艾滋病毒感染者的肝脏代谢健康和代谢综合征的组成部分——它们与“健康”人群不同吗?

IF 1.8 4区 医学 Q3 INFECTIOUS DISEASES
HIV Research & Clinical Practice Pub Date : 2025-12-01 Epub Date: 2025-09-15 DOI:10.1080/25787489.2025.2555065
Michał Biały, Marcin Czarnecki, Małgorzata Inglot
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引用次数: 0

摘要

背景:代谢功能障碍相关脂肪变性肝病(MASLD)在人类免疫缺陷病毒(HIV)感染者中的患病率高于普通人群。造成这种情况的原因与艾滋病毒感染者中存在的其他危险因素有关,例如感染本身具有慢性免疫系统刺激和艾滋病毒治疗的不良影响。目的:我们旨在比较在弗罗茨瓦夫诊所接受抗逆转录病毒治疗的艾滋病毒感染者和对照组之间的代谢综合征组成和masld相关参数。方法:对计划于2021年4月至10月就诊的患者进行病例对照观察研究。我们收集了患者的血液样本和调查,并检查了代谢和肝脏相关参数。结果:在弗罗茨瓦夫一家门诊诊所接受治疗的60名患者被纳入研究。从健康志愿者中挑选了30名对照者。HIV感染者肝功能参数和HbA1c水平正常;他们的血脂异常患病率更高(68.33%比40%,p = 0.01),胰岛素抵抗的稳态模型评估(HOMA-IR)更高(2.16比1.24,p = 0.001)。在几个masld预测模型(FIB-4、NFS、NAFLD-LFS、Forns、TyG、MACK-3)中,HIV感染者和对照组之间存在差异;然而,它没有超过定义艾滋病毒感染者中脂肪变性/纤维化风险的较低临界值。结论:我们发现艾滋病毒感染者比对照组更容易受到代谢问题的困扰;然而,艾滋病毒感染者的代谢疾病似乎并不比一般波兰人口更严重。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liver metabolic health and the components of metabolic syndrome in people living with HIV - do they differ from those in a 'healthy' population?

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) has a greater prevalence in people living with human immunodeficiency virus (HIV) than in the general population. Reasons for this are connected with the presence of additional risk factors in people living with HIV, such as the infection itself with chronic immune system stimulation and HIV therapy adverse effects.

Objective: We aimed to compare metabolic syndrome components and MASLD-related parameters between people living with HIV on antiretroviral treatment at the clinic in Wroclaw and controls.

Methods: We conducted a case-control observational study on patients scheduled for visits from April to October 2021. We gathered blood samples and surveys from the patients and checked for metabolic and liver-related parameters.

Results: Sixty patients treated at an outpatient clinic in Wroclaw were enrolled into the study. Thirty controls were picked from healthy volunteers. People living with HIV had normal liver function parameters and HbA1c levels; they had a greater prevalence of dyslipidaemia (68.33% vs. 40%, p = 0.01), and higher homeostatic model assessment for insulin resistance (HOMA-IR) (2.16 vs. 1.24; p = 0.001). There was a difference between people living with HIV and controls in several MASLD-predictive models (FIB-4, NFS, NAFLD-LFS, Forns, TyG, MACK-3); however, it did not exceed the lower cut-off values for defining the risk of steatosis/fibrosis among people living with HIV.

Conclusions: We found people living with HIV to be more burdened by metabolic issues than our controls; however, people living with HIV did not appear to be more metabolically ill than the general Polish population.

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CiteScore
2.90
自引率
6.20%
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