Searched for: school:SOM
Department/Unit:Child and Adolescent Psychiatry
Preference for digital media use, biobehavioral attention bias, and anxiety symptoms in adolescents
Myruski, Sarah; de Rutte, Jennifer; Findley, Abigail; Roy, Amy K; Dennis-Tiwary, Tracy A
Adolescence is a critical developmental period of biological and social change during which 1 in 3 youth experience significant anxiety symptoms. The social-emotional lives of the majority of adolescents are largely conducted via digital media use (DMU; e.g., social media, text messaging). Yet the past decade of research on DMU and anxiety has yielded mixed results (e.g., Keles et al., 2020 review), leaving the complex role that DMU might play in the emergence and maintenance of anxiety poorly understood. A key step forward is to leverage psychophysiology to identify individual differences in cognitive and emotional processes that confer vulnerability to potential negative effects of DMU. Further, given the ubiquity of DMU, a greater focus is needed on measurements that move beyond sheer frequency to capture DMU in comparison to face-to-face (FTF) social interactions. This study examined attention bias (AB), characterized by selective and exaggerated attention toward or away from threat, as a moderator of the link between DMU and anxiety in adolescents (N = 75; 42 female) aged 12-14 years (M = 13.28, SD = 0.87). AB was indexed during a dot probe task using reaction time metrics (i.e., trial-level bias) and via ERPs capturing attentional selection and discrimination (N170) and cognitive control (N2) to threat compared to neutral faces. AB moderated associations between DMU and anxiety. A greater preference to use DMU vs FTF predicted greater anxiety among those with a greater behavioral bias away from threat, blunted N170, and blunted N2 in the presence of threat. Future research should examine potential causal and bidirectional links between DMU and anxiety and explore whether preferences for technology-mediated interactions and individual differences in threat processing increase risk.
PMCID:11391916
PMID: 39268514
ISSN: 2451-9588
CID: 5690742
Early-life prefrontal cortex inhibition and early-life stress lead to long-lasting behavioral, transcriptional, and physiological impairments
Menezes, Edênia C; Geiger, Heather; Abreu, Fabiula F; Rachmany, Lital; Wilson, Donald A; Alldred, Melissa J; Castellanos, Francisco X; Fu, Rui; Sargin, Derya; Corvelo, André; Teixeira, Cátia M
Early-life stress has been linked to multiple neurodevelopmental and neuropsychiatric deficits. Our previous studies have linked maternal presence/absence from the nest in developing rat pups to changes in prefrontal cortex (PFC) activity. Furthermore, we have shown that these changes are modulated by serotonergic signaling. Here we test whether changes in PFC activity during early life affect the developing cortex leading to behavioral alterations in the adult. We show that inhibiting the PFC of mouse pups leads to cognitive deficits in the adult comparable to those seen following maternal separation. Moreover, we show that activating the PFC during maternal separation can prevent these behavioral deficits. To test how maternal separation affects the transcriptional profile of the PFC we performed single-nucleus RNA-sequencing. Maternal separation led to differential gene expression almost exclusively in inhibitory neurons. Among others, we found changes in GABAergic and serotonergic pathways in these interneurons. Interestingly, both maternal separation and early-life PFC inhibition led to changes in physiological responses in prefrontal activity to GABAergic and serotonergic antagonists that were similar to the responses of more immature brains. Prefrontal activation during maternal separation prevented these changes. These data point to a crucial role of PFC activity during early life in behavioral expression in adulthood.
PMID: 38486048
ISSN: 1476-5578
CID: 5644132
Unraveling unmet needs in ketogenic dietary services: An ERN EpiCARE survey
De Giorgis, Valentina; Pasca, Ludovica; Aznar-Lain, Gemma; Bibic, Irena; Bibic, Vedrana; Darra, Francesca; Dianin, Alice; Dressler, Anastasia; Jonsson, Henna; Komulainen-Ebrahim, Jonna; Kverneland, Magnhild; Molteberg, Ellen; Ragona, Francesca; de Saint-Martin, Anne; Varesio, Costanza; Cross, J Helen; ,
The implementation and potential of ketogenic dietary therapies (KDTs) have changed over time. The organization of KDT services, the availability of multidisciplinary teams, resources and support for patients and families still vary widely around the world. This diversity is reflected by a lack of consistency in reported outcomes, optimization of using KDT and KDT compliance. To highlight the unmet needs for KDT services, the ERN EpiCARE Ketogenic Dietary Therapy Special Interest Group (KDT SIG) conducted an online survey on KDT implementation and utilization, addressing the following topics: Use and completeness of guidelines and protocols; assessment of compliance and outcome parameters, sustainability and inclusivity in daily life. Consistently reported unmet needs included the lack of psychological support and resources to measure and improve adherence to KDT, the lack of inclusion strategies, and shared guidelines and protocols adapting to specific needs. Future interventions should focus primarily on educational and informative measures together with creation of shared protocols for complex care. PLAIN LANGUAGE SUMMARY: This study provides the results of a survey compiled by clinicians and patients representatives belonging to ERN Epicare, designed to unravel unmet needs from both patients' and healthcare practitioners' perspectives during ketogenic dietary therapies (KDT) provision. Importantly, results show the need to create new shared protocols and guidelines meant for KDT use in complex care situations and to develop future strategies initiatives to support patients improving their social inclusivity.
