Searched for: school:SOM
Department/Unit:Child and Adolescent Psychiatry
Behavioral Parent Training for Preschool ADHD: Family-Centered Profiles Predict Changes in Parenting and Child Outcomes
Dale, Chelsea; Parent, Justin; Forehand, Rex; DiMarzio, Karissa; Sonuga-Barke, Edmund; Long, Nicholas; Abikoff, Howard B
Objective: Behavioral parent training (BPT) is the first line of treatment for preschool-aged children with attention-deficit hyperactivity disorder (ADHD); however, clinically significant improvements are not universal. In the current study, we employ a person-centered approach to create subgroups of families based on the intersection of multiple parent, child, and family pre-treatment factors. Further, we explore the utility of pre-treatment family profiles in predicting post-treatment differences in observed parenting behavior (i.e., behavioral control, parental warmth) and clinically significant change in child ADHD and oppositional symptoms. Method: Longitudinal data were collected using observational and parent-, teacher- and clinician-reported assessments from 130 parent-child dyads (Mage= 3.57, range = 3.0- 4.11, 73.8% male, 69.2% White, 25.6% Hispanic) participating in BPT. Results: Findings from the current study suggest three distinct family profiles, which consisted of one profile with high family stress (HFS) as evidenced by elevated symptomatology across parent, child, and family-level domains, a second profile with elevated parental anxiety (PA), and a final profile with elevated parental depression (PD). These family-centered profiles were differentially associated with changes in observed parenting practices. Specifically, the PD profile (39%) demonstrated minimal improvements in behavioral control and warmth following treatment. In contrast, the HFS profile (30%) only improved in behavioral control and the PA profile (31%) improved in both parenting domains following treatment. In addition, marginally significant differences in child oppositional and ADHD symptoms were observed across profiles. Conclusions: Family-centered approaches may be useful for selecting and implementing interventions.
PMID: 33492172
ISSN: 1537-4424
CID: 4766952
Suubi+Adherence-Round 2: A study protocol to examine the longitudinal HIV treatment adherence among youth living with HIV transitioning into young adulthood in Southern Uganda
Ssewamala, Fred M; Sensoy Bahar, Ozge; Nabunya, Proscovia; Thames, April D; Neilands, Torsten B; Damulira, Christopher; Mukasa, Barbara; Brathwaite, Rachel; Mellins, Claude; Santelli, John; Brown, Derek; Guo, Shenyang; Namatovu, Phionah; Kiyingi, Joshua; Namuwonge, Flavia; McKay, Mary M
BACKGROUND:Youth living with HIV (YLHIV) in Sub-Saharan African (SSA) are less likely to adhere to antiretroviral therapy (ART) and other health-related regimens. As a consequence, YLHIV are not only at risk for health problems and mental health comorbidities, but are also at risk for cognitive deficits, including in areas of memory and executive functioning. The Suubi+Adherence study followed 702 adolescents (10-16 years of age) receiving bolstered standard of care and a family economic empowerment intervention comprising an incentivized youth financial savings account (YSA) augmented with financial literacy training (FLT) and peer mentorship. The study findings pointed to superior short-term viral suppression and positive adolescent health and mental health functioning among participants receiving the intervention. The original group of adolescents who received Suubi+Adherence are now transitioning into young adulthood. This paper presents a protocol for the follow-up phase titled Suubi+Adherence Round 2. METHODS:The original cohort in Suubi+Adherence will be tracked for an additional five years (2020-2025). Specifically, the long term follow-up will allow to: 1) ascertain the extent to which the short term outcomes identified in the first 6 years of the intervention are maintained as the same group transitions through young adulthood; and 2) address new scientific questions regarding ART adherence; HIV care engagement; protective health behaviors; and the potential of FEE to mitigate the development of HIV-associated neurocognitive disorders in YLHIV. Additionally, the team examines the potential mechanisms through which the observed long-term outcomes happen. Moreover, the Suubi+Adherence-Round 2 adds a qualitative component and extends the cost effectiveness component. DISCUSSION/CONCLUSIONS:Guided by asset and human development theories, Suubi+Adherence-R2 will build on the recently concluded Suubi+Adherence study to conduct one of the largest and longest running studies of YLHIV in SSA as they transition into young adulthood. The study will address new scientific questions regarding long-term ART adherence, HIV care engagement, protective health behaviors, and the potential of FEE to mitigate the development of HIV-associated neurocognitive disorders in YLHIV. The findings may inform efforts to improve HIV care among Uganda's YLHIV, with potential replicability in other low-resource countries. TRIAL REGISTRATION/BACKGROUND:ClinicalTrials.gov , ID: NCT01790373.
