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Tackling the epidemic of obesity and hypertension in children and young people. 解决儿童和青少年肥胖和高血压流行问题。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2026-01-09 DOI: 10.1097/MNH.0000000000001156
Emily Haseler, Manish D Sinha

Purpose of review: The prevalence of both obesity and hypertension is increasing in childhood, with considerable overlap in disease and causative factors. Evidence from studies over the past decade suggests both obesity and hypertension have summative effects on both cardiac remodelling in childhood and major adverse cardiovascular events in adulthood.

Recent findings: We highlight recent high-quality evidence reporting epidemiology of obesity, hypertension and hypertension-mediated organ damage (HMOD) in those with obesity-related hypertension. We discuss the early life influences on BP and BMI trajectory and the clustering of cardiovascular risk factors (CVRFs) seen in obesity hypertension. We discuss management options highlighting key contributors to compounding risk for obesity-associated hypertension across the first two decades of life, with potential windows for both individual and population-level intervention.

Summary: Currently, a large and expanding cohort of young people with multiple CVRFs is progressing toward adulthood, where they are likely to experience disproportionate cardiovascular morbidity when compared with age-matched healthy peers. These trends underscore the urgent need for co-ordinated healthcare responses to manage affected children and for robust governmental and public-health interventions to mitigate the environmental and societal drivers of this convergent epidemic.

综述目的:儿童肥胖和高血压的患病率都在增加,在疾病和致病因素上有相当大的重叠。过去十年的研究证据表明,肥胖和高血压对儿童时期的心脏重塑和成年期的主要不良心血管事件都有总结性影响。最近的发现:我们强调了最近高质量的证据报道肥胖相关高血压患者肥胖、高血压和高血压介导的器官损伤(HMOD)的流行病学。我们讨论了早期生活对血压和BMI轨迹的影响以及肥胖高血压中心血管危险因素(cvrf)的聚类。我们讨论了在生命的头二十年中,肥胖相关高血压的复合风险的关键因素的管理选择,以及个人和人群水平干预的潜在窗口。摘要:目前,一个庞大且不断扩大的患有多种cvrf的年轻人群体正在走向成年,与年龄匹配的健康同龄人相比,他们可能会出现不成比例的心血管发病率。这些趋势突出表明,迫切需要协调一致的保健对策,以管理受影响的儿童,并迫切需要强有力的政府和公共卫生干预措施,以减轻这一趋同流行病的环境和社会驱动因素。
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引用次数: 0
Cuffless blood pressure in 2025: from promise to practice: a narrative review. 2025年的无袖血压:从承诺到实践:叙述性回顾。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2025-12-29 DOI: 10.1097/MNH.0000000000001150
Farah Wehbe, Swapnil Hiremath

Purpose of review: Cuffless blood pressure (BP) technologies have moved from concept to everyday wearables, spurred by consumer adoption and recent regulatory milestones. Yet clinicians face mixed signals on accuracy, calibration stability, and clinical use. This review synthesizes current evidence and emerging standards to clarify where cuffless data can add value.

Recent findings: Most devices estimate BP from surrogate signals and require periodic calibration, making outputs reliable for trends around the last calibration but less so for absolute values. New cuffless-specific validation frameworks mandate dynamic testing (position/hydrostatics, activity/exercise, awake-sleep, pharmacologic response, and prerecalibration drift). Professional bodies currently advise against diagnosis or drug titration using cuffless readings unless a device passes such protocols. Real-world studies show feasibility and patient preference but only moderate agreement with cuffs and limited outcomes data. Special populations (chronic kidney disease/dialysis, pregnancy, pediatrics/frail, diverse skin tones) introduce additional accuracy and equity concerns.

Summary: Cuffless wearables may be used as adjuncts to surface patterns and support engagement; diagnosis and treatment decisions must be confirmed with validated upper-arm measurements. A pragmatic "good-enough" checklist includes stable calibration over weeks, accuracy across dynamic states and subgroups, and transparent multisite validation. Priorities include harmonized standards, inclusive datasets, and trials linking cuffless monitoring to clinical outcomes.

