Inverse association of alanine aminotransferase within normal range with prognosis in patients with coronary artery disease

医学 内科学 危险系数 冠状动脉疾病 置信区间 经皮冠状动脉介入治疗 丙氨酸转氨酶 心脏病学 胃肠病学 心肌梗塞
作者
Gjin Ndrepepa,Stefan Holdenrieder,Róisín Colleran,Salvatore Cassese,Erion Xhepa,Massimiliano Fusaro,Karl‐Ludwig Laugwitz,Heribert Schunkert,Adnan Kastrati
出处
期刊:Clinica Chimica Acta [Elsevier BV]
卷期号:496: 55-61 被引量:18
标识
DOI:10.1016/j.cca.2019.06.021
摘要

Data regarding the association between alanine aminotransferase (ALT) and prognosis of patients with coronary artery disease (CAD) are limited. The aim of this study was to assess the association of ALT with the prognosis of patients with CAD. The study included 9523 patients with angiography-proven CAD who underwent percutaneous coronary intervention. Baseline ALT activity measurements were available for analysis in all patients. The primary outcome was 3-year cardiac mortality. Patients were divided into three groups: a group with ALT within the 1st tertile (ALT 2.0 U/L to ≤17.0 U/L; n = 3276 patients), a group with ALT within the 2nd tertile (ALT >17.0 U/L to ≤26.0 U/L; n = 3075 patients) and a group with ALT within 3rd tertile (>26 U/L to ≤50.0 U/L; n = 3172 patients). Cardiac death (primary outcome) occurred in 441 patients: 201 (7.1%), 126 (4.7%) and 114 (4.0%) of these occurring in patients in the 1st, 2nd and 3rd ALT tertiles, respectively (with percentages representing Kaplan–Meier estimates of 3-year cardiac mortality); adjusted hazard ratio = 1.43, 95% confidence interval 1.11 to 1.85, P = 0.006 calculated for 1 unit decrement in the logarithmic scale of ALT. The multivariable model for cardiac mortality with baseline variables without ALT had a C-statistic of 0.827 [0.801–0.853], P < 0.001, which increased to 0.832 [0.806–0.857], P < 0.001 after incorporation of ALT (P = 0.020). In patients with CAD, ALT was inversely and independently associated with the risk of 3-year cardiac mortality. Low ALT may reflect cardiovascular risk that is poorly mediated by traditional cardiovascular risk factors.
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