Papademetriou Vasilios, Lovato Laura, Tsioufis Costas, Cushman William, Applegate William B, Mottle Amy, Punthakee Zubin, Nylen Eric, Doumas Michael
Veteran Affairs Medical Center and Georgetown University, Washington, DC, USA.
Am J Nephrol. 2017;45(2):136-145. doi: 10.1159/000453626. Epub 2016 Dec 17.
The role of high density lipoprotein-raising interventions in addition to statin therapy in patients with diabetes remains controversial. Chronic kidney disease (CKD) is a strong modifier of cardiovascular (CV) outcomes. We therefore investigated the impact of CKD status at baseline on outcomes in patients with diabetes randomized to standard statin or statin plus fenofibrate treatment in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) lipid trial.
Among 5,464 participants in the ACCORD lipid trial, 3,554 (65%) were free of CKD at baseline, while 1,910 (35%) had mild to moderate CKD. Differences in CV outcomes during follow-up between CKD and non-CKD subgroups were examined. In addition, the effect of fenofibrate as compared to placebo on CV outcomes was examined for both subgroups.
All CV outcomes were 1.4-3 times higher among patients with CKD as compared to non-CKD patients. In patients with CKD, the addition of fenofibrate had no effect on any of the primary or secondary outcomes. In patients without CKD, however, the addition of fenofibrate was associated with a significant 36% reduction of CV mortality (hazards ratio [HR] 0.64; 95% CI 0.42-0.97; p value for treatment interaction <0.05) and 44% lower rate of fatal or non-fatal congestive heart failure (CHF; HR 0.56; 95% CI 0.37-0.84; p value treatment interaction <0.03).
For patients with type 2 diabetes at high CV risk but no CKD, fenofibrate therapy added to statin reduced the CV mortality and the rate of fatal and non-fatal CHF.
除他汀类药物治疗外,提高高密度脂蛋白的干预措施在糖尿病患者中的作用仍存在争议。慢性肾脏病(CKD)是心血管(CV)结局的一个重要影响因素。因此,我们在糖尿病控制心血管风险行动(ACCORD)血脂试验中,研究了基线时CKD状态对随机接受标准他汀类药物或他汀类药物加非诺贝特治疗的糖尿病患者结局的影响。
在ACCORD血脂试验的5464名参与者中,3554名(65%)在基线时无CKD,而1910名(35%)患有轻度至中度CKD。检查了CKD和非CKD亚组在随访期间CV结局的差异。此外,还检查了非诺贝特与安慰剂相比对两个亚组CV结局的影响。
与非CKD患者相比,CKD患者的所有CV结局高出1.4至3倍。在CKD患者中,添加非诺贝特对任何主要或次要结局均无影响。然而,在无CKD的患者中,添加非诺贝特与CV死亡率显著降低36%相关(风险比[HR]0.64;95%CI 0.42-0.97;治疗交互作用p值<0.05),致命或非致命性充血性心力衰竭(CHF)发生率降低44%(HR 0.56;95%CI 0.37-0.84;治疗交互作用p值<0.03)。
对于CV风险高但无CKD的2型糖尿病患者,在他汀类药物基础上加用非诺贝特治疗可降低CV死亡率以及致命和非致命性CHF的发生率。