PMCID:11296111
PMID: 38952082
ISSN: 2470-9239
CID: 5965312
Epigenome-Wide Association Study of Depressive Symptoms in Black Women in the InterGEN Study
Taylor, Brittany; Zhao, Yihong; Perez, Nicole B; Potts-Thompson, Stephanie; Crusto, Cindy; Creber, Ruth Masterson; Taylor, Jacquelyn Y
(1) The prevalence of depression is two times higher in women than men. Black women have an increased risk of depression due to stressors such as low socioeconomic status and perceived discrimination. Depression is likely influenced by both genetic and environmental factors. Psychosocial stressors can influence DNA methylation (DNAm), leading to changes in gene expression and ultimately, depression. The objective of this study was to examine associations between DNAm and depressive symptoms in Black women. (2) This study was a secondary analysis of data from the Intergenerational Impact of Genetic and Psychological Factors on Blood Pressure (InterGEN) Study. Perceived discrimination was assessed using Krieger's Experiences of Discrimination and Waelde's Race-Related Events Scale, and participants were screened for depressive symptoms with the Beck Depression Inventory. Raw data from saliva samples were analyzed using the Illumina Infinium Epic (850 K) BeadChip and then preprocessed in RStudio. (3) Differential methylation analysis identified DNAm sites and regions associated with depressive symptoms. Six DNAm sites had a q-value less than 0.05. Additionally, of the 25 regions identified, 12 were associated with neurological diseases or disorders. (4) These findings suggest that there is a neurological component to depression, which should be considered during treatment.
PMCID:11277114
PMID: 39062924
ISSN: 1422-0067
CID: 5696222
Appearance Dissatisfaction and Body Dysmorphic Disorder in the Dermatology Patient
Sejdiu, Zane; Stitzlein, Erin; Rieder, Evan A; Andriessen, Anneke; Greenberg, Jennifer L; Oza, Vikash S; Cutler, Vanessa; Gonzalez, Mercedes E; Lio, Peter; Love, Elyse M; Park, Joyce; Andriessen, Hinke; Phillips, Katharine A
Dermatologists routinely see patients with inflammatory skin conditions and aesthetic concerns that involve substantial psychological comorbidity. However, most dermatologists do not receive formal training in this area, and many are unsure how to best help treat certain patients holistically. Body dysmorphic disorder (BDD) is a common and distressing psychiatric condition that disproportionately impacts dermatology patients, including patients living with chronic inflammatory skin conditions such as acne and atopic dermatitis. BDD is characterized by preoccupation with nonexistent or minimally noticeable flaws in physical appearance that cause clinically significant distress or impairment in functioning. Adolescent populations may be particularly vulnerable to clinically significant body image dissatisfaction, including BDD, due to the high prevalence of acne and the pervasive role of social media platforms. The rise of social media may exacerbate body image issues through repetitive exposure to idealized and often unrealistic beauty standards. Though screening questionnaires can assist dermatologists in recognizing BDD, dermatologists must collaborate with mental health providers to provide comprehensive care to vulnerable patients, including adolescents.J Drugs Dermatol. 2024;23(7):545-550. doi:10.36849/JDD.8156.
PMID: 38954625
ISSN: 1545-9616
CID: 5698282
Mapping the neural mechanism that distinguishes between holistic thinking and analytic thinking
Teng, Yue; Li, Hui-Xian; Chen, Sylvia Xiaohua; Castellanos, Francisco Xavier; Yan, Chao-Gan; Hu, Xiaomeng
Holistic and analytic thinking are two distinct modes of thinking used to interpret the world with relative preferences varying across cultures. While most research on these thinking styles has focused on behavioral and cognitive aspects, a few studies have utilized functional magnetic resonance imaging (fMRI) to explore the correlations between brain metrics and self-reported scale scores. Other fMRI studies used single holistic and analytic thinking tasks. As a single task may involve processing in spurious low-level regions, we used two different holistic and analytic thinking tasks, namely the frame-line task and the triad task, to seek convergent brain regions to distinguish holistic and analytic thinking using multivariate pattern analysis (MVPA). Results showed that brain regions fundamental to distinguish holistic and analytic thinking include the bilateral frontal lobes, bilateral parietal lobes, bilateral precentral and postcentral gyrus, bilateral supplementary motor areas, bilateral fusiform, bilateral insula, bilateral angular gyrus, left cuneus, and precuneus, left olfactory cortex, cingulate gyrus, right caudate and putamen. Our study maps brain regions that distinguish between holistic and analytic thinking and provides a new approach to explore the neural representation of cultural constructs. We provide initial evidence connecting culture-related brain regions with language function to explain the origins of cultural differences in cognitive styles.
