Irreversible Pulmonary Hypertension Associated with the use of Interferon Alpha for Chronic Hepatitis C
- First Online:
- Cite this article as:
- Dhillon, S., Kaker, A., Dosanjh, A. et al. Dig Dis Sci (2010) 55: 1785. doi:10.1007/s10620-010-1220-7
- 375 Views
The interferons are a complex group of virally induced proteins produced by activated macrophages and lymphocytes, which have become the mainstay of therapy for hepatitis C infection. Sustained viral response (SVR) rates in noncirrhotic patients vary from 40–80% with interferon-based therapy. This, along with transplantation, has drastically changed the course of hepatitis C virus (HCV) infection over the last two decades. Numerous side effects associated with interferon therapy have been reported. These range from transient flu-like symptoms to serious effects such as cardiac arrhythmias, cardiomyopathy, renal and liver failure, polyneuropathy, and myelosuppression. Pulmonary side effects including pneumonitis, pulmonary fibrosis, and reversible pulmonary hypertension have been reported. Herein, we present four cases in which irreversible pulmonary hypertension was diagnosed after prolonged treatment with interferon alpha. In each case, other causes of pulmonary hypertension were systematically eliminated. Pulmonary artery hypertension, which may be irreversible, should be considered in patients being treated with interferon alpha who present with exertional dyspnea and do not have a readily identifiable inflammatory or thromboembolic cause.
KeywordsHCVInterferon alphaPulmonary hypertensionLiverLung
The interferons are a complex group of virally induced host proteins produced by activated macrophages and lymphocytes. They were first described in 1957 by Isaacs and Lindenmann . Alpha, beta, and gamma interferons have been identified and characterized. Interferon alpha (IFNα) has been used extensively in the treatment of hepatitis viruses, as well as a few hematologic, nephrologic, and dermatologic malignancies. Although the exact mechanism of action of IFNα remains unclear, its usefulness in clinical practice is well established. It is most commonly used to treat chronic hepatitis C virus (HCV), either as monotherapy or in conjunction with ribavirin. In the past, the dose used for this purpose has ranged from 3 to 5 million units daily with 800–1,200 mg/day of oral ribavirin for 1 year . Two pegylated IFNα preparations enabling weekly dosing are now available and, along with ribavirin, are the current standard of care. A biosynthetic alpha interferon, consensus IFN (cIFN), is also available.
A sustained viral response (SVR) rate is defined as clearance of virus after 6 months following completion of active treatment. SVR rates currently vary from 40–80% in noncirrhotic patients depending upon the viral load, genotype, dosage, and formulation of IFNα utilized . IFNα has also been used in the treatment of chronic myelogenous leukemia (CML), multiple myeloma, and renal cell carcinoma. The doses used for these nonhepatic diseases, especially CML, are much higher than those used for the treatment of HCV. Typical dosages range from 10 to 20 million units/day for 12–18 months. Nearly a third of IFNα-treated patients with CML achieve complete cytologic remission and often remain disease-free for years [3, 4].
Numerous side effects have been reported as a consequence of interferon therapy. Almost all patients experience transient flu-like symptoms with fever, weakness, myalgias, headache, and tachycardia. These symptoms typically subside over the next 24 hours and are less prominent with treatment continuation. More serious effects include cardiac arrhythmias, cardiomyopathy, polyneuropathy, and myelosuppression, as well as liver and renal failure. Furthermore, various autoimmune diseases such as psoriasis, sprue, diabetes mellitus, thyroid disorders, and various forms of arthritis can be exacerbated or precipitated by IFNα therapy . Pulmonary side effects include pneumonitis, pulmonary fibrosis, and a single report of new onset pulmonary hypertension [6, 7]. Resolution of these numerous untoward effects with discontinuation of the agent has been the rule.
Herein is reported a series of four individuals, who developed an irreversible, progressive, and severe form of pulmonary hypertension during treatment with IFNα for chronic HCV. This complication has not been reported previously and should be considered as a rare but important adverse effect of IFNα therapy.
Case No. 1
GB was a 35-year-old white male who initially presented with lower extremity edema and weakness and was found to have end-stage liver disease due to HCV and alcohol abuse. Over the next several months, he developed decompensated liver disease with ascites. His past medical history was significant for a cholecystectomy for gallstones. His family history was significant for a mother who died of lung cancer and a father with coronary artery disease. He started drinking excessively at the age of 16 and occasionally used other illegal drugs, including amphetamines, heroin, and intranasal cocaine. He abstained from drug and alcohol use from the time of his initial presentation.