点评目的:在消费者的采用和最近的监管里程碑的推动下,无袖带血压(BP)技术已经从概念转变为日常可穿戴设备。然而,临床医生在准确性、校准稳定性和临床使用方面面临着复杂的信号。这篇综述综合了目前的证据和新出现的标准,以阐明无约束数据可以在哪里增加价值。最近的发现:大多数设备从替代信号估计BP,并需要定期校准,使输出可靠的趋势围绕上次校准,但不太可靠的绝对值。新的无袖带特异性验证框架要求动态测试(位置/流体静力学、活动/运动、觉醒-睡眠、药理学反应和校准前漂移)。专业机构目前不建议使用无袖口读数进行诊断或药物滴定,除非设备通过此类协议。现实世界的研究显示了可行性和患者偏好,但与袖口只有中等程度的一致,而且结果数据有限。特殊人群(慢性肾病/透析、怀孕、儿科/虚弱、不同肤色)带来了额外的准确性和公平性问题。总结:无袖可穿戴设备可以作为表面图案的辅助物和支持参与;诊断和治疗决定必须通过有效的上臂测量来确认。实用的“足够好”检查表包括数周的稳定校准,跨动态状态和子组的准确性,以及透明的多站点验证。优先事项包括协调标准、包容性数据集以及将无约束监测与临床结果联系起来的试验。
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引用次数: 0
Medullary sponge kidney and chronic pain: is there a role for renal denervation. 髓质海绵对肾脏慢性疼痛:是否有肾去神经作用。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2025-12-29 DOI: 10.1097/MNH.0000000000001148
Fatima Ayotunde, David S Goldfarb

Purpose of review: Medullary sponge kidney (MSK) is a congenital disorder of the distal nephron, characterized by cystic dilatation of the papillary and medullary tubules. It commonly presents with recurrent calcium nephrolithiasis and often, severe, life-altering chronic pain syndromes, often independent of urinary obstruction and of uncertain etiology. Management focuses on stone prevention and symptomatic care, but these measures are frequently inadequate. No studies of management of this pain syndrome in these patients have been performed. There are essentially no studies evaluating renal denervation in MSK specifically, although the technique has been utilized with some benefit in other disorders, underscoring a major therapeutic gap. In this review, we describe patients with MSK and chronic pain syndrome and review the role of renal denervation as a potential therapy.

Recent findings: Renal denervation may represent a promising strategy for chronic kidney pain syndrome. It could provide pain relief and improve quality of life in affected patients.

Summary: The optimal management strategy for chronic pain in MSK has not been elucidated. Renal denervation has recently been utilized and approved for the management of blood pressure. It could be useful for managing chronic kidney pain in this condition as well.

回顾目的:髓质海绵肾(MSK)是一种先天性肾远端疾病,其特征是乳头状小管和髓质小管的囊性扩张。它通常表现为复发性钙性肾结石和严重的、改变生活的慢性疼痛综合征,通常与尿路梗阻无关,病因不明。管理的重点是结石的预防和症状护理,但这些措施往往是不够的。在这些患者中没有对这种疼痛综合征的处理进行过研究。基本上没有研究专门评估MSK的肾去神经支配,尽管该技术已用于其他疾病,并有一些益处,强调了一个主要的治疗差距。在这篇综述中,我们描述了MSK和慢性疼痛综合征的患者,并回顾了肾去神经支配作为一种潜在的治疗方法的作用。最近发现:肾去神经支配可能是治疗慢性肾痛综合征的一种有希望的策略。它可以缓解疼痛,提高患者的生活质量。摘要:MSK慢性疼痛的最佳管理策略尚未阐明。肾去神经术最近已被应用并被批准用于控制血压。在这种情况下,它可能对治疗慢性肾痛也很有用。
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引用次数: 0
Hypertension guidelines need to be patient oriented. 高血压指南需要以病人为导向。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2026-01-05 DOI: 10.1097/MNH.0000000000001154
Nayanatara Nadeesha Tantirige, Joanna M Gray, Ian B Wilkinson

Purpose of review: There is growing evidence that personalisation of hypertension treatment leads to better blood pressure control. This review will explore current evidence for individualised treatment of hypertension, and application of this in future guidelines.

