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.

ABCC8 c.2500C>T 突变引起的青年起病型糖尿病急性肾损伤的遗传和临床见解:与 SGLT2 抑制剂相关的潜在风险因素

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作者:Zou Jing, Chen Xiang, Yu Hong-Ping, Chen Ying, He Kai-Ying, Ruan Dan-Dan, Zhu Juan, Chen Qian, Zhang Jian-Hui, Zhang Li, Gan Yu-Mian, Gao Mei-Zhu, Chen Li, Liang Ji-Xing, Wu Tian-Min, Liao Li-Sheng, Luo Jie-Wei
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 AKI in these patients may be pseudo-AKI associated with the use of SGLT2is. However, the proband exhibited symptoms indicative of rapidly progressing diabetic nephropathy. This study demonstrates that clinicians managing patients with MODY should be aware of the risk of acute and serious complications, particularly as SGLT2i may induce pseudo-AKI, which could ultimately compromise patients' long-term renal prognosis.

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