Managing portal hypertension in patients with liver cirrhosis

Introduction

Portal hypertension is defined as the pathological increase of portal venous pressure, mainly due to chronic end-stage liver disease, leading to augmented hepatic vascular resistance and congestion of the blood in the portal venous system. This pathology may result in a series of complications, such as the formation of collateral vessels for return of the blood to the right atrium with potential for intestinal bleeding, formation of ascites, encephalopathy, and development of a hyperdynamic circulation involving peripheral and splanchnic vessels^1,2 associated with dysfunction of the kidneys³, the heart⁴, the lungs⁵, and the brain⁶ (Figure 1 and Figure 2). A complex interplay among inflammatory stimuli, vasoregulatory molecules, neurotransmitters, and ion channels maintains and drives these processes. Thus, portal hypertension is one cause and a part of a dynamic process triggered by chronic liver disease and systemic inflammation⁷. In the stage of advanced liver disease, mostly fixed structural changes, such as fibrosis or the formation of regenerative nodules, are responsible for developing and sustaining portal hypertension. In addition, dynamic components involving the regulation of blood flow in different vascular beds play a decisive role in the modulation of portal pressure and its associated pathophysiology. Systemic therapy is aimed at the modulation of these dynamic parts. Most likely, they are more or less similar in end-stage liver disease, regardless of the etiology of hepatic damage. However, in the early stages of liver disease, the pathological chain of events depends more on the causative factors, be they metabolic, infectious, or autoimmune. Thus, early and specific treatment is the foremost aim. During later stages of liver disease, distinct treatment of the initiating factors may still be pivotal, i.e. interruption of viremia or alcohol abuse (Figure 1 and Figure 2). However, this must be combined with measures to prevent or treat complications due to liver cirrhosis.

Figure 1. Two main pathways in the development of liver disease.

A. The liver (L) is primarily affected (mainly by chronic infection with hepatotropic viruses). This leads to liver cirrhosis and portal hypertension causing leakiness of the intestine (I) and dysbiosis, affecting the brain (B), and altering the splanchnic and systemic circulation, including the heart (H) and the kidneys (K). Prevention and therapy is interruption and/or suppression of viremia. B. Increasingly, nutrition has become the main culprit in liver disease. Here, inflammatory and metabolic stimuli from the gut affect the liver, visceral fat (VF), and cardiovascular system, including the heart and the kidneys, but also, concomitantly and early on in the process, the brain, which may support a vicious cycle of craving more food and liquids. Prevention and therapy is modification of food and liquid intake. Only in the later stages of liver disease do the complications of liver cirrhosis and portal hypertension determine pathogenesis, diagnosis, and therapy similar to A).

Figure 2. Stages of chronic liver disease and portal hypertension.

The figure depicts the diagnostic and therapeutic procedures during the pathogenesis and aggravation of portal hypertension for patients with suspected fibrosis/cirrhosis of the liver (A), compensated cirrhosis (B), and decompensated cirrhosis (C). Asc, ascites; EV, esophageal varices; FXR, farnesoid X receptor; HCC, hepatocellular carcinoma; HVPG, hepatic venous pressure gradient; IB, intestinal barrier; IH, intrahepatic; IHR, intrahepatic resistance; M, microbiome; MRI, magnet resonance imaging; NSBB, non-selective beta-blocker; SVB, splanchnic vascular bed; US, ultrasound.

This review focuses on portal hypertension in patients with advanced liver disease. It will address some open questions and new approaches on how to stage chronic liver disease and portal hypertension and how to prevent some of its complications.

Staging of chronic liver disease and portal hypertension

For staging of chronic liver disease, a variety of different tools are available, including physical examination, laboratory tests, imaging techniques, and hemodynamic measurements (Figure 2). Imaging techniques comprise endoscopy, ultrasound, determination of liver stiffness, computed tomography, and magnetic resonance imaging (MRI). Physical examination includes important parameters of the Child–Pugh classification⁸. If there are no signs of jaundice, ascites, or encephalopathy, the patient has a good chance of being in a compensated stage of cirrhosis with a 10-year survival of above 50%, while clinical signs of decompensation indicate a mortality of more than 75% within the next 5 years⁹.