Recent findings: Recent studies demonstrate considerable inter-individual variability in responses to specific antihypertensives. Factors such as ethnicity, sex, age, BMI and genetics contribute to differences in blood pressure and cardiovascular risk. There is emerging ethnicity data that may help to support targeted pharmacotherapy. Advances in genetics, particularly through large-scale genome-wide association studies (GWAS), have given us insight into individual genetic determinants of blood pressure. The development of polygenic risk scores (PRS) also show promise for future precision-guided treatment. This review will examine both intra-individual and inter-individual variability in blood pressure control and treatment response using evidence to date.

Summary: Personalised hypertension care is an evolving field. Our review highlights the importance of refining clinical guidelines to better account for individual differences in blood pressure and treatment response.

综述目的:越来越多的证据表明,个体化高血压治疗可以更好地控制血压。这篇综述将探讨个体化高血压治疗的现有证据,以及在未来指南中的应用。最近的发现:最近的研究表明,对特定抗高血压药物的反应存在相当大的个体差异。种族、性别、年龄、身体质量指数和基因等因素会导致血压和心血管风险的差异。新出现的种族数据可能有助于支持靶向药物治疗。遗传学的进步,特别是通过大规模全基因组关联研究(GWAS),使我们深入了解了血压的个体遗传决定因素。多基因风险评分(PRS)的发展也显示了未来精确指导治疗的希望。本综述将使用迄今为止的证据来研究血压控制和治疗反应的个体内和个体间变异性。个体化高血压护理是一个不断发展的领域。我们的综述强调了完善临床指南的重要性,以更好地解释血压和治疗反应的个体差异。
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引用次数: 0
Time-limited trials for acute dialysis decision-making for critically ill older patients: rationale, communication strategies, and future research. 危重老年患者急性透析决策的限时试验:理论基础、沟通策略和未来研究。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2026-01-05 DOI: 10.1097/MNH.0000000000001155
Fahad Saeed, Paul R Duberstein, Douglas B White, Kathleen D Liu, Ronald M Epstein, Kevin A Fiscella

Purpose of review: Provide an overview of the rationale for implementing time-limited dialysis trials (TLT-Ds) in critically ill older adults with acute kidney injury treated with dialysis, the communication strategies required for proper implementation, and future research directions.

Recent findings: AKI-D is linked to high mortality, reduced renal recovery, and a substantial chance of discharge to nursing homes in older adults. Many older people value independence and quality of life over longevity. Yet acute dialysis often remains the reflexive treatment option, while patients and families face prognostic uncertainty in the face of mortality. A TLT-D is an ethically sound, person-centered approach that aligns with many patients' preferences. Its benefits include providing a structured opportunity for clinicians, families, and patients to assess the biomedical efficacy of dialysis while allowing time for deliberation, prognostic clarity, and emotional processing. This can inform whether to continue acute dialysis or transition to comfort care or chronic dialysis within prespecified or evolving goals.

Summary: Acute dialysis decision-making for critically ill older adults needs improvement. Reflexive initiation followed by automatic transition to chronic dialysis may not align with many patients' goals. TLT-Ds can promote goal-concordant care. Further research is needed to guide their implementation and evaluate person-centered outcomes.

