Palazzuoli Alberto, Maisel Alan, Caputo Maria, Fineschi Massimo, Quatrini Ilaria, Calabrò Anna, Campagna Maria Stella, Franci Beatrice, Grothgar Stefanie, Pierli Carlo, Nuti Ranuccio
Department of Internal Medicine and Metabolic Disease Cardiology Section, University of Siena, Italy.
Regul Pept. 2011 Feb 25;167(1):129-33. doi: 10.1016/j.regpep.2010.12.011. Epub 2011 Jan 13.
B-type natriuretic peptide (BNP) has been used recently as a biological marker in patients with coronary artery disease (CAD) with ST-elevation, as well as without ST-elevation. BNP is able to predict systolic dysfunction, adding new prognostic information to existing traditional markers. However is not known if there is a relation between the quantity of BNP levels and the severity of coronary artery disease.
This study compared B-type natriuretic peptide (BNP) levels in patients with stable angina (SA) and acute coronary syndromes (ACS) without ST-elevation in relation to angiographic lesions using TIMI and Gensini Scores. We studied 282 patients with CAD without ST elevation and preserved systolic function. BNP samples were measured in all recruited patients within 24 hours of hospitalization.
BNP values were progressively increased in relation to the severity of diagnosis: SA (52.6±49.4 pg/mL ) UA (243.3±212 pg/mL) NSTE-ACS (421.7±334 pg/mL) (p<0.0001 and p<0.007 respectively). No statistically significant difference was observed between patients with SA and controls (21.2±6.8 pg/mL). The analysis of BNP levels in relation to the number of involved vessels demonstrated significantly increased levels in patients with multivessel disease compared to patients with 1 or 2 vessel disease (1-86.2±46.3 pg/mL; 2-127±297 pg/mL; 3-295±318 pg/mL; 4-297±347 pg/mL p<0.001 and p<0.003). Evaluation of BNP using Gensini Score showed a strong relation between BNP and coronary disease extension (r=0.38 p<0.0001).This trend was maintained in all CAD groups (SA=r 0.54; UA r=0.36 NSTE-ACS r=0.28).
Circulating BNP levels appear elevated in ACS with diffuse coronary involvement, even in the absence of systolic dysfunction. BNP is also associated with multi-vessel disease and the extension of coronary disease.
B型利钠肽(BNP)最近已被用作ST段抬高型和非ST段抬高型冠状动脉疾病(CAD)患者的生物标志物。BNP能够预测收缩功能障碍,为现有的传统标志物增添了新的预后信息。然而,BNP水平的数量与冠状动脉疾病的严重程度之间是否存在关联尚不清楚。
本研究使用TIMI和Gensini评分,比较了稳定型心绞痛(SA)和无ST段抬高的急性冠状动脉综合征(ACS)患者的B型利钠肽(BNP)水平与血管造影病变的关系。我们研究了282例无ST段抬高且保留收缩功能的CAD患者。在所有招募患者住院24小时内测量BNP样本。
BNP值随着诊断严重程度的增加而逐渐升高:SA(52.6±49.4 pg/mL)、不稳定型心绞痛(UA,243.3±212 pg/mL)、非ST段抬高型急性冠状动脉综合征(NSTE-ACS,421.7±334 pg/mL)(分别为p<0.0001和p<0.007)。SA患者与对照组(21.2±6.8 pg/mL)之间未观察到统计学上的显著差异。与单支或双支血管病变患者相比,多支血管病变患者的BNP水平分析显示显著升高(单支血管病变-86.2±46.3 pg/mL;双支血管病变-127±297 pg/mL;三支血管病变-295±318 pg/mL;四支血管病变-297±347 pg/mL,p<0.001和p<0.003)。使用Gensini评分评估BNP显示BNP与冠状动脉疾病范围之间存在密切关系(r=0.38,p<0.0001)。这种趋势在所有CAD组中均保持(SA,r=0.54;UA,r=0.36;NSTE-ACS,r=0.28)。
即使在没有收缩功能障碍的情况下,弥漫性冠状动脉受累的ACS患者循环BNP水平似乎也会升高。BNP还与多支血管病变和冠状动脉疾病范围相关。