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  1. Artikel ; Online: Empirical evidence for psychopharmacologic treatment in early-onset psychosis and schizophrenia.

    Maloney, Ann E / Yakutis, Lauren J / Frazier, Jean A

    Child and adolescent psychiatric clinics of North America

    2012  Band 21, Heft 4, Seite(n) 885–909

    Abstract: Psychotic symptoms presenting in youth can be clinically complex and require that a child and adolescent psychiatrist use significant skill in making a diagnosis and initiating treatment. There are a number of illnesses to rule out before making a ... ...

    Abstract Psychotic symptoms presenting in youth can be clinically complex and require that a child and adolescent psychiatrist use significant skill in making a diagnosis and initiating treatment. There are a number of illnesses to rule out before making a diagnosis of early-onset schizophrenia in particular. Psychosis in youth has significant associated morbidity and places high demands not only on families but also on the medical and educational systems. More effective pharmacologic and nonpharmacologic treatments for psychosis are needed. Nonpharmacologic therapies targeting relatively treatment-resistant domains of dysfunction such as neurocognition are also necessary as adjunctive treatments to our extant pharmacologic agents.
    Mesh-Begriff(e) Adolescent ; Age of Onset ; Antipsychotic Agents/administration & dosage ; Antipsychotic Agents/adverse effects ; Child ; Clinical Trials as Topic ; Humans ; Psychotic Disorders/diagnosis ; Psychotic Disorders/drug therapy ; Schizophrenia/diagnosis ; Schizophrenia/drug therapy
    Chemische Substanzen Antipsychotic Agents
    Sprache Englisch
    Erscheinungsdatum 2012-10
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1313996-4
    ISSN 1558-0490 ; 1056-4993
    ISSN (online) 1558-0490
    ISSN 1056-4993
    DOI 10.1016/j.chc.2012.07.011
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Neurocognitive outcomes in the Treatment of Early-Onset Schizophrenia Spectrum Disorders study.

    Frazier, Jean A / Giuliano, Anthony J / Johnson, Jacqueline L / Yakutis, Lauren / Youngstrom, Eric A / Breiger, David / Sikich, Linmarie / Findling, Robert L / McClellan, Jon / Hamer, Robert M / Vitiello, Benedetto / Lieberman, Jeffrey A / Hooper, Stephen R

    Journal of the American Academy of Child and Adolescent Psychiatry

    2012  Band 51, Heft 5, Seite(n) 496–505

    Abstract: Objective: To assess neurocognitive outcomes following antipsychotic intervention in youth enrolled in the National Institute of Mental Health (NIMH)-funded Treatment of Early-Onset Schizophrenia Spectrum Disorders (TEOSS).: Method: Neurocognitive ... ...

