Combined Treatment With Lipoprotein Apheresis and Hemodialysis in Patients With Severe Cardiovascular Disease, High Lipoprotein(a) and End Stage Renal Disease
Tilmann Röseler, Daniel Kayser, Georg Schlieper, Wanja M. Bernhardt
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引用次数: 0
Abstract
Elevated Lipoprotein(a) (Lp(a)) is a known independent cardiovascular risk factor. Lp(a) Lipoprotein Apheresis (LA) substantially reduces the number of cardiovascular events. The effect of LA treatment in hemodialysis (HD) patients remains unknown. Retrospective analysis of nine patients undergoing LA and HD. Cardiovascular risk factors and the efficacy of treatment were assessed. Adverse cardiac or vascular events (ACVE) were recorded. Median (range) years on HD were 4.2 (1.5 to 23.6) years and median years on LA were 4.0 (1.6 to 12.4) years. Before initiation of LA, median (range) Lp(a) level was 242.67 (164.0 to 400.10) nmol/L and mean LDL-C level (±SD) 2.49 (±1.14) mmol/L. Under treatment, mean acute reduction rates, comparing concentrations before and after LA sessions, were 64.15 (±5.45)% for Lp(a) and 57.26 (±7.93)% for LDL-C. Before initiation of LA, 14 ACVE occurred; after initiation, only 6 (57.2% reduction rate). In this small cohort, LA appears to be effective in reducing ACVE in patients on HD with elevated Lp(a) levels. Further studies are needed to evaluate the effect of LA on cardiovascular outcomes in dialysis patients.
脂蛋白(a)(Lp(a))升高是一种已知的独立心血管风险因素。脂蛋白(a)脂蛋白吸附术(LA)可大大减少心血管事件的发生。血液透析(HD)患者接受 Lp(a) 脂蛋白吸附治疗的效果尚不清楚。对九名接受 LA 和 HD 治疗的患者进行了回顾性分析。评估了心血管风险因素和治疗效果。记录了心脏或血管不良事件(ACVE)。接受 HD 治疗的中位年数(范围)为 4.2(1.5 至 23.6)年,接受 LA 治疗的中位年数为 4.0(1.6 至 12.4)年。开始使用 LA 之前,脂蛋白(a)水平的中位数(范围)为 242.67(164.0 至 400.10)纳摩尔/升,低密度脂蛋白胆固醇的平均水平(±SD)为 2.49(±1.14)毫摩尔/升。在治疗过程中,比较 LA 治疗前后的浓度,脂蛋白(a)的平均急性降低率为 64.15 (±5.45) %,低密度脂蛋白胆固醇的平均急性降低率为 57.26 (±7.93) %。开始使用 LA 前,有 14 例 ACVE;开始使用 LA 后,仅有 6 例(降低率为 57.2%)。在这一小型队列中,LA 似乎能有效减少 Lp(a) 水平升高的 HD 患者的 ACVE。还需要进一步研究来评估 LA 对透析患者心血管预后的影响。
期刊介绍:
The Journal of Clinical Apheresis publishes articles dealing with all aspects of hemapheresis. Articles welcomed for review include those reporting basic research and clinical applications of therapeutic plasma exchange, therapeutic cytapheresis, therapeutic absorption, blood component collection and transfusion, donor recruitment and safety, administration of hemapheresis centers, and innovative applications of hemapheresis technology. Experimental studies, clinical trials, case reports, and concise reviews will be welcomed.