The impact of childhood maltreatment, HIV status, and their interaction on mental health outcomes and markers of systemic inflammation in women.

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Biology of Sex Differences Pub Date : 2025-03-28 DOI:10.1186/s13293-025-00704-9
Amanda Arnold, Heqiong Wang, C Christina Mehta, Paula-Dene C Nesbeth, Brahmchetna Bedi, Caitlin Kirkpatrick, Caitlin A Moran, Abigial Powers, Alicia K Smith, Kimbi Hagen, M Neale Weitzmann, Ighovwerha Ofotokun, Cecile D Lahiri, Jessica A Alvarez, Arshed A Quyyumi, Gretchen N Neigh, Vasiliki Michopoulos
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Abstract

Background: Childhood maltreatment and HIV are both associated with a greater risk for adverse mental health, including posttraumatic stress disorder (PTSD), depression, and increased systemic inflammation. However, it remains unknown whether childhood maltreatment and HIV interact to exacerbate PTSD, depression, and inflammation in a manner that may further increase the risk of adverse health outcomes in people living with HIV. This study investigated the interaction between childhood maltreatment and HIV status on PTSD and depression symptom severity, and on peripheral concentrations of lipopolysaccharide (LPS) and high sensitivity C-reactive protein (hsCRP) in women. We hypothesized that women living with HIV (WLWH) who report high levels of childhood maltreatment exposure would show the greatest PTSD and depressive symptoms, as well as the highest concentrations of LPS and hsCRP.

Methods: We conducted a cross-sectional study of 116 women (73 WLWH and 43 women without HIV). Participants completed interviews to measure trauma exposure, including childhood maltreatment, and PTSD and depression symptoms. They also provided blood samples that were analyzed for LPS and hsCRP concentrations.

Results: Both women living with and without HIV reported high rates of trauma exposure and showed no statistically significant differences in overall rates of childhood maltreatment. Moderate to severe childhood maltreatment was associated with higher PTSD symptom severity (p =.005), greater depression severity (p =.005), and elevated plasma LPS concentrations (p =.045), regardless of HIV status. There were no effects of childhood maltreatment on hsCRP concentrations. There were no detectable significant effects of HIV status, or interactions between HIV status and childhood maltreatment, on PTSD and depression symptoms, or LPS and hsCRP concentrations (all p's > 0.05).

Conclusions: Our findings highlight the impact of childhood maltreatment on depression and PTSD symptoms and LPS concentrations in women. These results underscore the importance of trauma-informed health care in addressing childhood maltreatment to potentially improve both mental and physical health outcomes of adult women.

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儿童虐待、艾滋病毒状况及其相互作用对妇女心理健康结果和全身性炎症标志物的影响
背景:儿童虐待和艾滋病毒都与更大的不良心理健康风险相关,包括创伤后应激障碍(PTSD)、抑郁和全身性炎症增加。然而,尚不清楚儿童虐待和艾滋病毒是否以一种可能进一步增加艾滋病毒感染者不良健康结果风险的方式相互作用,从而加剧创伤后应激障碍、抑郁和炎症。本研究探讨儿童虐待与HIV感染状况对女性PTSD和抑郁症状严重程度的影响,以及外周脂多糖(LPS)和高敏c反应蛋白(hsCRP)浓度的影响。我们假设感染HIV的女性(WLWH)报告高水平的童年虐待暴露会表现出最大的创伤后应激障碍和抑郁症状,以及最高浓度的LPS和hsCRP。方法:我们对116名妇女进行了横断面研究,其中73名妇女患有艾滋病,43名妇女没有艾滋病毒。参与者完成了访谈,以测量创伤暴露,包括童年虐待、创伤后应激障碍和抑郁症状。他们还提供了血液样本,用于分析LPS和hsCRP浓度。结果:感染和未感染艾滋病毒的妇女都报告了较高的创伤暴露率,并且在儿童虐待的总体比率上没有统计学上的显着差异。中度至重度儿童虐待与较高的创伤后应激障碍症状严重程度(p = 0.005)、较高的抑郁严重程度(p = 0.005)和血浆LPS浓度升高(p = 0.045)相关,与HIV感染状况无关。儿童虐待对hsCRP浓度没有影响。在PTSD和抑郁症状、LPS和hsCRP浓度方面,HIV状态或HIV状态与儿童虐待之间的相互作用均未发现显著影响(p值均为0.05)。结论:我们的研究结果强调了童年虐待对女性抑郁、PTSD症状和LPS浓度的影响。这些结果强调了创伤知情卫生保健在解决儿童虐待问题方面的重要性,以潜在地改善成年妇女的身心健康结果。
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来源期刊
Biology of Sex Differences
Biology of Sex Differences ENDOCRINOLOGY & METABOLISM-GENETICS & HEREDITY
CiteScore
12.10
自引率
1.30%
发文量
69
审稿时长
14 weeks
期刊介绍: Biology of Sex Differences is a unique scientific journal focusing on sex differences in physiology, behavior, and disease from molecular to phenotypic levels, incorporating both basic and clinical research. The journal aims to enhance understanding of basic principles and facilitate the development of therapeutic and diagnostic tools specific to sex differences. As an open-access journal, it is the official publication of the Organization for the Study of Sex Differences and co-published by the Society for Women's Health Research. Topical areas include, but are not limited to sex differences in: genomics; the microbiome; epigenetics; molecular and cell biology; tissue biology; physiology; interaction of tissue systems, in any system including adipose, behavioral, cardiovascular, immune, muscular, neural, renal, and skeletal; clinical studies bearing on sex differences in disease or response to therapy.
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