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Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level

BACKGROUND: Type 2 Diabetes Mellitus is one of the most common metabolic diseases worldwide. The most common complication of DM is diabetic neuropathy (DN), especially diabetic polyneuropathy (DPN). Vitamin D plays an important role in the pathogenesis of DN, thus affecting its severity which can be...

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Autores principales: Fitri, Aida, Sjahrir, Hasan, Bachtiar, Adang, Ichwan, Muhammad, Fitri, Fasihah Irfani, Rambe, Aldy Safruddin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Republic of Macedonia 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876802/
https://www.ncbi.nlm.nih.gov/pubmed/31777620
http://dx.doi.org/10.3889/oamjms.2019.454
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author Fitri, Aida
Sjahrir, Hasan
Bachtiar, Adang
Ichwan, Muhammad
Fitri, Fasihah Irfani
Rambe, Aldy Safruddin
author_facet Fitri, Aida
Sjahrir, Hasan
Bachtiar, Adang
Ichwan, Muhammad
Fitri, Fasihah Irfani
Rambe, Aldy Safruddin
author_sort Fitri, Aida
collection PubMed
description BACKGROUND: Type 2 Diabetes Mellitus is one of the most common metabolic diseases worldwide. The most common complication of DM is diabetic neuropathy (DN), especially diabetic polyneuropathy (DPN). Vitamin D plays an important role in the pathogenesis of DN, thus affecting its severity which can be assessed using nerve conduction study (NCS). AIM: This study aimed to develop a predictive model of DPN severity based on vitamin D level. METHODS: This was a prospective cohort study involving 50 subjects with DM which was conducted in Haji Adam Malik General Hospital Medan. All subjects were fulfilling inclusion criteria underwent laboratory examination to determine HbA1c and 25 (OH) D levels. Predictive variables were sex, age, duration of DM, smoking status, type and number of anti-diabetic drugs, the presence of metabolic syndrome, HbA1c and vitamin D levels. A scoring system was developed to determine a predictive model. The DPN severity was assessed using NCS and was re-evaluated after 3 months. RESULTS: Most of the subjects were female (60%), belonged to ≥ 50 years old age-group (88%), with DM duration < 5 years (56%), were non-smoker (90%), we’re using one anti-diabetic drug (60%), were using insulin (50%), had metabolic syndrome (68%), had HbA1c level > 6.5% (94%), and had vitamin D level < 20 ng/ml (56%). A score of > 4 on this predictive model of DPN severity had a relative risk (RR) of 2.70. The predictive model had a sensitivity of 82.8% and specificity of 61.9%. CONCLUSION: A score of higher than 4 on this predictive model showed a 2.7 times higher risk of severe DPN. A predictive model of DPN severity based on vitamin D level had high sensitivity and specificity.
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spelling pubmed-68768022019-11-27 Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level Fitri, Aida Sjahrir, Hasan Bachtiar, Adang Ichwan, Muhammad Fitri, Fasihah Irfani Rambe, Aldy Safruddin Open Access Maced J Med Sci Neuroscience, Neurology and Psychiatry BACKGROUND: Type 2 Diabetes Mellitus is one of the most common metabolic diseases worldwide. The most common complication of DM is diabetic neuropathy (DN), especially diabetic polyneuropathy (DPN). Vitamin D plays an important role in the pathogenesis of DN, thus affecting its severity which can be assessed using nerve conduction study (NCS). AIM: This study aimed to develop a predictive model of DPN severity based on vitamin D level. METHODS: This was a prospective cohort study involving 50 subjects with DM which was conducted in Haji Adam Malik General Hospital Medan. All subjects were fulfilling inclusion criteria underwent laboratory examination to determine HbA1c and 25 (OH) D levels. Predictive variables were sex, age, duration of DM, smoking status, type and number of anti-diabetic drugs, the presence of metabolic syndrome, HbA1c and vitamin D levels. A scoring system was developed to determine a predictive model. The DPN severity was assessed using NCS and was re-evaluated after 3 months. RESULTS: Most of the subjects were female (60%), belonged to ≥ 50 years old age-group (88%), with DM duration < 5 years (56%), were non-smoker (90%), we’re using one anti-diabetic drug (60%), were using insulin (50%), had metabolic syndrome (68%), had HbA1c level > 6.5% (94%), and had vitamin D level < 20 ng/ml (56%). A score of > 4 on this predictive model of DPN severity had a relative risk (RR) of 2.70. The predictive model had a sensitivity of 82.8% and specificity of 61.9%. CONCLUSION: A score of higher than 4 on this predictive model showed a 2.7 times higher risk of severe DPN. A predictive model of DPN severity based on vitamin D level had high sensitivity and specificity. Republic of Macedonia 2019-08-20 /pmc/articles/PMC6876802/ /pubmed/31777620 http://dx.doi.org/10.3889/oamjms.2019.454 Text en Copyright: © 2019 Aida Fitri, Hasan Sjahrir, Adang Bachtiar, Muhammad Ichwan, Fasihah Irfani Fitri, Aldy Safruddin Rambe. http://creativecommons.org/licenses/CC BY-NC/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
spellingShingle Neuroscience, Neurology and Psychiatry
Fitri, Aida
Sjahrir, Hasan
Bachtiar, Adang
Ichwan, Muhammad
Fitri, Fasihah Irfani
Rambe, Aldy Safruddin
Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level
title Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level
title_full Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level
title_fullStr Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level
title_full_unstemmed Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level
title_short Predictive Model of Diabetic Polyneuropathy Severity Based on Vitamin D Level
title_sort predictive model of diabetic polyneuropathy severity based on vitamin d level
topic Neuroscience, Neurology and Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876802/
https://www.ncbi.nlm.nih.gov/pubmed/31777620
http://dx.doi.org/10.3889/oamjms.2019.454
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