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1.
J Pediatr ; 214: 60-65.e2, 2019 11.
Artigo em Inglês | MEDLINE | ID: mdl-31474426

RESUMO

OBJECTIVES: To evaluate salivary biomarkers that elucidate the molecular mechanisms by which in utero opioid exposure exerts sex-specific effects on select hypothalamic and reward genes driving hyperphagia, a hallmark symptom of infants suffering from neonatal opioid withdrawal syndrome (NOWS). STUDY DESIGN: We prospectively collected saliva from 50 newborns born at ≥34 weeks of gestational age with prenatal opioid exposure and 50 sex- and gestational age-matched infants without exposure. Saliva underwent transcriptomic analysis for 4 select genes involved in homeostatic and hedonic feeding regulation (neuropeptide Y2 receptor [NPY2R], proopiomelanocortin [POMC], leptin receptor [LEPR], dopamine type 2 receptor [DRD2]). Normalized gene expression data were stratified based on sex and correlated with feeding volume on day of life 7 and length of stay in infants with NOWS requiring pharmacotherapy. RESULTS: Expression of DRD2, a hedonistic/reward regulator, was significantly higher in male newborns compared with female newborns with NOWS (Δ threshold cycle 10.8 ± 3.8 vs 13.9 ± 3.7, P = .01). In NOWS requiring pharmacotherapy expression of leptin receptor, an appetite suppressor, was higher in male subjects than female subjects (Δ threshold cycle 8.4 ± 2.5 vs 12.4 ± 5.1, P = .05), DRD2 expression significantly correlated with intake volume on day of life 7 (r = 0.58, P = .02), and expression of NPY2R, an appetite regulator, negatively correlated with length of stay (r = -0.24, P = .05). CONCLUSIONS: Prenatal opioid exposure exerts sex-dependent effects on hypothalamic feeding regulatory genes with clinical correlations. Neonatal salivary gene expression analyses may predict hyperphagia, severity of withdrawal state, and length of stay in infants with NOWS.


Assuntos
Analgésicos Opioides/efeitos adversos , Expressão Gênica , Hiperfagia/etiologia , Síndrome de Abstinência Neonatal/genética , Saliva/química , Estudos de Casos e Controles , Feminino , Perfilação da Expressão Gênica , Marcadores Genéticos , Humanos , Recém-Nascido , Masculino , Síndrome de Abstinência Neonatal/complicações , Projetos Piloto , Pró-Opiomelanocortina/genética , Estudos Prospectivos , Receptores de Dopamina D2/genética , Receptores para Leptina/genética , Receptores de Neuropeptídeo Y/genética , Índice de Gravidade de Doença , Fatores Sexuais
2.
J Pediatr ; 166(4): 890-896.e1, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25556020

RESUMO

OBJECTIVE: To determine the clinical presentation, diagnostic variables, risk factors, and disease burden in children with chronic pancreatitis. STUDY DESIGN: We performed a cross-sectional study of data from the International Study Group of Pediatric Pancreatitis: In Search for a Cure, a registry of children with acute recurrent pancreatitis and chronic pancreatitis. Between-group differences were compared using Wilcoxon rank-sum test. RESULTS: Among 170 subjects in the registry, 76 (45%) had chronic pancreatitis; 57% were female, 80% were white; median age at diagnosis was 9.9 years. Pancreatitis-predisposing genetic mutations were identified in 51 (67%) and obstructive risk factors in 25 (33%). Toxic/metabolic and autoimmune factors were uncommon. Imaging demonstrated ductal abnormalities and pancreatic atrophy more commonly than calcifications. Fifty-nine (77%) reported abdominal pain within the past year; pain was reported as constant and receiving narcotics in 28%. Children with chronic pancreatitis reported a median of 3 emergency department visits and 2 hospitalizations in the last year. Forty-seven subjects (70%) missed 1 day of school in the past month as the result of chronic pancreatitis; 26 (34%) missed 3 or more days. Children reporting constant pain were more likely to miss school (P = .002), visit the emergency department (P = .01), and experience hospitalizations (P = .03) compared with children with episodic pain. Thirty-three children (43%) underwent therapeutic endoscopic retrograde pancreatography; one or more pancreatic surgeries were performed in 30 (39%). CONCLUSIONS: Chronic pancreatitis occurs at a young age with distinct clinical features. Genetic and obstructive risk factors are common, and disease burden is substantial.


