Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 62
Filter
1.
PLoS One ; 15(6): e0234074, 2020.
Article in English | MEDLINE | ID: mdl-32502218

ABSTRACT

Data from the Czech part of the European Longitudinal Study of Pregnancy and Childhood offer a unique opportunity to examine a period of changing socioeconomic structure of the country. Our aim was to analyse the association between socioeconomic status, family structure and children's psychosocial problems at the age of 7, 11, 15 and 18 years in 3,261 subjects and compare our results with findings from western settings. The Strengths and Difficulties Questionnaire (SDQ) and its five subscales were used to assess individual problem areas (emotional symptoms, peer problems, hyperactivity, conduct problems) and prosocial behaviour. Socioeconomic status was represented by maternal education and three forms of family structure were identified: nuclear family, new partner family and single parent family. The SDQ subscale score over time was modelled as a quadratic growth curve using a linear mixed-effects model. Maternal university education was associated with a faster decline in problems over time for all five SDQ subscales. Problems in children from nuclear families were found to be significantly lower than in children from single parent families for all SDQ subscales with the exception of peer problems. Compared to nuclear families, children from new partner families scored significantly higher in hyperactivity and conduct problems subscales. The nuclear family structure and higher maternal education have been identified as protective factors for children's psychosocial problems, in agreement with findings from western settings. Adopting a longitudinal perspective was shown as essential for providing a more complex view of children's psychosocial problems over time.


Subject(s)
Child Behavior Disorders/pathology , Family , Socioeconomic Factors , Adolescent , Child , Educational Status , Emotions , Female , Humans , Longitudinal Studies , Male , Problem Behavior , Social Behavior , Social Class , Surveys and Questionnaires
2.
PLoS One ; 14(4): e0215220, 2019.
Article in English | MEDLINE | ID: mdl-30973924

ABSTRACT

AIM: The aim of this study was to evaluate long-term behavioural and neurodevelopmental complications of neonatal necrotizing enterocolitis at school age. METHOD: This was a historic cohort study comparing all surviving children born in Denmark between 1st of January 2002 and 31st of December 2011 with a diagnosis of necrotizing enterocolitis to a group of children without necrotizing enterocolitis, but same gestational age, birth weight and year of birth. Outcomes were investigated through a parental questionnaire. The primary outcome was the Strength and Difficulties Questionnaire score and secondary outcomes were cerebral palsy and impaired head growth. RESULTS: Response rates were 50% (163 of 328) and 36% (237 of 652) among children with and without necrotizing enterocolitis, respectively. There was a higher rate of abnormal Strength and Difficulties score (23.9 versus 17.8%), moderate/severe cerebral palsy (3.1 versus 0.9%) and small head circumference for age (11.7 versus 7.2%) among children with necrotizing enterocolitis. However, these differences were all statistically insignificant and did not change significantly by adjustment for potential confounders. CONCLUSION: To our knowledge, this study includes the largest cohort of necrotizing enterocolitis children evaluated for possible long-term complications at school age. The increased risks of behavioural- and neurodevelopmental impairments were statistically insignificant, moderate in magnitude and may be of little clinical importance for management in the neonatal period or when planning follow-up.


Subject(s)
Child Behavior Disorders/etiology , Enterocolitis, Necrotizing/complications , Neurodevelopmental Disorders/etiology , Adolescent , Age Factors , Cerebral Palsy/epidemiology , Cerebral Palsy/etiology , Cerebral Palsy/pathology , Child , Child Behavior Disorders/epidemiology , Child Behavior Disorders/pathology , Child, Preschool , Cohort Studies , Denmark/epidemiology , Developmental Disabilities/epidemiology , Developmental Disabilities/etiology , Developmental Disabilities/pathology , Female , Follow-Up Studies , Head/pathology , Humans , Infant, Newborn , Male , Neurodevelopmental Disorders/epidemiology , Neurodevelopmental Disorders/pathology , Risk Factors , Surveys and Questionnaires
3.
Eur Child Adolesc Psychiatry ; 28(9): 1169-1181, 2019 Sep.
Article in English | MEDLINE | ID: mdl-30684088

