儿童易怒:我们知道什么,我们需要学习什么

IF 60.5 1区 医学 Q1 PSYCHIATRY World Psychiatry Pub Date : 2017-02-01 DOI:10.1002/wps.20397
E. Leibenluft
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In the 1990s, American researchers suggested that pediatric bipolar disorder does not present with distinct manic episodes as in adults, but instead with severe, chronic irritability. However, post-hoc analyses of epidemiological studies found associations between pediatric irritability and risk for subsequent anxiety and depression, but not for bipolar disorder. Similarly, in studies comparing the two dimensions of oppositional defiant disorder (ODD) (i.e., irritability and headstrong behavior), irritability predicts subsequent anxiety and depression, while headstrong behavior predicts attention-deficit/hyperactivity disorder (ADHD) and conduct disorder. Thus, the diagnosis of bipolar disorder should be reserved for youth (and adults) with distinct manic episodes, rather than chronic irritability. Genetically informative studies link irritability and depression. Twin studies document that longitudinal associations between irritability and both anxiety and depression have a genetic component. These studies also find that the heritability of irritability is approximately 40-60%, similar to anxiety or unipolar depression. Irritability is a diagnostic criterion for multiple disorders in youth, including anxiety disorders, major depressive disorder, and ODD. It is also common in youth with ADHD, bipolar disorder, conduct disorder, and autism. However, for children and adolescents, the validity and clinical utility of a diagnostic category characterized primarily by irritability remains an important and unanswered question. Historically, that category has been ODD, which is conceptualized as a disruptive behavior disorder. However, ODD consists of two dimensions, only one of which, irritability, has genetically mediated longitudinal associations with depression and anxiety. Also, severe irritability has significant cross-sectional associations with anxiety disorders. These considerations call into question the appropriateness of combining irritable and headstrong features into one disorder, and of categorizing a diagnosis characterized primarily by irritability as an externalizing, disruptive behavior disorder, rather than as a mood disorder. Given these complexities, it is not surprising that DSM-5 and ICD-11 take different approaches to diagnosing youth whose primary problem is severe irritability. Reflecting the American controversy about pediatric bipolar disorder, the mood disorder section of DSM-5 includes a new diagnosis, disruptive mood dysregulation disorder (DMDD), characterized by severe, chronic irritability. DMDD captures youth whose irritability causes impairment comparable to that of youth with bipolar disorder and, hence, is more severe than that of most youth with ODD. Given overlap between DMDD and ODD, ICD-11 instead includes a specifier to the diagnosis of ODD denoting chronic irritability. To evaluate these different nosologic strategies, future research should focus on their utility in predicting treatment response. Two neuroscience-based formulations can guide research on the pathophysiology of irritability. One conceptualizes irritability as an aberrant response to frustration, the emotion elicited when goal attainment is blocked, as when an expected reward is withheld. The second conceptualizes irritability as an aberrant approach response to threat: whereas healthy organisms approach a threat (i.e., attack) only when it is inescapable, irritable individuals may attack in a broader range of contexts. In an animal model with translational potential for studying irritability, threat and frustration were found to interact in determining an animal’s behavior. Specifically, compared to non-frustrated rodents, those who experienced “frustrative non-reward” (i.e., did not receive an expected reward) showed increased motor activity and were more likely to attack a conspecific. Such hyperactivity and increased propensity for aggression may be analogous to the behavior exhibited by a frustrated child experiencing a temper outburst. Functional magnetic resonance imaging research has examined associations between irritability and neural responses to frustration (e.g., rigged