Pub Date : 2025-10-29DOI: 10.1016/j.aohep.2025.102110
Yuquan Qian, Qiao-Yuan Lu, Isaac Rodriguez, Michael Vácha, Xiangde Min, Muzaffer Reha Ümütlü, German A Castrillon, Andreas Georg Schreyer, Michael Haimerl, Philipp Wiggermann, Stefan Schönberg, Matthias P Ebert, Abhinay Vellala, Carlos Romero-Alaffita, Juan Alberto Garay Mora, Zhiqiang Guo, Jürgen Hesser, Christel Weiss, Matthias Froelich, Ying-Shi Sun, Andreas Teufel
Introduction and objectives: Primary liver cancer (PLC), comprising hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA), is a leading cause of cancer mortality globally. The combined hepatocellular-cholangiocarcinoma (cHCCCC) subtype may be less common but is relevant to treatment efficacy. We therefore evaluated the diagnostic accuracy of various approaches in distinguishing these liver cancers.
Materials and methods: Patients diagnosed with HCC, CCA, and cHCCCC at Beijing University Cancer Hospital and Institute, China were included. Radiologists of varying expertise independently assessed MRI scans, and we measured their diagnostic consistency. Radiomic features were extracted from MRI scans, and machine learning was applied to differentiate the cancer types.
Results: Standard imaging was insufficient to reliably characterize cHCCCC. Abdominal imaging experts (AIEs) had a higher mean sensitivity for HCC and CCA, 88% and 84% respectively, while non-experts (NIEs) had a lower sensitivity of 50% for HCC and 38% for CCA (HCC: p = 0.03, CCA: p = 0.008). Radiomic analysis found 'Sphericity' and 'ClusterShade' as the most relevant features. However, radiomics algorithms were also not sufficient to distinguish cHCCCC from either HCC or CCA. Regarding sensitivity, the radiomic-based model was not better than radiologists for any of the three classes (p = 0.065 for HCC, p = 0.426 for CCA, and p = 1.0 for cHCCCC). The random forest algorithm yielded an accuracy of 76% in the test set, since it correctly classified most HCC and CCA, while only one quarter of cHCCCC tumors.
Conclusions: Histopathological analysis, complemented by imaging as indicated, remains essential for accurate detection, diagnosis, and treatment of liver cancers.
{"title":"MRI imaging and machine learning based radiomics for detection of mixed HCC and CCA tumors.","authors":"Yuquan Qian, Qiao-Yuan Lu, Isaac Rodriguez, Michael Vácha, Xiangde Min, Muzaffer Reha Ümütlü, German A Castrillon, Andreas Georg Schreyer, Michael Haimerl, Philipp Wiggermann, Stefan Schönberg, Matthias P Ebert, Abhinay Vellala, Carlos Romero-Alaffita, Juan Alberto Garay Mora, Zhiqiang Guo, Jürgen Hesser, Christel Weiss, Matthias Froelich, Ying-Shi Sun, Andreas Teufel","doi":"10.1016/j.aohep.2025.102110","DOIUrl":"10.1016/j.aohep.2025.102110","url":null,"abstract":"<p><strong>Introduction and objectives: </strong>Primary liver cancer (PLC), comprising hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA), is a leading cause of cancer mortality globally. The combined hepatocellular-cholangiocarcinoma (cHCCCC) subtype may be less common but is relevant to treatment efficacy. We therefore evaluated the diagnostic accuracy of various approaches in distinguishing these liver cancers.</p><p><strong>Materials and methods: </strong>Patients diagnosed with HCC, CCA, and cHCCCC at Beijing University Cancer Hospital and Institute, China were included. Radiologists of varying expertise independently assessed MRI scans, and we measured their diagnostic consistency. Radiomic features were extracted from MRI scans, and machine learning was applied to differentiate the cancer types.</p><p><strong>Results: </strong>Standard imaging was insufficient to reliably characterize cHCCCC. Abdominal imaging experts (AIEs) had a higher mean sensitivity for HCC and CCA, 88% and 84% respectively, while non-experts (NIEs) had a lower sensitivity of 50% for HCC and 38% for CCA (HCC: p = 0.03, CCA: p = 0.008). Radiomic analysis found 'Sphericity' and 'ClusterShade' as the most relevant features. However, radiomics algorithms were also not sufficient to distinguish cHCCCC from either HCC or CCA. Regarding sensitivity, the radiomic-based model was not better than radiologists for any of the three classes (p = 0.065 for HCC, p = 0.426 for CCA, and p = 1.0 for cHCCCC). The random forest algorithm yielded an accuracy of 76% in the test set, since it correctly classified most HCC and CCA, while only one quarter of cHCCCC tumors.</p><p><strong>Conclusions: </strong>Histopathological analysis, complemented by imaging as indicated, remains essential for accurate detection, diagnosis, and treatment of liver cancers.</p>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":" ","pages":"102110"},"PeriodicalIF":4.4,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145420957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-27DOI: 10.1016/j.aohep.2025.102149
Jorge Emilio Lira-Vera , Ángel Daniel Santana-Vargas , Gabriela Gutiérrez-Reyes , Oscar Morales-Gutiérrez , María de Fátima Higuera-de la Tijera , Diana Montemira-Orozco , Christian Hinojosa-Segura , Moisés Martínez-Castillo , Samantha Sánchez-Valle , María de los Ángeles Lemus-Peña , Daniel Montes de Oca-Ángeles , Abigail Hernández-Barragán , Marisela Hernández-Santillán , Yadira Lilian Béjar-Ramírez , José Luis Pérez-Hernández
Introduction and Objectives
The concept of Metabolic dysfunction and alcohol-associated steatotic liver disease (MetALD) is recent. Patients with MetALD may have a higher risk of developing steatosis, inflammation, fibrosis, and cirrhosis than Metabolic dysfunction-associated steatotic liver disease (MASLD) or Alcohol-associated liver disease (ALD) patients. This study aims to evaluate the presence and grade of steatosis and liver fibrosis in the open Mexican population to determine the frequency and stage of MASLD, ALD, and MetALD.
