Tonstad Serena, Lawrence David
Section for Preventive Cardiology, Oslo University Hospital, Oslo, Norway.
Pfizer Inc., New York City, New York, USA.
J Diabetes Investig. 2017 Jan;8(1):93-100. doi: 10.1111/jdi.12543. Epub 2016 Jul 14.
AIMS/INTRODUCTION: Stopping smoking deserves high priority in preventing complications of diabetes; however, only sparse data are available regarding the efficacy of pharmacotherapy in smokers with diabetes. We assessed the efficacy and safety of varenicline in smokers with diabetes who participated in 15 double-blind, randomized, placebo-controlled studies.
This retrospective pooled analysis included data from smokers of ≥10 cigarettes per day with diabetes. Participants received varenicline 1 mg b.i.d. or placebo for 12 weeks. We examined carbon monoxide-confirmed continuous abstinence rates (CARs) for weeks 9-12, 9-24 and 9-52, and compared safety in participants with and without diabetes.
Of 6,771 participants, 323 had diabetes (varenicline n = 162; placebo n = 161). Week 9-12 CAR was higher with varenicline than placebo (43.8% vs 24.8%; odds ratio 2.36, 95% CI 1.47-3.79), as was week 9-24 CAR (27.5% vs 14.4%; odds ratio 2.25, 95% CI 1.27-4.00). Week 9-52 CAR was 18.4% for varenicline and 10.1% for placebo (odds ratio 2.00, 95% CI 0.90-4.49). The most commonly-reported adverse events in participants with diabetes for varenicline vs placebo were: nausea (27.2% vs 8.1%); headache (9.3% vs 9.9%); and insomnia (8.6% vs 5.6%), incidences that were similar in participants without diabetes (29.6% vs 9.7%; 13.4% vs 10.9%; and 11.4% vs 7.1%, respectively). Weight gain in quitters with diabetes (1.7 kg) was similar to that of those without diabetes (2.1 kg).
Varenicline was an effective and well-tolerated aid for smoking cessation in individuals with diabetes. Safety was comparable with participants without diabetes.
目的/引言:戒烟在预防糖尿病并发症方面应被高度重视;然而,关于药物疗法对糖尿病吸烟者疗效的可用数据却很少。我们评估了参与15项双盲、随机、安慰剂对照研究的糖尿病吸烟者使用伐尼克兰的疗效和安全性。
这项回顾性汇总分析纳入了每天吸烟≥10支的糖尿病吸烟者的数据。参与者接受1毫克伐尼克兰,每日两次,或安慰剂,为期12周。我们检查了第9至12周、第9至24周和第9至52周经一氧化碳确认的持续戒烟率(CARs),并比较了有糖尿病和无糖尿病参与者的安全性。
在6771名参与者中,323人患有糖尿病(伐尼克兰组n = 162;安慰剂组n = 161)。伐尼克兰组第9至12周的CAR高于安慰剂组(43.8%对24.8%;优势比2.36,95%置信区间1.47 - 3.79),第9至24周的CAR也是如此(27.5%对14.4%;优势比2.25,95%置信区间1.27 - 4.00)。伐尼克兰组第9至52周的CAR为18.4%,安慰剂组为10.1%(优势比2.00,95%置信区间0.90 - 4.49)。糖尿病参与者中,伐尼克兰组与安慰剂组最常报告的不良事件为:恶心(27.2%对8.1%);头痛(9.3%对9.9%);失眠(8.6%对5.6%),在无糖尿病参与者中的发生率分别为29.6%对9.7%;13.4%对10.9%;11.4%对7.1%,两者相似。糖尿病戒烟者的体重增加(1.7千克)与无糖尿病者(2.1千克)相似。
伐尼克兰是糖尿病患者戒烟的一种有效且耐受性良好的辅助药物。安全性与无糖尿病参与者相当。