Relationship of continuous glucose monitoring-related metrics with HbA1c and residual β-cell function in Japanese patients with type 1 diabetes.
Relationship of continuous glucose monitoring-related metrics with HbA1c and residual β-cell function in Japanese patients with type 1 diabetes.
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DOI:
10.1038/s41598-021-83599-x
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发表时间:
2021-02-17
影响因子:
4.6
通讯作者:
Ikegami H
中科院分区:
文献类型:
--
作者:
Babaya N;Noso S;Hiromine Y;Taketomo Y;Niwano F;Yoshida S;Yasutake S;Kawabata Y;Ikegami H
The targets for continuous glucose monitoring (CGM)-derived metrics were recently set; however, studies on CGM data over a long period with stable glycemic control are limited. We analyzed 194,279 CGM values obtained from 19 adult Japanese patients with type 1 diabetes. CGM data obtained during stable glycemic control over four months were analyzed. CGM-related metrics of different durations “within 120, 90, 60, 30, and 7 days” were calculated from baseline. Time in range (TIR; glucose 70–180 mg/dL), time above range (TAR; glucose ≥ 181 mg/dL), and average glucose levels, but not time below range (TBR; glucose ≤ 69 mg/dL), strongly correlated with glycated hemoglobin (HbA1c) values (P < 0.0001). TBR correlated with glucose coefficient of variation (CV) (P < 0.01). Fasting serum C-peptide levels negatively correlated with glucose CV (P < 0.01). HbA1c of approximately 7% corresponded to TIR of 74% and TAR of 20%. The shorter the CGM period, the weaker was the relationship between HbA1c and CGM-related metrics. TIR, TAR, and average glucose levels accurately reflected HbA1c values in Japanese patients with type 1 diabetes with stable glycemic control. Glucose CV and TBR complemented the limitation of HbA1c to detect glucose variability and hypoglycemia. Stable glycemic control with minimal hypoglycemia depended on residual β-cell function.
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影响因子:
7.7
作者:
Keenan HA;Sun JK;Levine J;Doria A;Aiello LP;Eisenbarth G;Bonner-Weir S;King GL
通讯作者:
King GL
影响因子:
39.2
作者:
Bergenstal, Richard M.;Gal, Robin L.;Beck, Roy W.
通讯作者:
Beck, Roy W.
影响因子:
7.7
作者:
FUKUDA, M;TANAKA, A;SHIMA, K
通讯作者:
SHIMA, K
影响因子:
16.2
作者:
Riddle, Matthew C.;Gerstein, Hertzel C.;Cefalu, William T.
通讯作者:
Cefalu, William T.
影响因子:
8.2
作者:
Gibb, Fraser W.;McKnight, John A.;Strachan, Mark W. J.
通讯作者:
Strachan, Mark W. J.