PMID: 33478469
ISSN: 1471-2458
CID: 4760922
Early changes in synaptic and intrinsic properties of dentate gyrus granule cells in a mouse model of Alzheimer's disease neuropathology and atypical effects of the cholinergic antagonist atropine
Alcantara-Gonzalez, David; Chartampila, Elissavet; Criscuolo, Chiara; Scharfman, Helen E
It has been reported that hyperexcitability occurs in a subset of patients with Alzheimer's disease (AD) and hyperexcitability could contribute to the disease. Several studies have suggested that the hippocampal dentate gyrus (DG) may be an important area where hyperexcitability occurs. Therefore, we tested the hypothesis that the principal DG cell type, granule cells (GCs), would exhibit changes at the single-cell level which would be consistent with hyperexcitability and might help explain it. We used the Tg2576 mouse, where it has been shown that hyperexcitability is robust at 2-3 months of age. GCs from 2 to 3-month-old Tg2576 mice were compared to age-matched wild type (WT) mice. Effects of muscarinic cholinergic antagonism were tested because previously we found that Tg2576 mice exhibited hyperexcitability in vivo that was reduced by the muscarinic cholinergic antagonist atropine, counter to the dogma that in AD one needs to boost cholinergic function. The results showed that GCs from Tg2576 mice exhibited increased frequency of spontaneous excitatory postsynaptic potentials/currents (sEPSP/Cs) and reduced frequency of spontaneous inhibitory synaptic events (sIPSCs) relative to WT, increasing the excitation:inhibition (E:I) ratio. There was an inward NMDA receptor-dependent current that we defined here as a novel synaptic current (nsC) in Tg2576 mice because it was very weak in WT mice. Intrinsic properties were distinct in Tg2576 GCs relative to WT. In summary, GCs of the Tg2576 mouse exhibit early electrophysiological alterations that are consistent with increased synaptic excitation, reduced inhibition, and muscarinic cholinergic dysregulation. The data support previous suggestions that the DG contributes to hyperexcitability and there is cholinergic dysfunction early in life in AD mouse models.
PMID: 33484828
ISSN: 1095-953x
CID: 4766672
Determinants of using children's mental health research in policymaking: variation by type of research use and phase of policy process
Purtle, Jonathan; Nelson, Katherine L; Horwitz, Sarah Mc Cue; McKay, Mary M; Hoagwood, Kimberly E
BACKGROUND:Research use in policymaking is multi-faceted and has been the focus of extensive study. However, virtually no quantitative studies have examined whether the determinants of research use vary according to the type of research use or phase of policy process. Understanding such variation is important for selecting the targets of implementation strategies that aim to increase the frequency of research use in policymaking. METHODS:A web-based survey of US state agency officials involved with children's mental health policymaking was conducted between December 2019 and February 2020 (n = 224, response rate = 33.7%, 49 states responding (98%), median respondents per state = 4). The dependent variables were composite scores of the frequency of using children's mental health research in general, specific types of research use (i.e., conceptual, instrumental, tactical, imposed), and during different phases of the policy process (i.e., agenda setting, policy development, policy implementation). The independent variables were four composite scores of determinants of research use: agency leadership for research use, agency barriers to research use, research use skills, and dissemination barriers (e.g., lack of actionable messages/recommendations in research summaries, lack of interaction/collaboration with researchers). Separate multiple linear regression models estimated associations between determinant and frequency of research use scores. RESULTS:Determinants of research use varied significantly by type of research use and phase of policy process. For example, agency leadership for research use was the only determinant significantly associated with imposed research use (β = 0.31, p < 0.001). Skills for research use were the only determinant associated with tactical research use (β = 0.17, p = 0.03) and were only associated with research use in the agenda-setting phase (β = 0.16, p = 0.04). Dissemination barriers were the most universal determinants of research use, as they were significantly and inversely associated with frequency of conceptual (β = -0.21, p = 0.01) and instrumental (β = -0.22, p = 0.01) research use and during all three phases of policy process. CONCLUSIONS:Decisions about the determinants to target with policy-focused implementation strategies-and the strategies that are selected to affect these targets-should reflect the specific types of research use that these strategies aim to influence.
