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Objective: To investigate how identifying factors associated with peripartum and postpartum intimate partner violence (IPV) may facilitate prioritizing women for psychosocial support. Methods: Pregnant women in Kenya were asked about IPV by their current partner at baseline (screening), during pregnancy and at 6 weeks and 6 months postpartum. IPV was defined as being physically hurt or forced to participate in sexual activities or being threatened or frightened by a partner. Results: A total of 502 women (11.8% HIV‐positive) enrolled during pregnancy and were successfully followed for 6 months postpartum, 430 (85.7%) reported never experiencing IPV, 32 (6.4%) reported IPV at least once in their lifetime but not in the past 6 months, and 31 (6.2%) reported IPV in the past 6 months but not in the past month. During pregnancy and postpartum, 61 (12.2%) reported incident IPV. Women who at baseline reported IPV in the past 6 months were at 2.7‐fold higher odds of experiencing IPV peripartum and postpartum (odds ratio 2.77; 95% confidence interval 1.17–6.53; P = 0.020) compared with women who had never experienced IPV. This association remained significant in multivariable analysis. Conclusion: Screening for recent IPV during antenatal care visits may be an effective means to identify women at highest risk of IPV and offer targeted prevention interventions. Screening for recent IPV during antenatal care may be an effective means to identify women at risk of IPV and offer targeted IPV prevention interventions. [ABSTRACT FROM AUTHOR]

Prostate cancer (PCa) is a very complex disease that is a major cause of death in men worldwide. Currently, PCa dependence on the androgen receptor (AR) has resulted in use of AR antagonists and antiandrogen therapies that reduce endogenous steroid hormone production. However, within two to three years of receiving first‐line androgen deprivation therapy, the majority of patients diagnosed with PCa progress to castration‐resistant prostate cancer (CRPC). There is an urgent need for therapies that are more durable than antagonism of the AR axis. Studies of runt‐related transcription factors (RUNX) and their heterodimerization partner, core‐binding factor subunit b (CBFβ), are revealing that the RUNX family are drivers of CRPC. In this review, we describe what is presently understood about RUNX members in PCa, including what regulates and is regulated by RUNX proteins, and the role of RUNX proteins in the tumor microenvironment and AR signaling. We discuss the implications for therapeutically targeting RUNX, the potential for RUNX as PCa biomarkers, and the current pressing questions in the field. [ABSTRACT FROM AUTHOR]

Premise: Herbaria are invaluable sources for understanding the natural world, and in recent years there has been a concerted effort to digitize these collections. To organize such efforts, a method for estimating the necessary labor is desired. This work analyzes digitization productivity reports of 105 participants from eight herbaria, deriving generalized labor estimates that account for human experience. Methods and Results: Individuals' rates of digitization were grouped based on cumulative time performing each task and then used to estimate a series of generalized labor projection models. In most cases, productivity was shown to improve with experience, suggesting longer technician retention can reduce labor requirements by 20%. Conclusions: Using student labor is a common tactic for digitization efforts, and the resulting outreach exposes future professionals to natural history collections. However, overcoming the learning curve should be considered when estimating the labor necessary to digitize a collection. [ABSTRACT FROM AUTHOR]

The article presents physiological form of depolarization during right ventricular (RV) pacing, a method of resynchronization therapy for bundle branch blocks, for pacing in advanced AV block and infranodal disease. Topic include present the case of a patient with permanent HB pacing with lead implanted proximal to the site of block, who subsequently lost HB pacing because of the progression of his‐purkinje disease.

Abstract: Background: This study aimed to describe parental perceptions of the causes of autism spectrum disorder (ASD) in an ethnically diverse sample and explore whether these perceptions relate to treatment choices. Methods: The sample consisted of White (n = 224), Hispanic (n = 85), and Asian (n = 21) mothers of a child with ASD. A mixed methods approach was used in this secondary analysis focusing on parental perceptions about the causes of ASD and the relationship of these to utilization of services and treatment. Results: Environmental and genetic factors were most often believed to be the cause or one of the causes of ASD by mothers across all ethnic groups studied. Asian mothers were more likely to cite multiple causes. Environmental causes were associated with receiving 20 or more hours of autism‐related services per week, whereas belief in environmental exposures and vaccines and medications as causes were associated with complementary–alternative medicine (CAM) use. Conclusion: Our findings suggest that ethnic differences in autism causal beliefs and treatment choices may exist. Future research should be conducted to specifically confirm the findings, to understand parental motivation behind their service and treatment choices, and to gain more insight into the types, usage, and sources of CAM treatments. Clinicians can use parental autism causal beliefs in discussions about treatment recommendations. [ABSTRACT FROM AUTHOR]

