Osteoarchaeological evidence for medical dissection in 18th to 19th century Aberdeen, Scotland

Open access via T&F agreement ACKNOWLEDGEMENTS: We would like to thank Police Scotland and Detective Sergeant Stephen Beattie for their initial response to the discovery, and to Jamie Grieve, Margaret Bruce and Leighanne Deboys for their assistance and expert advice in identifying the skeletal remains. Thanks to the owners of the property who allowed access. Aberdeenshire Council Archaeology Service kindly facilitated and funded the work.Peer reviewedPublisher PD

Revisiting funeral recordings during and beyond the COVID-19 pandemic in the UK

Peer reviewedPublisher PD

Hybrid funerals : how online attendance facilitates and impedes participation

This research was funded by the Economic and Social Research Council (ESRC), as part of UK Research and Innovation’s rapid response to Covid-19. Grant number: [ES/V017047/1].Peer reviewedPublisher PD

Why does funeral attendance matter? : Revisiting 'Configurational Eulogies' in light of the COVID-19 pandemic in the UK

Open Access via the Taylor & Francis Agreement Acknowledgements The authors thank Paul Kefford and Imogen Jones and two anonymous reviewers for their helpful feedback on earlier drafts of this paper. Funding This research was funded by the Economic and Social Research Council (ESRC), as part of UK Research and Innovation’s rapid response to Covid-19. Grant number: [ES/V017047/1].Peer reviewedPublisher PD

Identity and community structure in Neolithic Man Bac, Northern Vietnam

FUNDING This research was supported by JSPS fund 16H02527 and Australian Research Council grant DP0774079. ACKNOWLEDGEMENTS Many people have been involved in the excavation and post-excavation work associated with Man Bac over the years. Here we wish to pay special thanks to Nguyen Kim Dung (then of the Institute of Archaeology, Hanoi) who co-directed the excavations in 2004/5 and 2007. The following were involved in either one or several ways between 2004/5 and 2007 (facilitation of land access, excavation, post-excavation analysis, and ublication): Nguyen Hann Khang and Nguyen Cao Tan (Ninh Binh Provincial Museum, Vietnam), the landowner of Man Bac Nguyen Van Sai, the Chung Village community, Peter Bellwood and Lorna Tilley (Australian National University), Nguyen Giang Hai (former Director, Institute of Archaeology, Hanoi), Nguyen Kim Thuy, Nguyen An Tuan, Vu The Long, Tran Thi Thuy Ha, Bui Thu Phuong, Ha Manh Thang, Nguyen Ngoc Quy, Vo Thanh Huong, Nguyen Chi Tan, Nguyen Thi Mai Huong (Institute of Archaeology, Hanoi), Mariko Yamagata (Okayama Science University, Japan), Ken-ichi Shidoda (National Museum of Nature and Science, Japan), Yukio Dodo (formerly of Tohoku University, Japan), Takeji Toizumi (Meiji University, Japan), Junmei Sawada (Nigata University of Health and Welfare, Japan), Mark Lipson (Harvard Medical School, USA), Anna Willis (James Cook University, Australia). Many thanks to Jeff Oliver for reading and commenting on an earlier draft.Peer reviewedPostprin

xQSM: Quantitative Susceptibility Mapping with Octave Convolutional and Noise Regularized Neural Networks

Quantitative susceptibility mapping (QSM) is a valuable magnetic resonance imaging (MRI) contrast mechanism that has demonstrated broad clinical applications. However, the image reconstruction of QSM is challenging due to its ill-posed dipole inversion process. In this study, a new deep learning method for QSM reconstruction, namely xQSM, was designed by introducing modified state-of-the-art octave convolutional layers into the U-net backbone. The xQSM method was compared with recentlyproposed U-net-based and conventional regularizationbased methods, using peak signal to noise ratio (PSNR), structural similarity (SSIM), and region-of-interest measurements. The results from a numerical phantom, a simulated human brain, four in vivo healthy human subjects, a multiple sclerosis patient, a glioblastoma patient, as well as a healthy mouse brain showed that the xQSM led to suppressed artifacts than the conventional methods, and enhanced susceptibility contrast, particularly in the ironrich deep grey matter region, than the original U-net, consistently. The xQSM method also substantially shortened the reconstruction time from minutes using conventional iterative methods to only a few seconds.Comment: 37 pages, 10 figures, 3 tabl

Flavan-3-ol-methylxanthine interactions: Modulation of flavan-3-ol bioavailability in volunteers with a functional colon and an ileostomy

