Spoto Belinda, Mattace-Raso Francesco, Sijbrands Eric J, D'Arrigo Graziella, Tripepi Giovanni, Volpato Stefano, Bandinelli Stefania, Ferrucci Luigi, Zoccali Carmine
National Council of Research and Institute of Clinical Physiology CNR-IFC, Reggio Calabria Unit, Reggio Calabria, Italy.
Department of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.
J Am Geriatr Soc. 2017 Apr;65(4):e77-e82. doi: 10.1111/jgs.14566.
Gamma-glutamyltransferase (GGT) is a biomarker of liver disease and oxidative stress which was associated with all-cause and cardiovascular (CV) mortality in the general population and in patients with high risk conditions. This study aims at assessing whether oxLDL modifies the relationship between GGT, all-cause, and CV mortality in elderly individuals from the general population.
Observational longitudinal study.
Population-based cohort of older individuals (>65 years) free of liver disease.
One thousand and thirty-eight individuals from the Invecchiare in Chianti (InCHIANTI) study.
Serum GGT level, oxidized low-density lipoprotein (oxLDL), CV comorbidities, all-cause and CV mortality.
The median age of the study population (n = 1,038) was 74 years (inter-quartile range: 69-79), 152 individuals (15%) had past CV events. During a median follow-up of 9 years, 401 individuals died, 168 of them (42%) for CV causes. In adjusted analyses, GGT predicted all-cause mortality (HR for 20 U/L increase in serum GGT: 1.11, 95% CI: 1.02-1.21, P = .02) and CV mortality (HR: 1.17, 95% CI: 1.03-1.33; P = .02). Furthermore, in an analysis for interaction circulating oxLDL amplified the effect of GGT on all-cause mortality (P = .003).
Circulating oxLDL amplifies the effect of GGT on mortality in the elderly. The mechanism for this association remains unknown and requires further research, including studying the potential role of GGT in oxidative stress. These results are consistent with the hypothesis of a causal role of GGT in the CV morbidity and mortality in older individuals and indicate that oxLDL plays a crucial role in the interpretation of the link between GGT and the risk of adverse clinical events in this population.
γ-谷氨酰转移酶(GGT)是一种肝脏疾病和氧化应激的生物标志物,在普通人群和高危患者中与全因死亡率和心血管(CV)死亡率相关。本研究旨在评估氧化型低密度脂蛋白(oxLDL)是否会改变普通人群中老年个体中GGT、全因死亡率和CV死亡率之间的关系。
观察性纵向研究。
以无肝脏疾病的老年个体(>65岁)为基础的人群队列。
来自基安蒂地区老年化研究(InCHIANTI)的1038名个体。
血清GGT水平、氧化型低密度脂蛋白(oxLDL)、CV合并症、全因死亡率和CV死亡率。
研究人群(n = 1038)的中位年龄为74岁(四分位间距:69 - 79岁),152名个体(15%)有既往CV事件。在中位随访9年期间,401名个体死亡,其中168名(42%)死于CV原因。在多因素分析中,GGT可预测全因死亡率(血清GGT每增加20 U/L的HR:1.11,95% CI:1.02 - 1.21,P = 0.02)和CV死亡率(HR:1.17,95% CI:1.03 - 1.33;P = 0.02)。此外,在交互作用分析中,循环oxLDL增强了GGT对全因死亡率的影响(P = 0.003)。
循环oxLDL增强了GGT对老年人死亡率的影响。这种关联的机制尚不清楚,需要进一步研究,包括研究GGT在氧化应激中的潜在作用。这些结果与GGT在老年个体CV发病和死亡中起因果作用的假设一致,并表明oxLDL在解释该人群中GGT与不良临床事件风险之间的联系中起关键作用。