Suppr超能文献

美国青少年的纤维化和脂肪性肝病按新命名法分类。

Fibrosis and steatotic liver disease in US adolescents according to the new nomenclature.

机构信息

Division of Liver Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

J Pediatr Gastroenterol Nutr. 2024 Aug;79(2):229-237. doi: 10.1002/jpn3.12230. Epub 2024 May 1.

Abstract

OBJECTIVE

To apply the new nomenclature for steatotic liver diseases (SLD), replacing nonalcoholic fatty liver disease (NAFLD) with metabolic dysfunction-associated steatotic liver disease (MASLD), in adolescents using National Health and Nutrition Examination Survey (NHANES) data.

METHODS

Among 1410 adolescents (12-19 years) in NHANES (2017-March, 2020), the controlled attenuation parameter (CAP) of transient elastography (TE) was used to define steatosis and fibrosis (TE ≥ 7.4 kPa). Obesity and alanine aminotransferase (ALT) ≥ 80 U/L were used to identify adolescents qualifying for hepatology referral according to practice guidelines. NAFLD was defined as liver steatosis without a specific exposure; it has no cardiometabolic risk factor requirement, unlike MASLD.

RESULTS

Steatosis (yes/no) is the first decision point in the new diagnostic protocol; however, criteria for steatosis are undefined. At the supplier (EchoSens)-recommended CAP threshold of 240 dB/m, 30.5% (95% confidence interval [CI]: 27.1%-34.0%) of adolescents had SLD and about 85% of adolescents with NAFLD met criteria for MASLD. The other 15% would receive an ambiguous diagnosis of either cryptogenic SLD or possible MASLD. At higher CAP thresholds, MASLD/NAFLD concordance increased and approached 100%. Among adolescents with MASLD-fibrosis, only 8.8% (95% CI: 0%-19.3%) had overweight/obese and ALT ≥ 80 U/L.

CONCLUSIONS

The new nomenclature highlights the high prevalence of liver steatosis. At the CAP threshold of 240 dB/m, however, approximately 15% of adolescents would receive an ambiguous diagnosis, which could lead to confusion and worry. Fewer than 10% of adolescents with MASLD-fibrosis had overweight/obese and ALT ≥ 80 U/L. Revised guidelines are needed to ensure that the other 90% receive appropriate referral and liver disease care.

摘要

目的

应用新的脂肪性肝病命名法,将代谢相关脂肪性肝病(MASLD)取代非酒精性脂肪性肝病(NAFLD),并基于国家健康和营养调查(NHANES)数据对青少年进行研究。

方法

在 NHANES(2017 年 3 月至 2020 年)中,对 1410 名(12-19 岁)青少年进行了瞬时弹性成像(TE)的受控衰减参数(CAP)检测,以定义脂肪变性和纤维化(TE≥7.4kPa)。肥胖和丙氨酸氨基转移酶(ALT)≥80U/L 用于根据实践指南确定符合肝科转诊条件的青少年。NAFLD 被定义为无特定暴露的肝脏脂肪变性;它没有代谢相关心血管危险因素的要求,这与 MASLD 不同。

结果

脂肪变性(有/无)是新诊断方案的第一个决策点,但脂肪变性的标准尚未确定。在供应商(EchoSens)推荐的 CAP 阈值 240dB/m 下,30.5%(95%置信区间[CI]:27.1%-34.0%)的青少年患有 SLD,大约 85%的患有 NAFLD 的青少年符合 MASLD 的标准。其余 15%的患者将得到不确定的隐匿性 SLD 或可能的 MASLD 诊断。在更高的 CAP 阈值下,MASLD/NAFLD 的一致性增加,并接近 100%。在患有 MASLD-纤维化的青少年中,仅有 8.8%(95%CI:0%-19.3%)存在超重/肥胖和 ALT≥80U/L。

结论

新的命名法突出了肝脏脂肪变性的高患病率。然而,在 CAP 阈值 240dB/m 下,大约 15%的青少年会得到不确定的诊断,这可能会导致困惑和担忧。在患有 MASLD-纤维化的青少年中,仅有不到 10%的患者存在超重/肥胖和 ALT≥80U/L。需要修订指南,以确保其余 90%的患者得到适当的转诊和肝脏疾病护理。

相似文献

1
Fibrosis and steatotic liver disease in US adolescents according to the new nomenclature.
J Pediatr Gastroenterol Nutr. 2024 Aug;79(2):229-237. doi: 10.1002/jpn3.12230. Epub 2024 May 1.
2
The prevalence and predictors of metabolic dysfunction-associated steatotic liver disease and fibrosis/cirrhosis among adolescents/young adults.
J Pediatr Gastroenterol Nutr. 2024 Jul;79(1):110-118. doi: 10.1002/jpn3.12219. Epub 2024 Apr 16.
3
Prevalence of steatotic liver disease, MASLD, MetALD and significant fibrosis in people with HIV in the United States.
Aliment Pharmacol Ther. 2024 Mar;59(5):666-679. doi: 10.1111/apt.17849. Epub 2023 Dec 29.
4
Prevalence and Predictors of Suspected Metabolic Dysfunction-Associated Steatotic Liver Disease in Adolescents in the United States.
Aliment Pharmacol Ther. 2025 May;61(9):1479-1488. doi: 10.1111/apt.70022. Epub 2025 Feb 12.
6
Liver and atherosclerotic risks of patients with cryptogenic steatotic liver disease.
Hepatol Int. 2024 Jun;18(3):943-951. doi: 10.1007/s12072-023-10624-8. Epub 2024 Jan 16.
7
Current burden of steatotic liver disease and fibrosis among adults in the United States, 2017-2023.
Clin Mol Hepatol. 2025 Apr;31(2):382-393. doi: 10.3350/cmh.2024.0987. Epub 2024 Nov 29.
8
Exploring the landscape of steatotic liver disease in the general US population.
Liver Int. 2023 Nov;43(11):2425-2433. doi: 10.1111/liv.15695. Epub 2023 Aug 17.

本文引用的文献

1
A multisociety Delphi consensus statement on new fatty liver disease nomenclature.
J Hepatol. 2023 Dec;79(6):1542-1556. doi: 10.1016/j.jhep.2023.06.003. Epub 2023 Jun 24.
2
A call for unity: The path towards a more precise and patient-centric nomenclature for NAFLD.
Hepatology. 2023 Jul 1;78(1):3-5. doi: 10.1097/HEP.0000000000000412. Epub 2023 May 22.
3
Nonalcoholic Fatty Liver Disease Prevalence Trends Among Adolescents and Young Adults in the United States, 2007-2016.
Hepatol Commun. 2021 Oct;5(10):1676-1688. doi: 10.1002/hep4.1760. Epub 2021 Jul 1.
6
Controlled Attenuation Parameter (CAP) with the XL Probe of the Fibroscan: A Comparative Study with the M Probe and Liver Biopsy.
Dig Dis Sci. 2017 Sep;62(9):2569-2577. doi: 10.1007/s10620-017-4638-3. Epub 2017 Jun 2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验