{"title":"晚期慢性肝病肝脏脂肪含量低的预后意义:磁共振成像-PDFF的启示","authors":"Atsushi Nakamura, Tsubasa Yoshimura, Takeshi Ichikawa, Keiji Okuyama","doi":"10.1016/j.aohep.2024.101507","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction and Objectives</h3><p>The mechanisms of hepatic fat loss in late-stage metabolic dysfunction-associated fatty liver disease (MASLD) are enigmatic and the prognostic significance of low hepatic fat content (LHF) in chronic liver disease (CLD) is unknown. Proton density fat fraction (PDFF), measured by magnetic resonance imaging (MRI), is considered the most accurate noninvasive method for quantifying hepatic fat content. This study aimed to address these issues by evaluating PDFF.</p></div><div><h3>Patients and Methods</h3><p>This is a single-center, retrospective study involving 762 patients with CLD, measuring liver stiffness (LS) using MR elastography and PDFF using MRI. LHF was defined as a PDFF ≤ 2.7 % and hepatic reserve function was assessed using the albumin-bilirubin (ALBI) score. Multivariate analysis explored associations between variables.</p></div><div><h3>Results</h3><p>LHF was 27 % in the entire cohort, and PDFF was significantly decreased with LS ≥ 5.5 kPa (<em>p</em> < 0.05). On the multivariate analysis, low body mass index and ALBI score were independently associated with LHF (<em>p</em> < 0.05). In advanced CLD (<em>n</em> = 288), ALBI score and PDFF showed a significant negative correlation regardless of etiology (MASLD/non-MASLD: <em>r</em>= -0.613/-0.233), and the prevalence of LHF increased with progression of ALBI grade (<em>p</em> < 0.01 each). In addition, lower PDFF was associated with increased liver-related and all-cause mortality (<em>p</em> < 0.01), and Cox proportional hazards models extracted LHF as an independent prognostic factor, along with ALBI score and hepatocellular carcinoma (<em>p</em> < 0.05 each).</p></div><div><h3>Conclusions</h3><p>In ACLD, hepatic reserve dysfunction contributed to hepatic fat loss independent of nutritional status, suggesting that LHF may be a poor prognostic factor in all etiologies.</p></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"29 4","pages":"Article 101507"},"PeriodicalIF":3.7000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1665268124003016/pdfft?md5=5de8a56f03f73fecaabfdd25f91bea64&pid=1-s2.0-S1665268124003016-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Prognostic significance of low hepatic fat content in advanced chronic liver disease: MRI-PDFF insights\",\"authors\":\"Atsushi Nakamura, Tsubasa Yoshimura, Takeshi Ichikawa, Keiji Okuyama\",\"doi\":\"10.1016/j.aohep.2024.101507\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction and Objectives</h3><p>The mechanisms of hepatic fat loss in late-stage metabolic dysfunction-associated fatty liver disease (MASLD) are enigmatic and the prognostic significance of low hepatic fat content (LHF) in chronic liver disease (CLD) is unknown. Proton density fat fraction (PDFF), measured by magnetic resonance imaging (MRI), is considered the most accurate noninvasive method for quantifying hepatic fat content. This study aimed to address these issues by evaluating PDFF.</p></div><div><h3>Patients and Methods</h3><p>This is a single-center, retrospective study involving 762 patients with CLD, measuring liver stiffness (LS) using MR elastography and PDFF using MRI. LHF was defined as a PDFF ≤ 2.7 % and hepatic reserve function was assessed using the albumin-bilirubin (ALBI) score. Multivariate analysis explored associations between variables.</p></div><div><h3>Results</h3><p>LHF was 27 % in the entire cohort, and PDFF was significantly decreased with LS ≥ 5.5 kPa (<em>p</em> < 0.05). On the multivariate analysis, low body mass index and ALBI score were independently associated with LHF (<em>p</em> < 0.05). In advanced CLD (<em>n</em> = 288), ALBI score and PDFF showed a significant negative correlation regardless of etiology (MASLD/non-MASLD: <em>r</em>= -0.613/-0.233), and the prevalence of LHF increased with progression of ALBI grade (<em>p</em> < 0.01 each). In addition, lower PDFF was associated with increased liver-related and all-cause mortality (<em>p</em> < 0.01), and Cox proportional hazards models extracted LHF as an independent prognostic factor, along with ALBI score and hepatocellular carcinoma (<em>p</em> < 0.05 each).</p></div><div><h3>Conclusions</h3><p>In ACLD, hepatic reserve dysfunction contributed to hepatic fat loss independent of nutritional status, suggesting that LHF may be a poor prognostic factor in all etiologies.</p></div>\",\"PeriodicalId\":7979,\"journal\":{\"name\":\"Annals of hepatology\",\"volume\":\"29 4\",\"pages\":\"Article 101507\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-05-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1665268124003016/pdfft?md5=5de8a56f03f73fecaabfdd25f91bea64&pid=1-s2.0-S1665268124003016-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of hepatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1665268124003016\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of hepatology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1665268124003016","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
Prognostic significance of low hepatic fat content in advanced chronic liver disease: MRI-PDFF insights
Introduction and Objectives
The mechanisms of hepatic fat loss in late-stage metabolic dysfunction-associated fatty liver disease (MASLD) are enigmatic and the prognostic significance of low hepatic fat content (LHF) in chronic liver disease (CLD) is unknown. Proton density fat fraction (PDFF), measured by magnetic resonance imaging (MRI), is considered the most accurate noninvasive method for quantifying hepatic fat content. This study aimed to address these issues by evaluating PDFF.
Patients and Methods
This is a single-center, retrospective study involving 762 patients with CLD, measuring liver stiffness (LS) using MR elastography and PDFF using MRI. LHF was defined as a PDFF ≤ 2.7 % and hepatic reserve function was assessed using the albumin-bilirubin (ALBI) score. Multivariate analysis explored associations between variables.
Results
LHF was 27 % in the entire cohort, and PDFF was significantly decreased with LS ≥ 5.5 kPa (p < 0.05). On the multivariate analysis, low body mass index and ALBI score were independently associated with LHF (p < 0.05). In advanced CLD (n = 288), ALBI score and PDFF showed a significant negative correlation regardless of etiology (MASLD/non-MASLD: r= -0.613/-0.233), and the prevalence of LHF increased with progression of ALBI grade (p < 0.01 each). In addition, lower PDFF was associated with increased liver-related and all-cause mortality (p < 0.01), and Cox proportional hazards models extracted LHF as an independent prognostic factor, along with ALBI score and hepatocellular carcinoma (p < 0.05 each).
Conclusions
In ACLD, hepatic reserve dysfunction contributed to hepatic fat loss independent of nutritional status, suggesting that LHF may be a poor prognostic factor in all etiologies.
期刊介绍:
Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.