Clinical risk factors for portopulmonary hypertension

• Published in: Hepatology (Baltimore, Md.) Vol. 48; no. 1; pp. 196 - 203
• Main Authors: Kawut, Steven M., Krowka, Michael J., Trotter, James F., Roberts, Kari E., Benza, Raymond L., Badesch, David B., Taichman, Darren B., Horn, Evelyn M., Zacks, Steven, Kaplowitz, Neil, Brown, Robert S., Fallon, Michael B.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.07.2008; Wiley
• Subjects: Adult; Biological and medical sciences; Case-Control Studies; Cohort Studies; Female; Gastroenterology. Liver. Pancreas. Abdomen; Hepatitis C - complications; Hepatitis C - physiopathology; Hepatitis, Autoimmune - complications; Humans; Hypertension, Portal - etiology; Hypertension, Portal - prevention & control; Hypertension, Pulmonary - etiology; Hypertension, Pulmonary - prevention & control; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Male; Medical sciences; Middle Aged; Multivariate Analysis; Other diseases. Semiology; Prospective Studies; Risk Assessment; Risk Factors; Sex Factors; Vascular disease; Portal circulation disease; Risk factor; Gastroenterology; Portal hypertension; Cardiovascular disease; Digestive diseases; Portopulmonary hypertension
• ISSN: 0270-9139; 1527-3350
• DOI: 10.1002/hep.22275

Portopulmonary hypertension affects up to 6% of patients with advanced liver disease, but the predictors and biologic mechanism for the development of this complication are unknown. We sought to determine the clinical risk factors for portopulmonary hypertension in patients with advanced liver disease. We performed a multicenter case‐control study nested within a prospective cohort of patients with portal hypertension recruited from tertiary care centers. Cases had a mean pulmonary artery pressure > 25 mm Hg, pulmonary vascular resistance > 240 dynes · second · cm−5, and pulmonary capillary wedge pressure ≤ 15 mm Hg. Controls had a right ventricular systolic pressure < 40 mm Hg (if estimable) and normal right‐sided cardiac morphology by transthoracic echocardiography. The study sample included 34 cases and 141 controls. Female sex was associated with a higher risk of portopulmonary hypertension than male sex (adjusted odds ratio = 2.90, 95% confidence interval 1.20‐7.01, P = 0.018). Autoimmune hepatitis was associated with an increased risk (adjusted odds ratio = 4.02, 95% confidence interval 1.14‐14.23, P = 0.031), and hepatitis C infection was associated with a decreased risk (adjusted odds ratio = 0.24, 95% confidence interval 0.09‐0.65, P = 0.005) of portopulmonary hypertension. The severity of liver disease was not related to the risk of portopulmonary hypertension. Conclusion: Female sex and autoimmune hepatitis were associated with an increased risk of portopulmonary hypertension, whereas hepatitis C infection was associated with a decreased risk in patients with advanced liver disease. Hormonal and immunologic factors may therefore be integral to the development of portopulmonary hypertension. (HEPATOLOGY 2008.)