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突发性听力损失中的可溶性细胞间黏附分子1和可溶性血管细胞黏附分子1

Soluble intercellular adhesion molecule 1 and soluble vascular cell adhesion molecule 1 in sudden hearing loss.

作者信息

Quaranta Nicola, Ramunni Alfonso, Brescia Paola, D'Elia Alessandra, Vacca Angelo, Ria Roberto

机构信息

Otolaryngology G. Lugli, Otologic and Neurotologic Surgery, University of Bari, Bari, Italy.

出版信息

Otol Neurotol. 2008 Jun;29(4):470-4. doi: 10.1097/MAO.0b013e318170b650.

Abstract

HYPOTHESIS

The aim of the present study was to evaluate the concentration of soluble intercellular adhesion molecule 1 and soluble vascular cell adhesion molecule 1 in patients affected by sudden sensorineural hearing loss (SSHL).

STUDY DESIGN

Prospective study.

SETTING

Tertiary referral center.

PATIENTS

Patients affected by SSHL were evaluated. Inclusion criteria for this study were hearing loss of more than 30 dB hearing level affecting at least 3 contiguous frequencies, normal hearing on the contralateral ear, negative history of hearing loss or ear surgery in the affected ear, and magnetic resonance with gadolinium negative for VIII cranial nerve pathologic findings.

INTERVENTION

Circulating levels of soluble intercellular adhesion molecule 1 and soluble vascular cell adhesion molecule (VCAM) 1 were evaluated by means of enzyme-linked immunosorbent assay.

MAIN OUTCOME MEASURES

The levels of adhesion molecules in SSHL patients were compared with those of a control group.

RESULTS

Intercellular adhesion molecule 1 and VCAM-1 levels in sera of patients with SSHL were significantly higher than those of the matched control subjects (p < 0.001). Statistical analysis did not show significant differences between the 2 groups in terms of the known vascular risk factors such as total and fractionated cholesterol, triglycerides, fibrinogen, erythrocyte sedimentation rate smoking, and diabetes.

CONCLUSION

The results of this study show that in SSHL patients, there is an increased expression of circulating adhesion molecules confirming the existence of an endothelial dysfunction and supporting the vascular involvement in the pathogenesis of the disease. The identification of high levels of adhesion molecules and of the endothelial dysfunction open the way to selective pharmacologic treatments able to correct the activation of endothelial cells.

摘要

假设

本研究的目的是评估突发性感音神经性听力损失(SSHL)患者中可溶性细胞间黏附分子1和可溶性血管细胞黏附分子1的浓度。

研究设计

前瞻性研究。

研究地点

三级转诊中心。

患者

对受SSHL影响的患者进行评估。本研究的纳入标准为听力损失超过30 dB听力水平,影响至少3个连续频率,对侧耳听力正常,患耳无听力损失或耳部手术史,以及钆增强磁共振成像显示第八颅神经病理结果为阴性。

干预措施

通过酶联免疫吸附测定法评估可溶性细胞间黏附分子1和可溶性血管细胞黏附分子(VCAM)1的循环水平。

主要观察指标

将SSHL患者的黏附分子水平与对照组进行比较。

结果

SSHL患者血清中的细胞间黏附分子1和VCAM-1水平显著高于匹配的对照组(p < 0.001)。统计分析未显示两组在总胆固醇、胆固醇分级、甘油三酯、纤维蛋白原、红细胞沉降率、吸烟和糖尿病等已知血管危险因素方面存在显著差异。

结论

本研究结果表明,在SSHL患者中,循环黏附分子表达增加,证实存在内皮功能障碍,并支持血管参与该疾病的发病机制。黏附分子高水平和内皮功能障碍的识别为能够纠正内皮细胞激活的选择性药物治疗开辟了道路。

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