{"title":"将 FIB-4 作为代谢功能障碍相关性脂肪肝 (MASLD) 纤维化前期的筛查和疾病监测方法","authors":"Stewart G. Albert, Emily M. Wood","doi":"10.1016/j.jdiacomp.2024.108777","DOIUrl":null,"url":null,"abstract":"<div><h3>Aims</h3><p>Guidelines emphasize screening high-risk patients for metabolic dysfunction-associated steatotic liver disease (MASLD) with a calculated FIB-4 score for therapy to reverse fibrosis. We aimed to determine whether FIB-4 can effectively screen and monitor changes in steatohepatitis (MASH).</p></div><div><h3>Methods</h3><p>Data were retrieved from the NIDDK-CR R4R central repository, of the CRN/PIVENS (pioglitazone vs vitamin E vs placebo) trial of adult patients without diabetes mellitus and with MASLD.</p></div><div><h3>Results</h3><p>220 patients with MASLD had alanine transaminase (ALT), aspartate aminotransferase (AST) and platelet count, to calculate FIB-4, and repeat liver biopsies for histological MASLD activity scores (NAS). Compared to NAS score of 2, Fib-4 was higher at NAS 5) (<em>p</em> = 0.03), and NAS score of 6 (<em>p</em> = 0.02). FIB-4 correlated with cellular ballooning (<em>r</em> = 0.309, <em>p</em> < 0.001). Levels of ALT (ANOVA, <em>p</em> = 0.016) and AST (ANOVA <em>p</em> = 0.0008) were associated with NAS. NAS improved with pioglitazone by 39 %, <em>p</em> < 0.001 and with vitamin E by 36 %, <em>p</em> < 0.001. Pioglitazone and vitamin E both improved histological sub-scores for steatosis, and inflammation, without statistical changes in fibrosis grade. Changes in FIB-4 correlated with changes in NAS (<em>r</em> = 0.237, <em>p</em> < 0.001).</p></div><div><h3>Conclusions</h3><p>In this post hoc analysis, changes in FIB-4 were associated with changes of steatohepatitis. Medication known to treat steatohepatitis, may be considered, before the onset of advanced fibrosis.</p></div>","PeriodicalId":15659,"journal":{"name":"Journal of diabetes and its complications","volume":"38 7","pages":"Article 108777"},"PeriodicalIF":2.9000,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"FIB-4 as a screening and disease monitoring method in pre-fibrotic stages of metabolic dysfunction-associated fatty liver disease (MASLD)\",\"authors\":\"Stewart G. Albert, Emily M. Wood\",\"doi\":\"10.1016/j.jdiacomp.2024.108777\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aims</h3><p>Guidelines emphasize screening high-risk patients for metabolic dysfunction-associated steatotic liver disease (MASLD) with a calculated FIB-4 score for therapy to reverse fibrosis. We aimed to determine whether FIB-4 can effectively screen and monitor changes in steatohepatitis (MASH).</p></div><div><h3>Methods</h3><p>Data were retrieved from the NIDDK-CR R4R central repository, of the CRN/PIVENS (pioglitazone vs vitamin E vs placebo) trial of adult patients without diabetes mellitus and with MASLD.</p></div><div><h3>Results</h3><p>220 patients with MASLD had alanine transaminase (ALT), aspartate aminotransferase (AST) and platelet count, to calculate FIB-4, and repeat liver biopsies for histological MASLD activity scores (NAS). Compared to NAS score of 2, Fib-4 was higher at NAS 5) (<em>p</em> = 0.03), and NAS score of 6 (<em>p</em> = 0.02). FIB-4 correlated with cellular ballooning (<em>r</em> = 0.309, <em>p</em> < 0.001). Levels of ALT (ANOVA, <em>p</em> = 0.016) and AST (ANOVA <em>p</em> = 0.0008) were associated with NAS. NAS improved with pioglitazone by 39 %, <em>p</em> < 0.001 and with vitamin E by 36 %, <em>p</em> < 0.001. Pioglitazone and vitamin E both improved histological sub-scores for steatosis, and inflammation, without statistical changes in fibrosis grade. Changes in FIB-4 correlated with changes in NAS (<em>r</em> = 0.237, <em>p</em> < 0.001).</p></div><div><h3>Conclusions</h3><p>In this post hoc analysis, changes in FIB-4 were associated with changes of steatohepatitis. Medication known to treat steatohepatitis, may be considered, before the onset of advanced fibrosis.</p></div>\",\"PeriodicalId\":15659,\"journal\":{\"name\":\"Journal of diabetes and its complications\",\"volume\":\"38 7\",\"pages\":\"Article 108777\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of diabetes and its complications\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S105687272400103X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of diabetes and its complications","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S105687272400103X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
