From the Amyloidosis Center (J.L.S.H., C.M.K., J.L.B., F.L.R., T.P., L.H.C.), Department of Pathology and Laboratory Medicine (J.L.S.H., C.M.K., L.H.C.), Department of Medicine (M.A., J.L.B., F.L.R.), and Section of Cardiovascular Medicine, Department of Medicine (F.L.R.), Boston University School of Medicine, MA. The current affiliation for C.M.H. is the Department of Medicine, Division of Pulmonary and Critical Care, Northwestern University, Chicago, IL.
Circ Heart Fail. 2018 Feb;11(2):e004000. doi: 10.1161/CIRCHEARTFAILURE.117.004000.
Wild-type transthyretin amyloidosis (ATTRwt), an underappreciated cause of heart failure in older adults, is challenging to diagnose and monitor in the absence of validated, disease-specific biomarkers. We examined the prognostic use and survival association of serum TTR (transthyretin) concentration in ATTRwt.
Patients with biopsy-proven ATTRwt were retrospectively identified. Serum TTR, cardiac biomarkers, and echocardiographic parameters were assessed at baseline and follow-up evaluations. Statistical analyses included Kaplan-Meier method, Cox proportional hazard survival models, and receiver-operating characteristic curve analysis. Median serum TTR concentration at presentation was 23 mg/dL (n=116). Multivariate predictors of shorter overall survival were decreased TTR, left ventricular ejection fraction and elevated cTn-I (cardiac troponin I); an inclusive model demonstrated superior accuracy in 4-year survival prediction by receiver-operating characteristic curve analysis (area under the curve, 0.77). TTR values lower than the normal limit, <18 mg/dL, were associated with shorter survival (2.8 versus 4.1 years; =0.03). Further, TTR values at 1- and 2-year follow-ups were significantly lower (<0.001) in untreated patients (n=23) compared with those treated with TTR stabilizer, diflunisal (n=12), after baseline evaluation. During 2-year follow-up, unchanged TTR corresponded to increased cTn-I (=0.006) in untreated patients; conversely, the diflunisal-treated group showed increased TTR (=0.001) and stabilized cTn-I and left ventricular ejection fraction at 1 year.
In this series of biopsy-proven ATTRwt, lower baseline serum TTR concentration was associated with shorter survival as an independent predictor of outcome. Longitudinal analysis demonstrated that decreasing TTR corresponded to worsening cardiac function. These data suggest that TTR may be a useful prognostic marker and predictor of outcome in ATTRwt.
野生型转甲状腺素蛋白淀粉样变性(ATTRwt)是老年人心力衰竭的一个未被充分认识的原因,在缺乏经过验证的、特定于疾病的生物标志物的情况下,其诊断和监测具有挑战性。我们研究了血清 TTR(转甲状腺素蛋白)浓度在 ATTRwt 中的预后作用和与生存的关联。
回顾性确定了经活检证实的 ATTRwt 患者。在基线和随访评估时评估血清 TTR、心脏生物标志物和超声心动图参数。统计分析包括 Kaplan-Meier 法、Cox 比例风险生存模型和受试者工作特征曲线分析。在出现时,中位血清 TTR 浓度为 23mg/dL(n=116)。总生存时间较短的多变量预测因素包括 TTR 降低、左心室射血分数和 cTn-I(心肌肌钙蛋白 I)升高;受试者工作特征曲线分析显示,综合模型在 4 年生存预测方面具有更高的准确性(曲线下面积,0.77)。TTR 值低于正常值,<18mg/dL,与生存时间较短相关(2.8 年与 4.1 年;=0.03)。此外,与基线评估后接受 TTR 稳定剂双氯芬酸治疗的 12 例患者相比,未接受治疗的 23 例患者在 1 年和 2 年随访时的 TTR 值显著降低(<0.001)。在 2 年随访期间,未接受治疗的患者中,TTR 不变与 cTn-I 增加相关(=0.006);相反,双氯芬酸治疗组在 1 年时 TTR 增加(=0.001),并稳定了 cTn-I 和左心室射血分数。
在本系列经活检证实的 ATTRwt 中,基线时血清 TTR 浓度较低与生存时间较短相关,是预后的独立预测因素。纵向分析表明,TTR 降低与心功能恶化相关。这些数据表明,TTR 可能是 ATTRwt 的一种有用的预后标志物和预后预测指标。