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COL5A1基因的BstUI和DpnII变体与网球肘相关。

The BstUI and DpnII Variants of the COL5A1 Gene Are Associated With Tennis Elbow.

作者信息

Altinisik Julide, Meric Gokhan, Erduran Mehmet, Ates Omer, Ulusal Ali Engin, Akseki Devrim

机构信息

Department of Medical Biology, Balikesir University Medical Faculty, Balikesir, Turkey.

Department of Orthopaedics and Traumatology, Balikesir University Medical Faculty, Balikesir, Turkey

出版信息

Am J Sports Med. 2015 Jul;43(7):1784-9. doi: 10.1177/0363546515578661. Epub 2015 Apr 20.

Abstract

BACKGROUND

Tennis elbow entails pain and tenderness over the lateral epicondyle. The exact cause of the condition is not fully understood. Type V collagen is a minor fibrillar collagen that intercalates with type I collagen and forms collagen fibrils. It is encoded by the COL5A1 gene. Sequence variants within COL5A1 3'-UTR have been implicated in musculoskeletal diseases.

PURPOSE

To determine whether rs12722 (BstUI C414T polymorphism) and rs13946 (DpnII C230T polymorphism) of the COL5A1 gene are associated with an increased risk of tennis elbow.

STUDY DESIGN

Cohort study; Level of evidence, 3.

METHODS

A total of 152 patients with tennis elbow and 195 healthy participants were enrolled in this study. The rs12722 (BstUI C414T) and rs13946 (DpnII C230T) polymorphisms were investigated with the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method.

RESULTS

There was a significant difference in both BstUI and DpnII genotype frequencies between patients with tennis elbow and healthy participants. The A2 allele of BstUI and the B1 allele of DpnII were significantly underrepresented in the patient group.

CONCLUSION

Individuals with the BstUI A1 allele and DpnII B2 allele of the COL5A1 gene have a high likelihood of developing symptoms of the tennis elbow. This is the first study reporting that rs12722 and rs13946 SNPs (single nucleotide polymorphisms) are genetic risk factors for tennis elbow.

摘要

背景

网球肘表现为肱骨外上髁处疼痛和压痛。该病症的确切病因尚未完全明确。Ⅴ型胶原蛋白是一种少量的原纤维胶原蛋白,它与Ⅰ型胶原蛋白相互嵌入并形成胶原纤维。它由COL5A1基因编码。COL5A1基因3'-非翻译区内的序列变异与肌肉骨骼疾病有关。

目的

确定COL5A1基因的rs12722(BstUI C414T多态性)和rs13946(DpnII C230T多态性)是否与网球肘风险增加相关。

研究设计

队列研究;证据等级,3级。

方法

本研究共纳入152例网球肘患者和195名健康参与者。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法研究rs12722(BstUI C414T)和rs13946(DpnII C230T)多态性。

结果

网球肘患者与健康参与者之间的BstUI和DpnII基因型频率均存在显著差异。患者组中BstUI的A2等位基因和DpnII的B1等位基因明显较少。

结论

COL5A1基因具有BstUI A1等位基因和DpnII B2等位基因的个体发生网球肘症状的可能性很高。这是第一项报道rs12722和rs13946单核苷酸多态性(SNP)是网球肘遗传危险因素的研究。

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