Endoscopy is still the best method to assess the existence of varices in the upper intestinal tract as well as their size and potential to bleed or rebleed¹⁰. While in any patient with suspected liver cirrhosis a standard examination used to include endoscopy, new guidelines recommend abstaining from early endoscopy in patients with liver stiffness <20 kPa and platelet count >150 G/L^11,12. These patients have a high probability of being free of esophageal varices¹³. However, endoscopy retains its central role as the entrance test for the initiation of primary and secondary prophylaxis of variceal bleeding in patients with higher stiffness values or a lower platelet count, and it is still the central method for the assessment of variceal bleeding and hemostasis¹².

In addition, elastographic techniques enable estimation of the degree of liver fibrosis via transient elastography (TE), acoustic radiation force impulse imaging (ARFI), or shear wave elastography (SWE)^14,15. Determination of liver stiffness has by now become an important tool for screening of fibrosis and portal hypertension in patients with liver disease. Fibrosis leads to an increased stiffness of the liver. In organs with higher stiffness, shear waves travel with a higher speed through tissues. By delivering pulses, shear waves can be induced to assess their speed as an indirect measure of fibrosis. There are different systems using mechanical 50 Hz pulses (TE), a focused ultrasound pulse to deform internal tissue (AFRI and SWE), or a two-dimensional gradient-recalled-echo sequence analyzed by certain algorithms (magnetic resonance [MR] elastography).

The most extensive experience to date exists for TE, a stand-alone technique based on shear wave speed measurement, not integrated into ultrasound devices^16–18. Values below 5.2–9.5 kPa (TE) or 1.22–1.63 m/s (ARFI) can rule out significant liver fibrosis, whereas higher values may be falsely positive with respect to cirrhosis assessment because of obstructive cholestasis, liver congestion, severe liver inflammation, or infiltrative liver disease^16,17. However, many of these obscuring conditions can be assessed or ruled out by using ultrasound-based techniques such as SWE or AFRI. SWE has shown slightly better sensitivity and specificity for liver fibrosis and portal hypertension when compared to TE¹⁹. Nevertheless, observing standardized conditions like fasting state is important²⁰. By combining liver and spleen SWE, portal hypertension can be excluded with a very high probability²¹ on the one hand or assessed in its clinically significant form on the other²². Furthermore, ultrasound-based techniques allow for hepatocellular carcinoma (HCC) screening.

The different systems have pros and cons. TE is available in many centers and is excellently validated but may have a high failure rate in obese patients or in patients with ascites. AFRI allows ultrasound guidance for the region of interest but is less validated, and high body weight may also be a problem. MR elastography allows one to cover a large sampling volume, but it is affected by iron deposition, high body mass index, and massive ascites²³.

Ultrasound allows a more sensitive and specific assessment of ascites than clinical examination together with assessment of size, surface, and echotexture of the liver.

Similar to ultrasound, computed tomography and MRI are relevant for the diagnosis of HCC. This is important, since liver fibrosis or cirrhosis is a precancerous condition. Of all imaging devices, MRI has the broadest potential for staging liver disease with respect to morphology, including the biliary system, tissue texture, perfusion, formation of collaterals, function of hepatic cells^24–26, and quantification of steatosis or fibrosis^27,28. However, it is expensive and not always available. We recently showed how MRI can be used to measure fat-free muscle area as a prognostic marker of sarcopenia, correlated with survival²⁹ in patients with liver cirrhosis.

