Kristin Murtha, Samantha Perlstein, Yael Paz, Jakob Seidlitz, Adrian Raine, Samuel Hawes, Amy Byrd, Rebecca Waller
Background: Many studies show that both callous-unemotional (CU) traits (e.g., low empathy, lack of guilt) and cognitive difficulties increase risk for externalizing psychopathology across development. However, other work suggests that some aggression (e.g., relational, proactive) may rely on intact cognitive function, which could vary based on the presence of CU traits. Moreover, no prior research has adequately accounted for common risk factors shared by CU traits, cognitive difficulties, and externalizing problems, which confounds conclusions that can be drawn about their purported relationships. The current study addressed these knowledge gaps by leveraging rigorous propensity matching methods to isolate associations between CU traits and different dimensions of cognitive function and externalizing problems.
Methods: Associations between CU traits, cognitive functioning, and externalizing outcomes were tested within dimensional (n = 11,868) and propensity-matched group-based (n = 1,224) models using data from the Adolescent Brain Cognitive Development Study®, with rigorous statistical control for shared sociodemographic risk factors. Cross-sectional outcomes were parent-reported symptoms of conduct disorder (CD), oppositional defiant disorder (ODD), and attention deficit hyperactivity disorder (ADHD). Longitudinal outcomes were child-reported overt and relational aggression.
Results: CU traits were uniquely related to more parent-reported CD, ODD, ADHD symptoms, as well as more child-reported aggressive behaviors. Effects of cognitive difficulties were domain specific and were not consistent across dimensional and propensity matched models. There was minimal evidence for divergent associations between CU traits and externalizing outcomes as a function of cognition (i.e., no moderation).
Conclusions: Rigorous control for sociodemographic factors within propensity-matched models establish CU traits as a robust and unique risk factor for externalizing psychopathology, over and above difficulties with cognitive functioning.
背景:许多研究表明,"冷酷无情"(CU)特质(如移情能力低、缺乏负罪感)和认知困难都会增加儿童在整个成长过程中出现外化心理病态的风险。然而,其他研究表明,某些攻击行为(如关系攻击、主动攻击)可能依赖于完整的认知功能,而认知功能可能因 CU 特征的存在而不同。此外,之前的研究还没有充分考虑到CU特质、认知障碍和外化问题所共有的风险因素,这就混淆了关于它们之间所谓关系的结论。本研究利用严格的倾向匹配方法,分离出CU特质与认知功能和外化问题的不同维度之间的关联,从而填补了这些知识空白:利用青少年大脑认知发展研究(Adolescent Brain Cognitive Development Study®)的数据,在基于维度(n = 11,868 人)和倾向匹配组(n = 1,224 人)的模型中测试了CU特质、认知功能和外化结果之间的关联,并对共同的社会人口风险因素进行了严格的统计控制。横断面结果为家长报告的行为障碍 (CD)、对立违抗障碍 (ODD) 和注意缺陷多动障碍 (ADHD) 症状。纵向结果为儿童报告的公开攻击行为和关系攻击行为:结果:CU特质与家长报告的更多CD、ODD和ADHD症状以及儿童报告的更多攻击行为有着独特的关系。认知障碍的影响具有领域特异性,在维度模型和倾向匹配模型中并不一致。只有极少证据表明,认知障碍特质与外化结果之间存在不同的关联(即不存在调节作用):结论:在倾向匹配模型中对社会人口学因素的严格控制确立了CU特质是导致外部化心理病理学的一个强大而独特的风险因素,而不是认知功能方面的困难。
{"title":"Callous-unemotional traits, cognitive functioning, and externalizing problems in a propensity-matched sample from the ABCD study.","authors":"Kristin Murtha, Samantha Perlstein, Yael Paz, Jakob Seidlitz, Adrian Raine, Samuel Hawes, Amy Byrd, Rebecca Waller","doi":"10.1111/jcpp.14062","DOIUrl":"https://doi.org/10.1111/jcpp.14062","url":null,"abstract":"<p><strong>Background: </strong>Many studies show that both callous-unemotional (CU) traits (e.g., low empathy, lack of guilt) and cognitive difficulties increase risk for externalizing psychopathology across development. However, other work suggests that some aggression (e.g., relational, proactive) may rely on intact cognitive function, which could vary based on the presence of CU traits. Moreover, no prior research has adequately accounted for common risk factors shared by CU traits, cognitive difficulties, and externalizing problems, which confounds conclusions that can be drawn about their purported relationships. The current study addressed these knowledge gaps by leveraging rigorous propensity matching methods to isolate associations between CU traits and different dimensions of cognitive function and externalizing problems.</p><p><strong>Methods: </strong>Associations between CU traits, cognitive functioning, and externalizing outcomes were tested within dimensional (n = 11,868) and propensity-matched group-based (n = 1,224) models using data from the Adolescent Brain Cognitive Development Study®, with rigorous statistical control for shared sociodemographic risk factors. Cross-sectional outcomes were parent-reported symptoms of conduct disorder (CD), oppositional defiant disorder (ODD), and attention deficit hyperactivity disorder (ADHD). Longitudinal outcomes were child-reported overt and relational aggression.</p><p><strong>Results: </strong>CU traits were uniquely related to more parent-reported CD, ODD, ADHD symptoms, as well as more child-reported aggressive behaviors. Effects of cognitive difficulties were domain specific and were not consistent across dimensional and propensity matched models. There was minimal evidence for divergent associations between CU traits and externalizing outcomes as a function of cognition (i.e., no moderation).</p><p><strong>Conclusions: </strong>Rigorous control for sociodemographic factors within propensity-matched models establish CU traits as a robust and unique risk factor for externalizing psychopathology, over and above difficulties with cognitive functioning.</p>","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":" ","pages":""},"PeriodicalIF":6.5,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142575023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ekaterina Sadikova, David G Weissman, Maya L Rosen, Elise Robinson, Liliana J Lengua, Margaret A Sheridan, Henning Tiemeier, Katie A McLaughlin
Background: The mechanisms linking early-life adversity with psychopathology over the life-course are complex. In this prospective study, we collectively examined cognitive, affective, and developmental mediators previously found to individually link childhood threat and deprivation experiences to adolescent psychopathology to identify the most potent mechanisms.