games) and threat (e.g., angry faces). Work with frustrating tasks shows associations between irritability and dysfunction in striatum, anterior cingulate cortex, amygdala, and parietal lobe, consistent with irritable youths’ deficits in reward processing and in maintaining attentional control when frustrated. Irritable youth are also more likely than their non-irritable peers to view ambiguous faces as angry and, like youth with anxiety disorders, to attend preferentially to angry faces. One direction for future research would be identifying the extent to which abnormalities in reward or threat processing differentiate subtypes of irritable youth. Also, an important question is whether the brain mechanisms mediating irritability vary across diagnoses and/or when irritability co-occurs with another trait, such as anxiety. Early data suggest that the pathophysiology of irritability varies across such contexts. Given the very recent inclusion of DMDD in DSM-5, limited controlled trials exist. However, tentative recommendations stem from studies focused on treating irritability in the context of other disorders, including ADHD and major depressive disorder. Considerable data indicate that stimulants reduce irritability in youth with ADHD. 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Anger proneness has a defined developmental trajectory, peaking in the preschool period and declining thereafter, with a modest increase during adolescence. Irritability is a common reason for mental health evaluation in children, and pediatric irritability is associated with both concurrent and future impairment. In the 1990s, American researchers suggested that pediatric bipolar disorder does not present with distinct manic episodes as in adults, but instead with severe, chronic irritability. However, post-hoc analyses of epidemiological studies found associations between pediatric irritability and risk for subsequent anxiety and depression, but not for bipolar disorder. Similarly, in studies comparing the two dimensions of oppositional defiant disorder (ODD) (i.e., irritability and headstrong behavior), irritability predicts subsequent anxiety and depression, while headstrong behavior predicts attention-deficit/hyperactivity disorder (ADHD) and conduct disorder. 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However, ODD consists of two dimensions, only one of which, irritability, has genetically mediated longitudinal associations with depression and anxiety. Also, severe irritability has significant cross-sectional associations with anxiety disorders. These considerations call into question the appropriateness of combining irritable and headstrong features into one disorder, and of categorizing a diagnosis characterized primarily by irritability as an externalizing, disruptive behavior disorder, rather than as a mood disorder. Given these complexities, it is not surprising that DSM-5 and ICD-11 take different approaches to diagnosing youth whose primary problem is severe irritability. Reflecting the American controversy about pediatric bipolar disorder, the mood disorder section of DSM-5 includes a new diagnosis, disruptive mood dysregulation disorder (DMDD), characterized by severe, chronic irritability. DMDD captures youth whose irritability causes impairment comparable to that of youth with bipolar disorder and, hence, is more severe than that of most youth with ODD. Given overlap between DMDD and ODD, ICD-11 instead includes a specifier to the diagnosis of ODD denoting chronic irritability. To evaluate these different nosologic strategies, future research should focus on their utility in predicting treatment response. Two neuroscience-based formulations can guide research on the pathophysiology of irritability. One conceptualizes irritability as an aberrant response to frustration, the emotion elicited when goal attainment is blocked, as when an expected reward is withheld. The second conceptualizes irritability as an aberrant approach response to threat: whereas healthy organisms approach a threat (i.e., attack) only when it is inescapable, irritable individuals may attack in a broader range of contexts. 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引用次数: 45

摘要

