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1.
Arch Pediatr ; 30(5): 307-313, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-37236887

RESUMO

BACKGROUND: Collagen gastritis is a rare disease that manifests in children mainly as isolated gastric involvement associated with martial deficiency anemia. There are no recommendations for the management and follow-up of these patients. We aimed to describe the clinical data, endoscopic findings, and treatments deployed in France's children with collagenous gastritis. METHODS: All French pediatric gastroenterology centers and pediatric centers for rare digestive diseases (Centres de Maladies Rares Digestives) were contacted to collect cases of collagenous gastritis, defined on gastric biopsies and diagnosed before 18 years of age. RESULTS: A total of 12 cases diagnosed (4 males and 8 females) between 1995 and 2022 could be analyzed. The median age at diagnosis was 12.5 years (7-15.2). The most frequent clinical presentation was abdominal pain (6/11) and/or nonspecific symptomatology attributed to anemia (8/10). Anemia was present in all children (11/11; Hb 2.8-9.1 g/dL). Nodular gastritis was present in 10 patients (antrum: 2; fundus: 4; in antrum and fundus: 4). All patients had a basement membrane thickening (from 19 to 100 µm). The treatments received were PPI (11), oral or intravenous martial supplementation (12), budesonide (1), and prednisone (1). Martial supplementation improved anemia in all cases. At discontinuation, nine of 10 patients had a recurrence of anemia. CONCLUSION: Collagenous gastritis is an exceptional condition, clinically manifested in children as abdominal pain and iron deficiency anemia probably of hemorrhagic origin. Patients require long-term follow-up and monitoring of their disease to describe the risk of progression better.


Assuntos
Anemia , Gastrite , Síndromes de Malabsorção , Masculino , Feminino , Humanos , Criança , Gastrite/complicações , Gastrite/diagnóstico , Gastrite/terapia , Biópsia , Síndromes de Malabsorção/complicações , Anemia/complicações , Dor Abdominal/etiologia
2.
Rev Mal Respir ; 37(5): 355-363, 2020 May.
Artigo em Francês | MEDLINE | ID: mdl-32334966

RESUMO

INTRODUCTION: Chest computed tomography (CT) is essential to monitor lung disease in children with cystic fibrosis, but it involves recurrent exposure to ionizing radiation. The aim of this study was to compare the current complete CT protocol (volumetric end-inspiratory plus sequential expiratory acquisition) to a sequential expiratory acquisition protocol alone in terms of image analysis and ionizing radiation dose. METHODS: Seventy-eight CT scans from 57 children aged 5 to 18 years old were scored on the complete protocol images and on the expiratory sequential images only. Each CT protocol was scored independently, using the Brody scoring system, by two paediatric radiologists. RESULTS: Correlations between the Brody global scores of the two different CT protocols were very good (r=0.90 for both observers), for the bronchiectasis score (r=0.72 and 0.86), mucus plugging score (r=0.87 and 0.83), and expiratory trapped air (r=0.96 and 0.92). Total ionizing radiation dose was reduced, with the measured dose length product (DLP) reduced from 103.31mGy.cm (complete protocol) to 3.06mGy.cm (expiratory protocol) (P<0.001). CONCLUSION: An expiratory chest CT protocol was accurate in diagnosing early signs of CF disease and permitted significant reduction of radiation dose. This protocol would allow spacing out of complete CT scanning with its higher radiation dose and should be considered for the monitoring of lung disease severity in children with CF.


Assuntos
Fibrose Cística/diagnóstico , Expiração/fisiologia , Monitorização Fisiológica/métodos , Exposição Ocupacional/prevenção & controle , Doses de Radiação , Tomografia Computadorizada por Raios X , Adolescente , Criança , Pré-Escolar , Estudos de Coortes , Estudos Transversais , Fibrose Cística/fisiopatologia , Feminino , Humanos , Masculino , Exposição Ocupacional/efeitos adversos , Prognóstico , Radiografia Torácica/efeitos adversos , Radiografia Torácica/métodos , Respiração , Testes de Função Respiratória , Estudos Retrospectivos , Tomografia Computadorizada por Raios X/efeitos adversos , Tomografia Computadorizada por Raios X/métodos
3.
J Crohns Colitis ; 14(8): 1119-1148, 2020 Sep 07.
Artigo em Inglês | MEDLINE | ID: mdl-32115645

