Ahluwalia Vishwadeep, Heuman Douglas M, Feldman George, Wade James B, Thacker Leroy R, Gavis Edith, Gilles HoChong, Unser Ariel, White Melanie B, Bajaj Jasmohan S
Department of Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University and McGuire VA Medical Center, Richmond, VA, USA; Department of Radiology, Virginia Commonwealth University and McGuire VA Medical Center, Richmond, VA, USA.
Department of Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University and McGuire VA Medical Center, Richmond, VA, USA.
J Hepatol. 2015 Jan;62(1):75-82. doi: 10.1016/j.jhep.2014.07.033. Epub 2014 Aug 8.
BACKGROUND & AIMS: Hyponatraemia in cirrhosis is associated with impaired cognition and poor health-related quality of life (HRQOL). However, the benefit of hyponatraemia correction is unclear. The aim of this study was to evaluate the effect of tolvaptan on serum sodium (Na), cognition, HRQOL, companion burden, and brain MRI (volumetrics, spectroscopy, and diffusion tensor imaging) in cirrhotics with hyponatraemia.
Cirrhotics with Na <130 mEq/L were included for a four-week trial. At screening, patients underwent cognitive and HRQOL testing, serum/urine chemistries and companion burden assessment. Patients then underwent fluid restriction and diuretic withdrawal for two weeks after which cognitive tests were repeated. If Na was still <130 mEq/L, brain magnetic resonance imaging (MRI) was performed and tolvaptan was initiated for 14 days with frequent clinical/laboratory monitoring. After 14 days of tolvaptan, all tests were repeated. Comparisons were made between screen, pre-and post-drug periods Na, urine/serum laboratories, cognition, HRQOL and companion burden.
24 cirrhotics were enrolled; seven normalized Na without tolvaptan with improvement in cognition. The remaining 17 received tolvaptan of which 14 completed the study over 13 ± 2 days (age 58 ± 6 years, MELD 17, 55% HCV, median 26 mg/day of tolvaptan). Serum Na and urine free water clearance increased with tolvaptan without changes in mental status or liver function. Cognitive function, HRQOL and companion burden only improved in these 14 patients after tolvaptan, along with reduced total brain and white matter volume, increase in choline on magnetic resonance spectroscopy, and reduced cytotoxic oedema.
Short-term tolvaptan therapy is well tolerated in cirrhosis. Hyponatraemia correction is associated with cognitive, HRQOL, brain MRI and companion burden improvement.
肝硬化患者的低钠血症与认知功能受损及健康相关生活质量(HRQOL)较差有关。然而,纠正低钠血症的益处尚不清楚。本研究的目的是评估托伐普坦对低钠血症肝硬化患者血清钠(Na)、认知功能、HRQOL、照料者负担及脑磁共振成像(容积测量、波谱分析和扩散张量成像)的影响。
纳入血清钠<130 mEq/L的肝硬化患者进行为期四周的试验。在筛查时,患者接受认知和HRQOL测试、血清/尿液化学分析及照料者负担评估。然后患者进行两周的液体限制和停用利尿剂,之后重复认知测试。如果血清钠仍<130 mEq/L,则进行脑磁共振成像(MRI)检查,并开始使用托伐普坦治疗14天,同时进行频繁的临床/实验室监测。托伐普坦治疗14天后,重复所有测试。对筛查期、用药前和用药后阶段的血清钠、尿液/血清实验室检查结果、认知功能、HRQOL及照料者负担进行比较。
共纳入24例肝硬化患者;7例未使用托伐普坦血清钠恢复正常,认知功能改善。其余17例接受托伐普坦治疗,其中14例在13±2天内完成研究(年龄58±6岁,终末期肝病模型(MELD)评分为17,55%为丙型肝炎病毒感染,托伐普坦中位剂量为26 mg/天)。使用托伐普坦后血清钠和尿自由水清除率增加,精神状态和肝功能无变化。仅这14例患者在使用托伐普坦后认知功能、HRQOL和照料者负担得到改善,同时全脑和白质体积减小,磁共振波谱分析显示胆碱增加,细胞毒性水肿减轻。
肝硬化患者短期使用托伐普坦治疗耐受性良好。纠正低钠血症与认知功能、HRQOL、脑MRI及照料者负担改善有关。