Liu Jiamei, Wang Yidan, Chen Mulei, Zhao Wenshu, Wang Xin, Wang Hua, Zhang Zhiyong, Zhang Juan, Xu Lin, Chen Jin, Yang Xinchun, Zhang Lin
Heart Failure Center, Department of Cardiology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
PLoS One. 2014 Jan 23;9(1):e86770. doi: 10.1371/journal.pone.0086770. eCollection 2014.
Peripartum cardiomyopathy (PPCM) is characterized by left ventricular systolic dysfunction and heart failure. However, its pathogenesis is not clear. Our preliminary study revealed that autoantibodies against β1-adrenergic receptors (β1R-AABs) and M2-muscarinic receptors (M2R-AABs) participated in heart failure regardless of primary heart disease. Whether β1R-AABs and M2R-AABs participate in the pathogenesis of PPCM is still unknown.
Totally 37 diagnosed PPCM patients and 36 normal pregnant women were enrolled in this study. Clinical assessment and 2-dimensional echocardiographic studies as well as the measurement of β1R-AABs or M2R-AABs by enzyme linked immunosorbent assay (ELISA) were performed.
The positive rates for β1R-AABs and M2R-AABs were 59.5% (22/37) and 45.9% (17/37) in PPCM patients, and 19.4% (7/36) (P<0.001) and 16.67% (6/36) (P<0.001) in normal pregnant women, respectively. Both β1R-AABs and M2R-AABs had a positive correlation with serum expression level of NT-proBNP, left ventricular dimension and NYHA FC (rs: 0.496-0.892, P<0.01). In addition, a negative correlation between the activity of β1R-AABs and M2R-AABs and LVEF, LVFS was observed (rs: -0.488-0.568, P<0.01). Moreover, autoantibodies against cardiovascular receptors increased the risk of the onset of PPCM (OR = 18.786, 95% confidence interval 1.926-183.262, P = 0.012).
The β1R-AABs and M2R-AABs reveal a significant elevation and are correlated with the increased left ventricular dimension and worse cardiac contraction function. The autoantibodies of cardiovascular receptors are independent risk factors for the onset of PPCM.
围产期心肌病(PPCM)的特征是左心室收缩功能障碍和心力衰竭。然而,其发病机制尚不清楚。我们的初步研究表明,无论原发性心脏病如何,抗β1-肾上腺素能受体自身抗体(β1R-AABs)和M2-毒蕈碱受体自身抗体(M2R-AABs)均参与心力衰竭的发生。β1R-AABs和M2R-AABs是否参与PPCM的发病机制仍不清楚。
本研究共纳入37例确诊的PPCM患者和36例正常孕妇。进行了临床评估、二维超声心动图检查以及通过酶联免疫吸附测定(ELISA)检测β1R-AABs或M2R-AABs。
PPCM患者中β1R-AABs和M2R-AABs的阳性率分别为59.5%(22/37)和45.9%(17/37),正常孕妇中分别为19.4%(7/36)(P<0.001)和16.67%(6/36)(P<0.001)。β1R-AABs和M2R-AABs均与NT-proBNP的血清表达水平、左心室大小和NYHA心功能分级呈正相关(rs:0.496 - 0.892,P<0.01)。此外,观察到β1R-AABs和M2R-AABs的活性与左心室射血分数(LVEF)、左心室短轴缩短率(LVFS)呈负相关(rs:-0.488 - 0.568,P<0.01)。此外,抗心血管受体自身抗体增加了PPCM发病的风险(OR = 18.786,95%置信区间1.926 - 183.262,P = 0.0012)。
β1R-AABs和M2R-AABs显著升高,且与左心室大小增加和心脏收缩功能恶化相关。心血管受体自身抗体是PPCM发病的独立危险因素。