Literature DB >> 17852836

Butyrylcholinesterase K variants increase the risk of coronary artery disease in the population of western Iran.

A Vaisi-Raygani1, Z Rahimi, H Entezami, H Kharrazi, F Bahrhemand, H Tavilani, M Rezaei, A Kiani, B Nomanpour, T Pourmotabbed.   

Abstract

The conflicting results of several studies suggest that there is an association between the butyrylcholinesterase-K variant (BCHE-K, G1615A/Ala539Thr) and the risk of developing coronary artery disease (CAD) in diabetes and non-diabetic subjects. The objective of this study was to determine whether the presence of the BCHE-K variant exacerbates the risk of CAD in patients from western Iran with and without type 2 diabetes mellitus (T2DM). This case-control study comprised 464 subjects undergoing their first coronary angiography. They were matched and randomly assigned into four groups: CAD+T2DM+ (CAD/T2DM), CAD+DM(-) (CAD/ND), CAD(-)DM+ (T2DM/NCAD) and CAD(-)DM(-)(control). The BCHE-K variant was detected by PCR-RFLP. The BCHE-K allele frequency in CAD patients with and without T2DM [total CAD (TCAD)] and separately for each group (CAD/T2DM and CAD/ND) was significantly higher than in the control group (21.1 % versus 13.3 % (p = 0.001), 22.4 % versus 13.3 % (p = 0.001) and 19.7 % versus 13.3 % (p = 0.015), respectively). The odds ratios (ORs) for the BCHE-K heterozygous and homozygous variants in TCAD subjects were 1.65 (95 % CI 1.17-2.3; p = 0.004) and 4.3 (1.05-19.4; p = 0.048); for CAD/T2DM individuals 1.76 (1.2-2.6; p = 0.004) and 4.73 (0.96-23.3; p = 0.052); and for CAD/ND patients 1.53 (1.05-2.3; p = 0.029) and 3.88 (0.8-19.7; p = 0.7), respectively. The OR of the BCHE-K allele was found to be 1.74 (1.1-2.4; p = 0.001) in TCAD subjects, 1.87 (1.12-1.48; p = 0.001) in the CAD/T2DM group and 1.59 (1.04-1.4; p = 0.016) in CAD/ND subjects. These data suggest that the BCHE-K allele increases the risk of CAD in the population (with and without DM) in western parts of Iran, and its presence intensifies the risk of CAD in T2DM. The fact that the BCHE-K allele, even in the heterozygous form, exacerbates the risk of CAD in this population, suggests that a specific therapeutic intervention should be considered for this particular group of patients.

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Year:  2007        PMID: 17852836     DOI: 10.1080/00365510701576180

Source DB:  PubMed          Journal:  Scand J Clin Lab Invest        ISSN: 0036-5513            Impact factor:   1.713


  11 in total

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Authors:  Maryam Tanhapour; Shiva Shahmohamadnejad; Asad Vaisi-Raygani; Amir Kiani; Yadola Shakiba; Zohreh Rahimi; Fariborz Bahrehmand; Ebrahim Shakiba; Ali-Akbar Vaisi-Raygani; Reza Alibakhshi; Atefeh Eivazi; Tayebeh Pourmotabbed
Journal:  Mol Biol Rep       Date:  2018-12-01       Impact factor: 2.316

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Authors:  Beben Benyamin; Rita P Middelberg; Penelope A Lind; Anne M Valle; Scott Gordon; Dale R Nyholt; Sarah E Medland; Anjali K Henders; Andrew C Heath; Pamela A F Madden; Peter M Visscher; Daniel T O'Connor; Grant W Montgomery; Nicholas G Martin; John B Whitfield
Journal:  Hum Mol Genet       Date:  2011-08-23       Impact factor: 6.150

3.  Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease.

Authors:  Asad Vaisi-Raygani; Zohreh Rahimi; Haidar Tavilani; Hadiss Vaisi-Raygani; A Kiani; M Aminian; E Shakiba; Y Shakiba; Tayebeh Pourmotabbed
Journal:  Mol Biol Rep       Date:  2011-06-17       Impact factor: 2.316

4.  Butyrylcholinesterase Deficiency Promotes Adipose Tissue Growth and Hepatic Lipid Accumulation in Male Mice on High-Fat Diet.

Authors:  Vicky Ping Chen; Yang Gao; Liyi Geng; Michael B Stout; Michael D Jensen; Stephen Brimijoin
Journal:  Endocrinology       Date:  2016-06-14       Impact factor: 4.736

5.  Matrix metalloproteinase-9 functional promoter polymorphism 1562C>T increased risk of early-onset coronary artery disease.

Authors:  Massoud Saedi; Asad Vaisi-Raygani; Shahnaz Khaghani; Ahmad Shariftabrizi; M Rezaie; Parvin Pasalar; Zohreh Rahimi; Tayebeh Pourmotabbed
Journal:  Mol Biol Rep       Date:  2011-05-11       Impact factor: 2.316

6.  Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease.

Authors:  Asad Vaisi-Raygani; Hori Ghaneialvar; Zohreh Rahimi; Haidar Tavilani; Tayebeh Pourmotabbed; Ebrahim Shakiba; Aliakbar Vaisi-Raygani; Amir Kiani; Mahdi Aminian; Reza Alibakhshi; Cynthia Bartels
Journal:  Mol Biol Rep       Date:  2011-04-05       Impact factor: 2.316

7.  Butyrylcholinesterase K variant and the APOE-epsilon 4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients.

Authors:  Asad Vaisi-Raygani; Zohreh Rahimi; Haidar Tavilani; Tayebeh Pourmotabbed
Journal:  Mol Biol Rep       Date:  2009-08-15       Impact factor: 2.316

8.  Gestational diabetes mellitus (GDM) decreases butyrylcholinesterase (BChE) activity and changes its relationship with lipids.

Authors:  Larissa O Guimarães; Fabiana A de Andrade; Gleyse F Bono; Thaís E Setoguchi; Mariana B Brandão; Eleidi A Chautard-Freire-Maia; Izabella C R Dos Santos; Geraldo Picheth; Ana Cristina R de A Faria; Rosângela R Réa; Ricardo L R Souza; Lupe Furtado-Alle
Journal:  Genet Mol Biol       Date:  2013-02-28       Impact factor: 1.771

9.  Butyrylcholinesterase interactions with amylin may protect pancreatic cells in metabolic syndrome.

Authors:  Shani Shenhar-Tsarfaty; Tal Bruck; Estelle R Bennett; Tsafrir Bravman; Einor Ben Aassayag; Nir Waiskopf; Ori Rogowski; Natan Bornstein; Shlomo Berliner; Hermona Soreq
Journal:  J Cell Mol Med       Date:  2011-08       Impact factor: 5.310

10.  Vitamin D-binding protein and vitamin D receptor genotypes and 25-hydroxyvitamin D levels are associated with development of aortic and mitral valve calcification and coronary artery diseases.

Authors:  Amir Kiani; Ehsan Mohamadi-Nori; Asad Vaisi-Raygani; Maryam Tanhapour; Said Elahi-Rad; Fariborz Bahrehmand; Zohreh Rahimi; Tayebeh Pourmotabbed
Journal:  Mol Biol Rep       Date:  2019-07-29       Impact factor: 2.316

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