Unravelling the association between accelerometer-derived physical activity and adiposity among preschool children:A systematic review and meta-analyses

Evidence on the association between physical activity (PA) and adiposity in young children is inconclusive. A systematic review and meta-analyses were conducted to examine associations between accelerometer-derived PA and varying adiposity outcomes in preschool children. Searches were conducted in Embase, MEDLINE and Web of Science to identify studies on the association between total PA, sedentary behaviour or different PA intensities and adiposity in children aged 2 to 7 years. Separate random effects meta-analyses were performed for varying PA intensities and adiposity outcomes. Fifty-six articles were included in the review and 48 in the meta-analyses. There was substantial evidence of an inverse association between moderate-to-vigorous- or vigorous PA and body fat percentage (stdβ [SE] = −0.162[0.041]; 5 studies), weight status (r = −0.120, P<.001; 11 studies), fat mass (stdβ [SE] = −0.103[0.051]; 5 studies), fat mass index (stdβ [SE] = −0.121[0.036]; 2 studies) and skinfold thickness (stdβ [SE] = −0.145[0.036]; 4 studies). However, total PA, sedentary behaviour, and different PA intensities were not associated with body mass index (BMI) or waist circumference. Adiposity levels were lower among preschool children engaged in more (moderate-to-) vigorous PA compared with their peers, but no associations between PA and BMI or waist circumference were found

Complete Next to Leading Order QCD Corrections to the Photon Structure Functions F2γ(x,Q2)F^\gamma_2(x,Q^2) and FLγ(x,Q2)F_L^\gamma(x,Q^2)

We present the complete NLO QCD analysis of the photon structure functions $F_2^\gamma(x,Q^2)$ and $F_L^\gamma(x,Q^2)$ for a real photon target. In particular we study the heavy flavor content of the structure functions which is due to two different production mechanisms, namely collisions of a virtual photon with a real photon, and with a parton. We observe that the charm contributions are noticeable for $F_2^\gamma(x,Q^2)$ as well as $F_L^\gamma(x,Q^2)$ in the x-region studied.Comment: Latex 34 pages, 24 figures, uuencoded, attached at end, ITP-SB-93-46, FERMILAB-Pub-93/240-T, SMU HEP 93-1

Aeroallergen sensitisation for detecting asthma in primary care:a diagnostic test accuracy study

peer reviewe

Prevalence of Asthma Characteristics in COPD Patients in a Dutch Well-Established Asthma/COPD Service for Primary Care

Purpose: Primary care COPD guidelines indicate that COPD patients with asthma characteristics should be treated as having asthma. This study aims to describe the prevalence of asthma characteristics in patients with a pulmonologist-confirmed working diagnosis of COPD or ACO. Patients and Methods: This retrospective cross-sectional study used real-life data (collected between 2007 and 2017) from a Dutch asthma/COPD-service, a structured web-based system in which pulmonologists support general practitioners in their diagnosis of patients with suspicion of obstructive lung disease. The prevalence of asthma characteristics (history of asthma, atopy, symptoms, and reversibility) and blood eosinophil (Eos) counts were assessed in patients with a working diagnosis of COPD or ACO. Results: Of the 14,141 patients, ≥40 years in the dataset, 4475 (31.6%) were diagnosed with asthma, 3532 (25.0%) with COPD, and 1276 (9.0%) with ACO. Asthma characteristics were present in 65.6% (n=1956) of the COPD and 90.9% (n=1059) of the ACO patients. Eos counts of ≥ 300 cells per μL were found in 35.7% (n=924) of the COPD patients and 35.3% (n=341) of the ACO patients. Conclusion: In this group of COPD and ACO patients remotely diagnosed by pulmonologists, a substantial proportion would be considered to have asthma characteristics according to the guidelines. This may explain the high number of inhaled corticosteroid (ICS) prescriptions found in primary care COPD patients. Prospective studies are necessary to identify patients who may or may not benefit from ICS containing treatment. Hence, personalized care in primary care can be optimized

Lipase active site covalent anchoring of Rh(NHC) catalysts: Towards chemoselective artificial metalloenzymes

A Rh(NHC) phosphonate complex reacts with the lipases cutinase and Candida antarctica lipase B resulting in the first (soluble) artificial metalloenzymes formed by covalent active site-directed hybridization. When compared to unsupported complexes, these new robust hybrids show enhanced chemoselectivity in the (competitive) hydrogenation of olefins over ketones. This journal i

Charm quark and D^* cross sections in deeply inelastic scattering at DESY HERA

A next-to-leading order Monte Carlo program for the calculation of heavy quark cross sections in deeply inelastic scattering is described. Concentrating on charm quark and D^*(2010) production at HERA, several distributions are presented and their variation with respect to charm quark mass, parton distribution set, and renormalization-factorization scale is studied.Comment: 15 pages including 8 figures. Uses Latex, Revtex, and psfig. References added - others updated. Several sentences/words added for clarity. Results/conclusions unchanged. To appear in Phys. Rev.

Twist-2 Heavy Flavor Contributions to the Structure Function g2(x,Q2)g_2(x,Q^2)

The twist--2 heavy flavor contributions to the polarized structure function $g_2(x,Q^2)$ are calculated. We show that this part of $g_2(x,Q^2)$ is related to the heavy flavor contribution to $g_1(x,Q^2)$ by the Wandzura--Wilczek relation to all orders in the strong coupling constant. Numerical results are presented.Comment: 17 pages LATEX, 1 style files, 4 figure

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies.

BACKGROUND: The phenotypic severity of congenital muscular dystrophy-dystroglycanopathy (MDDG) syndromes associated with aberrant glycosylation of α-dystroglycan ranges from the severe Walker-Warburg syndrome or muscle-eye-brain disease to mild, late-onset, isolated limb-girdle muscular dystrophy without neural involvement. However, muscular dystrophy is invariably found across the spectrum of MDDG patients. METHODS: Using linkage mapping and whole-exome sequencing in two families with an unexplained neurodevelopmental disorder, we have identified homozygous and compound heterozygous mutations in B3GALNT2. RESULTS: The first family comprises two brothers of Dutch non-consanguineous parents presenting with mild ID and behavioral problems. Immunohistochemical analysis of muscle biopsy revealed no significant aberrations, in line with the absence of a muscular phenotype in the affected siblings. The second family includes five affected individuals from an Iranian consanguineous kindred with mild-to-moderate intellectual disability (ID) and epilepsy without any notable neuroimaging, muscle, or eye abnormalities. Complementation assays of the compound heterozygous mutations identified in the two brothers had a comparable effect on the O-glycosylation of α-dystroglycan as previously reported mutations that are associated with severe muscular phenotypes. CONCLUSIONS: In conclusion, we show that mutations in B3GALNT2 can give rise to a novel MDDG syndrome presentation, characterized by ID associated variably with seizure, but without any apparent muscular involvement. Importantly, B3GALNT2 activity does not fully correlate with the severity of the phenotype as assessed by the complementation assay