Kamrul-Hasan A B M, Mondal Sunetra, Dutta Deep, Nagendra Lakshmi, Kabir Mohammed Ruhul, Pappachan Joseph M
Department of Endocrinology Mymensingh Medical College Mymensingh Bangladesh.
Department of Endocrinology NRS Medical College Kolkata India.
Obes Sci Pract. 2024 Dec 24;10(6):e70032. doi: 10.1002/osp4.70032. eCollection 2024 Dec.
Endogenous glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) regulate islet cell function. GLP-1 receptor agonists (GLP-1RAs) have been associated with an elevated risk of acute pancreatitis. Data on the pancreatic safety of tirzepatide (a dual GLP-1 and GIP agonist) and its effects on islet cell function in randomized controlled trials (RCTs) are scarce. Moreover, no meta-analysis has comprehensively examined such effects of tirzepatide.
Electronic databases were searched for RCTs with tirzepatide as the intervention and a placebo or active comparator as the control. The primary outcome was adjudication-confirmed pancreatitis; secondary outcomes were the percent changes from baseline in serum pancreatic amylase, lipase, insulin, C-peptide, glucagon, and homeostasis model assessment of insulin resistance (HOMA2-IR).
Seventeen RCTs with 18 published reports involving 14,645 subjects were analyzed. Over a follow-up duration of 12-72 weeks, tirzepatide had identical risks of pancreatitis to placebo (tirzepatide 5 mg: RR 2.04, 95% CI [0.27-15.69], = 0.49; 10 mg: RR 0.63, 95% CI [0.08-5.12], = 0.67; and 15 mg: RR 1.26, 95% CI [0.36-4.98], = 0.72). Tirzepatide was also associated with comparable risks of pancreatitis to insulin and GLP-1RAs. However, tirzepatide (at all doses) caused greater increases in pancreatic amylase and lipase than placebo and insulin. Individuals on tirzepatide 15 mg and GLP-1RAs had similar risks of having increased lipase levels. The percent reductions in fasting insulin were greater with tirzepatide 10 and 15 mg than with placebo. All doses of tirzepatide caused greater percent reductions in fasting insulin, C-peptide, and glucagon than GLP-1RAs. Compared to placebo and GLP-1RAs, the percent reductions in HOMA2-IR were greater with all doses of tirzepatide.
The meta-analysis provides evidence of the safety of tirzepatide regarding pancreatitis and establishes its positive effect on islet cell functions and insulin resistance.
内源性胰高血糖素样肽-1(GLP-1)和葡萄糖依赖性促胰岛素多肽(GIP)调节胰岛细胞功能。GLP-1受体激动剂(GLP-1RAs)与急性胰腺炎风险升高有关。关于替尔泊肽(一种GLP-1和GIP双重激动剂)胰腺安全性及其在随机对照试验(RCTs)中对胰岛细胞功能影响的数据很少。此外,尚无荟萃分析全面研究替尔泊肽的此类作用。
检索电子数据库,查找以替尔泊肽为干预措施、以安慰剂或活性对照为对照的RCTs。主要结局是经判定确认的胰腺炎;次要结局是血清胰淀粉酶、脂肪酶、胰岛素、C肽、胰高血糖素以及胰岛素抵抗稳态模型评估(HOMA2-IR)较基线的变化百分比。
分析了17项RCTs,有18篇发表报告,涉及14645名受试者。在12至72周的随访期间,替尔泊肽发生胰腺炎的风险与安慰剂相同(替尔泊肽5mg:RR 2.04,95%CI[0.27 - 15.69],P = 0.49;10mg:RR 0.63,95%CI[0.08 - 5.12],P = 0.67;15mg:RR 1.26,95%CI[0.36 - 4.98],P = 0.72)。替尔泊肽发生胰腺炎的风险也与胰岛素和GLP-1RAs相当。然而,替尔泊肽(所有剂量)导致胰淀粉酶和脂肪酶较安慰剂和胰岛素有更大幅度升高。使用15mg替尔泊肽和GLP-1RAs的个体脂肪酶水平升高的风险相似。10mg和15mg替尔泊肽使空腹胰岛素降低的百分比大于安慰剂。所有剂量的替尔泊肽使空腹胰岛素、C肽和胰高血糖素降低的百分比均大于GLP-1RAs。与安慰剂和GLP-1RAs相比,所有剂量的替尔泊肽使HOMA2-IR降低的百分比更大。
该荟萃分析提供了替尔泊肽在胰腺炎方面安全性的证据,并证实了其对胰岛细胞功能和胰岛素抵抗的积极作用。