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慢性外侧踝关节不稳患者的前距腓韧带中存在细胞凋亡:一项体外研究。

Apoptosis Occurs in the Anterior Talofibular Ligament of Patients With Chronic Lateral Ankle Instability: An In Vitro Study.

机构信息

Department of Orthopaedic Surgery, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

Department of Orthopaedic Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

出版信息

Clin Orthop Relat Res. 2022 Dec 1;480(12):2420-2429. doi: 10.1097/CORR.0000000000002337. Epub 2022 Aug 16.

Abstract

BACKGROUND

Chronic lateral ankle instability is treated operatively, whereas most acute ankle sprains associated with acute anterior talofibular ligament injury are usually treated nonoperatively. This treatment strategy is widely accepted and has been validated using a variety of clinical or radiological methods. We suspected that there may be biological differences between chronic and acutely injured ligaments, particularly with respect to apoptosis. Apoptosis is known to cause ligament degeneration. If it could be demonstrated that apoptosis occurs more in the anterior talofibular ligament tissues of patients with chronic lateral ankle instability compared with patients with acute anterior talofibular ligament injury, biological evidence could be supported.

QUESTIONS/PURPOSES: We sought to (1) elucidate the difference in the extent of apoptosis between patients with chronic lateral ankle instability and those with acute anterior talofibular ligament injury. In addition, we asked: (2) What is the expression level of apoptotic enzymes such as caspases 3, 7, 8, and 9 and cytochrome c in each patient group? (3) Is there a correlation between apoptotic activities and the symptom duration period of chronic lateral ankle instability?

METHODS

Between March 2019 and February 2021, 50 patients were prospectively enrolled in this study. Anterior talofibular ligament tissues were harvested from patients who were divided into two groups: the chronic lateral ankle instability group and the acute anterior talofibular ligament injury group. Patients with insufficient remaining ligaments were excluded from the chronic lateral ankle instability group, and cases in which the tissue was severely damaged or the quality of collected tissue was insufficient because of severe impingement into the fracture site were excluded from the acute anterior talofibular ligament injury group. Tissues were collected from 21 patients (11 males and 10 females) in the chronic lateral ankle instability group with a mean age of 37 ± 14 years and from 17 patients (6 males and 11 females) in the acute anterior talofibular ligament injury group with a mean age of 49 ± 17 years. To investigate our first purpose, apoptotic cells were counted using a TUNEL assay. To answer our second question, Western blotting for apoptotic enzymes such as caspases 3, 7, 8, and 9 and cytochrome c was performed to investigate apoptotic activity. Immunohistochemistry was also used to detect apoptotic enzymes. To answer our third question, the time elapsed after the first symptom related to chronic lateral ankle instability occurred and the expression level of each enzyme was investigated.

RESULTS

More apoptotic cells were observed in the chronic lateral ankle instability group than in the acute anterior talofibular ligament injury group in the TUNEL assay. Western blotting revealed that the apoptotic activities of the chronic lateral ankle instability group were higher than those of the acute anterior talofibular ligament injury group: caspase 3 was 117 in the chronic lateral ankle instability group and 59 in the acute anterior talofibular ligament injury group (mean difference 58 [95% confidence interval (CI) 31 to 86]; p < 0.001), caspase 7 was 138 in the chronic lateral ankle instability group and 45 in the acute anterior talofibular ligament injury group (mean difference 93 [95% CI 58 to 128]; p < 0.001), caspase 8 was 126 in the chronic lateral ankle instability group and 68 in the acute anterior talofibular ligament injury group (mean difference 58 [95% CI 29 to 89]; p < 0.001), caspase 9 was 128 in the chronic lateral ankle instability group and 54 in the acute anterior talofibular ligament injury group (mean difference 74 [95% CI 44 to 104]; p < 0.001), and cytochrome c was 139 in the chronic lateral ankle instability group and 51 in the acute anterior talofibular ligament injury group (mean difference 88 [95% CI 46 to 129]; p < 0.001). Immunohistochemistry revealed higher expression of caspases 3, 7, 8, and 9 and cytochrome c in the chronic lateral ankle instability group compared with those in the acute anterior talofibular ligament injury group. Caspases 3, 7, and 9 showed no correlation with duration of chronic lateral ankle instability symptoms: the Pearson correlation coefficient was 0.22 [95% CI -0.25 to 0.69] for caspase 3 (p = 0.36), 0.29 [95% CI -0.16 to 0.74] for caspase 7 (p = 0.23), and 0.29 [95% CI -0.16 to 0.74] for caspase 9 (p = 0.23).

