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Volumn 18, Issue 2, 2014, Pages 274-282

KCNQ1 rs2237892 C→T gene polymorphism and type 2 diabetes mellitus in the Asian population: A meta-analysis of 15,736 patients

Author keywords

Asian; KCNQ1; Polymorphism; Rs2237892; Type 2 diabetes mellitus

Indexed keywords

KCNQ1 PROTEIN, HUMAN; POTASSIUM CHANNEL KCNQ1;

EID: 84893682991     PISSN: 15821838     EISSN: None     Source Type: Journal    
DOI: 10.1111/jcmm.12185     Document Type: Article
Times cited : (18)

References (23)
  • 1
    • 77950263954 scopus 로고    scopus 로고
    • Prevalence of diabetes among men and women in China
    • Yang W, Lu J, Weng J, et al. Prevalence of diabetes among men and women in China. N Engl J Med. 2010; 362: 1090-101.
    • (2010) N Engl J Med , vol.362 , pp. 1090-1101
    • Yang, W.1    Lu, J.2    Weng, J.3
  • 2
    • 50449085212 scopus 로고    scopus 로고
    • SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
    • Unoki H, Takahashi A, Kawaguchi T, et al. SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. Nat Genet. 2008; 40: 1098-102.
    • (2008) Nat Genet , vol.40 , pp. 1098-1102
    • Unoki, H.1    Takahashi, A.2    Kawaguchi, T.3
  • 3
    • 50449085998 scopus 로고    scopus 로고
    • Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
    • Yasuda K, Miyake K, Horikawa Y, et al. Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. Nat Genet. 2008; 40: 1092-7.
    • (2008) Nat Genet , vol.40 , pp. 1092-1097
    • Yasuda, K.1    Miyake, K.2    Horikawa, Y.3
  • 4
    • 57349191471 scopus 로고    scopus 로고
    • Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population
    • Lee YH, Kang ES, Kim SH, et al. Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population. J Hum Genet. 2008; 53: 991-8.
    • (2008) J Hum Genet , vol.53 , pp. 991-998
    • Lee, Y.H.1    Kang, E.S.2    Kim, S.H.3
  • 5
    • 67349097455 scopus 로고    scopus 로고
    • Variants in KCNQ1 are associated with susceptibility to type 2 diabetes in the population of mainland China
    • Liu Y, Zhou DZ, Zhang D, et al. Variants in KCNQ1 are associated with susceptibility to type 2 diabetes in the population of mainland China. Diabetologia. 2009; 52: 1315-21.
    • (2009) Diabetologia , vol.52 , pp. 1315-1321
    • Liu, Y.1    Zhou, D.Z.2    Zhang, D.3
  • 6
    • 77955365281 scopus 로고    scopus 로고
    • KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
    • Chen Z, Yin Q, Ma G, et al. KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population. Cardiovasc Diabetol. 2010; 9: 35.
    • (2010) Cardiovasc Diabetol , vol.9 , pp. 35
    • Chen, Z.1    Yin, Q.2    Ma, G.3
  • 7
    • 67349205597 scopus 로고    scopus 로고
    • Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population
    • Hu C, Wang C, Zhang R, et al. Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population. Diabetologia. 2009; 52: 1322-5.
    • (2009) Diabetologia , vol.52 , pp. 1322-1325
    • Hu, C.1    Wang, C.2    Zhang, R.3
  • 8
    • 77952701364 scopus 로고    scopus 로고
    • Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population
    • Han X, Luo Y, Ren Q, et al. Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population. BMC Med Genet. 2010; 11: 81.
    • (2010) BMC Med Genet , vol.11 , pp. 81
    • Han, X.1    Luo, Y.2    Ren, Q.3
  • 9
    • 78649526616 scopus 로고    scopus 로고
    • Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies
    • Xu M, Bi Y, Xu Y, et al. Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies. PLoS ONE. 2010; 5: e14022.
    • (2010) PLoS ONE , vol.5
    • Xu, M.1    Bi, Y.2    Xu, Y.3
  • 10
    • 78751647900 scopus 로고    scopus 로고
    • Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US
    • Been LF, Ralhan S, Wander GS, et al. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3, 310 subjects from India and the US. BMC Med Genet. 2011; 12: 18.
    • (2011) BMC Med Genet , vol.12 , pp. 18
    • Been, L.F.1    Ralhan, S.2    Wander, G.S.3
  • 11
    • 82955229603 scopus 로고    scopus 로고
    • KCNQ1 variants associate with type 2 diabetes in Malaysian Malay subjects
    • Saif-Ali R, Muniandy S, Al-Hamodi Z, et al. KCNQ1 variants associate with type 2 diabetes in Malaysian Malay subjects. Ann Acad Med Singapore. 2011; 40: 488-92.
    • (2011) Ann Acad Med Singapore , vol.40 , pp. 488-492
    • Saif-Ali, R.1    Muniandy, S.2    Al-Hamodi, Z.3
  • 12
    • 84860234285 scopus 로고    scopus 로고
