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首页> 外文期刊>Journal of Clinical Oncology >Serum cardiac troponins and N-terminal pro-brain natriuretic Peptide: a staging system for primary systemic amyloidosis.
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Serum cardiac troponins and N-terminal pro-brain natriuretic Peptide: a staging system for primary systemic amyloidosis.

机译:血清心肌肌钙蛋白和N端脑钠肽前体:原发性系统性淀粉样变性的分期系统。

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PURPOSE Primary systemic amyloidosis (AL) is a multisystemic disorder resulting from an underlying plasma cell dyscrasia. There is no formal staging system for AL, making comparisons between studies and treatment centers difficult. Our group previously identified elevated serum cardiac troponin T (cTnT) as the most powerful predictor of overall survival. Others have reported that N-terminal pro-brain natriuretic peptide (NT-proBNP) is a valuable prognostic marker. We sought to develop a staging system for patients with AL. PATIENTS AND METHODS Two hundred forty-two patients with newly diagnosed AL who were seen at the Mayo Clinic between April 1979 and November 2000, and who had echocardiograms and stored serum samples at presentation were eligible for this retrospective review. NT-proBNP measurements were performed on 242 patients in whom cTnT and cardiac troponin I (cTnI) had been previously run. Two prognostic models were designed using threshold values of NT-proBNP and either cTnT or cTnI (NT-proBNP < 332 ng/L, cTnT < 0.035 microg/L, and cTnI < 0.1 microg/L). Depending on whether NT-proBNP and troponin levels were both low, were high for only one level, or were both high, patients were classified as stage I, II, or III, respectively. Results Using the cTnT+NT-proBNP model 33%, 30%, and 37% of patients were stages I, II, and III, respectively, with median survivals of 26.4, 10.5, and 3.5 months, respectively. The alternate cTnI+NT-proBNP model predicted median survivals of 27.2, 11.1, and 4.1 months, respectively. CONCLUSION Stratification of AL patients into three stages is possible with two readily available and reproducible tests setting the stage for more consistent and reliable cross comparisons of therapeutic outcomes.
机译:目的原发性系统性淀粉样变性病(AL)是由潜在的浆细胞发育不良引起的多系统性疾病。没有针对AL的正式分期系统,因此很难在研究和治疗中心之间进行比较。我们的研究小组先前将血清心肌肌钙蛋白T(cTnT)升高确定为总体存活率的最有力预测指标。其他人已报道N末端脑利钠肽(NT-proBNP)是有价值的预后标志物。我们寻求为AL患者开发一个分期系统。患者与方法1979年4月至2000年11月在梅奥诊所就诊的242例新诊断为AL的患者,均具有超声心动图检查并在演示时存储了血清样本,符合这项回顾性研究的要求。 NT-proBNP测量在242例先前曾进行过cTnT和心肌肌钙蛋白I(cTnI)的患者中进行。使用NT-proBNP和cTnT或cTnI(NT-proBNP <332 ng / L,cTnT <0.035 microg / L,cTnI <0.1 microg / L)的阈值设计两个预后模型。根据NT-proBNP和肌钙蛋白水平是否低,仅高一个水平还是都高,分别将患者分为I,II或III期。结果使用cTnT + NT-proBNP模型,分别有33%,30%和37%的患者处于I,II和III期,中位生存期分别为26.4、10.5和3.5个月。替代性cTnI + NT-proBNP模型预测的中位生存期分别为27.2、11.1和4.1个月。结论通过两个易于获得且可重复的测试,可以将AL患者分为三个阶段,从而为治疗结果的更一致,更可靠的交叉比较奠定了基础。

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