Kondo Keiichiro, Minamino Hiroto, Murakami Takaaki, Okamura Emi, Hakata Takuro, Ueda Yohei, Taura Daisuke, Yabe Daisuke
Department of Diabetes, Endocrinology and Nutrition, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Diabetol Int. 2025 Mar 31;16(3):580-585. doi: 10.1007/s13340-025-00816-y. eCollection 2025 Jul.
We report two cases of diabetes mellitus treated with sacubitril/valsartan, whose urinary C-peptide dynamics exhibited significant difference. The first case is an 84-year-old Japanese man with type 2 diabetes and hypertension who exhibited significantly elevated urinary C-peptide levels during treatment with sacubitril/valsartan, an angiotensin receptor-neprilysin inhibitor (ARNi). Despite normal serum C-peptide levels, his urinary C-peptide excretion was disproportionately high, suggesting that sacubitril/valsartan may have altered C-peptide clearance through neprilysin inhibition. The discontinuation of sacubitril/valsartan demonstrated gradual decline of urinary C-peptide levels, although they remained elevated compared to serum ones. Daily longitudinal monitoring of urinary C-peptide revealed marked fluctuations of its levels, indicating a prolonged and potentially complex effect of neprilysin inhibition on C-peptide excretion. Additionally, we observed a corresponding decrease in atrial natriuretic peptide (ANP) levels after discontinuation of sacubitril/valsartan, further supporting the role of neprilysin inhibition in altering peptide metabolism. In contrast, the second case involves a 78-year-old Japanese woman with insulin-dependent type 1 diabetes and undetectable serum C-peptide levels. In her case, urinary C-peptide levels remained undetectable despite ARNi therapy. These cases highlight the need for careful clinical interpretation of urinary C-peptide levels in patients receiving neprilysin inhibitors. When evaluating pancreatic β-cell function using urinary C-peptide levels under ARNi therapy, it is crucial to consider extended monitoring of urinary C-peptide levels, the duration of drug withdrawal, and serum C-peptide levels to ensure accurate assessment.
我们报告了两例接受沙库巴曲缬沙坦治疗的糖尿病患者,其尿C肽动力学表现出显著差异。第一例是一名84岁的日本男性,患有2型糖尿病和高血压,在接受血管紧张素受体脑啡肽酶抑制剂(ARNi)沙库巴曲缬沙坦治疗期间,尿C肽水平显著升高。尽管血清C肽水平正常,但他的尿C肽排泄量却异常高,这表明沙库巴曲缬沙坦可能通过抑制脑啡肽酶改变了C肽清除率。停用沙库巴曲缬沙坦后,尿C肽水平逐渐下降,尽管与血清C肽水平相比仍处于升高状态。对尿C肽进行每日纵向监测发现其水平有明显波动,这表明脑啡肽酶抑制对C肽排泄有长期且可能复杂的影响。此外,我们观察到停用沙库巴曲缬沙坦后心房利钠肽(ANP)水平相应下降,进一步支持了脑啡肽酶抑制在改变肽代谢中的作用。相比之下,第二例是一名78岁的日本女性,患有胰岛素依赖型1型糖尿病,血清C肽水平检测不到。在她的病例中,尽管接受了ARNi治疗,但尿C肽水平仍检测不到。这些病例凸显了在接受脑啡肽酶抑制剂治疗的患者中对尿C肽水平进行仔细临床解读的必要性。在ARNi治疗下使用尿C肽水平评估胰腺β细胞功能时,至关重要的是要考虑对尿C肽水平进行延长监测、停药持续时间以及血清C肽水平,以确保准确评估。