Kalungi Allan, Womersley Jacqueline S, Kinyanda Eugene, Joloba Moses L, Ssembajjwe Wilber, Nsubuga Rebecca N, Seedat Soraya, Hemmings Sian M J
Department of Psychiatry, Stellenbosch University, Cape Town, South Africa.
Mental Health Project, MRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda.
Front Genet. 2021 Apr 23;12:649055. doi: 10.3389/fgene.2021.649055. eCollection 2021.
: Internalizing mental disorders (IMDs) among HIV-positive (HIV+) children and adolescents are associated with poor disease outcomes, such as faster HIV disease progression. Although it has been suggested that the development of IMDs is moderated by interaction of stressful life events and vulnerability factors, the underlying etiology is largely unknown. Serotonin transporter gene [solute carrier family 6 member A4 ()] and human tryptophan hydroxylase 2 gene () polymorphisms have been implicated in the development of IMDs. This study investigated the association between acute stress and IMDs, and moderation by chronic stress and genetic variants in and . : Acute stress acts through genetic and environmental vulnerability factors to increase the risk of developing IMDs. : Polymorphisms in (, rs25531, -rs25531, and VNTR) and (rs1843809, rs1386494, rs4570625, and rs34517220) were genotyped in 368 HIV+ children and adolescents (aged 5-17 years) with any internalizing mental disorder (depression, anxiety disorders, or posttraumatic stress disorder), and 368 age- and sex-matched controls, who were also HIV+. Chronic and acute stress categories were derived by hierarchical cluster analysis. Logistic regression analysis was used to assess the independent moderating effect of chronic stress and each selected polymorphism on the association between acute stress and IMDs. : We observed a statistically significant association between severe acute stress and IMDs ( = 0.001). Children and adolescents who experienced severe acute stress were twice as likely to develop IMDs, compared to children and adolescents who experienced mild acute stress ( = 0.001). Chronic stress interacted with severe acute stress to increase the risk of IMDs ( = 0.033). Acute stress was found to interact with -rs25531 haplotype to increase the risk for IMDs among Ugandan HIV+ children and adolescents ( = 0.049). We found no evidence for a combined interaction of acute stress, chronic stress, and -rs25531 on IMDs. : The odds of having an internalizing mental disorder (IMD) were higher among HIV+ children and adolescents who experienced severe acute stress compared to HIV+ children and adolescents who experienced mild acute stress. Chronic stress and -rs25531 independently moderated the association between acute stress and IMDs.
艾滋病毒呈阳性(HIV+)的儿童和青少年中的内化性精神障碍(IMDs)与不良疾病结局相关,如艾滋病毒疾病进展更快。尽管有人提出,应激性生活事件和脆弱因素的相互作用会调节IMDs的发生,但潜在病因在很大程度上尚不清楚。血清素转运体基因[溶质载体家族6成员A4()]和人类色氨酸羟化酶2基因()多态性与IMDs的发生有关。本研究调查了急性应激与IMDs之间的关联,以及慢性应激和基因变体在和中的调节作用。:急性应激通过遗传和环境脆弱因素起作用,增加患IMDs的风险。:对368名患有任何内化性精神障碍(抑郁症、焦虑症或创伤后应激障碍)的HIV+儿童和青少年(5 - 17岁)以及368名年龄和性别匹配的同样为HIV+的对照者进行了(,rs25531,-rs25531,和VNTR)和(rs1843809,rs1386494,rs4570625,和rs34517220)多态性的基因分型。慢性和急性应激类别通过层次聚类分析得出。采用逻辑回归分析来评估慢性应激和每个选定多态性对急性应激与IMDs之间关联的独立调节作用。:我们观察到严重急性应激与IMDs之间存在统计学上的显著关联( = 0.001)。与经历轻度急性应激的儿童和青少年相比,经历严重急性应激的儿童和青少年患IMDs的可能性是其两倍( = 0.001)。慢性应激与严重急性应激相互作用,增加了患IMDs的风险( = 0.033)。在乌干达HIV+儿童和青少年中,发现急性应激与-rs25531单倍型相互作用,增加了患IMDs的风险( = 0.049)。我们没有发现急性应激、慢性应激和-rs25531对IMDs存在联合相互作用的证据。:与经历轻度急性应激的HIV+儿童和青少年相比,经历严重急性应激的HIV+儿童和青少年患内化性精神障碍(IMD)的几率更高。慢性应激和-rs25531独立调节急性应激与IMDs之间的关联。