综述目的:概述在透析治疗急性肾损伤的危重老年人中实施限时透析试验(TLT-Ds)的基本原理、正确实施所需的沟通策略以及未来的研究方向。最近的研究发现:AKI-D与老年人的高死亡率、肾脏恢复减少和出院到养老院的大量机会有关。比起长寿,许多老年人更看重独立和生活质量。然而,急性透析往往仍然是反射性的治疗选择,而患者和家属在面对死亡率时面临预后的不确定性。TLT-D是一种合乎伦理的、以人为本的方法,符合许多患者的偏好。它的好处包括为临床医生、家庭和患者提供一个结构化的机会来评估透析的生物医学疗效,同时允许有时间进行审议、明确预后和情绪处理。这可以告知是否继续急性透析或过渡到舒适护理或慢性透析预先指定或发展的目标。危重老年人的急性透析决策需要改进。反身性开始后自动过渡到慢性透析可能不符合许多患者的目标。TLT-Ds可以促进目标和谐护理。需要进一步的研究来指导它们的实施和评估以人为本的结果。
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引用次数: 0
Updates in tolerance: future directions to improve kidney allograft survival. 耐受性的最新进展:改善同种异体肾移植生存的未来方向。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2026-01-12 DOI: 10.1097/MNH.0000000000001142
Opas Traitanon, Ekamol Tantisattamo, Suthiya Anumas, Pajaree Krisanapan, Thanee Eiamsitrakoon, Adis Tasanarong, Wiwat Chancharoenthana

Purpose of review: Long-term kidney allograft survival remains limited by chronic rejection and the toxicities of lifelong immunosuppression. Donor-specific tolerance, the acceptance of the graft without continuous pharmacological therapy, has long been considered the ultimate goal of transplantation. This review summarizes recent clinical advances in tolerance-inducing strategies and outlines future directions for clinical translation.

Recent findings: Clinical progress has accelerated in the past decade. Mixed hematopoietic chimerism protocols have matured from single-center feasibility studies to a recent phase 3 randomized trial in human leukocyte antigen (HLA)-identical recipients, achieving sustained immunosuppression-free survival with improved safety outcomes regulatory T cell therapies, tested across multiple early-phase trials, have consistently demonstrated safety, biological activity, and scalability in multicenter settings, with new approaches entering clinical development.

Summary: Tolerance in kidney transplantation is transitioning from conceptual aspiration to clinical feasibility. Landmark chimerism trials confirm that operational tolerance is possible in selected populations. Future priorities include refining conditioning regimens to reduce toxicity and extending eligibility to higher-risk recipients. Together, these developments suggest that tolerance-based strategies may ultimately transform kidney transplantation from chronic immunosuppression to durable immune re-education.

