Amino acid challenge in patients with cirrhosis: a model for the assessment of treatments for hepatic encephalopathy

被引:39
作者
Douglass, A [1 ]
Al Mardini, H [1 ]
Record, C [1 ]
机构
[1] Univ Newcastle Upon Tyne, Dept Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
amino acid challenge; psychometry; ammonia; electroencephalography; hepatic encephalopathy;
D O I
10.1016/S0168-8278(01)00004-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: To mimic episodic hepatic encephalopathy after gastrointestinal bleeding under controlled conditions, cirrhotic patients were challenged with an amino acid mixture of comparable composition to haemoglobin. Methods: Basal EEG, psychometric score (HE test), reaction times and venous blood ammonia were recorded. Following a 54 or 108 gm oral amino acid challenge, blood ammonia levels and EEG were recorded at 30-min intervals, and psychometric testing was repeated at 180 min. Ten controls (57 +/- 2) and 31 cirrhotics (52 +/- 2) of which 21 were Child's grade A or B and 10 grade C underwent the challenge. Nine had a transjugular intrahepatic porta-systemic shunt in situ. Results: Seventeen patients had abnormal baseline IIE scores. Basal blood ammonia and reaction time A were significantly greater in patients (52 +/- 5 mu mol/l and 478 +/- 20 ms, respectively) than controls (19 +/- 2 mu mol/l and 372 +/- 14 ms) (P < 0.001). Following the challenge, in patients with advanced liver disease (Child's grade B and C) the slowing of reaction time A (+85 +/- 38 and +71 +/- 31 ms, respectively; P < 0.03) and EEG (ratio of slow to fast wave activity +0.31 +/- 0.12 and +0.58 +/- 0.19; P < 0.02) were significantly greater than in controls (-3.3 +/- 8 ms and 0.00 +/- 0.03, respectively). Patients with an abnormal basal HE score had the most pronounced changes (reaction time A +110 +/- 39 ms, P < 0.01, EEG +0.52 +/- 13, P < 0.01, respectively). The change in EEG ratio correlated with the dose of amino acid administered (r = 0.96; P < 0.008). Conclusion: The amino acid challenge constitutes a reproducible human model of episodic, Type C hepatic encephalopathy unaffected by the complications usually encountered in clinical practice. (C) 2001 European Association for the Study of the Liver. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:658 / 664
页数:7
相关论文
共 34 条
[1]  
ADAMSONS RJ, 1978, SURG GYNECOL OBSTET, V146, P869
[2]   Visual attention in cirrhotic patients: A study on covert visual attention orienting [J].
Amodio, P ;
Marchetti, P ;
Del Piccolo, F ;
Campo, G ;
Rizzo, C ;
Iemmolo, RM ;
Gerunda, G ;
Caregaro, L ;
Merkel, C ;
Gatta, A .
HEPATOLOGY, 1998, 27 (06) :1517-1523
[3]  
[Anonymous], 1981, WAIS R MANUAL
[4]   Ammonia and GABA-ergic neurotransmission: Interrelated factors in the pathogenesis of hepatic encephalopathy [J].
Basile, AS ;
Jones, EA .
HEPATOLOGY, 1997, 25 (06) :1303-1305
[5]   Hepatic encephalopathy and brain edema in acute hepatic failure: Does glutamate play a role? [J].
Butterworth, RF .
HEPATOLOGY, 1997, 25 (04) :1032-1034
[6]  
CHEMMESEN JO, 1999, HEPATOLOGY, V29, P645
[7]  
COOPER AJL, 1990, ADV EXP MED BIOL, V272, P23
[8]  
Cordoba J, 1997, AM J GASTROENTEROL, V92, P1429
[9]  
Damink SWO, 1999, HEPATOLOGY, V30, p215A
[10]   Decreased plasma isoleucine concentrations after upper gastrointestinal haemorrhage in humans [J].
Dejong, CHC ;
Meijerink, WJHJ ;
vanBerlo, CLH ;
Deutz, NEP ;
Soeters, PB .
GUT, 1996, 39 (01) :13-17