Among hemodynamic measurements, assessment of the hepatic venous pressure gradient (HVPG)³⁰ is the most important in chronic liver disease. Developed in the 1950s³¹ and later modified by Groszmann et al.³², it has become the gold standard for indirect assessment of the degree of portal hypertension. The HVPG value closely correlates with the portal vein pressure, especially in alcoholic liver disease³³, which in turn shows a significant correlation with blood pressure in esophageal varices³⁴. HVPG values above 5 mmHg are regarded as portal hypertension. Measurement of the HVPG adds prognostic information to standard laboratory and clinical evaluations in advanced liver disease^35,36. Patients with compensated cirrhosis and HVPG <10 mmHg have a rather low risk of developing varices or decompensation of liver function³⁷. It is generally accepted that esophageal varices do not bleed if HVPG remains below 12 mmHg and that a reduction of HVPG by more than 20%, regardless of the baseline value, considerably reduces the risk of bleeding from varices. Thus, measurement of HVPG has repeatedly been advocated as a means to tailor the treatment for variceal bleeding^35,38. There is a good correlation between liver stiffness, as assessed by TE, and HVPG³⁹. Values below 14 kPa exclude clinically significant portal hypertension (HVPG ≥10 mmHg) with high sensitivity and specificity⁴⁰.

Since the introduction of the Child–Turcotte classification⁸ and its modification according to Pugh et al.⁴¹, it has been repeatedly shown that, in patients with liver cirrhosis, laboratory values reflecting hepatocyte function, e.g. uptake and secretion of bilirubin or synthesis of proteins, allow prediction of the probability of survival. Thus, serum levels of bilirubin, albumin, or clotting factors have been used for decades to stage chronic liver disease. They are part of the model for end-stage liver disease (MELD) system⁴² as well as of the Child–Pugh classification⁴¹.

The MELD consists of serum levels of bilirubin and creatinine and prothrombin time determined as an international normalized ratio (INR). Initially developed to determine the prognosis of patients receiving a transjugular intrahepatic portosystemic shunt (TIPS)^42,43, it is now used to assess organ allocation priority for liver transplantation. It can be calculated easily, has been validated prospectively in different cohorts, and contains no clinical parameters based on subjective assessment. Nevertheless, MELD is only slightly superior to the Child–Pugh model in the prediction of survival^44,45. The addition of further parameters such as sodium⁴⁶, hepatic encephalopathy⁴⁵, or sarcopenia⁴⁷ to MELD has been described to further improve prognosis with marginal effects.

Impairment of kidney function, such as sodium handling, occurs early in patients with liver disease⁴⁸, and elevated creatinine levels—or, more importantly, an increase in serum creatinine by ≥0.3 mg/dL - are independent markers for negative patient outcome⁴⁹.

Patients with liver cirrhosis are prone to systemic inflammation, where mostly cytokines of the innate immune system are involved⁵⁰. This paves the way towards fatal dysfunction of organs, now coined acute-on-chronic liver failure (ACLF)⁵¹. Thus, signs of inflammation, such as high leukocyte count and elevated C-reactive protein, are additional important prognostic parameters⁵². Interestingly, there is a subgroup of patients who, even after TIPS insertion, show an increased or unchanged liver stiffness. These are patients with high levels of proinflammatory cytokines. They have a bad outcome⁵³. Thus, dynamics in liver stiffness may be an easy read-out to assess inflammation and prognosis in TIPS patients. Furthermore, the individual genetic background with respect to genes coding for proteins involved in the immune response may predispose patients to infections, ACLF, and decompensation^54–58.

Many of the above-mentioned parameters are part of staging systems for liver cirrhosis designed to distinguish between compensated and decompensated disease at different states⁵⁹. If it is true that the intestine is important for the initiation and perpetuation of liver disease (see below), we will also need some sort of staging for intestinal dysfunction in patients with liver disease in the future.

