Management of Cirrhotic Ascites
Tolvaptan is a recently available diuretic that blocks arginine vasopressin receptor 2 in the renal collecting duct. Its diuretic mechanism involves selective water reabsorption by affecting the water reabsorption receptor aquaporin 2. Given that liver cirrhosis patients exhibit hyponatremia due to their pseudo-aldosteronism and usage of natriuretic agents, a sodium maintaining agent, such as tolvaptan, is physiologically preferable. However, large scale studies indicating the patients for whom this would be effective and describing management under its use have been insufficient. The appropriate management of cirrhosis patients treated with tolvaptan should be investigated. In the present review, we collected articles investigating the effectiveness of tolvaptan and factors associated with survival and summarized their management reports. Earlier administration of tolvaptan before increasing the doses of natriuretic agents is recommended because this may preserve effective arterial blood volume.
1. Ascites Management with Spironolactone and Furosemide
The first diuretic agent used for the management of cirrhotic ascites is spironolactone, which is a specific aldosterone antagonist. Given that cirrhotic patients have secondary aldosteronism due to RAAS activation via defected EABV, spironolactone is superior to furosemide in managing cirrhosis. Spironolactone was demonstrated to be more effective (response rate 95%) than furosemide (response rate 52%) in one study. When patients are refractory to spironolactone, furosemide may be added as a next step. However, given that both spironolactone and furosemide are sodium reabsorption restricting agents, severe hyponatremia may occur.
Hyponatremia is a common pathologic status in cirrhosis. Systemic vasodilation and arterial underfilling play a key role in the development of hyponatremia. As explained in the overload theory, sinusoidal obstruction-related sodium and water retention induce volume overload and—as explained in the underfilling theory—RAAS activation induces the same phenomenon. In addition, AVP-induced water retention affects hyponatremia. The majority of cirrhosis patients (90%) show hypervolemic dilutional hyponatremia. The administration of spironolactone and furosemide induces additional hyponatremia, resulting in a more severe state. The severity of hyponatremia has been shown to be correlated with mortality. The addition of spironolactone and furosemide results in a worsening of hyponatremia.
2. Ascites Management with AVP Targeting Agents
AVP is a nonapeptide synthesized by the neurosecretory cells in the supraoptic nucleus and the paraventricular nucleus of the hypothalamus. These nuclei have axons that terminate in the neural lobe of the posterior pituitary gland (neurohypophysis) where AVP is released. AVP is released into the systemic circulation in response to extracellular hyperosmolarity, and induces vasoconstriction and antidiuretic action. AVP is also released into the central nervous system (CNS) and acts as neuromodulator that affects many psychiatry functions, such as anxiety, social behavior, learning, and memory. There are three known AVP receptors: V1a, V1b, and V2. These receptors belong to the large rhodopsin-like class-A G-protein-coupled receptor family. V1a receptor is located on the vascular smooth muscle cells to induce vasoconstriction. V1a receptor is also expressed in the CNS to influence a wide variety of brain functions, such as social interaction, anxiety-like behavior, depression, and the circadian rhythm. V1b receptor is expressed in multiple brain regions and peripheral tissues, including the kidney, thymus, heart, lung, and spleen. V2 receptor is located on the basolateral membrane of the distal tubule and collecting ducts in the kidney. The activation of V1a receptors results in vascular constriction, while the activation of V2 receptors results in free water reabsorption in the principal collecting duct cells of the kidneys. After AVP binds to the V2 receptors, intracellular concentration of cyclic AMP (cAMP) increases via adenylyl cyclase activation. Cytoplasmic vesicles carrying the water channel aquaporin 2 (AQP2) are fused to the luminal membrane and increase its permeability to water, resulting in water re-absorption. AVP is increased in cirrhosis, especially in individuals who are hypo-responsive to water load, as assessed by water excretion via urine. Reduced EABV resulting from arterial vasodilation stimulates the secretion of AVP by baroreceptor-mediated non-osmotic stimulation.
