Efficacy and safety of canagliflozin compared with placebo in older patients with type 2 diabetes mellitus: a pooled analysis of clinical studies

被引:67
作者
Sinclair, Alan [1 ,2 ]
Bode, Bruce [3 ]
Harris, Stewart [4 ]
Vijapurkar, Ujjwala [5 ]
Mayer, Cristiana [6 ]
Fung, Albert [5 ]
Shaw, Wayne [5 ]
Usiskin, Keith [5 ]
Desai, Mehul [5 ]
Meininger, Gary [5 ]
机构
[1] Univ Bedfordshire, Luton & Dunstable Univ Hosp, Luton LU2 8LE, Beds, England
[2] Univ Bedfordshire, Bedfordshire & Hertfordshire Postgrad Med Sch, Luton LU2 8LE, Beds, England
[3] Atlanta Diabet Associates, Atlanta, GA 30309 USA
[4] Univ Western Ontario, London, ON N6G 4X8, Canada
[5] Janssen Res & Dev LLC, Raritan, NJ 08869 USA
[6] Janssen Res & Dev LLC, Titusville, NJ 08560 USA
关键词
Canagliflozin; Type 2 diabetes mellitus; Sodium glucose co-transporter 2 (SGLT2) inhibitor; Antihyperglycaemic agent; Older patients; POSITION STATEMENT; GLYCEMIC CONTROL; METFORMIN; MONOTHERAPY; SULFONYLUREA; ASSOCIATION; SITAGLIPTIN; THRESHOLD; PEOPLE; DIET;
D O I
10.1186/1472-6823-14-37
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Canagliflozin is a sodium glucose co-transporter 2 inhibitor developed for the treatment of patients with type 2 diabetes mellitus (T2DM). The efficacy and safety of canagliflozin were evaluated in patients with T2DM <65 and >= 65 years of age. Methods: Pooled data from 4 randomised, placebo-controlled, 26-week, Phase 3 studies (N = 2,313) evaluating canagliflozin 100 and 300 mg were analysed by age: <65 years (n = 1,868; mean age, 52.8 years) or >= 65 years (n = 445; mean age, 69.3 years). Efficacy evaluations included change from baseline in glycaemic parameters and systolic blood pressure (BP), and percent change from baseline in body weight. Assessment of safety/tolerability included adverse event (AE) reports, incidence of documented hypoglycaemia, and percent change from baseline in fasting plasma lipids. Results: Canagliflozin 100 and 300 mg reduced HbA(1c) and fasting plasma glucose relative to placebo in patients <65 and >= 65 years of age. Both canagliflozin doses reduced body weight and systolic BP relative to placebo in patients <65 and >= 65 years of age. Incidence of overall AEs was similar across all treatment groups in patients <65 and >= 65 years of age. Incidences of serious AEs and AE-related discontinuations were similar across all treatment groups in patients <65 years of age and higher with canagliflozin 100 mg than other groups in patients >= 65 years of age. As in patients <65 years of age, incidences of genital mycotic infections and osmotic diuresis-related AEs were higher with canagliflozin relative to placebo in those >= 65 years of age. Incidences of urinary tract infections (UTIs), renal-related AEs, AEs related to volume depletion, and documented hypoglycaemia episodes were similar across all treatment groups in patients >= 65 years of age; no notable trends were observed with canagliflozin 100 and 300 mg relative to placebo in these AEs among patients <65 years of age. Changes in lipid parameters with canagliflozin were similar in both age subsets. Conclusions: Canagliflozin improved glycaemic control, body weight, and systolic BP, and was generally well tolerated in older patients with T2DM.
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页数:11
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