The different staging systems mentioned above, such as the degree of fibrosis, HVPG, ongoing etiology, Child–Pugh, dynamics of kidney dysfunction, or signs of inflammation, are partly interrelated. Thus, HVPG increases with the degree of cirrhosis^60,61 or the degree of decompensation as assessed by the Child–Pugh score. However, the correlation is loose, and the prognostic value of HVPG is partly independent of the Child–Pugh system^62,63. Therefore, there is always the question of how to integrate different parameters or scores into an appropriate and simple bedside system. Clinical judgment is quite accurate for advanced liver disease. Jaundice and ascites are markers of bad prognosis. In this situation, bleeding, infections, overt encephalopathy, and deterioration of kidney function denote high risk of death. Determination of HVPG and/or of liver stiffness may improve long-term prognosis in patients with compensated cirrhosis⁵⁹, and HVPG alone is an independent prognostic marker in patients with decompensated cirrhosis and variceal bleeding^36,62,63. In the future, we will probably have to adapt to more complex systems^59,64 which might improve prognosis and therapy. No matter which stage of disease, the interruption of etiology, be it alcohol intake or viremia, is crucial.

As with all staging systems in medicine, the question arises as to whether these surrogates or biomarkers can guide the prevention or treatment of relevant clinical endpoints in patients with portal hypertension. The following sections will address some issues in this puzzle.

Decrease of portal pressure by shunt procedures

The most effective measure to reduce portal hypertension is to circumvent the increased intrahepatic resistance in liver cirrhosis and bypass the blood into the inferior vena cava by portacaval, mesocaval, or proximal splenorenal shunts. Controlled trials evaluating the potential of a surgical open shunt procedure were mainly performed to assess their effect on the prevention of bleeding from varices. They date back to the 1960s^65–67, but the most current long-term follow-up studies have been published as recently as 2012 and 2014^68,69. The indication for open shunt procedures was almost exclusively prevention of bleeding. Although open surgical shunts may have advantages in young patients with severe portal hypertension, recurrent bleeding, and good liver function, this surgical procedure has been more or less abandoned and surgical experience is waning. This is mainly owing to its invasiveness, perioperative mortality, and an increased risk of liver failure and/or encephalopathy due to loss of liver perfusion with portal venous blood. Accordingly, it has never been convincingly shown that surgical shunts improve survival. By contrast, transjugular insertion of an intrahepatic stent between a branch of the portal vein and a branch of the hepatic vein (TIPS) is less invasive and has become an established treatment approach in portal hypertension and its complications. After a learning period in different pioneering centers⁷⁰, the procedure is now established worldwide. In most patients, TIPS implantation reduces portal pressure by more than 50%, as assessed by the portal pressure gradient. The degree of reduction depends on the diameter of the stent^36,70. TIPS prevents variceal rebleeding in the vast majority of patients. According to many controlled trials and respective meta-analyses, TIPS is superior to ligation of varices with or without the addition of beta-blockers⁷¹. Yet the combination of ligation and beta-blockers (see below) is still considered the procedure of choice for rebleeding prophylaxis¹¹, mainly because TIPS patients with decompensated cirrhosis (bilirubin >3–5 mg/dL) are suboptimal candidates for shunt insertion, as they have a relatively high risk of liver and mental function deterioration. In the elective situation, TIPS implantation is therefore mainly used as a potential rescue procedure for the treatment of rebleeding of esophageal varices or the treatment of refractory ascites. According to randomized trials, around 20% of patients receiving local endoscopic rebleeding prophylaxis have to be switched to TIPS implantation because of refractory ascites or recurrent bleeding events^36,72–74. Thus, in patients with variceal bleeding and ascites, early placement of a small lumen-covered TIPS should be earnestly considered as early therapy.

One disadvantage of TIPS is shunt occlusions of bare stents, a rare event after shunt operation⁷⁵. However, this problem has been solved to a large extent by the introduction of polytetrafluoroethylene-covered stents^76,77. Furthermore, there is evidence that the placement of small-diameter, covered stents (8 mm) reduces the encephalopathy rate^36,78, while its protection from rebleeding remains. But, unfortunately, even small covered stents are still burdened with the risk of encephalopathy³⁶. Although TIPS insertion is now the most efficient method to reduce portal hypertension and to prevent bleeding in patients with liver cirrhosis, it does not improve survival as compared to patients receiving a non-shunt approach⁷¹, at least in the elective situation. This also holds true for the most recent trials comparing non-selective beta-blockers (NSBB) with or without ligation to TIPS with covered stents^36,73,79.

