RESUMEN
A gender gap exists in cystic fibrosis (CF). Here we investigate whether plasma microRNA expression profiles differ between the sexes in CF children. MicroRNA expression was quantified in paediatric CF plasma (n = 12; six females; Age range:1-6; Median Age: 3; 9 p.Phe508del homo- or heterozygotes) using TaqMan OpenArray Human miRNA Panels. Principal component analysis indicated differences in male versus female miRNA profiles. The miRNA array analysis revealed two miRNAs which were significantly increased in the female samples (miR-885-5p; fold change (FC):5.07, adjusted p value: 0.026 and miR-193a-5p; FC:2.6, adjusted p value: 0.031), although only miR-885-5p was validated as increased in females using specific qPCR assay (p < 0.0001). Gene ontology analysis of miR-885-5p validated targets identified cell migration, motility and fibrosis as processes potentially affected, with RAC1-mediated signalling featuring significantly. There is a significant increase in miR-885-5p in plasma of females versus males with CF under six years of age.
Asunto(s)
Fibrosis Quística/sangre , MicroARNs/sangre , Caracteres Sexuales , Niño , Preescolar , Fibrosis Quística/genética , Femenino , Ontología de Genes , Humanos , Lactante , Masculino , Pronóstico , Reacción en Cadena de la Polimerasa de Transcriptasa InversaRESUMEN
The risks of poor transition include delayed and inappropriate transfer that can result in disengagement with healthcare. Structured transition care can improve control of chronic digestive diseases and long-term health-related outcomes. These are the first nationally developed guidelines on the transition of adolescent and young persons (AYP) with chronic digestive diseases from paediatric to adult care. They were commissioned by the Clinical Services and Standards Committee of the British Society of Gastroenterology under the auspices of the Adolescent and Young Persons (A&YP) Section. Electronic searches for English-language articles were performed with keywords relating to digestive system diseases and transition to adult care in the Medline (via Ovid), PsycInfo (via Ovid), Web of Science and CINAHL databases for studies published from 1980 to September 2014. The quality of evidence and grading of recommendations was appraised using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system. The limited number of studies in gastroenterology and hepatology required the addition of relevant studies from other chronic diseases to be included.These guidelines deal specifically with the transition of AYP living with a diagnosis of chronic digestive disease and/or liver disease from paediatric to adult healthcare under the following headings;1. Patient populations involved in AYP transition. 2. Risks of failing transition or poor transition. 3. Models of AYP transition. 4. Patient and carer/parent perspective in AYP transition. 5. Surgical perspective.(AU)
Asunto(s)
Humanos , Adolescente , Adulto , Transición a la Atención de Adultos/normas , Enfermedades Gastrointestinales/terapia , Hepatopatías/terapia , Evaluación de Procesos y Resultados en Atención de Salud , Factores de Tiempo , Educación del Paciente como Asunto , Enfermedad Crónica , Enfoque GRADERESUMEN
Late-onset LAL deficiency, previously referred to as cholesteryl ester storage disorder, is a rare lysosomal storage disorder characterized by accumulation of cholesteryl esters. It has a heterogeneous clinical phenotype including abdominal pain, poor growth, hyperlipidemia with vascular complications and hepatosplenomegaly. End-stage liver disease may occur, but there are few reports of successful LT. There are also concerns that systemic manifestations of the disease might persist post-LT. We report a case with excellent outcome eight yr following LT. The subject was noted to have asymptomatic hepatosplenomegaly during an intercurrent illness, and LAL deficiency was confirmed with compound heterozygosity in the LIPA. Despite dietary fat restriction, he developed signs of progressive liver disease and subsequently developed hepatopulmonary syndrome. He underwent cadaveric LT at the age of nine and a half yr and recovered with prompt resolution of hepatopulmonary syndrome. Eight yr post-transplant he has normal growth, normal lipid profile, and liver and renal function tests. Liver histology showed no evidence of disease recurrence at this stage. LT in this subject resulted in an excellent functional correction of late-onset LAL deficiency.