RESUMO

BACKGROUND AND AIMS: Inflammatory bowel disease [IBD] is often one of the most devastating and debilitating chronic gastrointestinal disorders in children and adolescents. The main objectives here were to systematically review the incidence and prevalence of paediatric IBD across all 51 European states. METHODS: We undertook a systematic review and meta-analysis based on PubMed, CINAHL, the Cochrane Library, searches of reference lists, grey literature and websites, covering the period from 1970 to 2018. RESULTS: Incidence rates for both paediatric Crohn's disease [CD] and ulcerative colitis [UC] were higher in northern Europe than in other European regions. There have been large increases in the incidence of both paediatric CD and UC over the last 50 years, which appear widespread across Europe. The largest increases for CD have been reported from Sweden, Wales, England, the Czech Republic, Denmark and Hungary, and for UC from the Czech Republic, Ireland, Sweden and Hungary. Incidence rates for paediatric CD have increased up to 9 or 10 per 100 000 population in parts of Europe, including Scandinavia, while rates for paediatric UC are often slightly lower than for CD. Prevalence reported for CD ranged from 8.2 per 100 000 to approximately 60 and, for UC, from 8.3 to approximately 30. CONCLUSIONS: The incidence of paediatric IBD continues to increase throughout Europe. There is stronger evidence of a north-south than an east-west gradient in incidence across Europe. Further prospective studies are needed, preferably multinational and based on IBD registries, using standardized definitions, methodology and timescales.


Assuntos
Colite Ulcerativa/epidemiologia , Doença de Crohn/epidemiologia , Criança , Europa (Continente)/epidemiologia , Humanos , Incidência , Avaliação das Necessidades , Prevalência
4.
Artigo em Inglês | MEDLINE | ID: mdl-27910234

RESUMO

BACKGROUND: The pathophysiology of infantile colic is poorly understood, though various studies report gut microbiota dysbiosis in colicky infants. We aimed to test the hypothesis that colic-related dysbiosis is associated with visceral hypersensitivity triggered by an altered luminal milieu. METHODS: Fecal samples from seven colicky and seven non-colicky infants were studied. Fecal supernatants (FS) were infused into the colons of C57/Bl6 mice (n=10/specimen). Visceral sensitivity was subsequently assessed in the animals by recording their abdominal muscle response to colorectal distension (CRD) by electromyography (EMG). Serine and cysteine protease activities were assessed in FS with specific substrates. Infant fecal microbiota composition was analyzed by DNA extraction and 16S rRNA gene pyrosequencing. KEY RESULTS: FS from colicky infants triggered higher EMG activity than FS from non-colicky infants in response to both the largest CRD volumes and overall, as assessed by the area under the curve of the EMG across all CRD volumes. Infant crying time strongly correlated with mouse EMG activity. Microbiota richness and phylogenetic diversity were increased in the colicky group, without showing prominent microbial composition alterations. Only Bacteroides vulgatus and Bilophila wadsworthia were increased in the colicky group. Bacteroides vulgatus abundance positively correlated with visceral sensitivity. No differences were found in protease activities. CONCLUSIONS & INFERENCES: Luminal contents from colicky infants trigger visceral hypersensitivity, which may explain the excessive crying behavior of these infants. Additional studies are required to determine the nature of the compounds involved, their mechanism of action, and the potential implications of intestinal microbiota in their generation.