Trials suggest that pre-emptive or “early” TIPS insertion is beneficial in high-risk patients, mainly those with active bleeding, decompensated liver cirrhosis, and/or HVPG >20 mmHg^62,80,81, with respect to not only hemostasis and early rebleeding but also long-term survival. However, this strategy still needs to be established and proven in broad clinical practice. Currently, early TIPS insertion for acute variceal hemorrhage is neither always available nor widely applied in the real-world scenario⁸². The positive effect of TIPS insertion for the prevention of bleeding in patients with liver cirrhosis declines with increasing temporal distance to the index bleeding event in the acute⁸³ and elective³⁶ situation, i.e. for the treatment of bleeding in patients with liver cirrhosis, suitable patients together with the appropriate time window⁸⁴ have to be identified.

TIPS has a positive impact on hemodynamic changes in liver cirrhosis. Central blood volume and cardiac output increase after shunt placement^85,86. This is associated with a deactivation of the renin–angiotensin–aldosterone system (RAAS) and improvement of impaired kidney sodium excretion in liver cirrhosis^70,85,87. It explains the positive effect of TIPS insertion for the mobilization of refractory ascites. While this method was initially developed to prevent intestinal hemorrhage in liver cirrhosis, the number of patients receiving stents for the treatment of ascites now surpasses the bleeding indication according to our own experience⁵³ (unpublished data of groups from Bonn/Freiburg). There is an ongoing debate on the role of TIPS, especially with respect to the survival of ascitic patients, in comparison to paracentesis with albumin infusion⁸⁸. Analysis of the early studies using bare stents already suggested that TIPS improves transplant-free survival in patients with refractory ascites⁸⁹. A recent randomized study with limited patient numbers using covered stents showed a highly significant improvement of transplant-free survival in patients who had received covered TIPS for recurrent ascites when compared to paracentesis with albumin⁹⁰.

Taken together, TIPS, especially with technically improved stents, has become well established in the prevention and treatment of intestinal bleeding and ascites in patients with liver cirrhosis. However, the selection of patients is key. By contrast, hardly any centers exist that still perform shunt surgery for portal hypertension.

Shunts, including TIPS, bypass the increased hepatic resistance in patients with liver cirrhosis and exert their beneficial effect by a shift of the blood pool from the splanchnic to the central venous compartment. Most drugs, by contrast, act more by blunting stimuli that are activated or overactivated in liver cirrhosis. Some of these are addressed in the following paragraphs.

Modification of portal pressure by non-specific drugs

New and old pathogenetic concepts showed that advanced liver cirrhosis with portal hypertension is a systemic disease involving most organs. It remains a challenge to counter this. The interruption of etiology is the most important step, mainly with respect to the progression of liver disease but also with respect to an immediate portal pressure-lowering effect. This holds true for the interruption of hepatitis C^91–93 or abstinence from alcohol⁹⁴. Since chronic alcoholism is now the most frequent cause of liver cirrhosis and portal hypertension in most countries, we need a more holistic approach to alcohol use disorders^95,96.

In the following sections, we refer to medical treatments that are not curative but may have beneficial adjuvant effects.

Modulation of the intestine

Intrahepatic resistance, portal tributary blood flow, and formation of spontaneous shunts determine portal pressure^116,138. Intrahepatic resistance has a structural (fibrosis, alteration of the vascular architecture) and a non-structural (intrahepatic vascular tone) component. Gut-derived stimuli such as certain pathogen-associated molecular patterns (PAMPS) (lipopolysaccharide, endotoxin) may play an important role in this interplay. They impair intrahepatic endothelial function by influencing nitric oxide release^138,139 or stimulate signaling pathways of intrahepatic contractile cells and of fibrogenesis by inducing inflammation, e.g. activation of Kupffer cells and other macrophages^140,141 using sensing protein families such as Nod-like receptors or Toll-like receptors^142,143. Especially in fatty liver disease, an early increase in portal pressure may be caused by functional non-structural changes of the intrahepatic vascular bed¹⁴⁴. Many questions in this context are not resolved. We will touch on some aspects in the following paragraphs.