易怒可以被定义为相对于同龄人更容易生气。在临床上,它表现为发育不适当的脾气爆发和阴沉、易怒的情绪;因此,它包括行为和情绪成分。相关的构念是情绪失调,它比易怒更广泛,以及攻击,它只包括行为表现。愤怒倾向有一个明确的发展轨迹,在学龄前达到顶峰,随后下降,在青春期适度增加。易怒是儿童心理健康评估的常见原因,儿童易怒与当前和未来的损害有关。20世纪90年代,美国研究人员认为,儿童双相情感障碍不像成人那样表现为明显的躁狂发作,而是表现为严重的慢性烦躁。然而,流行病学研究的事后分析发现,儿童易怒与随后的焦虑和抑郁风险之间存在关联,但与双相情感障碍无关。同样,在比较对立违抗性障碍(ODD)的两个维度(即易怒和任性行为)的研究中,易怒预示着随后的焦虑和抑郁,而任性行为预示着注意力缺陷/多动障碍(ADHD)和品行障碍。因此,双相情感障碍的诊断应该保留给有明显躁狂发作的年轻人(和成年人),而不是慢性烦躁。基因信息研究将易怒和抑郁联系起来。双胞胎研究证明,易怒与焦虑和抑郁之间的纵向联系有遗传成分。这些研究还发现,易怒的遗传性约为40-60%,与焦虑或单相抑郁症相似。易怒是青少年多种疾病的诊断标准,包括焦虑症、重度抑郁症和ODD。在患有多动症、双相情感障碍、品行障碍和自闭症的青少年中也很常见。然而,对于儿童和青少年,主要以易怒为特征的诊断类别的有效性和临床效用仍然是一个重要的和未解决的问题。从历史上看,这一类别一直是ODD,它被概念化为破坏性行为障碍。然而,ODD由两个维度组成,其中只有一个维度,易怒,与抑郁和焦虑有遗传介导的纵向关联。此外,严重易怒与焦虑症有显著的横断面关联。这些考虑让人质疑将易怒和任性特征合并为一种疾病的适当性,以及将主要以易怒为特征的诊断归类为外化的破坏性行为障碍,而不是情绪障碍。考虑到这些复杂性,DSM-5和ICD-11采用不同的方法来诊断主要问题是严重易怒的青少年也就不足为奇了。反映了美国关于儿童双相情感障碍的争议,DSM-5的情绪障碍部分包括了一个新的诊断,破坏性情绪失调障碍(DMDD),其特征是严重的慢性烦躁。DMDD捕获的年轻人易怒导致的损害与双相情感障碍的年轻人相当,因此,比大多数患有ODD的年轻人更严重。考虑到DMDD和ODD之间的重叠,ICD-11在ODD的诊断中加入了一个指示符,表示慢性易怒。为了评估这些不同的病理性策略,未来的研究应侧重于它们在预测治疗反应方面的应用。两个基于神经科学的公式可以指导易怒的病理生理学研究。人们将易怒定义为对挫折的一种异常反应,当目标实现受阻时,当预期的奖励被扣留时,就会产生这种情绪。第二种理论将易怒定义为对威胁的异常反应:健康的生物体只在不可避免的情况下才会接近威胁(即攻击),而易怒的个体可能会在更广泛的情况下攻击。在一个具有研究易怒的转化潜力的动物模型中,发现威胁和挫折在决定动物行为方面相互作用。具体来说,与没有沮丧的啮齿动物相比,那些经历了“沮丧的无奖励”(即没有得到预期的奖励)的啮齿动物表现出更多的运动活动,更有可能攻击同型动物。这种多动和增加的攻击倾向可能类似于一个沮丧的孩子在经历脾气爆发时所表现出的行为。功能性磁共振成像研究已经检查了烦躁和对挫折(例如,操纵游戏)和威胁(例如,愤怒的脸)的神经反应之间的联系。 处理令人沮丧的任务显示出易怒与纹状体、前扣带皮层、杏仁核和顶叶功能障碍之间的联系,这与易怒的年轻人在受挫时奖励处理和保持注意力控制方面的缺陷是一致的。易怒的年轻人也比不易怒的同龄人更有可能把模棱两可的脸看作是愤怒的,而且和患有焦虑症的年轻人一样,他们更倾向于关注愤怒的脸。未来研究的一个方向将是确定奖励或威胁处理异常在多大程度上区分易激惹青年的亚型。此外,一个重要的问题是,在不同的诊断和/或当易怒与另一种特征(如焦虑)共存时,调节易怒的大脑机制是否会有所不同。早期的数据表明,在这种情况下,易怒的病理生理是不同的。鉴于最近将DMDD纳入DSM-5,存在有限的对照试验。然而,初步的建议来自于在其他疾病的背景下治疗易怒的研究,包括多动症和重度抑郁症。大量数据表明,兴奋剂可以减少青少年多动症患者的易怒。这表明,尽管
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Irritability in children: what we know and what we need to learn
Irritability can be defined as increased proneness to anger, relative to peers. Clinically, it manifests as developmentally inappropriate temper outbursts and sullen, grouchy mood; thus, it includes both behavioral and mood components. Related constructs are mood dysregulation, which is broader than irritability, and aggression, which encompasses only behavioral manifestations. Anger proneness has a defined developmental trajectory, peaking in the preschool period and declining thereafter, with a modest increase during adolescence. Irritability is a common reason for mental health evaluation in children, and pediatric irritability is associated with both concurrent and future impairment. In the 1990s, American researchers suggested that pediatric bipolar disorder does not present with distinct manic episodes as in adults, but instead with severe, chronic irritability. However, post-hoc analyses of epidemiological studies found associations between pediatric irritability and risk for subsequent anxiety and depression, but not for bipolar disorder. Similarly, in studies comparing the two dimensions of oppositional defiant disorder (ODD) (i.e., irritability and headstrong behavior), irritability predicts subsequent anxiety and depression, while headstrong behavior predicts attention-deficit/hyperactivity disorder (ADHD) and conduct disorder. Thus, the diagnosis of bipolar disorder should be reserved for youth (and adults) with distinct manic episodes, rather than chronic irritability. Genetically informative studies link irritability and depression. Twin studies document that longitudinal associations between irritability and both anxiety and depression have a genetic component. These studies also find that the heritability of irritability is approximately 40-60%, similar to anxiety or unipolar depression. Irritability is a diagnostic criterion for multiple disorders in youth, including anxiety disorders, major depressive disorder, and ODD. It is also common in youth with ADHD, bipolar disorder, conduct disorder, and autism. However, for children and adolescents, the validity and clinical utility of a diagnostic category characterized primarily by irritability remains an important and unanswered question. Historically, that category has been ODD, which is conceptualized as a disruptive behavior disorder. However, ODD consists of two dimensions, only one of which, irritability, has genetically mediated longitudinal associations with depression and anxiety. Also, severe irritability has significant cross-sectional associations with anxiety