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Long-term effects on glycaemic control and beta-cell preservation of early intensive treatment in patients with newly diagnosed type 2 diabetes: A multicentre randomized trial
DC Field | Value | Language |
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dc.contributor.author | Chon, S | - |
dc.contributor.author | Rhee, SY | - |
dc.contributor.author | Ahn, KJ | - |
dc.contributor.author | Baik, SH | - |
dc.contributor.author | Park, Y | - |
dc.contributor.author | Nam, MS | - |
dc.contributor.author | Lee, KW | - |
dc.contributor.author | Yoo, SJ | - |
dc.contributor.author | Koh, G | - |
dc.contributor.author | Lee, DH | - |
dc.contributor.author | Kim, YS | - |
dc.contributor.author | Woo, JT | - |
dc.contributor.author | KIIT study investigators | - |
dc.date.accessioned | 2019-11-13T04:28:19Z | - |
dc.date.available | 2019-11-13T04:28:19Z | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1462-8902 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/17690 | - |
dc.description.abstract | AIM: To determine the effects of early intensive glycaemic control with intensive insulin treatment (IIT) or initial combined oral antidiabetic drug (COAD) therapy on long-term glycaemic control and the preservation of beta-cell function in people with type 2 diabetes mellitus (T2DM).
METHODS: Newly diagnosed drug-naive patients with T2DM from 8 outpatient diabetes centres were randomized to receive either IIT (n = 50: glargine/glulisine) or COAD (n = 47: glimepiride/metformin) as intensive treatment until the termination criteria to ensure euglycaemia were met. After intensive treatment, the patients completed a follow-up period with either lifestyle modification (LSM) alone or rescue therapy to maintain target glycated haemoglobin levels of <7% (53 mmol/mol) up to week 104. The primary outcomes were analysed after excluding participants who were anti-glutamic acid decarboxylase autoantibody-positive. RESULTS: Both intensive treatment methods were effective for short-term glycaemic control, but improvements in the disposition index (DI) were significantly greater in the IIT group than in the COAD group (P = .021). During the follow-up period after intensive treatment, the two groups significantly differed in rescue method regarding the maintenance of comparable levels of glycaemic control (P = .010) and more participants who received IIT exhibited well-controlled glycaemia with LSM alone. Additionally, the IIT group maintained a higher DI than the COAD group during the follow-up period. Cox regression analysis showed that the IIT method was associated with a 52.5% lower risk of failing to maintain drug-free glycaemic remission compared with the COAD method (P = .015). CONCLUSIONS: The findings indicate that outpatient clinic-based IIT to ensure euglycaemia in newly diagnosed patients with T2DM might be an effective initial therapeutic option for improvements in beta-cell function and glycaemic control over the long term, without serious adverse events. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Diabetes Mellitus, Type 2 | - |
dc.subject.MESH | Drug Resistance, Multiple | - |
dc.subject.MESH | Drug Therapy, Combination | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Follow-Up Studies | - |
dc.subject.MESH | Glycated Hemoglobin A | - |
dc.subject.MESH | Hospitals, University | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hyperglycemia | - |
dc.subject.MESH | Hypoglycemia | - |
dc.subject.MESH | Hypoglycemic Agents | - |
dc.subject.MESH | Insulin | - |
dc.subject.MESH | Insulin Resistance | - |
dc.subject.MESH | Insulin Secretion | - |
dc.subject.MESH | Insulin-Secreting Cells | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Metformin | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Outpatient Clinics, Hospital | - |
dc.subject.MESH | Republic of Korea | - |
dc.subject.MESH | Sulfonylurea Compounds | - |
dc.title | Long-term effects on glycaemic control and beta-cell preservation of early intensive treatment in patients with newly diagnosed type 2 diabetes: A multicentre randomized trial | - |
dc.type | Article | - |
dc.identifier.pmid | 29272062 | - |
dc.subject.keyword | blood glucose | - |
dc.subject.keyword | combination | - |
dc.subject.keyword | drug therapy | - |
dc.subject.keyword | glimepiride | - |
dc.subject.keyword | hyperglycaemia | - |
dc.subject.keyword | hypoglycaemic agents | - |
dc.subject.keyword | insulin glargine | - |
dc.subject.keyword | insulin glulisine | - |
dc.subject.keyword | Korea | - |
dc.subject.keyword | type 2 diabetes mellitus | - |
dc.contributor.affiliatedAuthor | 이, 관우 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1111/dom.13196 | - |
dc.citation.title | Diabetes, obesity & metabolism | - |
dc.citation.volume | 20 | - |
dc.citation.number | 5 | - |
dc.citation.date | 2018 | - |
dc.citation.startPage | 1121 | - |
dc.citation.endPage | 1130 | - |
dc.identifier.bibliographicCitation | Diabetes, obesity & metabolism, 20(5). : 1121-1130, 2018 | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.identifier.eissn | 1463-1326 | - |
dc.relation.journalid | J014628902 | - |
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