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炎症生物标志物与抑郁症状之间的关联——糖尿病类型与抑郁症状簇之间的潜在差异

Associations between biomarkers of inflammation and depressive symptoms-potential differences between diabetes types and symptom clusters of depression.

作者信息

Herder Christian, Zhu Anna, Schmitt Andreas, Spagnuolo Maria C, Kulzer Bernhard, Roden Michael, Hermanns Norbert, Ehrmann Dominic

机构信息

Institute for Clinical Diabetology, German Diabetes Center (DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany.

German Center for Diabetes Research (DZD), München-Neuherberg, Germany.

出版信息

Transl Psychiatry. 2025 Jan 11;15(1):9. doi: 10.1038/s41398-024-03209-y.

Abstract

Inflammation is a probable biological pathway underlying the relationship between diabetes and depression, but data on differences between diabetes types and symptom clusters of depression are scarce. Therefore, this cross-sectional study aimed to compare associations of a multimarker panel of biomarkers of inflammation with depressive symptoms and its symptom clusters between people with type 1 diabetes (T1D) and type 2 diabetes (T2D). This cross-sectional study combined data from five studies including 1260 participants (n = 706 T1D, n = 454 T2D). Depressive symptoms were assessed using the Center for Epidemiological Studies-Depression Scale (CES-D). Serum levels of 92 biomarkers of inflammation were quantified with proximity extension assay technology. After quality control, 76 biomarkers of inflammation remained for statistical analysis. Associations between biomarkers and depressive symptom scores and clusters (cognitive-affective, somatic, anhedonia) were estimated with multivariable linear regression models. Nine biomarkers were positively associated with depressive symptoms in the total sample (CCL11/eotaxin, CCL25, CDCP1, FGF-21, IL-8, IL-10RB, IL-18, MMP-10, TNFRSF9; all p < 0.05) without interaction by diabetes type. Associations differed for eight biomarkers (p < 0.05). TNFβ was inversely associated with depressive symptoms in T1D, whereas three biomarkers (GDNF, IL-18R1, LIF-R) were positively associated with depressive symptoms in T2D. For the remaining four biomarkers (CD6, CD244, FGF-5, IFNγ) associations were not significant in either subgroup. Biomarker associations were more pronounced with somatic and anhedonia than with cognitive-affective symptoms. These results indicate that different proinflammatory pathways may contribute to depression in T1D and T2D and that there may be a symptom specificity in the link between subclinical inflammation and depression.

摘要

炎症可能是糖尿病与抑郁症之间关系的潜在生物学途径,但关于糖尿病类型与抑郁症症状群差异的数据却很匮乏。因此,这项横断面研究旨在比较1型糖尿病(T1D)和2型糖尿病(T2D)患者中,炎症生物标志物多指标组合与抑郁症状及其症状群之间的关联。这项横断面研究合并了五项研究的数据,包括1260名参与者(n = 706名T1D患者,n = 454名T2D患者)。使用流行病学研究中心抑郁量表(CES-D)评估抑郁症状。采用邻位延伸分析技术对92种炎症生物标志物的血清水平进行定量。经过质量控制后,保留76种炎症生物标志物用于统计分析。使用多变量线性回归模型估计生物标志物与抑郁症状评分及症状群(认知情感、躯体、快感缺失)之间的关联。在总样本中,9种生物标志物与抑郁症状呈正相关(CCL11/嗜酸性粒细胞趋化因子、CCL25、CDCP1、FGF-21、IL-8、IL-10RB、IL-18、MMP-10、TNFRSF9;所有p < 0.05),且不受糖尿病类型的交互影响。8种生物标志物的关联存在差异(p < 0.05)。TNFβ与T1D患者的抑郁症状呈负相关,而3种生物标志物(GDNF、IL-18R1、LIF-R)与T2D患者的抑郁症状呈正相关。对于其余4种生物标志物(CD6、CD244、FGF-5、IFNγ),在任一亚组中的关联均不显著。生物标志物与躯体及快感缺失症状的关联比与认知情感症状的关联更为明显。这些结果表明,不同的促炎途径可能导致T1D和T2D患者出现抑郁症,并且亚临床炎症与抑郁症之间的联系可能存在症状特异性。

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