Patients and Methods
Subjects aged 18 years or older, of any gender, and with a body mass index (BMI) of 18.5 or higher, who were healthy and without pre-existing chronic diseases, liver disease, or cancer, and who donated blood to our center's blood bank between June 1, 2021, and March 31, 2022, were included. To estimate the grade of steatosis and liver fibrosis, vibration-controlled transient elastography (VCTE) was performed. The subjects were classified according to VCTE and alcohol consumption pattern into one of four groups: healthy subjects (HS), ALD, MASLD, and MetALD.
Results
The prevalence of MASLD, ALD, and MetALD was 45.3%, 17.5%, and 5.8%, respectively. Only 31.4% were considered as HS. However, the average BMI was out of range in all four groups, including HS. Grade 3 steatosis was observed in the MASLD and MetALD groups. Liver stiffness showed higher values in the MetALD group.
Conclusions
MetALD has the lowest prevalence compared to MASLD and ALD. However, MetALD has the highest grade of steatosis and liver fibrosis. High BMI and risky alcohol consumption were associated with the severity of liver disease.
{"title":"Assessment of metabolic dysfunction-associated steatotic liver disease, alcohol-associated liver disease, and metabolic dysfunction and alcohol-associated steatotic liver disease in open Mexican population","authors":"Jorge Emilio Lira-Vera , Ángel Daniel Santana-Vargas , Gabriela Gutiérrez-Reyes , Oscar Morales-Gutiérrez , María de Fátima Higuera-de la Tijera , Diana Montemira-Orozco , Christian Hinojosa-Segura , Moisés Martínez-Castillo , Samantha Sánchez-Valle , María de los Ángeles Lemus-Peña , Daniel Montes de Oca-Ángeles , Abigail Hernández-Barragán , Marisela Hernández-Santillán , Yadira Lilian Béjar-Ramírez , José Luis Pérez-Hernández","doi":"10.1016/j.aohep.2025.102149","DOIUrl":"10.1016/j.aohep.2025.102149","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>The concept of Metabolic dysfunction and alcohol-associated steatotic liver disease (MetALD) is recent. Patients with MetALD may have a higher risk of developing steatosis, inflammation, fibrosis, and cirrhosis than Metabolic dysfunction-associated steatotic liver disease (MASLD) or Alcohol-associated liver disease (ALD) patients. This study aims to evaluate the presence and grade of steatosis and liver fibrosis in the open Mexican population to determine the frequency and stage of MASLD, ALD, and MetALD.</div></div><div><h3>Patients and Methods</h3><div>Subjects aged 18 years or older, of any gender, and with a body mass index (BMI) of 18.5 or higher, who were healthy and without pre-existing chronic diseases, liver disease, or cancer, and who donated blood to our center's blood bank between June 1, 2021, and March 31, 2022, were included. To estimate the grade of steatosis and liver fibrosis, vibration-controlled transient elastography (VCTE) was performed. The subjects were classified according to VCTE and alcohol consumption pattern into one of four groups: healthy subjects (HS), ALD, MASLD, and MetALD.</div></div><div><h3>Results</h3><div>The prevalence of MASLD, ALD, and MetALD was 45.3%, 17.5%, and 5.8%, respectively. Only 31.4% were considered as HS. However, the average BMI was out of range in all four groups, including HS. Grade 3 steatosis was observed in the MASLD and MetALD groups. Liver stiffness showed higher values in the MetALD group.</div></div><div><h3>Conclusions</h3><div>MetALD has the lowest prevalence compared to MASLD and ALD. However, MetALD has the highest grade of steatosis and liver fibrosis. High BMI and risky alcohol consumption were associated with the severity of liver disease.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102149"},"PeriodicalIF":4.4,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145399785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-26DOI: 10.1016/j.aohep.2025.102150
Xiaohui Ye , Lingling He , Caihong Deng , Junru Yang , Ping Li , Hongshan Wei
Introduction and Objectives
Transient elastography (TE) has been widely used in clinical practice, but noninvasive prediction models based on TE for the assessment of liver fibrosis in primary biliary cholangitis (PBC) has not been reported before. The aim of this study is to develop the simple, accurate and noninvasive prediction models for the histologic staging of PBC based on TE.
Patients and Methods
Serologic testing, liver stiffness measurement (LSM), and histological assessment of 144 patients with PBC were collected retrospectively. In model group consisted of 96 patients, LSM and alkaline phosphatase (ALP) were identified as two independent predictors of PBC histological stage, which were used to establish two noninvasive models, Model A and Model B, to predict significant fibrosis (Ludwig stage ≥ 2) and advanced fibrosis (Ludwig stage ≥ 3), respectively. The performance of noninvasive models was then validated in the validation group (48 patients).
Results
The area under the ROC curve (AUROC) of Model A was 0.870 (95 % CI, 0.802-0.939) in the model group and 0.914 (95 % CI, 0.803-1.000) in the validation group. The AUROC of Model B was 0.948 (95 % CI, 0.888-0.998) in the model group and 0.906 (95 % CI, 0.824-0.987) in validation group. The above results were higher than the other five serologic markers.
Conclusions
The Model A and Model B were the efficient noninvasive models with high accuracy in predicting the histological stages of PBC.