Assuntos
Cólica/fisiopatologia , Fezes , Trato Gastrointestinal/fisiopatologia , Dor Visceral/induzido quimicamente , Dor Visceral/fisiopatologia , Animais , Cólica/complicações , Colo/microbiologia , Colo/fisiopatologia , Eletromiografia/métodos , Fezes/microbiologia , Trato Gastrointestinal/microbiologia , Humanos , Lactente , Recém-Nascido , Masculino , Camundongos , Camundongos Endogâmicos C57BL
5.
Arch Pediatr ; 23(12S): 12S15-12S20, 2016 Dec.
Artigo em Francês | MEDLINE | ID: mdl-28231889

RESUMO

In cystic fibrosis (CF), approximately 5-8% of the patients develop multilobular cirrhosis during the first decade of life. Annual screening (clinical examination, liver biochemistry, ultrasonography) is recommended in order to identify early signs of liver involvement, initiate ursodeoxycholic acid therapy and detect complications (portal hypertension and liver failure). Management should focus on nutrition and prevention of variceal bleeding. The gut may also be involved in children with CF. Gastroesophageal reflux is frequent, although often neglected and should be investigated by pH monitoring and impedancemetry, if available. Acute pancreatitis occurs in patients with persistent exocrine pancreatic activity. Intussusception, appendicular mucocele, distal intestinal occlusion syndrome, small bowel bacterial overgrowth and Clostridium difficile colitis should be considered in case of abdominal pain. Preventive nutritional support should be started as soon as possible after diagnosis of CF. Attainment of normal growth is one of the main goals and can be achieved with hypercaloric and salt supplemented food. Pancreatic enzyme replacement therapy should be started as soon as exocrine pancreatic insufficiency is confirmed and ingested immediately prior to meals with intake of fat-soluble vitamins. Curative nutritional interventions are more likely to be effective in the early stages of pulmonary disease. Feeding disorders, related to the physiopathology and the psychologic aspects of the disease are frequent. Repeated corporeal aggressions, associated with inappropriate medical and parental pressure, may increase the child's refusal of food. The multidisciplinary team should guide parents in order to avoid all intrusive feeding practices and promote pleasant mealtimes.


Assuntos
Fibrose Cística/complicações , Fibrose Cística/terapia , Doenças do Sistema Digestório/etiologia , Doenças do Sistema Digestório/terapia , Transtornos de Alimentação na Infância/etiologia , Transtornos de Alimentação na Infância/terapia , Cirrose Hepática/etiologia , Cirrose Hepática/terapia , Criança , Pré-Escolar , Terapia Combinada , Fibrose Cística/diagnóstico , Doenças do Sistema Digestório/diagnóstico , Diagnóstico Precoce , Intervenção Médica Precoce , Transtornos de Alimentação na Infância/diagnóstico , Humanos , Lactente , Comunicação Interdisciplinar , Colaboração Intersetorial , Cirrose Hepática/diagnóstico , Relações Pais-Filho
6.
Arch Pediatr ; 23(12S): 12S47-12S53, 2016 Dec.
Artigo em Francês | MEDLINE | ID: mdl-28231894

RESUMO

Since the discovery of chloride secretion by the Cystic Fibrosis Transport regulator CFTR in 1983, and CFTR gene in 1989, knowledge about CFTR synthesis, maturation, intracellular transfer and function has dramatically expanded. These discoveries have led to the distribution of CF mutations into 6 classes with different pathophysiological mechanisms. In this article we will explore the state of art on CFTR synthesis and its chloride secretion function. We will then explore the consequences of the 6 classes of mutations on CFTR protein function and we will describe the new therapeutic developments aiming at correcting these defects.


Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Fibrose Cística/genética , Fibrose Cística/terapia , Análise Mutacional de DNA , Cloretos/metabolismo , Fibrose Cística/fisiopatologia , Regulador de Condutância Transmembrana em Fibrose Cística/fisiologia , Humanos
7.
Arch Pediatr ; 22(12): 1240-6, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26596857

RESUMO

BACKGROUND: Pseudomonas aeruginosa and Staphylococcus aureus toothbrush contamination in cystic fibrosis (CF) is unknown. This pilot study aimed to determine their prevalence and the potential involvement of toothbrushes in pulmonary infection. METHODS: Toothbrush bacteriological analysis for children aged 8-18 years was conducted on 27 CF patients, 15 healthy siblings, and 15 healthy children from the general population. RESULTS: S. aureus was detected on 22% of the patients' toothbrushes, and 13% of healthy children's toothbrushes and P. aeruginosa on 15% of patients' toothbrushes and 0-13% of healthy children's toothbrushes. There was no statistical correlation between pulmonary colonization and toothbrush contamination. P. aeruginosa genotyping showed two identical clones on the patients' toothbrushes and in their sputum, and between one patient's sputum and his sibling's toothbrush. CONCLUSION: S. aureus and P. aeruginosa can colonize CF patients' toothbrushes. The impact on pulmonary colonization remains unknown. Toothbrush decontamination methods need to consider these bacteria in CF patients.


