2009
DOI: 10.1111/j.1464-5491.2009.02691.x
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Nateglinide combination therapy with basal insulin and metformin in patients with Type 2 diabetes

Abstract: Addition of a short-acting insulin secretagogue at main meals improves postprandial hyperglycaemia during combination therapy with basal insulin and metformin, but increases the frequency of hypolycaemia.

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Cited by 9 publications
(2 citation statements)
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References 19 publications
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“…Moreover, certain patients are not able to achieve even more modest HbA1c targets with basal insulin alone . In most circumstances, when additional therapies, including non‐insulin agents, are used in combination with basal insulin, hypoglycaemia rates increase compared with the use of insulin monotherapy . One drug class, the dipeptidyl peptidase‐4 (DPP‐4) inhibitors, increases ambient concentrations of the endogenously secreted incretins of the gastrointestinal tract, glucagon‐like peptide‐1 (GLP‐1) and glucose‐dependent insulinotropic peptide (GIP) .…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, certain patients are not able to achieve even more modest HbA1c targets with basal insulin alone . In most circumstances, when additional therapies, including non‐insulin agents, are used in combination with basal insulin, hypoglycaemia rates increase compared with the use of insulin monotherapy . One drug class, the dipeptidyl peptidase‐4 (DPP‐4) inhibitors, increases ambient concentrations of the endogenously secreted incretins of the gastrointestinal tract, glucagon‐like peptide‐1 (GLP‐1) and glucose‐dependent insulinotropic peptide (GIP) .…”
Section: Introductionmentioning
confidence: 99%
“…In older people, treatment with nateglinide, alone or in combination with metformin, is well tolerated and produces significant improvements in glycaemic control . Similarly, nateglinide improves postprandial hyperglycaemia when added to the combination of basal insulin and metformin, but increases the frequency of hypoglycaemia . Interestingly, the glucose‐lowering effect of nateglinide is less potent than that for repaglinide, despite their similar postprandial glycaemic effects.…”
Section: Oral Agentsmentioning
confidence: 99%