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Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus
OBJECTIVE: Type 1 diabetes mellitus (T1DM) is a chronic immune-mediated disease. Diabetic peripheral neuropathy (DPN) is an important microvascular complication of T1DM. One of the most important risk factors for the development of DPN is poor glycemic control. We evaluated the prevalence of DPN amo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shahid Beheshti University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904742/ https://www.ncbi.nlm.nih.gov/pubmed/29696049 |
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author | GHAEMI, Nosrat HASANABADI, Hossein ASHRAFZADEH, Farah SARVARI, Somaye RAHIMI, Hamidreza HASHEMIAN, Somayyeh |
author_facet | GHAEMI, Nosrat HASANABADI, Hossein ASHRAFZADEH, Farah SARVARI, Somaye RAHIMI, Hamidreza HASHEMIAN, Somayyeh |
author_sort | GHAEMI, Nosrat |
collection | PubMed |
description | OBJECTIVE: Type 1 diabetes mellitus (T1DM) is a chronic immune-mediated disease. Diabetic peripheral neuropathy (DPN) is an important microvascular complication of T1DM. One of the most important risk factors for the development of DPN is poor glycemic control. We evaluated the prevalence of DPN among T1DM patients and determined the association between DPN and glycated hemoglobin (HbA1c) level. MATERIALS & METHODS: The subjects were recruited prospectively upon initial evaluation at Imam Reza Hospital, Mashhad, Iran from Jan 2013 to Jan 2015. Patients with T1DM were selected based on the inclusion criteria (i.e., age of 6≤yr and absence of other co-morbidities). DPN was assessed through electrodiagnostic studies and neurological examinations, while diabetes control was evaluated by measuring the HbA1c level. RESULTS: Fifty patients with T1DM were enrolled in this study. The mean diabetes duration of patients was 8.38±3.79 yr (mean age16.68±6.68 yr). The mean HbA1c level was 8.6±2.1% in patients without DPN and 10.5±3 in those with DPN (P=0.016). Overall, 24% of the subjects were presented with DPN according to nerve conduction velocity study (NCV) findings. A positive correlation was found between NCV and clinical symptoms with signs (P<0.001, r=0.45 and P<0.001, r=0.644, respectively). Sensitivity and specificity of neurological examination for DPN diagnosis were 91.7% and 63.2%, respectively. Poor diabetes control is associated with DPN. Moreover, HbA1c level was used as an index for glycemic control over the past 3 months. CONCLUSION: Rigid blood glucose control and periodic neurological examinations were the best strategies to prevent DPN. |
format | Online Article Text |
id | pubmed-5904742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Shahid Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-59047422018-06-01 Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus GHAEMI, Nosrat HASANABADI, Hossein ASHRAFZADEH, Farah SARVARI, Somaye RAHIMI, Hamidreza HASHEMIAN, Somayyeh Iran J Child Neurol Original Article OBJECTIVE: Type 1 diabetes mellitus (T1DM) is a chronic immune-mediated disease. Diabetic peripheral neuropathy (DPN) is an important microvascular complication of T1DM. One of the most important risk factors for the development of DPN is poor glycemic control. We evaluated the prevalence of DPN among T1DM patients and determined the association between DPN and glycated hemoglobin (HbA1c) level. MATERIALS & METHODS: The subjects were recruited prospectively upon initial evaluation at Imam Reza Hospital, Mashhad, Iran from Jan 2013 to Jan 2015. Patients with T1DM were selected based on the inclusion criteria (i.e., age of 6≤yr and absence of other co-morbidities). DPN was assessed through electrodiagnostic studies and neurological examinations, while diabetes control was evaluated by measuring the HbA1c level. RESULTS: Fifty patients with T1DM were enrolled in this study. The mean diabetes duration of patients was 8.38±3.79 yr (mean age16.68±6.68 yr). The mean HbA1c level was 8.6±2.1% in patients without DPN and 10.5±3 in those with DPN (P=0.016). Overall, 24% of the subjects were presented with DPN according to nerve conduction velocity study (NCV) findings. A positive correlation was found between NCV and clinical symptoms with signs (P<0.001, r=0.45 and P<0.001, r=0.644, respectively). Sensitivity and specificity of neurological examination for DPN diagnosis were 91.7% and 63.2%, respectively. Poor diabetes control is associated with DPN. Moreover, HbA1c level was used as an index for glycemic control over the past 3 months. CONCLUSION: Rigid blood glucose control and periodic neurological examinations were the best strategies to prevent DPN. Shahid Beheshti University of Medical Sciences 2018 /pmc/articles/PMC5904742/ /pubmed/29696049 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article GHAEMI, Nosrat HASANABADI, Hossein ASHRAFZADEH, Farah SARVARI, Somaye RAHIMI, Hamidreza HASHEMIAN, Somayyeh Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus |
title | Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus |
title_full | Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus |
title_fullStr | Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus |
title_full_unstemmed | Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus |
title_short | Peripheral Neuropathy in Children and Adolescents with Insulin-dependent Diabetes Mellitus |
title_sort | peripheral neuropathy in children and adolescents with insulin-dependent diabetes mellitus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904742/ https://www.ncbi.nlm.nih.gov/pubmed/29696049 |
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