Asunto(s)
Trasplante de Hígado , Enfermedad de Wolman/cirugía , Niño , Humanos , Masculino , Enfermedad de WolmanRESUMEN
Propionic acidemia (PA) is a severe metabolic disorder with cardiac and neurologic complications and a poor quality of life. Liver transplantation (LT) was thus proposed in PA to increase enzyme activity. We studied retrospectively LT in PA in two European centers. Twelve patients underwent 17 LTs between 1991 and 2013. They developed severe, unusual and unexpected complications, with high mortality (58%). When present, the cardiomyopathy resolved and no acute metabolic decompensation occurred allowing dietary relaxation. Renal failure was present in half of the patients before LT and worsened in all of them. We suggest that cardiac and renal functions should be assessed before LT and monitored closely afterward. A renal sparing immunosuppression should be used. We speculate that some complications may be related to accumulated toxicity of the disease and that earlier LT could prevent some of these consequences. As kidney transplantation has been performed successfully in methylmalonic acidemia, a metabolic disease in the same biochemical pathway, the choice of the organ to transplant could be further discussed.
Asunto(s)
Trasplante de Hígado/efectos adversos , Acidemia Propiónica/cirugía , Niño , Femenino , Humanos , Inmunosupresores/administración & dosificación , Masculino , Acidemia Propiónica/fisiopatologíaRESUMEN
BACKGROUND: Nitisinone has transformed the management of hereditary tyrosinaemia type 1 (HT1). However, the risk of developing hepatocellular carcinoma is related to the age at which treatment is commenced. Little data on the outcome of children treated pre-emptively exist. AIM: To describe the outcome of children with HT1 treated with nitisinone following selective newborn screening (NBS) and to compare their outcome with index siblings who had presented clinically. SUBJECTS: 12 children with HT1 were detected by NBS. Seven children were screened for HT1 because of an affected sibling (n=5). Four children were detected due to raised tyrosine concentrations on routine NBS and one child was born in a country with universal NBS for HT1. OUTCOME: Nitisinone was commenced at 4 (1-52) days old. 6 children had an initial coagulopathy which resolved after 4 (1-7) days treatment. Currently at median age 8.5 (3-12.5) years all are clinically normal, with normal liver function tests and imaging. Those of school age are in normal classes but four have reported learning difficulties. Five index siblings presented clinically with acute liver failure (four) and chronic liver disease (one) at median 4 (1.5-17) months. One died of liver failure prior to nitisinone's availability. Four were treated with nitisinone; one failed to respond and underwent liver transplantation and three responded. One responder died from complications of prematurity and the remaining two have compensated liver disease. SUMMARY: Children with HT1 treated with nitisinone following NBS have an excellent outcome. CONCLUSIONS: Universal NBS for HT1 should be introduced in the UK.
Asunto(s)
Ciclohexanonas/uso terapéutico , Inhibidores Enzimáticos/uso terapéutico , Tamizaje Neonatal , Nitrobenzoatos/uso terapéutico , Tirosinemias/diagnóstico , Tirosinemias/tratamiento farmacológico , Femenino , Genotipo , Humanos , Hidrolasas/genética , Recién Nacido , Masculino , Mutación , Tiempo de Protrombina , Resultado del Tratamiento , Tirosinemias/sangre , Tirosinemias/genética , alfa-Fetoproteínas/metabolismoRESUMEN
INTRODUCTION: The terminal ileum (TI) is important for the active reabsorption of bile salts and is the site of allograft rejection; disruption of enterohepatic circulation (EHC) may give insights to inflammatory and other physiologic processes at the TI. SUBJECTS AND METHODS: Four children aged 5 to 12 years who had received small bowel transplantation (SBTx), 3 recovering from post-transplant lymphoproliferative disease (PTLD) and 1 with acute rejection, were studied. Two of the 4 had stoma reversal. Another child (15 years) with progressive familial intrahepatic cholestasis (PFIC) and pruritus, despite liver transplantation and biliary diversion, was studied. Selenium homocholic acid taurocholate scanning ((75)SeHCAT) capsule was given orally (n = 3) or via introducer during endoscopy (n = 2); a baseline whole-body gamma camera scan was done 4 hours later and on days 1 to 5. RESULTS: The normal 3-day bile salt retention is 30% to 70% of baseline and normal adult biological half-life, t½ is 62 ± 17 hours. The results in children with a stoma were very low (0.1% at 7.6 hours; 5% at 17 hours). The children with reversed stoma had retention and t½ closer to the reference range (18% at 29 hours; 22% at 33 hours). The child with PFIC + biliary diversion had an initial very high gamma emission from the stoma bag suggesting excellent reabsorption of bile salts from his TI, but retention was 0.6% and t½ 9.8 hours, demonstrating efficient biliary diversion. CONCLUSION: These results confirm children with stomas malabsorb bile acids, which can be ameliorated after stoma closure. SeHCAT demonstrated that the biliary diversion was working well and may be helpful in preoperative assessment of abnormal EHC. The role of SeHCAT in SBTx requires further evaluation.
