Longitudinal monitoring of urinary C-peptide levels following discontinuation of sacubitril/valsartan in a type 2 diabetes patient: a case report and literature review.

IF 1.2 Q4 ENDOCRINOLOGY & METABOLISM
Diabetology International Pub Date : 2025-03-31 eCollection Date: 2025-07-01 DOI:10.1007/s13340-025-00816-y
Keiichiro Kondo, Hiroto Minamino, Takaaki Murakami, Emi Okamura, Takuro Hakata, Yohei Ueda, Daisuke Taura, Daisuke Yabe
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Abstract

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.

1例2型糖尿病患者停用苏比里尔/缬沙坦后尿c肽水平的纵向监测:1例报告和文献综述
我们报告两例糖尿病患者用苏比里尔/缬沙坦治疗,其尿c肽动力学表现出显著差异。第一个病例是一名84岁的日本男性2型糖尿病和高血压患者,他在接受血管紧张素受体-neprilysin抑制剂(ARNi)苏比里尔/缬沙坦治疗期间尿c肽水平明显升高。尽管血清c肽水平正常,但尿c肽排泄异常高,提示sacubitril/缬沙坦可能通过抑制neprilysin改变了c肽清除。停用苏比里尔/缬沙坦后尿c肽水平逐渐下降,但仍高于血清c肽水平。每日对尿c肽的纵向监测显示其水平有明显的波动,表明奈普利菌素对c肽排泄的抑制作用是长期的,可能是复杂的。此外,我们观察到停用苏比里尔/缬沙坦后,心房钠尿肽(ANP)水平相应下降,进一步支持奈普利素抑制在改变肽代谢中的作用。相比之下,第二个病例涉及一名78岁的日本妇女,患有胰岛素依赖型1型糖尿病,血清c肽水平未检测到。在她的病例中,尽管ARNi治疗,尿c肽水平仍未检测到。这些病例强调需要仔细的临床解释尿c肽水平的患者接受奈普利素抑制剂。在ARNi治疗下使用尿c肽水平评估胰腺β细胞功能时,重要的是要考虑延长监测尿c肽水平、停药时间和血清c肽水平,以确保准确评估。
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来源期刊
Diabetology International
Diabetology International ENDOCRINOLOGY & METABOLISM-
CiteScore
3.90
自引率
4.50%
发文量
42
期刊介绍: Diabetology International, the official journal of the Japan Diabetes Society, publishes original research articles about experimental research and clinical studies in diabetes and related areas. The journal also presents editorials, reviews, commentaries, reports of expert committees, and case reports on any aspect of diabetes. Diabetology International welcomes submissions from researchers, clinicians, and health professionals throughout the world who are interested in research, treatment, and care of patients with diabetes. All manuscripts are peer-reviewed to assure that high-quality information in the field of diabetes is made available to readers. Manuscripts are reviewed with due respect for the author''s confidentiality. At the same time, reviewers also have rights to confidentiality, which are respected by the editors. The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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