The complexity of neurodevelopment, the rapidity of early neurogenesis, and over 100 years of research identifying environmental influences on neurodevelopment serve as backdrop to understanding factors that influence risk and severity of autism spectrum disorder (ASD). This Keynote Lecture, delivered at the May 2016 annual meeting of the International Society for Autism Research, describes concepts of causation, outlines the trajectory of research on nongenetic factors beginning in the 1960s, and briefly reviews the current state of this science. Causal concepts are introduced, including root causes; pitfalls in interpreting time trends as clues to etiologic factors; susceptible time windows for exposure; and implications of a multi‐factorial model of ASD. An historical background presents early research into the origins of ASD. The epidemiologic literature from the last fifteen years is briefly but critically reviewed for potential roles of, for example, air pollution, pesticides, plastics, prenatal vitamins, lifestyle and family factors, and maternal obstetric and metabolic conditions during her pregnancy. Three examples from the case‐control CHildhood Autism Risks from Genes and the Environment Study are probed to illustrate methodological approaches to central challenges in observational studies: capturing environmental exposure; causal inference when a randomized controlled clinical trial is either unethical or infeasible; and the integration of genetic, epigenetic, and environmental influences on development. We conclude with reflections on future directions, including exposomics, new technologies, the microbiome, gene‐by‐environment interaction in the era of –omics, and epigenetics as the interface of those two. As the environment is malleable, this research advances the goal of a productive and fulfilling life for all children, teen‐agers and adults. Autism Res2018, 11: 554–586. © 2018 International Society for Autism Research, Wiley Periodicals, Inc. Lay Summary: This Keynote Lecture, delivered at the 2016 meeting of the International Society for Autism Research, discusses evidence from human epidemiologic studies of prenatal factors contributing to autism, such as pesticides, maternal nutrition and her health. There is no single cause for autism. Examples highlight the features of a high‐quality epidemiology study, and what comprises a compelling case for causation. Emergent research directions hold promise for identifying potential interventions to reduce disabilities, enhance giftedness, and improve lives of those with ASD. [ABSTRACT FROM AUTHOR]

Fragile histidine triad protein (Fhit) is a protein which primarily hydrolyses dinucleoside polyphosphates. To investigate possible interactions between the protein and a substrate, we used a nonhydrolyzable phosphorothioate analog of Ap4A, containing 5-bromo-2′-deoxyuridine instead of one adenosine residue. Photocrosslinking, followed by LC- MS experiments, determined a complex in which the probe was covalently linked to the NDSIYEELQK peptide (residues 110-119). The peptide was located within the 'disordered' region, which is invisible in the known crystal structures of Fhit. This invisible and flexible part seems to play a role in the stabilization of the Fhit-substrate complex, which may be important for its tumor suppressor activity. [ABSTRACT FROM AUTHOR]

Approximately 23% of mothers of children with autism spectrum disorder (ASD) produce specific patterns of autoantibodies to fetal brain proteins that have been detected in only 1% of mothers of typically developing children. The biological mechanisms underlying the development of ASD-specific maternal autoantibodies are poorly understood. We sought to determine whether ASD-specific maternal autoantibodies identified postnatally were associated with metabolic conditions (MCs) during gestation. Participants were 227 mothers of 2-5 year old children with confirmed ASD, enrolled in CHARGE (Childhood Autism Risk from Genetics and the Environment) between January 2003 and April 2008, and from whom blood samples were collected and analyzed for anti-fetal brain autoantibodies (Ab+). MCs included diabetes, hypertensive disorders, and prepregnancy obesity or overweight, ascertained from medical records or structured telephone interviews. Log-linear regression models were performed to estimate prevalence ratios and 95% confidence intervals (CI) based on robust standard errors. Fifty-six (25%) mothers were Ab+. Ab+ prevalence was higher among mothers with diabetes, hypertensive disorders, or overweight compared to healthy mothers, but differences were not statistically significant. In a subset of 145 mothers whose children exhibited severe ASD (31 Ab+), those diagnosed with type 2 or gestational diabetes were 2.7-fold more likely to be Ab+ (95% CI 1.1, 6.6), controlling for delivery payer and smoking. Gestational diabetes specifically was associated with a 3.2-fold increased Ab+ prevalence (95% CI 1.2, 8.6). In this exploratory study, mothers whose children had severe ASD and who experienced diabetes were more likely to have anti-fetal brain autoantibodies 2-5 years later. Autism Res 2017, 10: 89-98. © 2016 International Society for Autism Research, Wiley Periodicals, Inc. [ABSTRACT FROM AUTHOR]