PMCID:7815190
PMID: 33468166
ISSN: 1748-5908
CID: 4798712
Synaptic processes and immune-related pathways implicated in Tourette syndrome
Tsetsos, Fotis; Yu, Dongmei; Sul, Jae Hoon; Huang, Alden Y; Illmann, Cornelia; Osiecki, Lisa; Darrow, Sabrina M; Hirschtritt, Matthew E; Greenberg, Erica; Muller-Vahl, Kirsten R; Stuhrmann, Manfred; Dion, Yves; Rouleau, Guy A; Aschauer, Harald; Stamenkovic, Mara; Schlögelhofer, Monika; Sandor, Paul; Barr, Cathy L; Grados, Marco A; Singer, Harvey S; Nöthen, Markus M; Hebebrand, Johannes; Hinney, Anke; King, Robert A; Fernandez, Thomas V; Barta, Csaba; Tarnok, Zsanett; Nagy, Peter; Depienne, Christel; Worbe, Yulia; Hartmann, Andreas; Budman, Cathy L; Rizzo, Renata; Lyon, Gholson J; McMahon, William M; Batterson, James R; Cath, Danielle C; Malaty, Irene A; Okun, Michael S; Berlin, Cheston; Woods, Douglas W; Lee, Paul C; Jankovic, Joseph; Robertson, Mary M; Gilbert, Donald L; Brown, Lawrence W; Coffey, Barbara J; Dietrich, Andrea; Hoekstra, Pieter J; Kuperman, Samuel; Zinner, Samuel H; Wagner, Michael; Knowles, James A; Jeremy Willsey, A; Tischfield, Jay A; Heiman, Gary A; Cox, Nancy J; Freimer, Nelson B; Neale, Benjamin M; Davis, Lea K; Coppola, Giovanni; Mathews, Carol A; Scharf, Jeremiah M; Paschou, Peristera; Barr, Cathy L; Batterson, James R; Berlin, Cheston; Budman, Cathy L; Cath, Danielle C; Coppola, Giovanni; Cox, Nancy J; Darrow, Sabrina; Davis, Lea K; Dion, Yves; Freimer, Nelson B; Grados, Marco A; Greenberg, Erica; Hirschtritt, Matthew E; Huang, Alden Y; Illmann, Cornelia; King, Robert A; Kurlan, Roger; Leckman, James F; Lyon, Gholson J; Malaty, Irene A; Mathews, Carol A; McMahon, William M; Neale, Benjamin M; Okun, Michael S; Osiecki, Lisa; Robertson, Mary M; Rouleau, Guy A; Sandor, Paul; Scharf, Jeremiah M; Singer, Harvey S; Smit, Jan H; Sul, Jae Hoon; Yu, Dongmei; Aschauer, Harald Aschauer Harald; Barta, Csaba; Budman, Cathy L; Cath, Danielle C; Depienne, Christel; Hartmann, Andreas; Hebebrand, Johannes; Konstantinidis, Anastasios; Mathews, Carol A; Müller-Vahl, Kirsten; Nagy, Peter; Nöthen, Markus M; Paschou, Peristera; Rizzo, Renata; Rouleau, Guy A; Sandor, Paul; Scharf, Jeremiah M; Schlögelhofer, Monika; Stamenkovic, Mara; Stuhrmann, Manfred; Tsetsos, Fotis; Tarnok, Zsanett; Wolanczyk, Tomasz; Worbe, Yulia; Brown, Lawrence; Cheon, Keun-Ah; Coffey, Barbara J; Dietrich, Andrea; Fernandez, Thomas V; Garcia-Delgar, Blanca; Gilbert, Donald; Grice, Dorothy E; Hagstrøm, Julie; Hedderly, Tammy; Heiman, Gary A; Heyman, Isobel; Hoekstra, Pieter J; Huyser, Chaim; Kim, Young Key; Kim, Young-Shin; King, Robert A; Koh, Yun-Joo; Kook, Sodahm; Kuperman, Samuel; Leventhal, Bennett L; Madruga-Garrido, Marcos; Mir, Pablo; Morer, Astrid; Münchau, Alexander; Plessen, Kerstin