Cognitive Assessment and Brain Function Evaluation in Patients With Non-alcoholic Fatty Liver Disease

Sponsor
Yan Bi (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05563259
Collaborator
(none)
500
1
64
7.8

Study Details

Study Description

Brief Summary

The purpose of this study is to explore the relationship between Non-alcoholic fatty liver disease and cognitive impairment and evaluate the effect of metabolic surgery or lifestyle intervention on cognition.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Cognitive assessment, functional magnetic resonance imaging

Detailed Description

Previous research has shown that Non-alcoholic fatty liver disease (NAFLD) is associated with an increased risk of cognitive impairment. Even though there are many noninvasive tests available, a liver biopsy is still required for the accurate diagnosis of NAFLD. However, there are now few studies on cognitive function in patients with NAFLD based on pathological diagnosis. On one hand, in the cross-sectional study, biometric measurements, cognitive assessment, magnetic resonance imaging (MRI) results are analysed to explore the differences among control subjects and NAFLD patients undergoing liver biopsy. One the other hand, in the longitudinal study, changes in cognitive scales and MRI results in NAFLD patients both at baseline and 12-48 months after intervention are collected to investigate whether surgical intervention and weight control benefit brain function.

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
The Cross-sectional and Longitudinal Study of Relationship Between Non-alcoholic Fatty Liver Disease and Cognitive Impairment
Actual Study Start Date :
May 1, 2020
Actual Primary Completion Date :
Sep 30, 2022
Anticipated Study Completion Date :
Sep 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Groups/Cohorts Interventions Control

patients with steatosis < 5%

Radiation: Cognitive assessment, functional magnetic resonance imaging
Our study investigated cognitive function, MRI measures of brain structure and activation in patients undergoing liver biopsy. We aimed to evaluate the changes of cognition during the process of NAFLD and explore the association between brain alterations and cognition.
Other Names:
  • fMRI
  • non-NASH

    patients with steatosis ≥ 5% and did not achieve the criteria for NASH

    Radiation: Cognitive assessment, functional magnetic resonance imaging
    Our study investigated cognitive function, MRI measures of brain structure and activation in patients undergoing liver biopsy. We aimed to evaluate the changes of cognition during the process of NAFLD and explore the association between brain alterations and cognition.
    Other Names:
  • fMRI
  • NASH

    patients with NAFLD Activity Score (NAS) ≥ 5

    Radiation: Cognitive assessment, functional magnetic resonance imaging
    Our study investigated cognitive function, MRI measures of brain structure and activation in patients undergoing liver biopsy. We aimed to evaluate the changes of cognition during the process of NAFLD and explore the association between brain alterations and cognition.
    Other Names:
  • fMRI
  • Outcome Measures

    Primary Outcome Measures

    1. Participants' personal information [1 day]

      Self-reported information (age in years, gender, education in years)

    2. Physical assessments. [1 day]

      BMI (body mass index) in kg/m^2

    3. Cognitive Assessment (MMSE) [1 day]

      Mini-Mental State Examination (MMSE) scores from 0-30, and the test means better cognition with a higher score.

    4. Cognitive Assessment (MoCA) [1 day]

      he Montreal Cognitive Assessment (MoCA) scores from 0-30, and the test means better cognition with a higher score.

    5. Cognitive Assessment (RBANS) [1 day]

      The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) scores from 0-800, and the test means better cognition with a higher score.

    6. brain activation in fMRI [1 day]

      All patients underwent odor-induced task fMRI on a 3.0T MR scanner with 222 volumes for task fMRI and 230 volumes for resting-state and functional fMRI. The odor-induced task consisted of "fresh air" "rest" and "scent". Odor-induced brain activation was assessed by a general linear model using Statistical Parametric Mapping 12 (SPM12) software. Following extraction of the three separate conditions "fresh air," "scent," and "rest" from the whole sequence, contrasts were made for each participant between "fresh air > rest" and "scent > rest." Odor-induced fMRI data were analyzed in the mask of the olfactory network, including the regions of bilateral parahippocampus, amygdala, piriform cortex, insula, orbitofrontal cortex, hippocampus, and entorhinal cortices.

    Secondary Outcome Measures

    1. Change of weight from baseline [12-48 months]

      whether body weight (kg) changes during follow-up

    2. Change of Cognitive Assessment (MMSE) from baseline [12-48 months]

      Whether Mini-Mental State Examination (MMSE, scores from 0-30) changes during follow-up, and the test means better cognition with a higher score.

    3. Change of Cognitive Assessment (MoCA) from baseline [12-48 months]

      Whether the Montreal Cognitive Assessment (MoCA, scores from 0-30) change during follow-up, and the test means better cognition with a higher score.

    4. Change of Cognitive Assessment (RBANS) from baseline [12-48 months]

      Whether the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS, scores from 0-800) changes during follow-up, and the test means better cognition with a higher score.

    5. Change of brain MRI measurement from baseline [12-48 months]

      whether brain activation changes during follow-up

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • history of liver biopsy within 1 year

    • 6 years of education

    • right handed

    Exclusion Criteria:
    • consumed excessive alcohol (≥140 g/week for males or ≥ 70 g/week for females)

    • with history of other liver diseases including chronic hepatitis, biliary obstructive diseases or autoimmune hepatitis

    • with thyroid diseases

    • in a state of anxiety or depression

    • inability to complete cognitive function scales

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 at Division of Endocrinology, the Affiliated Drum Tower Hospital of Nanjing University Nanjing Jiangsu China 210008

    Sponsors and Collaborators

    • Yan Bi

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yan Bi, Chief Physician, The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
    ClinicalTrials.gov Identifier:
    NCT05563259
    Other Study ID Numbers:
    • NAFLDCOG
    First Posted:
    Oct 3, 2022
    Last Update Posted:
    Oct 12, 2022
    Last Verified:
    Oct 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Yan Bi, Chief Physician, The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 12, 2022