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非酒精性脂肪性肝病或代谢功能障碍相关脂肪性肝病患者的血浆致动脉粥样硬化指数与全因死亡率和心血管疾病之间的关联

Association between atherogenic index of plasma and all-cause mortality and cardiovascular disease among individuals with non-alcoholic fatty liver disease or metabolic dysfunction-associated steatotic liver disease.

作者信息

Lv Jialu, Yao Jiangnan, Zheng Leyi, Shao Jiaxin, Jin Jijie, Zheng Qianrong, Teng Jiayi, Zhou Jianghua, Cai Fuman, Huang Pan, Jiang Xuepei

机构信息

College of Nursing, Wenzhou Medical University, Wenzhou, Zhejiang province, 325000, China.

Department of Cardiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, 325000, China.

出版信息

Diabetol Metab Syndr. 2025 May 14;17(1):153. doi: 10.1186/s13098-025-01715-7.

Abstract

BACKGROUND

Non-alcoholic fatty liver disease (NAFLD) and metabolic dysfunction-associated steatotic liver disease (MASLD) are common chronic liver diseases worldwide, both of which are closely associated with an increased risk of cardiovascular disease (CVD). Atherogenic index of plasma (AIP), as a biomarker of dyslipidemia, may predict CVD risk and mortality in these patients, but its specific role in patients with NAFLD and MASLD has not been studied in detail. This study adopted a cohort design, using data from the National Health and Nutrition Examination Survey (NHANES, 1988-1994) database, which was conducted by the Centers for Disease Control and Prevention. A total of 12,929 adult participants were analyzed. After participants were grouped according to AIP quartiles, the relationship between AIP levels and CVD risk was explored using multivariate logistic regression models and restricted cubic splines. The relationship between AIP levels and all-cause and CVD mortality was analyzed using multivariate Cox regression models.

RESULTS

Participants with the higher AIP quartiles showed high rates of CVD among participants with NAFLD (Quartile 1: 7.57%; Quartile 2: 10.00%; Quartile 3: 11.63%; Quartile 4: 15.08%). Participants with the higher AIP quartiles showed high rates of CVD among participants with MASLD (Quartile 1: 9.71%; Quartile 2: 11.30%; Quartile 3: 11.14%; Quartile 4: 15.00%). The findings suggested a linear association between the AIP index and the risk of CVD in participants with NAFLD or MASLD. AIP was significantly associated with CVD in the highest quartile of NAFLD or MASLD patients, and the adjusted hazard ratio indicated that high AIP levels were associated with high risk of CVD among participants with NAFLD (HR: 1.77, 95% CI: 1.24, 2.52) and MASLD (HR 1.76, 95% CI: 1.04, 2.98). In addition, higher AIP levels were also associated with increased all-cause mortality and CVD mortality among participants with NAFLD or MASLD.

CONCLUSION

This study showed that AIP is an effective tool for predicting CVD risk and mortality in patients with NAFLD and MASLD. Regular monitoring of AIP levels can help identify high-risk patients early and provide clinical risk assessment before intervention, thereby improving patient management and prognosis. Future studies need to further explore the role of AIP in different ethnic and economic conditions to optimize cardiovascular disease prevention and treatment strategies.

摘要

背景

非酒精性脂肪性肝病(NAFLD)和代谢功能障碍相关脂肪性肝病(MASLD)是全球常见的慢性肝病,二者均与心血管疾病(CVD)风险增加密切相关。血浆致动脉粥样硬化指数(AIP)作为血脂异常的生物标志物,可能预测这些患者的CVD风险和死亡率,但其在NAFLD和MASLD患者中的具体作用尚未得到详细研究。本研究采用队列设计,使用疾病控制和预防中心进行的美国国家健康和营养检查调查(NHANES,1988 - 1994)数据库中的数据。共分析了12,929名成年参与者。在根据AIP四分位数对参与者进行分组后,使用多变量逻辑回归模型和受限立方样条探讨AIP水平与CVD风险之间的关系。使用多变量Cox回归模型分析AIP水平与全因死亡率和CVD死亡率之间的关系。

结果

在NAFLD参与者中,AIP四分位数较高的参与者CVD发生率较高(四分位数1:7.57%;四分位数2:10.00%;四分位数3:11.63%;四分位数4:15.08%)。在MASLD参与者中,AIP四分位数较高的参与者CVD发生率较高(四分位数1:9.71%;四分位数2:11.30%;四分位数3:11.14%;四分位数4:15.00%)。研究结果表明,AIP指数与NAFLD或MASLD参与者的CVD风险之间存在线性关联。在NAFLD或MASLD患者的最高四分位数中,AIP与CVD显著相关,调整后的风险比表明,高AIP水平与NAFLD参与者(HR:1.77,95%CI:1.24,2.52)和MASLD参与者(HR 1.76,95%CI:1.04,2.98)的高CVD风险相关。此外,较高的AIP水平也与NAFLD或MASLD参与者的全因死亡率和CVD死亡率增加相关。

结论

本研究表明,AIP是预测NAFLD和MASLD患者CVD风险和死亡率的有效工具。定期监测AIP水平有助于早期识别高危患者,并在干预前提供临床风险评估,从而改善患者管理和预后。未来的研究需要进一步探索AIP在不同种族和经济条件下的作用,以优化心血管疾病的预防和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fa/12076888/8367befb97c5/13098_2025_1715_Fig1_HTML.jpg

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