Achievement of target A1C levels with negligible hypoglycemia and low glucose variability in youth with short-term type 1 diabetes and residual β-cell function.
Achievement of target A1C levels with negligible hypoglycemia and low glucose variability in youth with short-term type 1 diabetes and residual β-cell function.
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DOI:
10.2337/dc11-2190
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发表时间:
2012-04
期刊:
影响因子:
16.2
通讯作者:
Diabetes Research in Children Network (DirecNet) Study Group
中科院分区:
文献类型:
--
作者:
Sherr J;Tamborlane WV;Xing D;Tsalikian E;Mauras N;Buckingham B;White NH;Arbelaez AM;Beck RW;Kollman C;Ruedy K;Diabetes Research in Children Network (DirecNet) Study Group
To determine exposure to hyper- and hypoglycemia using blinded continuous glucose monitoring (CGM) profiles in youth with type 1 diabetes (T1D) with residual β-cell function during the first year of insulin treatment. Blinded, 3–7 day CGM profiles were obtained in 16 short-term T1D patients (age 8–18 years, T1D duration 6–52 weeks) who had peak C-peptide levels ranging from 0.46 to 1.96 nmol/L during a mixed-meal tolerance test. Results in this short-term group were compared with those in 34 patients with well-controlled, longer-term T1D (duration ≥5 years), matched for age and A1C with the short-term T1D group, and with those in 26 age-matched nondiabetic individuals. Despite matching for A1C, and therefore similar mean sensor glucose levels in the two T1D groups, short-term T1D participants had a lower frequency of hypoglycemia (0.3 vs. 7.6%, P < 0.001), a trend toward less hyperglycemia (17 vs. 32%, P = 0.15), and a greater percentage in the target range (median 77 vs. 60%, P = 0.02). Indeed, the percentage of sensor glucose levels ≤70 mg/dL in the short-term T1D group (0.3%) did not differ from those in the nondiabetic group (1.7%, P = 0.73). The coefficient of variation of sensor glucose levels (an index of glucose variability) was lower in short-term vs. longer-term T1D participants (27 vs. 42%, respectively, P < 0.001). In youth with short-term T1D who retain residual β-cell function, there is negligible exposure to hypoglycemia and lower glucose variability than in youth with well-controlled T1D of longer duration.
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影响因子:
16.2
作者:
Beck, Roy W.
通讯作者:
Beck, Roy W.
影响因子:
8
作者:
Weinzimer, SA;Ahern, JH;Tamborlane, WV
通讯作者:
Tamborlane, WV
影响因子:
16.2
作者:
Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study Group;Fox LA;Beck RW;Xing D
通讯作者:
Xing D
影响因子:
16.2
作者:
Wilson, Darrell M.;Beck, Roy W.;Weinzimer, Stuart A.
通讯作者:
Weinzimer, Stuart A.
影响因子:
158.5
作者:
Herold, KC;Hagopian, W;Bluestone, JA
通讯作者:
Bluestone, JA