90 research outputs found

    Manipulation du métabolisme énergétique dans les leucémies aiguës myéloïdes : mitochondrie, apoptose et mécanisme d'action de la metformine

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    La metformine, utilisĂ©e pour le traitement du diabĂšte de type 2, a Ă©tĂ© dĂ©crite comme pouvant rĂ©duire le risque de cancer. Cependant, les mĂ©canismes responsables de cette activitĂ© n'ont pas encore Ă©tĂ© Ă©lucidĂ©s. Nous avons ici dĂ©cidĂ© d'Ă©tudier les effets de la metformine dans les cellules de leucĂ©mie aiguĂ« myĂ©loĂŻde (LAM). La metformine bloque la progression dans le cycle cellulaire, inhibe la prolifĂ©ration et la formation de colonies in vitro. In vivo, un traitement quotidien Ă  la metformine induit l'apoptose et rĂ©duit la progression tumorale. Toutefois, cette induction d'apoptose est variable en fonction des cellules leucĂ©miques. La metformine induit une inhibition de mTORC1 indĂ©pendante de l'AMPK, qui peut ĂȘtre responsable des effets anti-tumoraux observĂ©s. Par ailleurs, la metformine rĂ©duit fortement l'activitĂ© du complexe I de la chaĂźne respiratoire, la consommation d'oxygĂšne et la production d'ATP par la mitochondrie alors qu'elle stimule la glycolyse pour la production d'ATP et de lactate (effet Pasteur). Les cellules leucĂ©miques avec une forte glycolyse ou activation d'AKT montrent une rĂ©duction significative de l'induction de l'effet Pasteur et de l'apoptose en rĂ©ponse Ă  la metformine. Ainsi, la dĂ©privation en glucose ou un inhibiteur de la glycolyse ou d'AKT sensibilisent ces cellules Ă  la metformine. Nous proposons que le mĂ©canisme d'apoptose est bloquĂ© par la phosphorylation et la translocation au pore mitochondrial VDAC1 de l'hexokinase-II en aval d'AKT. En conclusion, ces travaux ont permis de mieux caractĂ©riser la signalisation et le mĂ©tabolisme impliquĂ©s dans la rĂ©ponse anti-tumorale induite par la metformine dans des lignĂ©es cellulaires de LAM.Normoglycemic agent, metformin, decreases the risk of cancer in type 2 diabetics and inhibits cell growth in various cancers. Metformin activates AMPK and inhibits electron transport chain complex I (ETCI), but its mechanism of action in cancer cells is unknown. Thus, we investigated metformin's activity in human acute myeloid leukemia (AML) cells. Metformin significantly blocks cell cycle progression and inhibits cell proliferation and colony formation. However, the apoptotic response to metformin varies among AML cell types. Furthermore, daily treatment with metformin induces apoptosis and reduces tumor growth in vivo. Metformin induces an AMPK-independent inhibition of mTORC1, which could be responsible for metformin's anti-tumoral activities. Additionally, metformin decreases ETCI activity, oxygen consumption and mitochondrial ATP synthesis, while stimulating glycolysis for ATP and lactate production (so-called Pasteur Effect). AML cells with high basal AKT phosphorylation or glycolysis exhibit a markedly reduced induction of the Pasteur effect in response to metformin and are resistant to metformin-induced apoptosis. Accordingly, glucose starvation or treatment with deoxyglucose or an AKT inhibitor induces sensitivity to metformin. Thus, we propose that activation of AKT, which can phosphorylate hexokinase-II to induce its translocation to the mitochondrial outer membrane pore, VDAC1, blocks cytochrome c release and mitochondrial-induced apoptosis. Overall, this work has allowed us to decipher the role of certain signaling and metabolic pathways in the anti-tumoral response to metformin in AML

    Cost of fertility treatment and live birth outcome in women of different ages and BMI

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    Acknowledgements We thank the Aberdeen Fertility Centre Database Committee and the Aberdeen Maternal and Neonatal Databank Committee for giving us approval to use their databases. We thank the Data Management Team for extracting the required information from these databases. The views expressed in this paper represent the views of the authors and not necessarily the views of the funding bodies. Funding This study was partly funded by an NHS endowment grant (Grant Number 12/48) and DM by a Chief Scientist Office Postdoctoral Fellowship (Ref PDF/12/06).Peer reviewedPostprin

    Predicted COVID-19 positive cases, hospitalisations, and deaths associated with the Delta variant of concern, June-July, 2021

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    Funding: EAVE II is funded by the Medical Research Council (MR/R008345/1) with the support of BREATHE - The Health Data Research Hub for Respiratory Health [MC_PC_19004], which is funded through the UK Research and Innovation Industrial Strategy Challenge Fund and delivered through Health Data Research UK. Additional support has been provided through Public Health Scotland and Scottish Government DG Health and Social Care and the Data and Connectivity National Core Study, led by Health Data Research UK in partnership with the Office for National Statistics and funded by UK Research and Innovation. SVK is funded by a NHS Research Scotland Senior Clinical Fellowship (SCAF/15/02), the Medical Research Council (MC_UU_00022/2), and the Scottish Government Chief Scientist Office (SPHSU17).Publisher PDFNon peer reviewe

    Revising acute care systems and processes to improve breastfeeding and maternal postnatal health: a pre and post intervention study in one English maternity unit