Physical examination was significant for a nontender but distended abdomen. The liver edge was 3 cm below the costal margin and a palpable spleen tip was present. Shifting dullness was present and pedal edema was noted to the level of the knees. The lungs were clear bilaterally. Cardiac examination revealed a normal rate and rhythm with no murmurs or gallop sounds.
Initial laboratory evaluation revealed normal electrolytes, normal renal function, and a prothrombin time of 15.8 s (normal 10.8–12.8 s). Serum aminotransferase levels (AST/ALT) were 226/183 IU/L, with a normal alkaline phosphatase and total bilirubin level. The serum albumin level was 3.3 mg/dl. A complete blood count documented a platelet count of 89,000/mm3. Serum tests were positive for HCV-RNA genotype 1a infection with a viral load > 1 × 106 copies/mL.
An abdominal computed tomography scan revealed a nodular cirrhotic liver with a volume of 1,600 cm3. The presence of prominent perigastric varices and periumbilical collaterals consistent with portal hypertension were noted also. Abdominal ultrasound documented the liver to have increased echogenicity. The portal and hepatic veins as well as the hepatic arteries were patent. A echocardiogram documented a left ventricular ejection fraction of 60% with normal heart valves and a normal estimated pulmonary artery pressure (PAP).
A liver biopsy was obtained and interpreted as showing grade 4, stage 4 disease. He was started on IFNα 3 million units daily in May 1999 in an effort to clear his viremia prior to transplantation. His viral load rapidly decreased and became undetectable at 8 weeks. He underwent orthotopic liver transplant 6 months later.
Postoperatively, he was found to have recurrent HCV with a viral load of 8.5 × 105 copies/mL. He was started on cIFN at a dose of 15 ug/day. He again responded rapidly and was HCV polymerase chain reaction (PCR)-negative by 8 weeks. His only complaint during the treatment period was persistent fatigue, which was attributed to the IFNα therapy.
After approximately 1 year of therapy, he began to experience progressive dyspnea on exertion, fatigue, and edema. An examination at this time revealed a resting tachycardia; a new grade III/VI systolic ejection murmur which increased in intensity with inspiration. He was admitted to hospital for further evaluation and was found to have severe pulmonary hypertension with right heart failure.
Cardiac catheterization revealed PAP of 81/30 mmHg, a cardiac output of 8.33 L/min, pulmonary vascular resistance (PVR) of 8.26 cm H2O/L/min, and a cardiac index of 2.61 L/min/m2. He experienced no change in his symptoms with the use of short-acting vasodilators. A ventilation perfusion scan was reported as having low probability for pulmonary emboli. A diagnosis of pulmonary hypertension of unknown etiology was made. He was classified as NYHC III and was started on bosentan, an endothelin receptor blocker, as well as a calcium channel blocker, a diuretic, and digitalis.
He failed bosentan as well as treprostinil, a prostacyclin analog, but had a minor response to epoprostenol. He required repeated admissions for progressive cardiac decompensation and the development of a persistent right-sided pleural effusion. Ultimately, he died in November 2002. The family refused an autopsy.
Case No. 2
DS was a 40-year-old female who was found to have an HCV infection while attempting to donate blood. Her past medical history included mild asthma, depression, a panic disorder, and multiple orthopedic surgeries related to a motor vehicle accident 20 years earlier, at which time she received 3 units of packed red blood cells. Her only medication was an inhaled bronchodilator. Social history included a 30-pack-year smoking history with occasional alcohol use. No intravenous drug use was reported.
A review of systems was unremarkable. Physical examination revealed clear lungs, and cardiac examination was with regular heart rate and no murmur or gallop. Abdominal examination revealed normal bowel sounds, no tenderness, and no hepatosplenomegaly. No pedal edema was appreciated. Laboratory examination included normal electrolytes, renal function, and liver function tests. The patient was found to have a genotype 1b infection with a viral load of 1.2 × 106 copies/mL. A liver biopsy was obtained and interpreted as showing grade 1 stage 1 disease. Mild steatosis was noted also. An upper gastrointestinal endoscopy was unremarkable. She was started on IFNα therapy (3 million units daily) with ribavirin (800 mg daily). The ribavirin was discontinued after 4 months because of profound anemia (Hgb 4.5 gm/dL). She failed to achieve viral clearance, despite being on maintenance therapy for 32 months.
