 without AD were analyzed. Patients with AD compared to those without AD showed significantly lower scores in all domains of the SF-36 questionnaire and mean (SD) higher scores in the HADS questionnaire for anxiety (10.06 [3.04] vs. 6.92 [2.98], p  less then  0.001) and depression (6.39 [3.89] vs. 2.74 [2.01], p  less then  0.002). Significant differences (p  less then  0.001) were also found for the percentages of absenteeism (12.2% vs. 1.1%), presenteeism (31.1% vs. 11.4%), overall work productivity loss (38.2% vs. 12.4%), and activity impairment (55.7% vs. 9.9%). The presence of AD was associated with higher yearly estimated indirect costs of €5161.32 (€7928.0 vs. €2460.8, p  less then  0.001). Conclusions AD negatively affects women's health-related quality of life, psychological health, and work productivity, with impairment at work and daily activities, and higher risk for anxiety and depression.

Human endogenous retrovirus (HERV) expression in multiple sclerosis (MS) brain lesions may contribute to chronic inflammation, but expression of genome-wide HERVs in different MS lesions is unknown.

We examined the HERV expression landscape in different MS lesions compared to control brains.

Transcripts from 71 MS brain samples and 25 control WM were obtained by next-generation RNA sequencing and mapped against HERV transcripts across the human genome. Differential expression of mapped HERV-W and HERV-H reads between MS lesion types and controls was analysed.

Out of 6.38 billion high-quality paired end reads, 174 million reads (2.73%) mapped to HERV transcripts. There was no difference in HERVs expression level between MS and control brains, but HERV-W transcripts were significantly reduced in chronic active lesions. Of the four HERV-W transcripts exclusively present in MS, ERV3633503 located on chromosome 7q21.13 close to the MS genetic risk locus had the highest number of reads. In the HERV-H family, 75% of transcripts located to nearby 7q21-22 were overrepresented in MS, and ERV3643914 was expressed more than 16 times in MS compared to control brains.