{"title":"Noninvasive elastography-based assessment of liver fibrosis in primary biliary cholangitis","authors":"Xiaohui Ye , Lingling He , Caihong Deng , Junru Yang , Ping Li , Hongshan Wei","doi":"10.1016/j.aohep.2025.102150","DOIUrl":"10.1016/j.aohep.2025.102150","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>Transient elastography (TE) has been widely used in clinical practice, but noninvasive prediction models based on TE for the assessment of liver fibrosis in primary biliary cholangitis (PBC) has not been reported before. The aim of this study is to develop the simple, accurate and noninvasive prediction models for the histologic staging of PBC based on TE.</div></div><div><h3>Patients and Methods</h3><div>Serologic testing, liver stiffness measurement (LSM), and histological assessment of 144 patients with PBC were collected retrospectively. In model group consisted of 96 patients, LSM and alkaline phosphatase (ALP) were identified as two independent predictors of PBC histological stage, which were used to establish two noninvasive models, Model A and Model B, to predict significant fibrosis (Ludwig stage ≥ 2) and advanced fibrosis (Ludwig stage ≥ 3), respectively. The performance of noninvasive models was then validated in the validation group (48 patients).</div></div><div><h3>Results</h3><div>The area under the ROC curve (AUROC) of Model A was 0.870 (95 % CI, 0.802-0.939) in the model group and 0.914 (95 % CI, 0.803-1.000) in the validation group. The AUROC of Model B was 0.948 (95 % CI, 0.888-0.998) in the model group and 0.906 (95 % CI, 0.824-0.987) in validation group. The above results were higher than the other five serologic markers.</div></div><div><h3>Conclusions</h3><div>The Model A and Model B were the efficient noninvasive models with high accuracy in predicting the histological stages of PBC.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102150"},"PeriodicalIF":4.4,"publicationDate":"2025-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145385889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1016/j.aohep.2025.102146
Martine A.M.C. Baven-Pronk , Camiel J.M. Marijnissen , Maaike Biewenga , Albert F. Stättermayer , Maarten E. Tushuizen , Bart van Hoek
Introduction and Objectives
Monitoring liver fibrosis during treatment of autoimmune hepatitis (AIH) is important to guide treatment. Transient elastography (TE) is not always available. Existing non-invasive fibrosis scores have been assessed primarily at diagnosis but not during treatment. This study aims to develop a non-invasive AIH fibrosis score (AIHFS) and validate its performance - alongside with existing fibrosis scores - for excluding advanced fibrosis (≥F3 on TE) and cirrhosis (F4 on TE) during AIH treatment.
Patients and Methods
This study included adult patients with AIH and variant syndromes from Leiden (derivation cohort, n = 73) and Vienna (validation cohort, n = 81). All patients had been treated for at least 6 months and had valid TE and routine laboratory tests within 1 months of TE. Existing fibrosis scores were calculated and a novel AIHFS was developed using multivariate regression. TE served as the reference standard.
Results
The aspartate aminotransferase-to-platelet ratio index (APRI) and AIHFS (comprising APRI and albumin) were the only fibrosis scores significantly associated with liver stiffness during treatment. AIHFS did not outperform APRI. APRI demonstrated a high negative predictive value for advanced fibrosis (≥F3 on TE) and cirrhosis (F4 on TE): 86 % and 93 % in the derivation cohort and 84 % and 95 % in the validation cohort, respectively. Based on an APRI threshold of 0.4874, only 22–40 % of patients would require further diagnostic assessment.
Conclusions
APRI is a simple, non-invasive, widely applicable score that reliably excludes advanced fibrosis (≥F3 on TE) and cirrhosis (F4 on TE) during AIH treatment, potentially reducing the need for additional investigations.
{"title":"Aspartate aminotransferase‑to‑platelet ratio index (APRI) reliably excludes advanced fibrosis and cirrhosis in treated autoimmune hepatitis","authors":"Martine A.M.C. Baven-Pronk , Camiel J.M. Marijnissen , Maaike Biewenga , Albert F. Stättermayer , Maarten E. Tushuizen , Bart van Hoek","doi":"10.1016/j.aohep.2025.102146","DOIUrl":"10.1016/j.aohep.2025.102146","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>Monitoring liver fibrosis during treatment of autoimmune hepatitis (AIH) is important to guide treatment. Transient elastography (TE) is not always available. Existing non-invasive fibrosis scores have been assessed primarily at diagnosis but not during treatment. This study aims to develop a non-invasive AIH fibrosis score (AIHFS) and validate its performance - alongside with existing fibrosis scores - for excluding advanced fibrosis (≥F3 on TE) and cirrhosis (F4 on TE) during AIH treatment.</div></div><div><h3>Patients and Methods</h3><div>This study included adult patients with AIH and variant syndromes from Leiden (derivation cohort, <em>n</em> = 73) and Vienna (validation cohort, <em>n</em> = 81). All patients had been treated for at least 6 months and had valid TE and routine laboratory tests within 1 months of TE. Existing fibrosis scores were calculated and a novel AIHFS was developed using multivariate regression. TE served as the reference standard.</div></div><div><h3>Results</h3><div>The aspartate aminotransferase-to-platelet ratio index (APRI) and AIHFS (comprising APRI and albumin) were the only fibrosis scores significantly associated with liver stiffness during treatment. AIHFS did not outperform APRI. APRI demonstrated a high negative predictive value for advanced fibrosis (≥F3 on TE) and cirrhosis (F4 on TE): 86 % and 93 % in the derivation cohort and 84 % and 95 % in the validation cohort, respectively. Based on an APRI threshold of 0.4874, only 22–40 % of patients would require further diagnostic assessment.</div></div><div><h3>Conclusions</h3><div>APRI is a simple, non-invasive, widely applicable score that reliably excludes advanced fibrosis (≥F3 on TE) and cirrhosis (F4 on TE) during AIH treatment, potentially reducing the need for additional investigations.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102146"},"PeriodicalIF":4.4,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145457605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1016/j.aohep.2025.102147
Ahmad Yahia , Fadi Abu Baker , Mifleh Tatour , Rawi Hazzan
Introduction and Objectives
The long-term clinical significance of anti-mitochondrial antibody (AMA)-positive patients with normal liver enzymes remains unclear. Despite increasing detection of AMA positivity in asymptomatic individuals, clinicians lack evidence-based protocols for long-term surveillance, and guidelines offer no clear recommendations. This study, the largest of its kind, investigates the natural history, prognostic implications, and risk factors for disease progression in this population.
