Wass Sojin Y, Barnard John, Kim Hyun Su, Sun Han, Telfer William, Schilling Taylor, Barzilai Benico, Bruemmer Dennis, Cho Leslie, Huang Julie, Hussein Ayman, Kashyap Sangeeta R, Laffin Luke, Mehra Reena, Moravec Chris, Saliba Walid, Sanders Prashanthan, Nissen Steven, Varma Niraj, Smith Jonathan, Van Wagoner David, Chung Mina K
Department of Cardiovascular Medicine, Heart, Vascular & Thoracic Institute, Cleveland, USA.
Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, USA.
J Interv Card Electrophysiol. 2025 Jan;68(1):9-19. doi: 10.1007/s10840-024-01955-z. Epub 2024 Dec 13.
Despite advances in ablation and other therapies for AF, progression of atrial fibrillation (AF) remains a significant clinical problem, associated with worse prognosis and worse treatment outcomes. Upstream therapies targeting inflammatory or antifibrotic mechanisms have been disappointing in preventing AF progression, but more recently genetic and genomic studies in AF suggest novel cellular and metabolic stress targets, supporting prior studies of lifestyle and risk factor modification (LRFM) for AF. However, while obesity is a significant risk factor, weight loss and risk factor modification have not been successfully applied in a US population with AF. Metformin, a common drug that targets metabolic stress pathways, has demonstrated potential in reducing the burden of AF.
The Targeting Risk Interventions and Metformin for Atrial Fibrillation (TRIM-AF, NCT03603912) is a randomized clinical trial designed to examine reduction of AF burden and progression, targeting metabolic upstream therapies. This single center trial, at the Cleveland Clinic, is designed as a prospective randomized open-label blinded endpoint (PROBE) 2 × 2 factorial study of metformin extended release up to 750 mg twice daily and lifestyle and risk factor modification (LRFM) in patients with a cardiovascular implantable electronic device (CIED) that have had at least one ≥ 5-min episode of atrial fibrillation (AF) over the prior 3 months. Randomization is stratified by pacemaker vs. ICD and rhythm at enrollment (sinus rhythm/atrial paced vs. AF).
TRIM-AF trial aims to determine if metformin, lifestyle, and risk factor modification (LRFM) reduce AF burden and its progression and assess whether combined therapy outperforms individual treatments.
URL: https://clinicaltrials.gov/ ; Unique Identifier: NCT03603912.
尽管房颤的消融及其他治疗方法取得了进展,但房颤进展仍是一个重大的临床问题,与更差的预后和治疗结果相关。针对炎症或抗纤维化机制的上游治疗在预防房颤进展方面效果不佳,但最近房颤的基因和基因组研究提示了新的细胞和代谢应激靶点,这支持了先前关于房颤生活方式和危险因素修正(LRFM)的研究。然而,虽然肥胖是一个重要的危险因素,但体重减轻和危险因素修正尚未成功应用于美国的房颤患者群体。二甲双胍是一种针对代谢应激途径的常用药物,已显示出减轻房颤负担的潜力。
房颤的靶向风险干预与二甲双胍(TRIM-AF,NCT03603912)是一项随机临床试验,旨在研究针对代谢上游治疗减轻房颤负担和进展情况。这项在克利夫兰诊所进行的单中心试验,设计为一项前瞻性随机开放标签盲终点(PROBE)2×2析因研究,对象为植入心血管植入式电子设备(CIED)且在过去3个月内至少有一次≥5分钟房颤发作的患者,给予每日两次最高750毫克的缓释二甲双胍以及生活方式和危险因素修正(LRFM)。随机分组按起搏器与植入式心律转复除颤器以及入组时的心律(窦性心律/心房起搏与房颤)进行分层。
TRIM-AF试验旨在确定二甲双胍、生活方式和危险因素修正(LRFM)是否能减轻房颤负担及其进展,并评估联合治疗是否优于单一治疗。
网址:https://clinicaltrials.gov/ ;唯一标识符:NCT03603912。