key: cord-0831945-qzpbtr1l
authors: Lotersztajn, Sophie
title: Celebrating the third year of JHEP Reports in the COVID-19 era
date: 2021-01-11
journal: JHEP Rep
DOI: 10.1016/j.jhepr.2021.100225
sha: 66aadd3c227b10d3e109cf37b1c22bc325910133
doc_id: 831945
cord_uid: qzpbtr1l

nan

When I celebrated the second year of JHEP Reports in the editorial of the first 2020 issue 1 , I could not imagine the year we would go through. But the 14 th issue of the journal is now associated with new hopes arising from vaccines that were developed at an unprecedented speed, thanks to previous solid research on related viruses and technologies, and huge financial investment. During this strange period, JHEP Reports has continued to expand, as illustrated in this issue gathering 11 basic, translational and clinical articles and 4 reviews covering liver cancer, autoimmune liver diseases, liver transplantation, non-alcoholic fatty liver disease (NAFLD) and viral hepatitis.

Amaddeo et al. 2 , studied the impact of the COVID-19 pandemic on the management of hepatocellular carcinoma (HCC) in Paris, in a multicentric cross-sectional study comparing the COVID-19 period to the same period in 2019. The study showed that COVID-19 clearly impacted the care of patients with liver diseases, especially those with HCC, with less patients being discussed in multidisciplinary tumor boards, especially newly diagnosed patients, and longer treatment delays. These data highlight the negative impact of the COVID-19 pandemic on HCC management. Moreover, although additional data on survival are needed to appreciate the impact of COVID-19 on liver disease progression, maintaining the usual care of patients in a J o u r n a l P r e -p r o o f pandemic is a major issue. A study by Azoulay et al. 3 aimed to reevaluate the fate of liver resection for HCC in patients with cirrhosis and significant portal hypertension, performed in highly specialized liver centers. They show that these patients can undergo liver resection with acceptable mortality, morbidity, and liver decompensation rates. The laparoscopic approach was the sole predictor of a textbook outcome. Finally, Gregory et al. 4 Three studies in this issue are related to cholestatic liver diseases. In the first study, Harms et al. 6 show that obeticholic acid (OCA) treatment is associated with a reduction in the predicted risk of liver-related complications in patients with primary biliary cholangitis (PBC). Ursodeoxycholic acid (UDCA) is the standard first-line therapy and is associated with reduced mortality. However, UDCA does not prevent pro-J o u r n a l P r e -p r o o f gression to cirrhosis and liver failure in all patients, and those with an incomplete biochemical response to UDCA are most at risk of an unfavorable outcome. The POISE trial was a randomized, double-blind, placebo-controlled, pivotal phase III trial evaluating the efficacy, safety and tolerability of the farnesoid X receptor agonist OCA as a monotherapy in patients who were intolerant to UDCA, or combined with UDCA, in patients with PBC who had an incomplete response to UDCA. Compared with placebo, OCA treatment was associated with a significant improvement in liver biochemistry in patients with PBC and an inadequate response to UDCA. Harms et al. show that OCA treatment was associated with a reduction in the predicted risk of liverrelated complications in patients with PBC, using data from the POISE trial to calculate GLOBE score and APRI. These findings strongly suggest that the biochemical effects of OCA may translate into clinical benefit. In another study, Vesterhus et al. 7 provide a comprehensive assessment of extracellular matrix (ECM) turnover profiles, establishing PBC as a high-turnover autoimmune liver disease. In a case-control retrospective study, they quantified the serum levels of a panel of ECM and fibrosis remodeling markers across different autoimmune liver diseases (primary sclerosing cholangitis [PSC], PBC, and autoimmune hepatitis [AIH]), in a test cohort from the UK and a validation cohort from Norway. Although small-sized subgroups were studied, the data show that the levels of ECM markers were associated with disease stage and were higher in PBC than in PSC or AIH, suggesting a higher ECM turnover in PBC than in PSC or AIH. A third study by Dyson et al. 8 explores the impact of potential environmental contributors to cholestatic disease and investigates whether the geo-epidemiology of PBC and PSC are disease-specific or pertain to cholestatic autoimmune liver diseases in general. The study, performed in a population-based cohort in north England, shows that PBC was prevalent in the urban, post-industrial ar-J o u r n a l P r e -p r o o f ea with coal-mine heritage and associated with cadmium levels, whereas PSC was more common in the rural, sheep farming west and inversely associated with social deprivation. The study is welcomed since in contrast to genetic studies, the role of environmental factors in cholestatic diseases has been poorly explored.

