• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非酒精性脂肪性肝病正常体重患者的体重变化与脂肪肝的缓解。

Weight change and resolution of fatty liver in normal weight individuals with nonalcoholic fatty liver disease.

机构信息

Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine.

Department of Clinical Research Design and Evaluation, SAIHST.

出版信息

Eur J Gastroenterol Hepatol. 2021 Dec 1;33(1S Suppl 1):e529-e534. doi: 10.1097/MEG.0000000000002158.

DOI:10.1097/MEG.0000000000002158
PMID:33867441
Abstract

OBJECTIVES

Obesity is a well-known risk factor for nonalcoholic fatty liver disease (NAFLD), and weight reduction is primarily recommended for managing the disease. However, some NAFLD patients have a normal weight (lean NAFLD), and whether weight reduction is also recommendable for lean NAFLD patients remains unclear.

METHODS

We conducted a longitudinal study of 16 738 adults (average age, 50.5 years; lean NAFLD, 2383 participants) with NAFLD at baseline who underwent repeated health check-up examinations, including bodyweight measurements and abdominal ultrasonography from January 2003 through December 2013.

RESULTS

During 68 389 person-years of follow-up (median follow-up of 3.00 years), 5819 patients had a fatty liver resolution. Compared with participants who had no weight reduction or increased weight, the fully adjusted hazard ratios for fatty liver resolution in participants with 0-4.9, 5-9.9 and 10% or more weight reduction were 1.67 [95% confidence interval (CI), 1.57-1.77], 3.36 (95% CI, 3.09-3.65) and 5.50 (95% CI, 4.83-6.27), respectively. The association between weight reduction and the fatty liver resolution was stronger in overweight/obese NAFLD participants but was also evident in lean NAFLD participants in a dose-dependent manner. In spline regression models, the association between weight change and the fatty liver resolution was linear among participants with normal weight.

CONCLUSION

There was a dose-dependent association between weight reduction and fatty liver resolution in both lean and overweight/obese NAFLD patients. This finding suggests weight reduction as a primary recommendation for lean NAFLD patients as in overweight/obese NAFLD patients.

摘要

目的

肥胖是众所周知的非酒精性脂肪性肝病(NAFLD)的危险因素,主要推荐减轻体重来治疗这种疾病。然而,一些 NAFLD 患者体重正常(瘦型 NAFLD),对于瘦型 NAFLD 患者是否也推荐减轻体重尚不清楚。

方法

我们对 16738 名基线时患有 NAFLD 的成年人(平均年龄为 50.5 岁;瘦型 NAFLD 患者 2383 名)进行了一项纵向研究,这些患者在 2003 年 1 月至 2013 年 12 月期间接受了重复的健康检查,包括体重测量和腹部超声检查。

结果

在 68389 人年的随访期间(中位随访时间为 3.00 年),5819 名患者的脂肪肝得到了缓解。与没有减轻体重或体重增加的参与者相比,体重减轻 0-4.9%、5-9.9%和 10%或更多的参与者,脂肪肝缓解的全调整风险比分别为 1.67(95%置信区间[CI],1.57-1.77)、3.36(95%CI,3.09-3.65)和 5.50(95%CI,4.83-6.27)。体重减轻与脂肪肝缓解之间的关联在超重/肥胖的 NAFLD 患者中更强,但在瘦型 NAFLD 患者中也呈剂量依赖性。在样条回归模型中,在体重正常的参与者中,体重变化与脂肪肝缓解之间的关系呈线性。

结论

在瘦型和超重/肥胖的 NAFLD 患者中,体重减轻与脂肪肝缓解之间存在剂量依赖性关联。这一发现表明,对于瘦型 NAFLD 患者,与超重/肥胖的 NAFLD 患者一样,减轻体重是主要推荐的治疗方法。