Terlipressin (Na-tryglycl-8-lysine-vasopressin) is a synthetic vasopressin analogue that shows vasoconstrictor activity in the splanchnic and systemic vasculature. It is a pro-drug for the endogenous/natural porcine hormone [Lys8]-vasopressin (LVP). Terlipressin has a substitution of lysine for arginine at the eighth position of natural AVP and also has three glycyl residues at the amino terminus. Terlipressin, and especially LVP show high affinity for the V1a receptor. However, terlipressin and LVP also show definite V2 receptor binding affinity. This means that in cirrhosis, terlipressin and its metabolite LVP constrict pathogenic dilated splanchnic vessels, resulting in renal EABV recovery. However, the V2 receptor binding and the activating collecting duct AQP2 pathway induce water reabsorption.
Figure 1. A schematic illustration of the mechanisms underlying the effects of terlipressin in cirrhosis. Splanchnic vascular dilatation is one characteristic of the vascular status in cirrhosis. Terlipressin, a synthetic arginine/vasopressin (AVP) analogue, constricts these dilated vessels and improves effective arterial blood volume (EABV). Although the activation of V2 receptors by vasopressin and terlipressin induces water reabsorption via the water channel aquaporin (AQP)-2 receptor, terlipressin is acknowledged to be a supportive agent for the management of acute kidney injury in cirrhosis.
Terlipressin is now recognized as effective in controlling acute kidney injury by hepatorenal syndrome (HRS-AKI), especially with the concomitant use of albumin infusion, as prescribed in the EASL clinical practice guidelines. Beyond the standard AKI, such as pre-renal, intra-renal, and post-renal, cirrhosis-related renal dysfunction is known as HRS. HRS is defined as renal dysfunction due to reduced EABV, or overactivity of vasoactive agents (e.g., AVP). HRS-AKI has been newly defined based on the following criteria.
HRS has been classified into two clinical types: types 1 (HRS-1) and 2 (HRS-2). HRS-1 is defined as the rapid progression of renal dysfunction with a doubling of the initial creatinine to >2.5 mg/dL or a 50% reduction in the initial 24 h creatinine clearance to <20 mL/min in less than 2 weeks. HRS-2 is defined as slowly progressive renal dysfunction in which refractory ascites is the main clinical finding.
Recently, the International Club of Ascites (ICA) renamed HRS-1 as HRS-AKI and HRS-2 as HRS-NAKI, according to the new definition of AKI in The Kidney Disease: Improving Global Outcomes (KDIGO) guidelines. HRS-AKI is defined by the following criteria: (a) absolute increase in creatinine of ≥0.3 mg/dL within 48 h; and/or (b) urinary output of ≤0.5 mL/kg body weight at ≥6 h; or (c) a ≥ 50% increase in creatinine, using the last available value of outpatient creatinine within 3 months as the baseline value. HRS-AKI is precipitated by bacterial infection, gastrointestinal hemorrhage, large-volume paracentesis without the administration of albumin, or an acute exacerbation of alcoholic liver injury.
Several placebo-controlled studies of terlipressin have shown a significant effect on recovery of HRS . The effectiveness is definite; however, terlipressin induced several adverse events, including severe respiratory failure. In the newest prospective study, respiratory failure was predominant in the terlipressin group; the incidence was nearly three times that in the placebo group. This effect must be in part associated with the activation of the V2 receptor by terlipressin, followed by increased water reabsorption.
