Literature DB >> 17922473

Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes.

Osama Alsmadi1, Khalid Al-Rubeaan, Salma M Wakil, Faiqa Imtiaz, Gamal Mohamed, Haya Al-Saud, Nouran Abu Al-Saud, Nasser Aldaghri, Shahinaz Mohammad, Brian F Meyer.   

Abstract

BACKGROUND: The E23K variant of KCNJ11 has been associated with type 2 diabetes (T2D) in several but not all populations studied. Thus far, despite a high incidence of T2D, the role of this variant in Arabs has not been established.
METHODS: We performed a case-control association study using 550 T2D Saudi patients (WHO criteria), and 335 controls (age>or=60; fasting plasma glucose<7 mmol/L). E23K genotyping was performed by using molecular beacon-based real time PCR assays.
RESULTS: The difference in K or risk allele frequency of cases and controls was significant with an OR of 1.7 (p=0.0001). The K allele is more common among T2D patients (21%) than in the age and sex matched controls (13.6%). This was consistent with a likely eventual conversion to T2D of younger normoglycemic individuals as they grow older.
CONCLUSIONS: Our results report for the first time a positive association of the E23K variant with T2D in an Arab population. Confirmation by a larger study is indicated. Copyright (c) 2007 John Wiley & Sons, Ltd.

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Year:  2008        PMID: 17922473     DOI: 10.1002/dmrr.777

Source DB:  PubMed          Journal:  Diabetes Metab Res Rev        ISSN: 1520-7552            Impact factor:   4.876


  17 in total

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Journal:  World J Diabetes       Date:  2015-03-15

3.  The KCNJ11 E23K gene polymorphism and type 2 diabetes mellitus in the Chinese Han population: a meta-analysis of 6,109 subjects.

Authors:  Yan-Yan Li
Journal:  Mol Biol Rep       Date:  2012-10-11       Impact factor: 2.316

4.  Genetic variations in magnesium-related ion channels may affect diabetes risk among African American and Hispanic American women.

Authors:  Kei Hang K Chan; Sara A Chacko; Yiqing Song; Michele Cho; Charles B Eaton; Wen-Chih H Wu; Simin Liu
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5.  Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population.

Authors:  Rosalind J Neuman; Jon Wasson; Gil Atzmon; Julio Wainstein; Yair Yerushalmi; Joseph Cohen; Nir Barzilai; Ilana Blech; Benjamin Glaser; M Alan Permutt
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6.  The ATP-sensitive K(+) channel ABCC8 S1369A type 2 diabetes risk variant increases MgATPase activity.

Authors:  Mohammad Fatehi; Mobeen Raja; Christian Carter; Daniel Soliman; Andrew Holt; Peter E Light
Journal:  Diabetes       Date:  2012-01       Impact factor: 9.461

7.  Association of KCNJ11 (E23K) gene polymorphism with susceptibility to type 2 diabetes in Iranian patients.

Authors:  Ali Rastegari; Mohammad Rabbani; Hamid Mirmohammad Sadeghi; Elham Faghih Imani; Akbar Hasanzadeh; Fatemeh Moazen
Journal:  Adv Biomed Res       Date:  2015-01-06

8.  FitSNPs: highly differentially expressed genes are more likely to have variants associated with disease.

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9.  Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population.

Authors:  Osama Alsmadi; Khalid Al-Rubeaan; Gamal Mohamed; Fadi Alkayal; Haya Al-Saud; Nouran Abu Al-Saud; Nasser Al-Daghri; Shahinaz Mohammad; Brian F Meyer
Journal:  BMC Med Genet       Date:  2008-07-26       Impact factor: 2.103

Review 10.  KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus.

Authors:  Polin Haghvirdizadeh; Zahurin Mohamed; Nor Azizan Abdullah; Pantea Haghvirdizadeh; Monir Sadat Haerian; Batoul Sadat Haerian
Journal:  J Diabetes Res       Date:  2015-09-13       Impact factor: 4.011

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