相似文献

1
Weight change and resolution of fatty liver in normal weight individuals with nonalcoholic fatty liver disease.非酒精性脂肪性肝病正常体重患者的体重变化与脂肪肝的缓解。
Eur J Gastroenterol Hepatol. 2021 Dec 1;33(1S Suppl 1):e529-e534. doi: 10.1097/MEG.0000000000002158.
2
Association between the lean nonalcoholic fatty liver disease and risk of incident type 2 diabetes in a healthy population of Northwest China: a retrospective cohort study with a 2-year follow-up period.瘦型非酒精性脂肪性肝病与中国西北地区健康人群 2 型糖尿病发病风险的关联:一项 2 年随访期的回顾性队列研究。
Front Endocrinol (Lausanne). 2023 Jun 26;14:1173757. doi: 10.3389/fendo.2023.1173757. eCollection 2023.
3
Liver and Cardiovascular Damage in Patients With Lean Nonalcoholic Fatty Liver Disease, and Association With Visceral Obesity.瘦型非酒精性脂肪性肝病患者的肝脏和心血管损伤,及其与内脏肥胖的关系。
Clin Gastroenterol Hepatol. 2017 Oct;15(10):1604-1611.e1. doi: 10.1016/j.cgh.2017.04.045. Epub 2017 May 26.
4
Nonalcoholic Fatty Liver Disease in Lean Subjects: Associations With Metabolic Dysregulation and Cardiovascular Risk-A Single-Center Cross-Sectional Study.瘦素型非酒精性脂肪性肝病:与代谢失调和心血管风险的相关性——一项单中心横断面研究。
Clin Transl Gastroenterol. 2021 Apr 5;12(4):e00326. doi: 10.14309/ctg.0000000000000326.
5
Lean non-alcoholic fatty liver disease and development of diabetes: a cohort study.瘦型非酒精性脂肪性肝病与糖尿病的发生:队列研究。
Eur J Endocrinol. 2019 Aug;181(2):185-192. doi: 10.1530/EJE-19-0143.
6
Relative fat mass at baseline and its early change may be a predictor of incident nonalcoholic fatty liver disease.基线时的相对脂肪量及其早期变化可能是非酒精性脂肪性肝病发病的一个预测指标。
Sci Rep. 2020 Oct 15;10(1):17491. doi: 10.1038/s41598-020-74659-9.
7
Risk of Cardiovascular Disease in Individuals With Nonobese Nonalcoholic Fatty Liver Disease.非肥胖非酒精性脂肪性肝病患者的心血管疾病风险。
Hepatol Commun. 2022 Feb;6(2):309-319. doi: 10.1002/hep4.1818. Epub 2021 Sep 2.
8
Association between weight change, waist circumference change, and the risk of nonalcoholic fatty liver disease in individuals with metabolically healthy overweight or obesity and metabolically unhealthy overweight or obesity.体重变化、腰围变化与代谢健康超重或肥胖与代谢不健康超重或肥胖个体中非酒精性脂肪性肝病风险的关系。
Obes Res Clin Pract. 2024 Mar-Apr;18(2):109-117. doi: 10.1016/j.orcp.2024.02.007. Epub 2024 Mar 4.
9
Systematic review with meta-analysis: the significance of histological disease severity in lean patients with nonalcoholic fatty liver disease.系统评价与荟萃分析:非酒精性脂肪性肝病瘦型患者组织学疾病严重程度的意义。
Aliment Pharmacol Ther. 2018 Jan;47(1):16-25. doi: 10.1111/apt.14401. Epub 2017 Oct 30.
10
Lean nonalcoholic fatty liver disease and risk of incident type 2 diabetes mellitus: A literature review and meta-analysis.非酒精性脂肪肝与 2 型糖尿病发病风险的关系:文献综述和荟萃分析。
Diabetes Res Clin Pract. 2023 Jun;200:110699. doi: 10.1016/j.diabres.2023.110699. Epub 2023 May 9.

引用本文的文献

1
Diagnosis and Management of Lean Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD): A Systematic Review.瘦素代谢功能障碍相关脂肪性肝病(MASLD)的诊断与管理:一项系统评价
Cureus. 2024 Oct 14;16(10):e71451. doi: 10.7759/cureus.71451. eCollection 2024 Oct.
2
Metabolic dysfunction associated fatty liver disease in healthy weight individuals.代谢功能障碍相关的健康体重个体的脂肪肝疾病。
Hepatol Int. 2024 Oct;18(Suppl 2):884-896. doi: 10.1007/s12072-024-10662-w. Epub 2024 Jul 25.
3
EASL-EASD-EASO Clinical Practice Guidelines on the Management of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).
EASL-EASD-EASO 临床实践指南:代谢功能障碍相关脂肪性肝病(MASLD)的管理。
Obes Facts. 2024;17(4):374-444. doi: 10.1159/000539371. Epub 2024 Jun 7.
4
MAFLD: an ideal framework for understanding disease phenotype in individuals of normal weight.MAFLD:理解正常体重个体疾病表型的理想框架。
Ther Adv Endocrinol Metab. 2024 May 27;15:20420188241252543. doi: 10.1177/20420188241252543. eCollection 2024.
5
Update in lean metabolic dysfunction-associated steatotic liver disease.瘦素代谢功能障碍相关脂肪性肝病的最新进展。
World J Hepatol. 2024 Mar 27;16(3):452-464. doi: 10.4254/wjh.v16.i3.452.
6
Hypercaloric low-carbohydrate high-fat diet protects against the development of nonalcoholic fatty liver disease in obese mice in contrast to isocaloric Western diet.与等热量的西方饮食相比,高热量低碳水化合物高脂肪饮食可预防肥胖小鼠非酒精性脂肪性肝病的发生。
Front Nutr. 2024 Mar 20;11:1366883. doi: 10.3389/fnut.2024.1366883. eCollection 2024.
7
Restoring skeletal muscle mass as an independent determinant of liver fat deposition improvement in MAFLD.恢复骨骼肌质量作为 MAFLD 肝脂肪沉积改善的独立决定因素。
Skelet Muscle. 2023 Dec 19;13(1):23. doi: 10.1186/s13395-023-00333-z.
8
Lifestyle interventions in nonalcoholic fatty liver disease.非酒精性脂肪性肝病的生活方式干预。
Nat Rev Gastroenterol Hepatol. 2023 Nov;20(11):708-722. doi: 10.1038/s41575-023-00800-4. Epub 2023 Jul 4.
9
The Role of Choline, Soy Isoflavones, and Probiotics as Adjuvant Treatments in the Prevention and Management of NAFLD in Postmenopausal Women.胆碱、大豆异黄酮和益生菌作为辅助治疗在绝经后妇女非酒精性脂肪性肝病的预防和管理中的作用。
Nutrients. 2023 Jun 8;15(12):2670. doi: 10.3390/nu15122670.
10
Weigh change across adulthood is related to the presence of NAFLD: results from NHANES III.成年后的体重变化与 NAFLD 的存在有关:来自 NHANES III 的结果。
J Transl Med. 2023 Feb 23;21(1):142. doi: 10.1186/s12967-023-04007-8.