Potential Hepatic Lipid Markers Associated with Nonalcoholic Steatohepatitis and Fibrosis in Morbid Obesity Patients

Author:

Wu Hua-Chien1,Hsieh Yin-Ru2,Wang Weu3456ORCID,Chang Ching-Wen67,Chang I-Wei891011ORCID,Chen Chi-Long89ORCID,Chang Chun-Chao1512ORCID,Chang Chia-Hsuan2,Kao Wei-Yu156111213ORCID,Huang Shih-Yi25614ORCID

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan

2. School of Nutrition and Health Sciences, Taipei Medical University, Taipei 110, Taiwan

3. Division of Digestive Surgery, Department of Surgery, Taipei Medical University Hospital, Taipei 110, Taiwan

4. Department of Surgery, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan

5. TMU Research Center for Digestive Medicine, Taipei Medical University, Taipei 110, Taiwan

6. Graduate Institute of Metabolism and Obesity Sciences, Taipei Medical University, Taipei 110, Taiwan

7. Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD 247202, USA

8. Department of Pathology, Taipei Medical University Hospital, Taipei 110, Taiwan

9. Department of Pathology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan

10. Department of Clinical Pathology, Wan Fang Hospital, Taipei Medical University, Taipei 110, Taiwan

11. Department of Pathology, Shuang Ho Hospital, Taipei Medical University, Taipei 110, Taiwan

12. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Taipei Medical University Hospital, Taipei 110, Taiwan

13. Taipei Cancer Center, Taipei Medical University, Taipei 110, Taiwan

14. Nutrition Research Center, Taipei Medical University Hospital, Taipei 110, Taiwan

Abstract

This study investigated differences in lipidomic profile features in nonalcoholic steatohepatitis (NASH) between mild and significant liver fibrosis cases among patients with morbid obesity. Wedge liver biopsy was performed during sleeve gastrectomy and significant liver fibrosis was defined as a fibrosis score ≥ 2. We selected patients with NASH with non/mild fibrosis (stage F0–F1; n = 30) and NASH with significant fibrosis (stage F2–F4; n = 30). The results of the liver tissue lipidomic analysis revealed that the fold changes of triglyceride (TG) (52:6); cholesterol ester (CE) (20:1); phosphatidylcholine (PC) (38:0) and (50:8); phosphatidic acid (PA) (40:4); phosphatidylinositol (PI) (49:4); phosphatidylglycerol (PG) (40:2); and sphingomyelin (SM) (35:0) and (37:0) were significantly lower in patients with NASH with F2–F4 than those with NASH with F0–F1 (p < 0.05). However, the fold changes of PC (42:4) were relatively higher in patients with NASH with stage 2–4 fibrosis (p < 0.05). Moreover, predictive models incorporating serum markers levels, ultrasonographic studies, and levels of specific lipid components [PC (42:4) and PG (40:2)] yielded the highest area under receiver operating curve (0.941), suggesting a potential correlation between NASH fibrosis stages and liver lipid accumulation among specific lipid species subclasses. This study demonstrated that the concentrations of particular lipid species in the liver correlate with NASH fibrosis stages and may indicate hepatic steatosis regression or progression in patients with morbid obesity.

Funder

Taiwan National Science and Technology Council

Publisher

MDPI AG

Subject

General Medicine

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