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

Identifieur interne : 000399 ( Main/Exploration ); précédent : 000398; suivant : 000400

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

Auteurs : Marco Armando [Suisse] ; Mariasole Ciampoli [Italie] ; Maria Carmela Padula [Suisse] ; Paul Amminger [Australie] ; Franco De Crescenzo [Italie] ; Johanna Maeder [Suisse] ; Maude Schneider [Suisse] ; Marie Schaer [Suisse] ; Francesca Manag [Italie] ; Stephan Eliez [Suisse] ; Francesco Papaleo [Italie]

Source :

RBID : pubmed:32057798

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.

DOI: 10.1016/j.neuropharm.2020.107995
PubMed: 32057798


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<div type="abstract" xml:lang="en">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.</div>
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<AbstractText>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.</AbstractText>
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<Affiliation>Department of Psychiatry, University of Oxford, Oxford, UK; Pediatric University Hospital-Department (DPUO), Bambino Gesù Children's Hospital, Rome, Italy; Department of Epidemiology, Lazio Regional Health Service, Rome, Italy.</Affiliation>
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<Affiliation>Genetics of Cognition Laboratory, Neuroscience Area, Istituto Italiano di Tecnologia, Via Morego, 30, 16163, Genova, Italy. Electronic address: francesco.papaleo@iit.it.</Affiliation>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<Year>2020</Year>
<Month>02</Month>
<Day>10</Day>
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<Country>England</Country>
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<Keyword MajorTopicYN="Y">Adolescence</Keyword>
<Keyword MajorTopicYN="Y">Attention</Keyword>
<Keyword MajorTopicYN="Y">Distractibility</Keyword>
<Keyword MajorTopicYN="Y">LgDel/+ mutant mice</Keyword>
<Keyword MajorTopicYN="Y">Translational pharmacology</Keyword>
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<CoiStatement>Declaration of competing interest The authors declare no competing financial interests.</CoiStatement>
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<li>Australie</li>
<li>Italie</li>
<li>Suisse</li>
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<li>Canton de Genève</li>
<li>Latium</li>
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<name sortKey="Padula, Maria Carmela" sort="Padula, Maria Carmela" uniqKey="Padula M" first="Maria Carmela" last="Padula">Maria Carmela Padula</name>
<name sortKey="Schaer, Marie" sort="Schaer, Marie" uniqKey="Schaer M" first="Marie" last="Schaer">Marie Schaer</name>
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<name sortKey="De Crescenzo, Franco" sort="De Crescenzo, Franco" uniqKey="De Crescenzo F" first="Franco" last="De Crescenzo">Franco De Crescenzo</name>
<name sortKey="Manag, Francesca" sort="Manag, Francesca" uniqKey="Manag F" first="Francesca" last="Manag">Francesca Manag</name>
<name sortKey="Papaleo, Francesco" sort="Papaleo, Francesco" uniqKey="Papaleo F" first="Francesco" last="Papaleo">Francesco Papaleo</name>
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