Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27853
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dc.contributor.authorHamblin, Peter S-
dc.contributor.authorWong, Rosemary-
dc.contributor.authorEkinci, Elif I-
dc.contributor.authorSztal-Mazer, Shoshana-
dc.contributor.authorBalachandran, Shananthan-
dc.contributor.authorFrydman, Aviva S-
dc.contributor.authorHanrahan, Timothy P-
dc.contributor.authorHu, Raymond T C-
dc.contributor.authorKet, Shara N-
dc.contributor.authorMoss, Alan-
dc.contributor.authorNg, Mark-
dc.contributor.authorRagunathan, Sashikala-
dc.contributor.authorBach, Leon A-
dc.date2021-10-26-
dc.date.accessioned2021-11-03T00:35:00Z-
dc.date.available2021-11-03T00:35:00Z-
dc.date.issued2022-
dc.identifier.citationClinical Endocrinology 2022; 96(4): 549-557en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27853-
dc.description.abstractSodium-glucose cotransporter 2 inhibitors (SGLT2i) have been associated with diabetic ketoacidosis at the time of colonoscopy. This study aimed to identify factors associated with ketone concentrations in SGLT2i-treated type 2 diabetes compared with non-SGLT2i-treated diabetes, and those with impaired fasting glycaemia (IFG) and normoglycaemia. Cross-sectional, multicentre, observational study June-December 2020 in four Australian tertiary hospitals. Capillary glucose and ketones were measured in people undergoing colonoscopy: 37 SGLT2i-treated and 105 non-SGLT2i-treated type 2 diabetes, 65 IFG and 151 normoglycaemia. Body mass index (BMI), age, glucose, fasting duration and where relevant, HbA1c and time since last SGLT2i dose. In SGLT2i-treated diabetes, BMI (ρ = -0.43 [95% confidence interval: -0.67, -0.11]) and duration since last SGLT2i dose (ρ = -0.33 [-0.60, 0.00]) correlated negatively with increasing ketones, but there was no correlation with fasting duration. In non-SGLT2i-treated diabetes, BMI correlated negatively (ρ = -0.24 [-0.42, -0.05]) and fasting duration positively (ρ = 0.26 [0.07, 0.43]) with ketones. In IFG participants, only fasting duration correlated with ketones (ρ = 0.28 [0.03, 0.49]). In normoglycaemic participants, there were negative correlations with BMI (ρ = -0.20 [-0.35, -0.04]) and fasting glucose (ρ = -0.31 [-0.45, -0.15]) and positive correlations with fasting duration (ρ = 0.20 [0.04, 0.35]) and age (ρ = 0.19 [0.03, 0.34]). Multiple regression analysis of the entire cohort showed BMI, age and fasting glucose remained independently associated with ketones, but in SGLT2i-treated participants only BMI remained independently associated. In SGLT2i-treated diabetes, lower BMI was a novel risk factor for higher ketones precolonoscopy. Pending larger confirmatory studies, extra vigilance for ketoacidosis is warranted in these people.en
dc.language.isoeng-
dc.subjectcolonoscopyen
dc.subjectdiabetes mellitus, type 2en
dc.subjectdiabetic ketoacidosisen
dc.subjectimpaired fasting glycaemiaen
dc.subjectketonesen
dc.subjectketosisen
dc.subjectsodium-glucose transporter 2 inhibitorsen
dc.titleBody mass index is inversely associated with capillary ketones at the time of colonoscopy: Implications for SGLT2i use.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical Endocrinologyen
dc.identifier.affiliationAnaesthesiaen
dc.identifier.affiliationEndocrinologyen
dc.identifier.affiliationDepartment of Medicine, Melbourne Medical School, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationGastroenterology and Hepatologyen
dc.identifier.affiliationDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Endoscopic Services, Western Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Anaesthesia, Pain and Perioperative Medicine, Eastern Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationGastroenterological Nurses College of Australia, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine (Alfred), Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, Western Health, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationVictorian Liver Transplant Uniten
dc.identifier.affiliationDepartment of Endocrinology and Diabetes, Alfred Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Public Health and Preventive Medicine, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Endocrinology and Diabetes, Western Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Endocrinology and Diabetes, Eastern Health, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1111/cen.14621en
dc.type.contentTexten
dc.identifier.orcid0000-0002-6280-865Xen
dc.identifier.orcid0000-0002-6381-2458en
dc.identifier.orcid0000-0003-2372-395Xen
dc.identifier.orcid0000-0002-3837-0125en
dc.identifier.orcid0000-0002-3682-7400en
dc.identifier.orcid0000-0002-0169-0600en
dc.identifier.orcid0000-0002-9062-1518en
dc.identifier.pubmedid34697809-
local.name.researcherEkinci, Elif I
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptEndocrinology-
crisitem.author.deptEndocrinology-
crisitem.author.deptAnaesthesia-
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