In February 2001, she reported progressive dyspnea on exertion, edema, and weight gain. This required hospitalization and the IFNα therapy was discontinued. On physical examination, an elevated jugulo-venous pressure was appreciated, the lungs were clear, and cardiac examination revealed a grade 2/6 systolic ejection murmur at the left lower sternal border with a prominent pulmonic second sound that increased with inspiration. Pedal edema was present up to her knees. Neurologic examination was unremarkable.
An EKG showed sinus rhythm with voltage criteria for right ventricular hypertrophy and left atrial enlargement. Her chest X-ray was unremarkable. Pulmonary function studies were consistent with minimal asthma. She had unremarkable arterial blood gas on room air (pH 7.42, pO2 102, pCO2 33). A cardiac echocardiogram demonstrated normal left ventricular ejection fraction (59%), diffusely dilated, hypertrophied, and hypokinetic right ventricle, severe tricuspid regurgitation, and a small pericardial effusion without evidence of cardiac tamponade. A ventilation perfusion scan was interpreted as having an intermediate probability of pulmonary embolism. A subsequent pulmonary angiogram revealed no evidence of thromboembolic disease. Right heart catheterization documented a right atrial pressure of 24 mm Hg, right ventricle systolic pressure of 67 mm Hg, right ventricle end diastolic pressure of 11 mm Hg, PAP of 71/34 mm Hg with a mean pulmonary arterial pressure of 52 mm Hg, and pulmonary artery wedge pressure of 24 mm Hg.
Severe pulmonary hypertension with NYHC III heart failure of uncertain etiology was diagnosed. She was started on a diuretic and a calcium channel blocker and experienced a gradual worsening of her symptoms. Subsequently, she was started on treprostinil, with stabilization but no reversal of her pulmonary hypertension.
Case No. 3
FM was a 50-year-old male who presented initially with a pericardial effusion in 1997. At that time, the effusion was drained, with no specific etiology being identified, although he was known to be HCV-positive. Subsequent workup revealed advanced liver disease with decompensated cirrhosis. He underwent liver transplantation soon thereafter. The post-transplant course was uncomplicated, except for recurrent HCV. His past medical history was significant for obstructive sleep apnea, hyperthyroidism, and hypertriglyceridemia. Social history revealed 40-pack-year tobacco use, which he terminated approximately 10 years earlier, and a distant history of alcohol and cocaine use. He was married and worked in a soft drink bottling factory. A review of systems was noncontributory. Physical examination revealed an obese man in no distress. The lungs were clear to auscultation bilaterally and the cardiac examination was unremarkable. The abdomen was protuberant and nontender with palpable hepatosplenomegaly. No ascites was appreciated and he had no edema.
The laboratory data was remarkable for mild renal insufficiency (BUN/Cr 23 mg/dl/1.6 mg/dl) with a platelet count of 105,000/mm3 and a WBC count of 4.1 × 1,000 cells/mm3. Liver function tests were normal and he was found to have an HCV viral load of 2.5 × 105 copies/mL. A liver biopsy showed stage I disease with no portal or lobular inflammation and mild sinusoidal fibrosis.
IFNα therapy (5 million units/day) with ribavirin 200 mg BID was initiated. After being on therapy for 10 months, he developed progressive dyspnea on exertion with pedal edema. The patient was admitted to hospital and the IFNα and ribavirin were discontinued. Physical examination showed him to have clear lungs, and a cardiac examination revealed an early systolic murmur with a prominent pulmonic second sound. The abdomen was protuberant with easily palpable hepatomegaly and normoactive bowel sounds. Mild lower extremity edema was noted.
His evaluation included pulmonary function testing, which showed a significant restrictive defect with dramatic reduction in diffusion capacity. Computed tomography of the abdomen showed massive hepatomegaly (liver volume 3,448 cc3), splenomegaly, and ascites. A ventilation perfusion scan was negative for thromboembolic disease. An echocardiogram documented severe left ventricular hypertrophy, enlargement of the right heart chambers with severe tricuspid regurgitation, and an elevated PAP (80 mm Hg). A diagnosis of severe pulmonary hypertension with resultant cor pulmonale was made. The IFN therapy was discontinued and treatment was initiated with a diuretic and a calcium channel blocker with stabilization, but there was no improvement in his pulmonary hypertension.
