Psychiatric Center Copenhagen, Copenhagen Affective Disorder Research Center (CADIC) Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Psychiatric Center Copenhagen, Copenhagen Affective Disorder Research Center (CADIC) Rigshospitalet, University of Copenhagen, Copenhagen, Denmark; Department of Psychology, University of Copenhagen, Copenhagen, Denmark.
Eur Neuropsychopharmacol. 2018 Mar;28(3):361-368. doi: 10.1016/j.euroneuro.2018.01.008. Epub 2018 Feb 10.
Cognitive deficits are common in patients with bipolar disorder (BD) in remission and may be associated with glycogen synthase kinase-3 (GSK-3) activity, which is inhibited by lithium. GSK-3 may be a relevant treatment target for interventions tailored at cognitive disturbances in BD but the relation between GSK-3 activity, cognition and lithium treatment is unknown. We therefore investigated the possible association between GSK-3 activity and cognition and whether lithium treatment moderates this association in patients with BD. In a prospective 6-12 month follow-up study, GSK- 3β activity in peripheral blood mononuclear cells was measured concurrently with cognitive performance assessed using a comprehensive test battery in 27 patients with BD-I in early and late remission following a manic or mixed episode. The GSK-3β activity, measured as serine-9 phosphorylated GSK-3β (pGSK-3β) and the GSK-3β ratio (serine-9-pGSK-3β /total GSK-3β), was negatively associated with sustained attention (p = 0.009 and p = 0.042, respectively), but not with other cognitive domains or global cognition. A crossover interaction between lithium treatment and the GSK activity was observed, indicating that lower pGSK-3β levels (p = 0.015) and GSK ratio (p = 0.010) were associated with better global cognition in lithium users whereas the opposite association was observed in non-lithium treated patients. Findings were not statistically significant after Bonferroni correction. In conclusion, cognitive functioning may be associated with GSK-3 activity in patients with BD-I and lithium treatment may modulate this relationship. Future studies in larger sample sizes are warranted to confirm these associations.
认知缺陷在缓解期的双相情感障碍(BD)患者中很常见,可能与糖原合酶激酶-3(GSK-3)活性有关,锂可抑制 GSK-3 活性。GSK-3 可能是针对 BD 认知障碍进行干预的一个相关治疗靶点,但 GSK-3 活性、认知和锂治疗之间的关系尚不清楚。因此,我们研究了 GSK-3 活性与认知之间的可能关联,以及锂治疗是否调节了 BD 患者中的这种关联。在一项前瞻性的 6-12 个月随访研究中,我们在 27 例双相情感障碍 I 型患者处于躁狂或混合发作缓解后的早期和晚期,同时测量外周血单个核细胞中的 GSK-3β 活性和使用综合测试套件评估认知表现,以评估 GSK-3β 活性与认知之间的关系。GSK-3β 活性,以丝氨酸-9 磷酸化 GSK-3β(pGSK-3β)和 GSK-3β 比值(丝氨酸-9-pGSK-3β/总 GSK-3β)表示,与持续注意力呈负相关(分别为 p = 0.009 和 p = 0.042),但与其他认知域或总体认知无关。锂治疗和 GSK 活性之间存在交叉相互作用,表明锂使用者的 pGSK-3β 水平(p = 0.015)和 GSK 比值(p = 0.010)较低与更好的总体认知相关,而在未接受锂治疗的患者中则观察到相反的关联。经过 Bonferroni 校正后,结果无统计学意义。总之,认知功能可能与 BD-I 患者的 GSK-3 活性有关,锂治疗可能调节这种关系。需要在更大的样本量中进行进一步的研究来证实这些关联。