Natural History of Noncirrhotic Portal Hypertension

Study Description:

Up to 400 subjects with noncirrhotic portal hypertension or at risk for developing noncirrhotic portal hypertension by virtue of their

underlying disease (as well as sporadic cases of noncirrhotic portal hypertension as referred to in this protocol) will be offered inclusion

in the study.

Objectives:

Primary Objective:

• The goal of this natural history study is to generate understanding of the development and progression of NCPH. We will use our

findings to generate novel biomarkers that will enable improved follow-up of patients, assist in preventing complications, and

enhance transplant decision.

Secondary Objectives:

• Measurement of the bile acids and lipids to understand NCPH and porto-systemic shunting.
• Identification of the genetic modifiers of NCPH.
• Evaluation of hepatic transcriptome in absence and presence of NCPH.
• Characterization of microbiome signatures in NCPH.

Endpoints:

Primary Endpoints:

• Establish surveillance methods and guidelines for evaluation of NCPH.
• Develop an understanding of the biological mechanisms of the progression of NCPH.
• Identification of novel biomarkers correlating with NCPH progression.

Secondary Endpoints:

• Measurement of bile acids fractionated and total, as well as lipid panel to establish cut-off levels correlating with NCPH severity.
• Establishment of positive or negative correlation between candidate susceptible genes and disease phenotype.
• Identification of novel markers of fibrosis or the development of hepatic neoplasia from transcriptome analysis.
• Characterization of microbiome signatures (taxonomic and functional), as well as identification of specific species.

• INCLUSION CRITERIA:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

• Male or female, aged >= 18 years of age, and minors 12-17 years of age.
• Women of childbearing potential must agree to use birth control unless they are menopausal or had hysterectomy.
• Known diagnosis of NCPH, or to be at the risk for NCPH by virtue of underlying disease processes such as but not limited to; CGD, SCD, Mastocytosis, CVID, CF, and CHF.

Exclusion criteria

An individual who meets any of the following criteria will be excluded from participation in this study:

• Pregnancy.
• Evidence of other forms of liver disease that typically result in cirrhosis.
• Evidence of active Chronic Hepatitis B infection as defined by the presence of hepatitis B surface antigen (HBsAg) in serum and elevated HBV DNA (>10,000 IU/mL).
• Hepatitis C as defined by the presence of hepatitis C RNA in serum.
• Evidence of other liver disease such as primary sclerosing cholangitis, primary biliary cirrhosis, Wilson s disease, autoimmune hepatitis as defined by either liver histology or laboratory abnormalities.
• Hemochromatosis as defined by presence of 3+ or 4+ stainable iron on liver biopsy or homozygosity for C282Y. Patients with iron saturation indices of >45% and serum ferritin levels of >300 ng/ml for men and >250 ng/ml for women will undergo genetic testing for hemochromatosis.
• Bile duct obstruction as suggested by imaging studies done within the previous six months.
• The presence of cirrhosis confirmed by liver biopsy.
• Active substance abuse, such as alcohol, inhaled or injection drugs within the previous one year (assessed during subject interviews by subject self-report).
• Evidence of hepatocellular carcinoma; either alpha-fetoprotein (AFP) levels greater than 50 ng/ml (normal <6.6ng/ml) and/or ultrasound (or other imaging study) demonstrating a mass suggestive of liver cancer.
• Evidence of cholangiocarcinoma as suggested by liver histology.
• Any other severe condition, which in the opinion of the investigators would impede the patient s participation or compliance in the study.
• Inability to comply or give written informed consent.