1.Advanced Pharmacotherapy Evidenced by Pathogenesis of Autism Spectrum Disorder.
Yeon Jung LEE ; Soo Hyun OH ; Chanmin PARK ; Minha HONG ; Ah Rah LEE ; Hee Jeong YOO ; Chan Young SHIN ; Keun Ah CHEON ; Geon Ho BAHN
Clinical Psychopharmacology and Neuroscience 2014;12(1):19-30
In clinical practice, pharmacological treatment is mostly focused on behavioral symptoms in everyday life. Nevertheless, persistent effort continues to develop medication for causal treatment. Recent changes in diagnostic criteria from Diagnostic and Statistical Manual of Mental Disorders, 4th edition, text revision (DSM-IV-TR) to DSM-5 would affect not only diagnosing approaches, but also therapeutic approaches. Because previous pervasive developmental disorders have been integrated into a single entity, the autism spectrum disorder (ASD), we have to prepare for what medications are valuable for the ASD. In this article, we reviewed the following etiological treatment: acetylcholine and glutamate related medicine; amino acid medicine such as secretin, endogenous opioid, and oxytocin; complementary and alternative medicine such as chelating agents, vitamins, and omega-3; promising drugs related to the scope of pharmacogenetics currently under study.
Acetylcholine
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Behavioral Symptoms
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Chelating Agents
;
Child
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Autism Spectrum Disorder*
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Complementary Therapies
;
Diagnostic and Statistical Manual of Mental Disorders
;
Drug Therapy*
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Glutamic Acid
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Oxytocin
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Pharmacogenetics
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Secretin
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Vitamins
2.Altered Brain Activation in Ventral Frontal-Striatal Regions Following a 16-week Pharmacotherapy in Unmedicated Obsessive-Compulsive Disorder.
Ji Yeon HAN ; Do Hyung KANG ; Bon Mi GU ; Wi Hoon JUNG ; Jung Seok CHOI ; Chi Hoon CHOI ; Joon Hwan JANG ; Jun Soo KWON
Journal of Korean Medical Science 2011;26(5):665-674
Recent studies have reported that cognitive inflexibility associated with impairments in a frontal-striatal circuit and parietal region is a core cognitive deficit of obsessive-compulsive disorder (OCD). However, few studies have examined progressive changes in these regions following clinical improvement in obsessive-compulsive symptoms. To determine if treatment changes the aberrant activation pattern associated with task switching in OCD, we examined the activation patterns in brain areas after treatment. The study was conducted on 10 unmedicated OCD patients and 20 matched controls using event-related functional magnetic resonance imaging. Treatment improved the clinical symptoms measured by the Yale-Brown Obsessive Compulsive Scale and behavioral flexibility indicated by the switching cost. At baseline, OCD showed significantly less activation in the dorsal and ventral frontal-striatal circuit and parietal regions under the task-switch minus task-repeat condition compared with controls. After treatment, the neural responses in the ventral frontal-striatal circuit in OCD were partially normalized, whereas the activation deficit in dorsal frontoparietal regions that mediate shifting attention or behavioral flexibility persisted. It is suggested that altered brain activation in ventral frontal-striatal regions in OCD patients is associated with their cognitive flexibility and changes in these regions may underlie the pathophysiology of OCD.
Adult
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Basal Ganglia/*metabolism
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Behavioral Symptoms/drug therapy
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Female
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Frontal Lobe/*drug effects/physiopathology
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Humans
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Magnetic Resonance Imaging
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Male
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Obsessive-Compulsive Disorder/*drug therapy/physiopathology
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Parietal Lobe/*drug effects/physiopathology
3.Prescription Trends of Psychotropics in Children and Adolescents with Autism Based on Nationwide Health Insurance Data.
Minha HONG ; Seung Yup LEE ; Juhee HAN ; Jin Cheol PARK ; Yeon Jung LEE ; Ram HWANGBO ; Hyejung CHANG ; Seong Woo CHO ; Soo Young BHANG ; Bongseog KIM ; Jun Won HWANG ; Geon Ho BAHN
Journal of Korean Medical Science 2017;32(10):1687-1693
Children with autism are often medicated to manage emotional and behavioral symptoms; yet, data on such pharmacotherapy is insufficient. In this study, we investigated the Korean National Health Insurance Claims Database (NHICD) information related to autism incidence and psychotropic medication use. From the 2010–2012 NHICD, we selected a total of 31,919,732 subjects under 19 years old. To examine the diagnostic incidence, we selected patients who had at least one medical claim containing an 10th revision of International Statistical Classification of Diseases and Related Health Problems (ICD-10) code for pervasive developmental disorder, F84, not diagnosed in the previous 360 days. Psychotropics were categorized into seven classes. Then, we analyzed the data to determine the mean annual diagnostic incidence and psychotropic prescription trends. Diagnostic incidence was 17,606 for the 3 years, with a mean annual incidence per 10,000 population of 5.52. Among them, 5,348 patients were prescribed psychotropics. Atypical antipsychotics were the most commonly used, followed by antidepressants. An older age, male sex, and the availability of medical aid were associated with a higher rate of prescription than observed for a younger age, female sex, and the availability of health insurance. Psychotropic drugs were used for less than one-third of patients newly diagnosed with autism, and prescription differed by sex and age. Increased diagnostic incidence is associated with an increased prescription of psychotropic drugs. Therefore, medication-related safety data and policies for psychotropic drugs in autism should be prepared.
Adolescent*
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Antidepressive Agents
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Antipsychotic Agents
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Autistic Disorder*
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Behavioral Symptoms
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Central Nervous System Stimulants
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Child*
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Drug Therapy
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Drug Utilization
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Female
;
Humans
;
Incidence
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Insurance, Health*
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International Classification of Diseases
;
Male
;
National Health Programs
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Prescriptions*
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Psychotropic Drugs