Obesity is associated with higher levels of circulating cytokines involved in the development of cardiovascular disease in people living with HIV.

IF 2.9 3区 医学 Q3 IMMUNOLOGY JAIDS Journal of Acquired Immune Deficiency Syndromes Pub Date : 2024-08-15 DOI:10.1097/QAI.0000000000003508
Stefano Savinelli, Pádraig McGettrick, Alejandro A Garcia Leon, Willard Tinago, Emma Haran, Elena Alvarez Barco, Alan L Landay, Patrick Wg Mallon, Eoin R Feeney
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Abstract

Background: Obesity is increasingly described in people living with HIV (PLWH), but its impact on immune activation and inflammation in HIV is still poorly characterised. We aimed to analyse the difference in circulating cytokines involved in pathways associated with co-morbidities in PLWH according to the presence or absence of obesity.

Methods: Age and sex matched PLWH with and without obesity (BMI ≥30 kg/m2) from a multicentre, prospective cohort were recruited with a 1:2 ratio. Twenty-three biomarkers covering pathways associated with systemic inflammation (hsCRP, IL-2, IL-6, TNFR1, TNFR2, TNF-α, IFN-γ, IL-18), coagulation (vWF, D-dimer, sCD40L), endothelial function (E-selectin, P-selectin, sICAM-1, sVCAM-1), atherosclerosis (MPO, Lp-PLA2), immune regulation (IL-1RA), innate immune activation (MIP-1, MCP-1, sCD163, sCD14) and microbial translocation (LBP) were measured in the two groups. Between-group difference in biomarkers were assessed using Mann-Whitney test. Associations between obesity and biomarkers were assessed using logistic regression adjusted for age, gender, ethnicity, smoking status, and antiretroviral therapy (ART).

Results: Ninety-nine ART-treated PLWH were included in the analysis (33 with obesity, 66 without obesity). PLWH with obesity had higher levels of hsCRP, IL-6, vWF, D-dimer, E-selectin, MPO, IL-1RA, and LBP. Six markers (hsCRP, IL-6, vWF, E-selectin, MPO, IL-1RA), reflecting systemic inflammation, coagulation and atherosclerosis pathways were associated with increased odds of obesity in the adjusted logistic regression model: hsCRP (aOR 2.7, 95% CI [1.7, 4.29]), IL-6 (3.77 [1.43, 9.93]), vWF (5.33 [1.51, 18.75]), E-selectin (6.28 [1.36, 29.04]), MPO (6.85 [1.87, 25.04]), IL-1RA (6.45 [2.28, 18.2]). No association was observed between obesity and markers of innate immune activation and gut microbial translocation.

Conclusions: Obesity in PLWH was associated with activation of systemic inflammatory, endothelial, atherosclerosis and coagulation pathways, rather than those associated with innate immune activation and gut microbial translocation. These pathways point towards an unfavourable cardiovascular profile in PLWH with obesity, which will have to be further explored in future studies on long-term outcomes.

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在艾滋病毒感染者中,肥胖与循环细胞因子水平升高有关,而循环细胞因子与心血管疾病的发生有关。
背景:越来越多的艾滋病病毒感染者(PLWH)患有肥胖症,但肥胖症对艾滋病病毒免疫活化和炎症的影响仍鲜为人知。我们的目的是根据肥胖与否,分析参与艾滋病病毒感染者共病相关途径的循环细胞因子的差异:方法:从一个多中心前瞻性队列中以 1:2 的比例招募了有肥胖症(体重指数≥30 kg/m2)和无肥胖症(体重指数≥30 kg/m2)的年龄和性别相匹配的 PLWH。23 种生物标记物涵盖了与全身炎症(hsCRP、IL-2、IL-6、TNFR1、TNFR2、TNF-α、IFN-γ、IL-18)、凝血(vWF、D-二聚体、sCD40L)、内皮功能(E-选择素、P-选择素、sICAM)相关的途径、P-选择素、sICAM-1、sVCAM-1)、动脉粥样硬化(MPO、Lp-PLA2)、免疫调节(IL-1RA)、先天性免疫激活(MIP-1、MCP-1、sCD163、sCD14)和微生物转位(LBP)。生物标志物的组间差异采用 Mann-Whitney 检验进行评估。采用逻辑回归评估肥胖与生物标志物之间的关系,并对年龄、性别、种族、吸烟状况和抗逆转录病毒疗法(ART)进行调整:99 名接受抗逆转录病毒疗法治疗的 PLWH 纳入了分析(肥胖 33 人,无肥胖 66 人)。肥胖 PLWH 的 hsCRP、IL-6、vWF、D-二聚体、E-选择素、MPO、IL-1RA 和 LBP 水平较高。在调整后的逻辑回归模型中,反映全身炎症、凝血和动脉粥样硬化途径的六种标记物(hsCRP、IL-6、vWF、E-选择素、MPO、IL-1RA)与肥胖几率增加有关:hsCRP(aOR 2.7,95% CI [1.7,4.29])、IL-6(3.77 [1.43,9.93])、vWF(5.33 [1.51,18.75])、E-选择素(6.28 [1.36,29.04])、MPO(6.85 [1.87,25.04])、IL-1RA(6.45 [2.28,18.2])。肥胖与先天性免疫激活和肠道微生物转位标志物之间没有关联:结论:白血病患者的肥胖与全身炎症、内皮、动脉粥样硬化和凝血途径的激活有关,而与先天性免疫激活和肠道微生物转位无关。这些途径表明,肥胖症 PLWH 患者的心血管状况不佳,这需要在今后的长期结果研究中进一步探讨。
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来源期刊
CiteScore
5.80
自引率
5.60%
发文量
490
审稿时长
3-6 weeks
期刊介绍: JAIDS: Journal of Acquired Immune Deficiency Syndromes​ seeks to end the HIV epidemic by presenting important new science across all disciplines that advance our understanding of the biology, treatment and prevention of HIV infection worldwide. JAIDS: Journal of Acquired Immune Deficiency Syndromes is the trusted, interdisciplinary resource for HIV- and AIDS-related information with a strong focus on basic and translational science, clinical science, and epidemiology and prevention. Co-edited by the foremost leaders in clinical virology, molecular biology, and epidemiology, JAIDS publishes vital information on the advances in diagnosis and treatment of HIV infections, as well as the latest research in the development of therapeutics and vaccine approaches. This ground-breaking journal brings together rigorously peer-reviewed articles, reviews of current research, results of clinical trials, and epidemiologic reports from around the world.
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