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Copyright ©ERS Journals Ltd 2005
Bosentan therapy for portopulmonary hypertension
1 Dept of Respiratory Medicine, Hanover Medical School, Hanover, 2 Dept of Respiratory Medicine, Carl Gustav Carus University of Dresden, Dresden, and 3 Dept of Respiratory Medicine, University of Leipzig, Leipzig, Germany
CORRESPONDENCE: M. M. Hoeper, Dept of Respiratory Medicine, Hannover Medical School, 30623 Hannover, Germany. Fax: 49 5115328536. E-mail: hoeper.marius@mh-hannover.de
Keywords: Cirrhosis, endothelin receptor antagonists, secondary pulmonary hypertension
Received: July 5, 2004
Accepted October 15, 2004
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ABSTRACT |
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 TOP ABSTRACT METHODSRESULTSDISCUSSIONREFERENCES |
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The dual endothelin receptor antagonist bosentan has been approved in several countries for pulmonary arterial hypertension, and patients with portopulmonary hypertension (PPHTN) have not specifically been excluded. However, no data have been published on the efficacy and safety of bosentan in this patient population. Here, the first clinical experiences with bosentan in patients with Child A cirrhosis and severe PPHTN are reported.
In total, 11 consecutive patients with cirrhosis and severe PPHTN in New York Heart Association Functional Classes III and IV were treated for >1 yr with bosentan.
After 1 yr of treatment with bosentan, all patients showed improved symptoms and exercise capacity. The 6-min walking distance increased from 310±102 m at baseline to 388±81 m at 1 yr. Cardiopulmonary exercise testing disclosed a significant increase in peak oxygen uptake, from 12.6±3.5 to 16.6±2.8 mL·min–1·kg–1. Pulmonary vascular resistance fell from 944±519 to 635±321 dynes·s·L–1. The medication was well tolerated by all patients, and there was no evidence of drug-related liver injury.
In conclusion, bosentan proved to be efficacious and safe in a small number of patients with portopulmonary hypertension.
The development of pulmonary arterial hypertension (PAH) in patients with portal hypertension is referred to as portopulmonary hypertension (PPHTN) 1. This complication predominantly affects patients with cirrhosis of various aetiologies accompanied by portal hypertension, but may also occur in noncirrhotic portal hypertension. Thus, it appears that portal hypertension rather than liver dysfunction triggers the occurrence of pulmonary hypertension 2.
The incidence of PPHTN varies widely in the medical literature. An autopsy study found vascular changes compatible with severe pulmonary hypertension in 0.7% of patients with cirrhosis 3, whereas most clinical series have described much higher incidences, ranging 2–16% 1, 4–9. These differences may be the result of different study populations, but also of different diagnostic criteria. In many cases, patients with cirrhosis develop only mild-to-moderate elevation of pulmonary vascular pressure in the presence of a high cardiac output and mildly elevated pulmonary vascular resistance. These patients usually show no symptoms related to pulmonary hypertension and specific treatment may not be required 2. However, for unknown reasons, some patients develop progressively symptomatic pulmonary hypertension with right heart dysfunction. In these patients, the prognosis is poor with 1-yr mortality rates ranging 24–60% 7, 10.
The only specific treatment available for PPHTN has been intravenous epoprostenol. There are no controlled trials of epoprostenol in this patient population, but several case series suggest a positive effect on exercise capacity and haemodynamics 11–15, although it has been questioned whether epoprostenol improves survival in PPHTN 16.
The dual endothelin receptor antagonist bosentan is efficacious in patients with idiopathic PAH and PAH related to connective tissue disease 17, 18. Elevation of hepatic aminotransferase levels is a common phenomenon in patients treated with bosentan, occurring in 
10% of patients receiving 125 mg twice daily 18. Owing to concerns about potential liver toxicity, patients with PPHTN have been excluded from clinical studies with bosentan, and physicians have been reluctant to prescribe the drug in patients with cirrhosis. However, the US Food and Drug Administration and the European Agency for the Evaluation of Medicinal Products have approved bosentan for all forms of PAH, not specifically excluding PPHTN, as long as liver function is stable.
The present article reports the first long-term clinical experiences with bosentan in patients with cirrhosis and severe PPHTN.
