Glucagon-like Peptide-1 receptor agonists versus dipeptidyl-peptidase 4 inhibitors in advanced chronic kidney disease and end stage kidney disease: Real world effectiveness and persistence of therapy.

IF 2.9 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
F N U Sidra, Shubham Agarwal, Paola Lockhart Pastor, Donglu Xie, Xilong Li, Ildiko Lingvay
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引用次数: 0

Abstract

Background: Atherosclerotic cardiovascular disease is the leading cause of death in people with type 2 diabetes (T2D) and chronic kidney disease (CKD) or end-stage kidney disease (ESKD). Glucagon-Like Peptide-1 receptor agonists (GLP-1RA) reduce cardiovascular events, improve glycemic control, promote weight loss, and slow progression of nephropathy. Despite these benefits and professional society treatment guidelines recommendations, GLP-1RAs remain under-utilized in people with advanced CKD and ESKD due to tolerability and safety concerns.

Methods: We conducted a retrospective cohort study comparing clinical outcomes and medication use details after initiating GLP-1RA or dipeptidyl-peptidase 4 inhibitor (DPP-4i) in people with T2D and advanced CKD or ESKD. Eligible patients were identified via electronic health record query with extraction of baseline demographics, vital signs, and laboratory values. A manual chart review was undertaken to confirm eligibility, medication use, and extract a detailed account of all side effects.

Results: A total of 236 eligible patients (149 in the GLP-1RA group and 87 in the DPP-4i group) were identified. The average duration of treatment was 1036 (±909.9) and 1109 (±1090.9) days for GLP-1RA and DPP-4i, respectively. The average percentage weight loss from baseline to 36 months of treatment in the GLP-1RA group was -9.6 % (95 % CI, -11.3 to -7.8) versus -2.4 % (95 % CI, -5.4 to 0.5) in the DPP-4i group (estimated treatment difference (ETD) -7.1 (95 % CI, -10.6 to -3.7) percentage-points, p < 0.001). The change in HbA1c from baseline to 36 months of treatment was significantly greater in the GLP-1RA (-1.0 %) compared with the DPP-4i group (0.2 %) (ETD -1.2 (95 % CI, -2.1 to -0.3) percentage-points, p = 0.04).

Conclusion: In patients with T2D and advanced CKD or ESKD, treatment with GLP-1RAs in a real-world setting had long treatment persistence, and compared to DPP-4is, was associated with greater weight loss and glycemic improvement.

胰高血糖素样肽-1受体激动剂与二肽基肽酶4抑制剂在晚期慢性肾病和终末期肾病中的疗效和治疗持久性
背景:动脉粥样硬化性心血管疾病是2型糖尿病(T2D)和慢性肾脏疾病(CKD)或终末期肾脏疾病(ESKD)患者死亡的主要原因。胰高血糖素样肽-1受体激动剂(GLP-1RA)减少心血管事件,改善血糖控制,促进体重减轻,减缓肾病的进展。尽管有这些益处和专业协会治疗指南的建议,由于耐受性和安全性问题,GLP-1RAs在晚期CKD和ESKD患者中的应用仍然不足。方法:我们进行了一项回顾性队列研究,比较T2D和晚期CKD或ESKD患者在启动GLP-1RA或二肽基肽酶4抑制剂(DPP-4i)后的临床结果和药物使用细节。通过提取基线人口统计学、生命体征和实验室值的电子健康记录查询确定符合条件的患者。进行了手动图表审查,以确认资格,药物使用,并提取所有副作用的详细说明。结果:共确定236例符合条件的患者(GLP-1RA组149例,DPP-4i组87例)。GLP-1RA和DPP-4i的平均治疗时间分别为1036(±909.9)天和1109(±1090.9)天。GLP-1RA组从基线到治疗36个月的平均体重下降百分比为- 9.6% (95% CI, -11.3至-7.8),而DPP-4i组为- 2.4% (95% CI, -5.4至0.5)(估计治疗差异(ETD) -7.1 (95% CI, -10.6至-3.7)个百分点,p。在T2D和晚期CKD或ESKD患者中,在现实环境中使用GLP-1RAs治疗具有较长的治疗持久性,并且与DPP-4is相比,与更大的体重减轻和血糖改善相关。
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来源期刊
Journal of diabetes and its complications
Journal of diabetes and its complications 医学-内分泌学与代谢
CiteScore
5.90
自引率
3.30%
发文量
153
审稿时长
16 days
期刊介绍: Journal of Diabetes and Its Complications (JDC) is a journal for health care practitioners and researchers, that publishes original research about the pathogenesis, diagnosis and management of diabetes mellitus and its complications. JDC also publishes articles on physiological and molecular aspects of glucose homeostasis. The primary purpose of JDC is to act as a source of information usable by diabetes practitioners and researchers to increase their knowledge about mechanisms of diabetes and complications development, and promote better management of people with diabetes who are at risk for those complications. Manuscripts submitted to JDC can report any aspect of basic, translational or clinical research as well as epidemiology. Topics can range broadly from early prediabetes to late-stage complicated diabetes. Topics relevant to basic/translational reports include pancreatic islet dysfunction and insulin resistance, altered adipose tissue function in diabetes, altered neuronal control of glucose homeostasis and mechanisms of drug action. Topics relevant to diabetic complications include diabetic retinopathy, neuropathy and nephropathy; peripheral vascular disease and coronary heart disease; gastrointestinal disorders, renal failure and impotence; and hypertension and hyperlipidemia.
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