回顾的目的:长期的肾移植存活仍然受到慢性排斥反应和终身免疫抑制的毒性的限制。供体特异性耐受,即不需要持续的药物治疗就能接受移植物,一直被认为是移植的最终目标。本文综述了耐受性诱导策略的最新临床进展,并概述了临床转化的未来方向。最近的发现:在过去的十年里,临床进展加快了。混合造血嵌合方案已经从单中心可行性研究成熟到最近在人类白细胞抗原(HLA)相同的受体中进行的3期随机试验,实现了持续的无免疫抑制生存,并改善了安全性结果,调节性T细胞疗法在多个早期试验中进行了测试,在多中心环境中一致证明了安全性、生物活性和可扩展性,新方法进入临床开发。摘要:肾移植的耐受性正从概念上的期望过渡到临床可行性。具有里程碑意义的嵌合试验证实,在选定的人群中,操作耐受是可能的。未来的优先事项包括改进调理方案以减少毒性,并将资格扩大到高风险接受者。总之,这些发展表明,基于耐受性的策略可能最终将肾移植从慢性免疫抑制转变为持久的免疫再教育。
{"title":"Updates in tolerance: future directions to improve kidney allograft survival.","authors":"Opas Traitanon, Ekamol Tantisattamo, Suthiya Anumas, Pajaree Krisanapan, Thanee Eiamsitrakoon, Adis Tasanarong, Wiwat Chancharoenthana","doi":"10.1097/MNH.0000000000001142","DOIUrl":"10.1097/MNH.0000000000001142","url":null,"abstract":"<p><strong>Purpose of review: </strong>Long-term kidney allograft survival remains limited by chronic rejection and the toxicities of lifelong immunosuppression. Donor-specific tolerance, the acceptance of the graft without continuous pharmacological therapy, has long been considered the ultimate goal of transplantation. This review summarizes recent clinical advances in tolerance-inducing strategies and outlines future directions for clinical translation.</p><p><strong>Recent findings: </strong>Clinical progress has accelerated in the past decade. Mixed hematopoietic chimerism protocols have matured from single-center feasibility studies to a recent phase 3 randomized trial in human leukocyte antigen (HLA)-identical recipients, achieving sustained immunosuppression-free survival with improved safety outcomes regulatory T cell therapies, tested across multiple early-phase trials, have consistently demonstrated safety, biological activity, and scalability in multicenter settings, with new approaches entering clinical development.</p><p><strong>Summary: </strong>Tolerance in kidney transplantation is transitioning from conceptual aspiration to clinical feasibility. Landmark chimerism trials confirm that operational tolerance is possible in selected populations. Future priorities include refining conditioning regimens to reduce toxicity and extending eligibility to higher-risk recipients. Together, these developments suggest that tolerance-based strategies may ultimately transform kidney transplantation from chronic immunosuppression to durable immune re-education.</p>","PeriodicalId":10960,"journal":{"name":"Current Opinion in Nephrology and Hypertension","volume":" ","pages":"262-269"},"PeriodicalIF":2.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145958954","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Methotrexate nephrotoxicity: a pragmatic approach. 甲氨蝶呤肾毒性:一个实用的方法。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2025-12-05 DOI: 10.1097/MNH.0000000000001144
Yara Mouawad, Jaya Kala

Purpose of review: High-dose methotrexate (HDMTX) is an integral component of treatment for multiple malignancies. However, preventive strategies often fail, resulting in renal impairment and delayed methotrexate elimination (DME), which increases the risk of systemic toxicity. This review aims to summarize past, current, and emerging strategies for the management of HDMTX-related toxicity.

Recent findings: Recent research has identified host genetic factors, hypoalbuminemia, and larger body surface area as contributors to DME. Animal studies have explored potential nephroprotective agents, including synthetic 1,3,4-oxadiazole (5b) and repurposed drugs such as empagliflozin and amlodipine. The preferred mitigation agent, glucarpidase, continues to demonstrate improved clinical and financial outcomes, with higher odds of renal recovery even at lower doses. Early therapeutic drug monitoring has shown promise as a biomarker for predicting acute kidney injury. In addition, the web-based clinical tool MTXPK.org now integrates population pharmacokinetic models with patient-specific data to guide interpretation and management of DME.

Summary: Identification of emerging risk factors, advances in pharmacogenomics, and timely methotrexate monitoring, combined with patient-specific pharmacokinetic modeling, underscore the importance of personalized therapeutic strategies to reduce renal toxicity and DME.

综述目的:大剂量甲氨蝶呤(HDMTX)是治疗多种恶性肿瘤的一个组成部分。然而,预防策略往往失败,导致肾功能损害和延迟甲氨蝶呤消除(DME),这增加了系统性毒性的风险。本综述旨在总结过去、现在和新兴的hdmtx相关毒性管理策略。最近的发现:最近的研究已经确定宿主遗传因素、低白蛋白血症和较大的体表面积是二甲醚的贡献者。动物研究已经探索了潜在的肾保护剂,包括合成的1,3,4-恶二唑(5b)和重新利用的药物,如恩格列净和氨氯地平。首选的缓解剂葡糖苷酶继续显示出改善的临床和财务结果,即使在较低剂量下,肾脏恢复的几率也较高。早期治疗药物监测已显示出作为预测急性肾损伤的生物标志物的希望。此外,基于网络的临床工具MTXPK.org现在整合了人群药代动力学模型和患者特定数据,以指导二甲醚的解释和管理。总结:识别新出现的危险因素,药物基因组学的进展,及时监测甲氨蝶呤,结合患者特异性药代动力学建模,强调了个性化治疗策略对减少肾毒性和二甲醚的重要性。
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引用次数: 0
Global trends in hypertension prevalence, awareness, treatment, and control. 高血压流行、认识、治疗和控制的全球趋势。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-03-01 Epub Date: 2026-01-06 DOI: 10.1097/MNH.0000000000001151
Samantha S O'Connell, Paul K Whelton, Katherine T Mills

