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预测扩张型心肌病患儿的预后:利用对预后危险因素的重复测量

Predicting outcome in children with dilated cardiomyopathy: the use of repeated measurements of risk factors for outcome.

作者信息

van der Meulen Marijke, den Boer Susanna, du Marchie Sarvaas Gideon J, Blom Nico, Ten Harkel Arend D J, Breur Hans M P J, Rammeloo Lukas A J, Tanke Ronald, Bogers Ad J J C, Helbing Willem A, Boersma Eric, Dalinghaus Michiel

机构信息

Department of Pediatric Cardiology, Erasmus MC, University Medical Center Rotterdam, Dr Molewaterplein 60, PO Box 2060, Rotterdam, 3000 CB, The Netherlands.

Department of Pediatric Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

ESC Heart Fail. 2021 Apr;8(2):1472-1481. doi: 10.1002/ehf2.13233. Epub 2021 Feb 5.

Abstract

AIMS

We aimed to determine whether in children with dilated cardiomyopathy repeated measurement of known risk factors for death or heart transplantation (HTx) during disease progression can identify children at the highest risk for adverse outcome.

METHODS AND RESULTS

Of 137 children we included in a prospective cohort, 36 (26%) reached the study endpoint (SE: all-cause death or HTx), 15 (11%) died at a median of 0.09 years [inter-quartile range (IQR) 0.03-0.7] after diagnosis, and 21 (15%) underwent HTx at a median of 2.9 years [IQR 0.8-6.1] after diagnosis. Median follow-up was 2.1 years [IQR 0.8-4.3]. Twenty-three children recovered at a median of 0.6 years [IQR 0.5-1.4] after diagnosis, and 78 children had ongoing disease at the end of the study. Children who reached the SE could be distinguished from those who did not, based on the temporal evolution of four risk factors: stunting of length growth (-0.42 vs. -0.02 length Z-score per year, P < 0.001), less decrease in N-terminal pro-B-type natriuretic peptide (NT-proBNP) (-0.26 vs. -1.06 2log pg/mL/year, P < 0.01), no decrease in left ventricular internal diastolic dimension (LVIDd; 0.24 vs. -0.60 Boston Z-score per year, P < 0.01), and increase in New York University Pediatric Heart Failure Index (NYU PHFI; 0.49 vs. -1.16 per year, P < 0.001). When we compared children who reached the SE with those with ongoing disease (leaving out the children who recovered), we found similar results, although the effects were smaller. In univariate analysis, NT-proBNP, length Z-score, LVIDd Z-score, global longitudinal strain (%), NYU PHFI, and age >6 years at presentation (all P < 0.001) were predictive of adverse outcome. In multivariate analysis, NT-proBNP appeared the only independent predictor for adverse outcome, a two-fold higher NT-proBNP was associated with a 2.8 times higher risk of the SE (hazard ratio 2.78, 95% confidence interval 1.81-3.94, P < 0.001).

CONCLUSIONS

The evolution over time of NT-proBNP, LVIDd, length growth, and NYU PHFI identified a subgroup of children with dilated cardiomyopathy at high risk for adverse outcome. In this sample, with a limited number of endpoints, NT-proBNP was the strongest independent predictor for adverse outcome.

摘要

目的

我们旨在确定在扩张型心肌病患儿疾病进展过程中,对已知的死亡或心脏移植(HTx)风险因素进行重复测量,是否能够识别出不良结局风险最高的患儿。

方法与结果

在我们纳入前瞻性队列研究的137名儿童中,36名(26%)达到了研究终点(SE:全因死亡或HTx),15名(11%)在诊断后中位数0.09年[四分位数间距(IQR)0.03 - 0.7]死亡,21名(15%)在诊断后中位数2.9年[IQR 0.8 - 6.1]接受了HTx。中位随访时间为2.1年[IQR 0.8 - 4.3]。23名儿童在诊断后中位数0.6年[IQR 0.5 - 1.4]恢复,78名儿童在研究结束时仍患有疾病。根据四个风险因素的时间演变情况,达到SE的儿童与未达到的儿童可以区分开来:身高增长迟缓(每年长度Z评分-0.42 vs. -0.02,P < 0.001)、N末端B型利钠肽原(NT-proBNP)下降较少(每年-0.26 vs. -1.06 2log pg/mL,P < 0.01)、左心室内径舒张末期(LVIDd)无减小(每年波士顿Z评分0.24 vs. -0.60,P < 0.01)以及纽约大学小儿心力衰竭指数(NYU PHFI)升高(每年0.49 vs. -1.16,P < 0.001)。当我们将达到SE的儿童与仍患有疾病的儿童(不包括恢复的儿童)进行比较时,发现了类似的结果,尽管影响较小。在单因素分析中,NT-proBNP、长度Z评分、LVIDd Z评分、整体纵向应变(%)、NYU PHFI以及就诊时年龄>6岁(所有P < 0.001)均为不良结局的预测因素。在多因素分析中,NT-proBNP似乎是不良结局的唯一独立预测因素,NT-proBNP升高两倍与SE风险高2.8倍相关(风险比2.78,95%置信区间1.81 - 3.94,P < 0.001)。

结论

NT-proBNP、LVIDd、身高增长和NYU PHFI随时间的演变情况,识别出了一组扩张型心肌病患儿不良结局风险较高。在这个终点数量有限的样本中,NT-proBNP是不良结局最强的独立预测因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2027/8006605/cae842149213/EHF2-8-1472-g002.jpg

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