To cite this article: Stelmach I, Podlecka D, Majak P, Jerzyńska J, Stelmach R, Janas A, Krakowiak J, Stelmach W. Validity of the Pediatric Asthma Quality of Life Questionnaire in Polish children. Pediatric Allergy Immunology 2011; 22: 660-666. Abstract Background: Although the Pediatric Asthma Quality of Life Questionnaire (PAQLQ) was translated for use in Polish asthmatic children, it is necessary to confirm that its validity, reliability, and the accuracy of the responses are not influenced by culture difference. Therefore, the objective of this study was to validate the Polish version of the Pediatric Asthma Quality of Life Questionnaire. Methods: This was a 9-week period cohort study. The patients were interviewed using the PAQLQ on four occasions: at baseline, 1 wk after inclusion, and after 5 and 9 wk. At each clinic visit, lung functions test and NO measurements were performed. Asthma control (according to GINA) was assessed throughout the study. Results: One hundred and one patients completed the study. At all visits, moderate correlations (from r = −0.51 to −0.68) between all PAQLQ domains and the asthma diary were observed. We noticed a significant improvement in the understanding of the questions during the last visit compared to baseline. The gradient of correlation coefficients between the symptoms domain of PAQLQ and asthma diary was observed across study visits. The standards of reliability defined by Cronbach's α-coefficient (from 0.75 to 0.91) were fulfilled in all domains of the questionnaire, at all visits. We found a higher increase in PAQLQ score in patients who obtained asthma control compared to those who lost control during the study. There was no relation between PAQLQ and FeNO. At all visits, moderate correlations (from r = −0.51 to −0.68) were shown between all PAQLQ domains and the asthma diary. Conclusions: We showed that Polish version of PAQLQ is valid and reliable among our study group. Moreover, as far as clinical practice is concerned, PAQLQ seems to be a useful tool for monitoring asthma in children especially based on the physician's grading of asthma severity according to GINA guidelines. [ABSTRACT FROM AUTHOR]

Despite the omnipresence of clay brick as construction material since thousands of years, fundamental knowledge about the link between composition, microstructure, and mechanical performance is still scarce. In this paper, we use a variety of advanced techniques of experimental mechanics and material characterization for extruded clay brick for masonry, that range from scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy, mercury intrusion porosimetry, to instrumented nanoindentation and macroscopic strength and durability tests. We find that extruded clay brick possesses a hierarchical microstructure: depending on the firing temperature, a 'glassy' matrix phase, which manifests itself at submicrometer scales in form of neo-crystals of mullite, spinel-type phase, and other accessory minerals, forms either a granular or a continuum matrix phase that hosts at submillimeter scale the porosity. This porous composite forms the backbone for macroscopic material performance of extruded brick, including anisotropic strength, elasticity, and water absorption behavior. [ABSTRACT FROM AUTHOR]

The article presents information on a research study which examines the ability of histidine triad nucleotide-binding protein 1 (HINT1) to bind various nucleotides and diadenosine polyphosphates. It describes HINT1 as playing an essential frole in myriad biological processes and can be found in many species. It reports on the first complete structure of HINT1-adenosine complex of a rabbit.