ABSTRACT

Selective mutism (SM) is classified under the category of anxiety disorders in DSM-5 [1], although concrete fears that underlie the condition are not specified contrary to all other anxiety disorders. Given the lack of studies systematically investigating fears in SM, content and frequency of concrete fears as well as related cognitions have remained unclear so far. One hundred and twenty-four participants [M = 13.25 years (SD = 3.24), range 8-18 years] with SM (n = 65), social phobia (SP n = 18) or with typical development (TD n = 51) took part in an online survey. Participants with SM (n = 65) answered an open-ended question concerning fears that might cause the consistent failure to speak in select situations. Additionally, participants with SM, SP and TD completed a survey containing 34 fear-related cognitions that might occur in speech-demanding situations. Open text answers were systematically evaluated by extracting higher-order categories using a Qualitative Content Analysis. Single item scores of the survey were compared between the three groups. 59% of all spontaneously reported fears were assigned to the cluster of social fears. Other reported fears represented the categories fear of mistakes (28%), language-related fears (8%) and voice-related fears (5%). The SM- and SP group only differed regarding the cognition that one's own voice might sound funny (SM > SP). Social fears and the fear of mistakes account for the majority of fears in SM. Therefore, future interventions should consider specifically targeting these types of fears.


Subject(s)
Anxiety Disorders/psychology , Child Behavior Disorders/diagnosis , Cognition/physiology , Diagnostic and Statistical Manual of Mental Disorders , Fear/psychology , Mutism/diagnosis , Phobia, Social/psychology , Adolescent , Child , Child Behavior Disorders/pathology , Female , Humans , Male , Mutism/pathology
4.
Int J Eat Disord ; 50(12): 1404-1412, 2017 12.
Article in English | MEDLINE | ID: mdl-29105808

ABSTRACT

OBJECTIVE: Previous studies evaluating the association between early childhood adversities and eating disorders have yielded conflicting results. The aim of this study is to examine the association between a range of adversities and risk of anorexia nervosa (AN), bulimia nervosa (BN), and eating disorder not otherwise specified (EDNOS) in 495,244 women. METHOD: In this nationwide, register-based cohort study, nine types of early childhood adversity (family disruption, residential instability, placement in out-of-home care, familial death, parental somatic illness, parental psychiatric illness, parental disability, severe parental criminality, and parental substance use disorder) were defined and exposure during the first 6 years of life was determined. Hazard ratios for eating disorders were calculated using Cox regression. RESULTS: Few adversities were significantly associated with AN, and for each, the presence of the adversity was associated with lower risk for AN. BN, and EDNOS were positively associated with several types of adversities. AN rates were unchanged or reduced by up to 54% by adversities, whereas rates of BN and EDNOS were unchanged or increased by adversities by up to 49 and 89%, respectively. DISCUSSION: Our findings indicate that childhood adversities appear to be associated with an increased risk of BN and in particular EDNOS, whereas they seem to be either unassociated or associated with a decreased risk of AN.


Subject(s)
Child Behavior Disorders/etiology , Child Behavior Disorders/psychology , Feeding and Eating Disorders/etiology , Feeding and Eating Disorders/psychology , Child Behavior Disorders/pathology , Child, Preschool , Cohort Studies , Feeding and Eating Disorders/pathology , Female , Humans , Infant , Infant, Newborn , Registries , Risk , Sweden
5.
Neuroimage Clin ; 15: 732-740, 2017.
Article in English | MEDLINE | ID: mdl-28702350

ABSTRACT

Mood disorders and behavioral are broad psychiatric diagnostic categories that have different symptoms and neurobiological mechanisms, but share some neurocognitive similarities, one of which is an elevated risk for reading deficit. Our aim was to determine the influence of mood versus behavioral dysregulation on reading ability and neural correlates supporting these skills in youth, using diffusion tensor imaging in 11- to 17-year-old children and youths with mood disorders or behavioral disorders and age-matched healthy controls. The three groups differed only in phonological processing and passage comprehension. Youth with mood disorders scored higher on the phonological test but had lower comprehension scores than children with behavioral disorders and controls; control participants scored the highest. Correlations between fractional anisotropy and phonological processing in the left Arcuate Fasciculus showed a significant difference between groups and were strongest in behavioral disorders, intermediate in mood disorders, and lowest in controls. Correlations between these measures in the left Inferior Longitudinal Fasciculus were significantly greater than in controls for mood but not for behavioral disorders. Youth with mood disorders share a deficit in the executive-limbic pathway (Arcuate Fasciculus) with behavioral-disordered youth, suggesting reduced capacity for engaging frontal regions for phonological processing or passage comprehension tasks and increased reliance on the ventral tract (e.g., the Inferior Longitudinal Fasciculus). The low passage comprehension scores in mood disorder may result from engaging the left hemisphere. Neural pathways for reading differ mainly in executive-limbic circuitry. This new insight may aid clinicians in providing appropriate intervention for each disorder.


