Department of Chemistry, College of Science, University of Kufa, Iraq.
Clinical Analysis Department, College of Pharmacy, Hawler Medical University, Havalan City, Erbil, Iraq.
J Affect Disord. 2021 Mar 1;282:644-655. doi: 10.1016/j.jad.2020.12.089. Epub 2020 Dec 28.
Transfusion dependent thalassemia (TDT) patients are treated with continued blood transfusions and show a higher prevalence of depression. TDT with consequent iron overload and inflammation is associated with increased severity of depressive symptoms in TDT children.
To construct a pathway-phenotype which combines iron overload and neuro-immune biomarkers with depressive symptom subdomains in TDT children.
We measured iron status parameters (iron, ferritin, transferrin saturation percentage) and inflammatory (interleukin-1β and tumour necrosis factor-α) biomarkers in TDT (n=111) and healthy (n=53) children and analyzed the results using machine learning.
Cluster analysis separated TDT children with depression from those without depression and revealed two depressive subgroups one with low self-esteem and another with increased social-irritability scores. Exploratory factor analysis validated four depressive symptom dimensions as reliable constructs, namely key depressive, physiosomatic, lowered self-esteem and social-irritability dimensions. Partial Least Squares showed that 73.0% of the variance in a latent vector extracted from those four clinical subdomains, immune-inflammatory and iron overload biomarkers was explained by exposure variables including the number of blood transfusions and hospitalizations and use of deferoxamine. The exposure data, iron and immune biomarkers, and symptom subdomains are reflective manifestations of a single latent trait, which shows internal consistency reliability and predictive relevance.
The nomological network combining exposure, pathways and behavioral phenome manifestations provides an index of overall severity and disease risk and, therefore, constitutes a new drug target, indicating that iron overload and immune activation should be targeted to treat depression due to TDT.
依赖输血的地中海贫血症(TDT)患者需要持续输血治疗,且更易出现抑郁症状。TDT 患者因铁过载和炎症,导致抑郁症状加重。
构建一个将铁过载和神经免疫生物标志物与 TDT 儿童抑郁症状亚领域相结合的途径表型。
我们测量了 TDT(n=111)和健康儿童(n=53)的铁状态参数(铁、铁蛋白、转铁蛋白饱和度)和炎症(白细胞介素-1β和肿瘤坏死因子-α)生物标志物,并使用机器学习分析结果。
聚类分析将有抑郁症状的 TDT 儿童与无抑郁症状的儿童区分开来,并揭示了两个具有不同抑郁亚组的儿童,一个表现为自尊心低下,另一个表现为社会激惹评分增加。探索性因子分析验证了四个抑郁症状维度是可靠的结构,即主要抑郁、生理躯体、自尊心降低和社会激惹维度。偏最小二乘法显示,从这四个临床亚领域、免疫炎症和铁过载生物标志物中提取的潜在向量的 73.0%的方差可由暴露变量解释,包括输血和住院次数以及去铁胺的使用。暴露数据、铁和免疫生物标志物以及症状亚领域是单一潜在特征的反映表现,具有内部一致性可靠性和预测相关性。
结合暴露、途径和行为表型表现的关联网络提供了整体严重程度和疾病风险的指标,因此构成了一个新的药物靶点,表明铁过载和免疫激活应成为治疗 TDT 相关抑郁的目标。