Orthopaedics and Traumatology Sports Center (CETE), Department of Orthopaedics and Traumatology, Paulista School of Medicine (EPM), Federal University of São Paulo, São Paulo, Brazil.
Am J Sports Med. 2018 Jun;46(7):1583-1591. doi: 10.1177/0363546518760577. Epub 2018 Mar 22.
Anterior cruciate ligament (ACL) reconstruction with remnant preservation has been described and related to potential advantages. Literature is lacking regarding gene expression of potential factors related to ligament healing in the ACL remnant and its relation to time from injury.
The mRNA expression of ligament healing factors in the ACL remnant would be higher in acute tears (<3 months from injury) than in intermediate (3-12 months) and chronic (>12 months) injuries.
Controlled laboratory study.
Gene expression of 21 genes related to ligament healing factors was analyzed in 46 ACL remnants biopsied during surgical reconstruction with quantitative real-time polymerase chain reaction technique. Specimens were divided into 3 groups according to time from injury: acute (<3 months from injury; n = 19), intermediate (3-12 months; n = 12), and chronic (>12 months; n = 15). Histological and immunohistochemical evaluation was performed by analysis of hematoxylin and eosin, CD-34, and S-100 staining.
Expression of COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, COL12A1, LOX, PLOD1, and TNC genes in ACL remnant was greater in acute compared with chronic injuries. COL1A1, COL5A1, COL12A1, and TNC genes were also expressed more in the acute group compared with the intermediate group. Furthermore, expression of the genes COL1A1 and COL5A2 was significantly higher in female than in male patients. No difference in the number of blood vessels and mechanoreceptors among groups was observed in the microscopic evaluation.
The present study demonstrates that expression of COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, COL12A1, LOX, PLOD1, and TNC genes in ACL remnant is greater in acute (<3 months from injury) compared with chronic (>12 months) injuries. Furthermore, COL1A1, COL5A1, COL12A1, and TNC genes were expressed more in the acute group compared with the intermediate group (3-12 months from injury).
ACL reconstructions with remnant preservation should be performed in patients with acute injuries, as in these cases the ACL remnant may present the greatest healing potential.
前交叉韧带(ACL)残端保留重建已经被描述过,并与潜在的优势相关。关于 ACL 残端中与韧带愈合相关的潜在因素的基因表达及其与受伤时间的关系,文献中还很缺乏。
ACL 残端中的韧带愈合因子的 mRNA 表达在急性撕裂(<3 个月)中高于亚急性(3-12 个月)和慢性(>12 个月)损伤。
对照实验室研究。
通过实时定量聚合酶链反应技术分析 46 个在手术重建过程中进行活检的 ACL 残端中 21 个与韧带愈合因子相关的基因的基因表达。根据受伤时间将标本分为 3 组:急性(<3 个月)(n=19)、亚急性(3-12 个月)(n=12)和慢性(>12 个月)(n=15)。通过对苏木精和伊红、CD-34 和 S-100 染色进行组织学和免疫组织化学评估。
ACL 残端中 COL1A1、COL1A2、COL3A1、COL5A1、COL5A2、COL12A1、LOX、PLOD1 和 TNC 基因的表达在急性组中高于慢性组。与慢性组相比,COL1A1、COL5A1、COL12A1 和 TNC 基因在急性组中的表达也更高。此外,COL1A1 和 COL5A2 基因在女性患者中的表达明显高于男性患者。在显微镜评估中,各组之间的血管和机械感受器数量没有差异。
本研究表明,与慢性(>12 个月)损伤相比,ACL 残端中 COL1A1、COL1A2、COL3A1、COL5A1、COL5A2、COL12A1、LOX、PLOD1 和 TNC 基因的表达在急性(<3 个月)损伤中更高。此外,与亚急性(3-12 个月)组相比,急性组中 COL1A1、COL5A1、COL12A1 和 TNC 基因的表达更高。
应在急性损伤患者中进行 ACL 残端保留重建,因为在这些情况下,ACL 残端可能具有最大的愈合潜力。