使用维格列汀单药治疗或联合治疗老年2型糖尿病患者的个体化治疗目标评估(INTERVAL):一项24周随机双盲安慰剂对照研究

"Individualised treatment targets for elderly patients with type 2 diabetes using vildagliptin add-on or lone therapy (INTERVAL): a 24 week, randomised, double-blind, placebo-controlled study "
作者:Strain WD, Lukashevich V, Kothny W, Hoellinger MJ,
期刊: Lancet2013年8月9890期382卷

BACKGROUND:

Guidelines suggest setting individualised targets for glycaemic control in elderly patients with type 2 diabetes, despite no evidence. We aimed to assess the feasibility of setting and achieving individualised targets over 24 weeks along with conventional HbA1c reduction usingvildagliptin versus placebo.

METHODS:

In this multinational, double-blind24 week study, we enrolled drug-naive or inadequately controlled (glycosylated haemoglobin A1c [HbA1c] ≥7·0% to ≤10·0%) patients with type 2 diabetes aged 70 years or older from 45 outpatient centres in Europe. Investigators set individualisedtreatment targets on the basis of age, baseline HbA1c, comorbidities, and frailty status before a validated automated system randomly assignedpatients (1:1) to vildagliptin (50 mg once or twice daily as per label) or placebo. Coprimary efficacy endpoints were proportion of patients reaching their investigator-defined HbA1c target and HbA1c reduction from baseline to study end. The study is registered with ClinicalTrials.gov, number NCT01257451, and European Union Drug Regulating Authorities Clinical Trials database, number 2010-022658-18.

FINDINGS:

Between Dec 22, 2010, and March 14, 2012, we randomly assigned 139 patients each to the vildagliptin and placebo groups. 37 (27%) of 137 patients in the placebo group achieved their individualised targets by education and interactions with the study team alone and 72 (52·6%) of 137patients achieved their target in the vildagliptin group (adjusted odds ratio 3·16, 96·2% CI 1·81-5·52; p<0·0001). This finding was accompanied by a clinically relevant 0·9% reduction in HbA1c from a baseline of 7·9% with vildagliptin and a between-group difference of -0·6% (98·8% CI -0·81 to -0·33; p<0·0001). The overall safety and tolerability was similar in the vildagliptin and placebo groups, with low incidence of hypoglycaemia and no emergence of new safety signals.

INTERPRETATION:

This study is the first to introduce and show the feasibility of using individualised HbA1c targets as an endpoint in any type 2diabetes population. Individualised glycaemic target levels are achievable with vildagliptin without any tolerability issues in the elderly type 2 diabetespopulation.

FUNDING:

Novartis Pharma AG.

学科代码:内分泌学与糖尿病   关键词:type 2 diabetes vildagliptin
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