Assuntos
Fibrose Cística , Dispositivos para o Cuidado Bucal Domiciliar/microbiologia , Contaminação de Equipamentos , Pseudomonas aeruginosa/isolamento & purificação , Staphylococcus aureus/isolamento & purificação , Adolescente , Criança , Feminino , Humanos , Pulmão/microbiologia , Masculino , Projetos Piloto , Escarro/microbiologia
8.
Rev Mal Respir ; 32(6): 566-85, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26001957

RESUMO

INTRODUCTION: The gastrointestinal tract is a major source of morbidity in adults with cystic fibrosis (CF), with a wide range of complications, some of them being specific to the underlying disease. STATE OF KNOWLEDGE: Abnormal CFTR function, with reduced bicarbonate and other ion transport levels through the apical surface of epithelial cells, affects the intestinal tract including the pancreas and the liver. Similarly to what is observed in the respiratory tract, gastrointestinal CFTR dysfunction leads to mucus accumulation, dysmotility, small bowel bacterial overgrowth and inflammation with alteration of innate immune responses, all of which being likely to be interrelated. In developed countries, almost half of patients with CF are adults followed in multidisciplinary CF care centres by pneumologists who often have to manage gastrointestinal complications. CONCLUSION: It therefore appears essential that adult gastroenterologists develop the expertise needed for managing CF gastrointestinal complications in close collaboration with multidisciplinary CF care centre teams to improve the quality of life of adults with CF.


Assuntos
Fibrose Cística/complicações , Fibrose Cística/terapia , Gastroenteropatias/terapia , Hepatopatias/terapia , Pancreatopatias/terapia , Adulto , Doenças Biliares/epidemiologia , Doenças Biliares/etiologia , Doenças Biliares/terapia , Fibrose Cística/epidemiologia , Gastroenteropatias/epidemiologia , Gastroenteropatias/etiologia , Humanos , Hepatopatias/epidemiologia , Hepatopatias/etiologia , Neoplasias/epidemiologia , Neoplasias/etiologia , Neoplasias/terapia , Pancreatopatias/epidemiologia , Pancreatopatias/etiologia
9.
Placenta ; 36(1): 34-40, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25468541

RESUMO

INTRODUCTION: Dietary supplementation with omega-3 long chain polyunsaturated fatty acids (n-3 PUFAs) may exert benefits in pregnancy through inhibition of placental inflammation. However, studies on the anti-inflammatory effects of n-3 PUFAs in the placenta are lacking. We compared the cytokine responses of human placental explants in vitro after 4 days pre-incubation with either: a) individual n-3 or n-6 PUFAs (20 µM), or b) physiologically relevant combinations of low, medium or high n-3 or n-6 PUFA concentrations. METHODS: Placental cytokine (IL-6 and TNF-α) mRNA expression and protein production were assessed at 4 h and 12 h, respectively. Cytokine and fatty acid concentrations were also measured in placentas delivered at term by women who ingested either low (n = 12) or high (n = 10) amounts of fish/fish oil in the month prior to delivery. RESULTS: Pre-exposure to n-3 PUFAs as individual fatty acids results in reduced placental IL-6 production (P < 0.05), whereas exposure to complex fatty acid mixtures enriched in n-3 PUFAs (high n-3:n-6 ratios) results in a significant stimulation of IL-6 production (P < 0.05). There were no differences in placental n-3 or n-6 PUFA levels between women with either high or low dietary fish oil intake and no differences in cytokine expression. DISCUSSION: In summary, data from our complex lipid explant model and an observational cohort study do not support a role for n3 PUFAs in the suppression of pro-inflammatory cytokine expression in the human placenta. Results from studies of placental tissues exposed to single n-3 and n-6 PUFAs should be interpreted with considerable caution.