Methods: Data came from a community sample of 227 children (mean child age 11.5 ± 0.5 years, 48.5% female) from the Seattle metro area with recruitment designed to reflect diversity in family income. Candidate mechanisms included self-rated pubertal development and task-measured attention bias to threat, emotion regulation, theory of mind, fear learning, inhibitory control, language ability, reasoning, and reward sensitivity. Using a high-dimensional mediation approach, we determined which mediating pathways linking threat and deprivation to psychopathology persisted after controlling for all candidate mechanisms associated with psychopathology. Models additionally controlled for the child's age, sex, early-childhood emotional and behavioral symptoms, poverty, and maternal depression.
Results: Blunted reward sensitivity mediated the prospective relationship between threat and internalizing psychopathology, explaining 17.25% (95% CI 1.08%, 69.96%) of this association. Advanced pubertal development was associated with increases in internalizing and externalizing symptoms (standardized associations of 0.16 (95% CI 0.03, 0.29) and 0.17 (95% CI 0.05, 0.29), respectively), but not with adversity. Although deprivation was strongly related to psychopathology, no mechanisms were empirically identified.
Conclusions: In a well-characterized community sample, we isolated reward sensitivity as a robust mediator of the prospective association between early-life threat and adolescent internalizing psychopathology. Interventions aimed at bolstering reward sensitivity may mitigate the impact of early-life threat experiences on internalizing problems.
背景:早期逆境与一生中的精神病理学之间的关联机制非常复杂。在这项前瞻性研究中,我们综合考察了认知、情感和发展方面的中介因素,这些因素以前曾被发现单独地将童年的威胁和匮乏经历与青少年心理病理学联系起来,从而找出最有效的机制:数据来自西雅图都会区的一个社区样本,样本中有 227 名儿童(平均年龄为 11.5 ± 0.5 岁,48.5% 为女性),样本的招募旨在反映家庭收入的多样性。候选机制包括自我评价的青春期发育和任务测量的对威胁的注意偏差、情绪调节、心智理论、恐惧学习、抑制控制、语言能力、推理和奖赏敏感性。利用高维中介方法,我们确定了在控制了所有与精神病理学相关的候选机制后,哪些中介途径将威胁和剥夺与精神病理学联系在一起。模型还控制了儿童的年龄、性别、儿童早期情绪和行为症状、贫困和母亲抑郁:结果:奖赏敏感性减弱在威胁与内化心理病理学之间的前瞻性关系中起中介作用,解释了17.25%(95% CI 1.08%,69.96%)的这种关联。青春期发育提前与内化和外化症状的增加有关(标准化关联分别为 0.16 (95% CI 0.03, 0.29) 和 0.17 (95% CI 0.05, 0.29)),但与逆境无关。虽然贫困与精神病理学密切相关,但没有发现经验机制:结论:在一个特征明确的社区样本中,我们发现奖赏敏感性是早期生活威胁与青少年内化心理病理学之间前瞻性关联的一个强有力的中介因素。旨在提高奖赏敏感性的干预措施可能会减轻早期生活威胁经历对内化问题的影响。
{"title":"Identifying cognitive, affective, and developmental mechanisms linking threat and deprivation with adolescent psychopathology.","authors":"Ekaterina Sadikova, David G Weissman, Maya L Rosen, Elise Robinson, Liliana J Lengua, Margaret A Sheridan, Henning Tiemeier, Katie A McLaughlin","doi":"10.1111/jcpp.14067","DOIUrl":"https://doi.org/10.1111/jcpp.14067","url":null,"abstract":"<p><strong>Background: </strong>The mechanisms linking early-life adversity with psychopathology over the life-course are complex. In this prospective study, we collectively examined cognitive, affective, and developmental mediators previously found to individually link childhood threat and deprivation experiences to adolescent psychopathology to identify the most potent mechanisms.</p><p><strong>Methods: </strong>Data came from a community sample of 227 children (mean child age 11.5 ± 0.5 years, 48.5% female) from the Seattle metro area with recruitment designed to reflect diversity in family income. Candidate mechanisms included self-rated pubertal development and task-measured attention bias to threat, emotion regulation, theory of mind, fear learning, inhibitory control, language ability, reasoning, and reward sensitivity. Using a high-dimensional mediation approach, we determined which mediating pathways linking threat and deprivation to psychopathology persisted after controlling for all candidate mechanisms associated with psychopathology. Models additionally controlled for the child's age, sex, early-childhood emotional and behavioral symptoms, poverty, and maternal depression.</p><p><strong>Results: </strong>Blunted reward sensitivity mediated the prospective relationship between threat and internalizing psychopathology, explaining 17.25% (95% CI 1.08%, 69.96%) of this association. Advanced pubertal development was associated with increases in internalizing and externalizing symptoms (standardized associations of 0.16 (95% CI 0.03, 0.29) and 0.17 (95% CI 0.05, 0.29), respectively), but not with adversity. Although deprivation was strongly related to psychopathology, no mechanisms were empirically identified.</p><p><strong>Conclusions: </strong>In a well-characterized community sample, we isolated reward sensitivity as a robust mediator of the prospective association between early-life threat and adolescent internalizing psychopathology. Interventions aimed at bolstering reward sensitivity may mitigate the impact of early-life threat experiences on internalizing problems.</p>","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":" ","pages":""},"PeriodicalIF":6.5,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142542365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E Caitlin Lloyd, Jonathan Posner, Janet Schebendach, Alexandra F Muratore, Susie Hong, Jessica Ojeda, Elizabeth Rafanello, Joanna E Steinglass, Karin Foerde
Background: Adolescence is a critical developmental period for the study of anorexia nervosa (AN), an illness characterized by extreme restriction of food intake. The maturation of the reward system during adolescence combined with recent neurobiological models of AN led to the hypothesis that early on in illness, restrictive food choices would be associated with activity in nucleus accumbens reward regions, rather than caudate regions identified among adults with AN.
Methods: Healthy adolescents (HC, n = 41) and adolescents with AN or atypical AN (atypAN, n = 76) completed a Food Choice Task during fMRI scanning. Selection of high-fat foods and choice-related activation in nucleus accumbens and anterior caudate regions-of-interest (ROIs) were compared between individuals with AN/atypAN and HC. Associations were examined between choice-related activation and choice preferences among the AN group. Exploratory analyses examined associations between choice-related activation and psychological assessments among the patient group.
