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1.
Korean Journal of Medicine ; : 104-108, 2009.
Artigo em Coreano | WPRIM | ID: wpr-154717

RESUMO

Hypertriglyceridemia-induced pancreatitis is a rare, but serious, complication of pregnancy. We report a case of acute pancreatitis associated with type V hyperlipoproteinemia in pregnancy. A 36-year-old primigravida was admitted at 16 weeks of gestation with severe abdominal pain. Chemical analysis showed high serum pancreatic enzymes and very high serum triglyceride. Abdominal magnetic resonance imaging (MRI) showed diffuse swelling of the pancreas and a peripancreatic fluid collection. A diagnosis of acute pancreatitis with type V hyperlipoproteinemia was made. She recovered from the acute pancreatitis with conservative management and the serum triglyceride decreased rapidly with dietary restriction of fat, insulin/glucose, fenofibrate, and omega-3. We review the management of hypertriglyceridemia-induced acute pancreatitis in pregnancy.


Assuntos
Adulto , Humanos , Gravidez , Dor Abdominal , Fenofibrato , Hiperlipoproteinemia Tipo V , Hipertrigliceridemia , Imageamento por Ressonância Magnética , Pâncreas , Pancreatite
2.
Korean Diabetes Journal ; : 402-408, 2008.
Artigo em Coreano | WPRIM | ID: wpr-99657

RESUMO

BACKGROUND: Peroxisome proliferators-activated receptor gamma (PPARgamma) is a member of the nuclear hormone receptor superfamily of ligand-activated transcription factors and known to play a role in regulating the expression of numerous genes involved in lipid metabolism, metabolic syndrome, inflammation, and atherosclerosis. The PPARgamma2 Pro12Ala polymorphism has recently been shown to be associated with diabetic nephropathy. In this study, we evaluated the relationship between PPARgamma2 Pro12Ala polymorphism and type 2 diabetic nephropathy whose duration of diabetes was over 10 years. METHODS: We conducted a case-control study, which enrolled 367 patients with type 2 diabetes. Genotyping of PPARgamma2 Pro12Ala polymorphism was performed using polymerase chain reaction followed by digestion with Hae III restriction enzyme. RESULTS: The genotype or allele frequencies of PPARgamma2 Pro12Ala polymorphism were not significantly different in diabetic patients with or without diabetic nephropathy. The genotype frequencies in terms of diabetic retinopathy and macrovascular complications such as coronary artery disease or stroke were not different either. Interestingly, nephropathy patients with Ala/Pro genotype showed lower C-peptide levels than those of Pro/Pro genotype. CONCLUSION: Our results suggest that PPARgamma2 Pro12Ala polymorphism is not associated with diabetic nephropathy in type 2 diabetic patients.


Assuntos
Humanos , Aterosclerose , Peptídeo C , Estudos de Casos e Controles , Doença da Artéria Coronariana , Nefropatias Diabéticas , Retinopatia Diabética , Digestão , Frequência do Gene , Genótipo , Inflamação , Metabolismo dos Lipídeos , Peroxissomos , Reação em Cadeia da Polimerase , PPAR gama , Acidente Vascular Cerebral , Fatores de Transcrição
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