Genetic and clinical insights into acute kidney injury in maturity‑onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitors

作者：Jing Zou, Xiang Chen, Hongping Yu, Ying Chen, Kai-Ying He, Dan‐dan Ruan, Juan Zhu, Qian Chen, Jianhui Zhang, Li Zhang, Yu‐Mian Gan, Mei-zhu Gao, Li Chen, Jixing Liang, Tong Wu, Lisheng Liao, Jie-wei Luo · 发表于：Experimental and Therapeutic Medicine · 年份：2025 · DOI：10.3892/etm.2025.12914 · 被引用次数：3 · 研究领域：Diabetes Treatment and Management、Pancreatic function and diabetes、Chronic Kidney Disease and Diabetes

Mature‑onset diabetes of the young (MODY) is an autosomal dominant genetic disease that is typically diagnosed during childhood or early adolescence. The primary pathogenesis of MODY involves gene mutations that impair insulin synthesis and/or secretion by islet β cells, rendering the condition independent of insulin resistance. A family with the MODY‑12 phenotype caused by an ATP‑binding cassette subfamily C member 8 ( ABCC8 ) gene mutation was investigated in the present study. Clinical data were collected from all family members, and second‑generation gene sequencing and Sanger sequencing were performed. The suspected pathogenic mutation was validated by Sanger sequencing, and the three‑dimensional structure of the pathogenic variant protein was predicted and simulated using the Swiss‑Model platform. Five individuals with MODY‑12, including the proband, were identified in this family. Second‑generation gene sequencing confirmed that all family members carried the ABCC8 c.2500C>T (p.Arg834Cys) mutation. Structural modeling revealed that the replacement of arginine at position 834 in the wild‑type protein with cysteine results in the formation of an additional hydrogen bond with the surrounding amino acids. In addition, the ABCC8 c.2500C>T carriers in this family experienced recurrent diabetic ketoacidosis and acute kidney involvement (AKI) phenotypes, and all patients had a history of sodium‑glucose transporter 2 inhibitor (SGLT2i) use. We hypothesize that AK...