Subject(s)
Child Behavior Disorders/pathology , Mood Disorders/pathology , Reading , White Matter/pathology , Adolescent , Child , Child Behavior Disorders/complications , Comprehension/physiology , Diffusion Tensor Imaging , Dyslexia/etiology , Dyslexia/pathology , Female , Humans , Male , Mood Disorders/complications , Neural Pathways/pathology , Neuroimaging/methods
7.
Pediatr Res ; 79(1-1): 87-95, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26372513

ABSTRACT

BACKGROUND: Preterm infants are at risk for white matter (WM) injury and adverse neurodevelopmental outcomes. METHODS: Serial diffusion tensor magnetic resonance imaging data were obtained from very preterm infants (N = 78) born <30 wk gestation imaged up to four times from 26-42 wk postmenstrual age. Slopes were calculated for fractional anisotropy (FA) and mean diffusivity (MD) within regions of interest for infants with ≥2 scans (N = 50). Sixty-five children underwent neurodevelopmental testing at 2 y of age. RESULTS: FA slope for the posterior limb of the internal capsule was greater than other regions. The anterior limb of the internal capsule (ALIC), corpus callosum, and optic radiations demonstrated greater FA slope with increasing gestational age. Infants with patent ductus arteriosus had lower FA slope in the ALIC. MD slope was lower with prolonged ventilation or lack of antenatal steroids. At 2 y of age, lower motor scores were associated with lower FA in the left but higher FA in the right inferior temporal lobe at term-equivalent age. Better social-emotional competence was related to lower FA in the left cingulum bundle. CONCLUSION: This study demonstrates regional variability in the susceptibility/sensitivity of WM maturation to perinatal factors and relationships between altered diffusion measures and developmental outcomes in preterm neonates.


Subject(s)
Infant, Extremely Premature/growth & development , Neurodevelopmental Disorders/pathology , White Matter/pathology , Adrenal Cortex Hormones/adverse effects , Adrenal Cortex Hormones/therapeutic use , Affective Symptoms/etiology , Affective Symptoms/pathology , Anisotropy , Child Behavior Disorders/etiology , Child Behavior Disorders/pathology , Comorbidity , Corpus Callosum/pathology , Diffusion Tensor Imaging , Ductus Arteriosus, Patent/epidemiology , Female , Follow-Up Studies , Gestational Age , Humans , Infant, Newborn , Infant, Premature, Diseases/epidemiology , Internal Capsule/pathology , Male , Movement Disorders/etiology , Movement Disorders/pathology , Neurodevelopmental Disorders/etiology , Organ Specificity , Parenteral Nutrition, Total/adverse effects , Pregnancy , Pregnancy Complications/drug therapy , Prenatal Exposure Delayed Effects , Prognosis , Respiration, Artificial/adverse effects , Temporal Lobe/pathology
8.
Eur Child Adolesc Psychiatry ; 24(8): 979-84, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25398390

ABSTRACT

Research into Pathological Demand Avoidance (PDA), which has been suggested to be a subgroup within the Autism Spectrum Disorder (ASD), is almost nonexistent in spite of the frequent reference to the condition in clinical practice. The total population of 15 to 24-year-olds in the Faroe Islands was screened for ASD, and 67 individuals were identified who met diagnostic criteria for ASD (corresponding to a general population prevalence of ASD of almost 1 %). Of these 67, 50 had parents who were interviewed using the Diagnostic Interview for Social and Communication Disorders (DISCO-11) which contains 15 "PDA-specific" items. Nine individuals met criteria for "possible clinical diagnosis of PDA", meaning that almost one in five of all with ASD also had indications of having had PDA in childhood, and that 0.18 % of the total population had had the combination of ASD and PDA. However, at the time of assessment, only one of the 9 individuals with possible PDA still met "full criteria". PDA possibly constitutes a considerable minority of all cases with ASD diagnosed in childhood, but criteria for the condition are unlikely to be still met in later adolescence and early adult life.


Subject(s)
Autism Spectrum Disorder/diagnosis , Autistic Disorder/diagnosis , Avoidance Learning , Child Behavior Disorders/pathology , Conduct Disorder/pathology , Adolescent , Adult , Autism Spectrum Disorder/epidemiology , Autistic Disorder/epidemiology , Child , Child Behavior Disorders/epidemiology , Conduct Disorder/epidemiology , Denmark/epidemiology , Female , Humans , Male , Minority Groups/statistics & numerical data , Population Surveillance , Prevalence , Social Behavior
9.
Australas Psychiatry ; 23(1): 63-5, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25520002

ABSTRACT

OBJECTIVE: Our objective was to report and describe a case of psychosocial short stature in an adolescent girl with psychotic features. Psychosocial short stature is a rare condition in which emotional stress or deprivation in childhood profoundly reduces growth, leading to persistent short stature. This disorder is variably known as psychosocial dwarfism, hyperphagic short stature or maternal deprivation dwarfism. In the literature, psychosocial short stature has not been associated previously with psychosis. CONCLUSIONS: We formulate that our patient's short stature, developmental regression and psychotic features were culminations of insecure mother-child attachment, personal traumatic experiences, immigrant status, high family expressed emotions and social isolation. Neuropsychiatric influences were critically regarded due to our patient's fluctuations in behaviour and affect, in the setting of cortical volume loss on brain MRI. Diagnostic hypotheses included childhood disintegrative disorder or childhood-onset schizophrenia. The management plan involved inpatient family psychoeducation, a pharmacological trial with an atypical antipsychotic and community mental health service follow-up for family therapy and psychotherapy.


