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Understanding where people with tuberculosis seek care to serve them better 了解结核病患者在哪里寻求治疗,以便更好地为他们服务
Pub Date : 2026-03-20 DOI: 10.1016/s0140-6736(26)00543-x
Charity Oga-Omenka, Arlene Rabvukwa, Obioma Chijioke-Akaniro, Nkirote Mwirigi, Madhukar Pai
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引用次数: 0
Semaglutide for Alzheimer's disease after evoke and evoke+ Semaglutide用于阿尔茨海默病后的evoke和evoke+
Pub Date : 2026-03-19 DOI: 10.1016/s0140-6736(26)00514-3
Lon S Schneider
No Abstract
没有抽象的
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引用次数: 0
Efficacy and safety of oral semaglutide 14 mg (flexible dose) in early-stage symptomatic Alzheimer's disease (evoke and evoke+): two phase 3, randomised, placebo-controlled trials 口服西马鲁肽14mg(灵活剂量)治疗早期症状性阿尔茨海默病(evoke和evoke+)的疗效和安全性:两项3期随机安慰剂对照试验
Pub Date : 2026-03-19 DOI: 10.1016/s0140-6736(26)00459-9
Jeffrey L Cummings, Alireza Atri, Mary Sano, Henrik Zetterberg, Philip Scheltens, Filip K Knop, Peter Johannsen, Christian A Wichmann, Rikke Mortensen Abschneider, Teresa Leon, Howard H Feldman
<h3>Background</h3>Evidence, including animal, clinical, and real-world studies in individuals with type 2 diabetes and/or obesity, suggests reduced risk of dementia and Alzheimer's disease after GLP-1 receptor agonist exposure. The evoke and evoke+ trials aimed to investigate the efficacy and safety of oral semaglutide in individuals with early Alzheimer's disease.<h3>Methods</h3>evoke and evoke+ were multicentre, randomised, double-blind, placebo-controlled phase 3 trials conducted across 566 sites in 40 countries. The trials assessed the efficacy and safety of oral semaglutide up to 14 mg once daily in participants with amyloid-confirmed Alzheimer's disease, aged 55–85 years, with mild cognitive impairment or mild dementia due to Alzheimer's disease. In evoke+, participants with significant small vessel pathology were included. Participants were randomly assigned (1:1) to once-daily semaglutide 14 mg (flexible dose) or placebo for up to 156 weeks. The primary endpoint was change in Clinical Dementia Rating—Sum of Boxes (CDR-SB) score from baseline to week 104, assessed in all randomised participants. Safety was assessed in all randomised participants and reported for those receiving at least one dose of study drug. These trials were registered at <span><span>ClinicalTrials.gov</span><svg aria-label="Opens in new window" focusable="false" height="20" viewbox="0 0 8 8"><path d="M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z"></path></svg></span> (<span><span>NCT04777396</span><svg aria-label="Opens in new window" focusable="false" height="20" viewbox="0 0 8 8"><path d="M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z"></path></svg></span> and <span><span>NCT04777409</span><svg aria-label="Opens in new window" focusable="false" height="20" viewbox="0 0 8 8"><path d="M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z"></path></svg></span>); both trials have been discontinued due to negative clinical outcome.<h3>Findings</h3>Between May 18, 2021, and Sept 8, 2023, 9981 participants were screened, of whom 3808 were randomly assigned; 1855 in evoke (semaglutide, n=928; placebo, n=927) and 1953 in evoke+ (semaglutide, n=976; placebo, n=977). Mean age was 72·2 years (SD 7·1), and mean CDR-SB score was 3·7 (SD 1·6) at baseline. In evoke+, 54 (2·8%) participants had small vessel pathology. In evoke and evoke+, mean changes in CDR-SB score from baseline to week 104 were 2·3 (SE 0·1) and 2·2 (0·1) with semaglutide, compared with 2·3 (0·1) and 2·1 (0·1) with placebo (estimated difference −0·08 [95% CI −0·35 to 0·20], p=0·57 in evoke and 0·10 [−0·17 to 0·38], p=0·46 in evoke+). Treatment-emergent adverse events were reported in 1729 (91·2%) of 1896 participants receiving semaglutide versus 1613 (84·8%) of 1902 receiving placebo. There were five fatalities considered treatment-related by the investigators (one in the semaglutide group and fo