Case No. 4
DM was a 49-year-old male who was noted to have elevated serum aminotransferase levels (AST/ALT 228/136 IU/L). Workup revealed chronic HCV infection. He was in good health and had no specific complaints. His past medical history was unremarkable. He had no allergies and was on no medications. Social history revealed a 40-pack-year tobacco history and occasional use of alcohol. He denied any intravenous drug use. Family history was negative. A review of systems was positive only for generalized malaise. Physical examination revealed clear lungs, cardiac examination with no murmurs, the abdomen was soft with a liver and a spleen palpable 3–4 finger breadths below the costal margins. No peripheral edema was present.
Laboratory evaluation revealed normal electrolytes and renal function. Complete blood count showed WBC 2.8 × 1,000 cells/mm3 and a platelet count of 80,000/mm3. Liver function tests documented serum aminotransferase elevations with a normal bilirubin level. HCV genotype 1 was found with a viral load of 1.8 × 106 copies.
A computed tomography scan of the abdomen revealed a cirrhotic liver with splenomegaly and evidence of portal hypertension with recanalization of the periumbilical veins. An upper endoscopy revealed grade II esophageal varices with portal hypertensive gastropathy.
He was started on IFNα therapy (PEG-Intron® 2 μg/kg/week) with ribavirin (200 mg BID). Eight months after the initiation of therapy, the patient developed progressive dyspnea on exertion with increasing abdominal girth and pedal edema. The IFNα and ribavirin therapy were discontinued. Re-evaluation at this time revealed a normal chest X-ray. Pulmonary function tests documented a moderate to severe decrease in diffusion capacity with a mild reversible obstructive ventilatory defect. A cardiac echogram documented normal left ventricular size and function (EF 60%) and a normal right ventricular size. Moderate tricuspid regurgitation was noted, with a markedly elevated PAP of 80 mm Hg. A ventilation perfusion scan was negative for thromboembolic disease. The patient was diagnosed as having severe pulmonary hypertension of unknown etiology and was treated with a diuretic and calcium channel blocker with good results. He remains clinically stable however, without improvement in his pulmonary hypertension.
In these four cases, each individual reported a new symptom of respiratory insufficiency after prolonged therapy with IFNα. Evaluation revealed pulmonary hypertension which was irreversible upon discontinuation of IFNα and with no identifiable etiology. There is no common variable other than HCV and IFNα therapy among these individuals. Three of four were noncirrhotic and 2/4 were postliver transplant with good hepatic function and uncomplicated postsurgical course. There was also no commonality in the preparation of the interferon used. The dosage and duration used were not unlike those used typically for hepatic or hematologic disease. The dosage of cIFN used was 15 μg daily, which was higher than the approved 9 μg/three times per week; however, this regimen is now commonly used. It was recently evaluated in a multicenter study, the DIRECT trial, with validation of its safety and efficacy in those who fail standard therapy . Also, it is unlikely that an interaction with any other medications, such as immunosuppressants, is contributory to this finding, but such an association cannot be ruled out categorically.
Potential mechanisms that might explain this sequence of events might include a pre-existing condition, IFNα-induced pulmonary hypertension, or the acceleration of a previously subclinical phenomenon caused by other factors such as human herpesvirus 8 (HHV8), HCV itself, or a previously unrecognized genetic predisposition.
The development of primary pulmonary hypertension secondary to portal hypertension, called portopulmonary hypertension, is a well-known entity . Cirrhosis has been reported to increase the risk of pulmonary hypertension 6–20-fold . This risk increases proportional to the duration of the portal hypertension, although there is no documented relationship to the severity of portal hypertension, degree of hepatic failure, or fraction of blood flow shunting through the lungs . It is most often seen in patients with end-stage liver disease and is considered as one of several rare sequelae of prolonged portal hypertension. In the present series, only case 4 had evidence of significant portal hypertension prior to the initiation of therapy. Patients 1 and 3 had a liver transplant prior to the time of diagnosis and patient 2 had only mild hepatic fibrosis on biopsy. In each case, other causes of portal hypertension were pursued vigorously and systematically ruled out.
