Weight Gain Was Associated With Worsening Glycemia and Cardiovascular and Kidney Outcomes in Patients With Type 2 Diabetes Independent of Diabetes Medication in the GRADE Randomized Controlled Trial.

IF 16.6
Diabetes care Pub Date : 2025-06-01 DOI:10.2337/dc24-2825
Deborah J Wexler, W Timothy Garvey, Alokananda Ghosh, Erin J Kazemi, Heidi Krause-Steinrauf, Andrew J Ahmann, Janet Brown-Friday, Sabina Casula, Andrea L Cherrington, Tom A Elasy, Stephen P Fortmann, Jonathan A Krakoff, Sunder Mudaliar, Margaret Tiktin, Naji Younes
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Abstract

Objective: Weight gain with glucose-lowering medications may interfere with effective type 2 diabetes (T2D) management. We evaluated weight change and the effect of weight gain on outcomes over 5 years on four diabetes medications.

Research design and methods: The Glycemia Reduction Approaches in Diabetes: A Comparative Effectiveness Study (GRADE) randomized trial compared the addition of insulin glargine, glimepiride, liraglutide, or sitagliptin to metformin in participants with T2D. We report weight change and hazard ratio (HR) per kilogram of weight change for HbA1c >7.5%; cardiovascular disease (CVD), kidney disease, and neuropathy outcomes; and diabetes treatment satisfaction.

Results: Participants (n = 4,980) were 57 ± 10 years, 44% non-White, with HbA1c 7.5% ± 0.5%, and BMI 34.3 ± 6.8 kg/m2. Mean (95% CI) weight change (kg) during the first year was -3.5 (-3.8,-3.2) with liraglutide,-1.07 (-1.4,-0.78) with sitagliptin, 0.45 (0.16, 0.74) with glargine, and 0.89 (0.60, 1.2) with glimepiride (P < 0.0001). Thereafter, weight decreased in all groups. Weight gain within the first 6 months was associated with increased risk of HbA1c >7.5%, with modest differences by treatment, and with subsequent CVD (HR 1.03 [95% CI 1.005, 1.06]). Weight gain at 1 year was associated with increased risk of HbA1c >7.5% (HR 1.05 [1.04, 1.07]) and kidney disease (HR 1.03 [1.01, 1.06]). Baseline weight, but not weight gain, was associated with new-onset neuropathy. Weight gain was associated with lower diabetes treatment satisfaction.

Conclusions: Liraglutide and sitagliptin were associated with initial weight loss and glargine and glimepiride with slight weight gain, followed by weight loss in metformin-treated T2D. Weight gain was associated with worsening glycemia and increased risk of cardiovascular and kidney outcomes largely independent of treatment.

在GRADE随机对照试验中,体重增加与2型糖尿病患者血糖、心血管和肾脏预后恶化相关,而非糖尿病药物治疗。
目的:体重增加与降糖药物可能会干扰有效的2型糖尿病(T2D)管理。我们评估了体重变化和体重增加对四种糖尿病药物5年疗效的影响。研究设计和方法:糖尿病降糖方法:一项比较效果研究(GRADE)随机试验比较了t2dm患者在二甲双胍基础上添加甘精胰岛素、格列美脲、利拉鲁肽或西格列汀的效果。我们报告了糖化血红蛋白(HbA1c)的体重变化和每公斤体重变化的风险比(HR)为7.5%;心血管疾病(CVD)、肾脏疾病和神经病变结局;糖尿病治疗满意度。结果:参与者(n = 4,980)年龄为57±10岁,44%非白种人,HbA1c为7.5%±0.5%,BMI为34.3±6.8 kg/m2。利拉鲁肽组第一年的平均体重变化(kg) (95% CI)为-3.5(-3.8,-3.2),西格列汀组为-1.07(-1.4,-0.78),甘精组为0.45(0.16,0.74),格列美脲组为0.89 (0.60,1.2)(P < 0.0001)。此后,各组体重均有所下降。前6个月内体重增加与HbA1c风险增加7.5%相关,治疗差异不大,与随后的CVD相关(HR 1.03 [95% CI 1.005, 1.06])。1年后体重增加与HbA1c bbb7.5% (HR 1.05[1.04, 1.07])和肾脏疾病(HR 1.03[1.01, 1.06])的风险增加相关。基线体重与新发神经病变相关,但与体重增加无关。体重增加与较低的糖尿病治疗满意度相关。结论:利拉鲁肽和西格列汀与初始体重减轻相关,甘精和格列美脲与轻度体重增加相关,随后二甲双胍治疗的T2D患者体重减轻。体重增加与血糖恶化、心血管和肾脏结局风险增加有关,这在很大程度上与治疗无关。
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CiteScore
29.50
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