TY - JOUR
T1 - Diabetes as a Risk Factor for Orthopedic Implant Surface Performance
T2 - A Retrieval and In Vitro Study
AU - Arteaga, Alexandra
AU - Qu, Jiayi
AU - Haynes, Sara
AU - Webb, Brian G.
AU - LaFontaine, Javier
AU - Rodrigues, Danieli C.
N1 - Funding Information:
Research reported in this manuscript was supported by the National Institute of Diabetes and Digestive and Kidney Disease (NIDDK/NIH) of the National Institutes of Health under the NIH Ruth L. Kirschstein National Research Service Award (NRSA) Individual Predoctoral Fellowship to Promote Diversity in Health-Related Research Award number F31DK121483 and the Eugene McDermott Fellowship. This project is also supported by the University of Texas at Dallas Office of Research Seed Grant, Collaborative Biomedical Research Award (CoBRA).
Funding Information:
The authors would like to acknowledge the Biomaterials for Osseointegration and Novel Engineering (BONE) lab at the University of Texas at Dallas for providing the facilities. The authors would also like to acknowledge the support from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK/NIH) F31 fellowship number F31DK121483. This project is also supported by the University of Texas at Dallas (UTD) Office of Research through a seed grant, Collaborative Biomedical Research Award (CoBRA). We thank Danyal Siddiqui for his expertise and manuscript edits.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Switzerland AG part of Springer Nature.
PY - 2021/6
Y1 - 2021/6
N2 - Orthopedic devices are often associated with increased risk for diabetic patients due to impaired wound healing capabilities. Adverse biological responses for immunocompromised patients at the implant–tissue interface can lead to significant bone resorption that may increase failure rates. The goal of this study was to characterize the surface of implants removed from diabetic patients to determine underlying mechanisms of diabetes-induced impaired osseointegration. Thirty-nine retrieved titanium and stainless-steel orthopedic devices were obtained from diabetic and non-diabetic patients, and compared to non-implanted controls. Optical Microscopy, Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and X-ray Photoelectron Spectroscopy revealed changes in morphology, chemical composition, oxidation state, and oxide thickness of the retrieval specimens, respectively. Additionally, titanium disks were immersed for 28 days in simulated in vitro diabetic conditions followed by Inductively Coupled Plasma-Optical Emission Spectroscopy to quantify metal dissolution. Electrochemical testing was performed on specimens from retrievals and in vitro study. Aside from biological deposits, retrievals demonstrated surface discoloration, pit-like formations, and oxide thinning when compared to non-implanted controls, suggesting exposure to unfavorable acidic conditions. Cyclic load-bearing areas on fracture-fixation screws and plates depicted cracking and delamination. The corrosion behavior was not significantly different between diabetic and non-diabetic conditions of immersed disks or implant type. However, simulated diabetic conditions elevated aluminum release. This elucidates orthopedic implant failures that potentially arise from diabetic environments at the implant–tissue interface. Design of new implant surfaces should consider specific strategies to induce constructive healing responses in immunocompromised patients while also mitigating corrosion in acidic diabetic environments.
AB - Orthopedic devices are often associated with increased risk for diabetic patients due to impaired wound healing capabilities. Adverse biological responses for immunocompromised patients at the implant–tissue interface can lead to significant bone resorption that may increase failure rates. The goal of this study was to characterize the surface of implants removed from diabetic patients to determine underlying mechanisms of diabetes-induced impaired osseointegration. Thirty-nine retrieved titanium and stainless-steel orthopedic devices were obtained from diabetic and non-diabetic patients, and compared to non-implanted controls. Optical Microscopy, Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and X-ray Photoelectron Spectroscopy revealed changes in morphology, chemical composition, oxidation state, and oxide thickness of the retrieval specimens, respectively. Additionally, titanium disks were immersed for 28 days in simulated in vitro diabetic conditions followed by Inductively Coupled Plasma-Optical Emission Spectroscopy to quantify metal dissolution. Electrochemical testing was performed on specimens from retrievals and in vitro study. Aside from biological deposits, retrievals demonstrated surface discoloration, pit-like formations, and oxide thinning when compared to non-implanted controls, suggesting exposure to unfavorable acidic conditions. Cyclic load-bearing areas on fracture-fixation screws and plates depicted cracking and delamination. The corrosion behavior was not significantly different between diabetic and non-diabetic conditions of immersed disks or implant type. However, simulated diabetic conditions elevated aluminum release. This elucidates orthopedic implant failures that potentially arise from diabetic environments at the implant–tissue interface. Design of new implant surfaces should consider specific strategies to induce constructive healing responses in immunocompromised patients while also mitigating corrosion in acidic diabetic environments.
KW - Diabetes
KW - Orthopedic implants
KW - Retrieval
KW - Stainless steel
KW - Titanium alloy
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U2 - 10.1007/s40735-021-00486-8
DO - 10.1007/s40735-021-00486-8
M3 - Article
C2 - 34150468
AN - SCOPUS:85101570617
SN - 2198-4220
VL - 7
JO - Journal of Bio- and Tribo-Corrosion
JF - Journal of Bio- and Tribo-Corrosion
IS - 2
M1 - 51
ER -