Early Identification of Myocardial Impairment in PBC
Launched by RENJI HOSPITAL · May 22, 2018
Trial Information
Current as of June 01, 2025
Completed
Keywords
ClinConnect Summary
Primary biliary cholangitis (PBC) is a progressive and uncommon inflammatory autoimmune cholesteric liver disease,which will contribute to cirrhosis. Symptoms and course of primary biliary cholangitis can be diverse, wherefore the targets of the current treatment are focused on the prevention of end-stage liver disease. Researches reported patients with PBC may involve abnormalities on skeleton, thyroid and exocrine glands. However, whether this autoimmune disease would cause cardiac impairment is scarcely investigated. From our clinical practice, the cardiac structural abnormal can be foun...
Gender
ALL
Eligibility criteria
- Inclusion Criteria for PBC group:
- • Age between 18-80 years old.
- * Definite primary biliary cirrhosis diagnosis which is consistent with European Association for the Study of the Liver (EASL) \[Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis (2017)\]. The following three diagnostic factors, at least meet two:
- • 1. History of elevated alkaline phosphatase (ALP) levels;
- • 2. Liver biopsy consistent with PBC;
- • 3. Positive antimitochondrial antibodies (AMA) or specific antinuclear antibodies;
- • Providing written informed consent
- Exclusion Criteria:
- * History or presence of other concomitant liver disease including:
- • 1. cirrhosis or viral hepatitis;
- • 2. Inherited metabolic liver disease;
- • 3. Drug-induced liver injury;
- • 4. Other systemic disease inducing liver change.
- • Subjects with life expectancy \< 6 months.
- • Subjects with known ischemic/non-ischemic cardiomyopathy or abnormal in cardiac-related examinations.
- • Subjects with standard metallic contraindications to CMR (i.e., estimated glomerular filtration rate \< 30 ml/min/1.73 m2, New York Heart Association functional capacity class IV)
- Inclusion Criteria for Control group:
- • Absence of known systemic diseases
- • Normal examinations in CMR/Echo/ECG
- • Age between 18-80 years old.
- • Providing written informed consent
- Exclusion Criteria:
- * Subjects with known heart disease including:
- • 1. Documented coronary artery disease;
- • 2. Ischemia/non-ischemia cardiomyopathy;
- • 3. Other systemic disease inducing heart change.
- * Subjects with known liver disease including:
- • 1. Viral hepatitis;
- • 2. Inherited metabolic liver disease;
- • 3. Drug-induced liver injury;
- • 4. Other systemic disease inducing liver change.
- • Subjects with standard metallic contraindications to CMR
About Renji Hospital
Renji Hospital, a prestigious medical institution affiliated with Shanghai Jiao Tong University School of Medicine, is dedicated to advancing healthcare through innovative clinical research. With a strong emphasis on patient-centered care, Renji Hospital conducts a wide range of clinical trials across various therapeutic areas, harnessing cutting-edge technology and evidence-based practices. The hospital's multidisciplinary team of experienced researchers and medical professionals collaborates closely to ensure rigorous study design and execution, aiming to contribute significantly to medical knowledge and improve treatment outcomes for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Shanghai, Shanghai, China
Patients applied
Trial Officials
Meng Jiang, MD
Study Chair
RenJi Hospital, School of Medicine, Shanghai Jiantong University
Xiong Ma, MD,PhD
Study Chair
RenJi Hospital, School of Medicine, Shanghai Jiantong University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials