Inflammatory profiles of severe treatment-resistant depression

被引:90
作者
Strawbridge, Rebecca [1 ]
Hodsoll, John [2 ]
Powell, Timothy R. [3 ]
Hotopf, Matthew [1 ,4 ]
Hatch, Stephani L. [1 ]
Breen, Gerome [3 ]
Cleare, Anthony J. [1 ,4 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychol Med, London, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Biostat, London, England
[3] Kings Coll London, Inst Psychiat Psychol & Neurosci, Social Genet & Dev Psychiat Ctr, London, England
[4] South London & Maudsley NHS Fdn Trust, London, England
基金
英国医学研究理事会;
关键词
Inflammation; Treatment-resistant depression; Cytokines; Treatment response; MAJOR DEPRESSION; RATING-SCALE; CYTOKINES; DISORDER; ESCITALOPRAM; VALIDATION; COMMUNITY; PATHWAYS; UNIPOLAR; MINI;
D O I
10.1016/j.jad.2018.12.037
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Treatment-resistant depression (TRD) contributes substantially to the burden of mood disorders and is undoubtedly an important subpopulation in whom there are clear unmet treatment needs. Despite a paucity of research focusing specifically on TRD, recent studies indicate that inflammatory activity may be particularly elevated in these patients. Methods: 36 patients with TRD were investigated longitudinally before and after undertaking a specialist inpatient treatment program. 27 inflammatory proteins were compared between patients and a matched sample of non-depressed controls, as well as between treatment responders and non-responders. Treatment outcomes were calculated from depression severity scores before and after admission, and at a long-term follow-up 3-12 months after discharge. Results: TRD patients had higher levels of numerous inflammatory proteins than controls, and elevated inter-leukins 6 and 8, tumour necrosis factor, c-reactive protein and macrophage inflammatory protein-1 were associated with poorer treatment outcomes. A separate set of proteins (either anti-inflammatory in nature or attenuated at baseline) showed increases during treatment, regardless of clinical response. Participants with the greatest elevations in inflammation tended to be older, more cognitively impaired and more treatment-resistant at baseline. Limitations: The small sample and large number of comparisons examined in this study must be taken into account when interpreting these results. Conclusions: However, this study provides empirical support for theories that more severe, chronic or treatment-resistant depressive disorders are associated with dysregulated inflammatory activity. If a predictor or predictors of response in TRD are established, improved and targeted care might be more reliably provided to this vulnerable population.
引用
收藏
页码:42 / 51
页数:10
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