{"title":"谷氨酸调节药物在强迫症中的应用。","authors":"F. Macmaster, D. Rosenberg","doi":"10.1521/CAPN.2010.15.6.1","DOIUrl":null,"url":null,"abstract":"Obsessive-compulsive disorder (OCD) is a chronic, severe and debilitating disorder, affecting over 3 million people in the United States. People afflicted with OCD have obsessions and compulsions that impair their functioning in life. According to the World Health Organization, OCD is among the ten most disabling medical conditions worldwide. The National Comorbidity Survey Replication, when examining anxiety disorders, found that OCD had the highest percentage of serious cases (50.6%) (Kessler et al., 2005). Lifetime prevalence estimates of OCD in pediatric and adult populations range from 1% to 3% (Kessler et al., 2005). The clinical presentation of OCD in childhood and adulthood is similar, making findings applicable across the age span. The mean age of onset for OCD in children is between 9 to 11 years in males and 11 to 13 years in females (Hanna, 1995). A more negative outcome is associated with an early age of onset. Furthermore, pediatric OCD was found to be chronic and unremitting in up to 87% of cases that failed to receive effective treatment (Stewart et al., 2004). Finally, an early diagnosis of OCD is associated with a higher risk for developing other psychiatric disorders into adulthood. \n \nTHE CASE FOR NOVEL TREATMENTS OF OCD \nSerotonin reuptake inhibitors (SRI) are the only FDA approved medications for OCD. While considered effective in the clinical trial literature, treatment of OCD with SRI’s has proven limited in clinical practice. SRIs are only effective in 40 to 60% of patients (Jenike, 2004). Obviously, this leaves a considerable number still ill. Additionally, studies often define treatment response as a 20 to 40% reduction in symptoms. Hence, many subjects who are classed as “responders” still have marked symptoms after treatment (Jenike, 2004). OCD symptom severity scores, as calculated by the Children’s Yale-Brown Obsessive-Compulsive Scale (CY-BOCS), normally range from 15 to 20 post-treatment. A score in this range is still indicative of significant impairment. In addition to SRIs, cognitive behavioral therapy (CBT), alone or in combination with SRI, is also considered effective for treating OCD (POTS, 2004). Nonetheless, one-third of pediatric patients remain markedly ill even after receiving the combination of CBT and medication (POTS, 2004). What is more, data indicates that an earlier onset of OCD may be associated with the illness being more treatment refractory (POTS, 2004). Indeed, OCD is one of the few remaining psychiatric disorders for which there is a neurosurgical treatment indication. The persistence of symptoms and the limited nature of treatment response indicates that the serotonin paradigm of understanding OCD cannot fully account for the underlying neurobiology of the illness. Therefore, novel, evidence based approaches are needed to advance treatment of OCD. The glutamate hypothesis of OCD, first developed over a decade ago (Rosenberg & Keshavan, 1998), and resulting biological evidence has recently translated to the application of glutamate modulating agents for the treatment of pediatric OCD.","PeriodicalId":89750,"journal":{"name":"Child & adolescent psychopharmacology news","volume":"23 1","pages":"1-5"},"PeriodicalIF":0.0000,"publicationDate":"2010-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"THE USE OF GLUTAMATE MODULATING DRUGS IN OBSESSIVE COMPULSIVE DISORDER.\",\"authors\":\"F. Macmaster, D. 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A more negative outcome is associated with an early age of onset. Furthermore, pediatric OCD was found to be chronic and unremitting in up to 87% of cases that failed to receive effective treatment (Stewart et al., 2004). Finally, an early diagnosis of OCD is associated with a higher risk for developing other psychiatric disorders into adulthood. \\n \\nTHE CASE FOR NOVEL TREATMENTS OF OCD \\nSerotonin reuptake inhibitors (SRI) are the only FDA approved medications for OCD. While considered effective in the clinical trial literature, treatment of OCD with SRI’s has proven limited in clinical practice. SRIs are only effective in 40 to 60% of patients (Jenike, 2004). Obviously, this leaves a considerable number still ill. Additionally, studies often define treatment response as a 20 to 40% reduction in symptoms. Hence, many subjects who are classed as “responders” still have marked symptoms after treatment (Jenike, 2004). OCD symptom severity scores, as calculated by the Children’s Yale-Brown Obsessive-Compulsive Scale (CY-BOCS), normally range from 15 to 20 post-treatment. A score in this range is still indicative of significant impairment. In addition to SRIs, cognitive behavioral therapy (CBT), alone or in combination with SRI, is also considered effective for treating OCD (POTS, 2004). Nonetheless, one-third of pediatric patients remain markedly ill even after receiving the combination of CBT and medication (POTS, 2004). What is more, data indicates that an earlier onset of OCD may be associated with the illness being more treatment refractory (POTS, 2004). Indeed, OCD is one of the few remaining psychiatric disorders for which there is a neurosurgical treatment indication. The persistence of symptoms and the limited nature of treatment response indicates that the serotonin paradigm of understanding OCD cannot fully account for the underlying neurobiology of the illness. 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引用次数: 1
