Prevalence of Metabolic Liver Diseases in Patients With Type 1 Diabetes Mellitus

Sponsor
Consorci Sanitari de l'Alt Penedès i Garraf (Other)
Overall Status
Recruiting
CT.gov ID
NCT05054712
Collaborator
(none)
250
2
28
125
4.5

Study Details

Study Description

Brief Summary

Nonalcoholic fatty liver disease (NAFLD) has been extensively studied in the context of type 2 diabetes mellitus (T2D) due to its higher prevalence and its association with obesity and syndrome metabolic, a well-established risk factor for NAFLD. Although several studies have reported the accumulation of liver fat in patients with type 1 diabetes mellitus (T1D), the prevalence, etiology, and the consequences of NAFLD in patients with T1D are poorly characterized, requiring more studies in this field. In addition, liver involvement at the metabolic level in patients with T1D raises the differential diagnosis between NAFLD and glycogen hepatopathy (GH), a rare complication associated with the poorly metabolic control of diabetes and probably underdiagnosed, since the ultrasound pattern is the same than the NAFLD. The investigators have designed a cross-sectional observational study with the objective of describing the prevalence of metabolic liver diseases (NAFLD and GH) in the population of patients with T1D in the healthcare area of Hospital del Mar and Hospital de Vilafranca, as well as studying the relationship of these pathologies with the degree of metabolic control, the presence of metabolic syndrome and the presence of micro and macrovascular complications.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    250 participants
    Observational Model:
    Case-Crossover
    Time Perspective:
    Cross-Sectional
    Official Title:
    Prevalence of Metabolic Liver Diseases in Patients With Type 1 Diabetes Mellitus: Non-alcoholic Fatty Liver Disease and Glycogenic Hepatopathy
    Actual Study Start Date :
    Sep 1, 2021
    Anticipated Primary Completion Date :
    Jan 1, 2023
    Anticipated Study Completion Date :
    Jan 1, 2024

    Outcome Measures

    Primary Outcome Measures

    1. To describe the prevalence of metabolic liver diseases (NAFLD and GH) by different diagnostic approaches in the population of patients with T1D. [2 years]

      To describe the prevalence of metabolic liver diseases (NAFLD and GH) by different diagnostic approaches (levels of transaminases, liver ultrasound, liver MRI and, in selected cases, liver biopsy) in the population of patients with T1D in the healthcare area of Hospital del Mar and Hospital de Vilafranca.

    Secondary Outcome Measures

    1. To study the relationship between metabolic liver diseases in patients with T1D and the degree of metabolic control of diabetes. [2 years]

    2. To study the relationship between metabolic liver diseases in patients with T1D and the presence of metabolic syndrome. [2 years]

    3. To study the relationship between metabolic liver diseases in patients with T1D and the presence of microvascular and macrovascular complications. [2 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 100 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Men and women aged ≥ 18 years.

    • Diagnosed with T1D of at least 6 months of evolution.

    • Patients who give their informed consent in writing.

    Exclusion Criteria:
    • Active alcoholism> 30 g / day in men and> 20 g / day in women.

    • Known non-metabolic liver disease: alcoholic hepatitis, viral hepatitis from HBV infection and / or HCV, hemochromatosis, Wilson's disease, α-1 antitrypsin deficiency, autoimmune hepatitis, hepatic granulomatous (tuberculosis, mycobacteria, histoplasmosis), hepatic lymphoma, primary neoplasia liver, liver metastasis.

    • Active treatment with hepatotoxic drugs: amiodarone, isoniazid, rifampicin, sulfa drugs, tetracyclines, amoxycline / clavulanate, ketoconazole, methotrexate, valproic acid, trazodone, tamoxifen, methyldopa, reverse transcriptase inhibitors, chemotherapy, immunotherapy.

    • Pregnant women.

    • Acute decompensation of T1D (ketoacidosis) in the 3 months prior to inclusion. The inclusion after this period.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital Comarcal de l'Alt Penedès Vilafranca Del Penedès Barcelona Spain 08720
    2 Hospital del Mar Barcelona Spain 08003

    Sponsors and Collaborators

    • Consorci Sanitari de l'Alt Penedès i Garraf

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Consorci Sanitari de l'Alt Penedès i Garraf
    ClinicalTrials.gov Identifier:
    NCT05054712
    Other Study ID Numbers:
    • 21-E5
    First Posted:
    Sep 23, 2021
    Last Update Posted:
    Sep 23, 2021
    Last Verified:
    Sep 1, 2021
    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
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 23, 2021