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Post-treatment renin status and cardiovascular, renal, and mortality outcomes in medically treated primary aldosteronism: a systematic review and meta-analysis 经药物治疗的原发性醛固酮增多症患者治疗后肾素状态与心血管、肾脏和死亡率的关系:一项系统回顾和荟萃分析
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-25 DOI: 10.1016/s2213-8587(25)00263-3
Sho Katsuragawa, Minh V Le, Peter J Fuller, Jun Yang
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引用次数: 0
The importance of science communication surrounding weight-loss drugs 关于减肥药的科学传播的重要性
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-25 DOI: 10.1016/s2213-8587(25)00320-1
Giles S H Yeo
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引用次数: 0
Safeguarding natural intelligence: the case for renewed action on iodine sufficiency in the UK 保护自然智力:在英国对碘的充足性采取新的行动
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-25 DOI: 10.1016/s2213-8587(25)00327-4
Peter N Taylor, Malcolm Prentice, Kristien Boelaert, John Lazarus
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引用次数: 0
The road towards standardisation in cyclic Cushing's syndrome 循环库欣综合征的标准化之路
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-25 DOI: 10.1016/s2213-8587(25)00258-x
Dan Alexandru Niculescu
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引用次数: 0
Cycle characterisation and clinical complications in patients with cyclic Cushing's syndrome: insights from an international retrospective cohort study 周期性库欣综合征患者的周期特征和临床并发症:来自国际回顾性队列研究的见解
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-25 DOI: 10.1016/s2213-8587(25)00249-9
Elisabeth Nowak, Qilin Zhang, Shuo Zhang, Yao Zhao, Hongying Ye, Márcio Carlos Machado, Caio Celio Santiago Moises, Miklós Tóth, Júlia Stark, Kevin C J Yuen, Mark Gurnell, James MacFarlane, Ann McCormack, Mauli Govinna, Aleksandra Gilis-Januszewska, Mari Minasyan, Ilaria Bonaventura, Mauro A Czepielewski, Amandine Ferriere, Monica Gadelha, Andrea M Isidori, Darko Kastelan, Dominique Maiter, Antoine Tabarin, Krystallenia I Alexandraki, Julia Chang, Eric D Frontera, Felicia A Hanzu, Niina Matikainen, Dragana Miljic, Robert Pichler, Vera Popovic, Joanna L Spencer-Segal, Karen Tordjman, Amit Akirov, Marta Araujo-Castro, Emanuela Arvat, Irina Bancos, Fabio Bioletto, Pia Burman, Frederic Castinetti, Mario Detomas, Martin Fassnacht, Richard A Feelders, Athanasios Fountas, Peter Igaz, Sasa Ilic, Kristina Isand, Gregory Kaltsas, Gesine Meyer, Mirko Parasiliti-Caprino, John Newell-Price, Oskar Ragnarsson, Elena Valassi, Greisa Vila, John Wass, Uri Yoel, Maria Fleseriu, Martin Reincke
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引用次数: 0
Correction to Lancet Diabetes Endocrinol 2022; 10: 623–33 《柳叶刀糖尿病内分泌》2022版修正;10: 623 - 33所示
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-15 DOI: 10.1016/s2213-8587(25)00325-0
Inagaki N, Takeuchi M, Oura T, et al. Efficacy and safety of tirzepatide monotherapy compared with dulaglutide in Japanese patients with type 2 diabetes (SURPASS J-mono): a double-blind, multicentre, randomised, phase 3 trial. Lancet Diabetes Endocrinol 2022; 10: 623–33—Appendix 2 of this Article has been corrected as of Oct 15, 2025.