Pennuto CM, Krakowiak PJ, Janik CE. Seasonal abundance, diet, and energy consumption of round gobies ( Neogobius melanostomus) in Lake Erie tributary streams. Ecology of Freshwater Fish 2010: 19: 206–215. © 2010 John Wiley & Sons A/S The invasive round goby ( Neogobius melanostomus) is a benthic invertivore that has become established in many lake and river systems of Europe and the United States, especially within the Great Lakes basin. Multiple reports document its negative impact on benthic macroinvertebrates and fishes in lakes and recent studies show fish and invertebrate communities in streams are equally at risk. We assessed the seasonal abundance of round gobies and their summer diet composition in tributary streams to Lake Erie. Populations of round gobies in the lower reaches of two tributary streams peaked in abundance in early fall, were absent in late winter, and reappeared in early spring, suggesting a possible out-migration to the lake in winter. Population size distributions show a peak recruitment of young round gobies in July and low-level recruitment through October. In this study, round gobies obtained most of their energy from amphipods, chironomids, and caddisflies compared to other invertebrates, and midges were consumed in greater proportion than their availability suggesting a preference for these prey. As the stream lacked molluscs, large round gobies remained generalist invertivores without a diet shift to molluscivory as has been reported in lake studies. The observations on recruitment and abundance, and possible out-migration suggest the lower reaches of tributary streams may act as source populations for lake-bound round gobies. It may be possible to take advantage of this out-migration behaviour as a control strategy to capture large numbers of round gobies each winter. [ABSTRACT FROM AUTHOR]

Background: The expression of a fragile histidine triad (FHIT) protein is lost in stomach tumors. The study aimed at determining whether FHIT expression is affected by Helicobacter pylori infection, strain virulence ( vacA and cagA genes) and histopathological changes in the gastric mucosa of patients with functional dyspepsia having first-degree relatives with gastric cancer. Materials and Methods: Eighty-eight never-smoking patients with functional dyspepsia were selected for the study, and 48 of them had first-degree relatives with gastric cancer. Bacterial DNA amplification was used to identify H. pylori colonization. The level of FHIT gene expression was determined by qRT-PCR (mRNA) and Western blot (FHIT protein) analyses. Results: For patients having first-degree relatives with gastric cancer FHIT expression was lower (mRNA by ca. 40–45% and protein by 30%) compared with the control patients ( p < .05). H. pylori infection decreased the FHIT mRNA level by 10–35% and the protein level by 10–20%. Bacterial strain vacA(+) cagA(+) lowered FHIT mRNA by ca. 30–35% in the antrum samples of both groups and in corpus samples of patients with first-degree relatives with gastric cancer ( p < .05). The FHIT mRNA level was twice as high in control H. pylori-negative patients with intestinal metaplasia, compared with those with non-atrophic gastritis. Conclusions: The decreased FHIT gene expression associated with hereditary factors and with H. pylori infection, especially with vacA(+) cagA(+)-positive strains, may be related to gastric carcinoma development. [ABSTRACT FROM AUTHOR]

Objectives: To assay if plasma antibody levels in children with autism or developmental delays (DD) differ from those with typical development as an indicator of immune function and to correlate antibody levels with severity of behavioral symptoms. Methods: Plasma was collected from children with autistic disorder (AU; n=116), DD but not autism ( n=32), autism spectrum disorder but not full autism ( n=27), and age-matched typically developing (TD) controls ( n=96). Samples were assayed for systemic levels of immunoglobulin (IgG, IgM, IgA, and IgE) by enzyme-linked immunosorbent assay. Subjects with autism were evaluated using the Autism Diagnostic Observation Schedule and the Autism Diagnostic Interview-Revised, and all subjects were scored on the Aberrant Behavior Checklist (ABC) by the parents. Numerical scores for each of the ABC subscales as well as the total scores were then correlated with Ig levels. Results: Children with AU have a significantly reduced level of plasma IgG (5.39±0.29 mg/mL) compared to the TD (7.72±0.28 mg/mL; P<0.001) and DD children (8.23±0.49 mg/mL; P<0.001). Children with autism also had a reduced level of plasma IgM (0.670.06mg/mL) compared to TD (0.79±0.05 mg/mL; P<0.05). Ig levels were negatively correlated with ABC scores for all children (IgG: r=−0.334, P<0.0001; IgM: r=−0.167, P=0.0285). Conclusion: Children with AU have significantly reduced levels of plasma IgG and IgM compared to both DD and TD controls, suggesting an underlying defect in immune function. This reduction in specific Ig levels correlates with behavioral severity, where those patients with the highest scores in the behavioral battery have the most reduced levels of IgG and IgM. [ABSTRACT FROM AUTHOR]