Purpose of review: High blood pressure is the leading risk factor for premature death and disability globally. Despite availability of effective treatment, prevention, and control of high blood pressure remain suboptimal worldwide. This review examines trends in hypertension prevalence, awareness, treatment, and control and highlights evidence-based strategies to improve hypertension care.

Recent findings: Hypertension awareness, treatment, and control remain inadequate globally. Recent evidence suggests that universal healthcare facility-based screening, increased accessibility and affordability of fixed-dose combination therapies, and team-based care approaches can improve the management of hypertension along the care cascade.

Summary: To prevent death and disability globally, the implementation of evidence-based strategies and policy recommendations targeting the multifactorial barriers to hypertension management and control is essential.

综述目的:高血压是全球过早死亡和残疾的主要危险因素。尽管有有效的治疗方法,但在世界范围内,预防和控制高血压的效果仍不理想。本文综述了高血压的流行、认识、治疗和控制趋势,并强调了改善高血压护理的循证策略。近期发现:全球范围内对高血压的认识、治疗和控制仍然不足。最近的证据表明,以医疗机构为基础的普遍筛查,增加固定剂量联合治疗的可及性和可负担性,以及以团队为基础的护理方法可以改善整个护理级联的高血压管理。摘要:为了在全球范围内预防死亡和残疾,实施以证据为基础的战略和政策建议至关重要,这些战略和政策建议针对高血压管理和控制的多因素障碍。
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引用次数: 0
Reimagining kidney value-based care: leveraging data science for dynamic, clinician-level risk prediction. 重新构想基于肾脏价值的护理:利用数据科学进行动态的临床水平的风险预测。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-30 DOI: 10.1097/MNH.0000000000001162
Derek J Baughman, Paul Nagy, Chirag R Parikh

Purpose of review: Chronic kidney disease (CKD) remains one of the costliest conditions in healthcare, yet value-based payment (VBP) reforms have produced limited improvements in cost or quality. Existing renal payment models rely on annual benchmarks that fail to reflect the longitudinal reality of CKD care. This precludes the possibility of observing a dose-response relationship in clinician-level interventions, effectively invisible in current VBP structures.

Recent findings: Advances in clinical informatics and predictive modeling demonstrate the feasibility of sub-annual, patient-level risk estimation for CKD outcomes and costs. Standardized electronic health record and claims data enable longitudinal, clinician-level analysis. This can transform retrospective, aggregate VBP into dynamic forecasting systems reflecting real-world care delivery. Short-horizon prediction reveals temporal, dose-response relationships between guideline-aligned interventions and downstream events that remain obscured by annualized VBP frameworks.

Summary: CKD is a clinically and economically compelling testbed for next-generation VBP design. Patient-level modeling with sub-annual risk prediction is the next step in modernizing payment frameworks to align incentives. Future VBP policy should shift models beyond static, annual metrics toward EHR-native, temporally precise evaluation frameworks that reward meaningful preventive care for patients, clinicians, and payers.

