Heart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Science, Peking Union Medical College, 10037, Beijing, China.
Key Laboratory of Clinical Research for Cardiovascular Medications, National Health Committee, 10037, Beijing, China.
ESC Heart Fail. 2022 Oct;9(5):3345-3357. doi: 10.1002/ehf2.14065. Epub 2022 Jul 13.
Evidence of the prognostic value of high-sensitivity troponin in patients with non-ischaemic heart failure (NIHF) is scarce. This study aimed to assess the predictive value of high-sensitivity cardiac troponin I (hs-cTnI) in NIHF patients.
Hs-cTnI was measured at baseline in 650 NIHF patients admitted to the Heart Failure Center. The prognostic value of hs-cTnI was assessed based on a well-established model (including age, sex, New York Heart Association class, left ventricular ejection fraction, haemoglobin, sodium, estimated glomerular filtration rate, diabetes mellitus, treatment with angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers, treatment with β-blockers, and NT-proBNP).
During a median follow-up of 1036 days, 163 patients died of various causes. In total, 46.92% of patients had high hs-cTnI (hs-cTnI >0.011 ng/ml). Over a 3-year follow-up, patients with high hs-cTnI (>0.011 ng/ml) had a 1.54 [95% confidence interval (95% CI) 1.11-2.15] fold higher all-cause mortality risk than those without. Increasing concertation of hs-cTnI was also associated with a 23.0% (95% CI 13-33%, per log increase) increment risk of all-cause mortality. The inclusion of hs-cTnI significantly improved the risk prediction and stratification of all-cause mortality (integrated discrimination improvement 1.58%, 95% CI 0.38-2.79%, absolute net reclassification improvement 23.41% 95% CI 4.52-44.49%, additive net reclassification improvement 27.8%, 95% CI 9.29-46.3%) of the well-established model.
Hs-cTnI provides significant prognostic value and could further remarkably improve risk stratification and prediction capabilities in NIHF patients.
高敏肌钙蛋白在非缺血性心力衰竭(NIHF)患者中的预后价值证据有限。本研究旨在评估高敏心肌肌钙蛋白 I(hs-cTnI)在 NIHF 患者中的预测价值。
在 650 例入住心力衰竭中心的 NIHF 患者中,于基线时测量 hs-cTnI。根据成熟模型(包括年龄、性别、纽约心脏协会(NYHA)心功能分级、左心室射血分数、血红蛋白、钠、估算肾小球滤过率、糖尿病、血管紧张素转换酶抑制剂或血管紧张素 II 受体阻滞剂治疗、β受体阻滞剂治疗和 NT-proBNP)评估 hs-cTnI 的预后价值。
中位随访 1036 天期间,163 例患者因各种原因死亡。共有 46.92%的患者 hs-cTnI 升高(hs-cTnI>0.011ng/ml)。在 3 年随访期间,hs-cTnI 升高(>0.011ng/ml)患者的全因死亡率风险比无 hs-cTnI 升高患者高 1.54 倍(95%置信区间[95%CI]为 1.11-2.15)。hs-cTnI 浓度的升高也与全因死亡率风险增加 23.0%(95%CI 为 13-33%,每增加 1 个对数单位)相关。hs-cTnI 的纳入显著改善了全因死亡率风险预测和分层(综合判别改善 1.58%,95%CI 为 0.38-2.79%;绝对净重新分类改善 23.41%,95%CI 为 4.52-44.49%;附加净重新分类改善 27.8%,95%CI 为 9.29-46.3%)。
hs-cTnI 提供了显著的预后价值,可进一步显著改善 NIHF 患者的风险分层和预测能力。