摘要
目的指南强调通过计算 FIB-4 评分筛查代谢功能障碍相关性脂肪性肝病 (MASLD) 的高危患者,以便进行逆转纤维化治疗。我们的目的是确定 FIB-4 是否能有效筛查和监测脂肪性肝炎 (MASH) 的变化。方法从 NIDDK-CR R4R 中央资料库中检索了 CRN/PIVENS(吡格列酮 vs 维生素 E vs 安慰剂)试验的数据,该试验的对象是无糖尿病且患有 MASLD 的成年患者。结果 220 名 MASLD 患者接受了丙氨酸转氨酶 (ALT)、天门冬氨酸转氨酶 (AST) 和血小板计数检查,以计算 FIB-4,并重复肝活检以进行组织学 MASLD 活性评分 (NAS)。与 NAS 评分为 2 分相比,FIB-4 在 NAS 评分为 5 分时更高(P = 0.03),在 NAS 评分为 6 分时更高(P = 0.02)。FIB-4 与细胞气球相关(r = 0.309,p < 0.001)。ALT(方差分析,p = 0.016)和 AST(方差分析,p = 0.0008)水平与 NAS 相关。服用吡格列酮后,NAS 的改善率为 39%,p <0.001;服用维生素 E 后,NAS 的改善率为 36%,p <0.001。吡格列酮和维生素 E 均能改善脂肪变性和炎症的组织学分项评分,但纤维化等级无统计学变化。结论在这项事后分析中,FIB-4 的变化与脂肪性肝炎的变化相关。在出现晚期纤维化之前,可以考虑使用已知的治疗脂肪性肝炎的药物。
FIB-4 as a screening and disease monitoring method in pre-fibrotic stages of metabolic dysfunction-associated fatty liver disease (MASLD)
Aims
Guidelines emphasize screening high-risk patients for metabolic dysfunction-associated steatotic liver disease (MASLD) with a calculated FIB-4 score for therapy to reverse fibrosis. We aimed to determine whether FIB-4 can effectively screen and monitor changes in steatohepatitis (MASH).
Methods
Data were retrieved from the NIDDK-CR R4R central repository, of the CRN/PIVENS (pioglitazone vs vitamin E vs placebo) trial of adult patients without diabetes mellitus and with MASLD.
Results
220 patients with MASLD had alanine transaminase (ALT), aspartate aminotransferase (AST) and platelet count, to calculate FIB-4, and repeat liver biopsies for histological MASLD activity scores (NAS). Compared to NAS score of 2, Fib-4 was higher at NAS 5) (p = 0.03), and NAS score of 6 (p = 0.02). FIB-4 correlated with cellular ballooning (r = 0.309, p < 0.001). Levels of ALT (ANOVA, p = 0.016) and AST (ANOVA p = 0.0008) were associated with NAS. NAS improved with pioglitazone by 39 %, p < 0.001 and with vitamin E by 36 %, p < 0.001. Pioglitazone and vitamin E both improved histological sub-scores for steatosis, and inflammation, without statistical changes in fibrosis grade. Changes in FIB-4 correlated with changes in NAS (r = 0.237, p < 0.001).
Conclusions
In this post hoc analysis, changes in FIB-4 were associated with changes of steatohepatitis. Medication known to treat steatohepatitis, may be considered, before the onset of advanced fibrosis.
期刊介绍:
Journal of Diabetes and Its Complications (JDC) is a journal for health care practitioners and researchers, that publishes original research about the pathogenesis, diagnosis and management of diabetes mellitus and its complications. JDC also publishes articles on physiological and molecular aspects of glucose homeostasis.
The primary purpose of JDC is to act as a source of information usable by diabetes practitioners and researchers to increase their knowledge about mechanisms of diabetes and complications development, and promote better management of people with diabetes who are at risk for those complications.
Manuscripts submitted to JDC can report any aspect of basic, translational or clinical research as well as epidemiology. Topics can range broadly from early prediabetes to late-stage complicated diabetes. Topics relevant to basic/translational reports include pancreatic islet dysfunction and insulin resistance, altered adipose tissue function in diabetes, altered neuronal control of glucose homeostasis and mechanisms of drug action. Topics relevant to diabetic complications include diabetic retinopathy, neuropathy and nephropathy; peripheral vascular disease and coronary heart disease; gastrointestinal disorders, renal failure and impotence; and hypertension and hyperlipidemia.