Assuntos
Ácidos Graxos Ômega-3/farmacologia , Ácidos Graxos Ômega-6/farmacologia , Interleucina-6/metabolismo , Placenta/efeitos dos fármacos , Fator de Necrose Tumoral alfa/metabolismo , Adulto , Suplementos Nutricionais , Feminino , Humanos , Estresse Oxidativo/efeitos dos fármacos , Placenta/metabolismo , Gravidez , Adulto Jovem
10.
Arch Pediatr ; 22(1): 32-8, 2015 Jan.
Artigo em Francês | MEDLINE | ID: mdl-25500066

RESUMO

Digestive complications related to the ingestion of magnetic foreign bodies in children are increasing, especially in Asia and North America. In France, several case reports have been reported since 2008. We conducted a retrospective multicentric study to evaluate the frequency of ingestion of magnet foreign bodies and to describe the complicated cases that have occurred in France over the last 5 years. We report 40 cases of which 60% were multiple magnet ingestions. Eighty-eight percent of the children of the group who had swallowed multiple magnets needed interventional management by endoscopy (33%) or surgery (58%). Only two children (12.5%) of the group who swallowed one magnet required removal. This problem is not uncommon in France (2% of the 1132 foreign bodies investigated in the Toulouse center over 5 years), which justifies clear information for healthcare professionals and caregivers in order to avoid potential intestinal complications. We suggest interventional management or very close monitoring in the cases of multiple magnet ingestion. Meanwhile, in the majority of confirmed cases of simple magnet ingestions, we propose home monitoring.


Assuntos
Corpos Estranhos/epidemiologia , Corpos Estranhos/cirurgia , Imãs , Distribuição por Idade , Criança , Pré-Escolar , Endoscopia/estatística & dados numéricos , Feminino , França/epidemiologia , Humanos , Lactente , Laparoscopia/estatística & dados numéricos , Masculino , Estudos Retrospectivos , Distribuição por Sexo
11.
Arch Pediatr ; 19(12): 1362-8, 2012 Dec.
Artigo em Francês | MEDLINE | ID: mdl-23141564

RESUMO

In children, caustic ingestion is due to accidents at home and inadequate storage of caustic agents. In emergency, it is useful to remove the soiled clothes, rinse the affected area, and prevent vomiting and feeding. Caustic ingestion (pH<2 or>12) induces burns of the upper gastrointestinal tract requiring esophagogastro-duodenoscopy between H12 and H24. Strong alkalis cause necrosis with liquefaction of the esophagus, penetrating deeply with a high-risk of perforation. Management of these children requires a specialized care center with an intensive care unit, endoscopic equipment, and a surgical team. Esophageal stricture is the main complication; no prophylactic treatment (steroids) is effective. Strictures occur after the 3rd week, and barium swallow should be performed by the end of the 1st month. Stricture are often multiple, long, and tortuous; endoscopic dilatation is difficult with a high-rate of perforation and a low-rate of success. In situ application of mitomycin C or injection of triamcinolone could reduce the recurrence rate of stricture. In recalcitrant or recurrent strictures, it is recommended to perform an esophageal replacement using a colonic interposition or a gastric tube. Endoscopy should also be performed 15-20years after caustic ingestion to screen for early neoplastic lesions. Prevention is very important for avoiding caustic ingestions. Information and education should be given specifically to the parents of toddlers; caustic products should be stored out of reach of children and they should not be kept with food.


