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Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes
BACKGROUND: Even though several oral anti-diabetic drugs (OAD) with various modes of action are replacing sulfonylurea (SU), some patients seem to be dependent on SU for adequate glycemic control. Therefore, we evaluated the clinical characteristics of such patients. METHODS: We selected the patient...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Endocrine Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722406/ https://www.ncbi.nlm.nih.gov/pubmed/26354492 http://dx.doi.org/10.3803/EnM.2015.30.4.509 |
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author | Min, Se Hee Kwak, Soo Heon Cho, Young Min Park, Kyong Soo Jung, Hye Seung |
author_facet | Min, Se Hee Kwak, Soo Heon Cho, Young Min Park, Kyong Soo Jung, Hye Seung |
author_sort | Min, Se Hee |
collection | PubMed |
description | BACKGROUND: Even though several oral anti-diabetic drugs (OAD) with various modes of action are replacing sulfonylurea (SU), some patients seem to be dependent on SU for adequate glycemic control. Therefore, we evaluated the clinical characteristics of such patients. METHODS: We selected the patients with type 2 diabetes who met following criteria from 2009 to 2014 at Seoul National University Hospital: glycated hemoglobin (HbA1c) was maintained below 7.5% for at least 6 months under small dose of SU (glimepiride ≤2 mg/day or equivalent dose); after discontinuation of SU, HbA1c increased ≥1.2% within 3 months or ≥1.5% within 6 months; and after resuming SU, HbA1c reduction was ≥0.8% or reduction of fasting plasma glucose was ≥40 mg/dL within 3 months. Patients with impaired hepatic or renal function, and steroid users were excluded. RESULTS: Nineteen subjects were enrolled: after averaged 4.8±1.5 months of SU-free period, HbA1c increased from 6.7%±0.4% to 8.8%±0.8% even though adding other OAD such as gliptins. However, HbA1c decreased to 7.4%±0.7% after resuming SU within 2.4±0.8 months. There was no sexual predominance. Despite their old age (67±11 years) and long duration of diabetes (18±10 years), fasting C-peptide was relatively well-reserved (3.9±2.6 ng/mL), and nephropathy was not observed (albumin-creatinine ratio 21.2±16.6 mg/g and estimated glomerular filtration rate 75.8±18.0 mL/min/1.73 m(2)). Strong family history was also noted (73.7%). CONCLUSION: Despite hypoglycemia risk of SU, it seemed indispensable for a subset of patients with regard to insulin secretion. Genetic influences would be evaluated. |
format | Online Article Text |
id | pubmed-4722406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47224062016-01-27 Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes Min, Se Hee Kwak, Soo Heon Cho, Young Min Park, Kyong Soo Jung, Hye Seung Endocrinol Metab (Seoul) Original Article BACKGROUND: Even though several oral anti-diabetic drugs (OAD) with various modes of action are replacing sulfonylurea (SU), some patients seem to be dependent on SU for adequate glycemic control. Therefore, we evaluated the clinical characteristics of such patients. METHODS: We selected the patients with type 2 diabetes who met following criteria from 2009 to 2014 at Seoul National University Hospital: glycated hemoglobin (HbA1c) was maintained below 7.5% for at least 6 months under small dose of SU (glimepiride ≤2 mg/day or equivalent dose); after discontinuation of SU, HbA1c increased ≥1.2% within 3 months or ≥1.5% within 6 months; and after resuming SU, HbA1c reduction was ≥0.8% or reduction of fasting plasma glucose was ≥40 mg/dL within 3 months. Patients with impaired hepatic or renal function, and steroid users were excluded. RESULTS: Nineteen subjects were enrolled: after averaged 4.8±1.5 months of SU-free period, HbA1c increased from 6.7%±0.4% to 8.8%±0.8% even though adding other OAD such as gliptins. However, HbA1c decreased to 7.4%±0.7% after resuming SU within 2.4±0.8 months. There was no sexual predominance. Despite their old age (67±11 years) and long duration of diabetes (18±10 years), fasting C-peptide was relatively well-reserved (3.9±2.6 ng/mL), and nephropathy was not observed (albumin-creatinine ratio 21.2±16.6 mg/g and estimated glomerular filtration rate 75.8±18.0 mL/min/1.73 m(2)). Strong family history was also noted (73.7%). CONCLUSION: Despite hypoglycemia risk of SU, it seemed indispensable for a subset of patients with regard to insulin secretion. Genetic influences would be evaluated. Korean Endocrine Society 2015-12 2015-12-31 /pmc/articles/PMC4722406/ /pubmed/26354492 http://dx.doi.org/10.3803/EnM.2015.30.4.509 Text en Copyright © 2015 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Min, Se Hee Kwak, Soo Heon Cho, Young Min Park, Kyong Soo Jung, Hye Seung Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes |
title | Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes |
title_full | Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes |
title_fullStr | Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes |
title_full_unstemmed | Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes |
title_short | Clinical Characteristics of Subjects with Sulfonylurea-Dependent Type 2 Diabetes |
title_sort | clinical characteristics of subjects with sulfonylurea-dependent type 2 diabetes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722406/ https://www.ncbi.nlm.nih.gov/pubmed/26354492 http://dx.doi.org/10.3803/EnM.2015.30.4.509 |
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