Materials and Methods
We conducted a retrospective cohort study using a national healthcare database to identify adults (aged 18 years or older) with a positive AMA and normal alkaline phosphatase (ALP) levels between 2002 and 2023. Demographics, laboratory data, and liver-related outcomes were assessed. Multivariate logistic and Cox regression models were used to evaluate predictors of primary biliary cholangitis (PBC), cirrhosis, and hepatic complications.
Results
Among 1018 patients (median follow-up 6.3 years (IQR 2.5–11.5), 76 (7.5 %) developed PBC and 30 (2.9 %) progressed to cirrhosis. Liver-related complications were infrequent: esophageal varices (1.1 %), ascites (1.8 %), hepatocellular carcinoma (0.2 %), and liver transplantation (0.1 %). Higher AMA titers were strongly associated with increased risk of PBC, cirrhosis, and complications, showing a clear titer-dependent gradient. Longitudinal analysis also demonstrated titer-associated increases in ALP and bilirubin over time.
Conclusions
AMA-positive individuals with normal liver enzymes typically experience a benign clinical course. However, high AMA titers identify a subgroup at increased risk for progression to PBC and advanced liver disease. These findings underscore the importance of risk-stratified surveillance strategies in clinical practice, guiding healthcare professionals in the management of their patients.
{"title":"Reevaluating the clinical course of AMA-positive patients with normal liver enzymes: A large retrospective cohort study","authors":"Ahmad Yahia , Fadi Abu Baker , Mifleh Tatour , Rawi Hazzan","doi":"10.1016/j.aohep.2025.102147","DOIUrl":"10.1016/j.aohep.2025.102147","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>The long-term clinical significance of anti-mitochondrial antibody (AMA)-positive patients with normal liver enzymes remains unclear. Despite increasing detection of AMA positivity in asymptomatic individuals, clinicians lack evidence-based protocols for long-term surveillance, and guidelines offer no clear recommendations. This study, the largest of its kind, investigates the natural history, prognostic implications, and risk factors for disease progression in this population.</div></div><div><h3>Materials and Methods</h3><div>We conducted a retrospective cohort study using a national healthcare database to identify adults (aged 18 years or older) with a positive AMA and normal alkaline phosphatase (ALP) levels between 2002 and 2023. Demographics, laboratory data, and liver-related outcomes were assessed. Multivariate logistic and Cox regression models were used to evaluate predictors of primary biliary cholangitis (PBC), cirrhosis, and hepatic complications.</div></div><div><h3>Results</h3><div>Among 1018 patients (median follow-up 6.3 years (IQR 2.5–11.5), 76 (7.5 %) developed PBC and 30 (2.9 %) progressed to cirrhosis. Liver-related complications were infrequent: esophageal varices (1.1 %), ascites (1.8 %), hepatocellular carcinoma (0.2 %), and liver transplantation (0.1 %). Higher AMA titers were strongly associated with increased risk of PBC, cirrhosis, and complications, showing a clear titer-dependent gradient. Longitudinal analysis also demonstrated titer-associated increases in ALP and bilirubin over time.</div></div><div><h3>Conclusions</h3><div>AMA-positive individuals with normal liver enzymes typically experience a benign clinical course. However, high AMA titers identify a subgroup at increased risk for progression to PBC and advanced liver disease. These findings underscore the importance of risk-stratified surveillance strategies in clinical practice, guiding healthcare professionals in the management of their patients.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102147"},"PeriodicalIF":4.4,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145457591","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1016/j.aohep.2025.102144
Yujiao Deng , Jingyue Tan , Jian Zu , Zixuan Xing , Zhanpeng Yang , Yue Zhang , Yajing Bo , Xu Gao , Enrui Xie , Yuan Wang , Meijuan Han , Fanpu Ji , Yang Yang
Introduction and Objectives
Liver cancer (LC) is a leading cause of cancer-related deaths worldwide. Hepatitis B/C virus -associated LC (HBC/HCC) remains the primary cause of liver cancer, and it imposes a heavy burden on public health. This study aimed to estimate the mortality and health inequalities of hepatitis B/C virus (HBV/HCV)-associated LC at the global, regional and national levels to provide guidance to reduce the mortality burden of LC.
Materials and Methods
We extracted the HBV/HCV-associated LC mortality data from the GBD 2021 study during 1990–2021 and analyzed its temporal and spatial trends and forecasted to 2050. Average annual percent change (AAPC) was calculated by joinpoint regression to evaluate the variation of ASMRs, and factors impacting mortality were evaluated through decomposition analysis. The Bayesian spatiotemporal model was used to fit the relationship between age-standardized mortality rate (ASMR) of 204 countries/territories and spatial effects, temporal effects, and spatio-temporal interaction effects. Frontier analysis was conducted to evaluate the minimum achievable ASMR in each country or territory by 2050 and its potential space for ASMR improvement in 2050.
Results
Globally, LC deaths doubled from 238,969 in 1990 to 483,875 in 2021. Compared with 1990, the proportions of HBV and HCV in the mortality rate of LC in 2021 were 37.45 % and 30.28 %, corresponding to a decrease of 7.13 % and an increase of 3.44 %, respectively. From 1990 to 2021, the global ASMR of LC (AAPC:0.11, 95 % CI:0.35 to 0.12) and LCC (AAPC: 0.05, 95 % CI:0.26 to 0.36) remained stable, while LCB decreased (AAPC:0.54, 95 % CI:0.81 to -0.27). ASMRs for LC and LCB was the highest in the Western Pacific Region (WPR), but significant declines were observed. The highest ASMR of LCB and LCC shifted from WPR to the Eastern Mediterranean Region (EMR). It is expected that the global ASMR of LC will decrease by 2050. From 1990 to 2021, population growth and age structure were the primary drivers for the increase of LC mortality globally and in Southeast Asia, and age structure is projected to remain a key factor until 2050.
