Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture: A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures

Research output: Contribution to journalJournal articleResearchpeer-review

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Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture : A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures. / Cramer, Allan; Moser, Claus; Fritz, Blaine Gabriel; Hölmich, Per; Barfod, Kristoffer Weisskirchner.

In: Orthopaedic Journal of Sports Medicine, Vol. 10, No. 8, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Cramer, A, Moser, C, Fritz, BG, Hölmich, P & Barfod, KW 2022, 'Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture: A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures', Orthopaedic Journal of Sports Medicine, vol. 10, no. 8. https://doi.org/10.1177/23259671221112138

APA

Cramer, A., Moser, C., Fritz, B. G., Hölmich, P., & Barfod, K. W. (2022). Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture: A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures. Orthopaedic Journal of Sports Medicine, 10(8). https://doi.org/10.1177/23259671221112138

Vancouver

Cramer A, Moser C, Fritz BG, Hölmich P, Barfod KW. Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture: A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures. Orthopaedic Journal of Sports Medicine. 2022;10(8). https://doi.org/10.1177/23259671221112138

Author

Cramer, Allan ; Moser, Claus ; Fritz, Blaine Gabriel ; Hölmich, Per ; Barfod, Kristoffer Weisskirchner. / Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture : A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures. In: Orthopaedic Journal of Sports Medicine. 2022 ; Vol. 10, No. 8.

Bibtex

@article{bc626c5048674df8a6a9cbf4c7807af5,
title = "Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture: A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures",
abstract = "Background: The source of the pathological changes that occur before an acute Achilles tendon rupture (ATR) is not fully understood. Bacterial DNA has previously been detected in samples from ruptured Achilles tendons, suggesting a pathogenic role of bacteria in ATR. Purpose/Hypothesis: The purpose of this study was to investigate if DNA from bacteria was present in acutely ruptured Achilles tendons. We hypothesized that 20% to 30% of the samples from the rupture site and no samples from healthy tissue would be positive for bacterial DNA. Study Design: Case series; Level of evidence, 4. Methods: This study included 20 consecutive patients scheduled for surgical repair of an acute ATR. Tendon biopsy specimens were taken from the rupture site and from the healthy tendon tissue proximal to the rupture to act as a control. Samples were blinded to the technician and analyzed using polymerase chain reaction targeted to the bacterial 16S rDNA gene and Sanger sequencing to identify the bacterial species present. McNemar test for paired proportions was performed to test for statistically significant differences in the number of samples positive for bacterial DNA between the ruptured and control regions of the Achilles tendon. Results: Of the 20 patients, 1 (5%) had a positive sample with bacterial DNA from the ruptured part of the Achilles tendon. The same patient also had a positive control sample, although with different bacterial DNA. An additional patient had a positive control sample. There was no statistically significant difference in the number of bacterial DNA–positive samples between the ruptured and control regions of the Achilles tendon. The bacteria found (Staphylococcus sp, Micrococcus sp, and Staphylococcus epidermidis) were normal commensal organisms on the human skin. Conclusion: Bacterial DNA was infrequent in tissue from ruptured Achilles tendons and, if identified, likely was a result of contamination. This suggests that bacteria are not involved in the pathological changes occurring before rupture of the Achilles tendon.",
keywords = "16S rDNA, Achilles tendon, bacteria, etiology, pathogenesis, risk factor, rupture, surgery",
author = "Allan Cramer and Claus Moser and Fritz, {Blaine Gabriel} and Per H{\"o}lmich and Barfod, {Kristoffer Weisskirchner}",
note = "Publisher Copyright: {\textcopyright} The Author(s) 2022.",
year = "2022",
doi = "10.1177/23259671221112138",
language = "English",
volume = "10",
journal = "Orthopaedic Journal of Sports Medicine",
issn = "2325-9671",
publisher = "SAGE Publications",
number = "8",

}

RIS

TY - JOUR

T1 - Involvement of Bacteria in the Pathological Changes Before Achilles Tendon Rupture

T2 - A Case Series Investigating 16S rDNA in 20 Consecutive Ruptures

AU - Cramer, Allan

AU - Moser, Claus

AU - Fritz, Blaine Gabriel

AU - Hölmich, Per

AU - Barfod, Kristoffer Weisskirchner

N1 - Publisher Copyright: © The Author(s) 2022.

