Effect of Patient Demographics, Comorbidities, and Medications on Severity of NASH Fibrosis

Sponsor
Methodist Health System (Other)
Overall Status
Completed
CT.gov ID
NCT05357352
Collaborator
(none)
263
1
22.5
11.7

Study Details

Study Description

Brief Summary

Few studies have evaluated an extensive list of possible risk factors for NAFLD for their association with presence and severity of histologic features. We wish to conduct a retrospective study on these possible factors (including demographics, comorbid diseases, and medications) for their association, if any, with severity of histopathologic findings. This study hypothesize that certain risk factors, specifically those contributing to or consisting of metabolic syndrome, will have higher NASH Fibrosis stages.

Condition or Disease Intervention/Treatment Phase
  • Other: NAFLD/NASH

Detailed Description

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in Western countries, and is projected to become one of the foremost indications for liver transplantation (2). Both NAFLD and its most severe histopathologic subtype, non-alcoholic steatohepatitis (NASH) can progress to cirrhosis and its complications including hepatic malignancy, and are thus an important target for study. It is well-known that several risk factors are associated with the development of NAFLD, including obesity, type 2 diabetes mellitus, and metabolic syndrome (1), however their association with the presence and severity of histologic features of NAFLD/NASH has not been extensively examined. This study can help determine prognostic indicators for NALFD/NASH which can be useful in its prevention and treatment.

This is a retrospective chart review and de-identified data analysis. Data will be extracted from the patient database from the Methodist Liver Institute from April 2013 - June 2020. Patients with confirmed NAFLD/NASH via liver biopsy will be selected and NAFLD Activity Score and Fibrosis stage will be assessed. Data will then be collected on demographics, comorbid diseases, and medications from EPIC EMR system used by Methodist Health System.

Study Design

Study Type:
Observational
Actual Enrollment :
263 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Effect of Patient Demographics, Comorbidities, and Medications on Severity of NASH Fibrosis
Actual Study Start Date :
May 24, 2019
Actual Primary Completion Date :
Apr 7, 2021
Actual Study Completion Date :
Apr 7, 2021

Outcome Measures

Primary Outcome Measures

  1. NAS score lover [April 2013 - June 2020]

    Severity of Nonalcoholic fatty liver disease and fibrosis staging. The NAS is a measure of grade and is the sum of numerical scores applied to steatosis (0-3), hepatocellular ballooning (0-2), and lobular inflammation (0-3). Accordingly, the NAS ranges from 0 to 8 (see Table 12.3). The NAS is one of the few grading systems for NAFLD that has been externally validated.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients identified to have biopsy-proven NASH within April 2013 - June 2020

  • Minimum age 18, no upper limit of age

  • Patients with complete records

Exclusion Criteria:
  • Age <18 years

  • Incomplete records

  • Diseases other than NASH

Contacts and Locations

Locations

Site City State Country Postal Code
1 Methodist Dallas Medical Center Dallas Texas United States 75203

Sponsors and Collaborators

  • Methodist Health System

Investigators

  • Principal Investigator: Mantry Parvez, MD, The Liver Institute at Methodist Dallas Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Methodist Health System
ClinicalTrials.gov Identifier:
NCT05357352
Other Study ID Numbers:
  • 002.HEP.2019.D
First Posted:
May 2, 2022
Last Update Posted:
May 2, 2022
Last Verified:
Apr 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 Methodist Health System
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 2, 2022