Results: Adolescents with AN or atypAN selected fewer high-fat foods than HC (t = -5.92, p < .001). Counter to predictions, there were no significant group differences in choice-related activation in the ROIs. Among individuals with AN or atypAN, choice-related neural activity in the anterior caudate was significantly negatively associated with high-fat food selections in the task (r = -.32, p = .024). In exploratory analyses, choice-related anterior caudate activation was positively associated with psychological measures of illness severity among patients (p's < .05, uncorrected).
Conclusions: In this large cohort of adolescents with AN/atypAN, there was no evidence of altered reward system engagement during food choice. While there was no group difference in choice-related caudate activation, the associations with choices and psychological measures continue to suggest that this neural region is implicated in illness. Longitudinal analyses will clarify whether neural variability relates to longer-term course.
{"title":"Food choice and neural reward systems in adolescents with anorexia nervosa and atypical anorexia nervosa.","authors":"E Caitlin Lloyd, Jonathan Posner, Janet Schebendach, Alexandra F Muratore, Susie Hong, Jessica Ojeda, Elizabeth Rafanello, Joanna E Steinglass, Karin Foerde","doi":"10.1111/jcpp.14066","DOIUrl":"10.1111/jcpp.14066","url":null,"abstract":"<p><strong>Background: </strong>Adolescence is a critical developmental period for the study of anorexia nervosa (AN), an illness characterized by extreme restriction of food intake. The maturation of the reward system during adolescence combined with recent neurobiological models of AN led to the hypothesis that early on in illness, restrictive food choices would be associated with activity in nucleus accumbens reward regions, rather than caudate regions identified among adults with AN.</p><p><strong>Methods: </strong>Healthy adolescents (HC, n = 41) and adolescents with AN or atypical AN (atypAN, n = 76) completed a Food Choice Task during fMRI scanning. Selection of high-fat foods and choice-related activation in nucleus accumbens and anterior caudate regions-of-interest (ROIs) were compared between individuals with AN/atypAN and HC. Associations were examined between choice-related activation and choice preferences among the AN group. Exploratory analyses examined associations between choice-related activation and psychological assessments among the patient group.</p><p><strong>Results: </strong>Adolescents with AN or atypAN selected fewer high-fat foods than HC (t = -5.92, p < .001). Counter to predictions, there were no significant group differences in choice-related activation in the ROIs. Among individuals with AN or atypAN, choice-related neural activity in the anterior caudate was significantly negatively associated with high-fat food selections in the task (r = -.32, p = .024). In exploratory analyses, choice-related anterior caudate activation was positively associated with psychological measures of illness severity among patients (p's < .05, uncorrected).</p><p><strong>Conclusions: </strong>In this large cohort of adolescents with AN/atypAN, there was no evidence of altered reward system engagement during food choice. While there was no group difference in choice-related caudate activation, the associations with choices and psychological measures continue to suggest that this neural region is implicated in illness. Longitudinal analyses will clarify whether neural variability relates to longer-term course.</p>","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":" ","pages":""},"PeriodicalIF":6.5,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142542364","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Robert B. Penfold, Abisola E. Idu, R. Yates Coley, Kara L. Cushing‐Haugen, Deborah King, Ashley Glass, Rebecca C. Phillips, Anne D. Renz, Chester J. Pabiniak, Vina F. Graham, Ella E. Thompson, James D. Ralston, Gregory E. Simon, Erin S. Gonzalez, Kathleen M. Myers, Arne Beck, LeeAnn M. Quintana, Arthur J. Runkle, Megan Rogers, Deirdre M. Foster, Gregory N. Clarke, Stefan Massimino, Phillip M. Crawford, Julie A. Cavese, Anthony R. Cordaro, Laura I. Chavez, Kelly J. Kelleher, Nadine Schwartz, Kristina R. Jiner, Swan Bee Liu, Sara Condrac, Robert J. Hilt
BackgroundAntipsychotic medications (AP) are inappropriately prescribed to young people. The goal of this pragmatic trial was to test a four‐component approach to improved targeting of antipsychotic prescribing to people aged ≥3 and <18 years.MethodsClinicians in four health systems were cluster randomized by the number of previous AP orders and service line – specialty mental health and all others. Intervention arm clinicians received a best practice alert and child psychiatrist consultation and feedback. Families received system navigation and expedited access to psychotherapy. Primary outcomes were total days' supply of AP medication and proportion of youth with any AP supply at 6 months. We estimated the log‐odds of AP use at 6 months and the relative rate of AP over 6 months. The Safer and Targeted Use of Antipsychotics in Youth (SUAY) trial took place between 3/2018 and 12/2020.ResultsThe trial enrolled 733 patients. The odds ratio (OR) comparing use at 6 months was 0.75 (95% CI: 0.52, 1.09). The mean number of days using AP was 118.5 for intervention patients and 128.2 for control patients (relative risk [RR] = 0.92; 95% CI: 0.81–1.04). Exploratory heterogeneity of treatment effects (HTE) was not detected in groups defined by age, gender, provider specialty, and insurance type. HTE by race/ethnicity was present: among youth of color, mean days' supply was 103.2 for intervention arm and 131.2 for the control arm (RR 0.79, 95% CI: 0.67–0.93). Among secondary outcomes, only new psychotherapy referrals differed with 44.3% (n = 154) of intervention participants having a new order for psychotherapy compared to 33.5% (n = 129) in the control arm (OR 1.47: 95% CI: 1.01–2.14).ConclusionsThis intervention did not result in less AP use at 6 months or a reduction in the days' supply of AP medication, although psychotherapy orders increased. The intervention may be effective for some subgroups.
