Biomarkers for Early Detection of Charcot Arthropathy: A Prospective Study on Type 2 Diabetes Patients with Severe Neuropathy
Background: Charcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic neuropathy (DN) patients. The debilitating prognosis demands early detection to prevent the development and progression of this disorder. Dy...
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Published in: | Foot & ankle international Vol. 45; no. 2; pp. 175 - 178 |
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Abstract | Background:
Charcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic neuropathy (DN) patients. The debilitating prognosis demands early detection to prevent the development and progression of this disorder. Dysregulated and persistent production of inflammatory cytokines is reported as the key element in initiating osteoclastogenesis in CA. The study analyzed the potential association of markers of inflammation and bone turnover of prediagnostic serum samples on CA.
Methods:
Seventy-one type 2 severe DN patients were selected based on inclusion-exclusion criteria. Serum samples of interleukin 6 (IL-6), osteoprotegerin (OPG), bone alkaline phosphatase (BALP), and C-reactive protein (CRP) were analyzed. These patients were followed for the development of symptoms of CA for 12 months. In the year of monitoring, 7 patients developed CA (group 1), whereas the remaining 64 patients did not develop CA (group 2).
Results:
The rate of development of CA in patients with severe DN was 9.8%. In this group, significantly increased median values of HbA1c (group 2: 8.00 [7.00-9.00], group 1: 10.00 [9.25-11.50], P = .013); IL-6 (group 2: 1.21 [0.72-2.16], group 1: 11.08 [6.65-63.64], P = .008); and CRP (group 2: 1.25 [0.78-3.20], group 1: 3.31 [1.18-41.33], P = .041) were found. The receiver operating characteristic analysis showed that IL-6 was more strongly associated with the onset of CA (IL-6: area under the curve = 0.808; P = .008) than CRP. Cut-off values of ≥6.6 for IL-6 show potential to rule out CA in high-risk patients, with a positive predictive value of 26.1%, a negative predictive value of 97.9%, a sensitivity of 85.7%, and a specificity of 73.4%.
Conclusion:
In our study population, we found that an exacerbated inflammatory state, reflected by IL-6 values, generally occurred in DN patients before the clinical detection of CA.
Level of Evidence:
Level II, prospective comparative study. |
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AbstractList | Background:
Charcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic neuropathy (DN) patients. The debilitating prognosis demands early detection to prevent the development and progression of this disorder. Dysregulated and persistent production of inflammatory cytokines is reported as the key element in initiating osteoclastogenesis in CA. The study analyzed the potential association of markers of inflammation and bone turnover of prediagnostic serum samples on CA.
Methods:
Seventy-one type 2 severe DN patients were selected based on inclusion-exclusion criteria. Serum samples of interleukin 6 (IL-6), osteoprotegerin (OPG), bone alkaline phosphatase (BALP), and C-reactive protein (CRP) were analyzed. These patients were followed for the development of symptoms of CA for 12 months. In the year of monitoring, 7 patients developed CA (group 1), whereas the remaining 64 patients did not develop CA (group 2).
Results:
The rate of development of CA in patients with severe DN was 9.8%. In this group, significantly increased median values of HbA1c (group 2: 8.00 [7.00-9.00], group 1: 10.00 [9.25-11.50], P = .013); IL-6 (group 2: 1.21 [0.72-2.16], group 1: 11.08 [6.65-63.64], P = .008); and CRP (group 2: 1.25 [0.78-3.20], group 1: 3.31 [1.18-41.33], P = .041) were found. The receiver operating characteristic analysis showed that IL-6 was more strongly associated with the onset of CA (IL-6: area under the curve = 0.808; P = .008) than CRP. Cut-off values of ≥6.6 for IL-6 show potential to rule out CA in high-risk patients, with a positive predictive value of 26.1%, a negative predictive value of 97.9%, a sensitivity of 85.7%, and a specificity of 73.4%.
Conclusion:
In our study population, we found that an exacerbated inflammatory state, reflected by IL-6 values, generally occurred in DN patients before the clinical detection of CA.
