Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
1.
Rev Med Interne ; 39(2): 122-126, 2018 Feb.
Artigo em Francês | MEDLINE | ID: mdl-29157755

RESUMO

The most common causes of high anion gap metabolic acidosis (HAGMA) are lactic acidosis, ketoacidosis, and intoxications. Nevertheless, clinicians can be faced with unexplained HAGMA, with a need to look for less common etiologies. We describe a case of 5-oxoproline (pyroglutamate) acidosis due to chronic acetaminophen ingestion at therapeutic dose in a 79-year-old inpatient. The pathophysiology of this condition is detailed, with abnormalities in the gamma-glutamyl cycle due to acetaminophen ingestion and severe chronic morbidities, resulting in glutathione and cysteine deficiency and then accumulation of 5-oxoproline. In HAGMA, when usual causes have been excluded, 5-oxoproline acidosis should be suspected in patients with chronic morbidities and acetaminophen ingestion. This diagnosis should be kept in mind because it generally resolves quickly with cessation of acetaminophen and administration of intravenous fluids.


Assuntos
Acetaminofen/efeitos adversos , Acidose/induzido quimicamente , Erros Inatos do Metabolismo dos Aminoácidos/induzido quimicamente , Analgésicos não Narcóticos/efeitos adversos , Glutationa Sintase/deficiência , Ácido Pirrolidonocarboxílico/sangue , Equilíbrio Ácido-Base , Idoso , Glutationa Sintase/efeitos dos fármacos , Humanos , Masculino
2.
J Gynecol Obstet Biol Reprod (Paris) ; 43(9): 671-9, 2014 Nov.
Artigo em Francês | MEDLINE | ID: mdl-25218268

RESUMO

Down syndrome maternal serum screening is largely used in France. The aim of this article is to specify and to explain the different comments applied on the reports in order to optimize the management of the patient. These comments represent the consensus of the study group of the biologist accredited for Down syndrome maternal serum screening.


Assuntos
Síndrome de Down/sangue , Diagnóstico Pré-Natal/métodos , Biomarcadores/sangue , Gonadotropina Coriônica Humana Subunidade beta/sangue , Consenso , Feminino , França , Humanos , Gravidez , Primeiro Trimestre da Gravidez , Proteína Plasmática A Associada à Gravidez/análise , Risco , alfa-Fetoproteínas/análise
3.
Mol Genet Metab ; 112(2): 177-82, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24742993

RESUMO

BACKGROUND: Trisomy 18 and Smith-Lemli-Opitz syndrome are two polymalformative conditions in which a cholesterol defect has been noted. When they occur prenatally, they are associated with a decreased maternal unconjugated estriol (uE(3)) level. Cholesterol plays an essential role in the Sonic Hedgehog pathway, allowing Shh protein maturation leading to its maximal activity. Many malformations in these two syndromes occur in Shh dependent tissues. We thus sought to assess whether a cholesterol defect could affect the Shh pathway and explain some of the observed malformations. MATERIALS AND METHODS: We selected 14 cases of trisomy 18 and 3 cases of SLO in which the maternal uE(3) level was decreased and reported malformations were observed after fetopathological examination. We correlated the number of malformations with maternal uE(3) level. We then carried out cholesterol concentrations in separate culture media consisting of trisomy 18, SLO and control amniocytes. Finally, we analyzed the Shh pathway by testing the gene expression of several Shh components: GLI transcription factors, BMP2, BMP4, TGFß1, COL1A1 and COL1A2. RESULTS AND DISCUSSION: There was an inverse correlation between phenotypic severity and maternal uE(3) levels in SLO and trisomy 18. The cholesterol levels in the amniocyte culture media were correlated with maternal uE3 levels and were significantly lower in T18 and SLO amniocytes, reflecting cholesterol defects. There was an alteration in the Shh pathway since expression of several genes was decreased in T18 and SLO amniocytes. However, these cholesterol defects were not solely responsible for the altered Shh pathway and the malformations observed.