Conclusions
Hepatitis virus-related LC remains a serious health issue worldwide, with regional variations. Asia contributes the most LC-related deaths. The WPR had the highest ASMR for LC and LCB. ASMR for LC showed the fastest decrease in WPR. For women, Africa had the highest ASMR for LC and LCB, while the Americas had the lowest ASMR for LC. The highest ASMR for LCC shifted from the WPR to the EMR during 1990–2021.
{"title":"Trends and health inequalities of hepatitis virus-associated liver cancer mortality during 1990–2050","authors":"Yujiao Deng , Jingyue Tan , Jian Zu , Zixuan Xing , Zhanpeng Yang , Yue Zhang , Yajing Bo , Xu Gao , Enrui Xie , Yuan Wang , Meijuan Han , Fanpu Ji , Yang Yang","doi":"10.1016/j.aohep.2025.102144","DOIUrl":"10.1016/j.aohep.2025.102144","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>Liver cancer (LC) is a leading cause of cancer-related deaths worldwide. Hepatitis B/C virus -associated LC (HBC/HCC) remains the primary cause of liver cancer, and it imposes a heavy burden on public health. This study aimed to estimate the mortality and health inequalities of hepatitis B/C virus (HBV/HCV)-associated LC at the global, regional and national levels to provide guidance to reduce the mortality burden of LC.</div></div><div><h3>Materials and Methods</h3><div>We extracted the HBV/HCV-associated LC mortality data from the GBD 2021 study during 1990–2021 and analyzed its temporal and spatial trends and forecasted to 2050. Average annual percent change (AAPC) was calculated by joinpoint regression to evaluate the variation of ASMRs, and factors impacting mortality were evaluated through decomposition analysis. The Bayesian spatiotemporal model was used to fit the relationship between age-standardized mortality rate (ASMR) of 204 countries/territories and spatial effects, temporal effects, and spatio-temporal interaction effects. Frontier analysis was conducted to evaluate the minimum achievable ASMR in each country or territory by 2050 and its potential space for ASMR improvement in 2050.</div></div><div><h3>Results</h3><div>Globally, LC deaths doubled from 238,969 in 1990 to 483,875 in 2021. Compared with 1990, the proportions of HBV and HCV in the mortality rate of LC in 2021 were 37.45 % and 30.28 %, corresponding to a decrease of 7.13 % and an increase of 3.44 %, respectively. From 1990 to 2021, the global ASMR of LC (AAPC:0.11, 95 % CI:0.35 to 0.12) and LCC (AAPC: 0.05, 95 % CI:0.26 to 0.36) remained stable, while LCB decreased (AAPC:0.54, 95 % CI:0.81 to -0.27). ASMRs for LC and LCB was the highest in the Western Pacific Region (WPR), but significant declines were observed. The highest ASMR of LCB and LCC shifted from WPR to the Eastern Mediterranean Region (EMR). It is expected that the global ASMR of LC will decrease by 2050. From 1990 to 2021, population growth and age structure were the primary drivers for the increase of LC mortality globally and in Southeast Asia, and age structure is projected to remain a key factor until 2050.</div></div><div><h3>Conclusions</h3><div>Hepatitis virus-related LC remains a serious health issue worldwide, with regional variations. Asia contributes the most LC-related deaths. The WPR had the highest ASMR for LC and LCB. ASMR for LC showed the fastest decrease in WPR. For women, Africa had the highest ASMR for LC and LCB, while the Americas had the lowest ASMR for LC. The highest ASMR for LCC shifted from the WPR to the EMR during 1990–2021.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102144"},"PeriodicalIF":4.4,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145370153","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1016/j.aohep.2025.102143
Bradley Jermy , Jack Brownrigg , Pavel Strnad , Rohit Loomba
Introduction and Objectives
Most investigational treatments for metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) show modest anti-fibrotic effects, likely due to a multifactorial aetiology. The Pi*Z mutation in SERPINA1 can lead to proteotoxic liver injury and progressive chronic liver disease. Here, we investigate whether the SERPINA1 Z mutation is associated with disease progression in MASLD/MASH.
Patients and Methods
A population of MASLD/MASH patients of European ancestry was identified in the UK Biobank using ICD-10 codes (N = 6319). We estimated odds ratios (OR) for advanced liver disease (composite of incident cirrhosis, hepatic decompensation, and liver-related death/transplant) with the MZ genotype. ORs were compared with metabolic risk factors (RFs; obesity, dyslipidaemia, hypertension, and type 2 diabetes) and established genetic RFs (PNPLA3, HSD17B13, and TM6SF2).
Results
Some individuals (7.9%) experienced advanced liver disease. The MZ genotype prevalence was greater in individuals who experienced advanced liver disease (7.6% vs 3.9%). After adjustment for established metabolic and genetic RFs, advanced liver disease was significantly associated with the MZ genotype (OR 2.01; 95% CI, 1.38–2.92). We replicated known associations in all genetic and metabolic RFs. The MZ genotype (OR 1.90; 1.33–2.73) was a risk equivalent to ≥2 metabolic RFs (OR 1.74; 1.44–2.09) and PNPLA3 (OR 1.32; 1.15–1.51).
Conclusions
Carriage of the Pi*Z mutation significantly affects the risk of future clinical outcomes among individuals with MASLD/MASH. The MZ genotype confers a risk equivalent to established RFs in MASLD/MASH, underscoring the importance of screening and further work to understand the underlying mechanisms.
