Older people living with HIV: a population with high prevalence and severity of metabolic dysfunction-associated steatotic liver disease ‒ A cross-sectional study

IF 2 4区 医学 Q2 INFECTIOUS DISEASES
Brazilian Journal of Infectious Diseases Pub Date : 2026-09-01 Epub Date: 2026-09-15 DOI:10.1016/j.bjid.2026.105967
Rafaella Italiano Peixoto, Andrea Dória Batista, Armando Ykaro Soares de Oliveira, Ana Lúcia Coutinho Domingues, Paulo Sérgio Ramos de Araújo
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引用次数: 0

Abstract

Background

Among People Living With Human immunodeficiency virus (PLWH) chronic liver disease is a major cause of non-HIV-related death. Factors related to HIV and its treatment may amplify the impact of metabolic risk factors and aging, thus leading to a high frequency of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) among this population. This study aimed to evaluate the frequency and associated factors of MASLD and its severity in older PLWH, and secondarily, to assess the frequency of MASLD-related fibrosis.

Methods

This cross-sectional study included older PLWH followed at a referral center in northeastern Brazil. Hepatic steatosis was assessed by abdominal ultrasonography and liver fibrosis by point Shear-Wave Elastography (pSWE). Multivariable Poisson regression was performed to identify factors independently associated with hepatic steatosis and steatosis severity.

Results

Ninety-two older PLWH were included. Hepatic steatosis was identified in 53.3% (n = 49) of participants, of whom 29 (53%) had moderate-to-severe steatosis. Significant fibrosis (F2 or greater) was identified in 10.6% of participants with steatosis who underwent elastography. Increased waist circumference, higher body mass index, metabolic syndrome, higher HbA1c and triglyceride levels were associated with hepatic steatosis. In multivariate analysis, increased waist circumference remained the factor most strongly associated with hepatic steatosis (PR = 4.69; 95% CI 1.53–14.38; p = 0.007). Factors associated with moderate-to-severe steatosis included metabolic and social factors, higher Alanine Aminotransferase (ALT) levels, dolutegravir use, absence of darunavir exposure and higher CD4 nadir. After adjustment, lipodystrophy (aPR = 1.63; 95% CI 1.04–2.56; p = 0.033) and higher Alanine Aminotransferase (ALT) levels (aPR = 1.03; 95% CI 1.01–1.04; p = 0.001) remained independently associated with greater steatosis severity.

Conclusions

MASLD was highly prevalent among older PLWH, with a substantial proportion presenting moderate-to-severe steatosis and significant fibrosis. Metabolic and adiposity-related factors were independently associated with hepatic steatosis, while lipodystrophy and higher ALT levels were associated with greater steatosis severity.
老年艾滋病毒感染者:代谢功能障碍相关脂肪变性肝病高发和严重程度人群——一项横断面研究
背景:在人类免疫缺陷病毒(PLWH)感染者中,慢性肝病是非hiv相关死亡的主要原因。与HIV及其治疗相关的因素可能会放大代谢危险因素和衰老的影响,从而导致该人群中代谢功能障碍相关脂肪变性肝病(MASLD)的高频率。本研究旨在评估老年PLWH中MASLD的发生频率和相关因素及其严重程度,其次评估MASLD相关纤维化的发生频率。方法:这项横断面研究包括在巴西东北部转诊中心随访的老年PLWH。腹部超声检查肝脂肪变性,点剪切波弹性成像(pSWE)检查肝纤维化。采用多变量泊松回归来确定与肝脂肪变性和脂肪变性严重程度独立相关的因素。结果:纳入92例老年PLWH。53.3% (n = 49)的参与者有肝脂肪变性,其中29人(53%)有中度至重度脂肪变性。10.6%的脂肪变性患者接受弹性成像后发现显著纤维化(F2或更大)。腰围增加、体重指数升高、代谢综合征、HbA1c升高和甘油三酯水平升高与肝脂肪变性有关。在多变量分析中,腰围增加仍然是与肝脂肪变性最密切相关的因素(PR = 4.69; 95% CI 1.53-14.38; p = 0.007)。与中度至重度脂肪变性相关的因素包括代谢和社会因素、较高的谷丙转氨酶(ALT)水平、多替格拉韦使用、缺乏达那韦暴露和较高的CD4最低点。调整后,脂肪营养不良(aPR = 1.63; 95% CI 1.04-2.56; p = 0.033)和较高的丙氨酸转氨酶(ALT)水平(aPR = 1.03; 95% CI 1.01-1.04; p = 0.001)仍然与脂肪变性严重程度独立相关。结论:MASLD在老年PLWH中非常普遍,其中相当大比例表现为中度至重度脂肪变性和显著纤维化。代谢和肥胖相关因素与肝脂肪变性独立相关,而脂肪营养不良和高ALT水平与脂肪变性严重程度相关。
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来源期刊
CiteScore
5.50
自引率
0.00%
发文量
925
审稿时长
41 days
期刊介绍: The Brazilian Journal of Infectious Diseases is the official publication of the Brazilian Society of Infectious Diseases (SBI). It aims to publish relevant articles in the broadest sense on all aspects of microbiology, infectious diseases and immune response to infectious agents. The BJID is a bimonthly publication and one of the most influential journals in its field in Brazil and Latin America with a high impact factor, since its inception it has garnered a growing share of the publishing market.
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