    Abstract Objective: To assess neurocognitive outcomes following antipsychotic intervention in youth enrolled in the National Institute of Mental Health (NIMH)-funded Treatment of Early-Onset Schizophrenia Spectrum Disorders (TEOSS).
    Method: Neurocognitive functioning of youth (ages 8 to 19 years) with schizophrenia or schizoaffective disorder was evaluated in a four-site, randomized, double-blind clinical trial comparing molindone, olanzapine, and risperidone. The primary outcomes were overall group change from baseline in neurocognitive composite and six domain scores after 8 weeks and continued treatment up to 52 weeks. Age and sex were included as covariates in all analyses.
    Results: Of 116 TEOSS participants, 77 (66%) had post-baseline neurocognitive data. No significant differences emerged in the neurocognitive outcomes of the three medication groups. Therefore, the three treatment groups were combined into one group to assess overall neurocognitive outcomes. Significant modest improvements were observed in the composite score and in three of six domain scores in the acute phase, and in four of six domain scores in the combined acute and maintenance phases. Partial correlation analyses revealed very few relationships among Positive and Negative Syndrome Scale (PANSS) baseline or change scores and neurocognition change scores.
    Conclusions: Antipsychotic intervention in youth with early-onset schizophrenia spectrum disorders (EOSS) led to modest improvement in measures of neurocognitive function. The changes in cognition were largely unrelated to baseline symptoms or symptom change. Small treatment effect sizes, easily accounted for by practice effects, highlight the critical need for the development of more efficacious interventions for the enduring neurocognitive deficits seen in EOSS. Clinical trial registry information-Treatment of Early-Onset Schizophrenia Spectrum Disorders (TEOSS); http://www.clinicaltrials.gov; NCT00053703.
    Mesh-Begriff(e) Adolescent ; Antipsychotic Agents/adverse effects ; Antipsychotic Agents/therapeutic use ; Benzodiazepines/adverse effects ; Benzodiazepines/therapeutic use ; Child ; Cognition Disorders/diagnosis ; Cognition Disorders/drug therapy ; Cognition Disorders/psychology ; Double-Blind Method ; Female ; Follow-Up Studies ; Humans ; Male ; Molindone/adverse effects ; Molindone/therapeutic use ; Neuropsychological Tests ; Olanzapine ; Psychotic Disorders/diagnosis ; Psychotic Disorders/drug therapy ; Psychotic Disorders/psychology ; Risperidone/adverse effects ; Risperidone/therapeutic use ; Schizophrenia/diagnosis ; Schizophrenia/drug therapy ; Schizophrenic Psychology
    Chemische Substanzen Antipsychotic Agents ; Benzodiazepines (12794-10-4) ; Risperidone (L6UH7ZF8HC) ; Olanzapine (N7U69T4SZR) ; Molindone (RT3Y3QMF8N)
    Sprache Englisch
    Erscheinungsdatum 2012-03-13
    Erscheinungsland United States
    Dokumenttyp Comparative Study ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 392535-3
    ISSN 1527-5418 ; 0890-8567
    ISSN (online) 1527-5418
    ISSN 0890-8567
    DOI 10.1016/j.jaac.2012.02.001
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.

    Bakken, Trygve E / Roddey, J Cooper / Djurovic, Srdjan / Akshoomoff, Natacha / Amaral, David G / Bloss, Cinnamon S / Casey, B J / Chang, Linda / Ernst, Thomas M / Gruen, Jeffrey R / Jernigan, Terry L / Kaufmann, Walter E / Kenet, Tal / Kennedy, David N / Kuperman, Joshua M / Murray, Sarah S / Sowell, Elizabeth R / Rimol, Lars M / Mattingsdal, Morten /
    Melle, Ingrid / Agartz, Ingrid / Andreassen, Ole A / Schork, Nicholas J / Dale, Anders M / Weiner, Michael / Aisen, Paul / Petersen, Ronald / Jack, Clifford R / Jagust, William / Trojanowki, John Q / Toga, Arthur W / Beckett, Laurel / Green, Robert C / Saykin, Andrew J / Morris, John / Liu, Enchi / Montine, Tom / Gamst, Anthony / Thomas, Ronald G / Donohue, Michael / Walter, Sarah / Gessert, Devon / Sather, Tamie / Harvey, Danielle / Kornak, John / Dale, Anders / Bernstein, Matthew / Felmlee, Joel / Fox, Nick / Thompson, Paul / Schuff, Norbert / Alexander, Gene / DeCarli, Charles / Bandy, Dan / Koeppe, Robert A / Foster, Norm / Reiman, Eric M / Chen, Kewei / Mathis, Chet / Cairns, Nigel J / Taylor-Reinwald, Lisa / Trojanowki, J Q / Shaw, Les / Lee, Virginia M Y / Korecka, Magdalena / Crawford, Karen / Neu, Scott / Foroud, Tatiana M / Potkin, Steven / Shen, Li / Kachaturian, Zaven / Frank, Richard / Snyder, Peter J / Molchan, Susan / Kaye, Jeffrey / Quinn, Joseph / Lind, Betty / Dolen, Sara / Schneider, Lon S / Pawluczyk, Sonia / Spann, Bryan M / Brewer, James / Vanderswag, Helen / Heidebrink, Judith L / Lord, Joanne L / Johnson, Kris / Doody, Rachelle S / Villanueva-Meyer, Javier / Chowdhury, Munir / Stern, Yaakov / Honig, Lawrence S / Bell, Karen L / Morris, John C / Ances, Beau / Carroll, Maria / Leon, Sue / Mintun, Mark A / Schneider, Stacy / Marson, Daniel / Griffith, Randall / Clark, David / Grossman, Hillel / Mitsis, Effie / Romirowsky, Aliza / deToledo-Morrell, Leyla / Shah, Raj C / Duara, Ranjan / Varon, Daniel / Roberts, Peggy / Albert, Marilyn / Onyike, Chiadi / Kielb, Stephanie / Rusinek, Henry / de Leon, Mony J / Glodzik, Lidia / De Santi, Susan / Doraiswamy, P Murali / Petrella, Jeffrey R / Coleman, R Edward / Arnold, Steven E / Karlawish, Jason H / Wolk, David / Smith, Charles D / Jicha, Greg / Hardy, Peter / Lopez, Oscar L / Oakley, MaryAnn / Simpson, Donna M / Porsteinsson, Anton P / Goldstein, Bonnie S / Martin, Kim / Makino, Kelly M / Ismail, M Saleem / Brand, Connie / Mulnard, Ruth A / Thai, Gaby / Mc-Adams-Ortiz, Catherine / Womack, Kyle / Mathews, Dana / Quiceno, Mary / Diaz-Arrastia, Ramon / King, Richard / Weiner, Myron / Martin-Cook, Kristen / DeVous, Michael / Levey, Allan I / Lah, James J / Cellar, Janet S / Burns, Jeffrey M / Anderson, Heather S / Swerdlow, Russell H / Apostolova, Liana / Lu, Po H / Bartzokis, George / Silverman, Daniel H S / Graff-Radford, Neill R / Parfitt, Francine / Johnson, Heather / Farlow, Martin R / Hake, Ann Marie / Matthews, Brandy R / Herring, Scott / van Dyck, Christopher H / Carson, Richard E / MacAvoy, Martha G / Chertkow, Howard / Bergman, Howard / Hosein, Chris / Black, Sandra / Stefanovic, Bojana / Caldwell, Curtis / Ging-Yuek / Hsiung, Robin / Feldman, Howard / Mudge, Benita / Assaly, Michele / Kertesz, Andrew / Rogers, John / Trost, Dick / Bernick, Charles / Munic, Donna / Kerwin, Diana / Mesulam, Marek-Marsel / Lipowski, Kristina / Wu, Chuang-Kuo / Johnson, Nancy / Sadowsky, Carl / Martinez, Walter / Villena, Teresa / Turner, Raymond Scott / Johnson, Kathleen / Reynolds, Brigid / Sperling, Reisa A / Johnson, Keith A / Marshall, Gad / Frey, Meghan / Yesavage, Jerome / Taylor, Joy L / Lane, Barton / Rosen, Allyson / Tinklenberg, Jared / Sabbagh, Marwan / Belden, Christine / Jacobson, Sandra / Kowall, Neil / Killiany, Ronald / Budson, Andrew E / Norbash, Alexander / Johnson, Patricia Lynn / Obisesan, Thomas O / Wolday, Saba / Bwayo, Salome K / Lerner, Alan / Hudson, Leon / Ogrocki, Paula / Fletcher, Evan / Carmichael, Owen / Olichney, John / Kittur, Smita / Borrie, Michael / Lee, T-Y / Bartha, Rob / Johnson, Sterling / Asthana, Sanjay / Carlsson, Cynthia M / Potkin, Steven G / Preda, Adrian / Nguyen, Dana / Tariot, Pierre / Fleisher, Adam / Reeder, Stephanie / Bates, Vernice / Capote, Horacio / Rainka, Michelle / Scharre, Douglas W / Kataki, Maria / Zimmerman, Earl A / Celmins, Dzintra / Brown, Alice D / Pearlson, Godfrey D / Blank, Karen / Anderson, Karen / Santulli, Robert B / Schwartz, Eben S / Sink, Kaycee M / Williamson, Jeff D / Garg, Pradeep / Watkins, Franklin / Ott, Brian R / Querfurth, Henry / Tremont, Geoffrey / Salloway, Stephen / Malloy, Paul / Correia, Stephen / Rosen, Howard J / Miller, Bruce L / Mintzer, Jacobo / Longmire, Crystal Flynn / Spicer, Kenneth / Finger, Elizabether / Rachinsky, Irina / Drost, Dick / Jernigan, Terry / McCabe, Connor / Grant, Ellen / Ernst, Thomas / Kuperman, Josh / Chung, Yoon / Murray, Sarah / Bloss, Cinnamon / Darst, Burcu / Pritchett, Lexi / Saito, Ashley / Amaral, David / DiNino, Mishaela / Eyngorina, Bella / Sowell, Elizabeth / Houston, Suzanne / Soderberg, Lindsay / Kaufmann, Walter / van Zijl, Peter / Rizzo-Busack, Hilda / Javid, Mohsin / Mehta, Natasha / Ruberry, Erika / Powers, Alisa / Rosen, Bruce / Gebhard, Nitzah / Manigan, Holly / Frazier, Jean / Kennedy, David / Yakutis, Lauren / Hill, Michael / Gruen, Jeffrey / Bosson-Heenan, Joan / Carlson, Heatherly

