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1.
Nutr Neurosci ; 22(12): 863-866, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29629638

RESUMO

Autism spectrum disorder (ASD) is a common neurodevelopmental disorder caused by complicated interactions between genetic and environmental factors. Clinical trials, including case reports, case-control studies, and a double-blinded randomized clinical study, have suggested that high-dose vitamin D3 regimens may ameliorate the core symptoms of ASD. Vitamin D3 supplementation was effective in about three-quarters of children with ASD. To further investigate the relationship between vitamin D and ASD symptoms in vitamin D-responsive autistic children, changes in symptoms were assessed in three children with ASD who were given vitamin D3 supplementation followed by a long interruption. The core symptoms of ASD were remarkably improved during the vitamin D3 supplementation period when serum 25-hydroxyvitamin D [25(OH)]D levels reached over 40.0 ng/mL. However, symptoms reappeared after the supplementation was stopped, when serum 25(OH)D levels fell below 30.0 ng/mL but were again improved with re-administration of vitamin D3 after the interruption, when serum 25(OH)D levels exceeded 40.0 ng/mL. Overall, these results showed that the core symptoms of ASD fluctuated in severity with changes in serum 25(OH)D levels in children, indicating that maintaining a responsive 25(OH)D level is important for treating ASD. Maintaining a serum 25(OH)D level between 40.0 and 100.0 ng/ml may be optimal for producing therapeutic effects in vitamin D-responsive individuals with ASD.


Assuntos
Transtorno do Espectro Autista/sangue , Transtorno do Espectro Autista/fisiopatologia , Colecalciferol/administração & dosagem , Vitamina D/análogos & derivados , Transtorno do Espectro Autista/tratamento farmacológico , Transtornos do Comportamento Infantil/sangue , Pré-Escolar , Suplementos Nutricionais , Humanos , Lactente , Transtornos da Linguagem/sangue , Masculino , Habilidades Sociais , Vitamina D/sangue
2.
Am J Clin Nutr ; 94(6): 1592-9, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22071708

RESUMO

BACKGROUND: Little is known about the effect of fatty acid (FA) concentrations in cord blood on long-term behavioral outcomes. OBJECTIVE: We assessed the effect of FAs in cord blood serum on children's behavioral difficulties at the age of 10 y. DESIGN: A longitudinal study of 416 children from the population-based Influences of Lifestyle-Related Factors on the Immune System and the Development of Allergies in Childhood (LISAplus) birth cohort from Munich was conducted. Individual glycerophospholipid FAs in blood were analyzed in venous cord blood. Data on children's behavior were collected with a parent-reported Strength and Difficulties Questionnaire at 10 y of age. Zero-inflated Poisson regression models were applied and adjusted for sex, parental income, smoking during pregnancy, and dietary intake of arachidonic acid (AA) and DHA at 10 y. RESULTS: A 1% increase in DHA in cord blood serum was found to decrease total difficulties by (exp)ß(adj) = 0.93 (SE = 0.02, P < 0.0001) and hyperactivity or inattention by (exp)ß(adj) = 0.94 (SE = 0.03, P < 0.04). Higher long-chain (LC) PUFA concentrations in cord blood serum were associated with fewer emotional symptoms [(exp)ß(adj) = 0.95, SE = 0.03, P = 0.01], and similarly higher AA concentrations were associated with fewer emotional symptoms [(exp)ß(adj) = 0.94, SE = 0.03, P = 0.03]. CONCLUSION: Increased concentrations of DHA, LC-PUFAs, and AA in cord blood serum were associated with lower scores on a parent-completed behavioral screen. An appropriate FA supply to the developing fetus may be essential for optimal long-term behavioral outcomes in children.


Assuntos
Transtorno do Deficit de Atenção com Hiperatividade/sangue , Transtornos do Comportamento Infantil/sangue , Ácidos Graxos Insaturados/sangue , Sangue Fetal/química , Fenômenos Fisiológicos da Nutrição do Lactente , Estado Nutricional , Ácido Araquidônico/sangue , Criança , Pré-Escolar , Ácidos Docosa-Hexaenoicos/sangue , Emoções , Feminino , Alemanha , Glicerofosfolipídeos/sangue , Glicerofosfolipídeos/química , Humanos , Lactente , Recém-Nascido , Estudos Longitudinais , Masculino , Gravidez , Inquéritos e Questionários
3.
J Neurosurg ; 100(2 Suppl Pediatrics): 212-6, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14758953

RESUMO

The authors describe a unique case of a 2-year-old boy with a hypothalamic hamartoma secreting corticotropin-releasing hormone (CRH). The patient presented with a history of behavioral disturbances progressing over 12 months. His neurological status was intact. Magnetic resonance imaging demonstrated a 1.8 x 1.6 x 1.2-cm isointense, nonenhancing hypothalamic lesion. Endocrinological workup revealed elevated serum CRH and adrenocorticotropic hormone levels, nonsuppression with low-dose dexamethasone, and partial suppression with high-dose dexamethasone. He underwent tumor resection via a right frontotemporal craniotomy. Pathological examination of the tissue confirmed a hypothalamic hamartoma with CRH immunostaining. Postoperatively, his hormone levels normalized and his behavioral disturbances abated. The radiographic and clinical characteristics of hypothalamic hamartomas are reviewed and therapeutic considerations discussed.


