FibroScan compared to liver biopsy for accurately staging recurrent hepatic steatosis and fibrosis after transplantation for MASH

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作者
Martinez-Arenas, Laura [1 ,2 ,3 ]
Vinaixa, Carmen [1 ,3 ,4 ]
Conde, Isabel [1 ,3 ,4 ]
Lorente, Sara [5 ]
Diaz-Fontenla, Fernando [6 ,7 ]
Marques, Patrice [1 ,3 ]
Perez-Rojas, Judith [8 ]
Montalva, Eva [1 ,3 ,9 ,10 ]
Carvalho-Gomes, Angela [1 ,3 ]
Berenguer, Marina [1 ,3 ,4 ,11 ]
机构
[1] Inst Invest Sanitaria Fe IIS Fe, Hepatobiliopancreat Surg & Transplant Lab, Hepatol, Valencia, Spain
[2] Univ Politecn Valencia, Dept Biotechnol, Valencia, Spain
[3] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid, Spain
[4] Hosp Univ & Politecn La Fe, Hepatol & Liver Transplantat Unit, 106 Fernando Abril Martorell Ave,F Tower,5th Floor, Valencia 46026, Spain
[5] Hosp Clin Univ Lozano Blesa, Hepatol & Liver Transplantat Unit, Inst Invest Sanitaria Aragon IIS Aragon, Zaragoza, Spain
[6] Hosp Gen Univ Gregorio Maranon, Liver Unit, Madrid, Spain
[7] Hosp Gen Univ Gregorio Maranon, Digest Dept, Madrid, Spain
[8] Hosp Univ & Politecn La Fe, Dept Pathol, Valencia, Spain
[9] Hosp Univ & Politecn La Fe, Hepatobiliopancreat Surg & Transplantat Unit, Valencia, Spain
[10] Univ Valencia, Dept Surg, Valencia, Spain
[11] Univ Valencia, Dept Med, Valencia, Spain
关键词
FibroScan; liver biopsy; liver transplantation; metabolic dysfunction-associated steatotic liver disease; metabolic factors; recurrent fibrosis; recurrent steatosis; METABOLIC SYNDROME; TRANSIENT ELASTOGRAPHY; SCORING SYSTEM; DISEASE; ASSOCIATION; PREVALENCE; DIAGNOSIS;
D O I
10.1111/liv.16085
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims Metabolic dysfunction-associated steatotic liver disease (MASLD) recurrence after liver transplantation (LT) seems unavoidable and gradual. We aimed to evaluate the diagnostic accuracy in the post-LT setting of patients transplanted for metabolic dysfunction-associated steatohepatitis (MASH) of recurrent hepatic steatosis and fibrosis identified with FibroScan, compared to biopsy findings. Methods This prospective cohort study included adults transplanted for MASH between 2010 and 2022 in three LT centres in Spain who underwent FibroScan and biopsy at least 1-year after LT. Results In total, 44 patients transplanted for MASH after LT were included. The median time from LT to biopsy and FibroScan was 24.5 (interquartile range [IQR]:16-46) and 26.0 (IQR: 16.8-41.5) months, respectively. The median time between biopsy and FibroScan was 2.0 (IQR: 0-5) months. On FibroScan, significant steatosis was diagnosed in about half of the patients (n = 21, 47.7%), yet advanced fibrosis in only two cases (4.6%). On biopsy, a quarter of biopsied patients (n = 11, 25%) had a MASH diagnosis, two (4.6%) with significant fibrosis and one (2.3%) with cirrhosis. All patients with liver stiffness measurement (LSM) values <8 kPa (n = 35, 79.5%) had a fibrosis stage <= F1 (negative predictive value = 100%). The combination of post-LT hypertension (odds ratio [OR]: 12.0, 95% confidence interval [CI]: 1.8-80.4, p = .010) and post-LT dyslipidaemia (OR: 7.9, 95% CI: 1.3-47.1, p = .024) with LSM (OR: 1.7, 95% CI: 1.1-2.8, p = .030) was independently associated with MASLD. Conclusions Although biopsy remains the gold standard for detecting fibrosis, our results suggest that LSM values <8 kPa after LT for MASH are strongly correlated with absence of significant/advanced fibrosis.
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