米德兰兹肝脏研究联盟-优化肥胖相关肝病研究的伙伴关系:针对高发地区和服务不足的社区。

NIHR open research Pub Date : 2024-12-12 eCollection Date: 2024-01-01 DOI:10.3310/nihropenres.13784.1
James King, Guruprasad Aithal, Louisa Herring, Scott Willis, Dimitris Papamargaritis, Kerry Hulley, Melanie Davies
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引用次数: 0

摘要

背景:在英国,肝脏疾病的患病率正在上升,肥胖是代谢功能障碍相关脂肪变性肝病(MASLD)激增的基础。MASLD与心脏代谢风险增加有关,特别是当与2型糖尿病共存时。进展为代谢功能障碍相关脂肪性肝炎(MASH)伴肝纤维化是与严重肝脏疾病和死亡率密切相关的一个临床里程碑。因此,临床上有意义且持续的体重减轻(≥10%)是MASLD患者的主要治疗目标。不幸的是,这对大多数采用传统生活方式的人来说是很困难的。然而,新的肥胖药物治疗在MASLD中有希望,因为它们能够产生显著的体重减轻(10-25%)并改善心脏代谢健康。这些药物改善晚期肝病患者肝纤维化和患者报告的预后/生活质量的能力仍然存在疑问。方法:由米德兰兹(英国)牵头,但具有全国代表性,我们建立了一个对肥胖相关肝脏疾病感兴趣的利益相关者网络(临床医生、学者、第三部门、行业和PPIE代表)。这个网络被称为米德兰兹肝脏研究联盟(MLRA),它寻求1)建立一个PPIE利益相关者网络,2)确定研究重点,3)绘制网络基础设施和专业知识。肝病方面的保健不平等是《肝病法》的核心优先事项。结果:MLRA与其他当地肝脏合作伙伴合作,建立了一个大型PPIE利益相关者网络。这些网络促进了关键研究优先事项的确定,从而促成了国家卫生研究院的三项资助申请。重点围绕:1)以患者为中心的结果在肥胖相关肝病研究中的重要性;2)基于胰高血糖素样肽1 (GLP-1)的肥胖药物治疗酒精使用障碍的潜力;3)初级保健/社区肝病的早期识别和管理。结论:MLRA已经建立了一个多学科的研究中心,专门研究肥胖相关肝病。该基础为该领域的研究活动提供了一个跳板。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Midlands Liver Research Alliance - A partnership to optimise obesity-related liver disease research: targeting areas of high incidence and underserved communities.

Background: The prevalence of liver disease is rising in the United Kingdom (UK), with obesity underpinning surging metabolic dysfunction-associated steatotic liver disease (MASLD). MASLD is associated with an increased cardiometabolic risk, particularly when co-existing with type 2 diabetes. Progression to metabolic dysfunction-associated steatohepatitis (MASH) with hepatic fibrosis represents a clinical milestone strongly linked to serious liver disease and mortality.Therefore, clinically meaningful and sustained weight loss (≥10%) is a primary therapeutic target for patients with MASLD. Unfortunately, this is difficult for most people who adopt traditional lifestyle approaches. However, new obesity pharmacotherapies hold promise in MASLD, given their ability to produce dramatic weight loss (10-25%) and improve cardiometabolic health. Questions remain about the ability of these agents to improve liver fibrosis and patient-reported outcomes/quality of life in patients with advanced liver disease.

Methods: Led from the Midlands (UK) but with national representation, we developed a network of stakeholders (clinicians, academics, third-sector, industry, and PPIE representatives) with an interest in obesity-related liver diseases. This network was called the Midlands Liver Research Alliance (MLRA), which sought to 1) establish a PPIE stakeholder network, 2) identify research priorities, and 3) map the network infrastructure and expertise. Health inequalities within liver disease are a core priority within the MLRA.

Results: The MLRA developed a large PPIE stakeholder network in collaboration with other local liver partnerships. These networks facilitated the identification of key research priorities that led to three NIHR funding applications. Priorities centered around: 1) the importance of patient-centered outcomes in obesity-related liver disease research; 2) the potential of glucagon-like peptide 1 (GLP-1)-based obesity pharmacotherapy in alcohol use disorder; and 3) early identification and management of liver disease in primary care/community.

Conclusions: The MLRA has created a multidisciplinary hub of research expertise in obesity-related liver disease. This foundation provides a springboard for research activities in this area.

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