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1.
Journal of Korean Diabetes ; : 303-309, 2015.
Article Dans Coréen | WPRIM | ID: wpr-726847

Résumé

BACKGROUND: The effects of dipeptidyl peptidase-4 inhibitors on adipokines remain obscure. The aim of this study was to evaluate the effect of the addition of vildagliptin on visfatin, an adipokine that represents inflammatory biomarkers of adipose tissue, in patients with type 2 diabetes inadequately controlled with prior metformin monotherapy. METHODS: In this 16-week, double-blind, randomized, parallel-group, placebo-controlled study, 71 patients were randomly assigned to vildagliptin 50 mg twice a day (n = 35) or placebo (n = 36) added to ongoing metformin therapy. Fasting plasma glucose (FPG), glycated hemoglobin (HbA1c), plasma lipids, and visfatin levels were measured at baseline and 16 weeks after treatment. RESULTS: After 16 weeks, significant reduction in HbA1c and FPG was observed with vildagliptin addon treatment compared to placebo (-0.54 +/- 0.52%, P = 0.001 and -14.80 +/- 19.21 mg/dL, P = 0.004, respectively). However, no other clinically meaningful changes in lipid parameters or visfatin were observed. CONCLUSION: Vildagliptin add-on to metformin significantly improved fasting blood glucose and HbA1c. However, in this study, no significant differences in lipid parameters or visfatin level were observed between the two groups.


Sujets)
Humains , Adipokines , Tissu adipeux , Marqueurs biologiques , Glycémie , Diabète , Jeûne , Hémoglobine glyquée , Metformine , Nicotinamide phosphoribosyltransferase , Plasma sanguin , Études prospectives
2.
Diabetes & Metabolism Journal ; : 507-511, 2015.
Article Dans Anglais | WPRIM | ID: wpr-149422

Résumé

BACKGROUND: An oral glucose tolerance test (OGTT) is the current method used for screening and diagnosis of gestational diabetes mellitus (GDM). OGTT is a relatively complicated procedure and is expensive. Thus, new strategies that do not require fasting or more than a single blood draw may improve the diagnosis of GDM and increase the rate of GDM testing. We investigated the utility of monitoring glycosylated hemoglobin (HbA1c) levels for the diagnosis of GDM. METHODS: The data from 992 pregnant women with estimated gestational ages ranging from 24 to 28 weeks were retrospectively reviewed. There were 367 women with plasma glucose levels > or =140 mg/dL 1 hour after a 50-g OGTT. GDM was diagnosed according to the Carpenter-Coustan criteria for a 3-hour 100 g OGTT. A HbA1c assessment was performed at the same time. RESULTS: We enrolled 343 women in this study, and there were 109 women with GDM. The area under the curve the receiver operating characteristic curve for HbA1c detection of GDM was 0.852 (95% confidence interval, 0.808 to 0.897). A HbA1c cutoff value > or =5.35% had maximal points on the Youden index (0.581). The sensitivity was 87.2% and the specificity was 70.9% for diagnosing GDM. A threshold value > or =5.35% indicated that 163 patients had GDM and that 68 (41.7%) were false positive. The positive predictive value was 58.3% at this threshold value. CONCLUSION: Despite substantial progress in methodology, HbA1c values cannot replace OGTT for the diagnosis of GDM.


Sujets)
Femelle , Humains , Grossesse , Glycémie , Diabète gestationnel , Diagnostic , Jeûne , Âge gestationnel , Hyperglycémie provoquée , Hémoglobine glyquée , Dépistage de masse , Femmes enceintes , Études rétrospectives , Courbe ROC , Sensibilité et spécificité
3.
Soonchunhyang Medical Science ; : 130-133, 2015.
Article Dans Anglais | WPRIM | ID: wpr-28806

Résumé

Extrapulmonary manifestations of Mycoplasma pneumoniae infection are not uncommon and involvement of every organ system has been reported. However, association of inflammatory myositis with M. pneumoniae infection is rare. Here, we describe a patient who developed polymyositis associated with mycoplasma infection, who was treated successfully with glucocorticoid, intravenous immunoglobulin, and methotrexate.


Sujets)
Adolescent , Femelle , Humains , Dermatomyosite , Immunoglobulines , Méthotrexate , Infections à Mycoplasma , Mycoplasma pneumoniae , Mycoplasma , Myosite , Pneumopathie infectieuse , Pneumopathie à mycoplasmes , Polymyosite
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