Proietti Riccardo, Rivera-Caravaca José Miguel, López-Gálvez Raquel, Harrison Stephanie L, Marín Francisco, Underhill Paula, Shantsila Eduard, McDowell Garry, Vinciguerra Manlio, Davies Rhys, Giebel Clarissa, Lane Deirdre A, Lip Gregory Y H
Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool L8 7TX, UK.
Department of Cardiovascular and Metabolic Medicine, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool L8 7TX, UK.
J Clin Med. 2023 Apr 11;12(8):2814. doi: 10.3390/jcm12082814.
Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are effective anti-diabetic drugs improving cardiovascular outcomes in type 2 diabetes mellitus (T2DM) patients. This study investigated cardiovascular, cerebrovascular and cognitive outcomes of SGLT2i therapy in patients with atrial fibrillation (AF) and T2DM.
Observational study using TriNetX, a global health research network of anonymised electronic medical records from real-world patients between January 2018 and December 2019. The network includes healthcare organisations globally but predominately in the United States. AF patients (ICD-10-CM code: I48) with T2DM were divided according to SGLT2i use or not, and balanced using propensity score matching (PSM). Patients were followed-up for 3-years. The primary endpoints were ischaemic stroke/transient ischemic attack (TIA), intracranial haemorrhage (ICH), and incident dementia. Secondary endpoints were incident heart failure and mortality.
We identified 89,356 AF patients with T2DM of which 5061 (5.7%) were taking a SGLT2i. After PSM, 5049 patients (mean age 66.7 ± 10.6 years; 28.9% female) were included in each group. At 3-years follow-up, the risk of ischaemic stroke/TIA was higher in patients not receiving SGLT2i (HR 1.12, 95% CI 1.01-1.24) and for ICH (HR 1.57, 95% CI 1.25-1.99) and incident dementia (HR 1.66, 95% CI 1.30-2.12). Incident heart failure (HR 1.50, 95% CI 1.34-1.68) and mortality (HR 1.77, 95% CI 1.58-1.99) risks were increased in AF patients not receiving SGLT2i.
In our large 'real world' analysis of patients with concomitant AF and T2DM, SGLT2i reduced the risk of cerebrovascular events, incident dementia, heart failure and death.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)是有效的抗糖尿病药物,可改善2型糖尿病(T2DM)患者的心血管结局。本研究调查了SGLT2i治疗对心房颤动(AF)合并T2DM患者的心血管、脑血管和认知结局的影响。
使用TriNetX进行观察性研究,TriNetX是一个全球健康研究网络,包含2018年1月至2019年12月期间真实世界患者的匿名电子病历。该网络包括全球的医疗机构,但主要在美国。将患有T2DM的AF患者(ICD-10-CM编码:I48)根据是否使用SGLT2i进行分组,并使用倾向评分匹配(PSM)进行平衡。对患者进行3年的随访。主要终点为缺血性卒中/短暂性脑缺血发作(TIA)、颅内出血(ICH)和新发痴呆。次要终点为新发心力衰竭和死亡率。
我们确定了89356例患有T2DM的AF患者,其中5061例(5.7%)正在服用SGLT2i。经过PSM后,每组纳入5049例患者(平均年龄66.7±10.6岁;28.9%为女性)。在3年的随访中,未接受SGLT2i治疗的患者发生缺血性卒中/TIA的风险更高(HR 1.12,95%CI 1.01-1.24),ICH(HR 1.57,95%CI 1.25-1.99)和新发痴呆(HR 1.66,95%CI 1.30-2.12)的风险也更高。未接受SGLT2i治疗的AF患者发生新发心力衰竭(HR 1.50,95%CI 1.34-1.68)和死亡率(HR 1.77,95%CI 1.58-1.99)的风险增加。
在我们对AF合并T2DM患者的大型“真实世界”分析中,SGLT2i降低了脑血管事件、新发痴呆、心力衰竭和死亡的风险。