Asunto(s)
Ácidos y Sales Biliares , Colestasis Intrahepática/cirugía , Íleon/trasplante , Radioisótopos de Selenio , Ácido Taurocólico/análogos & derivados , Receptores de Trasplantes , Adulto , Humanos , Íleon/diagnóstico por imagen , Íleon/fisiopatología , Masculino , Proyectos Piloto , CintigrafíaRESUMEN
To compare the incidence of acute histologically proven rejection in children who have had a liver transplant for hepatoblastoma with a control group of children transplanted for biliary atresia (EHBA). A retrospective case notes based study was performed. Twenty patients were identified with hepatoblastoma who were transplanted at a single unit between 1991 and 2008. These were matched as closely as possible for age, gender, year of transplant and type of immunosuppression used to the control group transplanted for biliary atresia (n = 60). There was a significant decrease in rate of acute rejection as assessed by the rejection activity index (RAI) in the hepatoblastoma group (75% vs. 50%, respectively, p < 0.04). Chronic rejection was rare in both groups, but twice as common in the biliary atresia group. Equal levels of immunosuppression were achieved in both groups. Renal function was noted to be reduced one yr post-transplant in both groups, as previously reported. A modified immunosuppression regimen could be considered in children with hepatoblastoma undergoing liver transplantation.
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Rechazo de Injerto/epidemiología , Hepatoblastoma/terapia , Neoplasias Hepáticas/terapia , Trasplante de Hígado , Atresia Biliar/terapia , Niño , Preescolar , Femenino , Humanos , Terapia de Inmunosupresión , Inmunosupresores/uso terapéutico , Masculino , Estudios Retrospectivos , Resultado del TratamientoAsunto(s)
Hígado Graso/cirugía , Trasplante de Hígado/normas , Cirugía Bariátrica , Medicina Basada en la Evidencia/métodos , Humanos , Inmunosupresores/uso terapéutico , Trasplante de Hígado/efectos adversos , Trasplante de Hígado/métodos , Monitoreo Fisiológico/métodos , Enfermedad del Hígado Graso no Alcohólico , Selección de Paciente , Atención Perioperativa/métodosAsunto(s)
Síndrome de Crigler-Najjar/terapia , Trasplante de Hígado/métodos , Trasplante de Hígado/estadística & datos numéricos , Enfermedades Metabólicas/terapia , Niño , Toma de Decisiones , Ética Médica , Familia , Humanos , Trasplante de Hígado/tendencias , Derivación y Consulta , Factores de Tiempo , Obtención de Tejidos y ÓrganosRESUMEN
BACKGROUND: Tyrosinaemia type 1 (HT1) is treated with a tyrosine and phenylalanine-restricted diet, amino acids free of phenylalanine and tyrosine, and nitisinone (NTBC). Treatment guidelines recommend plasma tyrosine between 200-400 µm and phenylalanine at least >30 µm. There is little information on the diurnal variation of plasma tyrosine or phenylalanine in HT1. Low plasma phenylalanine <30 µm may be associated with poor growth and cognitive delay. The present study aimed to document diurnal variation of tyrosine and phenylalanine plasma concentrations and growth in children with HT1. METHODS: Median tyrosine and phenylalanine plasma concentrations were reviewed retrospectively over 3 years in 11 subjects (median age 4 years) with HT1. Subjects routinely collected morning fasting blood samples but afternoon nonfasted samples were taken in the clinic (<10% of samples). Growth Z-scores were calculated. RESULTS: The percentage of all plasma phenylalanine concentrations <30 µm was 8.6% and <40 µm was 13.6%. Only 2% of fasting morning phenylalanine concentrations were <30 µm, compared to 83% of nonfasting afternoon samples. All but one child had a height Z-score <0. CONCLUSIONS: Blood phenylalanine concentrations were consistently lower in the afternoon. Taking blood samples at variable time points in the day may lead to variation in interpreting dietary control. A detailed study is necessary to examine the 24-h diurnal variation of plasma phenylalanine and tyrosine in HT1. It is possible that phenylalanine concentrations may be very low for a substantive time over 24 h and the potential impact that this may have on cognitive development and growth in children is unknown.