Tolvaptan is a highly selective antagonist of the AVP V2 receptor. It was first shown to be effective in body weight reduction and in recovering low sodium levels in patients with hyponatremic chronic heart failure. It was later shown to be effective in controlling the syndrome of inappropriate antidiuretic hormone (SIADH), and autosomal dominant polycystic kidney disease (ADPKD). It has been approved in many countries for the treatment of hyponatremia in heart failure, SIADH, and ADPKD. Although tolvaptan definitely prevented an increase in the size of the ADPKD kidney, a higher discontinuation rate was clearly observed due to adverse events (AEs), including increased transaminase. At doses of 60–120 mg/day in early-stage ADPKD (estimated creatinine clearance ≥ 60 mL/min), a significant increase was observed in the transaminase level in the experimental group compared with the placebo group (4.9% vs. 1.2%). In later-stage ADPKD (estimated glomerular filtration rate 25–65 mL/min/1.73 m2 in 18–55 years of age, 25–44 mL/min/1.73 m2 in 56–65 years of age), the administration of tolvaptan was also associated with a higher transaminase level in comparison with the administration of a placebo (5.6% vs. 1.2%). Based on these reports, US-FDA limits the duration of tolvaptan use to not more than 30 days and to patients with underlying liver disease. However, in Japan, tolvaptan was shown to be effective against cirrhotic ascites without severe AEs at low doses of 7.5 mg/day, and has received national health insurance coverage from 2013. Accumulating evidence suggests that it can even improve the prognosis of liver cirrhosis, and it is now recognized as an effective agent for the management of cirrhotic ascites.
The Mechanisms of Tolvaptan
Vaptans are non-peptide vasopressin receptor antagonists, which include V1 receptor antagonists and V2 receptor antagonists. V1 receptor antagonists, such as relcovaptan, have been shown to be effective in controlling Raynaud’s disease, dysmenorrhea, and tocolysis. When first produced in 1992 (when water diuresis in humans was limited), the V2 receptor antagonist mozavaptan was the first vaptan demonstrated to be effective for increasing the serum sodium level. Tolvaptan was shown to be effective for water diuresis in 1998. In addition to these agents, the use of lixivaptan and satavaptan have also been reported as effective in improving hyponatremia and/or ascites . Given that the V2 receptor is located on the principal collecting duct cells of the kidneys, its effects are believed to be specific for renal water reabsorption (Figure 2). Tolvaptan induces electrolyte-free water excretion without changing the total level of electrolyte excretion. In addition to these water-balance-related mechanisms, tolvaptan has been shown to activate antioxidant pathway Nrf2/HO-1 and to restore a damaged renal collecting duct cell line. Given that oxidative stress has been shown to induce renal damage in cirrhosis, the anti-oxidant function might be preferable for the kidneys in cirrhosis patients.
Figure 2. A schematic illustration of the mechanisms underlying the effects of tolvaptan in cirrhosis. Tolvaptan blocks the V2 receptor and reduces the effect of arginine/vasopressin (AVP) in the renal water channel. This does not reduce the preferable effect of AVP on the dilated splanchnic vascular bed.
The Clinical Efficacy of Tolvaptan in Cirrhosis
Tolvaptan (7.5-30 mg/day for 7 days) has been shown to have add-on effects to conventional diuretics on ascites in Japanese multicenter randomized control trials (RCTs) (Table 1). Significant body weight loss was also reported in a Chinese multicenter RCT. The effectiveness of tolvaptan has been defined differently in different studies. Recently, a Japanese multicenter study reported that body weight loss of 1.5 kg/week most accurately reflected a reduction of symptoms.
