P>Aims We assessed an extended interruption of subcutaneous insulin delivery during overnight closed-loop glucose control in children and adolescents with Type 1 diabetes (T1D). Methods In seven young subjects with T1D [age 14.2 +/- 2.1 years, diabetes duration 6.9 +/- 4.0 years, glycated haemoglobin (HbA(1c)) 8.0 +/- 1.5%, body mass index (BMI) 21.4 +/- 4.0 kg/m2, total daily insulin dose 0.9 +/- 0.2 units/kg/day; mean +/- sd) participating in overnight closed-loop glucose control studies, insulin delivery was interrupted for at least 90 min on the basis of predicted hypoglycaemia, low prevailing glucose levels or a too-steep decline in glucose levels. Results Insulin delivery was interrupted for 165 (105, 210) min [median, interquartile range (IQR)]. Plasma glucose was 6.2 +/- 3.2 mmol/l at the time of interruption and 5.5 +/- 2.0 mmol/l 105 min later (P = 0.15, paired t-test). Plasma glucose declined during the first hour of the interruption at a rate of 0.02 +/- 0.03 mmol/l per min and reached a nadir of 5.2 +/- 2.7 mmol/l; 105 min after the interruption, plasma glucose was increasing at a rate of 0.01 +/- 0.03 mmol/l per min. When insulin delivery restarted, plasma glucose was 6.4 +/- 2.2 mmol/l and peaked at 7.9 +/- 2.1 mmol/l in 60 min (P = 0.01). Physiological levels of plasma insulin were measured throughout with a nadir of 119 +/- 78 pmol/l. Conclusions A prolonged interruption of insulin delivery during overnight closed-loop glucose control to prevent hypoglycaemia was not associated with an increased risk of hyperglycaemia in young people with T1D.
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Stanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Univ Western Australia, Sch Paediat & Child Hlth, Perth, WA 6009, AustraliaStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Ly, Trang T.
Keenan, D. Barry
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Medtron Minimed, Northridge, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Keenan, D. Barry
Roy, Anirban
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Medtron Minimed, Northridge, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Roy, Anirban
Han, Jino
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Medtron Minimed, Northridge, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Han, Jino
Grosman, Benyamin
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Medtron Minimed, Northridge, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Grosman, Benyamin
Cantwell, Martin
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Medtron Minimed, Northridge, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Cantwell, Martin
Kurtz, Natalie
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Medtron Minimed, Northridge, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Kurtz, Natalie
von Eyben, Rie
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Stanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
von Eyben, Rie
Clinton, Paula
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Stanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Clinton, Paula
Wilson, Darrell M.
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Stanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA
Wilson, Darrell M.
Buckingham, Bruce A.
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Stanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USAStanford Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol & Diabet, Stanford, CA USA