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编码胶原 IX 和 XI 基因多态性在腰椎间盘疾病中的作用。

The role of polymorphisms of genes encoding collagen IX and XI in lumbar disc disease.

机构信息

Neurosurgery Ward of St. Rafael Hospital, Krakow, Poland.

Department of Genetics, Polish-American Institute of Pediatrics, Krakow, Poland.

出版信息

Neurol Neurochir Pol. 2014 Jan-Feb;48(1):60-2. doi: 10.1016/j.pjnns.2013.04.001. Epub 2014 Jan 23.

Abstract

The intervertebral disc disease (IDD) is one of the most common musculoskeletal disorders. A number of environment and anthropometric risk factors may contribute to it. The recent reports have suggested the importance of genetic factors, especially these which encode collagen types IX and XI. The allelic variants in the collagen IX genes - COL9A2 (Trp2) and COL9A3 (Trp3) have been identified as genetic risk factors for IDD, because they interfere the cross-linking between collagen types II, IX and XI and result in decreased stability of intervertebral discs. Type XI collagen is a minor component of cartilage collagen fibrils, but it is present in the annulus fibrosus and nucleus pulposus of intervertebral discs. Some studies have shown the association between gene COL11A1 polymorphism c.4603C>T and IDD. The frequency of 4603T allele was significantly higher in the patients with IDD than in the healthy controls.

摘要

椎间盘疾病(IDD)是最常见的肌肉骨骼疾病之一。许多环境和人体测量风险因素可能与之相关。最近的报告表明遗传因素的重要性,特别是编码胶原类型 IX 和 XI 的这些因素。COL9A2(色氨酸 2)和 COL9A3(色氨酸 3)基因中的等位基因变体已被确定为 IDD 的遗传风险因素,因为它们干扰了胶原类型 II、IX 和 XI 之间的交联,导致椎间盘稳定性降低。XI 型胶原是软骨胶原原纤维的次要成分,但存在于纤维环和椎间盘的髓核中。一些研究表明基因 COL11A1 多态性 c.4603C>T 与 IDD 之间存在关联。在 IDD 患者中,4603T 等位基因的频率明显高于健康对照组。

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