包括动物、临床和现实世界2型糖尿病和/或肥胖患者的研究在内的证据表明,GLP-1受体激动剂暴露后,痴呆和阿尔茨海默病的风险降低。evoke和evoke+试验旨在研究口服西马鲁肽对早期阿尔茨海默病患者的疗效和安全性。sevoke和evoke+是在40个国家的566个地点进行的多中心、随机、双盲、安慰剂对照的3期试验。这些试验评估了每日一次口服西马鲁肽最多14毫克的有效性和安全性,受试者为淀粉样蛋白确诊的阿尔茨海默病,年龄在55-85岁之间,患有阿尔茨海默病引起的轻度认知障碍或轻度痴呆。在evoke+中,包括有明显小血管病变的参与者。参与者被随机分配(1:1)至每日一次的西马鲁肽14mg(灵活剂量)或安慰剂,长达156周。主要终点是临床痴呆评分-盒和(CDR-SB)评分从基线到第104周的变化,对所有随机参与者进行评估。对所有随机受试者的安全性进行了评估,并报告了接受至少一剂研究药物的受试者的安全性。这些试验在ClinicalTrials.gov注册(NCT04777396和NCT04777409);由于临床结果阴性,两项试验均已停止。在2021年5月18日至2023年9月8日期间,筛查了9981名参与者,其中3808名随机分配;evoke组1855例(semaglutide, n=928; placebo, n=927), evoke+组1953例(semaglutide, n=976; placebo, n=977)。平均年龄72.2岁(SD 7.1),基线时平均CDR-SB评分3.7 (SD 1.6)。在evoke+中,54例(2.8%)参与者有小血管病变。在evoke和evoke+中,CDR-SB评分从基线到第104周的平均变化,semaglutide组为2.3 (SE为0.1)和2.2(0.1),而安慰剂组为2.3(0.1)和2.1(0.1)(估计差异为- 0.08 [95% CI为- 0.35 ~ 0.20],p= 0.57, evoke+组为0.10 [- 0.17 ~ 0.38],p= 0.46)。1896名接受西马鲁肽治疗的受试者中有1729名(91.2%)报告了治疗中出现的不良事件,而1902名接受安慰剂治疗的受试者中有1613名(84.8%)报告了治疗中出现的不良事件。研究者认为有5例死亡与治疗相关(1例在西马鲁肽组,4例在安慰剂组)。解释:口服西马鲁肽对减缓早期阿尔茨海默病患者的临床进展无效。西马鲁肽治疗早期阿尔茨海默病的安全性和耐受性与其他适应症的研究一致。FundingNovo诺。
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引用次数: 0
Katrina Jane Allen 卡特里娜·简·艾伦
Pub Date : 2026-03-19 DOI: 10.1016/s0140-6736(26)00517-9
Andrew Green
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引用次数: 0
Global challenges for research on gun violence 枪支暴力研究面临的全球挑战
Pub Date : 2026-03-19 DOI: 10.1016/s0140-6736(26)00361-2
Sandra Ley, Lorena Barberia, Aisha Jafri, Adnan A Hyder
No Abstract
没有抽象的
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引用次数: 0
Learning from swine influenza, Ebola virus disease, and Legionnaires' disease in 1976 从1976年的猪流感、埃博拉病毒病和军团病中学习
Pub Date : 2026-03-19 DOI: 10.1016/s0140-6736(26)00460-5
Daniel B Jernigan, Caitlin M Rivers
No Abstract
没有抽象的
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引用次数: 0
Early atheroma prevention: a cost-effective approach to healthy cardiovascular ageing 早期动脉粥样硬化预防:健康心血管老化的成本效益方法
Pub Date : 2026-03-16 DOI: 10.1016/s0140-6736(26)00419-8
Rachael Steinhauer, Joshua Y H Xu, Roger S Blumenthal, Aaron L Troy
No Abstract
没有抽象的
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引用次数: 0
Measuring progress in pregnancy planning and preconception health 衡量怀孕计划和孕前保健方面的进展
Pub Date : 2026-03-16 DOI: 10.1016/s0140-6736(26)00192-3
Danielle Schoenaker, Jennifer Hall, Sarah Verbiest, Engelbert A Nonterah, Wendy V Norman, Ghadir Fakhri Al-Jayyousi, Hanan F Abdul Rahim, Nadira Sultana Kakoly, Ana Luiza Vilela Borges, Danielle Mazza, Chee Wai Ku, Jerry Kok Yen Chan, Ilse Delbaere, Shane A Norris, Eric Steegers, Geraldine Barrett, Gabriella Conti, Judith Stephenson
As efforts to support pregnancy planning and improve preconception health are increasing at scale, appropriate systems to monitor progress are required. Despite developments in a few countries, no surveillance systems currently in operation are using a comprehensive set of indicators for monitoring preconception health. This Review describes relevant indicators, reflecting both system-level and individual-level factors, that can be drawn from routine data sources to form the basis for developing new surveillance systems. We present a new framework for national and international surveillance that incorporates, for the first time, community perspectives on the factors that matter most before pregnancy and parenthood. Finally, we describe an international collaboration working towards a core set of indicators that can be compared across low-income, middle-income, and high-income countries, and discuss future directions to enhance and expand international monitoring of pregnancy planning and preconception health.
由于支持怀孕计划和改善孕前健康的努力正在大规模增加,需要适当的系统来监测进展情况。尽管少数国家取得了进展,但目前运行的任何监测系统都没有使用一套全面的指标来监测孕前健康。本综述描述了反映系统级和个人级因素的相关指标,这些指标可以从常规数据来源中得出,以形成开发新的监测系统的基础。我们提出了一个新的国家和国际监测框架,首次纳入了社区对怀孕和生育前最重要因素的看法。最后,我们描述了一项旨在制定一套核心指标的国际合作,这些指标可以在低收入、中等收入和高收入国家之间进行比较,并讨论了加强和扩大妊娠计划和孕前健康国际监测的未来方向。
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引用次数: 0
US global health deals falter over sovereignty concerns 美国的全球医疗交易因主权担忧而步履蹒跚
Pub Date : 2026-03-12 DOI: 10.1016/s0140-6736(26)00509-x
Gilbert Nakweya
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引用次数: 0
Advancing Indigenous men's health equity in gender justice action 在性别正义行动中促进土著男子的健康平等
Pub Date : 2026-03-12 DOI: 10.1016/s0140-6736(25)01296-6
Bryce Brickley, Kootsy Canuto, Beau Cubillo, Jacob Prehn, James A Smith
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引用次数: 0
期刊
The Lancet
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