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language of document : English
Material Type : طرح تحقیقاتی/ پروژه لاتین
Record number : 51462
doc. No : R2998
main entry : Janghorban, Mohsen
title & author : Comparison of glycated hemoglobin with fasting plasma glucose in definition of glycemic component of the metabolic syndrome in an Iranian population [Research Project]/Executer: Mohsen Janghorban, Masoud Amini
Publication statement : Isfahan: Isfahan University of Medical Sciences, Vice Chancellery for Research, 2012.
Physical Description : [ No paging ].:tab
Notes : The aim of this study was to compare the utility of glycated hemoglobin (GHb) versus the fasting. plasma glucose (FPG) in definition of glycemic component of the metabolic syndrome (MetS) in a nondiabetic Iranian population. A cross-sectional study of first-degree relatives (FDRs) of patients with type 2 diabetes was conducted from 2003 to 2005. A total of 2410 non-diabetic FDRs of consecutive patients with type 2 diabetes 30 to 60 years old were examined. All subjects underwent a standard 75 g 2-h oral glucose tolerance test and GHb measurement. Consensus criteria in 2009 were used to identify MetS. Glycemic component of MetS was defined as either FPG 100 mg/dl or GHb 5.7 percent. The mean (SD) age of participants was 43.6 (6.5) years. The prevalence of MetS was 33.5 percent (95 percent) confidence interval (CI): 31.6, 35.4) based on FPG criterion alone and 28.6 percent (95 percent) CI: 26.8, 30.4) based on GHb criterion alone. Use of combination of both criteria increased the prevalence of MetS ( 36.7 percent, 95 percent, CI: 34.8, 38.6). There was 88.7 percent (95 percent CI: 87.5, 90.0) percent. agreement between the GHb and FPG when either was used to define MetS (k coefficient = 0.737). These data indicate that using GHb may be an acceptable surrogate of FPG to define glycemic component of MetS..
Notes : Print
descriptor : Diabetes Mellitus, Type 2- prevention and control
: Glycemic Index
: Blood Glucose
: Hypoglycemia
: Metabolic Syndrome X
Originating Source : IRIsfahan University of Medical Sciences
publication type : p
Source : Vice Chancellery for Research
Ended Date : 2012
Project code : 191064
 
 
 
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