Department of Cardiology, Center for Clinical Heart Research, Oslo University Hospital Ullevål, Oslo, Norway.
Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Scand Cardiovasc J. 2021 Aug;55(4):213-219. doi: 10.1080/14017431.2021.1889653. Epub 2021 Mar 2.
. Ageing is one of the strongest risk factors for atrial fibrillation (AF), and additional risk factors are also closely related to ageing. Remodeling is part of the pathophysiology of AF, and a possible common denominator of ageing and other AF risk factors. The aim of this study was to investigate any association between the presence of AF and the ageing biomarkers, leukocyte telomere length (LTL) and sirtuin-1 (SIRT-1), and the cardiac remodeling biomarkers Galectin-3 and sST2 in elderly myocardial infarction (MI) patients. Patients were included after admission for MI. Diagnosis of AF was retrieved from medical records and classified as either history of AF before MI or new onset from admission to study inclusion. SIRT-1, sST2 and Galectin-3 were analyzed by ELISAs and LTL by qPCR. In total, 299 patients were included, median age 75 years, 70.2% male. A history of AF was recorded in 38 patients and 30 patients experienced new onset AF. Higher levels of SIRT-1 were associated with lower risk of having a history of AF (OR = 0.46 (95% CI 0.26, 0.81), = 0.007), whereas higher sST2 levels were associated with higher risk of AF (OR = 4.13 (95% CI 1.69, 10.13), = 0.002). Results remained significant after adjustment for other AF risk factors. No significant associations with AF were found for Galectin-3 or LTL. None of the biomarkers associated with new onset AF. In elderly patients with MI, higher ST2 and lower SIRT-2 levels were associated with higher prevalence of AF, possibly reflecting both ageing and the remodeling phenomena in AF. ClinicalTrials.gov (NCT01841944).
衰老(ageing)是心房颤动(atrial fibrillation,AF)最强的危险因素之一,此外,其他的危险因素也与衰老密切相关。重构(remodeling)是 AF 病理生理学的一部分,也是衰老和其他 AF 危险因素的一个可能的共同因素。本研究旨在探讨 AF 与衰老生物标志物白细胞端粒长度(leukocyte telomere length,LTL)和 SIRT-1、心脏重构生物标志物半乳糖凝集素-3(Galectin-3)和可溶性 ST2(sST2)之间的关系,这些标志物在老年心肌梗死(myocardial infarction,MI)患者中都有体现。
MI 入院后,患者被纳入研究。AF 的诊断来源于病历,并分为 MI 前有 AF 病史或从入院到研究纳入期间新发 AF。通过 ELISA 分析 SIRT-1、sST2 和 Galectin-3,通过 qPCR 分析 LTL。
总共纳入 299 例患者,中位年龄 75 岁,70.2%为男性。38 例患者有 AF 病史,30 例患者新发 AF。较高的 SIRT-1 水平与 AF 病史的风险降低相关(OR = 0.46(95% CI 0.26, 0.81),= 0.007),而较高的 sST2 水平与 AF 的风险升高相关(OR = 4.13(95% CI 1.69, 10.13),= 0.002)。调整其他 AF 危险因素后,结果仍有统计学意义。Galectin-3 或 LTL 与 AF 无显著相关性。无任何生物标志物与新发 AF 相关。
在老年 MI 患者中,较高的 sST2 和较低的 SIRT-2 水平与 AF 患病率升高相关,这可能反映了衰老和 AF 重构现象。
ClinicalTrials.gov(NCT01841944)。