J; Roessner, Veit; Shin, Eun-Young; Song, Dong-Ho; Song, Jungeun; Tischfield, Jay A; Willsey, A Jeremy; Zinner, Samuel; Aschauer, Harald; Barr, Cathy L; Barta, Csaba; Batterson, James R; Berlin, Cheston; Brown, Lawrence; Budman, Cathy L; Cath, Danielle C; Coffey, Barbara J; Coppola, Giovanni; Cox, Nancy J; Darrow, Sabrina; Davis, Lea K; Depienne, Christel; Dietrich, Andrea; Dion, Yves; Fernandez, Thomas; Freimer, Nelson B; Gilbert, Donald; Grados, Marco A; Greenberg, Erica; Hartmann, Andreas; Hebebrand, Johannes; Heiman, Gary; Hirschtritt, Matthew E; Hoekstra, Pieter; Huang, Alden Y; Illmann, Cornelia; Jankovic, Joseph; King, Robert A; Kuperman, Samuel; Lee, Paul C; Lyon, Gholson J; Malaty, Irene A; Mathews, Carol A; McMahon, William M; Müller-Vahl, Kirsten; Nagy, Peter; Neale, Benjamin M; Nöthen, Markus M; Okun, Michael S; Osiecki, Lisa; Paschou, Peristera; Rizzo, Renata; Robertson, Mary M; Rouleau, Guy A; Sandor, Paul; Scharf, Jeremiah M; Schlögelhofer, Monika; Singer, Harvey S; Stamenkovic, Mara; Stuhrmann, Manfred; Sul, Jae Hoon; Tarnok, Zsanett; Tischfield, Jay; Tsetsos, Fotis; Willsey, A Jeremy; Woods, Douglas; Worbe, Yulia; Yu, Dongmei; Zinner, Samuel
Tourette syndrome (TS) is a neuropsychiatric disorder of complex genetic architecture involving multiple interacting genes. Here, we sought to elucidate the pathways that underlie the neurobiology of the disorder through genome-wide analysis. We analyzed genome-wide genotypic data of 3581 individuals with TS and 7682 ancestry-matched controls and investigated associations of TS with sets of genes that are expressed in particular cell types and operate in specific neuronal and glial functions. We employed a self-contained, set-based association method (SBA) as well as a competitive gene set method (MAGMA) using individual-level genotype data to perform a comprehensive investigation of the biological background of TS. Our SBA analysis identified three significant gene sets after Bonferroni correction, implicating ligand-gated ion channel signaling, lymphocytic, and cell adhesion and transsynaptic signaling processes. MAGMA analysis further supported the involvement of the cell adhesion and trans-synaptic signaling gene set. The lymphocytic gene set was driven by variants in FLT3, raising an intriguing hypothesis for the involvement of a neuroinflammatory element in TS pathogenesis. The indications of involvement of ligand-gated ion channel signaling reinforce the role of GABA in TS, while the association of cell adhesion and trans-synaptic signaling gene set provides additional support for the role of adhesion molecules in neuropsychiatric disorders. This study reinforces previous findings but also provides new insights into the neurobiology of TS.