Subject(s)
Dwarfism/complications , Psychotic Disorders/complications , Adolescent , Antipsychotic Agents/therapeutic use , Atrophy/pathology , Cerebral Cortex/pathology , Child Behavior Disorders/complications , Child Behavior Disorders/drug therapy , Child Behavior Disorders/pathology , Child Behavior Disorders/therapy , Developmental Disabilities/complications , Developmental Disabilities/drug therapy , Developmental Disabilities/pathology , Developmental Disabilities/therapy , Dwarfism/drug therapy , Dwarfism/pathology , Dwarfism/therapy , Family Therapy , Female , Humans , Magnetic Resonance Imaging , Neuroimaging , Psychotherapy , Psychotic Disorders/drug therapy , Psychotic Disorders/pathology , Psychotic Disorders/therapy
10.
PLoS One ; 9(10): e109342, 2014.
Article in English | MEDLINE | ID: mdl-25333762

ABSTRACT

BACKGROUND: On March 11, 2011, a massive undersea earthquake and tsunami struck East Japan. Few studies have investigated the impact of exposure to a natural disaster on preschool children. We investigated the association of trauma experiences during the Great East Japan Earthquake on clinically significant behavior problems among preschool children 2 years after the earthquake. METHOD: Participants were children who were exposed to the 2011 disaster at preschool age (affected area, n = 178; unaffected area, n = 82). Data were collected from September 2012 to June 2013 (around 2 years after the earthquake), thus participants were aged 5 to 8 years when assessed. Severe trauma exposures related to the earthquake (e.g., loss of family members) were assessed by interview, and trauma events in the physical environment related to the earthquake (e.g. housing damage), and other trauma exposure before the earthquake, were assessed by questionnaire. Behavior problems were assessed by caregivers using the Child Behavior Checklist (CBCL), which encompasses internalizing, externalizing, and total problems. Children who exceeded clinical cut-off of the CBCL were defined as having clinically significant behavior problems. RESULTS: Rates of internalizing, externalizing, and total problems in the affected area were 27.7%, 21.2%, and 25.9%, respectively. The rate ratio suggests that children who lost distant relatives or friends were 2.36 times more likely to have internalizing behavior problems (47.6% vs. 20.2%, 95% CI: 1.10-5.07). Other trauma experiences before the earthquake also showed significant positive association with internalizing, externalizing, and total behavior problems, which were not observed in the unaffected area. CONCLUSIONS: One in four children still had behavior problems even 2 years after the Great East Japan Earthquake. Children who had other trauma experiences before the earthquake were more likely to have behavior problems. These data will be useful for developing future interventions in child mental health after a natural disaster.


Subject(s)
Child Behavior Disorders/epidemiology , Earthquakes , Caregivers/psychology , Child , Child Behavior Disorders/pathology , Child, Preschool , Female , Humans , Interviews as Topic , Male , Surveys and Questionnaires
11.
PLoS One ; 9(8): e104793, 2014.
Article in English | MEDLINE | ID: mdl-25120014

ABSTRACT

Parental harsh disciplining, like corporal punishment, has consistently been associated with adverse mental health outcomes in children. It remains a challenge to accurately assess the consequences of harsh discipline, as researchers and clinicians generally rely on parent report of young children's problem behaviors. If parents rate their parenting styles and their child's behavior this may bias results. The use of child self-report on problem behaviors is not common but may provide extra information about the relation of harsh parental discipline and problem behavior. We examined the independent contribution of young children's self-report above parental report of emotional and behavioral problems in a study of maternal and paternal harsh discipline in a birth cohort. Maternal and paternal harsh discipline predicted both parent reported behavioral and parent reported emotional problems, but only child reported behavioral problems. Associations were not explained by pre-existing behavioral problems at age 3. Importantly, the association with child reported outcomes was independent from parent reported problem behavior. These results suggest that young children's self-reports of behavioral problems provide unique information on the effects of harsh parental discipline. Inclusion of child self-reports can therefore help estimate the effects of harsh parental discipline more accurately.


