Greater medial arterial supply revealed by 7-Tesla quantitative magnetic resonance imaging, histology and high-resolution computed tomography of the patellar tendon
- PMID: 41822380
- PMCID: PMC12975651
- DOI: 10.1002/jeo2.70668
Greater medial arterial supply revealed by 7-Tesla quantitative magnetic resonance imaging, histology and high-resolution computed tomography of the patellar tendon
Abstract
Purpose: To quantitatively assess relative arterial contributions to the patellar tendon (PT) across predefined anatomic regions with 7-Tesla quantitative magnetic resonance imaging (7T-qMRI), algorithm-based histological analysis and high-resolution computed tomography (micro-CT) in a cadaveric model.
Methods: Seven fresh-frozen human cadaveric knee pairs (mean age 41.9 ± 15.5 years) underwent limited vascular dissection and arterial cannulation. Pre- and post-contrast 7T-qMRI, with a volumetric interpolated breath-hold examination (VIBE) three-dimensional T1-weighted gradient echo pulse sequence, quantified tendonous vascularity by measuring contrast enhancement. Subsequent quantitative algorithm-based histologic analysis with hematoxylin and eosin (H&E) staining followed, and two additional specimens underwent high-resolution (98 μm) micro-CT for qualitative vascular assessment.
Results: In the transverse analysis, 7T-qMRI demonstrated the highest mean relative arterial contributions in the medial region (42.4%) compared with the middle region (30.2%; p = 0.035) and higher, though not significant, than the lateral region (32.0%). The central PT demonstrated greater relative arterial contributions (37.5%) than the proximal (26.5%) or distal (29.3%) thirds (p > 0.05) in the longitudinal analysis. At the patellar enthesis, the middle third exhibited higher contributions (35.3%) than medial (28.8%) or lateral (29.6%), without significance, while the tibial tuberosity showed greater contributions along the lateral region (37.2%; p > 0.05). Histology confirmed significantly greater medial arterial contribution, with 8.3% higher supply than lateral (p = 0.018). Micro-CT revealed a robust vascular network along the medial PT with smaller branches laterally. Distal to the inferior patellar pole, a peripatellar circular network, extending medially into the posterior PT layers, was qualitatively identified.
Conclusion: 7T-qMRI and histological analyses demonstrated significantly greater arterial supply along the medial border of the PT, while micro-CT revealed a medial and peripatellar circular vascular network extending from the medial margin and the inferior patellar pole into the posterior tendon layers. These findings identify the medial margin as the main vascular source for the PT, with implications for surgical preservation and reducing PT devascularization risk.
Level of evidence: N/A.
Keywords: arterial supply; parapatellar approach; patellar tendon; patellar tendon rupture; rupture; vascularity.
© 2026 The Author(s). Journal of Experimental Orthopaedics published by John Wiley & Sons Ltd on behalf of European Society of Sports Traumatology, Knee Surgery and Arthroscopy.
Conflict of interest statement
Unrelated to this study, Kevin G. Shea serves on the Board of POSNA, holds stock options in Sarcio, Medeloop and nView, and receives research materials from Arthrex, Stryker, Evolution Surgical and Allosource. Gregory S. DiFelice receives royalties, owns stock and is a paid consultant for Zimmer Biomet. Gregory S. DiFelice receives royalties from Arthrex. Gregory S. DiFelice received stock options, provides consulting services and participates in funded research with Miach Orthopaedics. Gregory S. DiFelice receives stock options and provides consulting services for OSSIO Inc. Peter K. Sculco consults for BICMD, Inc., Enovis and Zimmer Biomet; receives royalties from Enovis and Zimmer Biomet; research support from Zimmer Biomet; serves on the advisory board of Osgenic; and holds ownership interests in BetterPT, HS2, LLC, HSS ASC Development Network, LLC, Intellijoint Surgical, Inc., Joint Effort Administrative Services Organization, LLC, Parvizi Surgical Innovation, LLC and Osgenic. Scott A. Rodeo reports consulting for Novartis, Advance Medical/Teladoc and Enovis; research support from Virginia Toulmin Foundation, OREF, Arthritis Foundation, Angiocrine Biosciences, CTSC and NIH; and stock options in Jannu Therapeutics and Overture Medical. Daniel W. Green reports roles with AONA & AO, Arthrex (consulting, royalties, speakers' bureau), OrthoPediatrics (royalties) and Wolters Kluwer (authorship). The remaining authors declare no conflict of interest.
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