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Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications
BACKGROUND: Diagnosis of infection in diabetic foot ulcer (DFU) is not always simple. The analytic precision of procalcitonin (PCT) was evaluated to clarify the use of PCT for distinguish the presence of infection in DFU in comparison to other inflammatory markers. MATERIALS AND METHODS: This study...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583618/ https://www.ncbi.nlm.nih.gov/pubmed/28900451 http://dx.doi.org/10.4103/jrms.JRMS_906_16 |
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author | AL-Shammaree, Shatha Abdul Wadood Abu-ALkaseem, Banan Akram Salman, Isam N |
author_facet | AL-Shammaree, Shatha Abdul Wadood Abu-ALkaseem, Banan Akram Salman, Isam N |
author_sort | AL-Shammaree, Shatha Abdul Wadood |
collection | PubMed |
description | BACKGROUND: Diagnosis of infection in diabetic foot ulcer (DFU) is not always simple. The analytic precision of procalcitonin (PCT) was evaluated to clarify the use of PCT for distinguish the presence of infection in DFU in comparison to other inflammatory markers. MATERIALS AND METHODS: This study comprised 88 subjects distributed into four groups: 16 nondiabetic healthy subjects (group control), 17 patients with type 2 diabetes mellitus without foot Complication (group DM), 25 patients with noninfected diabetic foot (group NIDF), and 30 patients with infected diabetic foot (group IDF). Fasting blood samples were taken for measurement of glucose, hemoglobin A1C, lipid profile, renal function, erythrocyte sedimentation rate (ESR), and white blood cell (WBC) and its derivatives. Plasma PCT was determined using an enzyme-linked immunosorbent assay. RESULTS: PCT, WBC, ESR, and neutrophils (NEU) were found significantly higher in IDF group than other groups. The receiver operating characteristic analysis showed that sensitivity, specificity, the best cutoff value, and the area under the curve were for ESR (100%, 93%, 31.5 mm/h, 1; P < 0.001), for PCT (87.5%, 86.7%, 66.55 pg/dl, 0.977; P < 0.001), for NEU (93.8%, 93.3%, 5.35, 0.957; P < 0.001) and for WBC (93.8%, 90%, 9.29 × 10(9)/L, 0.942; P < 0.001), respectively. CONCLUSION: The outcomes of this study recommend that PCT can be an asymptomatic marker in the diagnosis of infection in DFU with higher Wagner grades in combination with different inflammatory markers. |
format | Online Article Text |
id | pubmed-5583618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55836182017-09-12 Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications AL-Shammaree, Shatha Abdul Wadood Abu-ALkaseem, Banan Akram Salman, Isam N J Res Med Sci Original Article BACKGROUND: Diagnosis of infection in diabetic foot ulcer (DFU) is not always simple. The analytic precision of procalcitonin (PCT) was evaluated to clarify the use of PCT for distinguish the presence of infection in DFU in comparison to other inflammatory markers. MATERIALS AND METHODS: This study comprised 88 subjects distributed into four groups: 16 nondiabetic healthy subjects (group control), 17 patients with type 2 diabetes mellitus without foot Complication (group DM), 25 patients with noninfected diabetic foot (group NIDF), and 30 patients with infected diabetic foot (group IDF). Fasting blood samples were taken for measurement of glucose, hemoglobin A1C, lipid profile, renal function, erythrocyte sedimentation rate (ESR), and white blood cell (WBC) and its derivatives. Plasma PCT was determined using an enzyme-linked immunosorbent assay. RESULTS: PCT, WBC, ESR, and neutrophils (NEU) were found significantly higher in IDF group than other groups. The receiver operating characteristic analysis showed that sensitivity, specificity, the best cutoff value, and the area under the curve were for ESR (100%, 93%, 31.5 mm/h, 1; P < 0.001), for PCT (87.5%, 86.7%, 66.55 pg/dl, 0.977; P < 0.001), for NEU (93.8%, 93.3%, 5.35, 0.957; P < 0.001) and for WBC (93.8%, 90%, 9.29 × 10(9)/L, 0.942; P < 0.001), respectively. CONCLUSION: The outcomes of this study recommend that PCT can be an asymptomatic marker in the diagnosis of infection in DFU with higher Wagner grades in combination with different inflammatory markers. Medknow Publications & Media Pvt Ltd 2017-08-16 /pmc/articles/PMC5583618/ /pubmed/28900451 http://dx.doi.org/10.4103/jrms.JRMS_906_16 Text en Copyright: © 2017 Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article AL-Shammaree, Shatha Abdul Wadood Abu-ALkaseem, Banan Akram Salman, Isam N Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
title | Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
title_full | Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
title_fullStr | Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
title_full_unstemmed | Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
title_short | Procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
title_sort | procalcitonin levels and other biochemical parameters in patients with or without diabetic foot complications |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583618/ https://www.ncbi.nlm.nih.gov/pubmed/28900451 http://dx.doi.org/10.4103/jrms.JRMS_906_16 |
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