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抗 M2 毒蕈碱型乙酰胆碱受体自身抗体对标准治疗围生期心肌病患者临床结局的影响。

Impact of autoantibodies against the M2-muscarinic acetylcholine receptor on clinical outcomes in peripartum cardiomyopathy patients with standard treatment.

机构信息

Department of Cardiology, Beijing Key Laboratory of Hypertension Research, Beijing Chao-Yang Hospital, Capital Medical University, 8# Gong-Ti South Road, Chaoyang District, Beijing, 100020, China.

HTRM Cardiologist Group, BENQ Medical Center, Nanjing Medical University, 181# Zhuyuan Road, Suzhou City, 215000, JiangSu Province, China.

出版信息

BMC Cardiovasc Disord. 2021 Dec 28;21(1):619. doi: 10.1186/s12872-021-02414-7.

DOI:10.1186/s12872-021-02414-7
PMID:34963460
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8713397/
Abstract

OBJECTIVES

To evaluate the impact of autoantibodies against the M2-muscarinic receptor (anti-M2-R) on the clinical outcomes of patients receiving the standard treatment for peripartum cardiomyopathy (PPCM).

METHODS

A total of 107 PPCM patients who received standard heart failure (HF) treatment between January 1998 and June 2020 were enrolled in this study. According to anti-M2-R reactivity, they were classified into negative (n = 59) and positive (n = 48) groups, denoted as the anti-M2-R (-) and anti-M2-R (+) groups. Echocardiography, 6-min walk distance, serum digoxin concentration (SDC), and routine laboratory tests were performed regularly for 2 years. The all-cause mortality, cardiovascular mortality, and rehospitalisation rate for HF were compared between the two groups.

RESULTS

A total of 103 patients were included in the final data analysis, with 46 in the anti-M2-R (+) group and 57 in the anti-M2-R (-) group. Heart rate was lower in the anti-M2-R (+) group than in the anti-M2-R (-) group at the baseline (102.7 ± 6.1 bpm vs. 96.0 ± 6.4 bpm, p < 0.001). The initial SDC was higher in the anti-M2-R (+) group than in the anti-M2-R (-) group with the same dosage of digoxin (1.25 ± 0.45 vs. 0.78 ± 0.24 ng/mL, p < 0.001). The dosages of metoprolol and digoxin were higher in the anti-M2-R (-) patients than in the anti-M2-R (+) patients (38.8 ± 4.6 mg b.i.d. vs. 27.8 ± 5.3 mg b.i.d., p < 0.0001, respectively, for metoprolol; 0.12 ± 0.02 mg/day vs. 0.08 ± 0.04 mg/day, p < 0.0001, respectively, for digoxin). Furthermore, there was a greater improvement in cardiac function in the anti-M2-R (-) patients than in the anti-M2-R (+) patients. Multivariate analysis identified negativity for anti-M2-R as the independent predictor for the improvement of cardiac function. Rehospitalisation for HF was lower in the anti-M2-R (-) group, but all-cause mortality and cardiovascular mortality were the same.

CONCLUSIONS

There were no differences in all-cause mortality or cardiovascular mortality between the two groups. Rehospitalisation rate for HF decreased in the anti-M2-R (-) group. This difference may be related to the regulation of the autonomic nervous system by anti-M2-R.

摘要

目的

评估抗 M2 毒蕈碱受体(anti-M2-R)自身抗体对接受围产期心肌病(PPCM)标准治疗的患者临床结局的影响。

方法

本研究共纳入 1998 年 1 月至 2020 年 6 月期间接受标准心力衰竭(HF)治疗的 107 例 PPCM 患者。根据抗 M2-R 反应性,将其分为阴性(n=59)和阳性(n=48)组,分别记为抗 M2-R(-)和抗 M2-R(+)组。定期进行超声心动图、6 分钟步行距离、血清地高辛浓度(SDC)和常规实验室检查,随访 2 年。比较两组患者的全因死亡率、心血管死亡率和 HF 再住院率。

结果

共有 103 例患者纳入最终数据分析,其中抗 M2-R(+)组 46 例,抗 M2-R(-)组 57 例。抗 M2-R(+)组患者的心率在基线时低于抗 M2-R(-)组(102.7±6.1bpm vs. 96.0±6.4bpm,p<0.001)。抗 M2-R(+)组患者初始 SDC 高于抗 M2-R(-)组患者,且地高辛剂量相同(1.25±0.45 vs. 0.78±0.24ng/mL,p<0.001)。与抗 M2-R(+)组患者相比,抗 M2-R(-)组患者的美托洛尔和地高辛剂量更高(38.8±4.6mg bid vs. 27.8±5.3mg bid,p<0.0001,分别为美托洛尔;0.12±0.02mg/day vs. 0.08±0.04mg/day,p<0.0001,分别为地高辛)。此外,抗 M2-R(-)组患者的心脏功能改善程度大于抗 M2-R(+)组患者。多变量分析表明,抗 M2-R 阴性是心脏功能改善的独立预测因素。抗 M2-R(-)组 HF 再住院率较低,但全因死亡率和心血管死亡率相同。

结论

两组患者的全因死亡率或心血管死亡率无差异。抗 M2-R(-)组 HF 再住院率降低。这种差异可能与抗 M2-R 对自主神经系统的调节有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/713e2bb86bb2/12872_2021_2414_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/6ac6cddb4122/12872_2021_2414_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/63d9d0b13e59/12872_2021_2414_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/531df7580876/12872_2021_2414_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/713e2bb86bb2/12872_2021_2414_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/6ac6cddb4122/12872_2021_2414_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/63d9d0b13e59/12872_2021_2414_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/531df7580876/12872_2021_2414_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9147/8713397/713e2bb86bb2/12872_2021_2414_Fig4_HTML.jpg

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