Assuntos
Proteína Morfogenética Óssea 2/metabolismo , Colesterol/metabolismo , Colágeno Tipo I/metabolismo , Estriol/metabolismo , Proteínas Hedgehog/metabolismo , Síndrome de Smith-Lemli-Opitz/patologia , Trissomia/patologia , Líquido Amniótico/metabolismo , Atorvastatina , Proteína Morfogenética Óssea 2/genética , Células Cultivadas , Cromossomos Humanos Par 18/metabolismo , Colágeno Tipo I/genética , Cadeia alfa 1 do Colágeno Tipo I , Meios de Cultura/química , Feminino , Regulação da Expressão Gênica , Proteínas Hedgehog/genética , Ácidos Heptanoicos/farmacologia , Humanos , Gravidez , Pirróis/farmacologia , Transdução de Sinais/efeitos dos fármacos , Síndrome de Smith-Lemli-Opitz/metabolismo , Síndrome da Trissomía do Cromossomo 18
5.
Ann Biol Clin (Paris) ; 60(4): 421-8, 2002.
Artigo em Francês | MEDLINE | ID: mdl-12147446

RESUMO

A lot of methods are now available for total plasma homocysteine (tHcy) determination. Commercial kits using immunoassay, easier to use, begin to supplant in-house laboratory methods. Our aim is to evaluate the interchangeability of tHcy measurements in 9 French hospital laboratories. Six different method types were used: 2 gas chromatography-mass spectrometry (GC-MS), 2 HPLC with fluorescence detection subdivided in one in-house method and one commercial kit (Bio-Rad ), 3 fluorescence polarization immunoassays (FPIA), 1 enzyme immunoassay, 1 amino acid analyser, 1 capillary electrophoresis coupled with laser-induced fluorescence detection (EC-LIF). Each laboratory analysed 41 patient's plasma samples in which 8 samples contained added homocystine. Results were analysed for imprecision, recovery, and methodological differences. The mean among-laboratory imprecision (CV) ranged from 12.5 to 18% in function of plasma sample type and was identical to the mean among-method variation. In terms of recovery, we obtained underestimated results with immunoassays. The bias relative to the GC-MS method was less than 12.5% except for two laboratories, one using FPIA assay and the other EC-LIF. In conclusion, the interchangeability of tHcy results between laboratories is not satisfactory and does not allow us to evaluate cardiovascular risk linked to moderate increases of tHcy.


Assuntos
Análise Química do Sangue/métodos , Homocisteína/sangue , Laboratórios Hospitalares , Análise Química do Sangue/normas , Cromatografia Gasosa , Cromatografia Líquida de Alta Pressão , Eletroforese Capilar , Fluorescência , Imunoensaio de Fluorescência por Polarização , França , Humanos , Técnicas Imunoenzimáticas , Laboratórios Hospitalares/normas , Lasers , Espectrometria de Massas , Kit de Reagentes para Diagnóstico
9.
Adolescence ; 23(91): 567-75, 1988.
Artigo em Inglês | MEDLINE | ID: mdl-2848400

RESUMO

Through school-sponsored health fairs, 398 adolescents (153 males and 245 females) between the ages of 14 and 18 completed a questionnaire on their compliance with six of the U.S. Dietary Guidelines. Results indicated that adolescents report highest compliance on "eat a variety of foods" and "eat foods with adequate starch and fiber." Conversely, they indicated low compliance on "reduce sugar intake" and "reduce fat, saturated fat and cholesterol intake." Sex differences were noted on two dietary guidelines. Females reported lower compliance with respect to "maintain desirable body weight." Males, on the other hand, reported lower compliance than females on "reduce salt intake." Given the fact that the dietary guidelines of "reduce fat, saturated fat and cholesterol," "maintain desirable body weight," and "reduce salt intake" are all aimed at reducing cardiovascular risk, the low compliance reported by adolescents may have long-range health implications.


Assuntos
Comportamento do Adolescente , Dieta , Adolescente , Peso Corporal , Comportamento Cooperativo , Gorduras na Dieta , Fibras na Dieta , Feminino , Comportamentos Relacionados com a Saúde , Educação em Saúde , Humanos , Masculino , Fatores Sexuais , Sacarose
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA