Low‐quality muscle mass rather than normal‐quality muscle mass determines fibrosis progression in biopsy‐proven NAFLD

Author:

Lee Yun Kyu1ORCID,Koo Bo Kyung12ORCID,Joo Sae Kyung3,Lee Dong Hyeon3ORCID,Jang Heejoon3,Chai Jee Won4,Lee Myoung Seok4,Jang Si Won4,So Young Ho4,Park Jeong Hwan5,Chang Mee Soo5,Kim Won13ORCID,

Affiliation:

1. Department of Internal Medicine Seoul National University College of Medicine Seoul Republic of Korea

2. Division of Endocrinology, Department of Internal Medicine Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center Seoul South Korea

3. Division of Gastroenterology and Hepatology, Department of Internal Medicine Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center Seoul South Korea

4. Department of Radiology Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center Seoul South Korea

5. Department of Pathology Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center Seoul South Korea

Abstract

SummaryBackground and aimsSarcopaenia is associated with advanced nonalcoholic fatty liver disease (NAFLD). However, the impact of the muscle mass categorised by muscle quality on fibrosis progression remains unclear.MethodsA total of 292 patients with biopsy‐proven NAFLD who underwent serial vibration‐controlled transient elastography assessments at least 1 year from baseline were selected. The skeletal muscle area (SMA) was determined on abdominal computed tomography (CT) at the third lumbar vertebra level and categorised to normal‐attenuation muscle area (NAMA), low‐attenuation muscle area (LAMA) and intermuscular adipose tissue (IMAT) using a muscle quality map. These SMAs were normalised by the height squared to obtain the skeletal muscle index (SMI).ResultsAt baseline, as the histological fibrosis stage increased, SMINAMA decreased and SMILAMA increased (p for trend = 0.014 and p for trend <0.001, respectively), which was not significant after adjustment for age, sex and obesity. During a median follow‐up of 41 months, fibrosis progression was detected in 48 out of 292 patients, and higher SMILAMA quartiles independently increased the risk of fibrosis progression in a dose‐dependent manner (hazard ratio [HR] per quartile: 1.41; 95% confidence interval [CI], 1.04–1.91). The highest quartile of SMILAMA increased the risk of fibrosis progression by 3.25 times compared to the lowest quartile of SMILAMA (95% CI, 1.18–8.90). SMINAMA quartiles were not associated with the risk of fibrosis progression.ConclusionIncreased low‐quality muscle mass, but not decreased normal‐quality muscle mass, as assessed by a muscle quality map in CT, predicts fibrosis progression in patients with NAFLD.

Funder

Korea Centers for Disease Control and Prevention

Korea Health Industry Development Institute

National Research Foundation of Korea

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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