Assuntos
Queimaduras Químicas/complicações , Esofagite/terapia , Esôfago/lesões , Esôfago/cirurgia , Anastomose Cirúrgica , Antibioticoprofilaxia , Cáusticos/toxicidade , Criança , Colo/transplante , Estenose Esofágica/induzido quimicamente , Estenose Esofágica/prevenção & controle , Esofagectomia , Esofagite/induzido quimicamente , Esofagoplastia , Esofagoscopia , Glucocorticoides/uso terapêutico , Humanos , Apoio Nutricional , Inibidores da Bomba de Prótons/uso terapêutico
12.
J Nutr Health Aging ; 16(2): 155-61, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22323351

RESUMO

OBJECTIVE: To investigate the effect of aerobic training in the context of antioxidant supplementation on systemic oxidative stress and leukocytes heat shock protein (Hsp)72 expression in the elderly. DESIGN: Sixteen septuagenarians (8 males and 8 females, mean age 74.6) were supplemented with Vitamin C and E (respectively 500 and 100mg per day) and randomly assigned either to sedentary (AS) or individualized aerobically trained (AT) group for 8 weeks. METHODS: Plasma Vitamin C and E concentrations and aerobic fitness, as well as resting and post graded exercise (GXT) Hsp72 expression in leukocytes, plasma levels of thiobarbituric acid reactive substances (TBARS) and advanced oxidation protein product (AOPP) were measured pre and post training / supplementation. RESULTS: At the end of the intervention, the two groups showed a significant increase in resting plasma vitamin C and E (approximately 50 and 20% increase respectively) and a significant decrease in both resting and post GXT plasma TBARS and AOPP (approximately 25 and 20% decrease respectively). These changes were of similar magnitude in the two groups. The reduced oxidative stress was concomitant with a 15% decreased expression of Hsp72 in monocytes and granulocytes in both groups. CONCLUSION: This study provides evidence that in elderly, increased concentration of antioxidant vitamins C and E is associated with a reduction in oxidative stress and leukocytes Hsp72. In this context, 8 weeks of aerobic training has no impact on oxidative stress or leukocytes Hsp72 expression in elderly people.


Assuntos
Antioxidantes/administração & dosagem , Exercício Físico/fisiologia , Proteínas de Choque Térmico HSP72/metabolismo , Leucócitos/metabolismo , Estresse Oxidativo , Idoso , Envelhecimento/metabolismo , Ácido Ascórbico/sangue , Relação Dose-Resposta a Droga , Feminino , Humanos , Masculino , Oxirredução , Estresse Oxidativo/efeitos dos fármacos , Estresse Oxidativo/fisiologia , Substâncias Reativas com Ácido Tiobarbitúrico/metabolismo , Vitamina E/sangue
13.
Ann Dermatol Venereol ; 137(10): 640-4, 2010 Oct.
Artigo em Francês | MEDLINE | ID: mdl-20932445

RESUMO

BACKGROUND: Porphyria cutanea tarda (PCT) is rare in childhood and association with bone marrow transplant has occasionally been reported. PATIENTS AND METHODS: A 13-year-old boy was referred to our department for bullous lesions on sun-exposed areas. His past medical history revealed acute biphenotypic leukaemia with complete remission after allogeneic hematopoietic stem cell transplantation (unrelated donor). Complications of bone marrow transplant comprised anaemia (treated by blood transfusions), primary cytomegalovirus (CMV) infection, pulmonary aspergillosis and acute digestive graft-versus-host disease. The diagnosis of type I sporadic PCT was based on high levels of porphyria and normal erythrocytic uroporphyrinogen decarboxylase activity. The bullous lesions disappeared on bleeding, but the patient subsequently developed sclerodermiform lesions. DISCUSSION: An association between PCT and bone marrow transplant has been reported previously in two independent cases, of which one involved a child. The causative role of bone marrow transplantation in the development of PCT could be related to several triggering factors: primary CMV infection, hepatotoxic drugs, blood transfusion and possible chronic hepatic graft-versus-host disease. CONCLUSION: We report the second case in a child of type I PCT associated with bone marrow transplantation. This new case reinforces the hypothesis of a non-random relationship between the two conditions.


Assuntos
Transplante de Medula Óssea/efeitos adversos , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Leucemia Aguda Bifenotípica/terapia , Porfiria Cutânea Tardia/diagnóstico , Porfiria Cutânea Tardia/terapia , Adolescente , Humanos , Masculino , Indução de Remissão
16.
Cancer Biol Ther ; 7(4): 523-31, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18296916

RESUMO

PURPOSE: Multiple biochemical and molecular alterations occur in pancreatic cancer cells. In the present study, attempts were made for the first time, to explore the level of expression of members of histone deacetylase encoding genes (HDACs) in four pancreatic tumor cell lines: Panc-1, BxPC-3, SOJ-6 and MiaPaCa-2; and two non-related tumor cells: Jurkat and HeLa. Furthermore, we examined the possible relationship between the levels of HDACs expression and the sensitivity/resistance to HDAC inhibitors (TSA, Nicotinamide and Sirtinol). RESULTS: We have found that although a slight variation in the profiles of gene expression among cell lines could be evidenced, HDACs protein synthesis seem to be similar. Furthermore, the cells were equally sensitive to inhibition by Sirtinol whereas some variation in the IC(50) could be seen in the case of TSA. We also demonstrate that the drugs had the capacity to induce the death of cells by apoptosis. METHODS: We have used four human pancreatic tumor cell lines and two-non related tumor cells, to evaluate the expression of HDAC encoding genes by RT-PCR and Western blot analysis. We also measured the effect of certain HDAC inhibitors (HDIs) on cell growth, cell cycle alteration, membrane phosphatidyl-serine exposure, DNA fragmentation and mitochondrial membrane potential loss. CONCLUSIONS: Taken together, our data support the notion that the level of cell sensitivity to the HDIs might be related to the level of expression of genes such as those encoding proteins playing a role in cell cycle checkpoints control but not HDAC per se.


Assuntos
Adenocarcinoma/enzimologia , Resistencia a Medicamentos Antineoplásicos/genética , Inibidores Enzimáticos/farmacologia , Inibidores de Histona Desacetilases , Histona Desacetilases/genética , Neoplasias Pancreáticas/enzimologia , Adenocarcinoma/genética , Benzamidas/farmacologia , Linhagem Celular , Linhagem Celular Tumoral , Expressão Gênica , Humanos , Naftóis/farmacologia , Neoplasias Pancreáticas/genética
17.
Arch Pediatr ; 14 Suppl 3: S152-5, 2007 Oct.
Artigo em Francês | MEDLINE | ID: mdl-17961807

RESUMO

The molecular characterization of gastroenteritis viruses has led to advances both in our understanding of the pathogens themselves and in development of a new generation of diagnostics. In developing countries, gastroenteritis is a common cause of death in children under 5 years that can be linked to a wide variety of pathogens. In developed countries, while deaths from diarrhoea are less common, much illness leads to hospitalization or doctor visits. Much of the gastroenteritis in children is caused by viruses belonging to four distinct families: rotaviruses, caliciviruses, astroviruses and adenoviruses. Viral gastroenteritis occurs with two epidemiologic patterns, diarrhoea that is endemic in children and outbreaks that affect people of all ages. Rotavirus infection causes severe gastroenteritis, particularly in infants under six months of age.


Assuntos
Diarreia/virologia , Doença Aguda , Criança , Pré-Escolar , Diarreia Infantil/virologia , Disenteria/virologia , Gastroenterite/virologia , Humanos , Lactente , Infecções por Rotavirus/diagnóstico
18.
Rev Neurol ; 44(2): 92-4, 2007.
Artigo em Espanhol | MEDLINE | ID: mdl-17236148

RESUMO

AIM: To report a case of cerebral gas embolism secondary to the withdrawal of a central venous line in a patient who had recently undergone abdominal surgery. CASE REPORT: An 82-year-old male who suddenly presented myoclonias in the right upper extremity and a sharp drop in the level of consciousness. A computerised tomography (CT) scan revealed air bubbles in the intracranial circulatory system and associated infarction in the right hemisphere. The patient's clinical progression was poor and he died some days later. CONCLUSIONS: Cerebral gas embolism can be diagnosed using a CT scan of the head if it is performed immediately after the entrance of air into the bloodstream inside the brain. In later phases, findings are unspecific and difficult to distinguish from ischaemic infarction or from diffuse leukoencephalopathy. Treatment is based on supportive measures and, in some cases, hyperbaric oxygen, although their true effectiveness is a controversial issue. Cerebral gas embolism is a potentially fatal and avoidable complication in patients with a central venous line or other iatrogenic procedures that can allow air to enter the arterial or venous circulatory systems.


