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1.
Pathol Biol (Paris) ; 61(2): e5-11, 2013 Apr.
Artigo em Francês | MEDLINE | ID: mdl-21616607

RESUMO

Celiac disease is an auto-immune enteropathy involving genetic factors. It is associated in almost all the patients, to specific susceptibility alleles encoding histocompatibility antigens (HLA for human leucocyte antigen), specifically certain variants of the HLA-DQ2, and the HLA-DQ8 HLA class II molecules. Its estimated prevalence is 1% in the european and north-american populations. However, although these alleles represent the main genetic factor for this disease, they do not explain it on their own, as they are expressed by up to 30% of the population. Recent immunological advances allowed identifying the immunodominant epitopes of gluten, to establish the role of tissue transglutaminase in the disease and to define at the atomic level the presentation of these antigens by the HLA-DQ molecule. It is noteworthy that the HLA susceptibility alleles only account for 40% of the whole genetic risk, and the challenge is now to explain the remaining 60%. Genome-wide association studies using the DNA arrays technology to screen single nucleotide polymorphisms to pinpoint candidate regions and genes, have started to provide answers, but contradictory results sometimes still persist. Most of the genes emerging as statistically significantly associated with celiac disease are involved in the immune response, and suggest that the situation is complex.


Assuntos
Doença Celíaca/genética , Doença Celíaca/imunologia , Fenômenos Imunogenéticos , Apresentação de Antígeno/genética , Apresentação de Antígeno/imunologia , Predisposição Genética para Doença , Estudo de Associação Genômica Ampla , Glutens/efeitos adversos , Glutens/imunologia , Antígenos HLA/genética , Antígenos HLA/imunologia , Humanos , Epitopos Imunodominantes/genética , Epitopos Imunodominantes/imunologia , Modelos Biológicos
2.
Pathol Biol (Paris) ; 61(3): e39-46, 2013 Jun.
Artigo em Francês | MEDLINE | ID: mdl-21621349

RESUMO

Screening studies using high-sensitivity and specificity markers indicate a prevalence of celiac disease of up to 1% in European and North-American populations. Celiac disease is a frequent condition that has become an important public health issue. Yet the majority of cases remain undiagnosed due to the polymorphism of its clinical manifestations. The new insight in the pathogenesis of celiac disease has lead to the development of new diagnostic tools. Early screening of symptomatic patients and pre-identified at-risk groups significantly improves the quality of life while reducing morbidity and mortality. However, prophylactic benefits of early diagnosis by assessing the general population have not been shown in any study. French and Northern American scientific societies have introduced serological testing in their newly revised strategies to diagnose celiac disease. Older markers judged insufficiently accurate like anti-gliadin and anti-reticulin antibodies have recently been withdrawn from the list of reimbursed medical expenses in France. Anti-endomysium and tissue transglutaminase IgA antibodies have proven to be at this day the most sensitive and specific markers for the diagnosis and follow-up of patients on gluten-free diet, at the exception of IgA-deficient patients. Assays testing for IgG antibodies are recommended upon IgA-deficiency. Although very accurate, a better standardisation of current assays may enable serological testing to replace in a near future histological confirmation brought by small bowel biopsies which remains today the gold standard test to diagnose celiac disease. Indeed, serological testing represents and attractive alternative as it is less invasive, less expansive, laboursaving and more objective in interpretation.


Assuntos
Doença Celíaca/diagnóstico , Doença Celíaca/imunologia , Autoanticorpos/imunologia , Doença Celíaca/epidemiologia , Proteínas de Ligação ao GTP/fisiologia , Gliadina/imunologia , Humanos , Programas de Rastreamento/métodos , Prevalência , Proteína 2 Glutamina gama-Glutamiltransferase , Reticulina/imunologia , Testes Sorológicos , Transglutaminases/fisiologia
3.
Artigo em Francês | MEDLINE | ID: mdl-2838545

RESUMO

The authors report a case of a tumour of the liver in a pregnant woman who had taken oral contraception for six years. Since oral contraceptives have become far more widely used the two benign tumours of the liver, namely a hepatocellular adenoma of the liver and focal nodular hyperplasia, have become far more common. The increased blood supply to the liver can make such a tumour symptomatic and increase the risk of it rupturing intraperitoneally, especially at the onset of labour. A course of management has been suggested according to the size of the tumour and the duration of the pregnancy.


Assuntos
Carcinoma Hepatocelular/patologia , Neoplasias Hepáticas/patologia , Complicações Neoplásicas na Gravidez/patologia , Adulto , Carcinoma Hepatocelular/terapia , Feminino , Humanos , Neoplasias Hepáticas/terapia , Gravidez , Complicações Neoplásicas na Gravidez/terapia
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