{"title":"Alpha-1 antitrypsin Pi*MZ variant increases the risk of liver disease progression in MASLD and MASH","authors":"Bradley Jermy , Jack Brownrigg , Pavel Strnad , Rohit Loomba","doi":"10.1016/j.aohep.2025.102143","DOIUrl":"10.1016/j.aohep.2025.102143","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>Most investigational treatments for metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) show modest anti-fibrotic effects, likely due to a multifactorial aetiology. The Pi*Z mutation in <em>SERPINA1</em> can lead to proteotoxic liver injury and progressive chronic liver disease. Here, we investigate whether the <em>SERPINA1</em> Z mutation is associated with disease progression in MASLD/MASH.</div></div><div><h3>Patients and Methods</h3><div>A population of MASLD/MASH patients of European ancestry was identified in the UK Biobank using ICD-10 codes (<em>N</em> = 6319). We estimated odds ratios (OR) for advanced liver disease (composite of incident cirrhosis, hepatic decompensation, and liver-related death/transplant) with the MZ genotype. ORs were compared with metabolic risk factors (RFs; obesity, dyslipidaemia, hypertension, and type 2 diabetes) and established genetic RFs (<em>PNPLA3, HSD17B13</em>, and <em>TM6SF2</em>).</div></div><div><h3>Results</h3><div>Some individuals (7.9%) experienced advanced liver disease. The MZ genotype prevalence was greater in individuals who experienced advanced liver disease (7.6% vs 3.9%). After adjustment for established metabolic and genetic RFs, advanced liver disease was significantly associated with the MZ genotype (OR 2.01; 95% CI, 1.38–2.92). We replicated known associations in all genetic and metabolic RFs. The MZ genotype (OR 1.90; 1.33–2.73) was a risk equivalent to ≥2 metabolic RFs (OR 1.74; 1.44–2.09) and <em>PNPLA3</em> (OR 1.32; 1.15–1.51).</div></div><div><h3>Conclusions</h3><div>Carriage of the Pi*Z mutation significantly affects the risk of future clinical outcomes among individuals with MASLD/MASH. The MZ genotype confers a risk equivalent to established RFs in MASLD/MASH, underscoring the importance of screening and further work to understand the underlying mechanisms.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102143"},"PeriodicalIF":4.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145367401","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1016/j.aohep.2025.102142
Fátima Higuera-de-la-Tijera , Mario Reis Alvares-da-Silva , Graciela Elia Castro-Narro , Josué Barahona-Garrido , Enrique Carrera-Estupiñán , Jorge Garavito-Rentería , Héctor Adolfo Henríquez-Meléndez , Geovanny Hernández-Cely , Javier Mora-Lazo , Manuel Mendizabal , Gabriel Alejandro Mezzano-Puentes , Claudia P. Oliveira , Mário Guimarães Pessoa , Yanette Suárez-Quintero , José Antonio Velarde-Ruiz Velasco
Introduction and Objectives
Hepatic encephalopathy (HE) is a frequent and severe complication of cirrhosis, leading to rapid deterioration and increased mortality. Management varies across Latin America due to differences in disease awareness, diagnostic and therapeutic resources, and healthcare system structures. Standardized guidelines are crucial to improve outcomes.
Materials and Methods
To evaluate therapeutic strategies and develop region-specific recommendations, the Latin American Association for the Study of the Liver (ALEH) convened 15 experts from 9 countries. The consensus process, conducted in 9 phases using the Nominal Group Technique, included virtual meetings, platform-based collaboration, virtual voting, and two in-person sessions to finalize recommendations and the publication draft.
Results
The panel issued 23 recommendations covering the treatment of minimal and overt HE, as well as the prophylaxis and management of recurrent HE in cirrhotic patients.
Conclusions
This consensus provides updated, evidence-based guidelines emphasizing early diagnosis and effective management. It aims to optimize clinical outcomes, standardize treatment approaches, and enhance patient quality of life. Additionally, these recommendations seek to reduce morbidity, mortality, and hospital readmissions, addressing key challenges in the Latin American healthcare landscape.
{"title":"First Latin American consensus on the treatment and prophylaxis of hepatic encephalopathy","authors":"Fátima Higuera-de-la-Tijera , Mario Reis Alvares-da-Silva , Graciela Elia Castro-Narro , Josué Barahona-Garrido , Enrique Carrera-Estupiñán , Jorge Garavito-Rentería , Héctor Adolfo Henríquez-Meléndez , Geovanny Hernández-Cely , Javier Mora-Lazo , Manuel Mendizabal , Gabriel Alejandro Mezzano-Puentes , Claudia P. Oliveira , Mário Guimarães Pessoa , Yanette Suárez-Quintero , José Antonio Velarde-Ruiz Velasco","doi":"10.1016/j.aohep.2025.102142","DOIUrl":"10.1016/j.aohep.2025.102142","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>Hepatic encephalopathy (HE) is a frequent and severe complication of cirrhosis, leading to rapid deterioration and increased mortality. Management varies across Latin America due to differences in disease awareness, diagnostic and therapeutic resources, and healthcare system structures. Standardized guidelines are crucial to improve outcomes.</div></div><div><h3>Materials and Methods</h3><div>To evaluate therapeutic strategies and develop region-specific recommendations, the Latin American Association for the Study of the Liver (ALEH) convened 15 experts from 9 countries. The consensus process, conducted in 9 phases using the Nominal Group Technique, included virtual meetings, platform-based collaboration, virtual voting, and two in-person sessions to finalize recommendations and the publication draft.</div></div><div><h3>Results</h3><div>The panel issued 23 recommendations covering the treatment of minimal and overt HE, as well as the prophylaxis and management of recurrent HE in cirrhotic patients.</div></div><div><h3>Conclusions</h3><div>This consensus provides updated, evidence-based guidelines emphasizing early diagnosis and effective management. It aims to optimize clinical outcomes, standardize treatment approaches, and enhance patient quality of life. Additionally, these recommendations seek to reduce morbidity, mortality, and hospital readmissions, addressing key challenges in the Latin American healthcare landscape.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102142"},"PeriodicalIF":4.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145367393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1016/j.aohep.2025.102145
Shiqi Zhu , Lihe Liu , Yiping Shen , Rui Li , Jiaxi Lin , Lu Liu , Xiaolin Liu , Hongpeng Sun , Jinzhou Zhu
Introduction and Objectives
While excessive sodium intake is associated with hepatic steatosis, its precise role in metabolic dysfunction-associated steatotic liver disease (MASLD) remains underexplored. This study investigated the relationship between different measures of sodium intake and the risk of MASLD.