Assuntos
Hormônio Liberador da Corticotropina/metabolismo , Hamartoma/diagnóstico , Doenças Hipotalâmicas/diagnóstico , Hormônio Adrenocorticotrópico/sangue , Transtornos do Comportamento Infantil/sangue , Transtornos do Comportamento Infantil/etiologia , Pré-Escolar , Dexametasona , Diagnóstico Diferencial , Hamartoma/sangue , Hamartoma/patologia , Hamartoma/cirurgia , Humanos , Hidrocortisona/sangue , Doenças Hipotalâmicas/sangue , Doenças Hipotalâmicas/patologia , Doenças Hipotalâmicas/cirurgia , Hipotálamo/patologia , Hipotálamo/cirurgia , Imageamento por Ressonância Magnética , Masculino
4.
Pediatrics ; 101(3): E10, 1998 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-9481029

RESUMO

OBJECTIVE: To assess whether small elevations in blood lead level were associated with measurable behavioral changes in a group of poor children between 1 and 3 years old. METHODS: The study population consisted of children presenting for routine well-child care to the pediatric clinic at Bellevue Hospital Center, a large urban public hospital. The following inclusion criteria were used for entry into the study: age 12 to 36 months; capillary lead screening result <1.21 micromol/L (25 microg/dL); no known prior history either of blood lead level >1.21 micromol/L (25 microg/dL) or lead exposure requiring chelation therapy; Latino or African-American; English or Spanish spoken in the home; biological mother as primary caretaker; child not presently attending day care; full-term, singleton gestation; birth weight at least 2500 g; no known neurologic or developmental disorder; and no severe chronic disease, including human immunodeficiency virus infection. Study enrollment was simultaneously stratified by capillary lead level and age. All children between 12 and 36 months attending the pediatric clinic during the study period received screening capillary blood measures of lead level following the recommendations of the Centers for Disease Control and Prevention and the American Academy of Pediatrics as part of routine primary care. During periods of enrollment, consecutive lead measurements performed in the pediatric clinic were reviewed by one of the researchers. For those children meeting entry criteria based on lead level and age, further eligibility based on the remainder of the inclusion criteria was determined through parental interview and review of the medical record. Lead exposure was assessed with a single capillary blood specimen, using atomic absorption spectrophotometry. Subjects were considered to be lead-exposed if their lead level was between 0.48 and 1.20 micromol/L (10 and 24.9 microg/dL) and nonexposed if their lead level was between 0 and 0.48 micromol/L (0 and 9.9 microg/dL). Behavior was assessed using the Behavior Rating Scale (BRS) of the Bayley Scales of Infant Development, second edition. The BRS in this age group consists of three components: an Emotional Regulation Factor that measures hyperactive/distractible/easy-frustration behaviors; an Orientation-Engagement Factor that measures fear/withdrawal/disinterest behaviors; and a Motor Quality Factor that assesses the appropriateness of movement and tone. The BRS is scored as a percentile; lower scores reflect more problematic behaviors. Researchers performing the BRS were blinded to capillary lead results. Information was collected concerning factors that might confound the relationship between lead and behavior. Demographic factors were collected, including: child's age, gender, and country of origin; mother's age, marital status, parity, country of origin, and primary language spoken; parental education, and occupation and receipt of public assistance. Socioeconomic status was determined using the Hollingshead Two-Factor Index of Social Position. Maternal verbal IQ was assessed using the Peabody Picture Vocabulary Test-Revised. Maternal depression was assessed using the Center for Epidemiologic Studies-Depression Scale. Cognitive stimulation provided in the home was assessed using a new office-based instrument, the StimQ, which measures the quantity and quality of play materials and parent-toddler activities in the child's home. To assess the child for iron deficiency, we performed a hematocrit and mean corpuscular volume at the time of the capillary lead evaluation. A presumptive diagnosis of iron deficiency was made if the child was either anemic (defined as a hematocrit <32) or had a mean corpuscular volume <72. RESULTS: The study sample consisted of 72 children. Children in the lead-exposed group (n = 41) had a mean BRS behavior score that was 15.8 points lower than that of children in the nonexposed group (n = 31), which was significant by the Stu


Assuntos
Transtornos do Comportamento Infantil/etiologia , Intoxicação por Chumbo/complicações , Comportamento Infantil , Transtornos do Comportamento Infantil/sangue , Transtornos do Comportamento Infantil/fisiopatologia , Pré-Escolar , Exposição Ambiental/efeitos adversos , Feminino , Humanos , Lactente , Chumbo/sangue , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/fisiopatologia , Masculino , Testes Psicológicos , Espectrofotometria Atômica , Inquéritos e Questionários
5.
J Autism Dev Disord ; 9(1): 73-82, 1979 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-438115

RESUMO

The recent upsurge in megavitamin therapy raises questions about the role of vitamin deficiencies and dependencies in mental health. With this in mind, the plasma levels of folic acid, ascorbic acid, pyridoxine, and riboflavin were studied in approximately 125 children admitted to a child psychiatric unit. There were no apparent decreased levels of vitamins in these children in terms of their age, race, or psychiatric diagnosis. It is postulated that vitamin deficiencies per se cannot be proposed as etiological factors in any of the psychiatric deficits represented. Megavitamin therapy, if successful, is not effective due to crrection of vitamin deficiencies as opposed to vitamin dependencies and may be due to the metabolic onus and consequent effects of such heavy doses of vitamins.


Assuntos
Sintomas Afetivos/sangue , Ácido Ascórbico/sangue , Ácido Fólico/sangue , Piridoxina/sangue , Riboflavina/sangue , Adolescente , Sintomas Afetivos/terapia , Transtorno Autístico/sangue , Criança , Transtornos do Comportamento Infantil/sangue , Pré-Escolar , Humanos , Deficiência Intelectual/sangue , Masculino , Terapia Ortomolecular , Transtornos Psicóticos/sangue , Esquizofrenia/sangue
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