Alcohol is the most common cause of progressive liver dysfunction and portal hypertension in the Western world¹⁴⁵, although only a minority of heavy drinkers develop liver cirrhosis^146,147. Early research on the mechanism of alcohol-induced liver damage focused on direct or indirect hepatotoxic effects of ethanol and its oxidative and non-oxidative metabolites, such as acetaldehyde or fatty acid ethyl esters¹⁴⁸. The handling of fatty acids by hepatocytes was also studied, since hepatic steatosis is an important pre-stage of alcoholic liver cirrhosis. There is abundant literature on this, but it is mostly based on animal and cell culture models. Later, endotoxin from the outer membrane of Gram-negative bacteria was more and more regarded as a cofactor for the pathogenesis of alcoholic liver disease^148,149 as a gut-derived stimulus. Further research showed that it mediates intrahepatic inflammation via Toll-like receptor 4 on macrophages¹⁵⁰, which in turn are a trigger for portal hypertension¹⁴⁰. Thus, the intestine has become a prime target for research on alcoholic liver disease and the catchword of today is gut–liver axis.

Our intestine, mainly the colon, is host to an enormous number of microorganisms, such as bacteria, fungi, Archaea, and viruses¹⁵¹. Most of these microorganisms are commensals with a symbiotic function. Their number equals the total amount of cells of our own body, and they create an internal ecosystem in addition to the surrounding world.

Although high-throughput techniques, as an essential new step, are now broadly available to investigate the association of intestinal microorganisms with physiological phenomena or disease, the topic remains extremely complex regarding sample collection, analytical procedure, and evaluation of their functions as well as their integration and numerous interactions with human organs. Also, many bacterial metabolites¹⁵², including dangerous ones, such as ammonia or hydrogen sulfide, and beneficial ones, such as short-chain fatty acids, must be considered. Last not least, T cells primed in the intestine can induce liver damage by aberrant homing in the liver¹⁵³. All of these different phenomena increase complexity. On the other hand, there is first evidence that common small molecules like N-acylamide with a signaling effect on G-protein-coupled receptors regulating metabolism are produced by human microbiota¹⁵⁴. Thus, in the end, a limited number of interacting biological structures may remain crucial.

It has been shown that alcohol intake affects the integrity of the gut from an early stage, on the one hand by altering the intestinal microbiota, including the small bowel and the oral cavity^155,156—often coined dysbiosis—and on the other hand by increasing intestinal permeability^157,158. As yet, it remains unclear which is the “chicken” and which is the “egg”, but both phenomena give rise to an increased transfer of inflammatory stimuli to the liver, mediated via Toll-like receptors, and to alteration of the bile acid pool and its enterohepatic circulation (for further reading, see 151,159,160). Moreover, fungal dysbiosis has been incriminated in the induction of liver damage in alcohol abuse¹⁶¹.

A change in the individual bile acids by bacterial enzymes may lead to hepatobiliary injury via the induction of nuclear and G-protein-coupled cell surface receptors (see 162,163). Based on these insights, numerous approaches, recently reviewed in depth^{159,164–166}, have been proposed to modulate the course of liver cirrhosis and portal hypertension.

Since a distinct change of the microbiota with a reduction of autochthonous bacteria has been found in patients with liver cirrhosis compared to healthy individuals^167,168, ongoing trials are targeting intestinal dysbiosis in patients with liver cirrhosis via antibiotics, probiotics, or synbiotics (see 164). Most of these trials study surrogate markers. Results on hard clinical endpoints, such as liver failure, bleeding, or death, are still far from being reached. One promising randomized study¹⁶⁹ showed that the probiotic VSL#3 reduced liver disease severity and hospitalization in patients with mainly alcoholic liver cirrhosis in India. Another study from India found that administration of this probiotic increased the response rate to propranolol with respect to a decrease in HVPG¹⁷⁰.