CONCLUSION

In chronic lateral ankle instability, apoptotic activity in the anterior talofibular ligament was higher than in acute anterior talofibular ligament injury.

CLINICAL RELEVANCE

Apoptosis occurs more in chronic injured ligaments than in acutely injured ligaments. Although urgent surgical repair is not required for acute anterior talofibular ligament injury, chronic lateral ankle instability may progress if the nonoperative treatment is not successful. Further research should focus not only on timing of apoptotic progression, but also on biological augmentation to reverse or prevent apoptosis within the anterior talofibular ligament.

摘要

背景

慢性外踝不稳定通常需要手术治疗,而大多数伴有急性前距腓韧带损伤的急性踝关节扭伤通常采用非手术治疗。这种治疗策略被广泛接受,并已通过各种临床或影像学方法得到验证。我们怀疑慢性和急性损伤的韧带之间可能存在生物学差异,特别是在细胞凋亡方面。已知细胞凋亡会导致韧带退化。如果能够证明慢性外踝不稳定患者的前距腓韧带组织中细胞凋亡比急性前距腓韧带损伤患者更常见,那么就可以提供生物学证据。

问题/目的:我们旨在:(1)阐明慢性外踝不稳定患者与急性前距腓韧带损伤患者之间细胞凋亡程度的差异。此外,我们还提出了以下问题:(2)每个患者组中凋亡酶(如 caspase 3、7、8 和 9 以及细胞色素 c)的表达水平如何?(3)慢性外踝不稳定的症状持续时间与细胞凋亡活性之间是否存在相关性?

方法

2019 年 3 月至 2021 年 2 月,前瞻性纳入 50 例患者。将前距腓韧带组织取自慢性外踝不稳定组和急性前距腓韧带损伤组的患者。慢性外踝不稳定组排除了剩余韧带不足的患者,急性前距腓韧带损伤组排除了韧带严重受损或因严重撞击骨折部位而导致采集的组织质量不足的病例。从慢性外踝不稳定组的 21 例患者(男性 11 例,女性 10 例)和急性前距腓韧带损伤组的 17 例患者(男性 6 例,女性 11 例)中采集组织。为了研究我们的第一个目的,使用 TUNEL 检测法计数凋亡细胞。为了回答我们的第二个问题,通过 Western 印迹法检测凋亡酶(如 caspase 3、7、8 和 9 以及细胞色素 c)来研究凋亡活性。还进行了免疫组织化学检测以检测凋亡酶。为了回答我们的第三个问题,研究了慢性外踝不稳定首次出现相关症状后的时间间隔以及每种酶的表达水平。

结果

TUNEL 检测法显示慢性外踝不稳定组中的凋亡细胞比急性前距腓韧带损伤组更多。Western 印迹法显示慢性外踝不稳定组的凋亡活性高于急性前距腓韧带损伤组:caspase 3 为 117,急性前距腓韧带损伤组为 59(平均差异 58 [95%置信区间(CI)31 至 86];p < 0.001),caspase 7 为 138,急性前距腓韧带损伤组为 45(平均差异 93 [95%CI 58 至 128];p < 0.001),caspase 8 为 126,急性前距腓韧带损伤组为 68(平均差异 58 [95%CI 29 至 89];p < 0.001),caspase 9 为 128,急性前距腓韧带损伤组为 54(平均差异 74 [95%CI 44 至 104];p < 0.001),细胞色素 c 为 139,急性前距腓韧带损伤组为 51(平均差异 88 [95%CI 46 至 129];p < 0.001)。免疫组织化学显示慢性外踝不稳定组中 caspase 3、7、8 和 9 以及细胞色素 c 的表达水平高于急性前距腓韧带损伤组。Caspase 3、7 和 9 与慢性外踝不稳定症状持续时间无相关性:caspase 3 的 Pearson 相关系数为 0.22 [95%CI -0.25 至 0.69](p = 0.36),caspase 7 的 Pearson 相关系数为 0.29 [95%CI -0.16 至 0.74](p = 0.23),caspase 9 的 Pearson 相关系数为 0.29 [95%CI -0.16 至 0.74](p = 0.23)。

结论

在慢性外踝不稳定中,前距腓韧带的凋亡活性高于急性前距腓韧带损伤。

临床意义

慢性损伤的韧带中细胞凋亡比急性损伤的韧带更常见。虽然急性前距腓韧带损伤不需要紧急手术修复,但如果非手术治疗不成功,慢性外踝不稳定可能会进展。未来的研究不仅应关注细胞凋亡进展的时间,还应关注生物增强以逆转或预防前距腓韧带内的细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e8/9653187/044229b3b8d2/abjs-480-2420-g001.jpg

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