PMID: 33462189
ISSN: 2158-3188
CID: 4760342
Sensing everyday activity: Parent perceptions and feasibility
Levin, Hannah I; Egger, Dominique; Andres, Lara; Johnson, Mckensey; Bearman, Sarah Kate; de Barbaro, Kaya
Mobile and wearable sensors provide a unique opportunity to capture the daily activities and interactions that shape developmental trajectories, with potential to revolutionize the study of development (de Barbaro, 2019). However, developmental research employing sensors is still in its infancy, and parents' comfort using these devices is uncertain. This exploratory report assesses parent willingness to participate in sensor studies via a nationally representative survey (N = 210) and live recruitment of a low-income, minority population for an ongoing study (N = 359). The survey allowed us to assess how protocol design influences acceptability, including various options for devices and datastream resolution, conditions of data sharing, and feedback. By contrast, our recruitment data provided insight into parents' true willingness to participate in a sensor study, with a protocol including 72 h of continuous audio, motion, and physiological data. Our results indicate that parents are relatively conservative when considering participation in sensing studies. However, nearly 41 % of surveyed parents reported that they would be at least somewhat willing to participate in studies with audio or video recordings, 26 % were willing or extremely willing, and 14 % reported being extremely willing. These results roughly paralleled our recruitment results, where 58 % of parents indicated interest, 29 % of parents scheduled to participate, and 10 % ultimately participated. Additionally, 70 % of caregivers stated their reason for not participating in the study was due to barriers unrelated to sensing while about 25 % noted barriers due to either privacy concerns or the physical sensors themselves. Parents' willingness to collect sensitive datastreams increased if data stayed within the household for individual use only, are shared anonymously with researchers, or if parents receive feedback from devices. Overall, our findings suggest that given the correct circumstances, mobile sensors are a feasible and promising tool for characterizing children's daily interactions and their role in development.
PMID: 33465730
ISSN: 1934-8800
CID: 4760492
Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders
Patel, Yash; Parker, Nadine; Shin, Jean; Howard, Derek; French, Leon; Thomopoulos, Sophia I; Pozzi, Elena; Abe, Yoshinari; Abé, Christoph; Anticevic, Alan; Alda, Martin; Aleman, Andre; Alloza, Clara; Alonso-Lana, Silvia; Ameis, Stephanie H; Anagnostou, Evdokia; McIntosh, Andrew A; Arango, Celso; Arnold, Paul D; Asherson, Philip; Assogna, Francesca; Auzias, Guillaume; Ayesa-Arriola, Rosa; Bakker, Geor; Banaj, Nerisa; Banaschewski, Tobias; Bandeira, Cibele E; Baranov, Alexandr; Bargalló, Núria; Bau, Claiton H D; Baumeister, Sarah; Baune, Bernhard T; Bellgrove, Mark A; Benedetti, Francesco; Bertolino, Alessandro; Boedhoe, Premika S W; Boks, Marco; Bollettini, Irene; Del Mar Bonnin, Caterina; Borgers, Tiana; Borgwardt, Stefan; Brandeis, Daniel; Brennan, Brian P; Bruggemann, Jason M; Bülow, Robin; Busatto, Geraldo F; Calderoni, Sara; Calhoun, Vince D; Calvo, Rosa; Canales-RodrÃguez, Erick J; Cannon, Dara M; Carr, Vaughan J; Cascella, Nicola; Cercignani, Mara; Chaim-Avancini, Tiffany M; Christakou, Anastasia; Coghill, David; Conzelmann, Annette; Crespo-Facorro, Benedicto; Cubillo, Ana I; Cullen, Kathryn R; Cupertino, Renata B; Daly, Eileen; Dannlowski, Udo; Davey, Christopher G; Denys, Damiaan; Deruelle, Christine; Di