disorders. These considerations call into question the appropriateness of combining irritable and headstrong features into one disorder, and of categorizing a diagnosis characterized primarily by irritability as an externalizing, disruptive behavior disorder, rather than as a mood disorder. Given these complexities, it is not surprising that DSM-5 and ICD-11 take different approaches to diagnosing youth whose primary problem is severe irritability. Reflecting the American controversy about pediatric bipolar disorder, the mood disorder section of DSM-5 includes a new diagnosis, disruptive mood dysregulation disorder (DMDD), characterized by severe, chronic irritability. DMDD captures youth whose irritability causes impairment comparable to that of youth with bipolar disorder and, hence, is more severe than that of most youth with ODD. Given overlap between DMDD and ODD, ICD-11 instead includes a specifier to the diagnosis of ODD denoting chronic irritability. To evaluate these different nosologic strategies, future research should focus on their utility in predicting treatment response. Two neuroscience-based formulations can guide research on the pathophysiology of irritability. One conceptualizes irritability as an aberrant response to frustration, the emotion elicited when goal attainment is blocked, as when an expected reward is withheld. The second conceptualizes irritability as an aberrant approach response to threat: whereas healthy organisms approach a threat (i.e., attack) only when it is inescapable, irritable individuals may attack in a broader range of contexts. In an animal model with translational potential for studying irritability, threat and frustration were found to interact in determining an animal’s behavior. Specifically, compared to non-frustrated rodents, those who experienced “frustrative non-reward” (i.e., did not receive an expected reward) showed increased motor activity and were more likely to attack a conspecific. Such hyperactivity and increased propensity for aggression may be analogous to the behavior exhibited by a frustrated child experiencing a temper outburst. Functional magnetic resonance imaging research has examined associations between irritability and neural responses to frustration (e.g., rigged games) and threat (e.g., angry faces). Work with frustrating tasks shows associations between irritability and dysfunction in striatum, anterior cingulate cortex, amygdala, and parietal lobe, consistent with irritable youths’ deficits in reward processing and in maintaining attentional control when frustrated. Irritable youth are also more likely than their non-irritable peers to view ambiguous faces as angry and, like youth with anxiety disorders, to attend preferentially to angry faces. One direction for future research would be identifying the extent to which abnormalities in reward or threat processing differentiate subtypes of irritable youth. Also, an important question is whether the brain mechanisms mediating irritability vary across diagnoses and/or when irritability co-occurs with another trait, such as anxiety. Early data suggest that the pathophysiology of irritability varies across such contexts. Given the very recent inclusion of DMDD in DSM-5, limited controlled trials exist. However, tentative recommendations stem from studies focused on treating irritability in the context of other disorders, including ADHD and major depressive disorder. Considerable data indicate that stimulants reduce irritability in youth with ADHD. This suggests that, while
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来源期刊
World Psychiatry
World Psychiatry 医学-精神病学
自引率
7.40%
发文量
124
期刊介绍: World Psychiatry is the official journal of the World Psychiatric Association. It is published in three issues per year. The journal is sent free of charge to psychiatrists whose names and addresses are provided by WPA member societies and sections. World Psychiatry is also freely accessible on Wiley Online Library and PubMed Central. The main aim of World Psychiatry is to disseminate information on significant clinical, service, and research developments in the mental health field. The journal aims to use a language that can be understood by the majority of mental health professionals worldwide.
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