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前白蛋白提高 BNP 附加西雅图心力衰竭模型的死亡风险预测:老年慢性心力衰竭患者的初步研究结果。

Prealbumin improves death risk prediction of BNP-added Seattle Heart Failure Model: results from a pilot study in elderly chronic heart failure patients.

机构信息

Cardiorenal Research Unit, Department of Clinical and Experimental Medicine, University of Parma Medical School, Via Gramsci 14, 43126 Parma, Italy.

出版信息

Int J Cardiol. 2013 Oct 9;168(4):3334-9. doi: 10.1016/j.ijcard.2013.04.039. Epub 2013 Apr 25.

Abstract

BACKGROUND

An accurate prognosis prediction represents a key element in chronic heart failure (CHF) management. Seattle Heart Failure Model (SHFM) prognostic power, a validated risk score for predicting mortality in CHF, is improved by adding B-type natriuretic peptide (BNP). We evaluated in a prospective study the incremental value of several biomarkers, linked to different biological domains, on death risk prediction of BNP-added SHFM.

METHODS

Troponin I (cTnI), norepinephrine, plasma renin activity, aldosterone, high sensitivity-C reactive protein (hs-CRP), tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6), interleukin 2 soluble receptor, leptin, prealbumin, free malondialdehyde, and 15-F2t-isoprostane were measured in plasma from 142 consecutive ambulatory, non-diabetic stable CHF (mean NYHA-class 2.6) patients (mean age 75±8years). Calibration, discrimination, and risk reclassification of BNP-added SHFM were evaluated after individual biomarker addition.

RESULTS

Individual addition of biomarkers to BNP-added SHFM did not improve death prediction, except for prealbumin (HR 0.49 CI: (0.31-0.76) p=0.002) and cTnI (HR 2.03 CI: (1.20-3.45) p=0.009). In fact, with respect to BNP-added SHFM (Harrell's C-statistic 0.702), prealbumin emerged as a stronger predictor of death showing the highest improvement in model discrimination (+0.021, p=0.033) and only a trend was observed for cTn I (+0.023, p=0.063). These biomarkers showed also the best reclassification statistic (Integrated Discrimination Improvement-IDI) at 1-year (IDI: cTnI, p=0.002; prealbumin, p=0.020), 2-years (IDI: cTnI, p=0.018; prealbumin: p=0.006) and 3-years of follow-up (IDI: cTnI p=0.024; prealbumin: p=0.012).

CONCLUSIONS

Individual addition of prealbumin allows a more accurate prediction of mortality of BNP enriched SHFM in ambulatory elderly CHF suggesting its potential use in identifying those at high-risk that need nutritional surveillance.

摘要

背景

准确的预后预测是慢性心力衰竭(CHF)管理的关键要素。西雅图心力衰竭模型(SHFM)的预后能力是预测心力衰竭患者死亡率的经过验证的风险评分,通过添加 B 型利钠肽(BNP)可以提高其预测能力。我们在一项前瞻性研究中评估了几种生物标志物的增量价值,这些标志物与不同的生物学领域相关联,可用于预测 BNP 加 SHFM 死亡风险。

方法

从 142 例连续的、非糖尿病的稳定 CHF(平均 NYHA 分级 2.6)患者(平均年龄 75±8 岁)的血浆中测量了肌钙蛋白 I(cTnI)、去甲肾上腺素、血浆肾素活性、醛固酮、高敏 C 反应蛋白(hs-CRP)、肿瘤坏死因子-α(TNF-α)、白细胞介素 6(IL-6)、白细胞介素 2 可溶性受体、瘦素、前白蛋白、游离丙二醛和 15-F2t-异前列腺素。在单独添加生物标志物后,评估了 BNP 加 SHFM 的校准、区分和风险再分类。

结果

除了前白蛋白(HR 0.49,CI:(0.31-0.76),p=0.002)和 cTnI(HR 2.03,CI:(1.20-3.45),p=0.009)外,其他生物标志物的单独添加并不能改善死亡预测。实际上,与 BNP 加 SHFM(Harrell 的 C 统计量为 0.702)相比,前白蛋白作为死亡的更强预测因子出现,显示出对模型区分度的最高改善(+0.021,p=0.033),而 cTnI 仅呈趋势(+0.023,p=0.063)。这些生物标志物在 1 年(IDI:cTnI,p=0.002;前白蛋白,p=0.020)、2 年(IDI:cTnI,p=0.018;前白蛋白,p=0.006)和 3 年随访(IDI:cTnI,p=0.024;前白蛋白,p=0.012)时的再分类统计数据(综合鉴别改善-ID)也显示出最佳效果。

结论

在非卧床老年 CHF 患者中,前白蛋白的单独添加可更准确地预测 BNP 富集 SHFM 的死亡率,提示其在识别高危患者并进行营养监测方面具有潜在应用价值。

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