Flavan-3-ols, including the flavan-3-ol monomer (-)-epicatechin, are dietary bioactives known to mediate beneficial cardiovascular effects in humans. Recent studies showed that flavan-3-ols could interact with methylxanthines, evidenced by an increase in flavan-3-ol bioavailability with a concomitant increase in flavan-3-ol intake-mediated vascular effects. This study aimed at elucidating flavan-3-ol-methylxanthine interactions in humans in vivo by evaluating the specific contributions of theobromine and caffeine on flavan-3-ol bioavailability. In ileostomists, the effect of methylxanthines on the efflux of flavan-3-ol metabolites in the small intestine was assessed, a parameter important to an understanding of the pharmacokinetics of flavan-3-ols in humans. In a randomized, controlled, triple cross-over study in volunteers with a functional colon (n = 10), co-ingestion of flavan-3-ols and cocoa methylxanthines, mainly represented by theobromine, increased peak circulatory levels (C ) of flavan-3-ols metabolites (+21 ± 8%; p < 0.05). Conversely, caffeine did not mediate a statistically significant effect on flavan-3-ol bioavailability (C = +10 ± 8%, p = n.s.). In a subsequent randomized, controlled, double cross-over study in ileostomists (n = 10), cocoa methylxanthines did not affect circulatory levels of flavan-3-ol metabolites, suggesting potential differences in flavan-3-ol bioavailability compared to volunteers with a functional colon. The main metabolite in ileal fluid was (-)-epicatechin-3'-sulfate, however, no differences in flavan-3-ol metabolites in ileal fluid were observed after flavan-3-ol intake with and without cocoa methylxanthines. Taken together, these results demonstrate a differential effect of caffeine and theobromine in modulating flavan-3-ol bioavailability when these bioactives are co-ingested. These findings should be considered when comparing the effects mediated by the intake of flavan-3-ol-containing foods and beverages and the amount and type of methylxanthines present in the ingested matrixes. Ultimately, these insights will be of value to further optimize current dietary recommendations for flavan-3-ol intake. CLINICAL TRIAL REGISTRATION NUMBER: This work was registered at clinicaltrials.gov as NCT03526107 (study part 1, volunteers with functional colon) and NCT03765606 (study part 2, volunteers with an ileostomy). [Abstract copyright: Copyright © 2023 Elsevier Inc. All rights reserved.

Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants.

Context: Single-nucleotide polymorphisms (SNPs) in genes related to vitamin D metabolism have been associated with serum 25-hydroxyvitamin D [25(OH)D] concentration, but these relationships have not been examined following antenatal cholecalciferol supplementation. Objective: To determine whether SNPs in DHCR7, CYP2R1, CYP24A1, and GC are associated with the response to gestational cholecalciferol supplementation. Design: Within-randomization group analysis of the Maternal Vitamin D Osteoporosis Study trial of antenatal cholecalciferol supplementation. Setting: Hospital antenatal clinics. Participants: In total, 682 women of white ethnicity (351 placebo, 331 cholecalciferol) were included. SNPs at rs12785878 (DHCR7), rs10741657 (CYP2R1), rs6013897 (CYP24A1), and rs2282679 (GC) were genotyped. Interventions: 1000 IU/d cholecalciferol from 14 weeks of gestation until delivery. Main Outcome Measure: 25(OH)D at randomization and 34 weeks of gestation were measured in a single batch (Liaison; Diasorin, Dartford, UK). Associations between 25(OH)D and the SNPs were assessed by linear regression using an additive model [β represents the change in 25(OH)D per additional common allele]. Results: Only rs12785878 (DHCR7) was associated with baseline 25(OH)D [β = 3.1 nmol/L; 95% confidence interval (CI), 1.0 to 5.2 nmol/L; P < 0.004]. In contrast, rs10741657 (CYP2R1) (β = -5.2 nmol/L; 95% CI, -8.2 to -2.2 nmol/L; P = 0.001) and rs2282679 (GC) (β = 4.2 nmol/L; 95% CI, 0.9 to 7.5 nmol/L; P = 0.01) were associated with achieved 25(OH)D status following supplementation, whereas rs12785878 and rs6013897 (CYP24A1) were not. Conclusions: Genetic variation in DHCR7, which encodes 7-dehyrocholesterol reductase in the epidermal vitamin D biosynthesis pathway, appears to modify baseline 25(OH)D. In contrast, the response to antenatal cholecalciferol supplementation was associated with SNPs in CYP2R1, which may alter 25-hydroxylase activity, and GC, which may affect vitamin D binding protein synthesis or metabolite affinity

Placental uptake and metabolism of 25(OH)vitamin D determine its activity within the fetoplacental unit

Pregnancy 25-hydroxyvitamin D [25(OH)D] concentrations are associated with maternal and fetal health outcomes. Using physiological human placental perfusion and villous explants, we investigate the role of the placenta in regulating the relationships between maternal 25(OH)D and fetal physiology. We demonstrate active placental uptake of 25(OH)D3 by endocytosis, placental metabolism of 25(OH)D3 into 24,25-dihydroxyvitamin D3 and active 1,25-dihydroxyvitamin D [1,25(OH)2D3], with subsequent release of these metabolites into both the maternal and fetal circulations. Active placental transport of 25(OH)D3 and synthesis of 1,25(OH)2D3 demonstrate that fetal supply is dependent on placental function rather than simply the availability of maternal 25(OH)D3. We demonstrate that 25(OH)D3 exposure induces rapid effects on the placental transcriptome and proteome. These map to multiple pathways central to placental function and thereby fetal development, independent of vitamin D transfer. Our data suggest that the underlying epigenetic landscape helps dictate the transcriptional response to vitamin D treatment. This is the first quantitative study demonstrating vitamin D transfer and metabolism by the human placenta, with widespread effects on the placenta itself. These data demonstrate a complex interplay between vitamin D and the placenta and will inform future interventions using vitamin D to support fetal development and maternal adaptations to pregnancy.</jats:p