Subject(s)
Child Behavior Disorders/etiology , Child Behavior Disorders/pathology , Child Rearing/psychology , Parent-Child Relations , Punishment/psychology , Stress, Psychological/psychology , Adult , Child , Child, Preschool , Cohort Studies , Humans , Linear Models , Prospective Studies , Self Report , Surveys and Questionnaires
12.
Epilepsia ; 54(12): 2116-24, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24304435

ABSTRACT

PURPOSE: Neurobehavioral comorbidities are common in pediatric epilepsy with enduring adverse effects on functioning, but their neuroanatomic underpinning is unclear. Striatal and thalamic abnormalities have been associated with childhood-onset epilepsies, suggesting that epilepsy-related changes in the subcortical circuit might be associated with the comorbidities of children with epilepsy. We aimed to compare subcortical volumes and their relationship with age in children with complex partial seizures (CPS), childhood absence epilepsy (CAE), and healthy controls (HC). We examined the shared versus unique structural-functional relationships of these volumes with behavior problems, intelligence, language, peer interaction, and epilepsy variables in these two epilepsy syndromes. METHODS: We investigated volumetric differences of caudate, putamen, pallidum, and thalamus in children with CPS (N = 21), CAE (N = 20), and HC (N = 27). Study subjects underwent structural magnetic resonance imaging (MRI), intelligence, and language testing. Parent-completed Child Behavior Checklists provided behavior problem and peer interaction scores. We examined the association of age, intelligence quotient (IQ), language, behavioral problems, and epilepsy variables with subcortical volumes that were significantly different between the children with epilepsy and HC. KEY FINDINGS: Both children with CPS and CAE exhibited significantly smaller left thalamic volume compared to HC. In terms of developmental trajectory, greater thalamic volume was significantly correlated with increasing age in children with CPS and CAE but not in HC. With regard to the comorbidities, reduced left thalamic volumes were related to more social problems in children with CPS and CAE. Smaller left thalamic volumes in children with CPS were also associated with poor attention, lower IQ and language scores, and impaired peer interaction. SIGNIFICANCE: Our study is the first to directly compare and detect shared thalamic structural abnormalities in children with CPS and CAE. These findings highlight the vulnerability of the thalamus and provide important new insights on its possible role in the neurobehavioral comorbidities of childhood-onset epilepsy.


Subject(s)
Child Behavior Disorders/epidemiology , Epilepsy, Absence/epidemiology , Epilepsy, Complex Partial/epidemiology , Thalamus/pathology , Adolescent , Age Factors , Case-Control Studies , Caudate Nucleus/pathology , Child , Child Behavior Disorders/pathology , Comorbidity , Epilepsy, Absence/pathology , Epilepsy, Complex Partial/pathology , Female , Humans , Intelligence , Interpersonal Relations , Language Development , Magnetic Resonance Imaging , Male , Neuroimaging , Organ Size , Putamen/pathology
13.
Cuad. psiquiatr. psicoter. niño adolesc ; (56): 47-58, jul.-dic. 2013. tab, ilus
Article in Spanish | IBECS | ID: ibc-127089

ABSTRACT

Este trabajo pretende evaluar las asociaciones de los factores de riesgo (ODAT) en los primeros años de vida y gravedad de la patología mental del niño, a través de un estudio trasversal, descriptivo y analítico de caso control, con una selección de los sujetos mediante un muestreo aleatorio estratificado. Se seleccionaron tres grupos de niños, uno con trastorno mental grave, otro con trastornos mentales no catalogados como graves y un último grupo de niños que acuden al reconocimiento del niño sano. Las alteraciones biológicas detectadas en los periodos iniciales de la vida se asocian sobre todo a la patología mental de mayor gravedad. La convivencia con ambos padres y parientes próximos, la patología mental y la situación laboral de los padres, las pérdidas de personas significativas también parecen contribuir significativamente en la patología mental del niño. Por contra factores como la incorporación temprana a guardería, no aparecen como relevantes (AU)


This work aims to evaluate the factors of risk (ODAT) associations in the first years of life and severity of mental pathology of the child, cross-sectional, descriptive and analytical case-control study, with a selection of subjects by means of a stratified random sampling. We selected three groups of children, one with serious mental disorder, other mental disorders not classified as serious and a last group of children who come to the recognition of the healthy child. Biological alterations detected in the initial periods of life are especially associated with more severe mental pathology. Living with both parents and close relatives, mental pathology and the employment situation of the parents, the loss of significant people also seem to contribute significantly in the child mental pathology. Against factors such as the early incorporation into child care, do not appear as relevant (AU)


