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Predictors of the Therapeutic Efficacy and Consideration of the Best Combination Therapy of Sodium-Glucose Co-transporter 2 Inhibitors

DC Field Value Language
dc.contributor.author강은석-
dc.contributor.author이민영-
dc.contributor.author이병완-
dc.contributor.author이용호-
dc.contributor.author이지연-
dc.contributor.author조용인-
dc.contributor.author차봉수-
dc.date.accessioned2019-07-11T03:30:03Z-
dc.date.available2019-07-11T03:30:03Z-
dc.date.issued2019-
dc.identifier.issn2233-6079-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/170002-
dc.description.abstractBACKGROUND: We investigated the predictive markers for the therapeutic efficacy and the best combination of sodium-glucose co-transporter 2 (SGLT2) inhibitors (empagliflozin, dapagliflozin, and ipragliflozin) therapy in patients with type 2 diabetes mellitus (T2DM). METHODS: A total of 804 patients with T2DM who had taken SGLT2 inhibitor as monotherapy or an add-on therapy were analyzed. Multivariate regression analyses were performed to identify the predictors of SGLT2 inhibitor response including the classes of baseline anti-diabetic medications. RESULTS: After adjusting for age, sex, baseline body mass index (BMI), diabetes duration, duration of SGLT2 inhibitor use, initial glycosylated hemoglobin (HbA1c) level, estimated glomerular filtration rate (eGFR), and other anti-diabetic agent usage, multivariate analysis revealed that shorter diabetes duration, higher initial HbA1c and eGFR were associated with better glycemic response. However, baseline BMI was inversely correlated with glycemic status; lean subjects with well-controlled diabetes and obese subjects with inadequately controlled diabetes received more benefit from SGLT2 inhibitor treatment. In addition, dipeptidyl peptidase 4 (DPP4) inhibitor use was related to a greater reduction in HbA1c in patients with higher baseline HbA1c ≥7%. Sulfonylurea users experienced a larger change from baseline HbA1c but the significance was lost after adjustment for covariates and metformin and thiazolidinedione use did not affect the glycemic outcome. CONCLUSION: A better response to SGLT2 inhibitors is expected in Korean T2DM patients who have higher baseline HbA1c and eGFR with a shorter diabetes duration. Moreover, the add-on of an SGLT2 inhibitor to a DPP4 inhibitor is likely to show the greatest glycemic response.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherKorean Diabetes Association-
dc.relation.isPartOfDIABETES & METABOLISM JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titlePredictors of the Therapeutic Efficacy and Consideration of the Best Combination Therapy of Sodium-Glucose Co-transporter 2 Inhibitors-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorJi-Yeon Lee-
dc.contributor.googleauthorYongin Cho-
dc.contributor.googleauthorMinyoung Lee-
dc.contributor.googleauthorYou Jin Kim-
dc.contributor.googleauthorYong-ho Lee-
dc.contributor.googleauthorByung-Wan Lee-
dc.contributor.googleauthorBong-Soo Cha-
dc.contributor.googleauthorEun Seok Kang-
dc.identifier.doi10.4093/dmj.2018.0057-
dc.contributor.localIdA00068-
dc.contributor.localIdA05491-
dc.contributor.localIdA02796-
dc.contributor.localIdA02989-
dc.contributor.localIdA03197-
dc.contributor.localIdA03866-
dc.contributor.localIdA03996-
dc.relation.journalcodeJ00720-
dc.identifier.eissn2233-6087-
dc.identifier.pmid30688052-
dc.subject.keywordBlood glucose-
dc.subject.keywordDiabetes mellitus, type 2-
dc.subject.keywordGlycated hemoglobin A-
dc.subject.keywordSodium-glucose transporter 2 inhibitors-
dc.contributor.alternativeNameKang, Eun Seok-
dc.contributor.affiliatedAuthor강은석-
dc.contributor.affiliatedAuthor이민영-
dc.contributor.affiliatedAuthor이병완-
dc.contributor.affiliatedAuthor이용호-
dc.contributor.affiliatedAuthor이지연-
dc.contributor.affiliatedAuthor조용인-
dc.contributor.affiliatedAuthor차봉수-
dc.citation.volume43-
dc.citation.number2-
dc.citation.startPage158-
dc.citation.endPage173-
dc.identifier.bibliographicCitationDIABETES & METABOLISM JOURNAL, Vol.43(2) : 158-173, 2019-
dc.identifier.rimsid62319-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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