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Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing
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 gl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270490/ https://www.ncbi.nlm.nih.gov/pubmed/37327293 http://dx.doi.org/10.1097/MD.0000000000033959 |
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author | Yang, Luyang Fan, Jinmeng Liu, Yunfeng Ren, Yi Liu, Zekun Fu, Hairui Qi, Hao Yang, Jing |
author_facet | Yang, Luyang Fan, Jinmeng Liu, Yunfeng Ren, Yi Liu, Zekun Fu, Hairui Qi, Hao Yang, Jing |
author_sort | Yang, Luyang |
collection | PubMed |
description | 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. PATIENT CONCERNS: A 51-year-old Chinese woman presented to emergency department because of intermittent fatigue for more than 10 years. DIAGNOSES: 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). INTERVENTIONS: She was given potassium and magnesium supplements, and dapagliflozin was used to control her blood glucose. OUTCOMES: After treatments, her fatigue symptoms were reduced, blood potassium and magnesium levels were increased, and blood glucose levels were well controlled. LESSONS: 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. |
format | Online Article Text |
id | pubmed-10270490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-102704902023-06-16 Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing Yang, Luyang Fan, Jinmeng Liu, Yunfeng Ren, Yi Liu, Zekun Fu, Hairui Qi, Hao Yang, Jing Medicine (Baltimore) 4300 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. PATIENT CONCERNS: A 51-year-old Chinese woman presented to emergency department because of intermittent fatigue for more than 10 years. DIAGNOSES: 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). INTERVENTIONS: She was given potassium and magnesium supplements, and dapagliflozin was used to control her blood glucose. OUTCOMES: After treatments, her fatigue symptoms were reduced, blood potassium and magnesium levels were increased, and blood glucose levels were well controlled. LESSONS: 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. Lippincott Williams & Wilkins 2023-06-16 /pmc/articles/PMC10270490/ /pubmed/37327293 http://dx.doi.org/10.1097/MD.0000000000033959 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 4300 Yang, Luyang Fan, Jinmeng Liu, Yunfeng Ren, Yi Liu, Zekun Fu, Hairui Qi, Hao Yang, Jing Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing |
title | Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing |
title_full | Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing |
title_fullStr | Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing |
title_full_unstemmed | Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing |
title_short | Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing |
title_sort | case report: gitelman syndrome with diabetes: confirmed by both hydrochlorothiazide test and genetic testing |
topic | 4300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270490/ https://www.ncbi.nlm.nih.gov/pubmed/37327293 http://dx.doi.org/10.1097/MD.0000000000033959 |
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