|determine the effects of tolvaptan||164 cirrhosis||Multicenter, double-blind, placebo-controlled. 7-day trial
placebo (n = 80),
add-on tolvaptan 7.5 mg/day (n = 84)
|Tolvaptan decreased the body weight
(−1.95 kg in tolvaptan vs. −0.44 kg in placebo)
|determine the optimal dose of tolvaptan||104 cirrhosis||Multicenter, double-blind, placebo-controlled. 7-day trial
placebo (n = 27),
7.5 mg/day (n = 26),
15 mg/day (n = 25),
30 mg/day (n = 26)
|Tolvaptan at 7.5 mg/day induced a maximum decrease in body weight with preferable tolerability
(−2.31 kg in 7.5 mg/day vs. −1.88 kg in 15 mg/day vs. −1.67 kg in 30 mg/day vs. −0.36 kg/day in placebo)
|determine the effects of tolvaptan||530 cirrhosis||Multicenter, double-blind, placebo-controlled. 7-day trial
placebo (n = 76),
7.5 mg/day (n = 153)
15 mg/day (n = 301)
|Tolvaptan decreased the body weight
(−2.0 kg in 7.5 mg/day, −2.2 kg in 15 mg/day
vs. −1.2 kg in placebo)
Given that the effect of tolvaptan has been shown to be around 60%, factors predicting its effect have been reported from several institutions. A prospective multicenter non-interventional, post-marketing surveillance study of 340 Japanese patients showed that body weight reduction was predominant in younger patients with a preserved renal function with low creatinine levels and a high estimated glomerular filtration rate (eGFR). A preserved renal function, as reflected by the eGFR or creatinine level, was shown to be important in several other reports and should therefore be considered a crucial factor predicting the effect of tolvaptan. While even in chronic kidney disease (CKD) patients (eGFR < 45 mL/min/1.73 m2), urinary volume increased and body weight decreased; however, the effect was somewhat lower than in non-CKD patients. A bad renal function is not a contraindication for tolvaptan.
Another later large-scale study with 1098 Japanese patients revealed that a lower serum urea nitrogen (UN) level (<22.4 mg/dL) was the only factor predicting an early tolvaptan response. UN has also been shown to be a predictor of the tolvaptan response in several reports, including a Chinese RCT study with 530 patients. Given that a high UN reflects dehydration or decreased renal EABV, maintaining EABV is crucial for drawing the tolvaptan response. UN and/or creatinine have been shown to be important markers in several studies; other markers also have been evaluated.
Low serum sodium levels have been shown to predict a non-response to tolvaptan in several studies . The main factor responsible for hyponatremia is the increased production of AVP due to nonosmotic hypersecretion in cirrhosis. In patients with high AVP levels, the standard doses of tolvaptan might be too low to achieve a clinical response. Given that hyponatremia is associated with an increased risk of mortality in cirrhosis, the administration of tolvaptan should be considered before severe hyponatremia occurs.
Patients with severe portal hypertension have also been reported to show a low re-sponse to tolvaptan. A high hepatic venous pressure gradient and serum hyaluronic acid levels have been shown to predict a low response to tolvaptan.
The spot urine Na/K ratio has been reported as a predictor in several studies. Urinary sodium excretion has been shown to be useful for the evaluation of standard na-triuretic agents. Urinary sodium excretion of <78 mmol/day with high-dose diuretic agents resulted in no weight loss in patients with refractory ascites. The urinary Na/K ratio has been shown to be the best candidate marker for defining the daily urinary excretion of sodium. The urinary spot Na/K ratio has been shown to be a marker for predicting the effectiveness of natriuretic agents. A spot urine Na/K ratio of ≥2.5 prior to the administration of tolvaptan has been shown to predict a positive response. Another study showed that a spot urine Na/K ratio of >3.09 indicated a response and that, in combination with a serum urea nitrogen/creatinine ratio of <17.5, predicted a response to tolvaptan in 100% of cases.
A greater rate of decrease in urinary osmolality at 4 h after the administration of tolvaptan has been shown to predict a response in several studies. Urinary osmolality is maintained with dissolved substances, such as creatinine, urea, urea nitrogen, and sodium. When tolvaptan is effective and the water content in urine increases, urinary osmolality should decrease. This marker is mechanistically sound; however, it does not predict a response prior to the administration of tolvaptan.
In addition to low creatinine levels, a high serum concentration of a vascular tonus-related marker, namely asymmetric dimethylarginine (ADMA), has been shown to be a significant marker in one study. ADMA is a vascular function-related marker reflecting reactive oxygen species (ROS) related vasoconstriction. As shown in Figure 3, ADMA is an endogenous inhibitor of endothelial nitric oxide synthase (NOS) and inhibits acetylcholine-induced vasodilation in endothelial cells. A high serum ADMA has been shown to be correlated with the progression of vascular diseases such as cerebral endothelial damage and cardiovascular diseases. ADMA is one of the molecules included in the oxidative stress-related vasoconstriction pathway. The concentration of ADMA levels is regulated by dimethylaminohydrolase (DDAH) activity. DDAH inactivates ADMA via hydrolyzing ADMA to citrulline and dimethylamines. One of the two isoforms of DDAH, DDAH-2 mainly exists in endothelial cells and is extremely sensitive to intracellular ROS. ROS can inhibit DDAH-2 activity, resulting in increased ADMA, which is followed by a reduction of vascular endothelial dilation-related NOS. The ROS-DDAH-ADMA-NOS pathway regulates NO production and endothelial motility. Although high serum ADMA is a marker of an advanced condition of a cerebrovascular disease, it predicts a positive response to tolvaptan. The vasoconstrictive status seems to be included in the tolvaptan-sensitive mechanism. This mechanistic analysis indicates that cirrhosis patients with higher serum ADMA levels might have a vasoconstrictive status with a large EABV and which is sensitive to tolvaptan. Tolvaptan might be effective in non-responsive patients with low ADMA levels when administered in combination with a vasoconstrictor, such as terlipressin.
Figure 3. A schematic diagram of oxidative stress in vasoconstriction. The red arrows indicate the changes of the vascular tonus-regulating pathway by oxidative stress. DDAH, dimethylaminohydrolase; ADMA, asymmetric dimethylarginine; NOS, nitric oxide synthase; NO, nitric oxided.
Long-Term Survival after Tolvaptan Administration
Long-term survival after tolvaptan administration has been shown in several reports. A tolvaptan-treated group showed better survival rates than patients who did not receive tolvaptan, although these data were from historical cases. A recent large scale retrospective cohort study using a Japan-wide hospital-based administrative claims database reported that the probability of survival was higher in patients who received tolvaptan. Other diuretics, especially furosemide, have been suggested to be correlated with a poor survival rate along with retardation of the renal function. A positive response to tolvaptan has been shown to predict a patient’s prognosis. This is convincing, because cirrhosis patients with hyponatremia or an impaired renal function show a poor prognosis , and tolvaptan is able to recover these bad conditions.
Several studies have shown that the administration of tolvaptan had no effect on survival. These studies showed prognostic factors, such as complications with HCC and low fractional excretion of sodium (FENa), complications with HCC and Child-Pugh class C, and a rapid and early decrease in a bioimpedance analysis (defined by intracellular water at 6 h after the first dose of tolvaptan). These factors are also convincing.
HCC and Child-Pugh class C are both clear factors that predict poor survival. The impact of HCC on survival is affected by the stages of the disease and this might influence the different results of reports on HCC.
FENa is calculated by (urine Na x serum creatinine)/(serum Na x urine creatinine), which reflects the sodium reabsorption status. Although the spot urine mineral concentration is affected by the urine concentration, FENa is relatively constant throughout the day because urinary sodium is adjusted by creatinine excretion. Low FENa is usually a marker of pre-renal low EABV-related AKI because renal Na+ and water reabsorption is induced in such situations. A reduced EABV, which indicates low FENa, reflects an advanced cirrhosis-related vascular disorder, which predicts a poor survival probability. A low FENa level has been reported to be a predictor of a poor probability of survival before tolvaptan became available. One means of achieving a better survival rate in patients with low FENa levels might be obtaining a recovery of EABV. Therefore, the administration of terlipressin or the infusion of albumin might be potentially effective approaches to improve EABV. For the management of cirrhosis, continuous human albumin administration has been shown to be effective for achieving long-term survival. The administration of human albumin (40 g twice weekly for 2 weeks, and then 40 g weekly) has been shown to be associated with an improved survival rate in comparison with standard medical treatment. Such an approach would also result in a reduction in UN, which would complement the treatment of tolvaptan in non-responsive patients with high UN values, potentially inducing a response followed by long-term survival.
The entry is from 10.3390/ijms22115582
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