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. 2024 Jan 3;19:4. doi: 10.1186/s13018-023-04512-y

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 8 — A The peri-tunnel bone marrow signal change in femoral and tibial bone in all groups together. B The peri-tunnel bone marrow signal change in femoral and tibial bone in control group, PRP group and BMAC + PRP group. The red arrow indicates significant difference between three groups by one way ANOVA. *p < 0.05 versus 6 weeks; **p < 0.01 versus 6 weeks; #p < 0.05 between weeks; ##p < 0.01 between weeks; N.S: no significant difference between weeks; §p < 0.05 vs reference femur bone marrow signal; §§ p < 0.01 versus reference femur bone marrow signal