HCV is a well-known cause of cardiopulmonary pathology. Numerous reports have linked HCV to idiopathic pulmonary fibrosis [11, 12], pneumonitis , and cardiomyopathy . In this setting, pulmonary hypertension is secondary to end-stage pulmonary fibrosis, which is easily recognized with standard radiologic evaluations. In this series, no evidence for the presence of pulmonary fibrosis was present in any of the four cases.
Thus, this series of cases suggests that an association between pulmonary hypertension and IFNα therapy may exist. IFNα is a powerful immunomodulator that has a variety of effects on the lungs. Though considered uncommon, most reported cases of adverse pulmonary side effects related to IFNα consist of an exacerbation of asthma , pleural effusion , an activation of sarcoidosis , bronchiolitis obliterans-organizing pneumonia , and bilateral pulmonary infiltrates and reversible pulmonary hypertension. Several reports have described the phenomenon of bilateral interstitial and alveolar infiltrates, which have been shown histologically to be interstitial pneumonitis [19–21]. In contrast, there is only one reported case of pulmonary hypertension which was reversible, having developed in a patient receiving IFNα for CML .
An association between IFNα and pulmonary hypertension has been described in sheep. Hanaoka et al. found that, 1 h after an infusion of IFNα directly into the lungs of sheep, PAP and PVR increased significantly and these events coincided with elevations of thromboxane B2 in the plasma. Furthermore, the administration of OKY-046, a selective thromboxane synthase inhibitor, prevented these IFNα-mediated pulmonary artery changes. This study suggests that the thromboxane cascade, a mediator of inflammation, is directly involved in the effect of IFN on the lungs  and may be a mediator in the development of pulmonary hypertension.
HCV itself has been reported to cause an occult inflammatory reaction in pulmonary air spaces. Idilman et al.  reported elevated levels of polymorphonuclear neutrophils in the bronchoalveolar lavage specimens of individuals with HCV. This suggests that a low-grade chronic inflammatory reaction may be present in the lungs of individuals with HCV infection and may contribute to the alveolar and pulmonary arterial changes. Shiomi et al. further demonstrated that IFNα exacerbates this inflammatory reaction in patients with HCV. Using gallium 67 citrate scans, they evaluated patients with HCV before and after IFN therapy and were able to quantitatively show increased radionucleotide uptake post-treatment. These investigators concluded that IFNα causes a gradual subclinical pulmonary inflammatory process in a majority of the individuals treated with the agent .
How then might irreversible pulmonary hypertension occur in an individual receiving IFNα therapy? Three possible mechanisms are worth considering.
As stated earlier, IFNα causes an acute increase in the PVR and PAP, which results in a transient hypoxia. This results in the local release of cytokines and arachidonic acid metabolites that promote further smooth-muscle contraction, resulting in a marked transient but reversible increase in the pulmonary vascular resistance. Over a prolonged period of time, this phenomenon may promote arterial smooth-muscle hypertrophy that may lead to irreversible pulmonary artery hypertension.
A second possibility is that HCV, like HIV, may have a direct effect on the pulmonary endothelium mediated by vasoactive amines, which leads to leukocyte adherence, inflammatory cytokine release, and endothelial cell proliferation. Additionally, it has been shown that certain vasculotropic viruses, such as HHV8, play a significant etiologic role in primary pulmonary hypertension . Co-infection with such viruses may yet be another etiologic factor in these individuals. This phenomenon may be subclinical initially but, with the added stress of prolonged IFNα exposure, may result in pulmonary hypertension which may be irreversible.
Finally, a genetic predisposition such as the novel mutation in the bone morphogenetic protein receptor type II (BMPR2) seen in certain familial forms of primary pulmonary hypertension  may have been present in these four cases. IFNα may promote the expression of this abnormal protein, which results in uncontrolled endothelial cell growth and proliferation alone or in response to insults such as HCV infection.
Regardless of the precise mechanism involved, these four cases suggest that pulmonary artery hypertension developing in individuals after prolonged IFN therapy may be irreversible and should be considered in individuals being treated with IFNα who present with exertional dyspnea and do not have a readily identifiable inflammatory or embolic cause for pulmonary artery hypertension. Further study is needed to identify the precise pathophysiology of this problem and the identification of individuals who might be at risk for developing this life-threatening complication of IFNα therapy.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.