Assuntos
Predisposição Genética para Doença , Pancreatite Crônica/genética , Criança , Colangiopancreatografia Retrógrada Endoscópica , Estudos Transversais , Regulador de Condutância Transmembrana em Fibrose Cística/genética , DNA/genética , Análise Mutacional de DNA , Feminino , Humanos , Incidência , Masculino , Mutação , Pancreatite Crônica/diagnóstico , Pancreatite Crônica/epidemiologia , Prevalência , Fatores de Risco , Estados Unidos/epidemiologia
3.
J Pediatr ; 162(3): 530-535.e1, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23062247

RESUMO

OBJECTIVES: To evaluate the relationship between nutritional status early in life and the timing and velocity of height growth, lung function, complications of cystic fibrosis, and survival. STUDY DESIGN: Prospective, observational study using data from the Cystic Fibrosis Foundation Registry (US) for patients born between 1989 and 1992 (n = 3142). RESULTS: Weight-for-age percentile (WAP) at 4 years of age was positively associated with height-for-age percentiles throughout childhood. Age 4 years WAP >10% was associated with better lung function from 6-18 years of age. In boys and girls with current WAP >50%, peak pubertal height velocities approximated but remained lower than that of the healthy reference population. By age 18 years, patients with an age 4 years WAP >50% suffered fewer acute pulmonary exacerbations, spent fewer days in the hospital, and had lower rates of impaired glucose tolerance or diabetes. Patients attaining higher age 4 years WAP and height-for-age percentiles had a survival advantage throughout childhood. CONCLUSION: For the population studied, greater weight at age 4 years is associated with greater height, better pulmonary function, fewer complications of cystic fibrosis, and better survival through age 18 years. Furthermore, greater weight-for-age in the peripubertal period is associated on average with improved tempo and timing of pubertal height growth.


Assuntos
Fibrose Cística/complicações , Pulmão/fisiopatologia , Estado Nutricional , Adolescente , Estatura , Peso Corporal , Criança , Pré-Escolar , Fibrose Cística/mortalidade , Fibrose Cística/fisiopatologia , Feminino , Intolerância à Glucose , Humanos , Masculino , Estudos Prospectivos , Testes de Função Respiratória , Análise de Sobrevida
4.
Arch Pediatr Adolesc Med ; 159(11): 1043-8, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16275795

RESUMO

OBJECTIVE: To describe 2 cases of lipoid pneumonia in Mexican American infants after administration of vegetable- or animal-derived oils and the cultural barriers to diagnosis. Various folk remedies have been documented in the international medical literature that involve the oral or nasal administration of vegetable- or animal-derived oils to children for the treatment of common ailments, including nasal stuffiness, constipation, and colic. Lipoid pneumonia is a known complication of such practices in Mexico, India, Saudi Arabia, and other countries. METHODS: Case reports of 2 Mexican American infants with respiratory distress and interviews with 30 immigrant families of Mexican origin. RESULTS: In both cases, language and cultural barriers resulted in a delayed diagnosis of lipoid pneumonia. Interviews with immigrant families confirmed that oil administration to children is a common traditional therapy in Mexican cultures. CONCLUSIONS: These findings underscore the need for primary care providers to be aware of the traditional practice of oil administration to infants in many cultures, its pathophysiological consequences, the potential cultural barriers to timely diagnosis, and the opportunity to prevent cases of lipoid pneumonia through anticipatory guidance.


Assuntos
Barreiras de Comunicação , Hispânico ou Latino , Óleos de Plantas/efeitos adversos , Pneumonia Lipoide/diagnóstico , Pneumonia Lipoide/etnologia , Broncoscopia , Diagnóstico Diferencial , Seguimentos , Humanos , Recém-Nascido , Masculino , Radiografia Torácica , Tomografia Computadorizada por Raios X
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