Level of Evidence:
Level II, prospective comparative study. BACKGROUNDCharcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic neuropathy (DN) patients. The debilitating prognosis demands early detection to prevent the development and progression of this disorder. Dysregulated and persistent production of inflammatory cytokines is reported as the key element in initiating osteoclastogenesis in CA. The study analyzed the potential association of markers of inflammation and bone turnover of prediagnostic serum samples on CA.METHODSSeventy-one type 2 severe DN patients were selected based on inclusion-exclusion criteria. Serum samples of interleukin 6 (IL-6), osteoprotegerin (OPG), bone alkaline phosphatase (BALP), and C-reactive protein (CRP) were analyzed. These patients were followed for the development of symptoms of CA for 12 months. In the year of monitoring, 7 patients developed CA (group 1), whereas the remaining 64 patients did not develop CA (group 2).RESULTSThe rate of development of CA in patients with severe DN was 9.8%. In this group, significantly increased median values of HbA1c (group 2: 8.00 [7.00-9.00], group 1: 10.00 [9.25-11.50], P = .013); IL-6 (group 2: 1.21 [0.72-2.16], group 1: 11.08 [6.65-63.64], P = .008); and CRP (group 2: 1.25 [0.78-3.20], group 1: 3.31 [1.18-41.33], P = .041) were found. The receiver operating characteristic analysis showed that IL-6 was more strongly associated with the onset of CA (IL-6: area under the curve = 0.808; P = .008) than CRP. Cut-off values of ≥6.6 for IL-6 show potential to rule out CA in high-risk patients, with a positive predictive value of 26.1%, a negative predictive value of 97.9%, a sensitivity of 85.7%, and a specificity of 73.4%.CONCLUSIONIn our study population, we found that an exacerbated inflammatory state, reflected by IL-6 values, generally occurred in DN patients before the clinical detection of CA.LEVEL OF EVIDENCELevel II, prospective comparative study. Charcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic neuropathy (DN) patients. The debilitating prognosis demands early detection to prevent the development and progression of this disorder. Dysregulated and persistent production of inflammatory cytokines is reported as the key element in initiating osteoclastogenesis in CA. The study analyzed the potential association of markers of inflammation and bone turnover of prediagnostic serum samples on CA. Seventy-one type 2 severe DN patients were selected based on inclusion-exclusion criteria. Serum samples of interleukin 6 (IL-6), osteoprotegerin (OPG), bone alkaline phosphatase (BALP), and C-reactive protein (CRP) were analyzed. These patients were followed for the development of symptoms of CA for 12 months. In the year of monitoring, 7 patients developed CA (group 1), whereas the remaining 64 patients did not develop CA (group 2). The rate of development of CA in patients with severe DN was 9.8%. In this group, significantly increased median values of Hb (group 2: 8.00 [7.00-9.00], group 1: 10.00 [9.25-11.50], = .013); IL-6 (group 2: 1.21 [0.72-2.16], group 1: 11.08 [6.65-63.64], = .008); and CRP (group 2: 1.25 [0.78-3.20], group 1: 3.31 [1.18-41.33], = .041) were found. The receiver operating characteristic analysis showed that IL-6 was more strongly associated with the onset of CA (IL-6: area under the curve = 0.808; = .008) than CRP. Cut-off values of ≥6.6 for IL-6 show potential to rule out CA in high-risk patients, with a positive predictive value of 26.1%, a negative predictive value of 97.9%, a sensitivity of 85.7%, and a specificity of 73.4%. In our study population, we found that an exacerbated inflammatory state, reflected by IL-6 values, generally occurred in DN patients before the clinical detection of CA. Level II, prospective comparative study. |
Author | Praveen, Valiyaparambil Pavithran Bal, Arun Dharmadas, Salini Kumar, Harish Sukumaran Mangalanandan, Thacho Pillay, Minnie Vivek, Lakshmanan |
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Cites_doi | 10.11622/smedj.2016074 10.17161/kjm.v11i4.8709 10.1038/s41598-017-00563-4 10.1016/j.diabres.2020.108337 10.1111/dme.12590 10.1177/107110070602701007 10.1053/j.jfas.2004.01.001 10.2337/dc09-0243 10.2337/db10-1220 |
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Keywords | Interleukin 6 Biomarkers Charcot arthropathy C reactive protein osteoprotegerin |
