Value of EZSCAN parameters for diabetes screening in Chinese.

Med Clin (Barc)

Department of Health Management, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.

Published: May 2017

AI Article Synopsis

  • The study examined EZSCAN as a screening method for diabetes in a large group of 6,270 Chinese participants.
  • Results indicated that higher EZSCAN scores correlated with an increased risk of diabetes, and there was a notable difference in diabetes prevalence across different risk groups.
  • EZSCAN demonstrated 73.2% sensitivity at a cut-off score of 44.5%, making it more effective than traditional glucose tests like FPG and HbA for diabetes screening.

Article Abstract

Objective: To study the parameters of EZSCAN as a screening tool for diabetes in Chinese.

Methods: A total of 6,270 subjects participated in the study. All subjects underwent tests of EZSCAN, fasting plasma glucose (FPG), oral glucose tolerance test and HbA.

Results: 1. All subjects were divided into 4 groups: the normal group, sugar metabolic abnormalities as low-risk group, middle-risk group and high-risk group. The difference of diabetes incidence among the 4 groups was statistically significant. With the increase of EZSCAN score, the prevalence of diabetes increased significantly. But there is no statistically difference between the low-risk group and the middle-risk group. 2. After adjustment for other variables, there is significantly positive relationship among EZSCAN risk score and the risk of diabetes. Meanwhile there is no statistically difference between the low-risk group and the middle-risk group. 3. The cut-off point of EZSCAN for diabetes was 44.5% with the sensitivity was 73.2% which was higher than of FPG and HbA.

Conclusion: As EZSCAN-diabetes risk score increases, the risk of diabetes increases. EZSCAN can be used as a tool for screening for diabetes. At the best screening diabetes cut-off point value 44.5%, the sensitivity is higher than traditional method of FPG and HbA.

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Source
http://dx.doi.org/10.1016/j.medcli.2016.11.037DOI Listing

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