Department of Endocrinology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China.
Shanxi Medical University, Taiyuan, Shanxi Province, China.
Medicine (Baltimore). 2023 Jun 16;102(24):e33959. doi: 10.1097/MD.0000000000033959.
Gitelman syndrome (GS) is an autosomal recessive tubulopathy caused by mutations of the SLC12A3 gene. It is characterized by hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria. Hypokalemia, hypomagnesemia, and increased renin-angiotensin-aldosterone system (RAAS) activity can cause glucose metabolism dysfunction. The diagnosis of GS includes clinical diagnosis, genetic diagnosis and functional diagnosis. The gene diagnosis is the golden criterion while as functional diagnosis is of great value in differential diagnosis. The hydrochlorothiazide (HCT) test is helpful to distinguish GS from batter syndrome, but few cases have been reported to have HCT testing.
A 51-year-old Chinese woman presented to emergency department because of intermittent fatigue for more than 10 years.
Laboratory test results showed hypokalemia, hypomagnesemia, hypocalciuria and metabolic alkalosis. The HCT test showed no response. Using next-generation and Sanger sequencing, we identified 2 heterozygous missense variants (c.533C > T:p.S178L and c.2582G > A:p.R861H) in the SLC12A3 gene. In addition, the patient was diagnosed with type 2 diabetes mellitus 7 years ago. Based on these findings, the patient was diagnosed with GS with type 2 diabetic mellitus (T2DM).
She was given potassium and magnesium supplements, and dapagliflozin was used to control her blood glucose.
After treatments, her fatigue symptoms were reduced, blood potassium and magnesium levels were increased, and blood glucose levels were well controlled.
When GS is considered in patients with unexplained hypokalemia, the HCT test can be used for differential diagnosis, and genetic testing can be continued to confirm the diagnosis when conditions are available. GS patients often have abnormal glucose metabolism, which is mainly caused by hypokalemia, hypomagnesemia, and secondary activation of RAAS. When a patient is diagnosed with GS and type 2 diabetes, sodium-glucose cotransporter 2 inhibitors (SGLT2i) can be used to control the blood glucose level and assist in raising blood magnesium.
Gitelman 综合征(GS)是一种常染色体隐性肾小管疾病,由 SLC12A3 基因突变引起。其特征为低钾性代谢性碱中毒、低镁血症和低钙尿症。低钾血症、低镁血症和肾素-血管紧张素-醛固酮系统(RAAS)活性增加可导致葡萄糖代谢功能障碍。GS 的诊断包括临床诊断、基因诊断和功能诊断。基因诊断是金标准,而功能诊断对鉴别诊断具有重要价值。氢氯噻嗪(HCT)试验有助于将 GS 与巴特综合征相鉴别,但报道的 HCT 试验病例较少。
一名 51 岁的中国女性因间歇性乏力 10 余年就诊于急诊科。
实验室检查结果显示低钾血症、低镁血症、低钙尿症和代谢性碱中毒。HCT 试验无反应。采用新一代测序和 Sanger 测序,我们在 SLC12A3 基因中发现 2 个杂合错义变异(c.533C>T:p.S178L 和 c.2582G>A:p.R861H)。此外,该患者 7 年前被诊断为 2 型糖尿病。基于这些发现,该患者被诊断为合并 2 型糖尿病的 GS。
给予补钾和补镁治疗,给予达格列净控制血糖。
治疗后,患者乏力症状减轻,血钾和血镁水平升高,血糖控制良好。
当不明原因低钾血症患者考虑 GS 时,可进行 HCT 试验进行鉴别诊断,有条件时可继续进行基因检测以明确诊断。GS 患者常存在葡萄糖代谢异常,主要由低钾血症、低镁血症和 RAAS 继发性激活引起。当患者被诊断为 GS 和 2 型糖尿病时,可使用钠-葡萄糖协同转运蛋白 2 抑制剂(SGLT2i)控制血糖水平并辅助升高血镁。