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Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease

Mutations in hepatocyte nuclear factor 1β gene (HNF1B) are responsible for a multisystemic syndrome where monogenic diabetes (classically known as MODY 5) and renal anomalies, mostly cysts, are the most characteristic findings. Urogenital malformations, altered liver function tests, hypomagnesemia o...

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Autores principales: Carrillo, Elena, Lomas, Amparo, Pinés, Pedro J, Lamas, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488326/
https://www.ncbi.nlm.nih.gov/pubmed/28680642
http://dx.doi.org/10.1530/EDM-17-0052
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author Carrillo, Elena
Lomas, Amparo
Pinés, Pedro J
Lamas, Cristina
author_facet Carrillo, Elena
Lomas, Amparo
Pinés, Pedro J
Lamas, Cristina
author_sort Carrillo, Elena
collection PubMed
description Mutations in hepatocyte nuclear factor 1β gene (HNF1B) are responsible for a multisystemic syndrome where monogenic diabetes (classically known as MODY 5) and renal anomalies, mostly cysts, are the most characteristic findings. Urogenital malformations, altered liver function tests, hypomagnesemia or hyperuricemia and gout are also part of the syndrome. Diabetes in these patients usually requires early insulinization. We present the case of a young non-obese male patient with a personal history of renal multicystic dysplasia and a debut of diabetes during adolescence with simple hyperglycemia, negative pancreatic autoimmunity and detectable C-peptide levels. He also presented epididymal and seminal vesicle cysts, hypertransaminasemia, hyperuricemia and low magnesium levels. In the light of these facts we considered the possibility of a HNF1B mutation. The sequencing study of this gene confirmed a heterozygous mutation leading to a truncated and less functional protein. Genetic studies of his relatives were negative; consequently, it was classified as a de novo mutation. In particular, our patient maintained good control of his diabetes on oral antidiabetic agents for a long period of time. He eventually needed insulinization although oral therapy was continued alongside, allowing reduction of prandial insulin requirements. The real prevalence of mutations in HNF1B is probably underestimated owing to a wide phenotypical variability. As endocrinologists, we should consider this possibility in young non-obese diabetic patients with a history of chronic non-diabetic nephropathy, especially in the presence of some of the other characteristic manifestations. LEARNING POINTS: HNF1B mutations are a rare cause of monogenic diabetes, often being a part of a multisystemic syndrome. The combination of young-onset diabetes and genitourinary anomalies with slowly progressive nephropathy of non-diabetic origin in non-obese subjects should rise the suspicion of such occurrence. A family history may not be present. Once diagnosis is made, treatment of diabetes with oral agents is worth trying, since the response can be sustained for a longer period than the one usually described. Oral treatment can help postpone insulinization and, once this is necessary, can help reduce the required doses.
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spelling pubmed-54883262017-07-05 Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease Carrillo, Elena Lomas, Amparo Pinés, Pedro J Lamas, Cristina Endocrinol Diabetes Metab Case Rep Insight into Disease Pathogenesis or Mechanism of Therapy Mutations in hepatocyte nuclear factor 1β gene (HNF1B) are responsible for a multisystemic syndrome where monogenic diabetes (classically known as MODY 5) and renal anomalies, mostly cysts, are the most characteristic findings. Urogenital malformations, altered liver function tests, hypomagnesemia or hyperuricemia and gout are also part of the syndrome. Diabetes in these patients usually requires early insulinization. We present the case of a young non-obese male patient with a personal history of renal multicystic dysplasia and a debut of diabetes during adolescence with simple hyperglycemia, negative pancreatic autoimmunity and detectable C-peptide levels. He also presented epididymal and seminal vesicle cysts, hypertransaminasemia, hyperuricemia and low magnesium levels. In the light of these facts we considered the possibility of a HNF1B mutation. The sequencing study of this gene confirmed a heterozygous mutation leading to a truncated and less functional protein. Genetic studies of his relatives were negative; consequently, it was classified as a de novo mutation. In particular, our patient maintained good control of his diabetes on oral antidiabetic agents for a long period of time. He eventually needed insulinization although oral therapy was continued alongside, allowing reduction of prandial insulin requirements. The real prevalence of mutations in HNF1B is probably underestimated owing to a wide phenotypical variability. As endocrinologists, we should consider this possibility in young non-obese diabetic patients with a history of chronic non-diabetic nephropathy, especially in the presence of some of the other characteristic manifestations. LEARNING POINTS: HNF1B mutations are a rare cause of monogenic diabetes, often being a part of a multisystemic syndrome. The combination of young-onset diabetes and genitourinary anomalies with slowly progressive nephropathy of non-diabetic origin in non-obese subjects should rise the suspicion of such occurrence. A family history may not be present. Once diagnosis is made, treatment of diabetes with oral agents is worth trying, since the response can be sustained for a longer period than the one usually described. Oral treatment can help postpone insulinization and, once this is necessary, can help reduce the required doses. Bioscientifica Ltd 2017-06-23 /pmc/articles/PMC5488326/ /pubmed/28680642 http://dx.doi.org/10.1530/EDM-17-0052 Text en © 2017 The authors http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en_GB This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en_GB) .
spellingShingle Insight into Disease Pathogenesis or Mechanism of Therapy
Carrillo, Elena
Lomas, Amparo
Pinés, Pedro J
Lamas, Cristina
Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
title Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
title_full Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
title_fullStr Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
title_full_unstemmed Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
title_short Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease
title_sort long-lasting response to oral therapy in a young male with monogenic diabetes as part of hnf1b-related disease
topic Insight into Disease Pathogenesis or Mechanism of Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488326/
https://www.ncbi.nlm.nih.gov/pubmed/28680642
http://dx.doi.org/10.1530/EDM-17-0052
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