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脂肪组织基因表达和血浆脂质组在HIV感染者心脏代谢疾病中的首要地位

The Primacy of Adipose Tissue Gene Expression and Plasma Lipidome in Cardiometabolic Disease in Persons With HIV.

作者信息

Bailin Samuel S, Ma Siyuan, Perry Andrew S, Terry James G, Carr John Jeffrey, Nair Sangeeta, Silver Heidi J, Shi Mingjian, Mashayekhi Mona, Kropski Jonathan A, Ferguson Jane F, Wanjalla Celestine N, Das Suman R, Shah Ravi, Koethe John R, Gabriel Curtis L

机构信息

Department of Medicine, Division of Infectious Diseases, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

出版信息

J Infect Dis. 2025 Feb 20;231(2):e407-e418. doi: 10.1093/infdis/jiae532.

Abstract

BACKGROUND

Persons with HIV (PWH) on contemporary antiretroviral therapy (ART) are at elevated risk for developing age-related cardiometabolic diseases. We hypothesized that integrative analysis of cross-tissue, multimodal data from PWH could provide insight into molecular programming that defines cardiometabolic phenotypes in this high-risk group.

METHODS

We enrolled 93 PWH without diabetes who were virologically suppressed on contemporary ART and obtained measures of insulin resistance, glucose intolerance, and adiposity. We performed circulating lipidomics, proteomics, and metabolomics, as well as subcutaneous adipose tissue (SAT) bulk transcriptomics, and used multiomics factor analysis (MOFA) to perform integrative analyses of these datasets.

RESULTS

The median age was 43 years, median body mass index 30.8 kg/m2, 81% were male, and 56% were self-identified non-Hispanic White. We identified a specific MOFA factor associated with visceral adipose tissue volume (ρ = -0.43), homeostasis model assessment 2 insulin resistance score (ρ = -0.52), liver density (ρ = 0.43), and other cardiometabolic risk factors, which explained more variance in the SAT transcriptome and circulating lipidome compared with the circulating proteome and metabolome. Gene set enrichment analysis of this factor showed extracellular matrix and inflammatory pathways that primarily mapped to SAT myeloid cells and adipose progenitor cells using single-cell deconvolution. Lipidomic analysis showed that this factor was significantly enriched for triacylglycerol and diacylglycerol species.

CONCLUSIONS

Our multiomic analysis demonstrated coordinated, multitissue molecular reprogramming in virologically suppressed PWH with elevated cardiometabolic disease risk. Longitudinal studies of PWH with assessments of adipose tissue and lipid handling are necessary to understand mechanisms of cardiometabolic disease in PWH. Clinical Trials Registration. NCT04451980.

摘要

背景

接受当代抗逆转录病毒疗法(ART)的艾滋病毒感染者(PWH)患与年龄相关的心脏代谢疾病的风险升高。我们假设,对PWH的跨组织多模态数据进行综合分析,能够深入了解在这一高危人群中定义心脏代谢表型的分子编程。

方法

我们招募了93名未患糖尿病且在当代ART治疗下病毒得到抑制的PWH,并测量了胰岛素抵抗、葡萄糖耐量和肥胖情况。我们进行了循环脂质组学、蛋白质组学和代谢组学分析,以及皮下脂肪组织(SAT)整体转录组学分析,并使用多组学因子分析(MOFA)对这些数据集进行综合分析。

结果

中位年龄为43岁,中位体重指数为30.8kg/m²,81%为男性,56%自我认定为非西班牙裔白人。我们确定了一个与内脏脂肪组织体积(ρ = -0.43)、稳态模型评估2胰岛素抵抗评分(ρ = -0.52)、肝脏密度(ρ = 0.43)和其他心脏代谢危险因素相关的特定MOFA因子,与循环蛋白质组和代谢组相比,该因子在SAT转录组和循环脂质组中解释了更多的变异。对该因子进行基因集富集分析,结果显示细胞外基质和炎症途径主要通过单细胞反卷积映射到SAT髓样细胞和脂肪祖细胞。脂质组学分析表明,该因子在三酰甘油和二酰甘油种类中显著富集。

结论

我们的多组学分析表明,在病毒得到抑制但心脏代谢疾病风险升高的PWH中存在协调的多组织分子重编程。有必要对PWH进行纵向研究,并评估脂肪组织和脂质处理情况,以了解PWH心脏代谢疾病的发病机制。临床试验注册。NCT04451980。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653d/11841643/9b9e3543a3e9/jiae532_ga.jpg

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