Subject(s)
Humans , Male , Female , Child , Child Behavior Disorders/pathology , Risk Factors , Mental Health , Psychology, Child
14.
Am J Med Genet A ; 161A(8): 1833-52, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23813913

ABSTRACT

Chromosome 17p13.3 is a gene rich region that when deleted is associated with the well-known Miller-Dieker syndrome. A recently described duplication syndrome involving this region has been associated with intellectual impairment, autism and occasional brain MRI abnormalities. We report 34 additional patients from 21 families to further delineate the clinical, neurological, behavioral, and brain imaging findings. We found a highly diverse phenotype with inter- and intrafamilial variability, especially in cognitive development. The most specific phenotype occurred in individuals with large duplications that include both the YWHAE and LIS1 genes. These patients had a relatively distinct facial phenotype and frequent structural brain abnormalities involving the corpus callosum, cerebellar vermis, and cranial base. Autism spectrum disorders were seen in a third of duplication probands, most commonly in those with duplications of YWHAE and flanking genes such as CRK. The typical neurobehavioral phenotype was usually seen in those with the larger duplications. We did not confirm the association of early overgrowth with involvement of YWHAE and CRK, or growth failure with duplications of LIS1. Older patients were often overweight. Three variant phenotypes included cleft lip/palate (CLP), split hand/foot with long bone deficiency (SHFLD), and a connective tissue phenotype resembling Marfan syndrome. The duplications in patients with clefts appear to disrupt ABR, while the SHFLD phenotype was associated with duplication of BHLHA9 as noted in two recent reports. The connective tissue phenotype did not have a convincing critical region. Our experience with this large cohort expands knowledge of this diverse duplication syndrome.


Subject(s)
1-Alkyl-2-acetylglycerophosphocholine Esterase/genetics , 14-3-3 Proteins/genetics , Brain/abnormalities , Child Behavior Disorders/pathology , Child Development Disorders, Pervasive/pathology , Chromosomes, Human, Pair 17/genetics , Gene Duplication , Microtubule-Associated Proteins/genetics , Adolescent , Adult , Brain/pathology , Child , Child Behavior Disorders/genetics , Child Development Disorders, Pervasive/genetics , Child, Preschool , Female , Humans , Infant , Male , Phenotype
15.
Eur Neuropsychopharmacol ; 23(7): 622-8, 2013 Jul.
Article in English | MEDLINE | ID: mdl-22824414

ABSTRACT

Adolescence is characterized by dynamic changes in structural brain maturation. At the same time, adolescence is a critical time for the development of affective and anxiety-related disorders. Individual differences in typically developing children and adolescents may prove more valuable for identifying which brain regions correspond with internalizing behavior problems (i.e., anxious/depressive, withdrawal and somatic symptoms) on a continuous scale compared to clinical studies. Participants were 179 (92 males, 87 females) typically developing children and adolescents between ages 8 and 17. Hippocampal and amygdala volumes were measured automatically with FreeSurfer. Internalizing behavior was assessed with the Child Behavior Checklist (CBCL) completed by the parent, and associated with hippocampal and amygdala volumes. Hippocampal volume was inversely related with the total internalizing problems scale of the CBCL, irrespective of gender, age, or informant (mother or father). The effects were most prominent for the withdrawal and anxiety/depression subscales and the left hippocampus: more withdrawal and anxiety/depression was related to smaller left hippocampal volume. No associations were found between internalizing behavior and amygdala volume. This study shows that typically developing children and adolescents with high internalizing behavior share some of the neuroanatomical features of adult depression and anxiety-related disorders.


Subject(s)
Adolescent Behavior/psychology , Child Behavior Disorders/pathology , Hippocampus/pathology , Internal-External Control , Adolescent , Amygdala/pathology , Atrophy/pathology , Child , Female , Humans , Male , Neuroimaging
16.
Dev Psychol ; 49(1): 92-108, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22448986

ABSTRACT

We assessed trajectories of children's internalizing symptoms, indexed through anxiety and depression, with a focus on the role of interactions between interparental marital conflict, children's sympathetic nervous system activity indexed by skin conductance level (SCL), and parasympathetic nervous system activity indexed by respiratory sinus arrhythmia (RSA) as predictors of growth. Children participated in 3 waves of data collection with a 1-year lag between each wave. At T1, 128 girls and 123 boys participated (M age = 8.23 years; SD = 0.73). The most important findings reveal that girls with either low RSA in conjunction with low SCL (i.e., coinhibition) at baseline or with increasing RSA and decreasing SCL in response to a challenging task (i.e., reciprocal parasympathetic activation) are susceptible to high or escalating anxiety and depression symptoms, particularly in the context of marital conflict. Findings support the importance of concurrent examinations of environmental risk factors and physiological activity for better prediction of the development of anxiety and depression symptoms.


