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Callous-unemotional traits, cognitive functioning, and externalizing problems in a propensity-matched sample from the ABCD study. ABCD研究中的倾向匹配样本中的冷漠-非情感特质、认知功能和外化问题。
IF 6.5 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-11-04 DOI: 10.1111/jcpp.14062
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。
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引用次数: 0
Identifying cognitive, affective, and developmental mechanisms linking threat and deprivation with adolescent psychopathology. 确定将威胁和剥夺与青少年心理病理学联系起来的认知、情感和发展机制。
IF 6.5 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-31 DOI: 10.1111/jcpp.14067
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。
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引用次数: 0
Food choice and neural reward systems in adolescents with anorexia nervosa and atypical anorexia nervosa. 神经性厌食症和非典型厌食症青少年的食物选择和神经奖赏系统。
IF 6.5 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-31 DOI: 10.1111/jcpp.14066
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.

背景:青春期是研究神经性厌食症(AN)的关键发育时期,这种疾病的特点是极度限制食物摄入。青春期奖赏系统的成熟与神经性厌食症的最新神经生物学模型相结合,导致了这样一种假设:在患病初期,限制性食物选择与伏隔核奖赏区的活动有关,而不是与成人神经性厌食症患者中发现的尾状核区有关。方法:健康青少年(HC,n = 41)和患有神经性厌食症或非典型神经性厌食症的青少年(atypAN,n = 76)在进行 fMRI 扫描时完成食物选择任务。对患有自闭症/非典型自闭症的青少年与患有自闭症/非典型自闭症的青少年进行了食物选择任务,并比较了自闭症/非典型自闭症青少年与患有自闭症/非典型自闭症的青少年选择高脂肪食物的情况以及与选择相关的凹凸核和尾状核前部感兴趣区(ROIs)的激活情况。研究还考察了AN组中选择相关激活与选择偏好之间的关联。探索性分析研究了患者组中选择相关激活与心理评估之间的关联:在这一大群患有自闭症/非自闭症的青少年中,没有证据表明在选择食物时奖赏系统的参与发生了改变。虽然在与选择相关的尾状核激活方面没有组间差异,但与选择和心理测量的关联继续表明,这一神经区域与疾病有关。纵向分析将明确神经变异是否与长期病程有关。
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引用次数: 0
Safer and targeted use of antipsychotics in youth: an embedded, pragmatic randomized trial 在青少年中更安全、更有针对性地使用抗精神病药物:嵌入式实用随机试验
IF 7.6 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-30 DOI: 10.1111/jcpp.14059
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 &lt;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}
引用次数: 0
Childhood trajectories of emotional and behavioral difficulties are related to polygenic liability for mood and anxiety disorders 情绪和行为障碍的童年轨迹与情绪和焦虑症的多基因责任有关
IF 7.6 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-27 DOI: 10.1111/jcpp.14063
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.
背景与情绪和焦虑障碍(情感障碍)有关的症状通常出现在儿童和青少年时期。精神障碍、情绪障碍和行为障碍的部分遗传责任似乎是共同的。然而,目前还不清楚情绪障碍和相关特征的遗传责任如何影响儿童行为和情绪障碍的发展轨迹,也不清楚特定的发展模式是否与这些障碍的较高遗传责任相关。我们使用潜在成长模型(1.5-5 岁)和潜在特征分析(1.5-8 岁)来量化儿童期情绪和行为障碍及诊断的轨迹和特征。我们研究了这些轨迹和特征与双相情感障碍(PGSBD)、焦虑(PGSANX)、抑郁(PGSDEP)和神经质(PGSNEUR)的多基因评分之间的关联。结果在整个幼儿期(1.5-5 岁),PGSDEP、PGSANX 和 PGSNEUR 与儿童期情绪和行为障碍之间的关联更具有持续性,而非年龄特异性。较高的 PGSANX 和 PGSDEP 与幼儿期行为障碍的急剧增加有关。潜特征分析确定了与情绪障碍诊断有不同关联的五个特征。结论情绪障碍及相关特质的遗传风险导致儿童早期和中期情绪和行为障碍的基线水平较高,且增加速度较快,并有一些迹象表明存在特定障碍的特征。我们的研究结果可为情绪障碍的发展途径研究以及早期识别和针对性干预措施的改进提供参考。
{"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}
引用次数: 0
Examining systemic inflammation as a pathway linking peer victimization to depressive symptoms in adolescence 研究全身性炎症是青春期同伴伤害与抑郁症状之间的联系途径
IF 7.6 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-25 DOI: 10.1111/jcpp.14060
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.
