Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus

<h4>Aims</h4> Inflammatory osteolysis is sine-qua-non of active Charcot neuroarthropathy (CN) causing decreased foot bone mineral density (BMD) and fractures. We aimed to explore the effect of anti-inflammatory or anti-resorptive agents for effect on foot bone mineral content (BMC) and c...

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Autores principales: Liza Das, Ashu Rastogi, Edward B. Jude, Mahesh Prakash, Pinaki Dutta, Anil Bhansali
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:5d6674ba331949af8f28faaffa493d0b2021-11-18T06:22:36ZLong-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus1932-6203https://doaj.org/article/5d6674ba331949af8f28faaffa493d0b2021-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575293/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Aims</h4> Inflammatory osteolysis is sine-qua-non of active Charcot neuroarthropathy (CN) causing decreased foot bone mineral density (BMD) and fractures. We aimed to explore the effect of anti-inflammatory or anti-resorptive agents for effect on foot bone mineral content (BMC) and consequent long-term outcomes of foot deformities, fractures and amputation. <h4>Methods</h4> Forty-three patients with active CN (temperature difference >2°C from normal foot) were evaluated. Patients were off-loaded with total contact cast and randomized to receive either methylprednisolone (1gm) (group A), zoledronate (5mg) (group B) or placebo (100ml normal saline) (group C) once monthly infusion for three consecutive months. Change in foot BMC was assessed at 6 months or at remission and followed subsequently up to 4 years for the incidence of new-onset fracture, deformities, or CN recurrence. <h4>Results</h4> Thirty-six participants (24 male, 12 female) were randomized (11 in group A, 12 group B, 13 group C). The mean age was 57.7± 9.9 years, duration of diabetes 12.3± 5.8 years and symptom duration 6.5± 2.8 weeks. BMC increased by 36% with zoledronate (p = 0.02) but reduced by 13% with methylprednisolone (p = 0.03) and 9% (p = 0.09) with placebo at remission. There were no incident foot fractures, however, two patients sustained ulcers, and 3 had new-onset or worsening deformities and none required amputation during 3.36 ± 0.89 years of follow-up. <h4>Conclusion</h4> Bisphosphonate for active CN is associated with an increase in foot bone mineral content as compared to decrease with steroids or total contact cast but long-term outcomes of foot deformities, ulceration and amputation are similar. <h4>Trial registration</h4> ClinicalTrials.gov:NCT03289338.Liza DasAshu RastogiEdward B. JudeMahesh PrakashPinaki DuttaAnil BhansaliPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Liza Das
Ashu Rastogi
Edward B. Jude
Mahesh Prakash
Pinaki Dutta
Anil Bhansali
Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus
description <h4>Aims</h4> Inflammatory osteolysis is sine-qua-non of active Charcot neuroarthropathy (CN) causing decreased foot bone mineral density (BMD) and fractures. We aimed to explore the effect of anti-inflammatory or anti-resorptive agents for effect on foot bone mineral content (BMC) and consequent long-term outcomes of foot deformities, fractures and amputation. <h4>Methods</h4> Forty-three patients with active CN (temperature difference >2°C from normal foot) were evaluated. Patients were off-loaded with total contact cast and randomized to receive either methylprednisolone (1gm) (group A), zoledronate (5mg) (group B) or placebo (100ml normal saline) (group C) once monthly infusion for three consecutive months. Change in foot BMC was assessed at 6 months or at remission and followed subsequently up to 4 years for the incidence of new-onset fracture, deformities, or CN recurrence. <h4>Results</h4> Thirty-six participants (24 male, 12 female) were randomized (11 in group A, 12 group B, 13 group C). The mean age was 57.7± 9.9 years, duration of diabetes 12.3± 5.8 years and symptom duration 6.5± 2.8 weeks. BMC increased by 36% with zoledronate (p = 0.02) but reduced by 13% with methylprednisolone (p = 0.03) and 9% (p = 0.09) with placebo at remission. There were no incident foot fractures, however, two patients sustained ulcers, and 3 had new-onset or worsening deformities and none required amputation during 3.36 ± 0.89 years of follow-up. <h4>Conclusion</h4> Bisphosphonate for active CN is associated with an increase in foot bone mineral content as compared to decrease with steroids or total contact cast but long-term outcomes of foot deformities, ulceration and amputation are similar. <h4>Trial registration</h4> ClinicalTrials.gov:NCT03289338.
format article
author Liza Das
Ashu Rastogi
Edward B. Jude
Mahesh Prakash
Pinaki Dutta
Anil Bhansali
author_facet Liza Das
Ashu Rastogi
Edward B. Jude
Mahesh Prakash
Pinaki Dutta
Anil Bhansali
author_sort Liza Das
title Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus
title_short Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus
title_full Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus
title_fullStr Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus
title_full_unstemmed Long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active Charcot neuroarthropathy in diabetes mellitus
title_sort long-term foot outcomes following differential abatement of inflammation and osteoclastogenesis for active charcot neuroarthropathy in diabetes mellitus
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/5d6674ba331949af8f28faaffa493d0b
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AT edwardbjude longtermfootoutcomesfollowingdifferentialabatementofinflammationandosteoclastogenesisforactivecharcotneuroarthropathyindiabetesmellitus
AT maheshprakash longtermfootoutcomesfollowingdifferentialabatementofinflammationandosteoclastogenesisforactivecharcotneuroarthropathyindiabetesmellitus
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AT anilbhansali longtermfootoutcomesfollowingdifferentialabatementofinflammationandosteoclastogenesisforactivecharcotneuroarthropathyindiabetesmellitus
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