Literature DB >> 18582459

PON1Q192R polymorphism is associated with lipid profile in Mexican men with Mayan ascendancy.

Norma Pérez-Herrera1, Carlos May-Pech, Isabel Hernández-Ochoa, Jorge Castro-Mañé, Elizabeth Rojas-García, Víctor Hugo Borja-Aburto, Teresa Castillo-Burguete, Betzabet Quintanilla-Vega.   

Abstract

Paraoxonase (PON1) enzyme is associated with high-density lipoproteins (HDL) that prevents low-density lipoprotein (LDL) oxidation. PON1Q192R polymorphism is associated with a risk of coronary heart disease and low HDL levels in case-control studies, but the issue is yet unresolved. Mexico has shown an increase in cardiovascular diseases, and some genetic factors may play a role. Our purpose was to evaluate the association between PON1Q192R and L55M polymorphisms and serum lipid profile in a healthy Mexican population. Ninety unrelated male inhabitants from southeastern Mexico with Mayan ascendancy agreed to participate. Demographic characteristics, lifestyle and medical history were obtained by questionnaire. Lipid profile was determined by enzymatic methods, PON1 activity by using paraoxon and phenylacetate and PON1 genotype by real-time PCR. HDL-cholesterol (HDL-C) levels were associated with genotype: 192RR homozygote subjects had lower HDL-C levels than 192QQ homozygotes, and individuals with 192RR and 192QR genotypes had an odds ratio (OR)=7.05 (95% confidence interval (CI)=1.29-38.34) of having HDL-C <60 mg/dL. Individuals with higher paraoxonase activity (>600.18 U/L) had a slight risk (OR=4.9, 95% CI=0.83-22.02) of having HDL-C <60 mg/dL. PON155LM polymorphism was associated with higher LDL-cholesterol. PON1Q192R polymorphism showed a role in modulating lipid profile: 192RR homozygotes showed the least favorable lipoprotein levels.

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Year:  2008        PMID: 18582459     DOI: 10.1016/j.yexmp.2008.05.003

Source DB:  PubMed          Journal:  Exp Mol Pathol        ISSN: 0014-4800            Impact factor:   3.362


  10 in total

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Journal:  Antioxidants (Basel)       Date:  2022-03-31

2.  Arylesterase activity of paraoxonase 1 (PON1) on HDL3 and HDL2: Relationship with Q192R, C-108T, and L55M polymorphisms.

Authors:  Sandra Y Valencia C; Carlos A Isaza M; Julieta Henao B; Leonardo Beltrán A; Nelsy Loango; Patricia Landázuri
Journal:  Biochem Biophys Rep       Date:  2021-03-18

3.  Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey.

Authors:  Man-huei Chang; Ajay Yesupriya; Renée M Ned; Patricia W Mueller; Nicole F Dowling
Journal:  BMC Med Genet       Date:  2010-04-20       Impact factor: 2.103

4.  Relationship between PON1L55M and Q192R gene polymorphisms and high APO B/APO A-I ratios.

Authors:  Amirhosein Khoshi; Yousof Mortazavi; Abbass Akbari; Sepideh Sokhanvar; Sadraddin Kalantari
Journal:  Indian J Clin Biochem       Date:  2009-12-30

5.  PON-1 haplotype (-108C>T, L55M, and Q192R) modulates the serum levels and activity PONase promoting an atherogenic lipid profile in rheumatoid arthritis patients.

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Review 7.  Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

Authors:  C S Paththinige; N D Sirisena; Vhw Dissanayake
Journal:  Lipids Health Dis       Date:  2017-06-02       Impact factor: 3.876

8.  Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia.

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9.  Genetic Variability of Antioxidative Mechanisms and Cardiotoxicity after Adjuvant Radiotherapy in HER2-Positive Breast Cancer Patients.

Authors:  Tanja Marinko; Jakob Timotej Stojanov Konda; Vita Dolžan; Katja Goričar
Journal:  Dis Markers       Date:  2020-12-19       Impact factor: 3.434

10.  A Genetic Biomarker of Oxidative Stress, the Paraoxonase-1 Q192R Gene Variant, Associates with Cardiomyopathy in CKD: A Longitudinal Study.

Authors:  E Dounousi; I Bouba; B Spoto; K Pappas; G Tripepi; I Georgiou; A Tselepis; M Elisaf; D Tsakiris; C Zoccali; K Siamopoulos
Journal:  Oxid Med Cell Longev       Date:  2016-05-30       Impact factor: 6.543

  10 in total

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