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Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana

OBJECTIVE: Peripheral sensory neuropathy (PSN) is a common complication of type 2 diabetes (T2DM) that can lead to frequent ulcerations, lower extremities, and reduced quality of life. Imbalance in the circulating levels of angiogenic growth factors, notably, angiopoietin (Ang)-1, Ang-2 and vascular...

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Autores principales: Agyekum, Jennifer A., Yeboah, Kwame
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563058/
https://www.ncbi.nlm.nih.gov/pubmed/37822668
http://dx.doi.org/10.1016/j.jcte.2023.100327
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author Agyekum, Jennifer A.
Yeboah, Kwame
author_facet Agyekum, Jennifer A.
Yeboah, Kwame
author_sort Agyekum, Jennifer A.
collection PubMed
description OBJECTIVE: Peripheral sensory neuropathy (PSN) is a common complication of type 2 diabetes (T2DM) that can lead to frequent ulcerations, lower extremities, and reduced quality of life. Imbalance in the circulating levels of angiogenic growth factors, notably, angiopoietin (Ang)-1, Ang-2 and vascular endothelial growth factor (VEGF) may be among the underlying mechanisms of PSN in T2DM patients. We studied the association between PSN and angiogenic growth factors, Ang-1, Ang-2 and VEGF in T2DM patients in Ghana. METHODS: In a case-control study design, PSN was evaluated in 160 patients with T2DM and 108 nondiabetic controls using vibration perception threshold (VPT) and diabetic neurological examination (DNE). The definition of PSN was abnormal VPT (≥25 mV) or the presence of neuropathic symptoms on examination (DNE score > 3). In addition, fasting venous blood samples were collected to measure circulating levels of Ang-1, Ang-2 and VEGF. RESULTS: Compared to non-diabetic controls, patients with T2DM had a higher prevalence of PSN using abnormal VPT (20.6 % vs 2.8 %, p < 0.001) or neuropathic symptoms (35.6 % vs 3.7 %, p < 0.001). Compared to nondiabetic controls, patients with T2DM had increased levels of Ang-2 [597 (274 – 1005) vs 838 (473 – 1241) ng/ml, p = 0.018] and VEGF [48.4 (17.4 – 110.1) vs 72.2 (28 – 201.8), p = 0.025] and decreased Ang-1 levels [41.1 (30 – 57.3) vs 36.1 (24.7 – 42.1) ng/ml, p = 0.01]. In regression analyses, an increase in Ang-1 levels was associated with decreased odds, while an increase in Ang-2 levels was associated with increased odds, of abnormal VPT and neuropathic symptoms in T2DM patients. CONCLUSION: In our study population, PSN was associated with reduced plasma levels of Ang-1 and increased plasma levels of Ang-2 in patients with T2DM. Therefore, an imbalance of angiopoietins may be associated with PSN in T2DM.
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spelling pubmed-105630582023-10-11 Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana Agyekum, Jennifer A. Yeboah, Kwame J Clin Transl Endocrinol Research Paper OBJECTIVE: Peripheral sensory neuropathy (PSN) is a common complication of type 2 diabetes (T2DM) that can lead to frequent ulcerations, lower extremities, and reduced quality of life. Imbalance in the circulating levels of angiogenic growth factors, notably, angiopoietin (Ang)-1, Ang-2 and vascular endothelial growth factor (VEGF) may be among the underlying mechanisms of PSN in T2DM patients. We studied the association between PSN and angiogenic growth factors, Ang-1, Ang-2 and VEGF in T2DM patients in Ghana. METHODS: In a case-control study design, PSN was evaluated in 160 patients with T2DM and 108 nondiabetic controls using vibration perception threshold (VPT) and diabetic neurological examination (DNE). The definition of PSN was abnormal VPT (≥25 mV) or the presence of neuropathic symptoms on examination (DNE score > 3). In addition, fasting venous blood samples were collected to measure circulating levels of Ang-1, Ang-2 and VEGF. RESULTS: Compared to non-diabetic controls, patients with T2DM had a higher prevalence of PSN using abnormal VPT (20.6 % vs 2.8 %, p < 0.001) or neuropathic symptoms (35.6 % vs 3.7 %, p < 0.001). Compared to nondiabetic controls, patients with T2DM had increased levels of Ang-2 [597 (274 – 1005) vs 838 (473 – 1241) ng/ml, p = 0.018] and VEGF [48.4 (17.4 – 110.1) vs 72.2 (28 – 201.8), p = 0.025] and decreased Ang-1 levels [41.1 (30 – 57.3) vs 36.1 (24.7 – 42.1) ng/ml, p = 0.01]. In regression analyses, an increase in Ang-1 levels was associated with decreased odds, while an increase in Ang-2 levels was associated with increased odds, of abnormal VPT and neuropathic symptoms in T2DM patients. CONCLUSION: In our study population, PSN was associated with reduced plasma levels of Ang-1 and increased plasma levels of Ang-2 in patients with T2DM. Therefore, an imbalance of angiopoietins may be associated with PSN in T2DM. Elsevier 2023-10-06 /pmc/articles/PMC10563058/ /pubmed/37822668 http://dx.doi.org/10.1016/j.jcte.2023.100327 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Agyekum, Jennifer A.
Yeboah, Kwame
Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana
title Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana
title_full Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana
title_fullStr Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana
title_full_unstemmed Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana
title_short Peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in Ghana
title_sort peripheral sensory neuropathy is associated with circulating angiopoietins in type 2 diabetes patients in ghana
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563058/
https://www.ncbi.nlm.nih.gov/pubmed/37822668
http://dx.doi.org/10.1016/j.jcte.2023.100327
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