In patients with liver cirrhosis and variceal bleeding¹⁷¹ and in patients with decompensated liver cirrhosis^172,173, systemic application of antibiotics, which affect other organs as well as the gut, increased survival. But direct studies on portal hemodynamics are sparse. Norfloxacin partially reversed the hyperdynamic state, while RAAS activation and portal hypertension were not influenced or only to a minor degree¹⁷⁴. Rifaximin is a non-absorbable antibiotic with proven effect on hepatic encephalopathy¹⁷⁵. While its effect in the intestine has not been fully elucidated, it has been found to reduce the production and absorption of gut-derived toxins and inflammatory stimuli, such as ammonia and endotoxin (see 176). Overall, its effects in the intestine may be more eubiotic than antibiotic¹⁷⁷. According to uncontrolled trials, rifaximin reduced plasma endotoxin levels and HVPG in alcohol-related decompensated liver cirrhosis¹⁷⁸. Furthermore, it lowered the 5-year cumulative probability of decompensation of cirrhosis, including bleeding and encephalopathy, and resulted in better survival¹⁷⁹. However, although the data are promising, they are from only one center and as yet remain uncontrolled. A randomized double-blind placebo-controlled trial consisting of a 4-week treatment with rifaximin found no effect on bacterial translocation, HVPG, systemic hemodynamics, kidney function, or vasoactive hormones, including plasma renin¹⁸⁰, and a further study found that there was no short-term effect of rifaximin on systemic inflammatory markers or intestinal bacterial composition¹⁸¹.

Alteration of the enterohepatic circulation of bile acids in liver and biliary disease^182–184 has also become a topic of research in portal hypertension (see above). Major regulators of bile acid homeostasis, such as the farnesoid X receptor (FXR) or TGR5^185,186, are addressed by specific drugs. Two different research groups found that in animal models of cirrhosis, farnesoid receptor agonists reduced portal hypertension^187,188. However, there is still a long way to go from proof of this concept in rats to an established treatment in the clinical situation. Bearing in mind that the FXR agonist obeticholic acid is already used in phase III trials¹⁸⁹ for primary biliary cholangitis, particular emphasis should be given to determining to what extent these drugs may blunt portal hypertension and its complications. Further non-bile acid and non-steroidal FXR agonists with or without concomitant TGR5 activity are being tested in animal models^188,190.

It has been shown in animals, and now even in a small series of humans, that transplant of fecal microbiota may reverse hepatic disease or its symptoms¹⁹¹. Furthermore, transplantation of stool from eubiotic rats to animals with a NASH model of portal hypertension significantly reduced portal pressure¹⁴⁴. However, to date, it is difficult to imagine that such an approach will have a future in clinical routine.

Dysbiosis of the gut and alteration of intestinal permeability, which are associated with alcohol intake, affect not only the liver but also adipose tissue and the brain, with involvement of the autonomic nervous system as a regulating circuit, at least according to studies in animal models^192–196. Activation of the immune system by the gut, including Toll-like receptor signaling, with release of proinflammatory cytokines is now regarded as a broad phenomenon that not only causes organ damage but also induces dysregulation in the brain, resulting in an unopposed craving for an unhealthy diet and liquids (see 197–199). In this vicious cycle, portal hypertension presents as a late link to disease. Thus, it is eminently worthwhile to support beneficial change in the eating or drinking habits of patients, which are controlled by the brain. It has been shown that in patients with liver cirrhosis, weight loss²⁰⁰ or abstinence from alcohol^94,201 significantly reduces portal hypertension. This appears to be the most important strategy to influence the gut–liver axis and portal hypertension (Figure 1).

