Literature DB >> 28835968

PON1 L55M and Q192R gene polymorphisms and CAD risks in patients with hyperlipidemia : Clinical study of possible associations.

H Chen1,2, S Ding3,4, M Zhou1, X Wu5, X Liu2, J Liu6, Y Wu2, D Liu5.   

Abstract

OBJECTIVE: A decreased plasma high density lipoprotein (HDL) cholesterol level is a strong risk factor for coronary artery disease (CAD). Antioxidant activity of HDL mainly lies in the activity of paraoxonase (PON). This study aimed to investigate the relationships between PON1 L55M and Q192R polymorphisms, and the risks of CAD in patients with hyperlipidemia.
METHODS: From January 2014 to January 2016, 244 patients were divided into hyperlipidemia, hyperlipidemia + CAD, and control groups. The hyperlipidemia and hyperlipidemia + CAD groups were designated as the case group. Serum PON1 concentrations were measured using the enzyme-linked immunosorbent assay. After isolating genomic DNA, the PON1 L55M and Q192R genes were amplified by polymerase chain reaction and sequenced.
RESULTS: In the case group, the genotypes LM and LL were detected significantly more often than in the control group, as were the alleles R (33.33%, 42.12%) and L (22.78%, 29.11%). The frequency of QR and RR genotypes was significantly higher in the hyperlipidemia + CAD group than in the hyperlipidemia group; the allele R in the hyperlipidemia + CAD group (42.77%) was more frequent than in the hyperlipidemia group (23.78%). The Q192R polymorphism was associated with low serum PON1 concentrations, and the lowest concentration was observed in the 192QR + 192RR genotype (P = 0.03). Logistic regression analysis showed a significant correlation between the 192R allele and smoking (P = 0.03), body mass index (P = 0.02), systolic blood pressure (P = 0.004), total cholesterol (P = 0.03), triglycerides (P = 0.01), HDL (P = 0.004), and low density lipoprotein (P = 0.02).
CONCLUSION: The PON1 alleles 192R and 55L are associated with CAD, and the Q192R polymorphism may be a risk factor for CAD.

Entities:  

Keywords:  Coronary artery disease; Gene polymorphism; High density lipoprotein cholesterol; Lipid metabolism; Paraoxonase-1

Mesh:

Substances:

Year:  2017        PMID: 28835968     DOI: 10.1007/s00059-017-4611-0

Source DB:  PubMed          Journal:  Herz        ISSN: 0340-9937            Impact factor:   1.443


  35 in total

1.  Paraoxonase Gln-Arg(192) and Leu-Met(55) gene polymorphisms and enzyme activity in a population with a low rate of coronary heart disease.

Authors:  Natàlia Ferré; Mònica Tous; Antoni Paul; Alberto Zamora; Juan J Vendrell; Alfredo Bardají; Jordi Camps; Cristobal Richart; Jorge Joven
Journal:  Clin Biochem       Date:  2002-05       Impact factor: 3.281

2.  Interaction of folate intake and the paraoxonase Q192R polymorphism with risk of incident coronary heart disease and ischemic stroke: the atherosclerosis risk in communities study.

Authors:  Hung N Luu; Pascal L Kingah; Kari North; Eric Boerwinkle; Kelly A Volcik
Journal:  Ann Epidemiol       Date:  2011-11       Impact factor: 3.797

3.  Low serum PON1 activity: an independent risk factor for coronary artery disease in North-West Indian type 2 diabetics.

Authors:  Nidhi Gupta; K B K Binu; Surjit Singh; Nagarjuna V Maturu; Yash P Sharma; Anil Bhansali; Kiran Dip Gill
Journal:  Gene       Date:  2012-02-04       Impact factor: 3.688

4.  The relationship of PON1 QR 192 and LM 55 polymorphisms with serum paraoxonase activities of Turkish diabetic patients.

Authors:  Durdu Altuner; Ilker Ates; Sinan H Suzen; Gonul Varan Koc; Yalcin Aral; Asuman Karakaya
Journal:  Toxicol Ind Health       Date:  2011-04-19       Impact factor: 2.273

5.  Paraoxonase 1 polymorphisms as the risk factor of coronary heart disease in a Thai population.

Authors:  Atip Likidlilid; Krittapoom Akrawinthawong; Saiphon Poldee; Charn Sriratanasathavorn
Journal:  Acta Cardiol       Date:  2010-12       Impact factor: 1.718

6.  Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus.

Authors:  Sudeshna Dasgupta; F Yesim Demirci; Amy S Dressen; Amy H Kao; Elisa Y Rhew; Rosalind Ramsey-Goldman; Susan Manzi; Candace M Kammerer; M Ilyas Kamboh
Journal:  BMC Med Genet       Date:  2011-01-11       Impact factor: 2.103

7.  Single nucleotide polymorphisms associated with abnormal coronary microvascular function.

Authors:  Satoshi Yoshino; Rebecca Cilluffo; Patricia J M Best; Elizabeth J Atkinson; Tatsuo Aoki; Julie M Cunningham; Mariza de Andrade; Byoung-Joo Choi; Lilach O Lerman; Amir Lerman
Journal:  Coron Artery Dis       Date:  2014-06       Impact factor: 1.439

Review 8.  Heart rate reduction in coronary artery disease and heart failure.

Authors:  Roberto Ferrari; Kim Fox
Journal:  Nat Rev Cardiol       Date:  2016-05-26       Impact factor: 32.419

Review 9.  The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis.

Authors:  Debbie A Lawlor; Ian N M Day; Tom R Gaunt; Lesley J Hinks; Patricia J Briggs; Matthew Kiessling; Nick Timpson; George Davey Smith; Shah Ebrahim
Journal:  BMC Genet       Date:  2004-06-23       Impact factor: 2.797

10.  Paraoxonase-1 is not associated with coronary artery calcification in type 2 diabetes: results from the PREDICT study.

Authors:  Bharti Mackness; Judit Marsillach; Robert S Elkeles; Ian F Godsland; Michael D Feher; Michael B Rubens; Marcus D Flather; Steve E Humphries; Jackie Cooper; Mike Mackness
Journal:  Dis Markers       Date:  2012       Impact factor: 3.434

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  3 in total

1.  Association between activity and genotypes of paraoxonase1 L55M (rs854560) increases the disease activity of rheumatoid arthritis through oxidative stress.

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

2.  Functional implications of single nucleotide polymorphisms rs662 and rs854860 on the antioxidative activity of paraoxonase1 (PON1) in patients with rheumatoid arthritis.

Authors:  Arkaitz Mucientes; Benjamín Fernández-Gutiérrez; Eva Herranz; Luis Rodriguez-Rodriguez; Jezabel Varadé; Elena Urcelay; José Ramón Lamas
Journal:  Clin Rheumatol       Date:  2018-12-26       Impact factor: 2.980

3.  Decreased serum PON1 arylesterase activity in familial hypercholesterolemia patients with a mutated LDLR gene.

Authors:  Muhammad Idrees; Abdul Rauf Siddiq; Muhammad Ajmal; Muhammad Akram; Rana Rehan Khalid; Alamdar Hussain; Raheel Qamar; Habib Bokhari
Journal:  Genet Mol Biol       Date:  2018-07-23       Impact factor: 1.771

  3 in total

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