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METHODS |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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Clinical data were retrospectively collected from all patients who were referred with newly diagnosed severe PPHTN (New York Heart Association (NYHA) Functional Class III or IV; mean pulmonary arterial pressure (Ppa) >40 mmHg), between January 2001 and February 2003, to three German university hospitals (Hanover Medical School, Hanover; Carl Gustav Carus University of Dresden, Dresden; and University Hospital Leipzig, Leipzig). At this time, all patients with PPHTN and Child A cirrhosis were treated with bosentan, since no other drug has gained approval for the treatment of this condition in Germany. All patients were carefully informed about the lack of clinical experience with bosentan in PPHTN and safety concerns about potential liver toxicity, and gave written informed consent. There was no formal study protocol, and the patients were treated at the discretion of their local physicians. This approach was approved by the institutional review boards of all the participating centres.
Bosentan was started at a dose of 62.5 mg twice daily in all patients, and the dose was increased to 125 mg twice daily after 4–8 weeks based on clinical judgement and tolerability. Liver enzyme, including alanine aminotransferase and aspartate aminotransferase, and bilirubin levels were monitored twice monthly during the first 3 months and monthly thereafter. All patients were seen in the outpatient clinics of the university hospitals at 3-monthly intervals for a thorough clinical investigation, including assessment of NYHA Functional Class, 6-min walking distance (6MWD), and pulmonary and liver function. Right heart catheter examinations were performed in all patients within 6 months before bosentan treatment was started and after 1 yr of treatment. Cardiac output was measured by thermodilution in triplicate and averaged. Samples for arterial and mixed venous blood gas analysis were obtained during heart catheterisation without supplemental oxygen. The alveolar–arterial oxygen tension difference (PAa,O2) was calculated by subtracting arterial oxygen tension (Pa,O2) from alveolar oxygen tension (PA,O2) (with PA,O2 = 150–arterial carbon dioxide tension (Pa,CO2)/0.8). Regular cardiopulmonary exercise testing, following a standardised protocol on a cycle ergometer 19, was part of the routine programme in two centres.
Statistics
All data are presented as mean±SD. A paired t-test (two-sided) was used to compare variables at baseline and after 1 yr of treatment. A p-value of <0.05 was considered significant.
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RESULTS |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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Between January 2001 and January 2003, bosentan treatment was initiated in 11 consecutive patients with PPHTN (at Hanover Medical School (n = 4), University Hospital Leipzig (n = 4) and Carl Gustav Carus University of Dresden (n = 3)), who presented with stable liver function (Child–Pugh class A) but severe functional limitation due to pulmonary hypertension (NYHA Functional Class III or IV). The final dose of bosentan was 125 mg b.i.d. in six patients and 62.5 mg b.i.d.in the remaining five. The demographics and baseline characteristics of these patients are shown in table 1
. The majority of the patients suffered from alcoholic liver disease, but all such patients had abandoned alcohol consumption 
6 months (median interval 38 months) before bosentan was introduced. The diagnosis of cirrhosis and portal hypertension was confirmed by expert hepatologists in all patients, and all patients had a history of one or more complications of portal hypertension, such as ascites, oesophagogastric varices or hypersplenism (table 1). Preliminary data from one patient (No. 2) have already been published as a case report 20.
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At baseline, pulmonary function testing revealed mild-to-moderate impairment of DL,CO in the majority of the patients as five patients had DL,CO of
50% of the predicted value and four of 50–70% pred. In addition, mild airflow obstruction, with a forced expiratory volume in one second/vital capacity ratio of <70%, was present in four patients (table 1
). The results of pulmonary function testing remained virtually unchanged after 1 yr of bosentan treatment (data not shown).
Outcome, functional classification and exercise capacity
No patient underwent transplantation or died during the observation period. All 11 patients reported subjective improvement in exercise capacity after initiation of bosentan treatment, and six patients improved by one functional class. The 6MWD increased from 310±102 m at baseline to 388±81 m after 1 yr (p = 0.0004). Data from cardiopulmonary exercise testing were available from seven patients and revealed a significant increase in peak oxygen uptake, from 12.6±3.5 to 16.6±2.8 mL·min–1·kg–1 (p = 0.01), as well as an increase in oxygen pulse, from 6.7±1.2 to 9.3±2.1 mL (p = 0.01). Ventilatory efficiency (minute ventilation/carbon dioxide production) at the anaerobic threshold showed a tendency to decrease from 57.7±22.1 to 46.9±11.7, but this change was not significant (p = 0.31). The individual NYHA classification at baseline and after 1 yr of treatment together with the change in 6MWD and variables obtained from cardiopulmonary exercise testing are shown in table 2.