Asunto(s)
Fenilalanina/sangre , Tirosina/sangre , Tirosinemias/sangre , Niño , Preescolar , Ritmo Circadiano , Proteínas en la Dieta/administración & dosificación , Proteínas en la Dieta/sangre , Femenino , Humanos , Masculino , Fenilalanina/administración & dosificación , Guías de Práctica Clínica como Asunto , Estudios Retrospectivos , Tirosina/administración & dosificación , Tirosinemias/dietoterapiaAsunto(s)
Trasplante de Hígado , Azatioprina/farmacología , Inhibidores de la Calcineurina , Niño , Continuidad de la Atención al Paciente , Glucocorticoides/farmacología , Rechazo de Injerto/inmunología , Rechazo de Injerto/prevención & control , Arteria Hepática , Humanos , Inmunosupresores/administración & dosificación , Cuidados a Largo Plazo , Monitoreo Fisiológico , Ácido Micofenólico/análogos & derivados , Ácido Micofenólico/farmacología , Vena Porta , Complicaciones Posoperatorias/epidemiología , Disfunción Primaria del Injerto/prevención & control , Recurrencia , Sobrevivientes , Trombosis de la Vena/prevención & control , Virosis/epidemiología , Virosis/inmunologíaRESUMEN
A male infant was diagnosed with atypical hemolytic uremic syndrome (aHUS) at the age of 5.5 months. Sequencing of the gene (CFH) encoding complement factor H revealed a heterozygous mutation (c.3644G>A, p.Arg1215Gln). Despite maintenance plasmapheresis he developed recurrent episodes of aHUS and vascular access complications while maintaining stable renal function. At the age of 5 years he received an isolated split liver graft following a previously established protocol using pretransplant plasma exchange (PE) and intratransplant plasma infusion. Graft function, renal function and disease remission are preserved 2 years after transplantation. Preemptive liver transplantation prior to the development of end stage renal disease is a valuable option in the management of aHUS associated with CFH mutations.
Asunto(s)
Factor H de Complemento/genética , Síndrome Hemolítico-Urémico/genética , Síndrome Hemolítico-Urémico/cirugía , Trasplante de Hígado , Mutación , Infecciones por Caliciviridae/etiología , Gastroenteritis/virología , Síndrome Hemolítico-Urémico/fisiopatología , Herpesvirus Humano 4 , Heterocigoto , Humanos , Recién Nacido , Riñón/fisiopatología , Trasplante de Hígado/efectos adversos , Masculino , Norovirus , Complicaciones Posoperatorias , Medición de Riesgo , Prevención Secundaria , Viremia/etiologíaRESUMEN
Citrin deficiency is a disorder with two phenotypes: neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD), and adult-onset type II citrullinaemia (CTLN2). NICCD presents in the first few weeks of life with prolonged cholestasis and metabolic abnormalities including aminoacidaemia (notably citrulline, tyrosine, threonine, arginine and methionine) and galactosuria. Symptoms resolve within the first year of life, thus making a diagnosis difficult after this time. Although patients subsequently remain generally healthy, some may develop more severe symptoms of CTLN2, characterized by neurological changes, one or more decades later. To date more than 400 cases have been reported, almost all from East Asia (mainly Japan). Here we describe the first two cases of NICCD in infants from the UK, one of caucasian origin and one of Pakistani origin. Both showed typical clinical and biochemical changes with a diagnosis confirmed by the presence of previously unreported mutations in the SLC25A13 gene. The presence of citrin deficiency in other ethnic groups means that NICCD needs to be considered in the diagnosis of any neonate with an unexplained cholestasis. We discuss both the difficulties in diagnosing these patients in populations where very few DNA mutations have been identified and the problems faced in the management of these patients. These findings also raise the possibility of adults with CTLN2 in whom a diagnosis has yet to be made.