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References | Petrova, Dew, Musto 2015; 32 Vopat, Nentwig, Chong, Agan, Shields, Yang 2018; 11 Anna, Anna, Marcelina, Bożena, Magdalena, Joanna 2020; 166 Foltz, Fallat, Schwartz 2004; 43 Baumhauer, O’Keefe, Schon, Pinzur 2006; 27 Fauzi, Chung, Latif 2016; 57 Ndip, Williams, Jude 2011; 60 Bruhn-Olszewska, Korzon-Burakowska, Węgrzyn, Jakobkiewicz-Banecka 2017; 7 Divyateja, Shu, Pearson, Scammell, Game, Jeffcoate 2011; 54 Pitocco, Zelano, Gioffre 2009; 32 bibr8-10711007231213645 bibr6-10711007231213645 bibr10-10711007231213645 bibr3-10711007231213645 bibr7-10711007231213645 bibr2-10711007231213645 bibr9-10711007231213645 bibr5-10711007231213645 bibr1-10711007231213645 Divyateja H (bibr4-10711007231213645) 2011; 54 |
References_xml | – volume: 43 start-page: 87 issue: 2 year: 2004 end-page: 92 article-title: Usefulness of a brief assessment battery for early detection of Charcot foot deformity in patients with diabetes publication-title: J Foot Ankle Surg contributor: fullname: Schwartz – volume: 32 start-page: 1694 issue: 9 year: 2009 end-page: 1697 article-title: Association between osteoprotegerin G1181C and T245G polymorphisms and diabetic charcot neuroarthropathy: a case-control study publication-title: Diabetes Care contributor: fullname: Gioffre – volume: 11 start-page: 114 issue: 4 year: 2018 end-page: 119 article-title: Initial diagnosis and management for acute Charcot neuroarthropathy publication-title: Kans J Med contributor: fullname: Yang – volume: 57 start-page: 198 issue: 4 year: 2016 end-page: 203 article-title: Risk factors of diabetic foot Charcot arthropathy: a case-control study at a Malaysian tertiary care center publication-title: Singapore Med J contributor: fullname: Latif – volume: 166 start-page: 108337 year: 2020 article-title: The role of genetic factors and monocyte-to-osteoclast differentiation in the pathogenesis of Charcot neuroarthropathy publication-title: Diabetes Res Clin Pract contributor: fullname: Joanna – volume: 60 start-page: 2187 issue: 8 year: 2011 end-page: 2196 article-title: The RANKL/RANK/OPG signaling pathway mediates medial arterial calcification in diabetic Charcot neuroarthropathy publication-title: Diabetes contributor: fullname: Jude – volume: 27 start-page: 797 issue: 10 year: 2006 end-page: 800 article-title: Cytokine-induced osteoclastic bone resorption in Charcot arthropathy: an immunohistochemical study publication-title: Foot Ankle Int contributor: fullname: Pinzur – volume: 7 start-page: 501 issue: 1 year: 2017 article-title: Prevalence of polymorphisms in OPG, RANKL, and RANK as potential markers for Charcot arthropathy development publication-title: Sci Rep contributor: fullname: Jakobkiewicz-Banecka – volume: 32 start-page: 267 issue: 2 year: 2015 end-page: 273 article-title: Inflammatory and bone turnover markers in a cross-sectional and prospective study of acute Charcot osteoarthropathy publication-title: Diabet Med contributor: fullname: Musto – volume: 54 year: 2011 article-title: Local and systemic concentration of pro-inflammatory cytokines, osteoprotegerin, sRANKL and bone turnover markers in acute Charcot foot and in controls publication-title: Diabetologia contributor: fullname: Jeffcoate – ident: bibr5-10711007231213645 doi: 10.11622/smedj.2016074 – volume: 54 year: 2011 ident: bibr4-10711007231213645 publication-title: Diabetologia contributor: fullname: Divyateja H – ident: bibr10-10711007231213645 doi: 10.17161/kjm.v11i4.8709 – ident: bibr3-10711007231213645 doi: 10.1038/s41598-017-00563-4 – ident: bibr1-10711007231213645 doi: 10.1016/j.diabres.2020.108337 – ident: bibr8-10711007231213645 doi: 10.1111/dme.12590 – ident: bibr2-10711007231213645 doi: 10.1177/107110070602701007 – ident: bibr6-10711007231213645 doi: 10.1053/j.jfas.2004.01.001 – ident: bibr9-10711007231213645 doi: 10.2337/dc09-0243 – ident: bibr7-10711007231213645 doi: 10.2337/db10-1220 |
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Snippet | Background:
Charcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic... Charcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic neuropathy... BACKGROUNDCharcot arthropathy (CA) is a progressive noninfectious inflammatory disease that causes irreversible destruction to pedal architecture in diabetic... |
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SubjectTerms | Arthropathy, Neurogenic - diagnosis Biomarkers C-Reactive Protein Diabetes Mellitus, Type 2 - complications Diabetic Neuropathies - diagnosis Humans Interleukin-6 Prospective Studies |
Title | Biomarkers for Early Detection of Charcot Arthropathy: A Prospective Study on Type 2 Diabetes Patients with Severe Neuropathy |
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