Giorgio, Annabella; Dickie, Erin W; Dima, Danai; Dohm, Katharina; Ehrlich, Stefan; Ely, Benjamin A; Erwin-Grabner, Tracy; Ethofer, Thomas; Fair, Damien A; Fallgatter, Andreas J; Faraone, Stephen V; Fatjó-Vilas, Mar; Fedor, Jennifer M; Fitzgerald, Kate D; Ford, Judith M; Frodl, Thomas; Fu, Cynthia H Y; Fullerton, Janice M; Gabel, Matt C; Glahn, David C; Roberts, Gloria; Gogberashvili, Tinatin; Goikolea, Jose M; Gotlib, Ian H; Goya-Maldonado, Roberto; Grabe, Hans J; Green, Melissa J; Grevet, Eugenio H; Groenewold, Nynke A; Grotegerd, Dominik; Gruber, Oliver; Gruner, Patricia; Guerrero-Pedraza, Amalia; Gur, Raquel E; Gur, Ruben C; Haar, Shlomi; Haarman, Bartholomeus C M; Haavik, Jan; Hahn, Tim; Hajek, Tomas; Harrison, Benjamin J; Harrison, Neil A; Hartman, Catharina A; Whalley, Heather C; Heslenfeld, Dirk J; Hibar, Derrek P; Hilland, Eva; Hirano, Yoshiyuki; Ho, Tiffany C; Hoekstra, Pieter J; Hoekstra, Liesbeth; Hohmann, Sarah; Hong, L E; Höschl, Cyril; Høvik, Marie F; Howells, Fleur M; Nenadic, Igor; Jalbrzikowski, Maria; James, Anthony C; Janssen, Joost; Jaspers-Fayer, Fern; Xu, Jian; Jonassen, Rune; Karkashadze, Georgii; King, Joseph A; Kircher, Tilo; Kirschner, Matthias; Koch, Kathrin; Kochunov, Peter; Kohls, Gregor; Konrad, Kerstin; Krämer, Bernd; Krug, Axel; Kuntsi, Jonna; Kwon, Jun Soo; Landén, Mikael; Landrø, Nils I; Lazaro, Luisa; Lebedeva, Irina S; Leehr, Elisabeth J; Lera-Miguel, Sara; Lesch, Klaus-Peter; Lochner, Christine; Louza, Mario R; Luna, Beatriz; Lundervold, Astri J; MacMaster, Frank P; Maglanoc, Luigi A; Malpas, Charles B; Portella, Maria J; Marsh, Rachel; Martyn, Fiona M; Mataix-Cols, David; Mathalon, Daniel H; McCarthy, Hazel; McDonald, Colm; McPhilemey, Genevieve; Meinert, Susanne; Menchón, José M; Minuzzi, Luciano; Mitchell, Philip B; Moreno, Carmen; Morgado, Pedro; Muratori, Filippo; Murphy, Clodagh M; Murphy, Declan; Mwangi, Benson; Nabulsi, Leila; Nakagawa, Akiko; Nakamae, Takashi; Namazova, Leyla; Narayanaswamy, Janardhanan; Jahanshad, Neda; Nguyen, Danai D; Nicolau, Rosa; O'Gorman Tuura, Ruth L; O'Hearn, Kirsten; Oosterlaan, Jaap; Opel, Nils; Ophoff, Roel A; Oranje, Bob; García de la Foz, Victor Ortiz; Overs, Bronwyn J; Paloyelis, Yannis; Pantelis, Christos; Parellada, Mara; Pauli, Paul; Picó-Pérez, Maria; Picon, Felipe A; Piras, Fabrizio; Piras, Federica; Plessen, Kerstin J; Pomarol-Clotet, Edith; Preda, Adrian; Puig, Olga; Quidé, Yann; Radua, Joaquim; Ramos-Quiroga, J Antoni; Rasser, Paul E; Rauer, Lisa; Reddy, Janardhan; Redlich, Ronny; Reif, Andreas; Reneman, Liesbeth; Repple, Jonathan; Retico, Alessandra; Richarte, Vanesa; Richter, Anja; Rosa, Pedro G P; Rubia, Katya K; Hashimoto, Ryota; Sacchet, Matthew D; Salvador, Raymond; Santonja, Javier; Sarink, Kelvin; Sarró, Salvador; Satterthwaite, Theodore D; Sawa, Akira; Schall, Ulrich; Schofield, Peter R; Schrantee, Anouk; Seitz, Jochen; Serpa, Mauricio H; Setién-Suero, Esther; Shaw, Philip; Shook, Devon; Silk, Tim J; Sim, Kang; Simon, Schmitt; Simpson, Helen Blair; Singh, Aditya; Skoch, Antonin; Skokauskas, Norbert; Soares, Jair C; Soreni, Noam; Soriano-Mas, Carles; Spalletta, Gianfranco; Spaniel, Filip; Lawrie, Stephen M; Stern, Emily R; Stewart, S Evelyn; Takayanagi, Yoichiro; Temmingh, Henk S; Tolin, David F; Tomecek, David; Tordesillas-Gutiérrez, Diana; Tosetti, Michela; Uhlmann, Anne; van Amelsvoort, Therese; van der Wee, Nic J A; van der Werff, Steven J A; van Haren, Neeltje E M; van Wingen, Guido A; Vance, Alasdair; Vázquez-Bourgon, Javier; Vecchio, Daniela; Venkatasubramanian, Ganesan; Vieta, Eduard; Vilarroya, Oscar; Vives-Gilabert, Yolanda; Voineskos, Aristotle N; Völzke, Henry; von Polier, Georg G; Walton, Esther; Weickert, Thomas W; Weickert, Cynthia Shannon; Weideman, Andrea S; Wittfeld, Katharina; Wolf, Daniel H; Wu, Mon-Ju; Yang, T T; Yang, Kun; Yoncheva, Yuliya; Yun, Je-Yeon; Cheng, Yuqi; Zanetti, Marcus V; Ziegler, Georg C; Franke, Barbara; Hoogman, Martine; Buitelaar, Jan K; van Rooij, Daan; Andreassen, Ole A; Ching, Christopher R K; Veltman, Dick J; Schmaal, Lianne; Stein, Dan J; van den Heuvel, Odile A; Turner, Jessica A; van Erp, Theo G M; Pausova, Zdenka; Thompson, Paul M; Paus, Tomáš
