Successful Transition to Sulfonylurea for Relapsed Monogenic Diabetes Due to Rare 6q23.3 Duplication.

JCEM case reports Pub Date : 2024-10-16 eCollection Date: 2024-10-01 DOI:10.1210/jcemcr/luae180
Doha Hassan, David B Allen, Melinda Chen
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Abstract

Transient neonatal diabetes mellitus (TNDM) due to 6q duplication usually presents in the first 4 months of life, resolves before 18 months of life, and recurs in adolescence or adulthood. Insulin is the first-line treatment for chromosome 6-related neonatal diabetes in infancy. While there is no ideal treatment for patients with relapsed TNDM, residual β-cell function after remission of neonatal diabetes indicates a potential role for insulin secretagogues. Patients with 6q24 duplication have been successfully transitioned from insulin to sulfonylureas (SUs) in adolescence. We present the first report to our knowledge of TNDM secondary to a rare 6q23.3 duplication for which reemergence of diabetes was successfully transitioned from insulin to SU treatment. The successful transition to SU improved glycemic control, cost-effectiveness, and overall quality of life, while decreasing occurrence of hypoglycemia.

因罕见的 6q23.3 重复而复发的单基因糖尿病患者成功转用磺脲类药物。
因 6q 染色体重复而导致的一过性新生儿糖尿病(TNDM)通常在出生后 4 个月内出现,在出生后 18 个月内缓解,并在青春期或成年期复发。胰岛素是治疗与 6 号染色体相关的新生儿糖尿病的一线疗法。虽然对复发的 TNDM 患者没有理想的治疗方法,但新生儿糖尿病缓解后残留的 β 细胞功能表明胰岛素促泌剂可能发挥作用。6q24基因重复的患者在青春期已成功地从胰岛素过渡到磺脲类药物(SUs)。我们首次报告了继发于罕见的 6q23.3 基因重复的 TNDM 患者,他们成功地从胰岛素治疗过渡到了磺脲类药物治疗。成功过渡到 SU 治疗改善了血糖控制、成本效益和整体生活质量,同时减少了低血糖的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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