背景受到伤害的青少年出现各种不良心理健康后果(包括抑郁症状)的风险增加。然而,人们对这些关联的生物学途径仍然知之甚少。方法207名青少年(基线年龄Mage = 12.69岁;SD = 0.49;43.5%为女性)参加了一项多波纵向研究,在1年半的时间里每6个月重复一次评估。在每次评估中,参与者都会自我报告其同伴受害经历和抑郁症状。在每次评估时,研究人员都会采用刺破手指的方法采集干血斑,以检测低度全身炎症的主要标志物白细胞介素-6(IL-6)。结果从IL-6到抑郁症状的交叉滞后路径在所有模型和波次中都是显著的(β12 = .13;β23 = .12;β34 = .08),这表明当青少年的低级全身炎症水平高于其特定人群的平均水平时,他们在随后几个月中的抑郁症状水平就会增加。然而,在同伴受害与 IL-6 或抑郁症状之间并没有出现明显的交叉滞后人际关联。尽管如此,研究结果表明,低度全身炎症水平的升高可预测青少年抑郁症状的发展,从而扩展了之前的研究。
{"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}
引用次数: 0
Editorial: An autism case series, vaccine hesitancy, and death by measles 社论:自闭症病例系列、疫苗犹豫不决和麻疹致死
IF 6.5 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-24 DOI: 10.1111/jcpp.14058
Eric Fombonne
<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,
因此,医疗服务提供者会给 VH 家长更多的时间和考虑,同意推迟麻腮风疫苗的免疫接种,或将其三个组成部分分开注射(众所周知,这种做法会导致免疫接种不完全),现在甚至会培训动机访谈技术以减少 "犹豫"。当疫苗接种规定放宽时(如在加利福尼亚州或得克萨斯州),出于个人信仰向 VH 父母慷慨发放非医疗性疫苗豁免,造成了社区内未接种疫苗儿童的小规模爆发(Bednarczyk, King, Lahijani, &amp; Omer, 2019)。对个人和社会而言,VH 的直接和间接成本一直在飙升。非 VH 父母因 VH 而增加的风险和成本没有得到同等的关注,这些风险和成本不仅对他们自己已接种疫苗的孩子,而且对他们生活的社区都造成了影响。婴儿、免疫抑制儿童、疫苗接种失败的儿童,以及那些来自服务不足、医疗条件有限的社会群体的儿童,都不必要地暴露在麻疹疫情中,并面临着感染麻疹的高风险。然而,因 VH 而产生的费用却全部由那些遵循疫苗接种建议的人分担。所有公共卫生计划都会遇到少数人的抵制,例如限制在公共场所吸烟或系安全带。然而,我们应该注意到,"安全带矛盾综合症 "并不能阻止不系安全带的司机被罚款;仅仅援引个人自由权也不会导致宽大处理。同样,吸烟者往往要支付更高的保险费。虽然强迫是不可取的,但可以考虑对 VH 实行某种形式的个人问责制。在此期间,出现了 12,000 例麻疹病例,数百人住院治疗,还有几例可预防的死亡。仅在 2017 年,欧洲的麻疹病例就增加了四倍,死亡人数达到 35 人。2000 年,美国的麻疹发病率为 0.03/100,000,2019 年上升到 0.39/100,000。2019年是美国自1992年以来麻疹最严重的一年,共报告了1282例病例,绝大多数是未接种疫苗的人。预计 2024 年的情况会更糟。麻疹不会导致儿童自闭症。麻疹不会导致儿童自闭症,但会导致他们死亡。
{"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":"&lt;p&gt;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.&lt;/p&gt;&lt;p&gt;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 &amp; Clothier, &lt;span&gt;2022&lt;/span&gt;). 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?&lt;/p&gt;&lt;p&gt;The saga started in 1998 with an editorial decision by the &lt;i&gt;Lancet&lt;/i&gt; to publish a case series of 12 children suggesting a new syndrome of autism triggered by MMR vaccination had been discovered (Wakefield et al., &lt;span&gt;1998&lt;/span&gt;). The publication of a case series in the &lt;i&gt;Lancet&lt;/i&gt; 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.&lt;/p&gt;&lt;p&gt;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 (&lt;span&gt;2011&lt;/span&gt;); Deer &lt;span&gt;2011a&lt;/span&gt;, &lt;span&gt;2011b&lt;/span&gt; and Deer (&lt;span&gt;2020&lt;/span&gt;)), 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}
引用次数: 0
The social skills of autistic boys in preschool: the contributions of their dyadic and triadic interactions with their parents. 学龄前自闭症男孩的社交技能:他们与父母的二元和三元互动的贡献。
IF 7.6 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-17 DOI: 10.1111/jcpp.14061
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.
