The Size of Intramedullary Fixation Affects Endochondral-Mediated Angiogenesis During Fracture Repair.


Journal

Journal of orthopaedic trauma
ISSN: 1531-2291
Titre abrégé: J Orthop Trauma
Pays: United States
ID NLM: 8807705

Informations de publication

Date de publication:
Oct 2019
Historique:
pubmed: 2 7 2019
medline: 30 10 2020
entrez: 2 7 2019
Statut: ppublish

Résumé

To explore the effect of intramedullary pin size on the biology of a healing fracture, specifically endochondral angiogenesis. We hypothesized that fracture fixation with a smaller pin would permit greater interfragmentary strain resulting in increased total amount of vascular endothelial growth factor within the callus and greater angiogenesis compared to fixation with a larger pin. Transverse mid-shaft femur fractures in 8-week-old mice were fixed with either a 23-gauge (G) or 30-G pin. Differences in interfragmentary strain at the fracture site were estimated between cohorts. A combination of histology, gene expression, serial radiography, and microcomputed tomography with and without vascular contrast agent were used to assess fracture healing and vascularity for each cohort. Larger soft-tissue callus formation increased vascular endothelial growth factor-A expression, and a corresponding increase in vascular volume was observed in the higher strain, 30-G cohort. Radiographic analysis demonstrated earlier hard callus formation with greater initial interfragmentary strain, similar rates of union between pin size cohorts, yet delayed callus remodeling in mice with the larger pin size. These findings suggest that the stability conferred by an intramedullary nail influences endochondral angiogenesis at the fracture.

Identifiants

pubmed: 31259800
doi: 10.1097/BOT.0000000000001555
doi:

Substances chimiques

Vascular Endothelial Growth Factor A 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e385-e393

Auteurs

Masato Yuasa (M)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.
Department of Orthopaedic Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Masanori Saito (M)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.
Department of Orthopaedic Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Deke M Blum (DM)

Vanderbilt University School of Medicine, Nashville, TN.

Alexander A Hysong (AA)

Vanderbilt University School of Medicine, Nashville, TN.

Satoru Egawa (S)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.
Department of Orthopaedic Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Sasidhar Uppuganti (S)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.

Toshitaka Yoshii (T)

Department of Orthopaedic Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Atsushi Okawa (A)

Department of Orthopaedic Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Herbert S Schwartz (HS)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.

Stephanie N Moore-Lotridge (SN)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.
Departments of Pharmacology, and.

Jeffry S Nyman (JS)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.
Biomedical Engineering, Vanderbilt University, Nashville, TN.
Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN.
Department of Veterans Affairs, Tennessee Valley Health Care System, Nashville, TN.

Jonathan G Schoenecker (JG)

Department of Orthopaedics and Rehabilitation, Vanderbilt University Medical Center, Nashville, TN.
Departments of Pharmacology, and.
Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN.
Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN.

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Classifications MeSH