2020
DOI: 10.1002/ccr3.3230
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Pasireotide‐induced hyperglycemia in a patient with Cushing's disease: Potential use of sodium‐glucose cotransporter 2 inhibitor and glucagon‐like peptide‐1 receptor agonist for treatment

Abstract: This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Cited by 5 publications
(2 citation statements)
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“…In summary, in patients with pasireotide-related hyperglycaemia we suggest starting GLP1-RA and metformin as a first-line approach and avoiding DPP4-i, in accordance with the findings of the previous studies ( 120 , 121 ) and to the mild anti-hyperglycaemic effects of DPP4-i ( Figure 3 ).…”
Section: Cushing’s Syndromesupporting
confidence: 90%
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“…In summary, in patients with pasireotide-related hyperglycaemia we suggest starting GLP1-RA and metformin as a first-line approach and avoiding DPP4-i, in accordance with the findings of the previous studies ( 120 , 121 ) and to the mild anti-hyperglycaemic effects of DPP4-i ( Figure 3 ).…”
Section: Cushing’s Syndromesupporting
confidence: 90%
“…In patients with pasireotide-related hyperglycaemia a significant decrease in HbA1c and fasting plasma glycaemia was obtained using GLP1-RA compared to other antidiabetic drugs such as metformin and DPP4-i ( 120 ). Further, a case of a man with pasireotide-induced hyperglycaemia successfully treated with a combination of GLP1-RA, insulin and empaglifozin was also reported ( 121 ). The most robust findings are those reported by Samson et al., who showed the superiority of the combination of sitagliptin and liraglutide in achieving glucose control ( 122 ).…”
Section: Cushing’s Syndromementioning
confidence: 99%