PY - 2022

Y1 - 2022

N2 - Background: The source of the pathological changes that occur before an acute Achilles tendon rupture (ATR) is not fully understood. Bacterial DNA has previously been detected in samples from ruptured Achilles tendons, suggesting a pathogenic role of bacteria in ATR. Purpose/Hypothesis: The purpose of this study was to investigate if DNA from bacteria was present in acutely ruptured Achilles tendons. We hypothesized that 20% to 30% of the samples from the rupture site and no samples from healthy tissue would be positive for bacterial DNA. Study Design: Case series; Level of evidence, 4. Methods: This study included 20 consecutive patients scheduled for surgical repair of an acute ATR. Tendon biopsy specimens were taken from the rupture site and from the healthy tendon tissue proximal to the rupture to act as a control. Samples were blinded to the technician and analyzed using polymerase chain reaction targeted to the bacterial 16S rDNA gene and Sanger sequencing to identify the bacterial species present. McNemar test for paired proportions was performed to test for statistically significant differences in the number of samples positive for bacterial DNA between the ruptured and control regions of the Achilles tendon. Results: Of the 20 patients, 1 (5%) had a positive sample with bacterial DNA from the ruptured part of the Achilles tendon. The same patient also had a positive control sample, although with different bacterial DNA. An additional patient had a positive control sample. There was no statistically significant difference in the number of bacterial DNA–positive samples between the ruptured and control regions of the Achilles tendon. The bacteria found (Staphylococcus sp, Micrococcus sp, and Staphylococcus epidermidis) were normal commensal organisms on the human skin. Conclusion: Bacterial DNA was infrequent in tissue from ruptured Achilles tendons and, if identified, likely was a result of contamination. This suggests that bacteria are not involved in the pathological changes occurring before rupture of the Achilles tendon.

AB - Background: The source of the pathological changes that occur before an acute Achilles tendon rupture (ATR) is not fully understood. Bacterial DNA has previously been detected in samples from ruptured Achilles tendons, suggesting a pathogenic role of bacteria in ATR. Purpose/Hypothesis: The purpose of this study was to investigate if DNA from bacteria was present in acutely ruptured Achilles tendons. We hypothesized that 20% to 30% of the samples from the rupture site and no samples from healthy tissue would be positive for bacterial DNA. Study Design: Case series; Level of evidence, 4. Methods: This study included 20 consecutive patients scheduled for surgical repair of an acute ATR. Tendon biopsy specimens were taken from the rupture site and from the healthy tendon tissue proximal to the rupture to act as a control. Samples were blinded to the technician and analyzed using polymerase chain reaction targeted to the bacterial 16S rDNA gene and Sanger sequencing to identify the bacterial species present. McNemar test for paired proportions was performed to test for statistically significant differences in the number of samples positive for bacterial DNA between the ruptured and control regions of the Achilles tendon. Results: Of the 20 patients, 1 (5%) had a positive sample with bacterial DNA from the ruptured part of the Achilles tendon. The same patient also had a positive control sample, although with different bacterial DNA. An additional patient had a positive control sample. There was no statistically significant difference in the number of bacterial DNA–positive samples between the ruptured and control regions of the Achilles tendon. The bacteria found (Staphylococcus sp, Micrococcus sp, and Staphylococcus epidermidis) were normal commensal organisms on the human skin. Conclusion: Bacterial DNA was infrequent in tissue from ruptured Achilles tendons and, if identified, likely was a result of contamination. This suggests that bacteria are not involved in the pathological changes occurring before rupture of the Achilles tendon.

KW - 16S rDNA

KW - Achilles tendon

KW - bacteria

KW - etiology

KW - pathogenesis

KW - risk factor

KW - rupture

KW - surgery

U2 - 10.1177/23259671221112138

DO - 10.1177/23259671221112138

M3 - Journal article

C2 - 35982829

AN - SCOPUS:85136212438

VL - 10

JO - Orthopaedic Journal of Sports Medicine

JF - Orthopaedic Journal of Sports Medicine

SN - 2325-9671

IS - 8

ER -

ID: 319162399