慢性炎症是否在经皮经静脉二尖瓣合并术后风湿性二尖瓣再狭窄中起作用?

A. Soesanto
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引用次数: 0

摘要

摘要背景:二尖瓣再狭窄是指PTMC后二尖瓣面积减少50%。它与时间相关,并与主要心血管不良事件(MACE)相关,如充血性心力衰竭、心脏病死亡、二尖瓣置换术和再行PTMC。其机制尚不清楚;然而,慢性炎症可能也有一定作用。目的:了解慢性炎症与PTMC术后二尖瓣再狭窄的关系。方法:将40例成功PTMC的二尖瓣狭窄患者进行配对,分为再狭窄/病例组(n=20)和无再狭窄/对照组(n=2 0)。次要数据取自电子医疗记录,如患者特征(性别、年龄和第二次预防)、PTMC前的超声心动图数据(PTMC前Wilkins评分和MVA)和PTMC后的超声心动图图数据(PT后MVA)。对所有患者进行随访超声心动图检查(随访MVA)和慢性炎症标志物(IL-6)的实验室评估。进行统计分析,寻找慢性炎症标志物和其他自变量水平与二尖瓣再狭窄之间的相关性。结果:IL-6的中位浓度为2.39(0.03–11.4)pg/mL。两组IL-6水平无统计学显著差异(p值>0.05)。MVA下降0.13(0–0.62)cm2/年,MVA下降率≥0.155 cm2/年是二尖瓣再狭窄的预测指标(p值<0.001,OR=46.72,95%CI 6.69–326.19)。结论:IL-6评估的慢性炎症与二尖瓣再狭窄无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does Chronic Inflammation Play a Role in Rheumatic Mitral Valve Restenosis after Percutaneous Transvenous Mitral Commissurotomy?
ABSTRACT Background: Mitral valve restenosis is defined as decreased mitral valve area (MVA) <1.5 cm2 or decreased MVA >50% after PTMC. It is time-dependent and associated with major adverse cardiovascular events (MACE), such as congestive heart failure, cardiac death, mitral valve replacement, and redo PTMC. The mechanism is not yet known; however, chronic inflammation may have a role. Objective: To know the association between chronic inflammation and mitral valve restenosis after PTMC. Methods: A total of 40 patients with mitral valve stenosis who underwent successful PTMC were matched and classified into restenosis/case group (n=20) and no restenosis/control group (n=20). Secondary data was taken from electronic medical records such as patient characteristics (gender, age & 2nd prophylaxis), echocardiography data before PTMC (Wilkins’ score and MVA before PTMC), and echocardiography data after PTMC (MVA after PTMC). Follow-up echocardiography examination (follow-up MVA) and laboratory assessment of chronic inflammation marker (IL-6) were done on all patients. Statistical analyses were done to look for an association between the level of chronic inflammation marker & other independent variables with mitral valve restenosis. Results: Median IL-6 concentration was 2.39 (0.03 – 11.4) pg/mL. There was no statistically significant difference in IL-6 levels between both groups (p-value >0.05). MVA decrement was 0.13 (0 – 0.62) cm2/year with rate of MVA decrement ≥0.155 cm2/year was predictor of mitral valve restenosis (p-value <0.001, OR = 46.72, 95% CI 6.69 – 326.19). Conclusion: Chronic inflammation assessed by IL-6 was not associated with mitral valve restenosis.
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