King James, Aithal Guruprasad, Herring Louisa, Willis Scott, Papamargaritis Dimitris, Hulley Kerry, Davies Melanie
Nottingham Digestive Diseases Center, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK.
NIHR Nottingham Biomedical Research Centre, Nottingham University Hospital NHS Trust, and the University of Nottingham, Nottingham, UK.
NIHR Open Res. 2024 Dec 12;4:75. doi: 10.3310/nihropenres.13784.1. eCollection 2024.
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.
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.
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.
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.
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性肝病(MASLD)激增的根本原因。MASLD与心血管代谢风险增加相关,尤其是与2型糖尿病共存时。进展为伴有肝纤维化的代谢功能障碍相关脂肪性肝炎(MASH)是一个临床里程碑,与严重肝病和死亡率密切相关。因此,具有临床意义的持续体重减轻(≥10%)是MASLD患者的主要治疗目标。不幸的是,对于大多数采用传统生活方式方法的人来说,这很难实现。然而,新的肥胖药物疗法在MASLD治疗中具有前景,因为它们能够显著减轻体重(10%-25%)并改善心血管代谢健康。对于这些药物改善晚期肝病患者肝纤维化以及患者报告的结局/生活质量的能力,仍存在疑问。
我们以英国中部地区为牵头,但有全国范围的代表参与,建立了一个对肥胖相关肝病感兴趣的利益相关者网络(包括临床医生、学者、第三部门、行业和患者及公众参与和参与研究代表)。这个网络被称为中部地区肝脏研究联盟(MLRA),其旨在:1)建立一个患者及公众参与和参与研究的利益相关者网络;2)确定研究重点;3)描绘网络基础设施和专业知识。肝病中的健康不平等是MLRA的核心优先事项。
MLRA与其他当地肝脏合作组织合作,建立了一个庞大的患者及公众参与和参与研究的利益相关者网络。这些网络促进了关键研究重点的确定,从而促成了三项向英国国家健康与护理研究委员会(NIHR)的资金申请。重点围绕:1)以患者为中心的结局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)的肥胖药物疗法在酒精使用障碍中的潜力;3)初级保健/社区中肝病的早期识别和管理。
MLRA创建了一个肥胖相关肝病研究专业知识的多学科中心。这一基础为该领域的研究活动提供了一个跳板。