Association of steatotic liver disease with all-cause and cardiovascular mortality among prehypertensive or hypertensive patients.

IF 4.5 3区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Journal of Global Health Pub Date : 2025-01-17 DOI:10.7189/jogh.15.04003
Shiwei Yan, Qian Li, Wenzhe Cao, Haolong Pei, Shihan Zhen, Qingyao Wu, Xueli Yang, Fengchao Liang
{"title":"Association of steatotic liver disease with all-cause and cardiovascular mortality among prehypertensive or hypertensive patients.","authors":"Shiwei Yan, Qian Li, Wenzhe Cao, Haolong Pei, Shihan Zhen, Qingyao Wu, Xueli Yang, Fengchao Liang","doi":"10.7189/jogh.15.04003","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Prehypertension and hypertension often coexist with non-alcoholic fatty liver disease (NAFLD) during the progression of cardiovascular disease (CVD). International academic liver societies have recently reached a consensus to replace NAFLD with the new term 'steatotic liver disease' (SLD). In this study, we aimed to evaluate the impact of different SLD subtypes on all-cause and CVD mortality in individuals with prehypertension or hypertension.</p><p><strong>Methods: </strong>We included 6074 adults from the National Health and Nutrition Examination Survey (2003-18). The US fatty liver index was used as the diagnostic criterion for SLD, and participants were classified into no SLD, metabolic dysfunction-associated steatotic liver disease (MASLD), metabolic dysfunction-associated and alcohol-related liver disease (MetALD), and alcohol-related liver disease (ALD). For cases of MASLD, MetALD, and ALD, we further assessed advanced fibrosis using the fibrosis-4 (FIB-4) index. Additionally, we calculated hazard ratios (HRs) and 95% confidence intervals (CIs) using Cox proportional hazards regression models to assess the associations of SLD subtypes and advanced fibrosis with all-cause and CVD mortality.</p><p><strong>Results: </strong>There were 3505 (57.7%) participants with no SLD, 1284 (21.1%) with MASLD, 777 (12.8%) with MetALD, and 508 (8.4%) with ALD. During a median follow-up period of 8.2 years, the risk of all-cause and CVD mortality progressively increased in participants with MASLD (HR = 1.28; 95% CI = 1.01-1.63 and HR = 1.55; 95% CI = 1.04-2.33, respectively), MetALD (HR = 1.41; 95% CI = 1.05-1.88 and HR = 1.78; 95% CI = 1.10-2.87, respectively), and ALD (HR = 1.83; 95% CI = 1.32-2.53 and HR = 1.80; 95% CI = 1.01-3.19, respectively). Among the individuals with MASLD, MetALD, and ALD, advanced fibrosis was also associated with an increased risk of all-cause and CVD mortality.</p><p><strong>Conclusions: </strong>Individuals with MASLD, MetALD, and ALD had a higher risk of all-cause and CVD mortality than those without SLD. Therefore, early intervention strategies targeting SLD prevention and management may help individuals with prehypertension and hypertension to improve their long-term health.</p>","PeriodicalId":48734,"journal":{"name":"Journal of Global Health","volume":"15 ","pages":"04003"},"PeriodicalIF":4.5000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11737813/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Global Health","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.7189/jogh.15.04003","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Prehypertension and hypertension often coexist with non-alcoholic fatty liver disease (NAFLD) during the progression of cardiovascular disease (CVD). International academic liver societies have recently reached a consensus to replace NAFLD with the new term 'steatotic liver disease' (SLD). In this study, we aimed to evaluate the impact of different SLD subtypes on all-cause and CVD mortality in individuals with prehypertension or hypertension.

Methods: We included 6074 adults from the National Health and Nutrition Examination Survey (2003-18). The US fatty liver index was used as the diagnostic criterion for SLD, and participants were classified into no SLD, metabolic dysfunction-associated steatotic liver disease (MASLD), metabolic dysfunction-associated and alcohol-related liver disease (MetALD), and alcohol-related liver disease (ALD). For cases of MASLD, MetALD, and ALD, we further assessed advanced fibrosis using the fibrosis-4 (FIB-4) index. Additionally, we calculated hazard ratios (HRs) and 95% confidence intervals (CIs) using Cox proportional hazards regression models to assess the associations of SLD subtypes and advanced fibrosis with all-cause and CVD mortality.

