Suppr超能文献

青少年特发性脊柱侧凸双曲与钙调蛋白 1 基因/雌激素受体-α 基因多态性的关系。

Association between adolescent idiopathic scoliosis with double curve and polymorphisms of calmodulin1 gene/estrogen receptor-α gene.

机构信息

Department of Orthopedic Surgery, Peking Union Medical College Hospital, Beijing, China.

出版信息

Orthop Surg. 2009 Aug;1(3):222-30. doi: 10.1111/j.1757-7861.2009.00038.x.

Abstract

OBJECTIVE

To investigate whether single nucleotide polymorphisms (SNP) of the calmodulin1 (CALM1) and estrogen receptor-α genes correlate with double curve in adolescent idiopathic scoliosis (AIS).

METHODS

A total of 67 Chinese patients with AIS with double curve and 100 healthy controls were recruited. Curve pattern and Cobb angle of each patient were recorded. The Cobb angle is at least 30°. There were 60 patients with Cobb angle ≥ 40°. According to the apical location of the major curve, there were 40 thoracic curve patients. Four polymorphic loci, including rs12885713 (-16C > T) and rs5871 in the CALM1 gene and rs2234693 (Pvu II) and rs9340799 (Xba I) in the estrogen receptor 1 (ER1) gene were analyzed by the ABI3730 genetic analyzer.

RESULTS

The current study indicates that: (i) there are statistical differences between patients with double curve, with Cobb angle ≥ 40° and with thoracic curve and healthy controls in the polymorphic distribution of the rs2234693 site of the ER1 gene, (P= 0.014, 0.0128, 0.0184 respectively); (ii) there is a difference between patients with double curve and controls in the polymorphic distribution of the rs12885713 site in the CALM1 gene (P= 0.034); and (iii) there is a difference between thoracic curve patients and controls in the polymorphic distribution of the rs5871 site in the CALM1 gene (P= 0.0102).

CONCLUSIONS

Different subtypes of AIS might be related to different SNP. A combination of CALM1 and ER1 gene polymorphisms might be related to double curve in patients with AIS. Further study is necessary to confirm these hypotheses.

摘要

目的

探讨钙调蛋白 1(CALM1)和雌激素受体-α基因的单核苷酸多态性(SNP)是否与青少年特发性脊柱侧凸(AIS)的双曲相关。

方法

共纳入 67 例双曲 AIS 中国患者和 100 例健康对照。记录每位患者的曲线类型和 Cobb 角。Cobb 角至少为 30°。60 例 Cobb 角≥40°。根据主要曲线的顶点位置,有 40 例胸弯患者。通过 ABI3730 遗传分析仪分析 CALM1 基因中的 rs12885713(-16C>T)和 rs5871 以及雌激素受体 1(ER1)基因中的 rs2234693(Pvu II)和 rs9340799(Xba I)四个多态性位点。

结果

本研究表明:(i)双曲、Cobb 角≥40°和胸弯患者与健康对照组在 ER1 基因 rs2234693 位点的多态性分布上存在统计学差异(P=0.014、0.0128、0.0184);(ii)CALM1 基因 rs12885713 位点的多态性分布在双曲患者与对照组之间存在差异(P=0.034);(iii)CALM1 基因 rs5871 位点的多态性分布在胸弯患者与对照组之间存在差异(P=0.0102)。

结论

不同亚型的 AIS 可能与不同的 SNP 有关。CALM1 和 ER1 基因多态性的组合可能与 AIS 患者的双曲有关。需要进一步的研究来证实这些假设。

相似文献

3
Association of calmodulin1 gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
Orthop Surg. 2009 Feb;1(1):58-65. doi: 10.1111/j.1757-7861.2008.00011.x.
5
Association of estrogen receptor gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
Spine (Phila Pa 1976). 2006 May 1;31(10):1131-6. doi: 10.1097/01.brs.0000216603.91330.6f.
6
Association of estrogen receptor beta gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
Spine (Phila Pa 1976). 2009 Apr 15;34(8):760-4. doi: 10.1097/BRS.0b013e31818ad5ac.
7
The association study of calmodulin 1 gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
Biomed Res Int. 2014;2014:168106. doi: 10.1155/2014/168106. Epub 2014 Jan 16.

引用本文的文献

1
A Pilot Study of and Gene Variants in Primary Hyperparathyroidism.
Balkan J Med Genet. 2025 Mar 6;27(2):33-39. doi: 10.2478/bjmg-2024-0011. eCollection 2024 Dec.
2
Genetics and pathogenesis of scoliosis.
N Am Spine Soc J. 2024 Sep 6;20:100556. doi: 10.1016/j.xnsj.2024.100556. eCollection 2024 Dec.
3
Prevalence of scoliosis in children and adolescents: a systematic review and meta-analysis.
Front Pediatr. 2024 Jul 23;12:1399049. doi: 10.3389/fped.2024.1399049. eCollection 2024.
4
Differential Regulation of POC5 by ERα in Human Normal and Scoliotic Cells.
Genes (Basel). 2023 May 19;14(5):1111. doi: 10.3390/genes14051111.
5
Exploring the association between specific genes and the onset of idiopathic scoliosis: a systematic review.
BMC Med Genomics. 2022 May 19;15(1):115. doi: 10.1186/s12920-022-01272-2.
7
Estrogen Receptors (ESRs) Mutations in Adolescent Idiopathic Scoliosis: A Cross-Sectional Study.
Med Sci Monit. 2020 Mar 16;26:e921611. doi: 10.12659/MSM.921611.
9
Etiology of Adolescent Idiopathic Scoliosis: A Literature Review.
Asian Spine J. 2019 Jun;13(3):519-526. doi: 10.31616/asj.2018.0096. Epub 2019 Feb 13.
10
Positive Association between Gene and Susceptibility to Idiopathic Scoliosis in Bulgarian Population.
Anal Cell Pathol (Amst). 2018 Jul 18;2018:6836092. doi: 10.1155/2018/6836092. eCollection 2018.

本文引用的文献

1
The effects of ABCB1 3'-untranslated region variants on mRNA stability.
Drug Metab Dispos. 2008 Jan;36(1):10-5. doi: 10.1124/dmd.107.017087. Epub 2007 Oct 16.
3
Association of estrogen receptor gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.
Spine (Phila Pa 1976). 2006 May 1;31(10):1131-6. doi: 10.1097/01.brs.0000216603.91330.6f.
4
Identification of candidate regions for familial idiopathic scoliosis.
Spine (Phila Pa 1976). 2005 May 15;30(10):1181-7. doi: 10.1097/01.brs.0000162282.46160.0a.
7
SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis.
Hum Genet. 2004 Jun;115(1):81-9. doi: 10.1007/s00439-004-1121-y. Epub 2004 Apr 16.
8
Aetiology of idiopathic scoliosis: current concepts.
Pediatr Rehabil. 2003 Jul-Dec;6(3-4):137-70. doi: 10.1080/13638490310001642757.
9
Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.
Spine (Phila Pa 1976). 2003 Sep 1;28(17):2025-8; discussion 2029. doi: 10.1097/01.BRS.0000083235.74593.49.
10
Poly(A)-binding proteins: multifunctional scaffolds for the post-transcriptional control of gene expression.
Genome Biol. 2003;4(7):223. doi: 10.1186/gb-2003-4-7-223. Epub 2003 Jul 1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验