So Wing Yee, Kong Alice P S, Ma Ronald C W, Ozaki Risa, Szeto Cheuk Chun, Chan Norman N, Ng Vanessa, Ho Chung Shun, Lam Christopher W K, Chow Chun Chung, Cockram Clive S, Chan Juliana C N, Tong Peter C Y
Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, N.T., Hong Kong SAR.
Diabetes Care. 2006 Sep;29(9):2046-52. doi: 10.2337/dc06-0248.
Chronic kidney disease (CKD) predicts cardiovascular disease (CVD) in the general population. We investigated the effects of stages of renal function using the estimated glomerular filtration rate (eGFR) on all-cause mortality and cardiovascular end points in a prospective cohort of Chinese type 2 diabetic patients.
Between 1995 and 2000, 4,421 patients without macrovascular disease or end-stage renal disease were recruited. Renal function was assessed by eGFR, as calculated by the abbreviated Modification of Diet in Renal Disease Study Group formula. Clinical end points included all-cause mortality, cardiovascular end point (cardiovascular death, new admissions due to angina, myocardial infarction, stroke, revascularization, or heart failure), and renal end point (reduction in eGFR by >50%, progression of eGFR to stage 5, or dialysis or renal death).
After a median follow-up period of 39.4 months (interquartile range 20.3-55), all-cause mortality rate increased from 1.2% (95% CI 0.8-1.7) to 18.3% (9.1-27.5) (P for trend <0.001) as renal function deteriorated from stage 1 (eGFR > or =90 ml/min per 1.73 m(2)) to stage 4 (15-29 ml/min per 1.73 m(2)). The respective rate of new cardiovascular end points also increased from 2.6% (2.0-3.3) to 25.3% (15.0-35.7) (P for trend <0.001). After adjustment for covariates (age, sex, albuminuria, use of renin-angiotensin-aldosterone system [RAAS] inhibitors, lipids, blood pressure, and glycemic control), hazard ratios across different stages of eGFR (> or =90, 60-89, 30-59, and 15-29 ml/min per 1.73 m(2)) for all-cause mortality were 1.00, 1.27, 2.34, and 9.82 (P for trend <0.001), for cardiovascular end points were 1.00, 1.04, 1.05, and 3.23 (P for trend <0.001), and for renal end points were 1.00, 1.36, 3.34, and 27.3 (P for trend <0.001), respectively.
Chinese type 2 diabetic patients with reduced eGFR were at high risk of developing cardiovascular end points and all-cause mortality, independent of albuminuria and metabolic control.
慢性肾脏病(CKD)可预测普通人群的心血管疾病(CVD)。我们在一个中国2型糖尿病患者前瞻性队列中,研究了使用估计肾小球滤过率(eGFR)评估的肾功能分期对全因死亡率和心血管终点事件的影响。
1995年至2000年期间,招募了4421例无大血管疾病或终末期肾病的患者。肾功能通过eGFR进行评估,eGFR由肾脏病饮食改良研究组简化公式计算得出。临床终点包括全因死亡率、心血管终点事件(心血管死亡、因心绞痛、心肌梗死、中风、血运重建或心力衰竭而新入院)以及肾脏终点事件(eGFR降低>50%、eGFR进展至5期、透析或肾脏死亡)。
在中位随访期39.4个月(四分位间距20.3 - 55)后,随着肾功能从1期(eGFR≥90 ml/min/1.73 m²)恶化至4期(15 - 29 ml/min/1.73 m²),全因死亡率从1.2%(95%CI 0.8 - 1.7)增至18.3%(9.1 - 27.5)(趋势P<0.001)。新发生心血管终点事件的相应发生率也从2.6%(2.0 - 3.3)增至25.3%(15.0 - 35.7)(趋势P<0.001)。在校正协变量(年龄、性别、蛋白尿、肾素 - 血管紧张素 - 醛固酮系统[RAAS]抑制剂的使用、血脂、血压和血糖控制)后,eGFR不同分期(≥90、60 - 89、30 - 59和15 - 29 ml/min/1.73 m²)的全因死亡率风险比分别为1.00、1.27、2.34和9.82(趋势P<0.001),心血管终点事件风险比分别为1.00、1.04、1.05和3.23(趋势P<0.001),肾脏终点事件风险比分别为1.00、1.36、3.34和27.3(趋势P<0.001)。
eGFR降低的中国2型糖尿病患者发生心血管终点事件和全因死亡的风险较高,且独立于蛋白尿和代谢控制情况。