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
Shiwei Yan, Qian Li, Wenzhe Cao, Haolong Pei, Shihan Zhen, Qingyao Wu, Xueli Yang, Fengchao Liang
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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.

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。
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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.
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