背景抗精神病药物(AP)被不适当地开具给年轻人。这项实用性试验的目的是测试一种由四部分组成的方法,以改进对年龄≥3 岁和 18 岁人群抗精神病药物处方的针对性。方法:四个医疗系统的临床医生按照之前的抗精神病药物处方数量和服务项目(专科精神卫生和其他)进行分组随机分配。干预组的临床医生会收到最佳实践提醒以及儿童精神科医生的咨询和反馈。家庭接受系统导航和快速心理治疗。主要结果为 AP 药物的总供应天数和 6 个月时有任何 AP 供应的青少年比例。我们估算了 6 个月内使用 AP 的对数,以及 6 个月内使用 AP 的相对比率。青少年更安全、更有针对性地使用抗精神病药物(SUAY)试验于2018年3月至2020年12月期间进行。6个月时使用抗精神病药物的几率比(OR)为0.75(95% CI:0.52,1.09)。干预患者使用 AP 的平均天数为 118.5 天,对照患者为 128.2 天(相对风险 [RR] = 0.92;95% CI:0.81-1.04)。在按年龄、性别、医疗机构专业和保险类型划分的组别中,未发现治疗效果的探索性异质性(HTE)。存在按种族/民族划分的异质性:在有色人种青少年中,干预组的平均治疗天数为 103.2 天,对照组为 131.2 天(RR 0.79,95% CI:0.67-0.93)。在次要结果中,只有新的心理治疗转介存在差异,44.3%(n = 154)的干预参与者有新的心理治疗订单,而对照组为 33.5%(n = 129)(OR 1.47:95% CI:1.01-2.14)。干预措施可能对某些亚群有效。
{"title":"Safer and targeted use of antipsychotics in youth: an embedded, pragmatic randomized trial","authors":"Robert B. Penfold, Abisola E. Idu, R. Yates Coley, Kara L. Cushing‐Haugen, Deborah King, Ashley Glass, Rebecca C. Phillips, Anne D. Renz, Chester J. Pabiniak, Vina F. Graham, Ella E. Thompson, James D. Ralston, Gregory E. Simon, Erin S. Gonzalez, Kathleen M. Myers, Arne Beck, LeeAnn M. Quintana, Arthur J. Runkle, Megan Rogers, Deirdre M. Foster, Gregory N. Clarke, Stefan Massimino, Phillip M. Crawford, Julie A. Cavese, Anthony R. Cordaro, Laura I. Chavez, Kelly J. Kelleher, Nadine Schwartz, Kristina R. Jiner, Swan Bee Liu, Sara Condrac, Robert J. Hilt","doi":"10.1111/jcpp.14059","DOIUrl":"https://doi.org/10.1111/jcpp.14059","url":null,"abstract":"BackgroundAntipsychotic medications (AP) are inappropriately prescribed to young people. The goal of this pragmatic trial was to test a four‐component approach to improved targeting of antipsychotic prescribing to people aged ≥3 and <18 years.MethodsClinicians in four health systems were cluster randomized by the number of previous AP orders and service line – specialty mental health and all others. Intervention arm clinicians received a best practice alert and child psychiatrist consultation and feedback. Families received system navigation and expedited access to psychotherapy. Primary outcomes were total days' supply of AP medication and proportion of youth with any AP supply at 6 months. We estimated the log‐odds of AP use at 6 months and the relative rate of AP over 6 months. <jats:italic>The Safer and Targeted Use of Antipsychotics in Youth</jats:italic> (SUAY) trial took place between 3/2018 and 12/2020.ResultsThe trial enrolled 733 patients. The odds ratio (OR) comparing use at 6 months was 0.75 (95% CI: 0.52, 1.09). The mean number of days using AP was 118.5 for intervention patients and 128.2 for control patients (relative risk [RR] = 0.92; 95% CI: 0.81–1.04). Exploratory heterogeneity of treatment effects (HTE) was not detected in groups defined by age, gender, provider specialty, and insurance type. HTE by race/ethnicity was present: among youth of color, mean days' supply was 103.2 for intervention arm and 131.2 for the control arm (RR 0.79, 95% CI: 0.67–0.93). Among secondary outcomes, only new psychotherapy referrals differed with 44.3% (<jats:italic>n</jats:italic> = 154) of intervention participants having a new order for psychotherapy compared to 33.5% (<jats:italic>n</jats:italic> = 129) in the control arm (OR 1.47: 95% CI: 1.01–2.14).ConclusionsThis intervention did not result in less AP use at 6 months or a reduction in the days' supply of AP medication, although psychotherapy orders increased. The intervention may be effective for some subgroups.","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":"53 1","pages":""},"PeriodicalIF":7.6,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142541233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nora R. Bakken, Nadine Parker, Laurie J. Hannigan, Espen Hagen, Pravesh Parekh, Alexey Shadrin, Piotr Jaholkowski, Evgeniia Frei, Viktoria Birkenæs, Guy Hindley, Laura Hegemann, Elizabeth C. Corfield, Martin Tesli, Alexandra Havdahl, Ole A. Andreassen
BackgroundSymptoms related to mood and anxiety disorders (emotional disorders) often present in childhood and adolescence. Some of the genetic liability for mental disorders, and emotional and behavioral difficulties seems to be shared. Yet, it is unclear how genetic liability for emotional disorders and related traits influence trajectories of childhood behavioral and emotional difficulties, and if specific developmental patterns are associated with higher genetic liability for these disorders.MethodsThis study uses data from a genotyped sample of children (n = 54,839) from the Norwegian Mother, Father, and Child Cohort Study (MoBa). We use latent growth models (1.5–5 years) and latent profile analyses (1.5–8 years) to quantify childhood trajectories and profiles of emotional and behavioral difficulties and diagnoses. We examine associations between these trajectories and profiles with polygenic scores for bipolar disorder (PGSBD), anxiety (PGSANX), depression (PGSDEP), and neuroticism (PGSNEUR).ResultsAssociations between PGSDEP, PGSANX, and PGSNEUR, and emotional and behavioral difficulties in childhood were more persistent than age‐specific across early childhood (1.5–5 years). Higher PGSANX and PGSDEP were associated with steeper increases in behavioral difficulties across early childhood. Latent profile analyses identified five profiles with different associations with emotional disorder diagnosis. All PGS were associated with the probability of classification into profiles characterized by some form of difficulties (vs. a normative reference profile), but only PGSBD was uniquely associated with a single developmental profile.ConclusionsGenetic risk for mood disorders and related traits contribute to both a higher baseline level of, and a more rapid increase in, emotional and behavioral difficulties across early and middle childhood, with some indications for disorder‐specific profiles. Our findings may inform research on developmental pathways to emotional disorders and the improvement of initiatives for early identification and targeted intervention.