Materials and Methods
The complete data of 286,073 participants on their self-reported frequency of adding salt to food and estimated 24-h urinary sodium excretion from the UK Biobank were analyzed. Cox proportional hazards models quantified hazard ratios (HRs) for incident MASLD, cirrhosis or liver cancer, and liver-related mortality. Mediation analyses evaluated potential mediating between sodium intake and MASLD. Energy-adjusted dietary sodium intake was evaluated in a sub-cohort of 119,073 participants with ≥2 dietary recalls.
Results
During a median follow-up of 13.3 years, 3147 MASLD, 1354 cirrhosis or liver cancer, and 523 liver-related mortality cases were identified. After adjusting for confounders, participants who reported “always” adding salt had an increased risk of MASLD (HR=1.36, 95 % CI=1.19–1.56). Higher urinary sodium excretion was also associated with incident MASLD (HR=1.62, 95 % CI=1.53–1.72), displaying a J-shaped nonlinear relationship with the threshold point at 1.93 g/d. Inflammatory dysregulation, insulin resistance and renal function impairment partly mediated this association. In the sub-cohort, every 1 g increase in energy-adjusted dietary sodium intake conferred a 14 % higher risk of MASLD (HR=1.14, 95 % CI=1.01–1.28).
Conclusions
The habit of always adding salt to food, a 24-h urinary sodium excretion above 1.93 g/day, and energy-adjusted dietary sodium intake above 1.49g/d increased the risk of MASLD, partly mediated through inflammation, insulin resistance, and renal dysfunction. It is recommended that public health strategies target reducing MASLD risk based on these findings.
{"title":"Different measures of sodium intake and the risk of metabolic dysfunction-associated steatotic liver disease: Evidence from the UK Biobank","authors":"Shiqi Zhu , Lihe Liu , Yiping Shen , Rui Li , Jiaxi Lin , Lu Liu , Xiaolin Liu , Hongpeng Sun , Jinzhou Zhu","doi":"10.1016/j.aohep.2025.102145","DOIUrl":"10.1016/j.aohep.2025.102145","url":null,"abstract":"<div><h3>Introduction and Objectives</h3><div>While excessive sodium intake is associated with hepatic steatosis, its precise role in metabolic dysfunction-associated steatotic liver disease (MASLD) remains underexplored. This study investigated the relationship between different measures of sodium intake and the risk of MASLD.</div></div><div><h3>Materials and Methods</h3><div>The complete data of 286,073 participants on their self-reported frequency of adding salt to food and estimated 24-h urinary sodium excretion from the UK Biobank were analyzed. Cox proportional hazards models quantified hazard ratios (HRs) for incident MASLD, cirrhosis or liver cancer, and liver-related mortality. Mediation analyses evaluated potential mediating between sodium intake and MASLD. Energy-adjusted dietary sodium intake was evaluated in a sub-cohort of 119,073 participants with ≥2 dietary recalls.</div></div><div><h3>Results</h3><div>During a median follow-up of 13.3 years, 3147 MASLD, 1354 cirrhosis or liver cancer, and 523 liver-related mortality cases were identified. After adjusting for confounders, participants who reported “always” adding salt had an increased risk of MASLD (HR=1.36, 95 % CI=1.19–1.56). Higher urinary sodium excretion was also associated with incident MASLD (HR=1.62, 95 % CI=1.53–1.72), displaying a J-shaped nonlinear relationship with the threshold point at 1.93 g/d. Inflammatory dysregulation, insulin resistance and renal function impairment partly mediated this association. In the sub-cohort, every 1 g increase in energy-adjusted dietary sodium intake conferred a 14 % higher risk of MASLD (HR=1.14, 95 % CI=1.01–1.28).</div></div><div><h3>Conclusions</h3><div>The habit of always adding salt to food, a 24-h urinary sodium excretion above 1.93 g/day, and energy-adjusted dietary sodium intake above 1.49<em>g</em>/d increased the risk of MASLD, partly mediated through inflammation, insulin resistance, and renal dysfunction. It is recommended that public health strategies target reducing MASLD risk based on these findings.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"31 1","pages":"Article 102145"},"PeriodicalIF":4.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145367415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-15DOI: 10.1016/j.aohep.2025.102141
Ignacio Roca, Cecilia Morales, Mariela De Santos, Nicolas Dominguez, Luciana Meza, Manuel Barbero, Lucia Navarro, Omar Galdame, Mario Altieri, Hongqun Liu, Samuel S Lee, Fernando Cairo, Graciela Reyes
Introduction and objectives: Cirrhotic cardiomyopathy (CCM) is defined as the presence of cardiac dysfunction in patients with cirrhosis in the absence of pre-existing heart disease. Reported prevalence thus far has varied between 17.5% and 35%, depending on the studies. In 2020, diagnostic criteria were revised based on imaging advances. The aim of this study was to evaluate the prevalence of CCM and its impact on overall mortality on the waiting list and post-transplantation.
Materials and methods: A prospectively recorded database was retrospectively analyzed. Consecutive adult patients who were evaluated and placed on the waiting list for liver transplantation (LT) from 2019 to 2023 were enrolled. Survival curves for patients with and without cirrhotic cardiomyopathy were constructed using the Kaplan-Meier method, and differences were compared by the Log-rank test. Multiple regression analysis was performed by the Cox proportional hazards model.