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    Background Most women in the UK give birth in a hospital labour ward, following which they are transferred to a postnatal ward and discharged home within 24 to 48 hours of the birth. Despite policy and guideline recommendations to support planned, effective postnatal care, national surveys of women’s views of maternity care have consistently found in-patient postnatal care, including support for breastfeeding, is poorly rated. Methods Using a Continuous Quality Improvement approach, routine antenatal, intrapartum and postnatal care systems and processes were revised to support implementation of evidence based postnatal practice. To identify if implementation of a multi-faceted QI intervention impacted on outcomes, data on breastfeeding initiation and duration, maternal health and women’s views of care, were collected in a pre and post intervention longitudinal survey. Primary outcomes included initiation, overall duration and duration of exclusive breastfeeding. Secondary outcomes included maternal morbidity, experiences and satisfaction with care. As most outcomes of interest were measured on a nominal scale, these were compared pre and post intervention using logistic regression. Results Data were obtained on 741/1160 (64%) women at 10 days post-birth and 616 (54%) at 3 months post-birth pre-intervention, and 725/1153 (63%) and 575 (50%) respectively postintervention. Post intervention there were statistically significant differences in the initiation (p = 0.050), duration of any breastfeeding (p = 0.020) and duration of exclusive breastfeeding to 10 days (p = 0.038) and duration of any breastfeeding to three months (p = 0.016). Post intervention, women were less likely to report physical morbidity within the first 10 days of birth, and were more positive about their in-patient care. Conclusions It is possible to improve outcomes of routine in-patient care within current resources through continuous quality improvement

    Disavowing 'the' prison

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    This chapter confronts the idea of ‘the’ prison, that is, prison as a fixed entity. However hard we, that is, prison scholars including ourselves, seek to deconstruct and critique specific aspects of confinement, there is a tendency to slip into a default position that envisions the prison as something given and pre-understood. When it comes to prison our imagination seems to clog up. It is the political solution to its own failure, and the preferred metaphor for its own representation

    The DUNDRUM Quartet: validation of structured professional judgement instruments DUNDRUM-3 assessment of programme completion and DUNDRUM-4 assessment of recovery in forensic mental health services

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    <p>Abstract</p> <p>Background</p> <p>Moving a forensic mental health patient from one level of therapeutic security to a lower level or to the community is influenced by more than risk assessment and risk management. We set out to construct and validate structured professional judgement instruments for consistency and transparency in decision making</p> <p>Methods</p> <p>Two instruments were developed, the seven-item DUNDRUM-3 programme completion instrument and the six item DUNDRUM-4 recovery instrument. These were assessed for all 95 forensic patients at Ireland's only forensic mental health hospital.</p> <p>Results</p> <p>The two instruments had good internal consistency (Cronbach's alpha 0.911 and 0.887). Scores distinguished those allowed no leave or accompanied leave from those with unaccompanied leave (ANOVA F = 38.1 and 50.3 respectively, p < 0.001). Scores also distinguished those in acute/high security units from those in medium or in low secure/pre-discharge units. Each individual item distinguished these levels of need significantly. The DUNDRUM-3 and DUNDRUM-4 correlated moderately with measures of dynamic risk and with the CANFOR staff rated unmet need (Spearman r = 0.5, p < 0.001).</p> <p>Conclusions</p> <p>The DUNDRUM-3 programme completion items distinguished significantly between levels of therapeutic security while the DUNDRUM-4 recovery items consistently distinguished those given unaccompanied leave outside the hospital and those in the lowest levels of therapeutic security. This data forms the basis for a prospective study of outcomes now underway.</p

    Risk of COVID-19 hospitalizations among school-aged children in Scotland : a national incident cohort study

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    Background There is considerable policy, clinical and public interest about whether children should be vaccinated against SARS-CoV-2 and, if so, which children should be prioritised (particularly if vaccine resources are limited). To inform such deliberations, we sought to identify children and young people at highest risk of hospitalization from COVID-19. Methods We used the Early Pandemic Evaluation and Enhanced Surveillance of COVID-19 (EAVE II) platform to undertake a national incident cohort analysis to investigate the risk of hospitalization among 5-17 years old living in Scotland in risk groups defined by the living risk prediction algorithm (QCOVID). A Cox proportional hazard model was used to derive hazard ratios (HR) and 95% confidence intervals (CIs) for the association between risk groups and COVID-19 hospital admission. Adjustments were made for age, sex, socioeconomic status, co-morbidity, and prior hospitalization. Results Between March 1, 2020 and November 22, 2021, there were 146 183 (19.4% of all 752 867 children in Scotland) polymerase chain reaction (PCR) confirmed SARS-CoV-2 infections among 5-17 years old. Of those with confirmed infection, 973 (0.7%) were admitted to hospital with COVID-19. The rate of COVID-19 hospitalization was higher in those within each QCOVID risk group compared to those without the condition. Similar results were found in age stratified analyses (5-11 and 12-17 years old). Risk groups associated with an increased risk of COVID-19 hospital admission, included (adjusted HR, 95% CIs): sickle cell disease 14.35 (8.48-24.28), chronic kidney disease 11.34 (4.61-27.87), blood cancer 6.32 (3.24-12.35), rare pulmonary diseases 5.04 (2.58-9.86), type 2 diabetes 3.04 (1.34-6.92), epilepsy 2.54 (1.69-3.81), type 1 diabetes 2.48 (1.47-4.16), Down syndrome 2.45 (0.96-6.25), cerebral palsy 2.37 (1.26-4.47), severe mental illness 1.43 (0.63-3.24), fracture 1.41 (1.02-1.95), congenital heart disease 1.35 (0.82-2.23), asthma 1.28 (1.06-1.55), and learning disability (excluding Down syndrome) 1.08 (0.82-1.42), when compared to those without these conditions. Although our Cox models were adjusted for a number of potential confounders, residual confounding remains a possibility. Conclusions In this national study, we observed an increased risk of COVID-19 hospital admissions among school-aged children with specific underlying long-term health conditions compared with children without these conditions
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