Yamaguchi Satoshi, Abe Masami, Arakaki Tomohiro, Arasaki Osamu, Shimabukuro Michio
Department of Cardiology, Tomishiro Central Hospital, Okinawa, Japan.
Department of Cardiology, Tomishiro Central Hospital, Okinawa, Japan.
Heart Lung Circ. 2020 Sep;29(9):1318-1327. doi: 10.1016/j.hlc.2019.11.013. Epub 2019 Dec 5.
Enzyme biomarkers-such as creatine phosphokinase, aspartate aminotransferase, and alanine aminotransferase-are associated with acute decompensated heart failure (ADHF) severity and, therefore, have a prognostic value in ADHF. However, the prognostic value of lactate dehydrogenase (LDH) is unclear. This study aimed to investigate the prognostic value of LDH in ADHF.
This single-centre observational retrospective study enrolled 396 patients with ADHF between June 2014 and July 2016. The patients were categorised into groups based on the tertile values of serum LDH (LDH-low [<196 U/L], LDH-intermediate [196≤ LDH <239 U/L] and LDH-high [LDH ≥239 U/L]). Survival analysis for all-cause mortality was performed. This study also examined the ability of adding log-transformed LDH (LogLDH) on Get With The Guideline score, which is an established risk score to predict 90-day, 180-day and 365-day mortality using time-dependent receiver operating characteristic curves.
During the follow-up (median, 204 days), 100 (25%) patients died. The LDH-intermediate and LDH-high groups had worse survival (LDH-low vs LDH-intermediate, log-rank p=0.019; LDH-low vs LDH-high, log-rank p<0.001). Log LDH improved the ability to predict 90-day, 180-day and 365-day all-cause mortality, which was statistically significant (90 days, area under curve [AUC] = 0.79, p=0.012; 180 days, AUC = 0.79, p=0.017; and 365 days, AUC = 0.79, p=0.025).
Lactate dehydrogenase may be an important predictor of 90-day, 180-day and 365-day all-cause mortality in ADHF patients; however, further studies are needed to confirm these findings.
酶生物标志物,如肌酸磷酸激酶、天冬氨酸氨基转移酶和丙氨酸氨基转移酶,与急性失代偿性心力衰竭(ADHF)的严重程度相关,因此在ADHF中具有预后价值。然而,乳酸脱氢酶(LDH)的预后价值尚不清楚。本研究旨在探讨LDH在ADHF中的预后价值。
这项单中心观察性回顾性研究纳入了2014年6月至2016年7月期间的396例ADHF患者。根据血清LDH的三分位数将患者分为几组(低LDH组[<196 U/L]、中LDH组[196≤LDH<239 U/L]和高LDH组[LDH≥239 U/L])。进行全因死亡率的生存分析。本研究还使用时间依赖性受试者工作特征曲线,检验了将对数转换的LDH(LogLDH)添加到“遵循指南”评分中的能力,该评分是一种既定的风险评分,用于预测90天、180天和365天的死亡率。
在随访期间(中位数为204天),100例(25%)患者死亡。中LDH组和高LDH组的生存率较差(低LDH组与中LDH组比较,对数秩检验p=0.019;低LDH组与高LDH组比较,对数秩检验p<0.001)。Log LDH提高了预测90天、180天和365天全因死亡率的能力,具有统计学意义(90天,曲线下面积[AUC]=0.79,p=0.012;180天,AUC=0.79,p=0.017;365天,AUC=0.79,p=0.025)。
乳酸脱氢酶可能是ADHF患者90天、180天和365天全因死亡率的重要预测指标;然而,需要进一步研究来证实这些发现。