Microbiota, Gender-Affirming Hormone Therapy, and Inflammatory Biomarkers in Transgender Women with HIV: Potential Implications for Cardiovascular Disease.

IF 1.8 Q2 PSYCHOLOGY, CLINICAL
Transgender health Pub Date : 2024-12-26 eCollection Date: 2026-04-01 DOI:10.1089/trgh.2024.0042
Tiffany R Glynn, Courtney A Broedlow, Violeta Rodriguez, Nicholas Fonseca Nogueira, Valeria Londono, Theodora Brophy, Suresh Pallikkuth, Margaret Roach, Savita Pahwa, Lydia A Fein, Barry E Hurwitz, Deborah Jones, Maria L Alcaide, Nichole Klatt, Claudia Martinez
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Abstract

Purpose: The intersecting disparities of human immunodeficiency virus (HIV) and cardiovascular disease (CVD) among transgender women have raised questions about the role of the gut microbiota and gender-affirming hormone therapy (GAHT) in the pathogenesis of CVD in the context of HIV. The purpose of this study was to provide an early exploration of the associations between these possible mechanisms driving inflammatory CVD risk markers among transgender women with HIV.

Methods: We conducted a preliminary study with 21 transgender women with HIV exploring the relationship between GAHT use (self-report), gut/rectal microbiota composition (rectal swabs), and inflammatory markers linked to CVD (plasma). Microbiota measures included alpha (richness, evenness, and Shannon diversity) and beta (Bray-Curtis, un/weighted UniFrac) diversity metrics. Inflammatory biomarkers included intestinal fatty-acid binding protein, monocyte chemoattractant protein-1, soluble CD163, intercellular adhesion molecule 1, tumor necrosis factor alpha (TNFa), soluble TNF receptor I (sTNF-I), sTNF-II, interleukin (IL)-6, IL-8, IL-1b, IL-1a, soluble CD14, d-dimer (domain dimer), vascular cell adhesion molecule 1, and high-sensitivity C-reactive protein. Wilcoxon rank sum test, log-level regression, Spearman's rho, permutational multivariate analysis of variance, and differential abundance testing assessed relationships between constructs.

Results: Key inflammatory markers linked to CVD were associated with GAHT use-an increased sTNF-I and sTNF-II levels and decreased IL-1a levels. Microbiota composition was not related to GAHT use but was variably associated with inflammatory biomarkers related to CVD risk.

Conclusions: Although preliminary, these findings suggest a potential association between inflammation linked to CVD risk and microbiota composition and GAHT. The results contribute to the characterization of interconnecting factors that may inform understanding and interventions to enhance overall health and well-being in transgender women with HIV. Further research is essential to elucidate the mechanisms underlying these associations, ultimately striving for health equity.

微生物群、性别确认激素治疗和感染艾滋病毒的跨性别妇女的炎症生物标志物:对心血管疾病的潜在影响
目的:人类免疫缺陷病毒(HIV)和心血管疾病(CVD)在跨性别女性中的交叉差异提出了关于肠道微生物群和性别确认激素治疗(GAHT)在HIV背景下CVD发病机制中的作用的问题。本研究的目的是对这些可能的机制之间的关联进行早期探索,这些机制驱动了感染艾滋病毒的跨性别女性炎症性心血管疾病风险标志物。方法:我们对21名感染HIV的跨性别女性进行了一项初步研究,探讨了GAHT使用(自我报告)、肠道/直肠微生物群组成(直肠拭子)和与CVD(血浆)相关的炎症标志物之间的关系。微生物群测量包括alpha(丰富度、均匀度和Shannon多样性)和beta (Bray-Curtis, UniFrac加权)多样性指标。炎症生物标志物包括肠道脂肪酸结合蛋白、单核细胞趋化蛋白-1、可溶性CD163、细胞间粘附分子1、肿瘤坏死因子α (TNFa)、可溶性TNF受体I (sTNF-I)、sTNF-II、白细胞介素(IL)-6、IL-8、IL-1b、IL-1a、可溶性CD14、d-二聚体(结构域二聚体)、血管细胞粘附分子1和高敏c反应蛋白。Wilcoxon秩和检验、对数水平回归、Spearman’s rho、多变量方差排列分析和差异丰度检验评估了构式之间的关系。结果:与CVD相关的关键炎症标志物与GAHT的使用相关——sTNF-I和sTNF-II水平升高,IL-1a水平降低。微生物群组成与GAHT的使用无关,但与CVD风险相关的炎症生物标志物有不同的相关性。结论:虽然是初步的,但这些发现表明与CVD风险相关的炎症与微生物群组成和GAHT之间存在潜在关联。这些结果有助于表征相互关联的因素,这些因素可能为了解和干预措施提供信息,以增强感染艾滋病毒的跨性别妇女的整体健康和福祉。进一步的研究对于阐明这些关联背后的机制,最终争取卫生公平至关重要。
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