One clinical and one basic article are related to NAFLD. The study by Linge et al. 9 provides a comprehensive assessment of the potential role of sarcopenia and myosteatosis in NAFLD. Sarcopenia (progressive and generalized loss of skeletal muscle mass, strength, and/or physical performance) is strongly associated with cirrhosis and commonly observed in end-stage liver disease. However, studies reporting associations between sarcopenia and NAFLD/NASH are not yet fully understood.

Using data from a large UK Biobank imaging study, the authors investigate the associations of MRI-measured adverse muscle composition (i.e low muscle volume and high muscle fat) with poor function, sarcopenia and metabolic comorbidity within NAFLD. The study shows that measuring muscle health could be included in the assessment of liver disease and could help identify the more vulnerable patients and enable early prevention of severe liver disease. In a preclinical study, Gwag et al. 10 investigate the role of the immunoregulatory protein thrombospondin 1 (TSP1) in NASH. They show that the hepatic expression of TSP1 is upregulated in patients and with NASH and in animal models. They demonstrate the crucial role of macrophages in NASH and NASH-related liver fibrosis, owing to the use of mice with specific deletion of TSP1 in myeloid cells exposed to a NASH diet. Mechanistically, they show that macrophage-derived TSP1 suppresses sphingomyelin phosphodiesterase acidlike 3B (SMPDL3B) expression in the liver, a negative regulator of the Toll-like receptor-4 signaling pathway. Although previous data argued for a role of TSP1 in NASH, the current study provides novel insights into the role of TSP1 and SMPDL3B in the to Hep-orgs (adult and foetal hepatocyte-derived organoids) and organoids derived from induced pluripotent stem cells. They also summarize the current knowledge on various liver diseases that have been modelled using this experimental approach, with a particular focus on monogenic diseases.

The first issue of 2021 is a fantastic vintage. I wish a long life to JHEP Reports, and our readers and all the team a happy, COVID-19-free and successful new year!

Happy 2020: JHEP Reports is starting its second year

Impact of COVID-19 on the management of hepatocellular carcinoma in a highprevalence area

Liver resection for hepatocellular carcinoma in patients with clinically significant portal hypertension

Published trials of TACE for HCC are often not registered and subject to outcome reporting bias

New insights into the pathophysiology and clinical care of rare primary liver cancers

Obeticholic acid is associated with improvements in AST-to-platelet ratio index and GLOBE score in patients with primary biliary cholangitis

Comprehensive assessment of ECM turnover using serum biomarkers establishes PBC as a high-turnover autoimmune liver disease

Geoepidemiology and environmental co-variate mapping of primary biliary cholangitis and primary sclerosing cholangitis

Adverse muscle composition is linked to poor functional performance and metabolic comorbidities in NAFLD

Macrophage-derived thrombospondin 1 promotes obesity-associated non-alcoholic fatty liver disease

Sex disparities in waitlisting and liver transplant for acute liver failure

De novo synthesis of hepatitis B virus nucleocapsids is dispensable for the maintenance and transcriptional regulation of cccDNA

Acute-on-chronic liver failure: Definitions, pathophysiology and principles of treatment

Our emerging understanding of the roles of long noncoding RNAs in normal liver function, disease, and malignancy

Organoids to model liver disease