Evidence map›Paper›PMID 42169057›Full record

ArticleJournal of orthopaedic surgery and research2026

Persistence of mechanoreceptors in ACL remnants: a histological and immunohistochemical analysis of 128 patients.

Cahit Ancar, Nilüfer Dönmezdil, Fırat Aşır

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Article in Journal of orthopaedic surgery and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Cahit AncarDivision of Orthopedics, Gazi Yasargil Training and Research Hospital, Health Sciences University, Diyarbakır, Turkey. dr_cahit2006@hotmail.com.ORCID http://orcid.org/0009-0000-1711-1311
Nilüfer DönmezdilDepartment of Histology and Embryology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey. nilufer.donmezdil@dicle.edu.tr.ORCID http://orcid.org/0000-0001-5543-1762
Fırat AşırDepartment of Histology and Embryology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey.ORCID http://orcid.org/0000-0002-6384-9146

Funding

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6 · The paper itself

Abstract

backgroundAnterior cruciate ligament (ACL) remnants may retain sensory neural elements after rupture, potentially contributing to proprioceptive function and graft reinnervation following reconstruction. However, the persistence of mechanoreceptors in remnant tissues and the factors influencing their preservation remain incompletely understood. This study aimed to evaluate the presence of neural structures in ACL remnants using histological and immunohistochemical methods and to determine the association between mechanoreceptor preservation, injury duration, and remnant attachment pattern.

methodsACL remnant tissues were obtained from 128 patients undergoing arthroscopic ACL reconstruction. Specimens were examined using hematoxylin-eosin (H&E) staining and immunohistochemistry with S100, myelin basic protein (MBP), and β-III-tubulin antibodies to identify neural elements. Patients were classified according to injury duration as subacute (≤ 3 months), chronic (3-12 months), and late chronic (> 12 months). Remnants were also categorized based on arthroscopic appearance as PCL-femur attachment or tibial stump. Mechanoreceptor presence and distribution were analyzed, and multivariate logistic regression was performed to evaluate factors associated with mechanoreceptor preservation.

resultsMechanoreceptors or neural structures were identified in 81 of 128 specimens (63.3%). Free nerve endings were the most frequently observed neural elements, whereas structured receptors such as Ruffini or Golgi-like endings were less common and Pacinian corpuscles were rare. Mechanoreceptor prevalence differed significantly according to injury duration, being highest in the subacute group (84.8%) and lower in the chronic (58.7%) and late chronic (53.1%) groups (p = 0.01). The remnant attachment pattern did not show a significant association with mechanoreceptor presence (p = 0.23). Logistic regression analysis demonstrated that longer injury duration was independently associated with reduced odds of mechanoreceptor detection.

conclusionsACL remnants frequently retain neural structures, particularly during the early post-injury period, but the prevalence of mechanoreceptors decreases with increasing injury duration. Remnant attachment pattern appears to have a limited influence on neural preservation. These findings support the biological rationale for remnant-preserving reconstruction strategies when technically feasible and highlight the potential importance of early surgical intervention for maintaining proprioceptive tissue integrity.

Indexed as

Anterior Cruciate LigamentAnterior Cruciate Ligament InjuriesAnterior Cruciate Ligament ReconstructionMechanoreceptorsAdolescentAdultArthroscopyFemaleHumansImmunohistochemistryMaleMiddle AgedYoung AdultACL remnantAnterior cruciate ligamentInjury chronicityMechanoreceptorsProprioceptionRemnant-preserving reconstructionSensory fibers

Identifiers

PMID42169057
PMCPMC13377717

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.