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The Long-Term Outcome of Patients with IgA Nephropathy Treated with Fish Oil in a Controlled Trial

鱼油 安慰剂 医学 临床终点 肾病 肾脏疾病 肌酐 内科学 肾功能 临床试验 安慰剂对照研究 终末期肾病 随机对照试验 外科 疾病 内分泌学 病理 生物 糖尿病 渔业 双盲 替代医学
作者
James V. Donadío,Joseph P. Grande,Erik J. Bergstralh,Richard A. Dart,Timothy S. Larson,Dorothy C. Spencer
出处
期刊:Journal of The American Society of Nephrology [American Society of Nephrology]
卷期号:10 (8): 1772-1777 被引量:202
标识
DOI:10.1681/asn.v1081772
摘要

Abstract. It was reported previously that dietary fish oil supplementation retarded the progression of renal disease in patients with IgA nephropathy in a multicenter, placebo-controlled, randomized, 2-yr clinical trial. The aim of this study was to determine the long-term influence of fish oil treatment on renal progression in observations on the study cohort of 106 patients extending beyond the 2-yr trial. Renal function was assessed by serial serum creatinine and 24-h urine protein measurements. Vital, end-stage renal disease (ESRD), and BP status and treatment beyond completion of the 2-yr trial were determined. As in the trial, the primary end point was an increase of 50% or more in the serum creatinine, and the secondary end point was ESRD. After a mean follow-up of 6.4 yr, 46 patients—17 in the fish oil group versus 29 in the placebo group—reached the primary end point ( P = 0.002), and 27 patients—eight in the fish oil group versus 19 in the placebo group—developed ESRD ( P = 0.009). At the end of the 2-yr trial, 75 patients (45 fish oil, 30 placebo) remained at risk for the primary end point. This is also when the double-blind part of the trial ended, allowing physicians to stop supplements, switch original placebo-assigned patients to fish oil, and continue fish oil in original fish oil-assigned patients. A significantly greater number of nonsupplemented placebo patients developed the primary end point ( P = 0.02) and ESRD ( P = 0.003) compared with long-term supplemented fish oil patients. Conversely, more fish oil-supplemented patients had stable renal function than nonsupplemented patients ( P = 0.02). By intention, BP control, primarily treated with angiotensin-converting enzyme inhibition, was equal in the fish oil and placebo groups. Proteinuria was modestly reduced in both groups. It is concluded that early and prolonged treatment with fish oil slows renal progression for high-risk patients with IgA nephropathy.
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