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Haemodynamic studies and blood gas analyses
The individual results of the haemodynamic studies are shown in table 3
. Treatment with bosentan caused a nonsignificant fall in Ppa from 53±9 to 48±14 mmHg (p = 0.23). Cardiac output rose, from 4.6±1.8 to 5.7±1.6 L·min–1 (cardiac index 2.5±1.0 and 3.1±0.8 L·min–1·m–2, respectively; p = 0.02), resulting in a significant fall in pulmonary vascular resistance, from 944±519 to 635±321 dynes·s·cm–5 (p = 0.007; fig. 1). The increase in cardiac output was due to a rise in stroke volume from 57±20 to 70±23 mL (p = 0.01), whereas the cardiac frequency remained unchanged (data not shown). Mixed venous oxygen saturation was 60±9% at baseline and 63±11% at 1 yr (p = 0.4). The right atrial pressure fell slightly, from 9±6 to 7±7 mmHg, a change that was also nonsignificant (p = 0.35). The mean systemic artery pressure dropped from 91±9 to 83±14 mmHg (p = 0.09).
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As shown in table 3
, blood gas analyses disclosed a significant worsening of arterial oxygenation. The Pa,O2 fell from 8.6±1.7 kPa (65±13 Torr) at baseline to 7.7±1.5 kPa (58±11 Torr) after 1 yr (p = 0.006); Pa,CO2 was unchanged; and the PAa,O2; increased from 5.7±1.7 kPa (43±13 mmHg) to 6.5±1.5 kPa (49±11 mmHg; p = 0.04). However, no patient complained of increasing dyspnoea at rest or during exertion.
Side-effects
Bosentan treatment was well tolerated by all of the patients. Although there was a decline in mean systemic artery pressure, there were no clinical signs or symptoms of hypotension and no episodes of syncope. Most notably, there was no evidence for drug-induced liver toxicity. Hepatic aminotransferase activities were normal or slightly abnormal (less than twice the upper limit of normal) in all patients at baseline and remained practically stable throughout the whole observation period (table 4). The same was true for bilirubin levels, which were 29±12 µmol·L–1 at baseline and 26±10 µmol·L–1 after 1 yr (p = 0.19). Parameters of liver synthesis, i.e. international normalised ratio and serum albumin activity levels remained unchanged (table 4). No encephalopathy and no episodes of variceal bleeding were observed. One patient developed increasing amounts of ascites 7 months after the introduction of bosentan. The patients had previously suffered from several episodes of ascites, and clinical judgement was that this complication was due to worsening of portal hypertension rather than causally linked to bosentan treatment.
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DISCUSSION |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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For many years the only specific drug treatment available for PPHTN has been continuous intravenous epoprostenol 1, 2, 11, 21. The present data suggest that the dual endothelin receptor antagonist bosentan may offer a safe and effective noninvasive alternative. All patients in the present series suffered from severe pulmonary hypertension at baseline (NYHA Functional Class III or IV; mean 6MWD 310 m; Ppa 53 mmHg; cardiac index (CI) 2.7 L·min–1·m–2; pulmonary vascular resistance 944 dyn·s·cm–5; right atrial pressure 7 mmHg; and mixed venous oxygen saturation 60%). In an earlier series of 49 patients with PPHTN of similar severity (Ppa 59 mmHg and CI 3.3 L·min–1·m–2), who did not receive specific treatment for pulmonary hypertension, Robalino and Moodie 10 reported a 1-yr mortality of >60%. Another series of 39 patients with PPHTN from France with comparable haemodynamics (Ppa 56 mmHg and CI 2.7 L·min–1·m–2) found a 1-yr mortality of 24% 7. During the 1-yr observation period reported here, no patient died, which is remarkable given the grave prognosis of this condition. However, the present data do not provide sufficient evidence to conclude that bosentan improves survival in PPHTN.