    • KCNQ1 gene polymorphisms are associated with the therapeutic efficacy of repaglinide in Chinese type 2 diabetic patients
    • Dai XP, Huang Q, Yin JY, et al. KCNQ1 gene polymorphisms are associated with the therapeutic efficacy of repaglinide in Chinese type 2 diabetic patients. Clin Exp Pharmacol Physiol. 2012; 39: 462-8.
    • (2012) Clin Exp Pharmacol Physiol , vol.39 , pp. 462-468
    • Dai, X.P.1    Huang, Q.2    Yin, J.Y.3
  • 13
    • 0031054075 scopus 로고    scopus 로고
    • A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    • Neyroud N, Tesson F, Denjoy I, et al. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nat Genet. 1997; 15: 186-9.
    • (1997) Nat Genet , vol.15 , pp. 186-189
    • Neyroud, N.1    Tesson, F.2    Denjoy, I.3
  • 14
    • 67349205529 scopus 로고    scopus 로고
    • Contribution of long-QT syndrome genetic variants in sudden infant death syndrome
    • Millat G, Kugener B, Chevalier P, et al. Contribution of long-QT syndrome genetic variants in sudden infant death syndrome. Pediatr Cardiol. 2009; 30: 502-9.
    • (2009) Pediatr Cardiol , vol.30 , pp. 502-509
    • Millat, G.1    Kugener, B.2    Chevalier, P.3
  • 15
    • 28344448471 scopus 로고    scopus 로고
    • Effects of I(Ks) channel inhibitors in insulin-secreting INS-1 cells
    • Ullrich S, Su J, Ranta F, et al. Effects of I(Ks) channel inhibitors in insulin-secreting INS-1 cells. Pflugers Arch. 2005; 451: 428-36.
    • (2005) Pflugers Arch , vol.451 , pp. 428-436
    • Ullrich, S.1    Su, J.2    Ranta, F.3
  • 16
    • 79955595167 scopus 로고    scopus 로고
    • Variants in KCNQ1, AP3S1, MAN2A1, and ALDH7A1 and the risk of type 2 diabetes in the Chinese Northern Han population: a case-control study and meta-analysis
    • Zhou JB, Yang JK, Zhao L, et al. Variants in KCNQ1, AP3S1, MAN2A1, and ALDH7A1 and the risk of type 2 diabetes in the Chinese Northern Han population: a case-control study and meta-analysis. Med Sci Monit. 2010; 16: BR179-83.
    • (2010) Med Sci Monit , vol.16
    • Zhou, J.B.1    Yang, J.K.2    Zhao, L.3
  • 17
    • 75149150236 scopus 로고    scopus 로고
    • Polymorphisms identified through genome-wide association studies and their associations with type 2 diabetes in Chinese, Malays, and Asian-Indians in Singapore
    • Tan JT, Ng DP, Nurbaya S, et al. Polymorphisms identified through genome-wide association studies and their associations with type 2 diabetes in Chinese, Malays, and Asian-Indians in Singapore. J Clin Endocrinol Metab. 2010; 95: 390-7.
    • (2010) J Clin Endocrinol Metab , vol.95 , pp. 390-397
    • Tan, J.T.1    Ng, D.P.2    Nurbaya, S.3
  • 18
    • 84868328459 scopus 로고    scopus 로고
    • The association between KCNQ1 gene polymorphism and type 2 diabetes risk: a meta-analysis
    • Doi: 10.1371/journal.pone.0048578.
    • Sun Q, Song K, Shen X, et al. The association between KCNQ1 gene polymorphism and type 2 diabetes risk: a meta-analysis. PLoS ONE. 2012; 7: e48578. Doi: 10.1371/journal.pone.0048578.
    • (2012) PLoS ONE , vol.7
    • Sun, Q.1    Song, K.2    Shen, X.3
  • 19
    • 84878416943 scopus 로고    scopus 로고
    • Meta-analysis of the effect of KCNQ1 gene polymorphism on the risk of type 2 diabetes
    • Liu J, Wang F, Wu Y, et al. Meta-analysis of the effect of KCNQ1 gene polymorphism on the risk of type 2 diabetes. Mol Biol Rep. 2013; 40: 3557-67.
    • (2013) Mol Biol Rep , vol.40 , pp. 3557-3567
    • Liu, J.1    Wang, F.2    Wu, Y.3
  • 20
    • 0014297593 scopus 로고
    • The effectiveness of adjustment by subclassification in removing bias in observational studies
    • Cochran WG. The effectiveness of adjustment by subclassification in removing bias in observational studies. Biometrics. 1968; 24: 295-313.
    • (1968) Biometrics , vol.24 , pp. 295-313
    • Cochran, W.G.1
  • 22
    • 84959801619 scopus 로고
    • Statistical aspects of the analysis of data from retrospective studies of disease
    • Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst. 1959; 22: 719-48.
    • (1959) J Natl Cancer Inst , vol.22 , pp. 719-748
    • Mantel, N.1    Haenszel, W.2
  • 23
    • 0030922816 scopus 로고    scopus 로고
    • Bias in meta-analysis detected by a simple, graphical test
    • Egger M, Davey Smith G, Schneider M, et al. Bias in meta-analysis detected by a simple, graphical test. Br Med J. 1997; 315: 629-34.
    • (1997) Br Med J , vol.315 , pp. 629-634
    • Egger, M.1    Davey Smith, G.2    Schneider, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.