Mitochondrial dysfunction is associated with the severity of liver fibrosis in patients after the Fontan operation

Author:

Sethasathien Saviga1ORCID,Leemasawat Krit2,Silvilairat Suchaya1,Sittiwangkul Rekwan1,Makonkawkeyoon Krit1,Leerapun Apinya3,Kongkarnka Sarawut4,Inmutto Nakarin5,Suksai Supanai67,Apaijai Nattayaporn678,Chattipakorn Siriporn C.679,Chattipakorn Nipon678ORCID

Affiliation:

1. Division of Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

2. Division of Cardiovascular Diseases, Department of Medicine, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

3. Division of Gastroenterology Diseases, Department of Medicine, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

4. Department of Pathology, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

5. Department of Radiology, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

6. Cardiac Electrophysiology Research and Training Center, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

7. Center of Excellence in Cardiac Electrophysiology Research Chiang Mai University Chiang Mai Thailand

8. Cardiac Electrophysiology Unit, Department of Physiology, Faculty of Medicine Chiang Mai University Chiang Mai Thailand

9. Department of Oral Biology and Diagnostic Sciences, Faculty of Dentistry Chiang Mai University Chiang Mai Thailand

Abstract

AbstractThe gold standard for determining the severity of liver disease in Fontan patients is now liver biopsy. Since it is an invasive procedure, this study determined the possibility of applying mitochondrial function from isolated peripheral blood mononuclear cells (PBMCs) as a non‐invasive indicator of liver fibrosis. Fontan patients (n = 37) without known liver disease were analysed cross‐sectionally. Patients were classified according to their histology using the METAVIR score as follows; F0/F1—no/mild fibrosis; F2—moderate fibrosis; and F3/F4—cirrhosis. Peripheral blood mononuclear cells were assessed for mitochondrial activity and apoptosis. This study did not find any significant differences in cardiac function among the groups according to liver histology. Interestingly, our findings indicated a significant decrease in maximal respiration and spare respiratory capacity, in both the moderate (F2) and cirrhosis (F3/F4) groups compared with the group without significant fibrosis (F0/F1). Moreover, the cirrhosis group exhibited higher levels of apoptosis and lower levels of live cells, compared with both the moderate and no significant fibrosis groups. In conclusion, the degree of liver fibrosis in Fontan patients is strongly correlated with mitochondrial dysfunction in PBMCs. Mitochondrial function and apoptosis could potentially serve as novel markers for tracking the progression of liver fibrosis in these patients.

Funder

National Research Council of Thailand

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

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