Importance/UNASSIGNED:Large-scale neuroimaging studies have revealed group differences in cortical thickness across many psychiatric disorders. The underlying neurobiology behind these differences is not well understood. Objective/UNASSIGNED:To determine neurobiologic correlates of group differences in cortical thickness between cases and controls in 6 disorders: attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), bipolar disorder (BD), major depressive disorder (MDD), obsessive-compulsive disorder (OCD), and schizophrenia. Design, Setting, and Participants/UNASSIGNED:Profiles of group differences in cortical thickness between cases and controls were generated using T1-weighted magnetic resonance images. Similarity between interregional profiles of cell-specific gene expression and those in the group differences in cortical thickness were investigated in each disorder. Next, principal component analysis was used to reveal a shared profile of group difference in thickness across the disorders. Analysis for gene coexpression, clustering, and enrichment for genes associated with these disorders were conducted. Data analysis was conducted between June and December 2019. The analysis included 145 cohorts across 6 psychiatric disorders drawn from the ENIGMA consortium. The numbers of cases and controls in each of the 6 disorders were as follows: ADHD: 1814 and 1602; ASD: 1748 and 1770; BD: 1547 and 3405; MDD: 2658 and 3572; OCD: 2266 and 2007; and schizophrenia: 2688 and 3244. Main Outcomes and Measures/UNASSIGNED:Interregional profiles of group difference in cortical thickness between cases and controls. Results/UNASSIGNED:A total of 12 721 cases and 15 600 controls, ranging from ages 2 to 89 years, were included in this study. Interregional profiles of group differences in cortical thickness for each of the 6 psychiatric disorders were associated with profiles of gene expression specific to pyramidal (CA1) cells, astrocytes (except for BD), and microglia (except for OCD); collectively, gene-expression profiles of the 3 cell types explain between 25% and 54% of variance in interregional profiles of group differences in cortical thickness. Principal component analysis revealed a shared profile of difference in cortical thickness across the 6 disorders (48% variance explained); interregional profile of this principal component 1 was associated with that of the pyramidal-cell gene expression (explaining 56% of interregional variation). Coexpression analyses of these genes revealed 2 clusters: (1) a prenatal cluster enriched with genes involved in neurodevelopmental (axon guidance) processes and (2) a postnatal cluster enriched with genes involved in synaptic activity and plasticity-related processes. These clusters were enriched with genes associated with all 6 psychiatric disorders. Conclusions and Relevance/UNASSIGNED:In this study, shared neurobiologic processes were associated with differences in cortical thickness across multiple psychiatric disorders. These processes implicate a common role of prenatal development and postnatal functioning of the cerebral cortex in these disorders.
PMCID:7450410
PMID: 32857118
ISSN: 2168-6238
CID: 4650132
Respiratory sinus arrhythmia correlates with depressive symptoms following mild traumatic brain injury. [Case Report]
Brandt, Emma; Wilson, J. Kevin; Rieger, Rebecca E.; Gill, Darbi; Mayer, Andrew R.; Cavanagh, James F.
ORIGINAL:0017721
ISSN: 0269-8803
CID: 5909692
Friendly Faces: Characteristics of Children and Adolescents With Repeat Visits to a Specialized Child Psychiatric Emergency Program
Marr, Mollie; Horwitz, Sarah M; Gerson, Ruth; Storfer-Isser, Amy; Havens, Jennifer F
OBJECTIVES/OBJECTIVE:Pediatric mental health emergency department (ED) visits continue to rise with 19% to 62% of youth presenting to the ED ultimately returning for a mental health-related complaint. To better understand the needs of children returning to the ED, this study examines the clinical, demographic, and environmental factors associated with revisits to a dedicated child psychiatric ED. METHODS:Clinical factors, home environment, and mental health service utilization of 885 children presenting to a dedicated child psychiatric ED over a 1-year period were abstracted by retrospective chart review. Bivariate analyses comparing demographic and clinical characteristics for children with and without revisits and a multivariable logistic regression were performed. RESULTS:Of the children presenting to the ED, 186 (21.0%) had at least 1 revisit in the subsequent 180 days. Thirty-one percent of initial visits presented as urgent, 55% presented as emergent. Children presenting with more severe symptoms at their initial visit were more likely to return within 6 months. Female gender, suicidal and disruptive behavioral symptomatology, and a diagnosis of oppositional defiant disorder were associated with repeat visits. Children with mental health system involvement were more likely to have revisits than those who were "treatment naive." CONCLUSIONS:Revisits to the ED are driven by both clinical factors, including severity and psychosocial complexity, and barriers to accessing services. Addressing the problem of return ED visits will require the development of a robust mental health service system that is accessible to children and families of all socioeconomic levels.
PMID: 29438124
ISSN: 1535-1815
CID: 2956152
An Equine-Assisted Therapy for Youth with Mild to Moderate Anxiety: Manual Development and Fidelity
Acri, Mary; Morrissey, Meghan; Peth-Pierce, Robin; Seibel, Lauren; Seag, Dana; Hamovitch, Emily K.; Guo, Fei; Horwitz, Sarah; Hoagwood, Kimberly E.
Childhood anxiety is common, yet approximately half of youth do not receive treatment due to stigma, mistrust of the mental health service system, extensive wait lists for services and provider shortages. Alternative models and modes of treatment are needed. This paper describes the development of an alternative treatment that incorporates cognitive behavioral components for anxiety into an adaptive/therapeutic riding program delivered by certified riding instructors in a horse stable that offers horseback riding and therapeutic horsemanship programs. Using PracticeWise®, a well-established database of evidence-based mental health practices for youth, we identified five therapeutic elements that are the most commonly examined in rigorous research for childhood anxiety, and integrated them into a manualized program of adaptive riding sessions. Excellent fidelity to the intervention (98.7% mean score) and high inter-rater reliability (k = 0.92) were achieved. This approach has implications for expanding access to and engagement in adaptive/therapeutic riding interventions.
SCOPUS:85108806607
ISSN: 1062-1024
CID: 4962732