Literature DB >> 23934357

The association of SCGB3A2 polymorphisms with the risk of Graves' disease: a meta-analysis.

Liqiong Xue1, Bing Han, Chunming Pan, Huaidong Song.   

Abstract

The aim of this study is to assess the association of the SCGB3A2 -112G>A promoter polymorphism with Graves' disease(GD) using a meta-analysis. Relevant studies were identified using PubMed and EMBASE electronic databases. A meta-analysis of relevant studies was performed. This meta-analysis included four case-control studies, containing 6,913 GD cases (Caucasian 3904, Han 3009) and 7,185 controls(Caucasian 4155, Han 3030). The combined results showed a significant difference in genotype distribution (-112A/G) between GD and control populations (A vs. G P = 1.53 × 10(-7); GG vs. AA+AG P = 6.78 × 10(-9)). Meta-analysis was performed using a fixed-effects model. Under the dominant model (GG/AA + GA), the AA and GA genotypes were significantly associated with GD (pooled OR = 1.24, 95 % CI 1.12-1.37). When the two European studies are combined, the AA and GA genotypes were also significantly associated with GD (pooled OR = 1.29, 95 % CI 1.20-1.39). This meta-analysis suggests that SCGB3A2 polymorphism at positions -112G>A was associated with GD both in Chinese and Caucasian population.

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Year:  2013        PMID: 23934357     DOI: 10.1007/s12020-013-0021-0

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.633


  32 in total

1.  Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease.

Authors:  Hironori Ueda; Joanna M M Howson; Laura Esposito; Joanne Heward; Hywel Snook; Giselle Chamberlain; Daniel B Rainbow; Kara M D Hunter; Annabel N Smith; Gianfranco Di Genova; Mathias H Herr; Ingrid Dahlman; Felicity Payne; Deborah Smyth; Christopher Lowe; Rebecca C J Twells; Sarah Howlett; Barry Healy; Sarah Nutland; Helen E Rance; Vin Everett; Luc J Smink; Alex C Lam; Heather J Cordell; Neil M Walker; Cristina Bordin; John Hulme; Costantino Motzo; Francesco Cucca; J Fred Hess; Michael L Metzker; Jane Rogers; Simon Gregory; Amit Allahabadia; Ratnasingam Nithiyananthan; Eva Tuomilehto-Wolf; Jaakko Tuomilehto; Polly Bingley; Kathleen M Gillespie; Dag E Undlien; Kjersti S Rønningen; Cristian Guja; Constantin Ionescu-Tîrgovişte; David A Savage; A Peter Maxwell; Dennis J Carson; Chris C Patterson; Jayne A Franklyn; David G Clayton; Laurence B Peterson; Linda S Wicker; John A Todd; Stephen C L Gough
Journal:  Nature       Date:  2003-04-30       Impact factor: 49.962

2.  The -112G>A polymorphism of the secretoglobin 3A2 (SCGB3A2) gene encoding uteroglobin-related protein 1 (UGRP1) increases risk for the development of Graves' disease in subsets of patients with elevated levels of immunoglobulin E.

Authors:  Dimitry A Chistiakov; Natalia V Voronova; Rust I Turakulov; Kirill V Savost'anov
Journal:  J Appl Genet       Date:  2010-12-18       Impact factor: 3.240

3.  Association study between the IL4, IL13, IRF1 and UGRP1 genes in chromosomal 5q31 region and Chinese Graves' disease.

Authors:  Yu Yang; Sun Lingling; Jin Ying; Li Yushu; Shan Zhongyan; Huang Wei; Teng Weiping
Journal:  J Hum Genet       Date:  2005-09-30       Impact factor: 3.172

4.  A polymorphism in the human UGRP1 gene promoter that regulates transcription is associated with an increased risk of asthma.

Authors:  Tomoaki Niimi; Mitsuru Munakata; Catherine L Keck-Waggoner; Nicholas C Popescu; Roy C Levitt; Michie Hisada; Shioko Kimura
Journal:  Am J Hum Genet       Date:  2002-01-25       Impact factor: 11.025

5.  Meta-analysis in clinical trials.

Authors:  R DerSimonian; N Laird
Journal:  Control Clin Trials       Date:  1986-09

6.  CD40 C/T(-1) and CTLA-4 A/G(49) SNPs are associated with autoimmune thyroid diseases in the Chinese population.

Authors:  Jing Yang; Qiu Qin; Ni Yan; Yuan-Feng Zhu; Cui Li; Xiang-Ju Yang; Xuan Wang; Madhu Pandey; Peng Hou; Jin-An Zhang
Journal:  Endocrine       Date:  2011-08-25       Impact factor: 3.633

7.  The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

Authors:  M R Velaga; V Wilson; C E Jennings; C J Owen; S Herington; P T Donaldson; S G Ball; R A James; R Quinton; P Perros; S H S Pearce
Journal:  J Clin Endocrinol Metab       Date:  2004-11       Impact factor: 5.958

8.  Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease.

Authors:  Hitomi Hiratani; Donald W Bowden; Satoshi Ikegami; Senji Shirasawa; Akira Shimizu; Yoshinori Iwatani; Takashi Akamizu
Journal:  J Clin Endocrinol Metab       Date:  2005-03-01       Impact factor: 5.958

9.  No evidence for association between the -112G/A polymorphism of UGRP1 and childhood atopic asthma.

Authors:  Z Jian; J Nakayama; E Noguchi; M Shibasaki; T Arinami
Journal:  Clin Exp Allergy       Date:  2003-07       Impact factor: 5.018

10.  Variation in Uteroglobin-Related Protein 1 (UGRP1) gene is associated with allergic rhinitis in Singapore Chinese.

Authors:  Anand Kumar Andiappan; Wei Sheng Yeo; Pallavi Nilkanth Parate; Ramani Anantharaman; Bani Kaur Suri; De Yun Wang; Fook Tim Chew
Journal:  BMC Med Genet       Date:  2011-03-16       Impact factor: 2.103

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  2 in total

1.  Increased chemokine (C-C motif) ligand 21 expression and its correlation with osteopontin in Graves' disease.

Authors:  Yicheng Qi; Xiaoli Li; Qianwei Zhang; Fengjiao Huang; Dongping Lin; Yulin Zhou; Jie Hong; Bin Cui; Weiqing Wang; Guang Ning; Shu Wang
Journal:  Endocrine       Date:  2015-03-15       Impact factor: 3.633

Review 2.  Emerging role of an immunomodulatory protein secretoglobin 3A2 in human diseases.

Authors:  Shioko Kimura; Shigetoshi Yokoyama; Aprile L Pilon; Reiko Kurotani
Journal:  Pharmacol Ther       Date:  2022-01-10       Impact factor: 13.400

  2 in total

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