跳至主要内容
临床试验/NCT00025935
NCT00025935招募中不适用

Characterization and Pathophysiology of Severe Mood and Behavioral Dysregulation in Children and Youth

National Institute of Mental Health (NIMH)1 个研究点 分布在 1 个国家目标入组 2,350 人开始时间: 2002年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
2,350
试验地点
1
主要终点
To examine between-group differences in clinical, behavioral, genetic, neuroanatomical, and neurophysiological variables

研究概览

简要总结

This study seeks to learn more about the symptoms of severe mood dysregulation in children and adolescents ages 7-17. Children and adolescents with severe mood dysregulation (SMD) display chronic anger, sadness, or irritability, as well as hyperarousal (such as insomnia, distractibility, hyperactivity) and extreme responses to frustration (such as frequent, severe temper tantrums). Researchers will describe the moods and behaviors of children with these symptoms and use specialized testing and brain imaging to learn about the brain changes associated with this disorder.

详细描述

Objective:

Irritability is a common and impairing clinical presentation in youth. Despite its significant public health impact, the clinical course and pathophysiology of irritability remains poorly understood. Chronic and severe irritability is the primary symptom of the new DSM-5 diagnosis, disruptive mood dysregulation disorder (DMDD), is an associated symptom of other pediatric disorders including Attention-Deficit/Hyperactivity Disorder (ADHD), and can be a clinical precursor to Major Depressive Disorder (MDD) and anxiety disorders. In addition, irritability is a trait distributed continuously in youth, thereby fitting well within the National Institute of Mental Health (NIMH) Research Domain Criteria (RDoC) initiative.

Clinically impairing irritability in children and adolescents began to gain more attention as interest grew in the diagnosis of pediatric bipolar disorder. Beginning in the 1990s, child psychiatry researchers suggested that while pediatric bipolar disorder can present with distinct episodes of mania or hypomania as in adults, the more typical pediatric presentation was chronic, severe irritability and hyperarousal symptoms. However, data collected under this protocol comprise a series of longitudinal, family, behavioral, and pathophysiological studies that differentiated classically defined episodic pediatric bipolar disorder from chronic irritability without distinct manic or hypomanic episodes. These findings are consistent with reports from other groups and meta-analyses.

Among the several strands of research designed to differentiate pediatric bipolar disorder from chronic irritability, longitudinal studies provide the strongest evidence that these two phenotypes are distinct. Children with chronic irritability are at elevated risk for later depression, but not manic episodes. Thus, youth with MDD (with and without prior DMDD) are an important comparison group to explore, and we are examining the developmental trajectory, phenomenology, behavioral correlates, and underlying neural mechanisms of chronic irritability and MDD in youth. Further, because irritability and ADHD symptoms are highly comorbid in youth, participants with ADHD are an important comparison group in our work on irritability.