Subject(s)
Autonomic Nervous System/physiopathology , Child Behavior Disorders/etiology , Child Behavior Disorders/pathology , Child Development , Marriage/psychology , Anxiety/pathology , Anxiety/physiopathology , Child , Depression/pathology , Depression/physiopathology , Electrocardiography , Electroencephalography , Female , Galvanic Skin Response , Humans , Longitudinal Studies , Male , Psychiatric Status Rating Scales , Statistics as Topic
17.
Actas esp. psiquiatr ; 40(3): 165-168, mayo-jun. 2012. ilus
Article in Spanish | IBECS | ID: ibc-101618

ABSTRACT

Introducción. Nuestro objetivo fue evaluar la eficacia, seguridad y tolerabilidad de duloxetina en el tratamiento de adolescentes con trastorno somatomorfo. Resultado. Describimos dos casos (chica 11 años y varón 17 años) evaluados en nuestro Departamento después de ser valorados por Pediatra y Neuropediatría por síntomas físicos complejos. Las evaluaciónes para descartar causas médicas fueron normales. Realizamos un diagnóstico de trastorno somatomorfo. El tratamiento farmacológico con antidepresivos, benzodiacepinas, estimulantes y estabilizadores del humor sólo produjouna mejoría breve y parcial. Tras cambiar el tratamiento aduloxetina (30 y 60 mg/día respectivamente) los pacientes experimentaron una mejoría gradual y se mantuvo 7 y 14meses. Conclusión. La duloxetina puede ser eficaz y bien tolerada en adolescentes con trastorno somatomorfo. Son necesarios ensayos controlados (AU)


Background. Our goal was to evaluate the effectiveness, safety and tolerability of duloxetine in the treatment of children and adolescents with somatoform disorder. Results. We describe two cases, those of an 11-year old girl and a 17-year old boy, evaluated in our Department after being studied by a Pediatrician and Neuropediatrician due to complex physical symptoms. The evaluations to rule out medical causes were normal. We diagnosed somatoform disorder. The pharmacological treatments with antidepressants, benzodiazepines, stimulants and mood stabilizers only produced brief and partial improvement. After switching the treatment to duloxetine (30 and 60 mg/day, respectively) both patients experienced a gradual improvement that was maintained at 7 and 14 months. Conclusion. Duloxetine may be effective and well tolerated in the treatment of adolescents with somatoform disorder. Controlled trials are need (AU)


Subject(s)
Humans , Male , Female , Child , Adolescent , Child Behavior Disorders/diagnosis , Child Behavior Disorders/pathology , Adolescent/legislation & jurisprudence , Adolescent Behavior/psychology , Child Behavior Disorders/therapy
18.
Behav Genet ; 41(3): 381-93, 2011 May.
Article in English | MEDLINE | ID: mdl-21279430

ABSTRACT

We investigated regional grey matter (GM) density in adolescents with Down syndrome (DS) compared to age-matched controls and correlated MRI data with neuropsychological measures in the DS group. Inter-group comparisons documented several GM concentration abnormalities in the participants with DS compared to controls. In the adolescents with DS, intra-group results also showed associations between regional GM density and the neuropsychological measures considered. In particular, GM density of the cerebellum and middle and inferior temporal gyrus was associated with linguistic measures. Short-term memory performances were correlated with the inferior parietal lobule, insula, superior temporal gyrus, medial occipital lobe, and cerebellum. Long-term memory abilities were correlated with GM density in the orbitofrontal cortex, lateral and medial temporal lobe regions, and anterior cingulum and visuo-perceptual abilities with GM density the left middle frontal gyrus. Results of this preliminary study are consistent with a not always efficient brain organization in DS.


Subject(s)
Cerebellum/pathology , Cerebral Cortex/pathology , Down Syndrome/genetics , Down Syndrome/pathology , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Adolescent , Brain Mapping , Child , Child Behavior Disorders/genetics , Child Behavior Disorders/pathology , DNA Mutational Analysis , Female , Humans , Male , Neuropsychological Tests , Organ Size/physiology , Phenotype , Young Adult
19.
Psychiatry Res ; 188(1): 96-101, 2011 Jun 30.
Article in English | MEDLINE | ID: mdl-21071098

