A Woman With HNF1A-Associated Monogenic Diabetes Treated Successfully With Repaglinide Monotherapy

Katherine Cuan DO , Ilana R. Bass MD
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Abstract

Background/Objective

Monogenic diabetes is a rare type of diabetes that is commonly misdiagnosed as type 1 or 2 diabetes mellitus, which adversely impacts patient care. Such cases are particularly challenging given the heterogeneity in presentation and overlap with other types of diabetes. As the sole use of meglitinides, especially repaglinide, to treat HNF1A-associated monogenic diabetes has been rarely reported in a few other observational studies, we describe a patient who was treated successfully with repaglinide.

Case Report

A 38-year-old woman with type 1 diabetes mellitus, congenital deafness, chronic kidney disease, and retinopathy presented with difficulty controlling her blood glucose levels. Although initially treated with insulin, she had periods of noncompliance with insulin without experiencing diabetic ketoacidosis. Although on insulin therapy, she experienced multiple episodes of hypoglycemia. The laboratory tests showed a hemoglobin A1c level of 10.8%, c-peptide level of 2.7 ng/mL (1.1-4.4 ng/mL), glucose level of 192 mg/dL, creatinine level of 1.23 ng/dL, and severely increased microalbumin-to-creatinine ratio of 638 mg/g (normal range, 0-29 mg/g). Pancreatic autoantibodies were negative. Genetic testing revealed a diagnosis of HNF1A-associated monogenic diabetes (c. 1340C>T (p.P447L)). She was ultimately treated with repaglinide after trials of sulfonylureas and dipeptidyl peptidase 4 inhibitors led to frequent hypoglycemia and a significant increase in the hemoglobin A1c level, respectively.

Discussion

This case highlights the importance of correctly diagnosing monogenic diabetes and reports the successful use of repaglinide to treat HNF1A-associated monogenic diabetes.

Conclusion

Patients with HNF1A-associated monogenic diabetes who do not achieve euglycemia with sulfonylureas and insulin may be successfully treated with repaglinide monotherapy.

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一名女性 Hnf1a 相关单基因糖尿病患者接受瑞格列奈单药治疗获得成功
背景/目的单基因糖尿病是一种罕见的糖尿病类型,通常会被误诊为 1 型或 2 型糖尿病,从而对患者护理造成不利影响。由于表现的异质性以及与其他类型糖尿病的重叠,这类病例尤其具有挑战性。病例报告一位 38 岁的女性患者患有 1 型糖尿病、先天性耳聋、慢性肾病和视网膜病变,她的血糖水平难以控制。虽然最初使用胰岛素治疗,但她曾有一段时间不按时使用胰岛素,而且没有出现糖尿病酮症酸中毒。虽然接受了胰岛素治疗,但她还是多次出现低血糖症状。实验室检查结果显示,血红蛋白 A1c 水平为 10.8%,c 肽水平为 2.7 纳克/毫升(1.1-4.4 纳克/毫升),葡萄糖水平为 192 毫克/分升,肌酐水平为 1.23 纳克/分升,微量白蛋白与肌酐比值严重升高,达到 638 毫克/克(正常范围为 0-29 毫克/克)。胰腺自身抗体呈阴性。基因检测显示,她被诊断为 HNF1A 相关单基因糖尿病(c. 1340C>T (p.P447L))。在试用磺脲类药物和二肽基肽酶 4 抑制剂分别导致频繁低血糖和血红蛋白 A1c 水平显著升高后,她最终接受了瑞格列奈治疗。讨论本病例强调了正确诊断单基因糖尿病的重要性,并报告了使用瑞格列奈治疗 HNF1A 相关单基因糖尿病的成功案例。
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来源期刊
AACE Clinical Case Reports
AACE Clinical Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
55 days
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