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ω-3多不饱和脂肪酸对22q11.2缺失综合征患者注意力控制及向精神病转化比率的有益影响。

Favorable effects of omega-3 polyunsaturated fatty acids in attentional control and conversion rate to psychosis in 22q11.2 deletion syndrome.

作者信息

Armando Marco, Ciampoli Mariasole, Padula Maria Carmela, Amminger Paul, De Crescenzo Franco, Maeder Johanna, Schneider Maude, Schaer Marie, Managò Francesca, Eliez Stephan, Papaleo Francesco

机构信息

Developmental Imaging and Psychopathology Lab, Department of Psychiatry, University of Geneva, 1202, Geneva, Switzerland.

Genetics of Cognition Laboratory, Neuroscience Area, Istituto Italiano di Tecnologia, Via Morego, 30, 16163, Genova, Italy.

出版信息

Neuropharmacology. 2020 May 15;168:107995. doi: 10.1016/j.neuropharm.2020.107995. Epub 2020 Feb 10.

Abstract

Omega-3-polyunsaturated-fatty-acids were suggested against cognitive dysfunctions and conversion to psychosis. However, a recent multicenter trial found no effect in reducing conversion rates in individuals at risk of developing schizophrenia. Patients' genetic heterogeneity and the timing of treatment might influence omega-3 efficacy. Here, we addressed the impact of omega-3 early treatment in both mice and human subjects with a 22q11.2 genetic hemi-deletion (22q11DS), characterized by cognitive dysfunctions and high penetrance of schizophrenia. We first tested the behavioural and cognitive consequences of adolescent exposure to normal or omega-3-enriched diets in wild-type and 22q11DS (LgDel/+) mice. We then contrasted mouse data with those gathered from sixty-two patients with 22q11DS exposed to a normal diet or supplemented with omega-3 during pre-adolescence/adolescence. Adolescent omega-3 exposure had no effects in wild-type mice. However, this treatment ameliorated distractibility deficits revealed in LgDel/+ mice by the Five Choice Serial Reaction Time Task (5CSRTT). The omega-3 improvement in LgDel/+ mice was selective, as no other generalized cognitive and non-cognitive effects were evident. Similarly, omega-3-exposed 22q11DS patients showed long-lasting improvements on distractibility as revealed by the continuous performance test (CPT). Moreover, omega-3-exposed 22q11DS patients showed less risk of developing an Ultra High Risk status and lower conversion rate to psychosis. Our convergent mouse-human findings represent a first analysis on the effects of omega-3 early treatment in 22q11DS. The beneficial effects in attentional control and transition to psychosis could support the early use of omega-3 supplementation in the 22q11DS population.

摘要

ω-3多不饱和脂肪酸被认为可预防认知功能障碍和转化为精神病。然而,最近的一项多中心试验发现,它对降低有患精神分裂症风险个体的转化率没有效果。患者的基因异质性和治疗时机可能会影响ω-3的疗效。在此,我们探讨了ω-3早期治疗对患有22q11.2基因半缺失(22q11DS)的小鼠和人类受试者的影响,该疾病的特征是认知功能障碍和精神分裂症的高外显率。我们首先测试了野生型和22q11DS(LgDel/+)小鼠在青春期接触正常饮食或富含ω-3饮食后的行为和认知后果。然后,我们将小鼠数据与从62名22q11DS患者收集的数据进行对比,这些患者在青春期前/青春期期间接受正常饮食或补充ω-3。青春期接触ω-3对野生型小鼠没有影响。然而,这种治疗改善了LgDel/+小鼠在五选择连续反应时任务(5CSRTT)中表现出的注意力分散缺陷。LgDel/+小鼠中ω-3的改善是选择性的,因为没有其他明显的普遍认知和非认知影响。同样,接受ω-3治疗的22q11DS患者在持续操作测试(CPT)中显示出注意力分散方面的长期改善。此外,接受ω-3治疗的22q11DS患者发展为超高风险状态的风险较低且转化为精神病的几率较低。我们在小鼠和人类中的一致发现代表了对22q11DS中ω-3早期治疗效果的首次分析。在注意力控制和向精神病转化方面的有益作用可能支持在22q11DS人群中早期使用ω-3补充剂。

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