51 research outputs found

    The Way of Death: Abortion’s Path to Criminalization During the Middle Ages

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    A lightning rod of controversy since the Middle Ages, abortion has both been condemned as the “way of death” and championed as a tool of female liberation (Elsakkers, “Reading Between the Lines” 468). Current debates over the legality of abortion rely on its religious characterization as an act of murder, a lingering stamp of ill fame from Europe’s medieval past. Remarkably, however, early medieval abortion laws were in some cases ambivalent toward early-term abortions (Elsakkers, “Abortion, Poisoning, Magic, and Contraception” 101). Frankish legal codes punished abortion as a poison, Frisian laws used a “hair and nails” criterion for abortion, and Old Germanic laws punished abortion more strongly for a male fetus. Intentional abortion went virtually unmentioned in Old Germanic law (Elsakkers, “Reading Between the Lines” 465). The Roman Catholic Church, by contrast, concentrated almost exclusively on intentional abortion. Church law vigorously denounced abortion as murder and warned women that they would be punished with “spiritual death,” excommunication, and hell if they obtained an abortion at any point in a pregnancy (Elsakkers, “Reading Between the Lines” 468). As the Middle Ages progressed, secular law began to echo these grim denunciations more and more frequently. The parallel development of the legal concept of criminalization and the religious concept of ensoulment at conception made possible the transfer of the Church’s condemnation of abortion into secular law.Biography:I am a freshman National Merit Scholar from Denver, Colorado, and I am double-majoring in Anthropology and Russian.University of Oklahoma Libraries Undergraduate Research Awardsundergraduat

    Sobrevivência e crescimento inicial em campo de espécies florestais nativas do Brasil Central indicadas para sistemas silvipastoris.

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    Objetivou-se, neste estudo, avaliar o índice de sobrevivência e o crescimento inicial de 11 espécies arbóreas nativas do Brasil central, plantadas diretamente em pastagem de Brachiaria brizantha cv. Marandu, em Campo Grande, MS. O solo foi classificado como Latossolo Vermelho, argiloso e distrófico, onde foi implantado um arboreto com 16 parcelas compostas, cada uma, por um indivíduo das 11 espécies selecionadas, em blocos casualizados (DBC) com quatro repetições. Os espaçamentos em campo foram de 10,0 x 4,0 m. Houve diferenças (P=0,05) entre as médias de sobrevivência das espécies estudadas, indicando influência do estágio sucessional da espécie. Os maiores índices foram de ocorrência nas seguintes espécies: ipê (Tabebuia impetiginosa), caroba (Jacaranda decurrens) e da aroeira (Myracrodruon urundeuva). As mais altas taxas de crescimento relativo nos 12 meses avaliados foram alcançadas por chico-magro (Guazuma ulmifolia), caroba (J. cuspidifolia) e canafístula (Peltophorum dubium). Houve diferença estatística (P=0,05) entre o crescimento das espécies de estágios sucessionais iniciais (pioneiras) e as de estádios tardios, e tais diferenças acentuaram-se com a idade e com a estação chuvosa. Três espécies que obtiveram as melhores combinações dos acréscimos em altura, diâmetro do colo e sobrevivência foram aptas para o cultivo em pastagens na região dos Cerrados: chicomagro (G. ulmifolia), caroba (J. cuspidifolias) e canafístula (P. dubium), sendo todas três de estágios sucessionais iniciais

    Exercise, cognition and Alzheimer’s disease: More is not necessarily better

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    Regional hypoperfusion, associated with a reduction in cerebral metabolism, is a hallmark of Alzheimer’s disease (AD) and contributes to cognitive decline. Cerebral perfusion and hence cognition can be enhanced by exercise. The present review describes first how the effects of exercise on cerebral perfusion in AD are mediated by nitric oxide (NO) and tissue-type plasminogen activator, the release of which is regulated by NO. A conclusion of clinical relevance is that exercise may not be beneficial for the cognitive functioning of all people with dementia if cardiovascular risk factors are present. The extent to which cardiovascular risk factors play a role in the selection of older people with dementia in clinical studies will be addressed in the second part of the review in which the effects of exercise on cognition are presented. Only eight relevant studies were found in the literature, emphasizing the paucity of studies in this field. Positive effects of exercise on cognition were reported in seven studies, including two that excluded and two that included patients with cardiovascular risk factors. These findings suggest that cardiovascular risk factors do not necessarily undo the beneficial effects of exercise on cognition in cognitively impaired people. Further research is called for, in view of the limitations of the clinical studies reviewed here.

