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抗磷脂综合征中除瓣膜性心脏病以外的左心室舒张功能异常:一项超声心动图研究。

Left ventricular diastolic abnormalities other than valvular heart disease in antiphospholipid syndrome: An echocardiographic study.

机构信息

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Department of Advanced Biomedical Sciences, Federico II University, Naples, Italy.

出版信息

Int J Cardiol. 2018 Nov 15;271:366-370. doi: 10.1016/j.ijcard.2018.05.040.

Abstract

BACKGROUND

Antiphospholipid syndrome (APS) can be primary or secondary to other autoimmune disorders. Besides valvular heart disease (VHD) and coronary artery disease (CAD), little is known about the impact of APS on left ventricular (LV) function.

METHODS

After excluding CAD, relevant VHD and heart failure, 69 patients (mean age = 43.9 years, 40 with primary and 29 with secondary APS) were assessed by echo-Doppler. Sixty-nine heathy controls, matched for age and sex, formed the control group. APS was diagnosed in presence of at least one clinical criteria and one confirmed laboratory criteria, including lupus anticoagulant (LA) titre. The adjusted global APS score (aGAPSS), derived from the combination of risk factors for thrombosis and autoimmune-antibody profile was calculated.

RESULTS

Patients had similar blood pressure and heart rate, but higher body mass index (BMI) than controls. LV mass index (p = 0.007) and left atrial volume index (p < 0.01) were greater, while early diastolic velocity (e') was lower (p = 0.003) and E/e' higher (p = 0.007) in APS. Primary APS patients had lower E/A and e' compared to both controls and secondary APS, while E/e' was higher in secondary APS than in controls. APS patients with diastolic dysfunction were older but did not differ for risk factors prevalence from those with normal/indeterminate diastolic function. In the pooled APS, LA positivity was independently associated with e' and E/e' after adjusting for age, BMI and aGAPSS in separate multivariate models.

CONCLUSION

In APS, LV diastolic abnormalities are detectable. They are more pronounced in primary APS and independently associated with LA positivity.

摘要

背景

抗磷脂综合征(APS)可分为原发性或继发性于其他自身免疫性疾病。除了心脏瓣膜病(VHD)和冠状动脉疾病(CAD)外,对于 APS 对左心室(LV)功能的影响知之甚少。

方法

在排除 CAD、相关 VHD 和心力衰竭后,对 69 名患者(平均年龄为 43.9 岁,其中 40 名原发性 APS,29 名继发性 APS)进行超声心动图-多普勒检查。69 名健康对照者,按年龄和性别匹配,作为对照组。APS 的诊断标准为至少存在一个临床标准和一个实验室标准,包括狼疮抗凝剂(LA)滴度。从血栓形成和自身抗体谱的危险因素组合中得出调整后的全局 APS 评分(aGAPSS)。

结果

患者的血压和心率相似,但体重指数(BMI)较高。LV 质量指数(p=0.007)和左心房容积指数(p<0.01)更高,而舒张早期速度(e')更低(p=0.003),E/e'更高(p=0.007)。原发性 APS 患者的 E/A 和 e'均低于对照组和继发性 APS 患者,而 E/e'在继发性 APS 患者中高于对照组。舒张功能障碍的 APS 患者年龄较大,但与舒张功能正常/不确定的患者相比,其危险因素的患病率并无差异。在合并的 APS 中,LA 阳性在分别调整年龄、BMI 和 aGAPSS 的多元模型中,与 e'和 E/e'独立相关。

结论

在 APS 中,可以检测到 LV 舒张异常。在原发性 APS 中更为明显,并与 LA 阳性独立相关。

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