背景典型发育(TD)儿童在家庭环境中的互动与他们在学前阶段的社交能力有关,本研究的重点是男孩,研究的问题是自闭症儿童是否也是如此。本研究的一个具体重点是,男孩参与三位一体的母子互动的重要性要高于他们参与两位一体的亲子互动的重要性。方法通过治疗中心和社交媒体招募了 75 名学龄前自闭症男孩(月龄:男 = 49.45,女 = 11.03)及其父母。通过观察男孩与母亲和父亲(分别)的互动来评估他们的二元参与度,通过观察母亲与父亲和孩子的互动来评估他们的三元参与度。通过观察员和教师填写的 Q-sort,以及教师填写的社会反应性问卷(SRS),对男童在学龄前的社交能力进行了评估。结果在控制了男童症状的严重程度和智商后,他们的双向参与与同时观察员填写的 Q-sort 和教师报告的 SRS 测量结果相关,而他们的三向参与并不能解释这些测量结果的额外差异。在预测一年后的情况时,双向参与又与观察者 Q-sort 和教师 SRS 测量结果相关,而男孩的三向参与则能解释这些测量结果以及教师 Q-sort 的额外差异。结论学龄前自闭症男孩在与父母的二元和三元互动中表现出的参与性似乎可以转移到学龄前环境中,三元互动尤其重要。
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引用次数: 0
Research Review: Pharmacological and non-pharmacological treatments for adolescents with attention deficit/hyperactivity disorder - a systematic review of the literature. 研究综述:针对注意力缺陷/多动症青少年的药物和非药物疗法--文献系统性综述。
IF 6.5 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-10-06 DOI: 10.1111/jcpp.14056
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.

背景:注意力缺陷/多动障碍(ADHD)在青少年时期表现出独特的发育特征,这对优化适龄治疗具有重要意义。本10年更新报告是对青少年注意力缺陷/多动障碍治疗的有效性和安全性进行的一系列系统性回顾中的第三篇。我们广泛考察了ADHD症状、损伤和其他报告结果的疗效。我们还考虑了急性和长期疗效以及治疗调节因素:我们在PubMed、EMBASE和PsycINFO上检索了2013年至2024年发表或出版的文章,并结合了手工检索和本系列早期综述中确定的随机对照试验(RCT)。研究对象包括被诊断为多动症的青少年(10.0-19.9 岁),研究内容为干预措施的安全性或有效性。对研究特征进行了提取和审查,使用 GRADE 对证据质量进行了评估,计算了单项研究的效应大小,并使用森林图进行了说明:结果:共确定了 63 项 RCT。证据质量从高(药物治疗;k = 29)到极低(营养补充剂、神经反馈、职业疗法;k = 1)不等。药物治疗对多动症症状的影响一致较强,而对障碍的影响则不一致。不同的认知/行为治疗(C/BTs)对多动症症状的影响不一致,但对功能障碍和执行功能技能的影响一致且很大,另外对内化症状也有适度的益处。没有任何干预措施显示出明显的安全性问题。C/BTs被证明具有长期维持性(治疗后长达3年),但由于不能对参与者接受治疗的情况完全盲目,因此证据质量中等:结论:C/BT 和药物治疗的效果似乎是互补的,而不是重复的。建议在治疗开始时将药物治疗和C/BT结合起来,以最大限度地提高参与度、维持度和反应广度(即同时改善ADHD症状/认知表现和应对技能/功能障碍)。参与策略(如动机访谈)可促进患者接受治疗。新疗法尚未显示出对青少年多动症症状或功能障碍的疗效,但仍是一个很有前景的研究领域。
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引用次数: 0
Treatments with versus without medication for children with behavioural difficulties in clinical practice: an economic evaluation with observational data. 临床实践中对有行为障碍的儿童采用药物治疗与不采用药物治疗的对比:利用观察数据进行经济评估。
IF 6.5 1区 医学 Q1 PSYCHIATRY Pub Date : 2024-09-30 DOI: 10.1111/jcpp.14057
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.

背景:针对儿童行为障碍(即注意力缺陷/多动障碍和/或对立违抗障碍的特征)的治疗方法的经济评估通常依赖于随机对照试验的数据或基于模型的数据。此类研究的结果可能无法代表临床实践中的成本效益和成本效用。本纵向研究旨在利用临床实践中获得的观察数据,对多动症、冲动行为、注意力不集中和/或行为障碍儿童的治疗方法进行经济评估:方法:209 名儿童(5-12 岁)的家长在三个时间点(基线、约 6 个月和约 12 个月后)填写了调查问卷,这些儿童被转介到荷兰 10 家青少年心理医疗机构中的一家,接受了药物治疗(108 人)或未接受药物治疗(101 人)。为使两组具有可比性,采用了倾向得分匹配法。研究结果包括质量调整生命年 (QALY)、ADHD 和 ODD 症状严重程度以及损伤程度。成本从社会角度进行衡量。估算了增量成本效益比(ICER),并绘制了成本效益可接受性曲线(CEAC),以显示ICER周围的不确定性:结果表明,接受药物治疗(单独或与非药物治疗相结合)的儿童与不接受药物治疗的儿童在成本和效果上没有明显的统计学差异。CEAC 认为,与不用药治疗相比,用药治疗在 8 万欧元阈值下具有成本效益的概率为 55%,在 2 万欧元阈值下为 36%:通过观察数据,我们的研究并未提供临床实践中用药治疗与不用药治疗的成本效益和成本效用的明确证据。
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Journal of Child Psychology and Psychiatry
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