Mikulic F L, Sagud M, Nikolac Perkovic M, Kudlek Mikulic S, Ganoci L, Bajs Janovic M, Janovic S, Filipcic Simunovic I, Mihaljevic Peles A, Bozicevic M, Bradas Z, Pivac N
University Hospital Centre Zagreb, Department of Emergency Medicine, Croatia.
School of Medicine, University of Zagreb, Croatia; University Hospital Center Zagreb, Department of Psychiatry and Psychological Medicine, Zagreb, Croatia.
Prog Neuropsychopharmacol Biol Psychiatry. 2025 Jan 10;136:111240. doi: 10.1016/j.pnpbp.2024.111240. Epub 2024 Dec 30.
Brain-derived neurotrophic factor (BDNF) is implicated in the etiology of schizophrenia, and peripheral BDNF levels are affected by the short-term antipsychotic treatment. However, the data on their long-term effects on BDNF levels are scarce, and there is no information whether BDNF levels change during sustained remission in relation to values in healthy individuals. The aim of the present study was to compare serum BDNF levels in patients in long-term remission and healthy controls. This study is an extension of our previous research on the effects of olanzapine and risperidone on serum BDNF in acute-episode patients with schizophrenia. Patients who remained in remission for at least 3 years on the same antipsychotic regimen (40 % of the initial cohort) were included. Symptoms were assessed by the Positive and Negative Syndrome Scale (PANSS). Serum BDNF levels were measured by ELISA in patients in remission (N = 20), evaluated at baseline, after 6 weeks of treatment and after 3 years of treatment, and in healthy individuals (N = 40). At baseline (p = 0.046) and after 6 weeks of treatment (p = 0.028), patients had significantly lower BDNF levels than controls. However, after 3 years of continuous antipsychotic maintenance treatment, serum BDNF levels were increased compared to baseline and values after 6 weeks of treatment in remitted patients, and were also significantly higher in patients than in healthy controls (p = 0.002). Antipsychotic medications appear to have distinct effects on serum BDNF levels in short-and long-term treatment. It remains to be determined if such finding may be related to potential neuroprotective effects of antipsychotic maintenance treatment.
脑源性神经营养因子(BDNF)与精神分裂症的病因有关,短期抗精神病药物治疗会影响外周BDNF水平。然而,关于它们对BDNF水平长期影响的数据很少,并且没有信息表明在持续缓解期间BDNF水平相对于健康个体的值是否会发生变化。本研究的目的是比较长期缓解患者和健康对照者的血清BDNF水平。本研究是我们之前关于奥氮平和利培酮对精神分裂症急性期患者血清BDNF影响研究的扩展。纳入了在相同抗精神病药物治疗方案下至少缓解3年的患者(初始队列的40%)。症状通过阳性和阴性症状量表(PANSS)进行评估。通过酶联免疫吸附测定法(ELISA)测量缓解期患者(N = 20)、健康个体(N = 40)在基线、治疗6周后和治疗3年后的血清BDNF水平。在基线时(p = 0.046)和治疗6周后(p = 0.028),患者的BDNF水平显著低于对照组。然而,在连续3年的抗精神病药物维持治疗后,缓解期患者的血清BDNF水平与基线和治疗6周后的水平相比有所升高,并且患者的BDNF水平也显著高于健康对照组(p = 0.002)。抗精神病药物在短期和长期治疗中似乎对血清BDNF水平有不同的影响。这种发现是否与抗精神病药物维持治疗的潜在神经保护作用有关还有待确定。