{"title":"Childhood trajectories of emotional and behavioral difficulties are related to polygenic liability for mood and anxiety disorders","authors":"Nora R. Bakken, Nadine Parker, Laurie J. Hannigan, Espen Hagen, Pravesh Parekh, Alexey Shadrin, Piotr Jaholkowski, Evgeniia Frei, Viktoria Birkenæs, Guy Hindley, Laura Hegemann, Elizabeth C. Corfield, Martin Tesli, Alexandra Havdahl, Ole A. Andreassen","doi":"10.1111/jcpp.14063","DOIUrl":"https://doi.org/10.1111/jcpp.14063","url":null,"abstract":"BackgroundSymptoms related to mood and anxiety disorders (emotional disorders) often present in childhood and adolescence. Some of the genetic liability for mental disorders, and emotional and behavioral difficulties seems to be shared. Yet, it is unclear how genetic liability for emotional disorders and related traits influence trajectories of childhood behavioral and emotional difficulties, and if specific developmental patterns are associated with higher genetic liability for these disorders.MethodsThis study uses data from a genotyped sample of children (<jats:italic>n</jats:italic> = 54,839) from the Norwegian Mother, Father, and Child Cohort Study (MoBa). We use latent growth models (1.5–5 years) and latent profile analyses (1.5–8 years) to quantify childhood trajectories and profiles of emotional and behavioral difficulties and diagnoses. We examine associations between these trajectories and profiles with polygenic scores for bipolar disorder (PGS<jats:sub>BD</jats:sub>), anxiety (PGS<jats:sub>ANX</jats:sub>), depression (PGS<jats:sub>DEP</jats:sub>), and neuroticism (PGS<jats:sub>NEUR</jats:sub>).ResultsAssociations between PGS<jats:sub>DEP</jats:sub>, PGS<jats:sub>ANX</jats:sub>, and PGS<jats:sub>NEUR</jats:sub>, and emotional and behavioral difficulties in childhood were more persistent than age‐specific across early childhood (1.5–5 years). Higher PGS<jats:sub>ANX</jats:sub> and PGS<jats:sub>DEP</jats:sub> were associated with steeper increases in behavioral difficulties across early childhood. Latent profile analyses identified five profiles with different associations with emotional disorder diagnosis. All PGS were associated with the probability of classification into profiles characterized by some form of difficulties (vs. a normative reference profile), but only PGS<jats:sub>BD</jats:sub> was uniquely associated with a single developmental profile.ConclusionsGenetic risk for mood disorders and related traits contribute to both a higher baseline level of, and a more rapid increase in, emotional and behavioral difficulties across early and middle childhood, with some indications for disorder‐specific profiles. Our findings may inform research on developmental pathways to emotional disorders and the improvement of initiatives for early identification and targeted intervention.","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":"44 1","pages":""},"PeriodicalIF":7.6,"publicationDate":"2024-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142490771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tamara Lorenz, Nathalie Michels, George M. Slavich, Matteo Giletta
BackgroundAdolescents exposed to victimization are at an increased risk for a variety of adverse mental health outcomes, including depressive symptoms. Yet, the biological pathways underlying these associations remain poorly understood. Focusing on within‐person processes, we examined whether low‐grade systemic inflammation mediated the longitudinal associations between peer victimization and depressive symptoms in adolescence.Methods207 adolescents (at baseline Mage = 12.69 years; SD = 0.49; 43.5% female) participated in a multi‐wave longitudinal study, with assessments repeated every 6 months over 1.5 years. At each assessment wave, participants self‐reported their peer victimization experiences and depressive symptoms. Dried blood spots were collected at each wave using a finger prick procedure to assay a key marker of low‐grade systemic inflammation, interkeukin‐6 (IL‐6). Data were analyzed using random‐intercept cross‐lagged panel models.ResultsThe cross‐lagged paths from IL‐6 to depressive symptoms were significant across all models and waves (β12 = .13; β23 = .12; β34 = .08), indicating that when adolescents' levels of low‐grade systemic inflammation were above their person‐specific average, they reported increased levels of depressive symptoms in the subsequent months. However, no significant cross‐lagged within‐person associations emerged between peer victimization and either IL‐6 or depressive symptoms.ConclusionsThe findings provide no evidence for the hypothesized mediating role of inflammation in the within‐person associations between peer victimization and depressive symptoms. Nevertheless, they extend prior research by indicating that elevated levels of low‐grade systemic inflammation predict the development of depressive symptoms in adolescence.
