Terlipressin improves renal function in patients with cirrhosis and ascites without hepatorenal syndrome

被引:113
作者
Krag, Aleksander [1 ]
Moller, Soren
Henriksen, Jens H.
Holstein-Rathlou, Niels-Henrik
Larsen, Fin Stolze
Bendtsen, Flemming
机构
[1] Hvidovre Univ Hosp, Dept Gastroenterol 439, DK-2650 Hvidovre, Denmark
[2] Hvidovre Univ Hosp, Dept Clin Physiol, Hvidovre, Denmark
[3] Univ Copenhagen, Panum Inst, Dept Biomed Sci, Copenhagen, Denmark
[4] Univ Copenhagen, Rigshosp, Dept Hepatol, Copenhagen, Denmark
关键词
D O I
10.1002/hep.21901
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Patients with advanced cirrhosis and ascites are characterized by circulatory dysfunction with splanchnic vasodilatation and renal vasoconstriction, which often lead to ascites. The vasoconstrictor terlipressin improves renal function in hepatorenal syndrome (FIRS). The aim of this study was to evaluate ifterlipressin also improves renal function in patients with ascites without HRS. Twenty-three patients with cirrhosis participated, 15 with nonrefractory ascites were randomized to either terlipressin (N group, n = 11) or a placebo (P group, n = 4), and 8 had refractory ascites and received terlipressin (R group). The glomerular filtration rate (GFR), sodium clearance (C-Na), lithium clearance (C-Li), osmolal clearance (C-Osm), and urine sodium concentration (U-Na) were assessed before and after the injection of 2 mg of terlipressin or the placebo. GFR increased in the N group (69 +/- 19 versus 92 +/- 25 mL/min, P < 0.005) and in the R group (31 +/- 19 versus 41 +/- 31 mL/min, P < 0.05) after terlipressin. In the N group, terlipressin induced an increase in C-Na (0.89 +/- 0.21 versus 1.52 +/- 1.45 mL/min, P < 0.05), C-Li (17.3 +/- 8.9 versus 21.5 +/- 11.6 mL/min, P < 0.05), and C-Osm (2.10 +/- 0.81 versus 3.06 +/- 2.0 mL/min, P < 0.05). In the Rgroup, terlipressin induced an increase in C-Na (0.11 +/- 0.18 versus 0.35 +/- 0.40 mL/min, P < 0.05) and C-Li (5.5 +/- 4.2 versus 9.5 +/- 8.55 mL/min, P < 0.05). U-Na increased in both groups after terlipressin (P < 0.005). Plasma norepinephrine (P < 0.05) and renin (P < 0.05) decreased after terlipressm. All parameters remained unchanged after the placebo. Conclusion: The vasopressin 1 receptor agonist terlipressin improves renal function and induces natriuresis in patients with cirrhosis and ascites without HRS. Vasoconstrictors may represent a novel future treatment modality for these patients.
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页码:1863 / 1871
页数:9
相关论文
共 39 条
[1]   Acute effects of the oral administration of midodrine, an α-adrenergic agonist, on renal hemodynamics and renal function in cirrhotic patients with ascites [J].
Angeli, P ;
Volpin, R ;
Piovan, D ;
Bortoluzzi, A ;
Craighero, R ;
Bottaro, S ;
Finucci, GF ;
Casiglia, E ;
Sticca, A ;
De Toni, R ;
Pavan, L ;
Gatta, A .
HEPATOLOGY, 1998, 28 (04) :937-943
[2]   EFFECTS OF AMILORIDE ON RENAL LITHIUM HANDLING IN NONAZOTEMIC ASCITIC CIRRHOTIC-PATIENTS WITH AVID SODIUM RETENTION [J].
ANGELI, P ;
DEBEI, E ;
PRIA, MD ;
CAREGARO, L ;
CEOLOTTO, G ;
ALBINO, G ;
GATTA, A .
HEPATOLOGY, 1992, 15 (04) :651-654
[3]  
Arroyo V, 1996, HEPATOLOGY, V23, P164, DOI 10.1002/hep.510230122
[4]   Ascites and hepatorenal syndrome in cirrhosis: pathophysiological basis of therapy and current management [J].
Arroyo, V ;
Colmenero, J .
JOURNAL OF HEPATOLOGY, 2003, 38 :S69-S89
[5]   INCREASED CIRCULATING CALCITONIN GENE-RELATED PEPTIDE (CGRP) IN CIRRHOSIS [J].
BENDTSEN, F ;
SCHIFTER, S ;
HENRIKSEN, JH .
JOURNAL OF HEPATOLOGY, 1991, 12 (01) :118-123
[6]   RENAL-FUNCTION AND EFFECTIVE BETA-BLOCKADE IN CIRRHOSIS WITH ASCITES - RELATIONSHIP WITH BASELINE SYMPATHOADRENERGIC TONE [J].
BERNARDI, M ;
DEPALMA, R ;
TREVISANI, F ;
TAME, MR ;
CIANCAGLINI, GC ;
PESA, O ;
LIGABUE, A ;
BARALDINI, M ;
GASBARRINI, G .
JOURNAL OF HEPATOLOGY, 1989, 8 (03) :279-286
[7]   ROLE OF VASOPRESSIN IN ABNORMAL WATER-EXCRETION IN CIRRHOTIC-PATIENTS [J].
BICHET, D ;
SZATALOWICZ, V ;
CHAIMOVITZ, C ;
SCHRIER, RW .
ANNALS OF INTERNAL MEDICINE, 1982, 96 (04) :413-417
[8]   POTENTIAL ROLE OF INCREASED SYMPATHETIC ACTIVITY IN IMPAIRED SODIUM AND WATER-EXCRETION IN CIRRHOSIS [J].
BICHET, DG ;
VANPUTTEN, VJ ;
SCHRIER, RW .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (25) :1552-1557
[9]   METABOLISM OF ALDOSTERONE IN NORMAL SUBJECTS AND IN PATIENTS WITH HEPATIC CIRRHOSIS [J].
COPPAGE, WS ;
COONER, AE ;
ISLAND, DP ;
LIDDLE, GW .
JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (08) :1672-&
[10]   SURVIVAL AND PROGNOSTIC INDICATORS IN COMPENSATED AND DECOMPENSATED CIRRHOSIS [J].
DAMICO, G ;
MORABITO, A ;
PAGLIARO, L ;
MARUBINI, E .
DIGESTIVE DISEASES AND SCIENCES, 1986, 31 (05) :468-475