The current translational model of irritability emphasizes the role of abnormal threat and reward processing, but also underlines the relevance of environmental factors in the emergence and maintenance of irritability. More precisely, it is assumed that irritable children experience environments, where rewards and punishments are inconsistently delivered leading to unintentional reinforcement of disruptive behavior through the parents. Reasons for this inconsistent parent behavior could be manifold spanning instrumental learning deficits and exaggerated responses to threat and frustrative non-reward in the parents themselves as well as lack of knowledge regarding learning principles and increased levels of stress. These factors might contribute to instrumental-learning deficits in the children increasing frequency and intensity of temper outbursts. Heightened levels of chronic irritability, another symptom of DMDD, might be more associated with features of the parent-child interaction. There is a rich literature within the framework of attachment theory showing that behavior of children with anxious-resistant insecure attachment is characterized by a general angry tone and is also associated with increased amygdala responses to negative social scenes. In addition, it was also shown that highly irritable infants are less sociable in terms of being less responsive and more fearful towards others and displaying an angry emotional tone in general as toddlers when they had been insecurely attached and more sociable when they had been securely attached. Adding another layer of complexity, it is also conceivable that inconsistent parent behavior diminishes parent's perceived trustworthiness. This could be of relevance as recent studies showed that persons are less willing to delay rewards - an action bound to increase levels of frustration - if their interaction partner is perceived as little reliable.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
7 Years 至 85 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • INCLUSION CRITERIA:
  • Inclusion criteria for children with DMDD, subthreshold DMDD:
  • 1.1.1 Ages 7-17 at the time of recruitment; will be followed in the longitudinal component of the study until age
  • 1.1.2 Abnormal mood (specifically, anger, sadness, and/or irritability), present at least half of the day most days (or at least half the day at least one day per week for subthreshold), and of sufficient severity to be noticeable by people in the child's environment (e.g. parents/caregivers, teachers, peers).
  • 1.1.3 Compared to his/her peers, the child exhibits markedly increased reactivity to negative emotional stimuli that is manifest verbally or behaviorally. For example, the child responds to frustration with extended temper tantrums (inappropriate for age and/or precipitating event), verbal rages, and/or aggression toward people or property. Such events occur, on average, at least three times a week. For subthreshold DMDD such tantrums occur on average at least once per month.
  • 1.1.4 The symptoms in # 1.1.2, and 1.1.3 above are currently present and have been present for at least 12 months without any symptom-free periods exceeding three months.
  • 1.1.5 The onset of symptoms must be prior to age 10 years.
  • 1.1.6 For DMDD the symptoms are severe in at least in one setting (e.g. violent outbursts, assaultiveness at home, school, or with peers) and at least mild (distractibility, intrusiveness) in a second setting. For subthreshold DMDD, there must be evidence of impairment causing distress to the child or to those around him/her in at least one setting.
  • Caregivers of children and adolescents with DMDD or subthreshold DMDD enrolled in 02-M-0021
  • Are capable of performing behavioral tasks and/or scanning.
  • Speaks English
  • Healthy Volunteer (Control) Children
  • Control subjects will be group matched to the patients.
  • Have an identified primary care physician.
  • Speaks English
  • Healthy Volunteer Adults
  • 4.1.1 Control subjects will be group matched to the patients.
  • They will have normal physical and neurological examinations by history or checklist
  • Have an identified primary care physician.
  • 4.1.4 Speaks English
  • Children with Major Depressive Disorder (MDD) Inclusion criteria (all must be met):
  • 5.1.1 Ages 11-17 at the time of recruitment; will be followed in the longitudinal component of the study until age
  • DSM-IV or DSM-5 Major Depressive Disorder
  • 5.1.2.1 Five or more of the following symptoms have been present during the same 2-week period and represent a change from previous functioning; at one of the symptoms is either (1) depressed mood or (2) loss of interest or pleasure.
  • 5.1.2.1.1 Depressed mood most of the day, nearly every day, as indicated by either subjective report (e.g., feeling sad, blue, "down in the dumps," or empty) or observation made by others (e.g., appears tearful or about to cry). (In children and adolescents, this may present as an irritable or cranky, rather than sad, mood.)
  • 5.1.2.1.2 Markedly diminished interest or pleasure in all, or almost all, activities every day, such as no interest in hobbies, sports, or other things the person used to enjoy doing.
  • Significant weight loss when not dieting or weight gain (e.g., a change of more than 5 percent of body weight in a month), or decrease or increase in appetite nearly every day.
  • Insomnia (inability to get to sleep or difficulty staying asleep) or hypersomnia (sleeping too much) nearly every day
  • Psychomotor agitation (e.g., restlessness, inability to sit still, pacing, pulling at clothes or clothes) or retardation (e.g., slowed speech, movements, quiet talking) nearly every day
  • Fatigue, tiredness, or loss of energy nearly every day (e.g., even the smallest tasks, like dressing or washing, seem difficult to do and take longer than usual).
  • Feelings of worthlessness or excessive or inappropriate guilt nearly every day (e.g., ruminating over minor past failings).
  • Diminished ability to think or concentrate, or indecisiveness, nearly every day (e.g. appears easily distracted, complains of memory difficulties).
  • Recurrent thoughts of death (not just fear of dying), recurrent suicidal ideas without a specific plan, or a suicide attempt or a specific plan for committing suicide
  • 5.1.2.1.10 Symptoms cause clinically significant distress or impairment in social, occupational/academic, or other important areas of functioning.
  • The episode is not attributable to the physiological effects of a substance or to another medical condition.
  • Youth with MDD who are continuing in research as adults must also be receiving psychiatric care for their MDD, if it is ongoing
  • Children with Attention-Deficit/Hyperactivity Disorder (ADHD)
  • Currently meets DSM-IV or DSM-5 criteria for ADHD
  • Subjects with other primary psychiatric disorders including anxiety disorders, dysthymic disorder, past major depression, oppositional defiant disorder, tic disorders, and the learning, communication, and elimination disorders may be accepted
  • Have an identified primary care physician.
  • Speaks English