{"title":"Examining systemic inflammation as a pathway linking peer victimization to depressive symptoms in adolescence","authors":"Tamara Lorenz, Nathalie Michels, George M. Slavich, Matteo Giletta","doi":"10.1111/jcpp.14060","DOIUrl":"https://doi.org/10.1111/jcpp.14060","url":null,"abstract":"BackgroundAdolescents exposed to victimization are at an increased risk for a variety of adverse mental health outcomes, including depressive symptoms. Yet, the biological pathways underlying these associations remain poorly understood. Focusing on within‐person processes, we examined whether low‐grade systemic inflammation mediated the longitudinal associations between peer victimization and depressive symptoms in adolescence.Methods207 adolescents (at baseline <jats:italic>M</jats:italic><jats:sub>age</jats:sub> = 12.69 years; <jats:italic>SD</jats:italic> = 0.49; 43.5% female) participated in a multi‐wave longitudinal study, with assessments repeated every 6 months over 1.5 years. At each assessment wave, participants self‐reported their peer victimization experiences and depressive symptoms. Dried blood spots were collected at each wave using a finger prick procedure to assay a key marker of low‐grade systemic inflammation, interkeukin‐6 (IL‐6). Data were analyzed using random‐intercept cross‐lagged panel models.ResultsThe cross‐lagged paths from IL‐6 to depressive symptoms were significant across all models and waves (<jats:italic>β</jats:italic><jats:sub><jats:italic>12</jats:italic></jats:sub> = .13; <jats:italic>β</jats:italic><jats:sub><jats:italic>23</jats:italic></jats:sub> = .12; <jats:italic>β</jats:italic><jats:sub><jats:italic>34</jats:italic></jats:sub> = .08), indicating that when adolescents' levels of low‐grade systemic inflammation were above their person‐specific average, they reported increased levels of depressive symptoms in the subsequent months. However, no significant cross‐lagged within‐person associations emerged between peer victimization and either IL‐6 or depressive symptoms.ConclusionsThe findings provide no evidence for the hypothesized mediating role of inflammation in the within‐person associations between peer victimization and depressive symptoms. Nevertheless, they extend prior research by indicating that elevated levels of low‐grade systemic inflammation predict the development of depressive symptoms in adolescence.","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":"60 1","pages":""},"PeriodicalIF":7.6,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142490598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p>Measles are back. Larger and more frequent measles outbreaks have been reported in 2024 in the United Kingdom and the United States, which predated the COVID-19 pandemic. Measles deaths worldwide rose to an estimated 136,000 in 2022, mostly children.</p><p>Immunizations have been one of the major contributor to the 20th century increased life expectancy alongside better nutrition, hygiene, and lifestyle, way ahead of medical technological prowess that keeps impressing us. Vaccination campaigns and other preventive policies (e.g. car safety belts and anti-tobacco campaigns) have saved and continue to save lives and reduce morbidity (remember tuberculosis or poliomyelitis) much more than da Vinci surgical robots or heart transplants. Vaccines are safe and post-licensure vaccine safety is continuously monitored with different overlapping population-based surveillance systems (Buttery & Clothier, <span>2022</span>). Vaccines achieved the total eradication of smallpox in the late 1970s. A worldwide campaign to eradicate measles was well under way in the 1990s. Then, a case series published in a prestigious medical journal triggered fears of vaccine-induced autism in the public. Despite rigorous science rapidly dismissing the original claim, the measles-mumps-rubella (MMR) vaccine scare and fear of autism propagated. Years later, it has morphed into what we now refer to as ‘vaccine hesitancy’ (VH), MMR vaccine uptake is still below optimal levels, fueling ongoing measles outbreaks. How did we get there?</p><p>The saga started in 1998 with an editorial decision by the <i>Lancet</i> to publish a case series of 12 children suggesting a new syndrome of autism triggered by MMR vaccination had been discovered (Wakefield et al., <span>1998</span>). The publication of a case series in the <i>Lancet</i> almost seems a contradiction in terms. As researchers and editors, we know how cautious we must remain before drawing causal inferences between two variables. There is an established hierarchy of research designs based on their relative strengths for causality assessment. Experimental designs are at the top (e.g. the RCT), followed by controlled observational (cohort and case–control) studies, and by much weaker ecological studies (relying on confounded correlations between group-level data); at the very bottom, lies the case series which, at most, helps generate hypotheses (especially when the knowledge base is quasi-inexistant) but is never sufficient to test causal ones.</p><p>While it is fair to assume that those who reviewed the 1998 manuscript and those who made the decision to publish it were unaware at the time of the fraudulent nature of the data (see: Godlee, Smith, and Marcovitch (<span>2011</span>); Deer <span>2011a</span>, <span>2011b</span> and Deer (<span>2020</span>)), multiple red flags were readily noticeable: its first author had spent previous years trying to prove that adult inflammatory bowel disorders were linked to measles vaccine,
{"title":"Editorial: An autism case series, vaccine hesitancy, and death by measles","authors":"Eric Fombonne","doi":"10.1111/jcpp.14058","DOIUrl":"10.1111/jcpp.14058","url":null,"abstract":"<p>Measles are back. Larger and more frequent measles outbreaks have been reported in 2024 in the United Kingdom and the United States, which predated the COVID-19 pandemic. Measles deaths worldwide rose to an estimated 136,000 in 2022, mostly children.</p><p>Immunizations have been one of the major contributor to the 20th century increased life expectancy alongside better nutrition, hygiene, and lifestyle, way ahead of medical technological prowess that keeps impressing us. Vaccination campaigns and other preventive policies (e.g. car safety belts and anti-tobacco campaigns) have saved and continue to save lives and reduce morbidity (remember tuberculosis or poliomyelitis) much more than da Vinci surgical robots or heart transplants. Vaccines are safe and post-licensure vaccine safety is continuously monitored with different overlapping population-based surveillance systems (Buttery & Clothier, <span>2022</span>). Vaccines achieved the total eradication of smallpox in the late 1970s. A worldwide campaign to eradicate measles was well under way in the 1990s. Then, a case series published in a prestigious medical journal triggered fears of vaccine-induced autism in the public. Despite rigorous science rapidly dismissing the original claim, the measles-mumps-rubella (MMR) vaccine scare and fear of autism propagated. Years later, it has morphed into what we now refer to as ‘vaccine hesitancy’ (VH), MMR vaccine uptake is still below optimal levels, fueling ongoing measles outbreaks. How did we get there?</p><p>The saga started in 1998 with an editorial decision by the <i>Lancet</i> to publish a case series of 12 children suggesting a new syndrome of autism triggered by MMR vaccination had been discovered (Wakefield et al., <span>1998</span>). The publication of a case series in the <i>Lancet</i> almost seems a contradiction in terms. As researchers and editors, we know how cautious we must remain before drawing causal inferences between two variables. There is an established hierarchy of research designs based on their relative strengths for causality assessment. Experimental designs are at the top (e.g. the RCT), followed by controlled observational (cohort and case–control) studies, and by much weaker ecological studies (relying on confounded correlations between group-level data); at the very bottom, lies the case series which, at most, helps generate hypotheses (especially when the knowledge base is quasi-inexistant) but is never sufficient to test causal ones.</p><p>While it is fair to assume that those who reviewed the 1998 manuscript and those who made the decision to publish it were unaware at the time of the fraudulent nature of the data (see: Godlee, Smith, and Marcovitch (<span>2011</span>); Deer <span>2011a</span>, <span>2011b</span> and Deer (<span>2020</span>)), multiple red flags were readily noticeable: its first author had spent previous years trying to prove that adult inflammatory bowel disorders were linked to measles vaccine,","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":"65 11","pages":"1403-1406"},"PeriodicalIF":6.5,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jcpp.14058","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142490594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
David Oppenheim,Michal Mottes-Peleg,Lior Hamburger,Michal Slonim,Yael Maccabi,Nurit Yirmiya
BACKGROUNDThe interactions of typically developing (TD) children within the family context are associated with their social skills in preschool, and the question guiding this study, which focused on boys, was whether the same would be true for autistic children. A specific focus was on the importance of the boys' engagement in triadic, mother-father-child interactions over and above their engagement in dyadic, parent-child interactions. The boys' social skills were assessed concurrently with their family interactions and one year later.METHODSSeventy-five autistic preschooler boys (Age in months: M = 49.45, SD = 11.03) and both of their parents were recruited through treatment centers and social media. The boys' dyadic engagement was assessed from observations of their interactions with their mothers and fathers (separately), and their triadic engagement from an observation of mother-father-child interactions. The boys' social skills in preschool were assessed using a Q-sort completed by observers and teachers and by the Social Responsiveness Questionnaire (SRS) completed by teachers.RESULTSControlling for the severity of the boys' symptoms and IQ, their dyadic engagement was associated with the concurrent observer Q-sort and teacher-reported SRS measures, and their triadic engagement did not explain additional variance in these measures. Predicting over one year, dyadic engagement was associated again with the observer Q-sort and teacher SRS measures, while the boys' triadic engagement accounted for additional variance in these measures as well as the teacher Q-sort. Finally, boys' dyadic engagement predicted gains in social skills on the observer Q-sort, and their triadic engagement was predictive of gains in the observer and teacher Q-sort.CONCLUSIONSThe engagement that autistic preschool-age boys displayed in the context of their dyadic and triadic interactions with their parents appears to be transferred to the preschool setting, and triadic interactions are of particular significance.
