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非瓣膜性心房颤动与老年退行性心脏瓣膜病的瓣膜结构与生化指标之间的关系

Relationship between valvular structure and biochemical indices of non-valvular atrial fibrillation and senile degenerative valvular heart disease.

作者信息

Chen Jian-Qin, Zeng Xin, Li Kun-Con, Huang Jing-Long, Guo Bing-Li, Zhou Xuan

机构信息

Department of Geriatrics, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.

Department of Cardiovascular Internal Medicine, Wuhan Fifth Hospital, Wuhan, China.

出版信息

J Thorac Dis. 2023 Feb 28;15(2):611-619. doi: 10.21037/jtd-23-61. Epub 2023 Feb 23.

Abstract

BACKGROUND

Valvular heart disease (VHD) is a common clinical condition in geriatric-related cardiovascular diseases that is connected to heart dysfunction. Atrial fibrillation (AF) is the most frequent arrhythmia. Considering these two common clinical conditions, so far no sufficient data on the relationship between degenerative VHD and non-valvular atrial fibrillation (NVAF). We aimed to explore the relationship between valvular structure and biochemistry of nonvalvular AF and degenerative valvular heart disease in the elderly.

METHODS

In our study, 234 VHD patients who were diagnosis evaluated by transthoracic echocardiography were enrolled in this retrospective study from January 2015 and December 2018. Significant valvular diseases were defined according to ACC/AHA Classification as any moderate or severe mitral regurgitation (MR), aortic regurgitation (AR), tricuspid stenosis, regurgitation, or aortic stenosis (AS). Data on relevant laboratory indicators were also collected.

RESULTS

A total of 234 patients with degenerative VHD were enrolled, of whom 81 had NVAF and 153 had sinus rhythm. Gender, smoking history, and some comorbidities, such as coronary artery disease, diabetes, and renal dysfunction, did not differ significantly between the two groups, but there were significant differences in age and hypertension {79 [74-83] 70 [65-79] years} After propensity-score matching (PSM), we identified 68 VHD patients with NVAF and 68 VHD patients without NVAF. The NVAF + VHD had higher low-density lipoprotein (LDL) cholesterol (2.94±0.84 2.26±1.33 mmol/L, P=0.001), lower high-density lipoprotein (HDL) cholesterol [1.03 (0.89-1.34) 1.56 (0.99-2.71) mmol/L, P<0.001], and higher uric acid (UA) (438.18±145.83 376.67±148.03 µmol/L, P=0.02) than the VHD group. The ejection fraction (EF) of the NVAF + VHD group was lower than that of the VHD group {63 [51-68] 66 [62-69], P=0.013}. In addition, the left atrial size, MR, and calcification of the NVAF + VHD group were higher than those of the VHD group.

CONCLUSIONS

Pronounced MR, valve calcification and hyperlipidemia were more likely in VHD patients with NVAF. These structures and biomarkers changes maybe important clinical parameters for disease prevention and management, which indicate early drug intervention to AF and hyperlipidemia is necessary.

摘要

背景

心脏瓣膜病(VHD)是老年相关心血管疾病中的一种常见临床病症,与心脏功能障碍相关。心房颤动(AF)是最常见的心律失常。考虑到这两种常见临床病症,目前尚无关于退行性VHD与非瓣膜性心房颤动(NVAF)之间关系的充分数据。我们旨在探讨老年非瓣膜性AF与退行性心脏瓣膜病的瓣膜结构及生物化学之间的关系。

方法

在我们的研究中,2015年1月至2018年12月期间,选取了234例经经胸超声心动图诊断评估的VHD患者纳入这项回顾性研究。根据美国心脏病学会/美国心脏协会(ACC/AHA)分类,将显著的瓣膜疾病定义为任何中度或重度二尖瓣反流(MR)、主动脉瓣反流(AR)、三尖瓣狭窄、反流或主动脉瓣狭窄(AS)。还收集了相关实验室指标的数据。

结果

共纳入234例退行性VHD患者,其中81例患有NVAF,153例为窦性心律。两组之间的性别、吸烟史以及一些合并症,如冠状动脉疾病、糖尿病和肾功能不全,差异均无统计学意义,但在年龄和高血压方面存在显著差异{79[74 - 83]岁对70[65 - 79]岁}。经过倾向评分匹配(PSM)后,我们确定了68例患有NVAF的VHD患者和68例未患有NVAF的VHD患者。与VHD组相比,NVAF + VHD组的低密度脂蛋白(LDL)胆固醇水平更高(2.94±0.84对2.26±1.33 mmol/L,P = 0.001),高密度脂蛋白(HDL)胆固醇水平更低[1.03(0.89 - 1.34)对1.56(0.99 - 2.71)mmol/L,P < 0.001],尿酸(UA)水平更高(438.18±145.83对376.67±148.03 µmol/L,P = 0.02)。NVAF + VHD组的射血分数(EF)低于VHD组{63[51 - 68]对66[62 - 69],P = 0.013}。此外,NVAF + VHD组的左心房大小、MR及钙化程度均高于VHD组。

结论

患有NVAF的VHD患者更易出现明显的MR、瓣膜钙化和高脂血症。这些结构和生物标志物的变化可能是疾病预防和管理的重要临床参数,这表明对AF和高脂血症进行早期药物干预是必要的。

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本文引用的文献

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Mitral valve diseases: Pathophysiology and interventions.二尖瓣疾病:病理生理学与干预措施。
Prog Cardiovasc Dis. 2021 Jul-Aug;67:98-104. doi: 10.1016/j.pcad.2021.03.008. Epub 2021 Apr 2.
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[Research progress in the pathogenesis of senile degenerated valvular heart diease].老年退行性心脏瓣膜病发病机制的研究进展
Zhonghua Xin Xue Guan Bing Za Zhi. 2017 Oct 24;45(10):895-898. doi: 10.3760/cma.j.issn.0253-3758.2017.10.018.

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