This study compared parent-reported sleep characteristics in 2- to 5-year-old children with autism spectrum disorders (ASD) to children with other developmental delays (DD) and typical development (TD). We included 529 children (303 ASD [167 males], 63 DD [46 males], and 163 TD [134 males]) enrolled in the CHARGE study, an ongoing population-based case–control study. The mean age of participants was 3.6 years (standard deviation, 0.8 years). ASD diagnosis was confirmed with Autism Diagnostic Interview-Revised (ADI-R) and Autism Diagnostic Observation Schedules (ADOS). Cognitive and adaptive functioning was assessed using Mullen Scales of Early Learning (MSEL) and Vineland Adaptive Behavior Scales (VABS), respectively. Demographic, medical and sleep history information were ascertained from California birth records, telephone interview, medical assessments at clinic visit, and parent-administered questionnaires. Fifty-three percent of children with ASD had at least one frequent sleep problem, followed by 46% of children with DD, and 32% of the TD group ( P < 0.0001). Exploratory factor analyses of sleep history data yielded two factors: sleep onset problems and night waking. Children with ASD had marginally higher sleep onset factor scores and significantly higher night waking factor scores compared with the TD group. Factor scores for children with DD were intermediate between the ASD and TD groups. Cognitive or adaptive development did not predict severity of sleep problems in the ASD group. [ABSTRACT FROM AUTHOR]

Background and Aim: The cytotoxic activity of Helicobacter pylori contributes significantly to the pathogenesis of gastric carcinoma. A preliminary study suggested that somatostatin receptor subtype 3 (SSTR3) might play a role in cell apoptosis and the growth of gastric cancer. The aim of the present study was to determine the influence of H. pylori infection and a family history of gastric cancer on the expression of SSTR3 in the gastric mucosa of non-cancer patients with dyspepsia. Methods: The expression of the SSTR3 gene in the gastric mucosa of the stomach antrum and corpus of 53 patients was determined by the use of quantitative reverse transcription–polymerase chain reaction. Results: The SSTR3 mRNA level was lower in the H. pylori-infected patients, as compared to the non-infected patients, independently of a family history of gastric cancer and stomach topography. The greatest decrease of approximately 40% and 35% ( P < 0.05) was observed for the antrum of the H. pylori-positive patients without and with a family history of gastric cancer, respectively. In the corpus, these differences were much smaller, regardless of a family history of gastric cancer. Interestingly, for H. pylori-negative patients, the density (at the mRNA level) of the SSTR3 receptor in the antrum was higher than in the corpus mucosa. Conclusions: A decrease in the density of SSTR3 (especially in the antrum) in individuals with H. pylori infection and particularly with a family history of gastric cancer may point to an environmental and inherited predisposition in the development of distal gastric cancer. [ABSTRACT FROM AUTHOR]

Today, mobility and persistence are important aspects of distributed computing. They have many fields of use such as load balancing, fault tolerance and dynamic reconfiguration of applications. In this context, Java provides many useful mechanisms for the mobility of code via dynamic class loading, and the mobility or persistence of data via object serialization. However, Java does not provide any mechanism for the mobility/persistence of computation (i.e. threads). We designed and implemented a new mechanism, called Java thread serialization, that is used to build thread mobility or thread persistence. Therefore, a running Java thread can, at an arbitrary state of its execution, migrate to a remote machine where it resumes its execution, or be checkpointed on disk for possible subsequent recovery. With our services, migrating a thread is simply performed by the call of our go primitive, and checkpointing/recovering a thread is performed by the call of our store and load primitives. Several projects have recently addressed the issue of Java thread serialization, e.g. Sumatra, Wasp, JavaGo, Brakes, JavaGoX, Merpati. Some of them have attempted to minimize the overhead incurred by the thread serialization mechanism on thread performance, but none of them has been able to completely avoid this overhead. We propose a generic Java thread serialization mechanism that does not impose any performance overhead on serialized threads. This is achieved thanks to the use of type inference and dynamic de-optimization techniques. In this paper, we describe the design and implementation details of our thread serialization prototype in Sun Microsystems' JDK. We report on experiments conducted with our prototype, present a comparative performance evaluation of the main thread serialization techniques, and confirm the elimination of the performance overhead with our thread serialization mechanism. Copyright © 2003 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]