{"title":"The social skills of autistic boys in preschool: the contributions of their dyadic and triadic interactions with their parents.","authors":"David Oppenheim,Michal Mottes-Peleg,Lior Hamburger,Michal Slonim,Yael Maccabi,Nurit Yirmiya","doi":"10.1111/jcpp.14061","DOIUrl":"https://doi.org/10.1111/jcpp.14061","url":null,"abstract":"BACKGROUNDThe interactions of typically developing (TD) children within the family context are associated with their social skills in preschool, and the question guiding this study, which focused on boys, was whether the same would be true for autistic children. A specific focus was on the importance of the boys' engagement in triadic, mother-father-child interactions over and above their engagement in dyadic, parent-child interactions. The boys' social skills were assessed concurrently with their family interactions and one year later.METHODSSeventy-five autistic preschooler boys (Age in months: M = 49.45, SD = 11.03) and both of their parents were recruited through treatment centers and social media. The boys' dyadic engagement was assessed from observations of their interactions with their mothers and fathers (separately), and their triadic engagement from an observation of mother-father-child interactions. The boys' social skills in preschool were assessed using a Q-sort completed by observers and teachers and by the Social Responsiveness Questionnaire (SRS) completed by teachers.RESULTSControlling for the severity of the boys' symptoms and IQ, their dyadic engagement was associated with the concurrent observer Q-sort and teacher-reported SRS measures, and their triadic engagement did not explain additional variance in these measures. Predicting over one year, dyadic engagement was associated again with the observer Q-sort and teacher SRS measures, while the boys' triadic engagement accounted for additional variance in these measures as well as the teacher Q-sort. Finally, boys' dyadic engagement predicted gains in social skills on the observer Q-sort, and their triadic engagement was predictive of gains in the observer and teacher Q-sort.CONCLUSIONSThe engagement that autistic preschool-age boys displayed in the context of their dyadic and triadic interactions with their parents appears to be transferred to the preschool setting, and triadic interactions are of particular significance.","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":"92 1","pages":""},"PeriodicalIF":7.6,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142448076","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Margaret H Sibley, Sabrina Flores, Madeline Murphy, Hana Basu, Mark A Stein, Steven W Evans, Xin Zhao, Maychelle Manzano, Shauntal van Dreel
Background: Attention Deficit/Hyperactivity Disorder (ADHD) demonstrates unique developmental manifestations in adolescence with implications for optimized, age-appropriate treatment. This 10-year update is the third in a series of systematic reviews examining the efficacy and safety of adolescent ADHD treatments. We broadly examined efficacy on ADHD symptoms, impairments, and other reported outcomes. Acute and long-term efficacy, and treatment moderators, were considered.
Method: We performed PubMed, EMBASE, and PsycINFO searches for articles published or in press from 2013 to 2024, integrated with hand search and randomized controlled trials (RCTs) identified in this series' earlier reviews. RCTs examining the safety or efficacy of interventions delivered to adolescents (ages 10.0-19.9) with a diagnosis of ADHD were included. Study characteristics were extracted and reviewed, quality of evidence was assessed using GRADE, and effect sizes were calculated for individual studies and illustrated using forest plots.
Results: Sixty-three RCTs were identified. Quality of evidence ranged from high (medication; k = 29) to very low (nutrient supplementation, neurofeedback, occupational therapy; k = 1 each). Medications demonstrated consistent strong impact on ADHD symptoms and inconsistent impact on impairment. Diverse cognitive/behavioral treatments (C/BTs) demonstrated inconsistent impact on ADHD symptoms but strong and consistent impact on impairment and executive function skills, plus moderate benefits on internalizing symptoms. No interventions demonstrated significant safety concerns. Long-term maintenance (up to 3 years post-treatment) was demonstrated for C/BTs, though moderate quality of evidence was noted because participants cannot be fully blinded to receipt of treatment.
Conclusions: The effects of C/BTs and medication appear complementary, not duplicative. Combining medication and C/BT is advised at treatment outset to maximize engagement, maintenance, and response breadth (i.e. improving both ADHD symptoms/cognitive performance and coping skills/functional impairments). Engagement strategies (e.g. motivational interviewing) may facilitate uptake. Novel treatments do not yet demonstrate effects on ADHD symptoms or impairments in adolescents but remain a promising area for research.
