Hill Michael C, Kim Noah, Galanter William, Gerber Ben S, Hubbard Colin C, Darbar Dawood, McCauley Mark D
Division of Cardiology, College of Medicine, University of Illinois at Chicago, United States.
Division of Academic Internal Medicine, College of Medicine, University of Illinois at Chicago, United States.
Int J Cardiol Heart Vasc. 2024 Jun 25;53:101450. doi: 10.1016/j.ijcha.2024.101450. eCollection 2024 Aug.
Obesity increases risk of atrial fibrillation (AF) at least in part due to pro-inflammatory effects, but has been paradoxically associated with improved mortality. Although statins have pleiotropic anti-inflammatory properties, their interaction with obesity and clinical outcomes in AF is unknown. We explored the relationship between BMI, statin use, and all-cause mortality and AF/congestive heart failure (CHF)-related encounters, hypothesizing that statin exposure may be differentially associated with improved outcomes in overweight/obesity.
This was a single center retrospective cohort study of adults with AF diagnosed between 2011-2018. Patients were grouped by body mass index (BMI) and statin use at time of AF diagnosis. Outcomes included all-cause mortality and ED or inpatient encounters for AF or CHF.
A total of 2503 subjects were included (median age 66 years, 43.4 % female, median BMI 29.8 kg/m, 54.6 % on baseline statin therapy). Increasing BMI was associated with decreased mortality hazard but not associated with AF/CHF encounter risk. Adjusting for statin-BMI interaction, demographics, and cardiovascular comorbidities, overweight non-statin users experienced improved mortality (adjusted hazard ratio [aHR] 0.55, 95 % CI 0.35-0.84) compared to statin users (aHR 0.98, 95 % CI 0.69-1.40; interaction P-value = 0.013). Mortality hazard was consistently lower in obese non-statin users than in statin users, however interaction was insignificant. No significant BMI-statin interactions were observed in AF/CHF encounter risk. In summary, statin use was not differentially associated with improved mortality or hospitalization risk in overweight/obese groups. These findings do not support statins for secondary prevention of adverse outcomes based on overweight/obesity status alone.
肥胖至少部分通过促炎作用增加心房颤动(AF)风险,但矛盾的是,肥胖与死亡率改善相关。尽管他汀类药物具有多效抗炎特性,但其与肥胖及房颤临床结局之间的相互作用尚不清楚。我们探讨了体重指数(BMI)、他汀类药物使用与全因死亡率以及房颤/充血性心力衰竭(CHF)相关就诊之间的关系,假设他汀类药物暴露可能与超重/肥胖人群结局改善存在差异关联。
这是一项对2011年至2018年间诊断为房颤的成年人进行的单中心回顾性队列研究。患者在房颤诊断时按体重指数(BMI)和他汀类药物使用情况分组。结局包括全因死亡率以及房颤或CHF的急诊或住院就诊情况。
共纳入2503名受试者(中位年龄66岁,43.4%为女性,中位BMI 29.8kg/m²,54.6%接受基线他汀类药物治疗)。BMI升高与死亡风险降低相关,但与房颤/CHF就诊风险无关。在对他汀类药物 - BMI相互作用、人口统计学特征和心血管合并症进行校正后,超重的非他汀类药物使用者与他汀类药物使用者相比,死亡率有所改善(校正风险比[aHR] 0.55,95%置信区间0.35 - 0.84)(aHR 0.98,95%置信区间0.69 - 1.40;相互作用P值 = 0.013)。肥胖的非他汀类药物使用者的死亡风险始终低于他汀类药物使用者,然而相互作用不显著。在房颤/CHF就诊风险方面未观察到显著的BMI - 他汀类药物相互作用。总之,在超重/肥胖人群中,他汀类药物使用与死亡率改善或住院风险降低无差异关联。这些发现不支持仅基于超重/肥胖状态使用他汀类药物进行不良结局的二级预防。