ABSTRACT

There exists an extensive terminology for defining the situation of children who, in varying circumstances, suffer from affective deprivation (AD), within an unsatisfactory family situation or in institutions. Nevertheless, the neuroendocrine mechanisms (if they exist) determining it have yet to be identified. Our objective was to determine if specific neuroendocrine markers, all of them previously implicated in affective disorders, could be modified, and in which sense, in affective deprivation syndrome of the child. For this purpose, we studied three separate groups of children: (1) control group (CG); (2) children suffering from AD; and (3) children with non-organic failure to thrive (NOFT). In every case, we studied the serum levels of melatonin, serotonin, ß-endorphins and adrenocorticotropic hormone (ACTH); and kynurenine pathway tryptophan metabolites (both during the day and at night). Significantly, there was a conspicuous reduction in the levels of each of the neuroendocrine markers (melatonin, serotonin, ß-endorphins and ACTH) in the group suffering from affective deficiency, a diminution which was even more noticeable in the group of patients presenting delayed growth. Furthermore, as also occurs in other affective disorders, there were corresponding modifications in the metabolisation of tryptophan. We report the existence of neuroendocrine mechanisms that are associated with the above-mentioned clinical manifestations in these patients, mechanisms that may underlie the close connection existing between AD syndrome and the cause of NOFT. These data suggest that the AD syndrome and NOFT comprise a single process, but one with a different evolutionary continuum of psychosocial dwarfism.


Subject(s)
Neurosecretory Systems/metabolism , Adolescent , Adrenocorticotropic Hormone/blood , Analysis of Variance , Chi-Square Distribution , Child , Child Behavior Disorders/metabolism , Child Behavior Disorders/pathology , Child Behavior Disorders/psychology , Child, Preschool , Circadian Rhythm/physiology , Developmental Disabilities/metabolism , Developmental Disabilities/pathology , Developmental Disabilities/psychology , Dwarfism , Failure to Thrive/metabolism , Failure to Thrive/psychology , Female , Humans , Kynurenine/urine , Male , Melatonin/blood , Psychopathology , Serotonin/blood , beta-Endorphin/blood
20.
Zhonghua Er Ke Za Zhi ; 48(5): 346-50, 2010 May.
Article in Chinese | MEDLINE | ID: mdl-20654034

ABSTRACT

OBJECTIVE: To find out the rate of comorbidities of depression, anxiety disorder and attention deficit hyperactivity disorder (ADHD) symptoms in children with epilepsy and to analyze the relevant affecting factors and impacts on quality of life. METHOD: Totally 142 children with various types of epilepsy underwent neuropsychological assessment with the Depression Self-rating Scale for Children, the Screen for Child Anxiety Related Emotional Disorders and the ADHD Rating Scale-IV, an 18-item parent-rated questionnaire based on the diagnostic criteria for ADHD, the quality of life was measured in 100 cases on antiepileptic medications by the Quality of Life in Epilepsy Inventory (QOLIE-31). The comorbidity rates were calculated using t-test, chi(2) test and multiple logistic analysis, the variables associated with psychiatric comorbidities were determined, and the impact on quality of life was analyzed. RESULT: (1) The total rate of emotional and behavioral comorbidities was 57.7% (82/142), the frequency of depressive disorder, anxiety disorder and ADHD was 14.8%, 44.4% and 17.6%, respectively. The suicidal ideation occasionally occurred in 5.6% of the cases and 0.7% of cases often had the ideation, but no suicidal action was found in any case. (2) Risk factors for the emotional and behavioral disorders: multiple logistic analysis indicated that age, gender and epilepsy illness-related variables were not relative to the comorbidities, P > 0.05, there were interactions among the disorders. (3) The impact on the quality of life: The emotional and behavioral conditions were associated with the low quality of life, which was significantly lower in epileptic children with co-morbid disorder compared to non-comorbidities epilepsy group. Especially negative impact on the total score of quality of life and four sub-items such as overall quality, emotional well-being, cognitive and social function, P < 0.001. There were also significant differences between the two groups in the other three sub-items including fear for seizure attack, energy/fatigue and medication effects (P < 0.05). CONCLUSIONS: The frequency of emotional and behavioral disorders including depress disorder, anxiety disorder and ADHD was considerably high in children with epilepsy. Age, gender and epilepsy illness-related variables are not associated with the emotional and behavioral comorbidities, which interfere with each other. Emotional and behavioral disorder is one of the negative factors to the quality of life in epileptic patients. Neuropsychological assessment and treatment are important for improvement of the quality of life in children with epilepsy.


Subject(s)
Epilepsy/epidemiology , Epilepsy/psychology , Quality of Life , Attention Deficit Disorder with Hyperactivity/epidemiology , Child , Child Behavior Disorders/epidemiology , Child Behavior Disorders/pathology , Comorbidity , Emotions , Female , Humans , Surveys and Questionnaires
SELECTION OF CITATIONS
SEARCH DETAIL
...