A Study Of Intestinal Permeability And Microbiota In HE

Overview

About this study

The purpose of this study is to determine the importance of intestinal permeability and microbiota in hepatic encephalopathy (HE).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Able to provide consent, with signed and dated informed consent form.

  • Stated willingness to comply with all study procedures and availability for the duration of the study.

  • Male or female, aged 18 years old or older.

  • Presenting clinically for an upper endoscopy +/- simultaneous colonoscopy.

Cases must additionally meet the following criteria in order to be eligible:

  • Diagnosis of cirrhosis based on liver biopsy, imaging, or evidence of clinical decompensation.

  • History of at least one episode of overt HE any time in the past, defined as HE requiring hospitalization and initiation or titration of HE therapy.

    • Can be precipitated HE episode

Cirrhosis Controls must additionally meet the following criteria in order to be eligible:

  • Diagnosis of cirrhosis based on liver biopsy, imaging, or evidence of clinical decompensation2. Childs Pugh Class B or C (marker of liver disease severity.3. Portal hypertension as evidenced by ascites or hydrothorax (current or controlled, in the prior year), varices, or platelet count < 80/nL (without hematological cause)

Exclusion Criteria:

  • Gut-absorbable or intravenous antibiotic therapy in the last 4 weeks (rifaximin not included in this list; rifaximin use is permissible in this study)

  • History of inflammatory bowel disease, short gut, gastrointestinal tract fistulas, intestinal ischemia, or any form of ongoing colitis.

  • Prior diagnosis of dementia or other primary neurocognitive disorder.

  • History of any prior gastric or duodenum surgery.

  • Any gastrointestinal surgery in the last year.

  • Substantial immune compromise/deficiency (e.g., uncontrolled HIV, active immune suppressive therapy including high doses of corticosteroids or medications to prevent graft rejection, recent myeloablative therapy, sustained neutropenia)

  • History of liver transplant.

  • Pregnancy or breast feeding.

  • Platelet count < 30/nL or INR > 2 at enrollment (OK to continue enrollment if these values develop during the study, but would preclude repeat endoscopic biopsy)

  • Active hepatitis C, B, or HIV virus viremia (detectable viral load)

Cirrhosis Controls will be excluded if they have a:

  • History of overt HE as defined by West Haven Criteria (but then could be study candidates as a “case”)

Healthy Controls will be excluded if they have a:

  • Diagnosis of cirrhosis based on liver biopsy, imaging, or evidence of portal hypertension.

  • Platelet count < 150/nL (as this may indicate portal hypertension and cirrhosis)

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 7/31/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Patricia Bloom, M.D.

Contact us for the latest status

More information

Publications

Publications are currently not available
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CLS-20598391

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