Laboratório de Neurociências Clínicas, Programa de Pós-Graduação em Saúde e Comportamento, Universidade Católica de Pelotas, Rua Gonçalves Chaves 373, CEP 96015560, Pelotas, RS, Brazil; Faculdade de Medicina, Universidade Federal de Pelotas, Avenida Duque de Caxias, 250, CEP 96030001, Fragata, Pelotas, RS, Brazil.
Laboratório de Neurociências Clínicas, Programa de Pós-Graduação em Saúde e Comportamento, Universidade Católica de Pelotas, Rua Gonçalves Chaves 373, CEP 96015560, Pelotas, RS, Brazil.
Gen Hosp Psychiatry. 2015 Jul-Aug;37(4):283-7. doi: 10.1016/j.genhosppsych.2015.03.016. Epub 2015 Mar 31.
Depressive symptoms have been frequently observed in association with immune activation. We prospectively evaluate depressive symptoms and risk factors for major depression in patients with hepatitis C virus treated with antiviral combined therapy.
Fifty patients were assessed during 1 year; the structured diagnostic interview - Mini International Neuropsychiatric Interview - was used to screen psychiatric disorders at the baseline and during the 4th and 12th week of antiviral therapy.
generalized estimating equations and pairwise comparisons with Bonferroni adjustment.
In our sample the prevalence of the Genotype 1 was 42%, and the pegylated interferon alpha plus ribavirin was the most prevalent treatment used for hepatitis C (86%). We found increased risk of depression in the 4th week (34%) but not in the 12th week (24%) compared with baseline values (20%) (P=0.040). In addition, we found differences between depression prevalence and hepatitis C genotypes, with higher odds in the 4th week compared to the baseline and 12th week [OR: 2.1(1.15-2.9); P=0.040]. Patients with the Genotype 2/3 had significantly lower odds of presenting depression compared to the Genotype 1 [OR: 0.3 (0.1-0.9); P=0.030].
This study provides evidence for an association between hepatitis C genotype and major depression, showing that besides immune activation, the Genotype 1 is associated with increased risk for psychiatric symptoms during the follow-up.
抑郁症状常与免疫激活有关。我们前瞻性评估了接受抗病毒联合治疗的丙型肝炎病毒患者的抑郁症状和重度抑郁症的危险因素。
50 名患者在 1 年内接受评估;在基线及抗病毒治疗第 4 周和第 12 周,使用结构化诊断访谈-迷你国际神经精神访谈-筛查精神障碍。
广义估计方程和 Bonferroni 调整后的两两比较。
在我们的样本中,基因型 1 的患病率为 42%,聚乙二醇干扰素α加利巴韦林是最常用于治疗丙型肝炎的药物(86%)。我们发现与基线值(20%)相比,第 4 周(34%)而非第 12 周(24%)的抑郁风险增加(P=0.040)。此外,我们发现抑郁患病率与丙型肝炎基因型之间存在差异,与基线和第 12 周相比,第 4 周的抑郁患病率更高[比值比:2.1(1.15-2.9);P=0.040]。与基因型 1 相比,基因型 2/3 的患者出现抑郁的可能性显著降低[比值比:0.3(0.1-0.9);P=0.030]。
本研究提供了丙型肝炎基因型与重度抑郁症之间存在关联的证据,表明除免疫激活外,基因型 1 与随访期间精神症状的发生风险增加有关。