排除标准

  • 1.3 Exclusion criteria for those with DMDD:
  • 1.3.1 The individual exhibits any of these cardinal bipolar symptoms:
  • 1.3.1.1 Elevated or expansive mood
  • 1.3.1.2 Grandiosity or inflated self-esteem
  • 1.3.1.3 Decreased need for sleep
  • 1.3.1.4 Increase in goal-directed activity (this can result in the excessive involvement in pleasurable activities that have a high potential for painful consequences)
  • Has BD symptoms in distinct periods lasting more than 1 day.
  • Meets criteria for schizophrenia, schizophreniform disorder, schizoaffective illness, PDD, or PTSD.
  • The symptoms are due to the direct physiological effects of a drug of abuse, or to a general medical or neurological condition.
  • Currently pregnant or lactating
  • Meets criteria for alcohol or substance abuse with the last three months
  • 2. Exclusion of caregivers of children and adolescents with DMDD or subthreshold DMDD
  • 2.1 Have an I.Q. < 70
  • 2.2 Have any serious medical condition or condition that interferes with participation
  • 3.2 Healthy Volunteer (Control) Children:
  • I.Q. < 70;
  • Any serious medical condition or condition that interferes with fMRI or MEG/EEG scanning, or fNIRS, pregnant or lactating;
  • Past or current diagnosis of any anxiety disorder (panic disorder, GAD, Separation Anxiety Disorder, Social Phobia), mood disorder (manic or hypomanic episode, major depression), OCD, PTSD, Conduct Disorder, psychosis, current suicidal ideation, Tourette Disorder, Autism Spectrum Disorder or ADHD.
  • Substance abuse within two months prior to study participation or present substance abuse
  • History of sexual abuse.
  • Parent or sibling with Bipolar Disorder, recurrent MDD, or any disorder with psychosis.
  • 4.2 Healthy Volunteer Adults:
  • Any past or current history of Bipolar Disorder (any manic or hypomanic episode), recurrent MDD, or any disorder with psychosis
  • 5.3 Exclusion criteria for those with MDD:
  • 5.3.1 The individual exhibits any of these cardinal bipolar symptoms:
  • 5.3.1.1 Elevated or expansive mood
  • 5.3.1.2 Grandiosity or inflated self-esteem
  • 5.3.1.3 Decreased need for sleep
  • 5.3.1.4 Increase in goal-directed activity (this can result in the excessive involvement in pleasurable activities that have a high potential for painful consequences)
  • Has BD symptoms in distinct periods lasting more than 1 day.
  • Meets criteria for schizophrenia, schizophreniform disorder, schizoaffective illness, PDD, or PTSD.
  • The symptoms are due to the direct physiological effects of a drug of abuse, or to a general medical or neurological condition.
  • Currently pregnant or lactating
  • Meets criteria for alcohol or substance abuse with the last three months
  • Exclusion criteria for those with ADHD:
  • Ongoing medical illness or neurological disorder other than ADHD
  • Any condition that would interfere with the participants' ability to perform research tasks
  • Current Major Depression
  • Any past or present manic or hypomanic episode

研究组 & 干预措施

Children/Adolescents with DMDD or subthreshold DMDD

Children/Adolescents with DMDD or subthreshold DMDD

干预措施: Lithium (Drug)

Children/adolescents with MDD

Children/adolescents with MDD

Children/adolescents with ADHD

Children/adolescents with ADHD

干预措施: Lithium (Drug)

Healthy volunteer adults

Healthy volunteer adults

Parents of children/adolescents with DMDD or subthreshold DMDD

Parents of children/adolescents with DMDD or subthresdhold DMDD

Healthy volunteer children/adolescents

Healthy volunteer children/adolescents

结局指标

主要结局

To examine between-group differences in clinical, behavioral, genetic, neuroanatomical, and neurophysiological variables

时间窗: 20 years

Individuals with full or subthreshold DMDD and/or MDD, ADHD, anxiety (see protocol 00-M-0192), and healthy volunteers (see protocol 00-M-0198).

To examine associations between irritability and clinical, behavioral, genetic, neuroanatomical, and neurophysiological variables

时间窗: 20 years

Individuals with full or subthreshold DMDD and/or MDD, ADHD, anxiety (see protocol 00-M-0192), and healthy volunteers (see protocol 00-M-0198).

次要结局

未报告次要终点

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (1)

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