Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Diabetes Care. 2013 Jun;36(6):1462-9. doi: 10.2337/dc12-1940. Epub 2012 Dec 28.
OBJECTIVE Long-chain n-3 polyunsaturated fatty acid (n-3 PUFA) supplements may have renoprotective effects in patients with diabetes, but previous trials have been inconsistent. We performed a randomized controlled trial of n-3 PUFA supplementation on urine albumin excretion and markers of kidney injury in adults with type 2 diabetes. RESEARCH DESIGN AND METHODS We conducted a randomized, placebo-controlled, two-period crossover trial to test the effects of 4 g/day of n-3 PUFA supplementation on markers of glomerular filtration and kidney injury in adults with adult-onset diabetes and greater than or equal to trace amounts of proteinuria. Each period lasted 6 weeks and was separated by a 2-week washout. The main outcome was urine albumin excretion and, secondarily, markers of kidney injury (kidney injury molecule-1, N-acetyl β-d-glucosaminidase [NAG], neutrophil gelatinase-associated lipocalin [NGAL], and liver fatty acid-binding protein [LFABP]), serum markers of kidney function (cystatin C, β2-microglobulin, and creatinine), and estimated glomerular filtration rate (eGFR). RESULTS Of the 31 participants, 29 finished both periods. A total of 55% were male, and 61% were African American; mean age was 67 years. At baseline, mean BMI was 31.6 kg/m(2), median eGFR was 76.9 mL/min/1.73 m(2), and median 24-h urine albumin excretion was 161 mg/day. Compared with placebo, n-3 PUFA had nonsignificant effects on urine albumin excretion (-7.2%; 95% CI -20.6 to 8.5; P = 0.35) and significant effects on urine NGAL excretion (-16% [-29.1 to -0.5%]; P = 0.04). There was no effect on serum markers of kidney function or eGFR. In subgroup analyses, there were significant decreases in 24-h urinary excretion of albumin, NGAL, LFABP, and NAG among participants taking medications that block the renin-angiotensin-aldosterone system (RAAS). CONCLUSIONS These results suggest a potential effect of n-3 PUFA supplementation on markers of kidney injury in patients with diabetes and early evidence of kidney disease. In the context of prior studies, these results provide a strong rationale for long-term trials of n-3 PUFA on chronic kidney disease progression.
长链 n-3 多不饱和脂肪酸(n-3 PUFA)补充剂可能对糖尿病患者具有肾脏保护作用,但先前的试验结果并不一致。我们进行了一项随机对照试验,以研究 n-3 PUFA 补充剂对 2 型糖尿病成人尿白蛋白排泄和肾脏损伤标志物的影响。
我们进行了一项随机、安慰剂对照、两周期交叉试验,以测试每天 4 克 n-3 PUFA 补充剂对成年发病且有微量蛋白尿的糖尿病患者肾小球滤过和肾脏损伤标志物的影响。每个周期持续 6 周,洗脱期为 2 周。主要结局是尿白蛋白排泄,其次是肾脏损伤标志物(肾损伤分子-1、N-乙酰-β-D-氨基葡萄糖苷酶[NAG]、中性粒细胞明胶酶相关脂质运载蛋白[NGAL]和肝脂肪酸结合蛋白[LFABP])、血清肾功能标志物(胱抑素 C、β2-微球蛋白和肌酐)和估计肾小球滤过率(eGFR)。
31 名参与者中,有 29 名完成了两个周期。共有 55%为男性,61%为非裔美国人;平均年龄为 67 岁。基线时,平均 BMI 为 31.6kg/m2,中位 eGFR 为 76.9mL/min/1.73m2,中位 24 小时尿白蛋白排泄量为 161mg/天。与安慰剂相比,n-3 PUFA 对尿白蛋白排泄量的影响无统计学意义(-7.2%[-20.6 至 8.5%];P=0.35),但对尿 NGAL 排泄量的影响有统计学意义(-16%[-29.1 至 0.5%];P=0.04)。血清肾功能标志物或 eGFR 无影响。亚组分析显示,在服用阻断肾素-血管紧张素-醛固酮系统(RAAS)药物的参与者中,24 小时尿白蛋白、NGAL、LFABP 和 NAG 的排泄量显著降低。
这些结果提示 n-3 PUFA 补充剂可能对糖尿病患者的肾脏损伤标志物有潜在影响,并初步证明对早期肾脏疾病有影响。在先前研究的背景下,这些结果为 n-3 PUFA 对慢性肾病进展的长期临床试验提供了强有力的依据。