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Combination Therapy With Exenatide Plus Pioglitazone Versus Basal/Bolus Insulin in Patients With Poorly Controlled Type 2 Diabetes on Sulfonylurea Plus Metformin: The Qatar Study.

基本信息

DOI:
10.2337/dc16-1738
发表时间:
2017-03
期刊:
影响因子:
16.2
通讯作者:
Jayyousi A
中科院分区:
医学1区
文献类型:
Journal Article;Randomized Controlled Trial
作者: Abdul-Ghani M;Migahid O;Megahed A;Adams J;Triplitt C;DeFronzo RA;Zirie M;Jayyousi A研究方向: -- MeSH主题词: --
关键词: --
来源链接:pubmed详情页地址

文献摘要

The Qatar Study was designed to examine the efficacy of combination therapy with exenatide plus pioglitazone versus basal/bolus insulin in patients with long-standing poorly controlled type 2 diabetes mellitus (T2DM) on metformin plus a sulfonylurea. The study randomized 231 patients with poorly controlled (HbA1c >7.5%, 58 mmol/mol) T2DM on a sulfonylurea plus metformin to receive 1) pioglitazone plus weekly exenatide (combination therapy) or 2) basal plus prandial insulin (insulin therapy) to maintain HbA1c <7.0% (53 mmol/mol). After a mean follow-up of 12 months, combination therapy caused a robust decrease in HbA1c from 10.0 ± 0.6% (86 ± 5.2 mmol/mol) at baseline to 6.1 ± 0.1% (43 ± 0.7 mmol/mol) compared with 7.1 ± 0.1% (54 ± 0.8 mmol/mol) in subjects receiving insulin therapy. Combination therapy was effective in lowering the HbA1c independent of sex, ethnicity, BMI, or baseline HbA1c. Subjects in the insulin therapy group experienced significantly greater weight gain and a threefold higher rate of hypoglycemia than patients in the combination therapy group. Combination exenatide/pioglitazone therapy is a very effective and safe therapeutic option in patients with long-standing poorly controlled T2DM on metformin plus a sulfonylurea.
卡塔尔研究旨在检验艾塞那肽联合吡格列酮与基础/餐时胰岛素在长期患有二甲双胍联合磺脲类药物控制不佳的2型糖尿病(T2DM)患者中的疗效。 该研究将231名服用磺脲类药物联合二甲双胍但控制不佳(糖化血红蛋白HbA1c>7.5%,即58 mmol/mol)的2型糖尿病患者随机分组,分别接受:1)吡格列酮联合每周一次的艾塞那肽(联合治疗);2)基础胰岛素加餐时胰岛素(胰岛素治疗),以将糖化血红蛋白维持在<7.0%(53 mmol/mol)。 平均随访12个月后,联合治疗使糖化血红蛋白从基线时的10.0±0.6%(86±5.2 mmol/mol)大幅降低至6.1±0.1%(43±0.7 mmol/mol),而接受胰岛素治疗的受试者为7.1±0.1%(54±0.8 mmol/mol)。联合治疗在降低糖化血红蛋白方面是有效的,且不受性别、种族、体重指数(BMI)或基线糖化血红蛋白的影响。胰岛素治疗组的受试者体重增加明显更多,低血糖发生率是联合治疗组的三倍。 对于长期服用二甲双胍联合磺脲类药物控制不佳的2型糖尿病患者,艾塞那肽/吡格列酮联合治疗是一种非常有效且安全的治疗选择。
参考文献(0)
被引文献(0)
Effects of pioglitazone and metformin on β-cell function in nondiabetic subjects at high risk for type 2 diabetes
DOI:
10.1152/ajpendo.00221.2006
发表时间:
2007-01-01
期刊:
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
影响因子:
5.1
作者:
Rasouli, Neda;Kern, Philip A.;Elbein, Steven C.
通讯作者:
Elbein, Steven C.
Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)
DOI:
10.1016/s0140-6736(98)07019-6
发表时间:
1998-09-12
期刊:
LANCET
影响因子:
168.9
作者:
Turner, RC;Holman, RR;Ward, JD
通讯作者:
Ward, JD
Secondary prevention of macrovascular events in patients with type 2 diabetes in the PROactive Study (PROspective pioglitAzone Clinical Trial In macroVascular Events):: a randomised controlled trial
DOI:
10.1016/s0140-6736(05)67528-9
发表时间:
2005-10-08
期刊:
LANCET
影响因子:
168.9
作者:
Dormandy, JA;Charbonnel, B;Taton, J
通讯作者:
Taton, J
Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes.
DOI:
10.1056/nejmoa1603827
发表时间:
2016-07-28
期刊:
The New England journal of medicine
影响因子:
0
作者:
Marso SP;Daniels GH;Brown-Frandsen K;Kristensen P;Mann JF;Nauck MA;Nissen SE;Pocock S;Poulter NR;Ravn LS;Steinberg WM;Stockner M;Zinman B;Bergenstal RM;Buse JB;LEADER Steering Committee;LEADER Trial Investigators
通讯作者:
LEADER Trial Investigators
A study comparing insulin lispro mix 25 with glargine plus lispro therapy in patients with Type 2 diabetes who have inadequate glycaemic control on oral anti-hyperglycaemic medication: results of the PARADIGM study
DOI:
10.1111/j.1464-5491.2012.03722.x
发表时间:
2012-09-01
期刊:
DIABETIC MEDICINE
影响因子:
3.5
作者:
Bowering, K.;Reed, V. A.;Oliveira, J.
通讯作者:
Oliveira, J.

数据更新时间:{{ references.updateTime }}

关联基金

Durability of Early Combination Therapy vs Conventional Therapy in New Onset T2DM
批准号:
9324995
批准年份:
2015
资助金额:
48.88
项目类别:
Jayyousi A
通讯地址:
--
所属机构:
--
电子邮件地址:
--
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