Results: A total of 451 patients were assessed, of whom 389 (86.3%) met inclusion criteria. The median age was 55 years (IQR 46-61) with 236 (60.7%) males. The most common etiology of cirrhosis was hepatitis C, 110/389 (28.3%). The prevalence of CCM was 16.2% (63/389). Thirty-seven patients (9.5%) met systolic criteria, and 27 (6.9%) met diastolic criteria for CCM. No mean differences were found in MELD-Na (15, IQR 11-19, vs 14, IQR 10-16.5, p0.1) or decompensations. The presence of hepatocellular carcinoma was higher in the CCM group (44.4% vs. 22.1% p<0.01).The median overall survival time on the waitlist was longer in the group without CCM compared to that in the CCM group (32 vs 22 months, p=0.04). In Cox regression analysis, the presence of CCM (HR 1.71 CI95% 1.09-2.68 p0.02), HCC (HR 2.37, CI95% 1.47-3.82 p<0.001) and higher MELD-Na (HR 1.14 CI95% 1.10-1.18, p<0.001) were predictors of mortality on the waiting list. There were no significant differences in survival between the groups post-transplantation.
Conclusions: Our study revealed a lower prevalence of CCM in liver transplant candidates compared with previous reports. Moreover, it underscores that CCM was an independent predictor of mortality on a liver transplantation waitlist, highlighting its significant clinical implications. Further research is imperative to elucidate its precise impact on post-transplant survival.
简介和目的:肝硬化心肌病(CCM)被定义为肝硬化患者在没有既往心脏病的情况下存在心功能障碍。到目前为止,根据不同的研究,报告的患病率在17.5%到35%之间。2020年,诊断标准根据影像学进展进行了修订。本研究的目的是评估CCM的患病率及其对等待名单和移植后总死亡率的影响。材料和方法:回顾性分析前瞻性记录的数据库。纳入了2019年至2023年连续评估并列入肝移植(LT)等待名单的成年患者。采用Kaplan-Meier法构建肝硬化和非肝硬化心肌病患者的生存曲线,并通过Log-rank检验比较差异。采用Cox比例风险模型进行多元回归分析。结果:共纳入451例患者,其中389例(86.3%)符合纳入标准。中位年龄55岁(IQR 46-61),男性236例(60.7%)。肝硬化最常见的病因是丙型肝炎,110/389(28.3%)。CCM患病率为16.2%(63/389)。37例(9.5%)患者符合CCM的收缩期标准,27例(6.9%)患者符合舒张期标准。MELD-Na无平均差异(15,IQR 11-19, vs 14, IQR 10-16.5, p0.1)或代偿。CCM组肝细胞癌的发生率更高(44.4% vs 22.1%)。结论:我们的研究显示,与之前的报道相比,CCM在肝移植候选者中的患病率较低。此外,它强调了CCM是肝移植等待名单上死亡率的独立预测因子,强调了其重要的临床意义。进一步的研究阐明其对移植后生存的确切影响是必要的。
{"title":"Prevalence of cirrhotic cardiomyopathy in liver transplant recipients: impact on pre- and post-transplant mortality.","authors":"Ignacio Roca, Cecilia Morales, Mariela De Santos, Nicolas Dominguez, Luciana Meza, Manuel Barbero, Lucia Navarro, Omar Galdame, Mario Altieri, Hongqun Liu, Samuel S Lee, Fernando Cairo, Graciela Reyes","doi":"10.1016/j.aohep.2025.102141","DOIUrl":"https://doi.org/10.1016/j.aohep.2025.102141","url":null,"abstract":"<p><strong>Introduction and objectives: </strong>Cirrhotic cardiomyopathy (CCM) is defined as the presence of cardiac dysfunction in patients with cirrhosis in the absence of pre-existing heart disease. Reported prevalence thus far has varied between 17.5% and 35%, depending on the studies. In 2020, diagnostic criteria were revised based on imaging advances. The aim of this study was to evaluate the prevalence of CCM and its impact on overall mortality on the waiting list and post-transplantation.</p><p><strong>Materials and methods: </strong>A prospectively recorded database was retrospectively analyzed. Consecutive adult patients who were evaluated and placed on the waiting list for liver transplantation (LT) from 2019 to 2023 were enrolled. Survival curves for patients with and without cirrhotic cardiomyopathy were constructed using the Kaplan-Meier method, and differences were compared by the Log-rank test. Multiple regression analysis was performed by the Cox proportional hazards model.</p><p><strong>Results: </strong>A total of 451 patients were assessed, of whom 389 (86.3%) met inclusion criteria. The median age was 55 years (IQR 46-61) with 236 (60.7%) males. The most common etiology of cirrhosis was hepatitis C, 110/389 (28.3%). The prevalence of CCM was 16.2% (63/389). Thirty-seven patients (9.5%) met systolic criteria, and 27 (6.9%) met diastolic criteria for CCM. No mean differences were found in MELD-Na (15, IQR 11-19, vs 14, IQR 10-16.5, p0.1) or decompensations. The presence of hepatocellular carcinoma was higher in the CCM group (44.4% vs. 22.1% p<0.01).The median overall survival time on the waitlist was longer in the group without CCM compared to that in the CCM group (32 vs 22 months, p=0.04). In Cox regression analysis, the presence of CCM (HR 1.71 CI95% 1.09-2.68 p0.02), HCC (HR 2.37, CI95% 1.47-3.82 p<0.001) and higher MELD-Na (HR 1.14 CI95% 1.10-1.18, p<0.001) were predictors of mortality on the waiting list. There were no significant differences in survival between the groups post-transplantation.</p><p><strong>Conclusions: </strong>Our study revealed a lower prevalence of CCM in liver transplant candidates compared with previous reports. Moreover, it underscores that CCM was an independent predictor of mortality on a liver transplantation waitlist, highlighting its significant clinical implications. Further research is imperative to elucidate its precise impact on post-transplant survival.</p>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":" ","pages":"102141"},"PeriodicalIF":4.4,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145311947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}