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Tissue Doppler imaging in systemic sclerosis: A 3-year longitudinal study

机译:系统性硬化症中的组织多普勒成像:一项为期3年的纵向研究

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Objectives: To investigate by standard echocardiography and pulsed-tissue Doppler imaging (TDI) the course of systemic sclerosis (SSc) heart disease and its correlation with epidemiological, clinical, and serological features of the disease and drug treatment. Methods: A total of 74 consecutive patients (69 females, between the ages of 19 and 71 years, and disease duration 1-43 years) and 71 controls underwent cardiac assessment at baseline and at 3-year follow-up. Results: At baseline, compared to controls, patients showed post-Bonferroni correction, impaired left (LV) and right ventricular (RV) diastolic function (Em/Am 0.85 ± 0.4 vs 1.5 ± 0.7, p = 0.0003; Et/At 0.9 ± 0.3 vs 1.3 ± 0.4, p = 0.0003), subtle LV and RV systolic dysfunction (Sm 13.7 ± 2.7 vs 15.4 ± 3.2cm/s, p = 0.031; St 11.5cm/s in 16/74 patients vs 0 controls, p = 0.0031), and higher pulmonary artery systolic pressure (sPAP) (26.1 ± 6.0 vs 24.1 ± 5.1, p = 0.040). At 3-year follow-up, SSc patients showed a further deterioration of biventricular diastolic and systolic function and a further sPAP increase. At multiple regression analysis of baseline data, Em/Am 1 was detected in 55/74 patients vs 25/71 controls (p 0.0001) and was associated with age (p = 0.030); Et/At 1 was detected in 16/74 patients vs 7/71 controls (p 0.0001), was associated with NYHA class ≥ II (p = 0.033), late capillaroscopic pattern (p = 0.029), and a baseline cardiac Medsger severity score ≥ 1 (p = 0.029). TDI evidence of new abnormalities in RV and/or LV diastolic function was associated with a baseline cardiac Medsger severity score ≥ 1 (p = 0.01). Neither diastolic or systolic abnormalities nor sPAP changes correlated with treatment. Conclusions: Our study confirms that SSc patients exhibit biventricular systolic and diastolic dysfunction and increased sPAP and reveals further deterioration at 3-year follow-up.
机译:目的:通过标准超声心动图和脉冲组织多普勒成像(TDI)研究系统性硬化症(SSc)心脏病的病程及其与疾病的流行病学,临床和血清学特征以及药物治疗的相关性。方法:在基线和3年随访期间,总共74例连续患者(69例女性,年龄在19至71岁之间,疾病持续时间为1-43岁)和71例对照组接受了心脏评估。结果:与对照组相比,患者基线时表现出邦弗朗尼矫正,左(LV)和右心室(RV)舒张功能受损(Em / Am 0.85±0.4 vs 1.5±0.7,p = 0.0003; Et / At 0.9± 0.3 vs 1.3±0.4,p = 0.0003),LV和RV收缩期功能不佳(Sm 13.7±2.7 vs 15.4±3.2cm / s,p = 0.031; 16/74患者的St <11.5cm / s vs 0对照,p = 0.0031)和更高的肺动脉收缩压(sPAP)(26.1±6.0 vs 24.1±5.1,p = 0.040)。在3年的随访中,SSc患者的双室舒张功能和收缩功能进一步恶化,sPAP进一步升高。在对基线数据进行多元回归分析时,在55/74例患者与25/71例对照中检测到Em / Am <1(p <0.0001),并且与年龄相关(p = 0.030);在16/74例患者和7/71例对照中检测到Et / At <1(p <0.0001),与NYHA≥II级(p = 0.033),晚期毛细血管镜检查模式(p = 0.029)和基线心脏Medsger相关严重性评分≥1(p = 0.029)。 RV和/或LV舒张功能新异常的TDI证据与基线心脏Medsger严重性评分≥1(p = 0.01)相关。舒张期或收缩期异常与sPAP变化均与治疗无关。结论:我们的研究证实SSc患者表现出双室收缩和舒张功能障碍和sPAP升高,并显示在3年的随访中进一步恶化。

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