PMID: 38723877
ISSN: 1095-9572
CID: 5658482
Pathways between parental depressed mood and child cognition in economically marginalized populations
Chad-Friedman, Simone; Kleiner, Jamie R.; Rich, Brendan A.
ORIGINAL:0017831
ISSN: 0193-3973
CID: 5964782
AACAP Endorses the Inclusion of Methylphenidate in the WHO Model Lists of Essential Medicines [Letter]
Cortese, Samuele; Coghill, David; Mattingly, Gregory W; Rohde, Luis Augusto; Thom, Robyn P; Wilens, Timothy E; Wong, Ian C K; Faraone, Stephen V
Despite decades of clinical use and a large body of evidence, the WHO continues to exclude methylphenidate for attention-deficit/hyperactivity disorder (ADHD) from its EML.1 The exclusion of methylphenidate has dire implications for millions of individuals with ADHD worldwide, especially those living in low and low-middle income countries (LMIC), where governmental decisions to make medicines available are contingent on EML listing.
PMID: 38428579
ISSN: 1527-5418
CID: 5722852
GLUT1DS focus on dysarthria
Corradini, Miriam; Zanaboni, Martina Paola; Varesio, Costanza; Celario, Massimiliano; Capelli, Elena; Giudice, Carla; Quaranta, Carlo Alberto; Mensi, Martina Maria; Pasca, Ludovica; De Giorgis, Valentina
RESEARCH PURPOSE/OBJECTIVE:GLUT1 deficiency syndrome (GLUT1DS) is a rare genetic disorder caused by a mutation in the SLC2A1 gene that limits the transport of glucose across the blood-brain barrier. Speech disorders and dysarthria are typical findings in patients with GLUT1DS, but have never been deeply phenotyped. The aim of the present study was to characterize speech abilities in a sample of patients with GLUT1DS. RESULTS:30 patients with GLUT1DS were recruited. We reported impairments in different speech and oromotor domains: the speech was characterized by dysarthria, inaccurate articulation of consonants, abnormal nasal resonance, errors in intonation and prosody and low intelligibility. We observed difficulties in motor planning and programming. Moreover, we observed a significant difference between the dysarthric level of impairment with genotype groups. CONCLUSIONS:The presence of a speech disorder in patients with GLUT1DS represents a core feature of the syndrome. Our findings suggest that patients with GLUT1DS would benefit from a comprehensive neurocognitive assessment to detect strengths and weaknesses of the speech profile. Understanding the speech and language phenotype in GLUT1DS is critical for planning early intervention to positively influence the global development of patients with GLUT1DS.
PMID: 38851145
ISSN: 1532-2130
CID: 5965302
White matter development and language abilities during infancy in autism spectrum disorder
McFayden, Tyler C; Rutsohn, Joshua; Cetin, Gizem; Forsen, Elizabeth; Swanson, Meghan R; Meera, Shoba S; Wolff, Jason J; Elison, Jed T; Shen, Mark D; Botteron, Kelly; Dager, Stephen R; Estes, Annette; Gerig, Guido; McKinstry, Robert C; Pandey, Juhi; Schultz, Robert; St John, Tanya; Styner, Martin; Truong, Young; Zwaigenbaum, Lonnie; Hazlett, Heather C; Piven, Joseph; Girault, Jessica B; ,
White matter (WM) fiber tract differences are present in autism spectrum disorder (ASD) and could be important markers of behavior. One of the earliest phenotypic differences in ASD are language atypicalities. Although language has been linked to WM in typical development, no work has evaluated this association in early ASD. Participants came from the Infant Brain Imaging Study and included 321 infant siblings of children with ASD at high likelihood (HL) for developing ASD; 70 HL infants were later diagnosed with ASD (HL-ASD), and 251 HL infants were not diagnosed with ASD (HL-Neg). A control sample of 140 low likelihood infants not diagnosed with ASD (LL-Neg) were also included. Infants contributed expressive language, receptive language, and diffusion tensor imaging data at 6-, 12-, and 24 months. Mixed effects regression models were conducted to evaluate associations between WM and language trajectories. Trajectories of microstructural changes in the right arcuate fasciculus were associated with expressive language development. HL-ASD infants demonstrated a different developmental pattern compared to the HL-Neg and LL-Neg groups, wherein the HL-ASD group exhibited a positive association between WM fractional anisotropy and language whereas HL-Neg and LL-Neg groups showed weak or no association. No other fiber tracts demonstrated significant associations with language. In conclusion, results indicated arcuate fasciculus WM is linked to language in early toddlerhood for autistic toddlers, with the strongest associations emerging around 24 months. To our knowledge, this is the first study to evaluate associations between language and WM development during the pre-symptomatic period in ASD.
PMCID:11336031
PMID: 38383768
ISSN: 1476-5578
CID: 5739222