    Proceedings of the National Academy of Sciences of the United States of America

    2012  Band 109, Heft 10, Seite(n) 3985–3990

    Abstract: Visual cortical surface area varies two- to threefold between human individuals, is highly heritable, and has been correlated with visual acuity and visual perception. However, it is still largely unknown what specific genetic and environmental factors ... ...

    Abstract Visual cortical surface area varies two- to threefold between human individuals, is highly heritable, and has been correlated with visual acuity and visual perception. However, it is still largely unknown what specific genetic and environmental factors contribute to normal variation in the area of visual cortex. To identify SNPs associated with the proportional surface area of visual cortex, we performed a genome-wide association study followed by replication in two independent cohorts. We identified one SNP (rs6116869) that replicated in both cohorts and had genome-wide significant association (P(combined) = 3.2 × 10(-8)). Furthermore, a metaanalysis of imputed SNPs in this genomic region identified a more significantly associated SNP (rs238295; P = 6.5 × 10(-9)) that was in strong linkage disequilibrium with rs6116869. These SNPs are located within 4 kb of the 5' UTR of GPCPD1, glycerophosphocholine phosphodiesterase GDE1 homolog (Saccharomyces cerevisiae), which in humans, is more highly expressed in occipital cortex compared with the remainder of cortex than 99.9% of genes genome-wide. Based on these findings, we conclude that this common genetic variation contributes to the proportional area of human visual cortex. We suggest that identifying genes that contribute to normal cortical architecture provides a first step to understanding genetic mechanisms that underlie visual perception.
    Mesh-Begriff(e) Adolescent ; Adult ; Aged ; Brain/pathology ; Brain Mapping/methods ; Cohort Studies ; Diagnostic Imaging/methods ; Female ; Genetic Variation ; Genome-Wide Association Study ; Genomics ; Genotype ; Humans ; Male ; Middle Aged ; Models, Genetic ; Phosphoric Diester Hydrolases/genetics ; Polymorphism, Single Nucleotide ; Saccharomyces cerevisiae/metabolism ; Visual Cortex/anatomy & histology ; Visual Cortex/pathology
    Chemische Substanzen Phosphoric Diester Hydrolases (EC 3.1.4.-) ; glycerophosphocholine phosphodiesterase (EC 3.1.4.2) ; glycerophosphodiester phosphodiesterase (EC 3.1.4.46)
    Sprache Englisch
    Erscheinungsdatum 2012-02-16
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.1105829109
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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