PT  - JOURNAL ARTICLE
AU  - Jung A Kim
AU  - Jinsil Kim
AU  - Eun Roh
AU  - So-hyeon Hong
AU  - You-Bin Lee
AU  - Sei Hyun Baik
AU  - Kyung Mook Choi
AU  - Eunjin Noh
AU  - Soon Young Hwang
AU  - Geum Joon Cho
AU  - Hye Jin Yoo
TI  - Association of fasting plasma glucose variability with gestational diabetes mellitus: a nationwide population-based cohort study
AID  - 10.1136/bmjdrc-2019-001084
DP  - 2020 Apr 01
TA  - BMJ Open Diabetes Research & Care
PG  - e001084
VI  - 8
IP  - 1
4099  - http://drc.bmj.com/content/8/1/e001084.short
4100  - http://drc.bmj.com/content/8/1/e001084.full
SO  - BMJ Open Diab Res Care2020 Apr 01; 8
AB  - Objective Long-term glycemic variability has recently been recognized as another risk factor for future adverse health outcomes. We aimed to evaluate the risk of gestational diabetes mellitus (GDM) according to the prepregnancy long-term fasting plasma glucose (FPG) variability.Research design and methods A total of 164 053 women who delivered their first baby between January 1, 2012 and December 31, 2015, were selected from the Korean National Health Insurance data. All women underwent at least three national health screening examinations, and the last examination should be conducted within 2 years before their first delivery. GDM was defined as the presence of more than four times of claim of GDM (International Classification of Disease, 10th Revision (ICD-10) O24.4 and O24.9) or prescription of insulin under the ICD-code of GDM. FPG variability was assessed by variability independent of the mean (FPG-VIM), coefficient of variation, SD, and average successive variability.Results Among the 164 053 women, GDM developed in 6627 (4.04%). Those in the higher quartiles of FPG-VIM showed a stepwise increased risk of GDM. In fully adjusted model, the ORs for GDM was 1.22 (95% CI 1.14 to 1.31) in women with the highest FPG-VIM quartile compared with those in the lowest quartile. The risk for GDM requiring insulin therapy was 48% increase in women in the highest quartile of FPG-VIM compared with those in the lowest quartile, while that for GDM not requiring insulin therapy was 19% increase. The association between high FPG variability and the risk of GDM was intensified in the obese and aged more than 35 years women.Conclusions Increased FPG variability in the prepregnancy state is associated with the risk of GDM independent of confounding factors. Therefore, prepregnancy FPG variability might be a surrogate marker of the risk of GDM.