Results: There were 3505 (57.7%) participants with no SLD, 1284 (21.1%) with MASLD, 777 (12.8%) with MetALD, and 508 (8.4%) with ALD. During a median follow-up period of 8.2 years, the risk of all-cause and CVD mortality progressively increased in participants with MASLD (HR = 1.28; 95% CI = 1.01-1.63 and HR = 1.55; 95% CI = 1.04-2.33, respectively), MetALD (HR = 1.41; 95% CI = 1.05-1.88 and HR = 1.78; 95% CI = 1.10-2.87, respectively), and ALD (HR = 1.83; 95% CI = 1.32-2.53 and HR = 1.80; 95% CI = 1.01-3.19, respectively). Among the individuals with MASLD, MetALD, and ALD, advanced fibrosis was also associated with an increased risk of all-cause and CVD mortality.

Conclusions: Individuals with MASLD, MetALD, and ALD had a higher risk of all-cause and CVD mortality than those without SLD. Therefore, early intervention strategies targeting SLD prevention and management may help individuals with prehypertension and hypertension to improve their long-term health.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
高血压前期或高血压患者脂肪变性肝病与全因死亡率和心血管死亡率的关系
背景:在心血管疾病(CVD)的发展过程中,高血压前期和高血压常与非酒精性脂肪性肝病(NAFLD)共存。国际学术肝脏学会最近达成共识,用新的术语“脂肪变性肝病”(SLD)取代NAFLD。在这项研究中,我们旨在评估不同SLD亚型对高血压前期或高血压患者全因死亡率和CVD死亡率的影响。方法:纳入2003-18年全国健康与营养调查6074名成年人。采用美国脂肪肝指数作为SLD的诊断标准,将参与者分为无SLD、代谢功能障碍相关脂肪变性肝病(MASLD)、代谢功能障碍相关和酒精相关肝病(MetALD)和酒精相关肝病(ALD)。对于MASLD、MetALD和ALD病例,我们使用纤维化-4 (FIB-4)指数进一步评估晚期纤维化。此外,我们使用Cox比例风险回归模型计算风险比(hr)和95%置信区间(CIs),以评估SLD亚型和晚期纤维化与全因和CVD死亡率的关系。结果:无SLD患者3505例(57.7%),MASLD患者1284例(21.1%),MetALD患者777例(12.8%),ALD患者508例(8.4%)。在8.2年的中位随访期间,MASLD患者的全因和CVD死亡风险逐渐增加(HR = 1.28;95% CI = 1.01 ~ 1.63, HR = 1.55;95% CI = 1.04-2.33), MetALD (HR = 1.41;95% CI = 1.05 ~ 1.88, HR = 1.78;95% CI = 1.10-2.87)和ALD (HR = 1.83;95% CI = 1.32 ~ 2.53, HR = 1.80;95% CI = 1.01-3.19)。在MASLD、MetALD和ALD患者中,晚期纤维化也与全因死亡率和CVD死亡率增加相关。结论:MASLD、MetALD和ALD患者的全因死亡率和CVD死亡率高于无SLD患者。因此,针对SLD预防和管理的早期干预策略可能有助于高血压前期和高血压患者改善其长期健康状况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Global Health
Journal of Global Health PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH -
CiteScore
6.10
自引率
2.80%
发文量
240
审稿时长
6 weeks
期刊介绍: Journal of Global Health is a peer-reviewed journal published by the Edinburgh University Global Health Society, a not-for-profit organization registered in the UK. We publish editorials, news, viewpoints, original research and review articles in two issues per year.
期刊最新文献
Assessing the global data availability and characteristics of eight risk factors for road traffic injury: an evaluation study across 194 countries/territories, 2000-2019. Building an effective coverage cascade for antenatal care: linking of household survey and health facility assessment data in eight low- and middle-income countries. Building capacity to treat childhood cancer in Papua New Guinea: 'It's a multidisciplinary village'. Building medical oxygen systems in a resource-limited setting: the case of Cameroon. Coal: in a burning world, the dark side of energy still rules.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1