Assuntos
Cateterismo Venoso Central , Remoção de Dispositivo/efeitos adversos , Embolia Aérea/etiologia , Embolia Intracraniana/etiologia , Complicações Pós-Operatórias/etiologia , Idoso de 80 Anos ou mais , Embolia Aérea/diagnóstico por imagem , Embolia Aérea/prevenção & controle , Evolução Fatal , Cálculos Biliares/complicações , Humanos , Íleus/etiologia , Íleus/cirurgia , Embolia Intracraniana/diagnóstico por imagem , Masculino , Complicações Pós-Operatórias/diagnóstico por imagem , Tomografia Computadorizada por Raios X
19.
Eur J Clin Nutr ; 59(5): 727-30, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15798774

RESUMO

OBJECTIVE: To assess the antioxidant/non-antioxidant effects of a hydroxytyrosol (HT)-rich phenolic extract from olive mill wastewaters administered with a breakfast. DESIGN, SETTING AND SUBJECTS: Five type I diabetic patients received 25 mg of HT the first day and 12.5 mg/day the following 3 days. Blood sampling was carried out at T(0) (baseline) and T(4d) just before the breakfast + HT administration and at time points 1, 2, 3 and 4 h after T(0). Urines (24-h) were collected from T(0) to T(4d). Baseline HbA1c was generally inferior to 10%, glycemia was within the range 6-24 mmol/l, whereas total cholesterol, HDL-chol and triglycerides were normal. RESULTS: The major finding was the 46% decrease in the serum TXB(2) production after blood clotting at T(4d). Plasma vitamin A, E, beta-carotene were not changed. Vitamin C tended to increase (P = 0.075). Plasma antioxidant capacity was enhanced at T(0)+1 h only, whereas its main determinants (albumin, bilirubin, uric acid) were not modified. Urinary 8-isoPGF(2alpha) levels were highly variable and were not affected significantly by HT administration. CONCLUSION: The major effect of HT accounts for an antiaggregating platelet action, leading to a possible prevention of thrombotic and microthrombotic processes.


Assuntos
Antioxidantes/farmacologia , Diabetes Mellitus Tipo 1/sangue , Álcool Feniletílico/análogos & derivados , Óleos de Plantas/farmacologia , Tromboxano B2/sangue , Resíduos , Adulto , Idoso , Diabetes Mellitus Tipo 1/tratamento farmacológico , Diabetes Mellitus Tipo 1/urina , Dinoprosta/análogos & derivados , Dinoprosta/urina , Relação Dose-Resposta a Droga , Humanos , Masculino , Pessoa de Meia-Idade , Azeite de Oliva , Álcool Feniletílico/farmacologia , Agregação Plaquetária/efeitos dos fármacos , Fatores de Tempo , Eliminação de Resíduos Líquidos/métodos
20.
An Med Interna ; 19(1): 16-8, 2002 Jan.
Artigo em Espanhol | MEDLINE | ID: mdl-11989074

RESUMO

Histiocytosis X or Langerhans cell histiocytosis is an infrequent disease, which consists on proliferation of Langerhans cells. The etiology is unknown. Diagnosis is reached by electron microscope study of the biopsy, in which the Birbeck intracytoplasmatic granules of the Langerhans cells are found and/or by immunohistochemistry procedures able to detect S-100 antigen and CD1 cells. Diagnosis can also be reached with a bronchoalveolar lavage in which CD1 cells will appear in a score higher than 5%. We present the case of a 16 year-old girl that first appeared with a pulmonary lesion with a honey comb X-ray pattern and unsyntomatic mandibular bone affectation. Diagnosis was reached by biopsy study using S-100 antigen detection procedures. We consider this case an important one due to the infrequency of this particular disease.


Assuntos
Histiocitose de Células de Langerhans/diagnóstico , Pneumopatias/diagnóstico , Adolescente , Feminino , Humanos
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