University College Dublin, Ireland; Children's Health Ireland - Crumlin Hospital, Ireland; Lucena Clinic, St. John of God Community Services, Ireland.
Children's Health Ireland - Crumlin Hospital, Ireland; Children's Health Ireland - Tallaght Hospital, Ireland; Trinity College Dublin, Ireland.
Psychoneuroendocrinology. 2023 Dec;158:106390. doi: 10.1016/j.psyneuen.2023.106390. Epub 2023 Sep 15.
The underlying psychobiology that contributes to Anorexia Nervosa (AN) onset and disease progression remains unclear. New research is emerging suggesting a possible link between inflammation and a variety of mental illnesses. Alterations of cytokines may play a role in the pathogenesis of AN. Some studies have found differences in the cytokine profile of those with AN compared to healthy controls, but results are heterogeneous. The aim of this work was to systematically review existing studies investigating in-vivo cytokine production in those with AN before and after weight restoration compared to controls.
A comprehensive literature search of four electronic databases (PubMed, PsychInfo, EMBASE and CINAH) was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines to identify human in-vivo studies investigating the relationship between AN and cytokine production. Data extracted from included studies related to population characteristics (e.g. age, gender, mean mBMI/%IBW), cytokine measurement and relevant findings. Confounding factors (e.g. smoking status, co-morbid mental illness, menstruation status) were also collected.
36 studies were eligible for this systematic review of which the majority were conducted in Europe (77.8%) and involved female subjects (97.2%). Those with AN ranged in age from 13 to 47 years and had an illness duration of 3 months to 24 years. 15 candidate cytokines and 3 receptors were identified (TNF-alpha, IL-6, IL-1B, CRP, IL-2, IL-7, IL-10, IFN-γ, TNF-R2, IL-1 α, IL-15, TNF-R1, IL-17, IL-18, TGF-B1, IL-12, IL-6R and TGF-B2) exploring in-vivo levels in patients with AN and comparing to controls. TNF-alpha and IL-6 were the most extensively studied with IL-6 being significantly elevated in 4 out of 8 (50%) of longitudinal studies when comparing AN patients at baseline compared to post weight restoration. Following weight restoration, there was no difference in IL-6 levels when comparing to HC in 7 of 8 (87.5%) longitudinal studies examined.
The most promising cytokine potentially involved in the pathogenesis of AN appears to be IL-6, and possibly TNF-alpha pathways. The heterogeneity of clinical and methodology factors impedes the generalizability of results. Future studies may wish to address these methodological shortcomings as alterations in cytokine levels in AN could act as therapeutic targets assisting with weight restoration and psychopathology and may offer diagnostic potential.
导致神经性厌食症(AN)发病和疾病进展的潜在心理生物学机制仍不清楚。新的研究表明,炎症与各种精神疾病之间可能存在联系。细胞因子的改变可能在 AN 的发病机制中起作用。一些研究发现,与健康对照组相比,AN 患者的细胞因子谱存在差异,但结果存在异质性。本研究旨在系统综述目前关于 AN 患者在体重恢复前后与对照组相比体内细胞因子产生的研究。
根据系统评价和荟萃分析的首选报告项目(PRISMA)指南,对四个电子数据库(PubMed、PsychInfo、EMBASE 和 CINAH)进行了全面的文献检索,以确定研究 AN 与细胞因子产生之间关系的人类体内研究。从纳入的研究中提取与人口统计学特征(如年龄、性别、平均 mBMI/%IBW)、细胞因子测量和相关发现相关的数据。还收集了混杂因素(如吸烟状况、合并精神疾病、月经状况)。
共有 36 项研究符合本系统综述的条件,其中大多数研究在欧洲进行(77.8%),涉及女性受试者(97.2%)。AN 患者的年龄从 13 岁到 47 岁不等,患病时间从 3 个月到 24 年不等。共确定了 15 种候选细胞因子和 3 种受体(TNF-α、IL-6、IL-1B、CRP、IL-2、IL-7、IL-10、IFN-γ、TNF-R2、IL-1α、IL-15、TNF-R1、IL-17、IL-18、TGF-B1、IL-12、IL-6R 和 TGF-B2),研究了 AN 患者体内的水平,并与对照组进行了比较。TNF-α和 IL-6 是研究最多的两种细胞因子,其中 8 项(50%)纵向研究在比较 AN 患者基线时与体重恢复后时发现 IL-6 显著升高。在 8 项(87.5%)纵向研究中,比较 AN 患者体重恢复后的结果显示,IL-6 水平与 HC 无差异。
在 AN 的发病机制中最有希望涉及的细胞因子似乎是 IL-6,可能还有 TNF-α 途径。临床和方法因素的异质性阻碍了结果的可推广性。未来的研究可能希望解决这些方法学上的缺陷,因为 AN 中细胞因子水平的改变可能作为治疗靶点,有助于体重恢复和精神病理学,并可能具有诊断潜力。