    X-chromosome and kidney function:evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

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    X-chromosomal genetic variants are understudied but can yield valuable insights into sexually dimorphic human traits and diseases. We performed a sex-stratified cross-ancestry X-chromosome-wide association meta-analysis of seven kidney-related traits (n = 908,697), identifying 23 loci genome-wide significantly associated with two of the traits: 7 for uric acid and 16 for estimated glomerular filtration rate (eGFR), including four novel eGFR loci containing the functionally plausible prioritized genes ACSL4, CLDN2, TSPAN6 and the female-specific DRP2. Further, we identified five novel sex-interactions, comprising male-specific effects at FAM9B and AR/EDA2R, and three sex-differential findings with larger genetic effect sizes in males at DCAF12L1 and MST4 and larger effect sizes in females at HPRT1. All prioritized genes in loci showing significant sex-interactions were located next to androgen response elements (ARE). Five ARE genes showed sex-differential expressions. This study contributes new insights into sex-dimorphisms of kidney traits along with new prioritized gene targets for further molecular research.</p

    Effects of a high-dose 24-h infusion of tranexamic acid on death and thromboembolic events in patients with acute gastrointestinal bleeding (HALT-IT): an international randomised, double-blind, placebo-controlled trial

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    Background: Tranexamic acid reduces surgical bleeding and reduces death due to bleeding in patients with trauma. Meta-analyses of small trials show that tranexamic acid might decrease deaths from gastrointestinal bleeding. We aimed to assess the effects of tranexamic acid in patients with gastrointestinal bleeding. Methods: We did an international, multicentre, randomised, placebo-controlled trial in 164 hospitals in 15 countries. Patients were enrolled if the responsible clinician was uncertain whether to use tranexamic acid, were aged above the minimum age considered an adult in their country (either aged 16 years and older or aged 18 years and older), and had significant (defined as at risk of bleeding to death) upper or lower gastrointestinal bleeding. Patients were randomly assigned by selection of a numbered treatment pack from a box containing eight packs that were identical apart from the pack number. Patients received either a loading dose of 1 g tranexamic acid, which was added to 100 mL infusion bag of 0·9% sodium chloride and infused by slow intravenous injection over 10 min, followed by a maintenance dose of 3 g tranexamic acid added to 1 L of any isotonic intravenous solution and infused at 125 mg/h for 24 h, or placebo (sodium chloride 0·9%). Patients, caregivers, and those assessing outcomes were masked to allocation. The primary outcome was death due to bleeding within 5 days of randomisation; analysis excluded patients who received neither dose of the allocated treatment and those for whom outcome data on death were unavailable. This trial was registered with Current Controlled Trials, ISRCTN11225767, and ClinicalTrials.gov, NCT01658124. Findings: Between July 4, 2013, and June 21, 2019, we randomly allocated 12 009 patients to receive tranexamic acid (5994, 49·9%) or matching placebo (6015, 50·1%), of whom 11 952 (99·5%) received the first dose of the allocated treatment. Death due to bleeding within 5 days of randomisation occurred in 222 (4%) of 5956 patients in the tranexamic acid group and in 226 (4%) of 5981 patients in the placebo group (risk ratio [RR] 0·99, 95% CI 0·82–1·18). Arterial thromboembolic events (myocardial infarction or stroke) were similar in the tranexamic acid group and placebo group (42 [0·7%] of 5952 vs 46 [0·8%] of 5977; 0·92; 0·60 to 1·39). Venous thromboembolic events (deep vein thrombosis or pulmonary embolism) were higher in tranexamic acid group than in the placebo group (48 [0·8%] of 5952 vs 26 [0·4%] of 5977; RR 1·85; 95% CI 1·15 to 2·98). Interpretation: We found that tranexamic acid did not reduce death from gastrointestinal bleeding. On the basis of our results, tranexamic acid should not be used for the treatment of gastrointestinal bleeding outside the context of a randomised trial
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