摘要
强迫症(OCD)是一种慢性的、严重的、使人衰弱的疾病,在美国影响着超过300万人。受强迫症折磨的人有影响他们生活功能的强迫和强迫。据世界卫生组织称,强迫症是世界上十大最致残的疾病之一。国家共病调查复制,当检查焦虑症时,发现强迫症的严重病例比例最高(50.6%)(Kessler et al., 2005)。强迫症在儿童和成人人群中的终生患病率估计在1%到3%之间(Kessler et al, 2005)。强迫症在儿童期和成人期的临床表现是相似的,这使得研究结果适用于整个年龄段。儿童强迫症的平均发病年龄男性为9 - 11岁,女性为11 - 13岁(Hanna, 1995)。更消极的结果与发病年龄较早有关。此外,在未能得到有效治疗的病例中,高达87%的儿童强迫症被发现是慢性和持续的(Stewart et al., 2004)。最后,强迫症的早期诊断与成年后发展为其他精神疾病的高风险相关。5 -羟色胺再摄取抑制剂(SRI)是FDA批准的唯一治疗强迫症的药物。虽然在临床试验文献中被认为是有效的,但在临床实践中,用SRI治疗强迫症被证明是有限的。SRIs仅对40% - 60%的患者有效(Jenike, 2004)。显然,这使得相当多的人仍然生病。此外,研究通常将治疗反应定义为症状减轻20%至40%。因此,许多被归类为“应答者”的受试者在治疗后仍有明显的症状(Jenike, 2004)。根据儿童耶鲁-布朗强迫症量表(CY-BOCS)计算的强迫症症状严重程度评分,治疗后通常在15到20之间。在这个范围内的分数仍然表明严重的损害。除了SRI,认知行为疗法(CBT),单独或与SRI联合,也被认为对治疗强迫症有效(POTS, 2004)。尽管如此,三分之一的儿科患者即使在接受CBT和药物治疗相结合后仍然明显不适(POTS, 2004)。更重要的是,数据表明,强迫症的早期发病可能与该疾病更难治疗有关(POTS, 2004)。事实上,强迫症是为数不多的需要神经外科治疗的精神疾病之一。症状的持续和治疗反应的有限性表明,理解强迫症的血清素范式不能完全解释该疾病的潜在神经生物学。因此,需要新的、基于证据的方法来推进强迫症的治疗。强迫症的谷氨酸假说最早是在十多年前提出的(Rosenberg & Keshavan, 1998),其产生的生物学证据最近被转化为谷氨酸调节剂在儿童强迫症治疗中的应用。
THE USE OF GLUTAMATE MODULATING DRUGS IN OBSESSIVE COMPULSIVE DISORDER.
Obsessive-compulsive disorder (OCD) is a chronic, severe and debilitating disorder, affecting over 3 million people in the United States. People afflicted with OCD have obsessions and compulsions that impair their functioning in life. According to the World Health Organization, OCD is among the ten most disabling medical conditions worldwide. The National Comorbidity Survey Replication, when examining anxiety disorders, found that OCD had the highest percentage of serious cases (50.6%) (Kessler et al., 2005). Lifetime prevalence estimates of OCD in pediatric and adult populations range from 1% to 3% (Kessler et al., 2005). The clinical presentation of OCD in childhood and adulthood is similar, making findings applicable across the age span. The mean age of onset for OCD in children is between 9 to 11 years in males and 11 to 13 years in females (Hanna, 1995). A more negative outcome is associated with an early age of onset. Furthermore, pediatric OCD was found to be chronic and unremitting in up to 87% of cases that failed to receive effective treatment (Stewart et al., 2004). Finally, an early diagnosis of OCD is associated with a higher risk for developing other psychiatric disorders into adulthood.
THE CASE FOR NOVEL TREATMENTS OF OCD
Serotonin reuptake inhibitors (SRI) are the only FDA approved medications for OCD. While considered effective in the clinical trial literature, treatment of OCD with SRI’s has proven limited in clinical practice. SRIs are only effective in 40 to 60% of patients (Jenike, 2004). Obviously, this leaves a considerable number still ill. Additionally, studies often define treatment response as a 20 to 40% reduction in symptoms. Hence, many subjects who are classed as “responders” still have marked symptoms after treatment (Jenike, 2004). OCD symptom severity scores, as calculated by the Children’s Yale-Brown Obsessive-Compulsive Scale (CY-BOCS), normally range from 15 to 20 post-treatment. A score in this range is still indicative of significant impairment. In addition to SRIs, cognitive behavioral therapy (CBT), alone or in combination with SRI, is also considered effective for treating OCD (POTS, 2004). Nonetheless, one-third of pediatric patients remain markedly ill even after receiving the combination of CBT and medication (POTS, 2004). What is more, data indicates that an earlier onset of OCD may be associated with the illness being more treatment refractory (POTS, 2004). Indeed, OCD is one of the few remaining psychiatric disorders for which there is a neurosurgical treatment indication. The persistence of symptoms and the limited nature of treatment response indicates that the serotonin paradigm of understanding OCD cannot fully account for the underlying neurobiology of the illness. Therefore, novel, evidence based approaches are needed to advance treatment of OCD. The glutamate hypothesis of OCD, first developed over a decade ago (Rosenberg & Keshavan, 1998), and resulting biological evidence has recently translated to the application of glutamate modulating agents for the treatment of pediatric OCD.