李建军,李建军,李建军,等。替西帕肽单药治疗与杜拉鲁肽在日本2型糖尿病患者中的疗效和安全性比较(transcend J-mono):一项双盲、多中心、随机、3期试验。Lancet Diabetes Endocrinol 2022;10:623 - 33本文附录2已于2025年10月15日更正。
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引用次数: 0
Addressing educational needs in older adults with type 1 diabetes 解决老年1型糖尿病患者的教育需求
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-14 DOI: 10.1016/s2213-8587(25)00259-1
Giuseppe Maltese, Partha Kar, Geraldine Gallen, Debbie Hicks, Alan J Sinclair
No Abstract
没有抽象的
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引用次数: 0
Managing adults with screen-detected islet autoantibody positivity: a pragmatic framework 管理筛查检测到胰岛自身抗体阳性的成人:一个实用的框架
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-14 DOI: 10.1016/s2213-8587(25)00260-8
Nicholas Thomas, Danijela Tatovic, Angus Jones, Parth Narendran
New disease-modifying therapies, such as teplizumab, offer opportunities to delay the clinical onset of type 1 diabetes but require islet autoantibody screening to identify individuals at increased risk of progression to diabetes. As type 1 diabetes screening programmes expand, clinicians will increasingly encounter a new group of people: adults who test positive for islet autoantibodies but have not yet been diagnosed with diabetes. Although international guidelines outline management for both children and adults, considerable uncertainties remain, particularly for adults. In adults with islet autoantibody positivity, the lower risk of progression to type 1 diabetes compared with children, combined with the high background prevalence of mild non-autoimmune dysglycaemia, presents substantial challenges for clinical management. This Personal View aims to add clarity to international consensus guidelines, proposing a pragmatic framework for managing adults with islet autoantibody positivity. Although fitting within a UK National Health Service setting, we feel this framework is also relevant to other health systems.
新的疾病改善疗法,如teplizumab,提供了延迟1型糖尿病临床发病的机会,但需要胰岛自身抗体筛查来识别糖尿病进展风险增加的个体。随着1型糖尿病筛查项目的扩大,临床医生将越来越多地遇到一个新的人群:胰岛自身抗体检测呈阳性但尚未被诊断为糖尿病的成年人。尽管国际准则概述了儿童和成人的管理,但仍存在相当大的不确定性,特别是对成人而言。成人胰岛自身抗体阳性,与儿童相比,进展为1型糖尿病的风险较低,加上轻度非自身免疫性血糖异常的高背景患病率,为临床管理带来了重大挑战。本个人观点旨在增加国际共识指南的清晰度,提出一个管理成人胰岛自身抗体阳性的实用框架。虽然适合英国国家卫生服务设置,我们认为这一框架也适用于其他卫生系统。
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引用次数: 0
Effects of empagliflozin on conventional and exploratory acute and chronic kidney outcomes: an individual participant-level meta-analysis 恩格列净对常规和探索性急慢性肾脏结局的影响:个体参与者水平的荟萃分析
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-11 DOI: 10.1016/s2213-8587(25)00222-0
William G Herrington, Zhaojing J Che, Rebecca Sardell, Alistair J Roddick, Parminder K Judge, Christoph Wanner, Sibylle J Hauske, Stefan Anker, Javed Butler, Gerasimos Filippatos, Milton Packer, Faiez Zannad, Dominik Steubl, Martina Brueckmann, Jennifer B Green, Jonathan R Emberson, Martin J Landray, Colin Baigent, Richard Haynes, Natalie Staplin

