Clinical and pathological characteristics of metabolic dysfunction-associated steatotic liver disease and the key role of epigenetic regulation: implications for molecular mechanism and treatment

医学 脂肪性肝炎 脂肪肝 非酒精性脂肪肝 生物标志物 肝硬化 疾病 生物信息学 表观遗传学 代谢综合征 肝病 重症监护医学 人口 糖尿病 病理 内科学 内分泌学 生物 环境卫生 遗传学 基因
作者
Yijing Li,Lijie Li,Yishuo Zhang,Jing Lü,Xiaolei Tang,Chaoran Bi,Yanan Qu,Jingmei Chai
出处
期刊:Therapeutic Advances in Endocrinology and Metabolism [SAGE Publishing]
卷期号:16: 20420188251321602-20420188251321602 被引量:7
标识
DOI:10.1177/20420188251321602
摘要

Nonalcoholic fatty liver disease (NAFLD), also called metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent syndrome marked by liver fat accumulation in the absence of significant alcohol consumption, encompassing simple fatty liver, nonalcoholic steatohepatitis (NASH), and advanced stages such as fibrosis and cirrhosis. Its incidence has surged globally, impacting up to 40% of the population, with a doubling of cases in China over a decade. NASH, a severe form, can progress to liver cirrhosis and cancer, posing a substantial health burden, especially among individuals with type 2 diabetes. Projections indicate a steep rise in NASH cases, necessitating urgent interventions beyond lifestyle modifications, such as innovative pharmaceuticals. Early diagnosis is crucial, yet current tools have limitations, highlighting the need for noninvasive, scalable diagnostic approaches. Advances in imaging and biomarker identification offer hope for early detection. Epigenetic factors play a significant role in MASLD pathogenesis, regulating key molecular mechanisms. Addressing MASLD requires a multifaceted approach, integrating lifestyle interventions, pharmacotherapy, and emerging therapeutics, against the backdrop of an evolving landscape in disease management.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
口腔飞飞完成签到 ,获得积分10
刚刚
1秒前
ralph_liu完成签到,获得积分10
1秒前
闭着眼数星星完成签到,获得积分20
4秒前
liubai完成签到,获得积分10
5秒前
6秒前
6秒前
9秒前
9秒前
10秒前
11秒前
务实的以松完成签到,获得积分10
11秒前
顾矜应助dodo采纳,获得10
12秒前
勿明发布了新的文献求助10
12秒前
stone发布了新的文献求助10
13秒前
22完成签到,获得积分10
13秒前
guochang完成签到,获得积分10
14秒前
wxw发布了新的文献求助10
14秒前
14秒前
15秒前
Yeeee发布了新的文献求助10
15秒前
15秒前
科研通AI6.2应助重要冷之采纳,获得10
15秒前
Hello应助采薇采纳,获得10
15秒前
XiaoShu发布了新的文献求助20
15秒前
17秒前
19秒前
RYY发布了新的文献求助10
19秒前
guochang发布了新的文献求助10
19秒前
丘比特应助无23223采纳,获得10
20秒前
20秒前
大心完成签到,获得积分10
20秒前
kk发布了新的文献求助10
21秒前
22秒前
22秒前
23秒前
stone完成签到,获得积分10
23秒前
24秒前
24秒前
abcd完成签到,获得积分10
24秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Reducing Compassion Fatigue, Secondary Traumatic Stress and Burnout 600
Comparative Elite Sport Development Systems, Structures and Public Policy 600
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Auslegungsgeschichte 500
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7637373
求助须知:如何正确求助?哪些是违规求助? 9210973
关于积分的说明 19757588
捐赠科研通 7204676
什么是DOI,文献DOI怎么找? 3275647
关于科研通互助平台的介绍 2437328
邀请新用户注册赠送积分活动 2272834