{"title":"Research Review: Pharmacological and non-pharmacological treatments for adolescents with attention deficit/hyperactivity disorder - a systematic review of the literature.","authors":"Margaret H Sibley, Sabrina Flores, Madeline Murphy, Hana Basu, Mark A Stein, Steven W Evans, Xin Zhao, Maychelle Manzano, Shauntal van Dreel","doi":"10.1111/jcpp.14056","DOIUrl":"https://doi.org/10.1111/jcpp.14056","url":null,"abstract":"<p><strong>Background: </strong>Attention Deficit/Hyperactivity Disorder (ADHD) demonstrates unique developmental manifestations in adolescence with implications for optimized, age-appropriate treatment. This 10-year update is the third in a series of systematic reviews examining the efficacy and safety of adolescent ADHD treatments. We broadly examined efficacy on ADHD symptoms, impairments, and other reported outcomes. Acute and long-term efficacy, and treatment moderators, were considered.</p><p><strong>Method: </strong>We performed PubMed, EMBASE, and PsycINFO searches for articles published or in press from 2013 to 2024, integrated with hand search and randomized controlled trials (RCTs) identified in this series' earlier reviews. RCTs examining the safety or efficacy of interventions delivered to adolescents (ages 10.0-19.9) with a diagnosis of ADHD were included. Study characteristics were extracted and reviewed, quality of evidence was assessed using GRADE, and effect sizes were calculated for individual studies and illustrated using forest plots.</p><p><strong>Results: </strong>Sixty-three RCTs were identified. Quality of evidence ranged from high (medication; k = 29) to very low (nutrient supplementation, neurofeedback, occupational therapy; k = 1 each). Medications demonstrated consistent strong impact on ADHD symptoms and inconsistent impact on impairment. Diverse cognitive/behavioral treatments (C/BTs) demonstrated inconsistent impact on ADHD symptoms but strong and consistent impact on impairment and executive function skills, plus moderate benefits on internalizing symptoms. No interventions demonstrated significant safety concerns. Long-term maintenance (up to 3 years post-treatment) was demonstrated for C/BTs, though moderate quality of evidence was noted because participants cannot be fully blinded to receipt of treatment.</p><p><strong>Conclusions: </strong>The effects of C/BTs and medication appear complementary, not duplicative. Combining medication and C/BT is advised at treatment outset to maximize engagement, maintenance, and response breadth (i.e. improving both ADHD symptoms/cognitive performance and coping skills/functional impairments). Engagement strategies (e.g. motivational interviewing) may facilitate uptake. Novel treatments do not yet demonstrate effects on ADHD symptoms or impairments in adolescents but remain a promising area for research.</p>","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":" ","pages":""},"PeriodicalIF":6.5,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142379582","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Caitlin K Kiernan, Hermien H Dijk, Barbara J van den Hoofdakker, Pieter J Hoekstra, Annabeth P Groenman
Background: Economic evaluations of treatments for children with behavioural difficulties (i.e., characteristics of attention-deficit/hyperactivity disorder (ADHD) and/or oppositional defiant disorder (ODD)) usually rely on data of randomised controlled trials or are model-based. Findings of such studies may not be representative of cost-effectiveness and cost-utility in clinical practice. The current longitudinal study aimed to perform an economic evaluation of treatments for children with hyperactivity, impulsive behaviours, inattention, and/or behavioural difficulties using observational data that were obtained in clinical practice.
Methods: Parents of 209 children (aged 5-12) who were referred to 1 of 10 Dutch youth mental healthcare institutions and who received treatment with (n = 108) or without (n = 101) the use of medication, filled out questionnaires at three timepoints (baseline, and ~ 6 and ~12 months later). Propensity score matching was used to make both groups comparable. Outcomes included quality-adjusted life years (QALYs), ADHD and ODD symptom severity, and impairment. Costs were measured from a societal perspective. Incremental cost-effectiveness ratios (ICERs) were estimated, and cost-effectiveness acceptability curves (CEACs) were derived to show uncertainty around the ICER.
Results: Results did not show statistically significant differences in costs and effects between children who were treated with medication (alone or in combination with non-medication treatment) and those who were treated without medication. CEAC suggested that medication treatment has a 55% probability of being cost-effective at the €80,000 threshold and 36% at the €20,000 threshold compared with treatment without medication.
Conclusions: Using observational data, our study did not provide clear evidence of the cost-effectiveness and cost-utility of treatment with medication compared with treatment without medication in clinical practice.
{"title":"Treatments with versus without medication for children with behavioural difficulties in clinical practice: an economic evaluation with observational data.","authors":"Caitlin K Kiernan, Hermien H Dijk, Barbara J van den Hoofdakker, Pieter J Hoekstra, Annabeth P Groenman","doi":"10.1111/jcpp.14057","DOIUrl":"https://doi.org/10.1111/jcpp.14057","url":null,"abstract":"<p><strong>Background: </strong>Economic evaluations of treatments for children with behavioural difficulties (i.e., characteristics of attention-deficit/hyperactivity disorder (ADHD) and/or oppositional defiant disorder (ODD)) usually rely on data of randomised controlled trials or are model-based. Findings of such studies may not be representative of cost-effectiveness and cost-utility in clinical practice. The current longitudinal study aimed to perform an economic evaluation of treatments for children with hyperactivity, impulsive behaviours, inattention, and/or behavioural difficulties using observational data that were obtained in clinical practice.</p><p><strong>Methods: </strong>Parents of 209 children (aged 5-12) who were referred to 1 of 10 Dutch youth mental healthcare institutions and who received treatment with (n = 108) or without (n = 101) the use of medication, filled out questionnaires at three timepoints (baseline, and ~ 6 and ~12 months later). Propensity score matching was used to make both groups comparable. Outcomes included quality-adjusted life years (QALYs), ADHD and ODD symptom severity, and impairment. Costs were measured from a societal perspective. Incremental cost-effectiveness ratios (ICERs) were estimated, and cost-effectiveness acceptability curves (CEACs) were derived to show uncertainty around the ICER.</p><p><strong>Results: </strong>Results did not show statistically significant differences in costs and effects between children who were treated with medication (alone or in combination with non-medication treatment) and those who were treated without medication. CEAC suggested that medication treatment has a 55% probability of being cost-effective at the €80,000 threshold and 36% at the €20,000 threshold compared with treatment without medication.</p><p><strong>Conclusions: </strong>Using observational data, our study did not provide clear evidence of the cost-effectiveness and cost-utility of treatment with medication compared with treatment without medication in clinical practice.</p>","PeriodicalId":187,"journal":{"name":"Journal of Child Psychology and Psychiatry","volume":" ","pages":""},"PeriodicalIF":6.5,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142337872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}