All patients in the present case series experienced functional improvement, with increasing exercise tolerance; six patients improved by one functional class. The 6MWD increased by a mean of 78 m, and, in those patients who were followed by cardiopulmonary exercise testing, there was a substantial increase in peak oxygen uptake and oxygen pulse, suggesting improved cardiopulmonary function during exercise. In addition, treatment with bosentan improved cardiopulmonary haemodynamics at rest; after 1 yr of bosentan treatment, Ppa had fallen by 10% from baseline, cardiac output had increased by 22% and pulmonary vascular resistance had fallen by 32%.
The present data confirm previous studies on the efficacy of bosentan in other forms of PAH 17–19, 22, 23. Together, these observations support the hypothesis that endothelin is a pathogenetically relevant mediator in pulmonary hypertension of various aetiologies. A recent study found significantly elevated plasma endothelin-1 levels in patients with PPHTN compared to cirrhotic patients with portal hypertension but without pulmonary hypertension 8. In addition, a large body of evidence suggests that endothelin-1 may also be involved in the pathogenesis of portal hypertension 24–28. A recent case report of a patient with PPHTN (who was included in the present study) described normalisation of portal venous pressures with bosentan treatment 20. Thus, the beneficial effects of bosentan in PPHTN could be related to a reduction in both pulmonary and portal hypertension. Unfortunately, no systematic follow-up information exists on portal hypertension in the present patients, but this aspect should be addressed in forthcoming trials.
There are serious safety concerns regarding the administration of bosentan in patients with coexisting liver disease since potential hepatotoxicity is a well-recognised side-effect of bosentan 18. Presumably, the underlying mechanism is inhibition by bosentan and its metabolites of a bile salt transporter pump 29. In order to prevent serious liver damage, regulatory agencies demand that hepatic aminotransferase levels be checked every 4 weeks before a new prescription of bosentan is filled. With these precautions in place, there have been no reports of serious or permanent liver damage associated with bosentan. It was hypothesised that the same precautions should prevent drug-related liver toxicity and worsening of liver function in patients with underlying liver disease. To date, this hypothesis seems to be correct, but it is important to note that great caution is still necessary when bosentan is given to patients with liver disease. It must be emphasised that all of the present patients exhibited stable liver function (Child class A). In these patients, it has been shown that metabolism of bosentan is not impaired 30. In patients with more advanced liver disease, metabolism of bosentan might be impaired, leading to increased plasma concentrations and potentially resulting in enhanced toxicity. Until more data are available, bosentan should probably not be used in patients with more advanced liver dysfunction (Child class B/C).
It is also noteworthy that a trend towards a fall in systemic blood pressure was observed with bosentan in the present PPHTN patients, an observation that has not been made in other populations of PAH patients. Although the decline in systemic blood pressure was not associated with any clinical symptoms in the present patients, it is important to be careful regarding use of bosentan in patients with pre-existing hypotension. The appropriate dosage of bosentan in patients with liver dysfunction should be addressed in forthcoming studies.
Similar considerations apply to potential worsening of arterial oxygenation, since a mild-but-significant fall in Pa,O2 was observed in most of the present patients after 1 yr of bosentan treatment. The reason for this finding is unclear, but presumably, worsening of arterial oxygenation may have been caused by nonselective intrapulmonary vasodilation, resulting in some degree of ventilation–perfusion mismatching. A fall in Pa,O2 was also reported with the use of epoprostenol in PPHTN 11, supporting the hypothesis that intrapulmonary vasodilation might be involved in this process.
The limitations of the present study are obvious. The number of patients investigated was small (11 patients treated at three university hospitals) and the study retrospective, patients and investigators were not blinded, and there was no control group. It needs to be emphasised that the presnt report describes all patients with PPHTN who were referred to the three participating centres over a 1-yr period, underscoring the fact that severe PPHTN is truly a rare condition. It is of note that there are also no controlled data on the use of epoprostenol in this condition, and most of the published case series with epoprostenol in PPHTN included even fewer patients 12, 14, 15, the largest published series consisting of 10 patients 11. To date, no randomised double-blind controlled clinical trials have ever been performed in PPHTN, but, given the evolving cooperation between pulmonary hypertension centres, such trials might be feasible in the future.
In conclusion, bosentan treatment was found to be safe and effective in the present case series of patients with severe portopulmonary hypertension. If these findings can be confirmed in future trials, bosentan would be the first noninvasive treatment option for this life-threatening disease.
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