综述目的:慢性肾脏疾病(CKD)仍然是医疗保健中最昂贵的疾病之一,但基于价值的支付(VBP)改革在成本或质量方面的改善有限。现有的肾脏支付模式依赖于年度基准,不能反映慢性肾病护理的纵向现实。这排除了在临床水平干预中观察到剂量-反应关系的可能性,这种关系在当前的VBP结构中实际上是不可见的。最新发现:临床信息学和预测模型的进展证明了分年度、患者水平的CKD预后和成本风险评估的可行性。标准化的电子健康记录和索赔数据支持纵向的临床级分析。这可以将回顾性的、汇总的VBP转变为反映现实世界护理交付的动态预测系统。短期预测揭示了与指南一致的干预措施与下游事件之间的时间、剂量-反应关系,这些关系仍然被年化VBP框架所掩盖。总结:CKD是下一代VBP设计的临床和经济上令人信服的测试平台。具有次年度风险预测的患者级建模是现代化支付框架以调整激励措施的下一步。未来的VBP政策应该将模型从静态的年度指标转向ehr原生的、暂时精确的评估框架,以奖励对患者、临床医生和支付方有意义的预防性护理。
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引用次数: 0
Microvascular inflammation in the kidney transplant, beyond acute antibody-mediated rejection. 肾移植中的微血管炎症,超越急性抗体介导的排斥反应。
IF 2.4 3区 医学 Q3 PERIPHERAL VASCULAR DISEASE Pub Date : 2026-01-30 DOI: 10.1097/MNH.0000000000001165
Aurélie Sannier, Louise Benning, Alexandre Loupy

Purpose of review: Microvascular inflammation (MVI) is a central feature of allograft rejection, traditionally associated with antibody-mediated rejection (AMR), but its mechanisms and clinical impact extend beyond this framework. This review highlights recent updates in the Banff classification, insights into the mechanisms underlying MVI, and how these developments may refine diagnostic approaches and guide the development of therapeutic strategies.

Recent findings: The spectrum of MVI has been refined, with DSA-negative C4d-negative MVI and probable AMR now recognized as distinct entities associated with adverse graft outcomes. Mechanistic studies highlight the complementary roles of non-HLA antibodies, NK-cell-driven alloreactivity, and T-cell mediated injury. Molecular diagnostics have advanced our understanding of rejection phenotypes, while donor-derived cell-free DNA has emerged as the most robust and noninvasive biomarker of active microvascular injury. Novel therapies, particularly CD38-directed treatments such as felzartamab, have shown promising results in AMR but their efficacy across all MVI phenotypes remains to be established.

Summary: MVI represents a heterogeneous spectrum of alloimmune injuries that extends beyond the traditional AMR framework. Combining histology with emerging artificial intelligence tools, molecular diagnostics, and noninvasive biomarkers, will offer a more integrated approach to diagnosis, risk stratification, and development of novel therapies.

综述目的:微血管炎症(MVI)是同种异体移植排斥反应的核心特征,传统上与抗体介导的排斥反应(AMR)有关,但其机制和临床影响超出了这一框架。这篇综述强调了Banff分类的最新进展,对MVI机制的深入了解,以及这些进展如何改进诊断方法和指导治疗策略的发展。最近的发现:MVI的频谱已经被完善,dsa阴性c4d阴性MVI和可能的AMR现在被认为是与不良移植结果相关的不同实体。机制研究强调了非hla抗体、nk细胞驱动的同种异体反应性和t细胞介导的损伤的互补作用。分子诊断提高了我们对排斥表型的理解,而供体来源的无细胞DNA已成为活动性微血管损伤最强大和无创的生物标志物。新疗法,特别是针对cd38的治疗,如非扎他单,已经在AMR中显示出有希望的结果,但它们对所有MVI表型的疗效仍有待确定。摘要:MVI代表了一种异质谱的同种免疫损伤,超出了传统的抗菌素耐药性框架。将组织学与新兴的人工智能工具、分子诊断和非侵入性生物标志物相结合,将为诊断、风险分层和新疗法的开发提供更综合的方法。
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引用次数: 0
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