Asunto(s)
Colestasis Intrahepática/genética , Citrulinemia/genética , Preescolar , Colestasis Intrahepática/epidemiología , Colestasis Intrahepática/etiología , Citrulinemia/complicaciones , Citrulinemia/epidemiología , Consanguinidad , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Proteínas de Transporte de Membrana Mitocondrial/genética , Mutación , Pakistán/epidemiología , Pakistán/etnología , Reino Unido/epidemiología , Población Blanca/genéticaRESUMEN
BACKGROUND: Little information is available on contemporary, prospectively collected data on the long-term outcome of national cohorts of children with biliary atresia. OBJECTIVE: This study aimed to describe the current outcome of a national cohort of children with biliary atresia. PATIENTS AND METHODS: All 93 cases of biliary atresia in the United Kingdom and Ireland diagnosed between March 1993 and February 1995 were followed up prospectively. RESULTS: A total of 91 children underwent Kasai portoenterostomy in 15 individual centres. Only 2 centres treated more than 5 children annually. Median age at last follow-up was 12 years (range 0.25-14). Fifteen children (16%) have died: 10 after unsuccessful portoenterostomy, 1 of sepsis after successful portoenterostomy, and 4 after liver transplantation. Forty-two (45%) underwent liver transplantation at a median age of 1 year (range 0.5-9), with 90% survival. All 41 children with failed portoenterostomy (and 2 without portoenterostomy) died or underwent liver transplantation at a median age of 0.8 years (range 0.25-6.5). When the portoenterostomy was successful, 40 of 50 patients (80%) are alive without liver transplantation. The 13-year actuarial survival without liver transplantation is 43.8% overall and is better in children treated at centres that treat more than 5 cases yearly (54% vs 27.3%, P = 0.005). CONCLUSIONS: If the portoenterostomy is successful, then few children with biliary atresia will need transplantation before adolescence. Children with biliary atresia should be treated in experienced centres to maximize the chance of successful surgery.
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Atresia Biliar/cirugía , Atresia Biliar/mortalidad , Niño , Preescolar , Estudios de Cohortes , Estudios de Seguimiento , Humanos , Lactante , Irlanda , Trasplante de Hígado , Portoenterostomía Hepática , Encuestas y Cuestionarios , Tasa de Supervivencia , Resultado del Tratamiento , Reino UnidoRESUMEN
We report the case of a 2-year-old boy with seizures who developed hepatic failure shortly after commencing sodium valproate. Unexpectedly, liver function returned to normal on stopping the drug. Sequencing of the mitochondrial polymerase γ gene (POLG1) revealed four heterozygous substitutions, two of which have been identified in cases of Alpers-Huttenlocher disease.
Asunto(s)
Enfermedad Hepática Inducida por Sustancias y Drogas , Hepatitis/complicaciones , Enfermedades Intestinales/terapia , Nutrición Parenteral/efectos adversos , Preescolar , Progresión de la Enfermedad , Humanos , Lactante , Hepatopatías/etiología , Hepatopatías/patología , Masculino , Factores de Riesgo , Factores de TiempoRESUMEN
BACKGROUND: Tyrosinaemia type I (TTI) is an inherited deficiency in the enzyme fumarylacetoacetate hydrolase and is frequently complicated by renal tubular dysfunction which may persist in some patients after hepatic transplantation. Nitisinone has revolutionized the management of TTI but its effect on renal tubular dysfunction has not been described in a large cohort of patients. AIMS: To document the incidence and progression of renal tubular dysfunction in children with TTI treated with nitisinone at a single centre. SUBJECTS: Twenty-one patients with TTI from a single centre were treated with nitisinone for at least 12 months. Median age at first treatment was 17 weeks (range 1 week to 27 months). Nine patients (43%) presented in acute liver failure, seven (33%) had a chronic presentation and five (24%) were detected pre-clinically. METHODS: A retrospective case analysis of plasma phosphate, urinary protein/creatinine ratio and tubular reabsorption of phosphate was performed for all patients as markers of tubular function. Renal ultrasounds were examined for evidence of nephrocalcinosis and where available, skeletal radiographs for rickets. RESULTS: All patients had biochemical evidence of renal tubular dysfunction at presentation. After nitisinone and dietary treatment were started, all three markers normalized within one year. Four children had clinical rickets at presentation (which improved), of whom one had nephrocalcinosis, which did not reverse on nitisinone. No child redeveloped tubular dysfunction after commencing nitisinone. All patients with TTI had evidence of tubular dysfunction at presentation and in all cases this resolved with nitisinone and dietary control. CONCLUSION: The tubulopathy associated with TTI is reversible.
Asunto(s)
Ciclohexanonas/uso terapéutico , Túbulos Renales/fisiopatología , Nitrobenzoatos/uso terapéutico , Tirosinemias/fisiopatología , Niño , Preescolar , Femenino , Humanos , Lactante , Recién Nacido , Riñón/diagnóstico por imagen , Masculino , Proteinuria/fisiopatología , Estudios Retrospectivos , Tirosinemias/tratamiento farmacológico , UltrasonografíaRESUMEN
We report the case of a 2-year-old boy with seizures who developed hepatic failure shortly after commencing sodium valproate. Unexpectedly, liver function returned to normal on stopping the drug. Sequencing of the mitochondrial polymerase gamma gene (POLG1) revealed four heterozygous substitutions, two of which have been identified in cases of Alpers-Huttenlocher disease.