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Molecular Psychiatry· 2016Q1· Derleme

Kronik inflamatuar durumların tedavisinde anti-sitokin tedavisinin antidepresan aktivitesi: Klinik çalışmaların sistematik derlemesi ve meta-analizi

Antidepressant activity of anti-cytokine treatment: a systematic review and meta-analysis of clinical trials of chronic inflammatory conditions

Nils Kappelmann, Glyn Lewis, Robert Dantzer, Peter B. Jones ve diğerleri

Kısa özet

Kronik inflamatuar durumlara sahip bireylerde, plaseboya kıyasla anti-sitokin tedavileri anlamlı derecede depresif semptomları orta düzeyde bir etki büyüklüğüyle (SMD=0.40) azaltmıştır.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Anti-sitokin tedavileri, 7 RCT'nin meta-analizinde anlamlı bir antidepresan etki göstermiştir (SMD=0.40, %95 GA, 0.22-0.59).
  • En sık incelenen anti-tümör nekroz faktörü ilaçları, 0.33'lük bir SMD (95% GA; 0.06-0.60) vermiştir.
  • Adalimumab, etanercept, infliximab ve tocilizumab ile depresif semptomlarda iyileşmeler gözlemlenmiştir.
  • Antidepresan etki, başlangıçtaki semptom şiddetiyle ilişkiliydi ancak fiziksel hastalık, cinsiyet, yaş veya çalışma süresindeki iyileşmelerle ilişkili değildi.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (abstract)

Inflammatory cytokines are commonly elevated in acute depression and are associated with resistance to monoaminergic treatment. To examine the potential role of cytokines in the pathogenesis and treatment of depression, we carried out a systematic review and meta-analysis of antidepressant activity of anti-cytokine treatment using clinical trials of chronic inflammatory conditions where depressive symptoms were measured as a secondary outcome. Systematic search of the PubMed, EMBASE, PsycINFO and Cochrane databases, search of reference lists and conference abstracts, followed by study selection process yielded 20 clinical trials. Random effect meta-analysis of seven randomised controlled trials (RCTs) involving 2370 participants showed a significant antidepressant effect of anti-cytokine treatment compared with placebo (standardised mean difference (SMD)=0.40, 95% confidence interval (CI), 0.22-0.59). Anti-tumour necrosis factor drugs were most commonly studied (five RCTs); SMD=0.33 (95% CI; 0.06-0.60). Separate meta-analyses of two RCTs of adjunctive treatment with anti-cytokine therapy and eight non-randomised and/or non-placebo studies yielded similar small-to-medium effect estimates favouring anti-cytokine therapy; SMD=0.19 (95% CI, 0.00-0.37) and 0.51 (95% CI, 0.34-0.67), respectively. Adalimumab, etanercept, infliximab and tocilizumab all showed statistically significant improvements in depressive symptoms. Meta-regression exploring predictors of response found that the antidepressant effect was associated with baseline symptom severity (P=0.018) but not with improvement in primary physical illness, sex, age or study duration. The findings indicate a potentially causal role for cytokines in depression and that cytokine modulators may be novel drugs for depression in chronically inflamed subjects. The field now requires RCTs of cytokine modulators using depression as the primary outcome in subjects with high inflammation who are free of other physical illnesses.

Yazarların özeti; kaynağından alınmıştır. Molecular Psychiatry, 2016 · DOI ↗

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