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1.
Immunol Allergy Clin North Am ; 43(4): 763-776, 2023 11.
Artigo em Inglês | MEDLINE | ID: mdl-37758412

RESUMO

This article reviews the effects of gender on anaphylaxis in general and focuses on mastocytosis-specific issues. Incidence of anaphylaxis is increased in female compared with male patients during the pubertal years through the fifth decade of life, in which these disparities decrease. Estrogen is thought to increase the severity of anaphylaxis through increased endothelial nitric oxide synthase release. Despite this, all-cause fatal anaphylaxis does not appear to show a gender predilection. Systemic mastocytosis incidence is higher in women; however, mortality is increased in men owing to increased molecular and cytogenetic abnormalities.


Assuntos
Anafilaxia , Mastocitose Sistêmica , Mastocitose , Humanos , Masculino , Feminino , Anafilaxia/epidemiologia , Anafilaxia/etiologia , Mastocitose/diagnóstico , Mastocitose/epidemiologia , Mastocitose Sistêmica/diagnóstico , Mastocitose Sistêmica/epidemiologia , Incidência , Triptases
2.
J Endocrinol ; 238(3): R131-R141, 2018 09.
Artigo em Inglês | MEDLINE | ID: mdl-29875163

RESUMO

The synthesis of glycogen represents a key pathway for the disposal of excess glucose while its degradation is crucial for providing energy during exercise and times of need. The importance of glycogen metabolism is also highlighted by human genetic disorders that are caused by mutations in the enzymes involved. In this review, we provide a basic summary on glycogen metabolism and some of the clinical aspects of the classical glycogen storage diseases. Disruptions in glycogen metabolism usually result in some level of dysfunction in the liver, muscle, heart, kidney and/or brain. Furthermore, the spectrum of symptoms observed is very broad, depending on the affected enzyme. Finally, we briefly discuss an aspect of glycogen metabolism related to the maintenance of its structure that seems to be gaining more recent attention. For example, in Lafora progressive myoclonus epilepsy, patients exhibit an accumulation of inclusion bodies in several tissues, containing glycogen with increased phosphorylation, longer chain lengths and irregular branch points. This abnormal structure is thought to make glycogen insoluble and resistant to degradation. Consequently, its accumulation becomes toxic to neurons, leading to cell death. Although the genes responsible have been identified, studies in the past two decades are only beginning to shed light into their molecular functions.


Assuntos
Doença de Depósito de Glicogênio/metabolismo , Doença de Depósito de Glicogênio/patologia , Glicogênio/metabolismo , Animais , Progressão da Doença , Glicogênio/efeitos adversos , Glicogênio/química , Doença de Depósito de Glicogênio/complicações , Doença de Depósito de Glicogênio/diagnóstico , Humanos , Corpos de Inclusão/química , Corpos de Inclusão/metabolismo , Doença de Lafora/metabolismo , Doença de Lafora/patologia , Neurônios/química , Neurônios/metabolismo , Neurônios/patologia , Síndromes Neurotóxicas/etiologia , Fosforilação
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