Other potential options and drugs

Patients with liver cirrhosis have an increased risk of portal vein thrombosis. The prevalence ranges from 10 to 20%, and the yearly incidence is estimated to be somewhat less than 10%²⁰². Anticoagulants reduce significantly the risk of occurrence²⁰³ and recurrence²⁰⁴. One small randomized study found not only a significantly reduced occurrence of portal vein thrombosis but also fewer events of decompensation and even improved survival in patients with advanced cirrhosis receiving low-molecular-weight heparin over a period of nearly one year²⁰³. The authors explain the positive effect by better microcirculation of the gut and less translocation of bacteria. Moreover, enoxaparin reduced intrahepatic vascular resistance and fibrosis in animal models of liver cirrhosis²⁰⁵. Further studies on the putative beneficial effect of anticoagulation in patients with liver cirrhosis are needed.

A recent comprehensive publication reviewed available studies on several other drugs that reduce portal hypertension, mostly in animal models²⁰⁶ and still in an experimental stage. In fact, many of these drugs reduce intrahepatic resistance. However, care has to be taken to prevent these drugs from aggravating hyperdynamic cardiovascular effects outside the liver^207–209 and from eliciting toxic effects inside the liver^210–214. We have addressed this problem for many years^{122,215–223}. Unfortunately, clinical trials in humans are lacking. A search for the one panacea seems futile. The actual stage of portal hypertension and its etiology have to be considered. Interruption or suppression of viremia as a cause of chronic liver disease and portal hypertension is now possible for the hepatitis B as well as the hepatitis C virus. Thus, advanced liver disease and portal hypertension increasingly appear to be food-induced disorders rather than chronic infectious diseases. Here, the modulation of behavior is key, as it is the case with so many of the diseases of modern civilization. Drugs and interventions, however, retain their importance in treating the decompensated stage no matter whether initial etiology could be stopped or not (see above).

Combined and stage-dependent treatment

At the stage of compensated cirrhosis without clinical signs of disease, it is crucial to halt progression. This is mainly achieved by interruption of an etiology that perpetuates inflammation and fibrogenesis leading to portal hypertension. Convincing examples include interruption or suppression of viremia, abstinence from alcohol abuse, immunosuppression of autoimmune liver disease, use of ursodeoxycholic acid in primary biliary cholangitis, or venesection for hemochromatosis. In all of these different etiologies, early diagnosis is important. However, co-factors (e.g. obesity, alcohol intake, or hepatotoxic drugs) which aggravate hepatic damage have to be considered and treated.

Once portal hypertension has developed, as documented by the invasive or non-invasive methods outlined above, it is desirable to blunt its interaction with systemic hemodynamics and to prevent further organ dysfunction. This applies not only to the liver but also to the heart, kidneys, brain, and lungs. At this stage, reduction of portal hypertension by modulation of the intestine as a source of inflammatory stimuli or retarding inflammatory pathways may be promising strategies. Here, statins, NSBB, FXR agonists, probiotics, and antibiotics have been established or appear to be promising.

In patients with ascites and variceal hemorrhage, early placement of a small lumen TIPS is an option because of its paramount effect on the prevention of bleeding and improvement of kidney function. However, once the stage of disease has become more advanced with threatening progress towards ACLF, survival is low and difficult to improve without liver transplantation. Thus, more effort must be put into early detection and prevention of liver disease, and more effective measures besides transplantation must be developed to treat decompensated cirrhosis. Combining small lumen TIPS with modulation of the systemic inflammatory response could be a possible approach.

Conclusion

Portal hypertension is a surrogate of advanced liver disease. Reduction of portal pressure is the most efficient step to prevent intestinal bleeding and treat ascites. But this has a limited impact on survival. Interruption or modulation of inflammatory stimuli leading to liver damage and dysfunction of other organs is key in order to prevent death or liver transplantation as ultimate rescue.

Abbreviations

ACLF, acute-on-chronic liver failure; ARFI, acoustic radiation force impulse imaging; FXR, farnesoid X receptor; HCC, hepatocellular carcinoma; HVPG, hepatic venous pressure gradient; MELD, model of end-stage liver disease; MR, magnetic resonance; MRI, magnetic resonance imaging; NSBB, non-selective beta-blockers; RAAS, renin–angiotensin–aldosterone system; SWE, shear wave elastography; TE, transient elastography; TIPS, transjugular intrahepatic portosystemic shunt.