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re are few other options for collecting these data in an ultra-rare setting.

Adolescence is a critical time for brain development. Findings from previous studies have been inconsistent, failing to distinguish the influence of pubertal status and aging on brain maturation. The current study sought to address these inconsistencies, addressing the trajectories of pubertal development and aging by longitudinally tracking structural brain development during adolescence.

Two cohorts of healthy children were recruited (cohort 1 9-10years old; cohort 2 12-13years old at baseline). MRI data were acquired for gray matter volume and white matter tract measures. To determine whether age, pubertal status, both or their interaction best modelled longitudinal data, we compared four multi-level linear regression models to the null model (general brain growth indexed by total segmented volume) using Bayesian model selection.

Data were collected at baseline (n = 116), 12months (n = 97) and 24months (n = 84) after baseline. Findings demonstrated that the development of most regional gray matter voume and white matter tract measures, we found age to best predict longitudinal changes. Further longitudinal studies investigating the differential influence of puberty status and age on brain development in more diverse samples are needed to replicate the present results and address mechanisms underlying norm-variants in brain development.Dissemination of antibiotic-resistant genes (ARGs) from hospital wastewaters (HWWs) is facilitated by the horizontal gene transfer (HGT) and involves association of ARGs with mobile genetic elements (MGEs). In our previous study, HWWs were found to have relatively high copy numbers of ARGs aadA, tetA, cmlA, sul1, and qnrS. In this study, therefore, the same HWWs were also monitored for 3 MGEs class 1 integron (intI1), insertion sequence common region 1 (ISCR1) and conjugative transposon Tn916/Tn1545 by using quantitative polymerase chain reaction. The gene intI1 with 7.4 × 102 average copy number/mL was found to be the most prevalent MGE and was up to two orders of magnitude higher than ISCR1 (5.5 × 100 average copy number/mL, p  less then  0.05) and Tn916/Tn1545 (2.3 × 100 average copy number/mL, p  less then  0.05) in all HWWs tested. Positive correlation between intI1 and the aadA, tetA, cmlA and sul1 genes indicated that the MGEs harbouring class1 integron most likely played major role in co-selecting all these ARGs together.The application of Sb, Pt and Hg in the development of new strategic technologies has increased significantly in recent years. This study evaluates the impact of vehicular traffic on the rise in emission of Sb, Pt and Hg in the atmospheric environmen of Mexico City and their correlation to Co, Cr, Cu, Ni, Pb, V and Zn. Ficus benjamina leaves were collected as biomonitor of atmospheric metals deposited in areas exposed to heavy vehicular traffic. High enrichment factor values (metal(loid) concentration/background values) were calculated 146 (Sb), 52.8 (Pb), 29.7 (Pt) and 25.1 (Cr). Enrichment factors of Ni, Zn, Co, V, Cu and Hg decrease in that order and are less then 10. Principal component analysis allows recognize that most of the analyzed metal(loids) are related to traffic sources; Ni and Cr are also attributable to an additional anthropogenic source. No relationship was found relating Pb to vehicular sources.The effects of potassium bromate (KBrO3), sodium bromate (NaBrO3), and potassium bromide (KBr) on the sexual reproduction of the rotifer Brachionus calyciflorus were studied by 2-d population growth, 4-d sexual reproduction, and 7-d resting egg production tests. The results showed that low concentrations of bromate promote 2-d and 4-d rotifer population growth, while high concentrations limit it. Bromate stress significantly affected parameters of rotifer sexual reproduction, including the ratio of mictic to amictic females, the mictic rate of rotifers, and the fertilization rate of mictic females. KBrO3 at 0.001, 0.01, 1, and 10 mg/L, NaBrO3 at 1 and 10 mg/L, and KBr at 100 and 200 mg/L significantly increased resting egg production, while KBrO3 at 100 and 200 mg/L, and NaBrO3 at 200 mg/L significantly decreased it. Resting egg production appears to provide a sensitive endpoint in evaluating the effect of bromate on rotifer sexual reproduction.

In metastatic breast cancer (MBC) population treated with capecitabine monotherapy, we investigated clinical-pathological features as possible biomarkers for the oncological outcome.

Retrospective study of consecutive MBC patients treated at University Hospitals Leuven starting capecitabine between 1999 and 2017. The primary endpoint was the durable response (DR), defined as non-progressive disease for > 52weeks. Other main endpoints were objective response rate (ORR), time to progression (TTP) and overall survival (OS).

We included 506 patients; mean age at primary breast cancer diagnosis was 51.2years; 18.2% had de novo MBC; 98.8% were pre-treated with taxanes and/or anthracycline. DR was reached in 11.6%. Patients with DR, as compared to those without DR, were more likely oestrogen receptor (ER) positive (91.5% vs. 76.8%, p = 0.010) at first diagnosis, had a lower incidence of lymph node (LN) involvement (35.6% vs. 49.9%, p = 0.039) before starting capecitabine, were more likely to present with metastases limited to ≤ 2 involved sites (54.2% vs. 38.5%, p = 0.020) and time from metastasis to start of capecitabine was longer (mean 3.5 vs. 2.7years, p = 0.020). see more ORR was 22%. Median TTP and OS were 28 and 58weeks, respectively. In multivariate analysis (only performed for TTP), ER positivity (hazard ratio (HR) = 0.529, p < 0.0001), HER2 negativity (HR = 0.582, p = 0.024), absence of LN (HR = 0.751, p = 0.008) and liver involvement (HR = 0.746, p = 0.013), older age at capecitabine start (HR = 0.925, p < 0.0001) and younger age at diagnosis of MBC (HR = 0.935, p = 0.001) were significant features of longer TTP.

Our data display relevant clinical-pathological features associated with DR and TTP in patients receiving capecitabine monotherapy for MBC.

Our data display relevant clinical-pathological features associated with DR and TTP in patients receiving capecitabine monotherapy for MBC.