Background

Uncertainty remains about effects of sodium–glucose co-transporter-2 (SGLT2) inhibition on kidney outcomes in individuals with slowly progressive chronic kidney disease (eg, low albuminuria) and those at risk of large acute estimated glomerular filtration rate (eGFR) dips on initiation of such treatment. We aimed to explore the effects of empagliflozin on a range of kidney outcomes in these population subtypes.

Methods

In this meta-analysis, we used individual-level data from 23 340 participants in four large placebo-controlled trials (EMPA-REG OUTCOME, EMPEROR-Reduced, EMPEROR-Preserved, and EMPA-KIDNEY) to assess the effects of empagliflozin on conventional and exploratory acute and chronic kidney outcomes. We then assessed whether effects varied by predicted size of the acute eGFR dip on treatment initiation or among other key population subtypes using tests for heterogeneity and trend. The individual-level data were requested from Boehringer Ingelheim (Ingelheim, Germany).

Findings

Compared with placebo, allocation to empagliflozin reduced the risk of a marker of acute kidney injury (a ≥50% increase in serum creatinine in consecutive follow-up samples) by 20% (hazard ratio 0·80 [95% CI 0·72–0·88]; 1573 outcomes), acute kidney injury adverse events by 27% (0·73 [0·63–0·85]; 694 outcomes), a categorical chronic kidney disease progression outcome by 30% (0·70 [0·63–0·78]; 1403 outcomes), and kidney failure by 34% (0·66 [0·55–0·79]; 490 outcomes). Empagliflozin slowed a chronic annual rate of eGFR decline by 64% (95% CI 59–69) and off-treatment dip-free slope—a post-hoc outcome using randomisation and off-treatment eGFR values available in a subset of 10 630 participants—by 64% (54–73). These kidney benefits were similar in subgroups divided by predicted size of acute eGFR dip, and were present irrespective of diabetes or heart failure status, level of kidney function, or albuminuria.

Interpretation

SGLT2 inhibition reduces risk of acute and chronic kidney outcomes irrespective of the size of the acute dip in eGFR. Kidney benefits are evident irrespective of diabetes status, heart failure status, primary cause of kidney disease, and markers of severity of these diseases.

Funding

None.
背景:钠-葡萄糖共转运蛋白-2 (SGLT2)抑制对缓慢进展的慢性肾病患者(如低蛋白尿)和有急性肾小球滤过率(eGFR)大幅下降风险的患者开始此类治疗时肾脏结局的影响仍不确定。我们的目的是探讨恩格列净对这些人群亚型的一系列肾脏结局的影响。方法在这项荟萃分析中,我们使用了来自4个大型安慰剂对照试验(EMPA-REG OUTCOME、emperr - reduced、emperr - preserved和EMPA-KIDNEY)的23340名参与者的个体水平数据来评估恩格列净对常规和探索性急慢性肾脏结局的影响。然后,我们通过异质性和趋势测试,评估急性eGFR下降对治疗开始或其他关键人群亚型的影响是否随预测大小而变化。从勃林格殷格翰公司(殷格翰,德国)获得了个人层面的数据。与安慰剂相比,分配恩格列净可使急性肾损伤标志物(连续随访样本中血清肌酐升高≥50%)的风险降低20%(风险比0.80 [95% CI 0.72 - 0.88]; 1573个结局),急性肾损伤不良事件发生率降低27%(0.73[0.63 - 0.85];694个结局),慢性肾脏疾病分类进展结局发生率降低30%(0.70[0.63 - 0.78];1403个结局),肾功能衰竭发生率降低34%(0.66[0.55 - 0.79];490个结局)。恩帕列净将慢性年eGFR下降率降低了64% (95% CI 59-69),治疗后无下降斜率(10630名参与者的随机化和治疗后eGFR值的随机结局)降低了64%(54-73)。这些肾脏益处在按急性eGFR下降预测大小划分的亚组中是相似的,并且与糖尿病或心力衰竭状态、肾功能水平或蛋白尿无关。sglt2抑制降低了急性和慢性肾脏结局的风险,与eGFR急性下降的大小无关。与糖尿病状况、心力衰竭状况、肾脏疾病的主要原因以及这些疾病的严重程度标志无关,对肾脏的益处是显而易见的。
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引用次数: 0
Empagliflozin in chronic kidney disease: evidence for early, inclusive, and confident use 恩格列净在慢性肾病中的应用:早期、全面和自信使用的证据
IF 44.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-10-11 DOI: 10.1016/s2213-8587(25)00224-4
Carmine Zoccali, Francesca Mallamaci
No Abstract
没有抽象的
{"title":"Empagliflozin in chronic kidney disease: evidence for early, inclusive, and confident use","authors":"Carmine Zoccali, Francesca Mallamaci","doi":"10.1016/s2213-8587(25)00224-4","DOIUrl":"https://doi.org/10.1016/s2213-8587(25)00224-4","url":null,"abstract":"No Abstract","PeriodicalId":48790,"journal":{"name":"The Lancet Diabetes & Endocrinology","volume":"104 5 1","pages":""},"PeriodicalIF":44.5,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145282669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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The Lancet Diabetes & Endocrinology
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