Assessment of the role of paraoxonase gene polymorphism (Q192R) and paraoxonase activity in the susceptibility to atherosclerosis among lead-exposed workers

被引:13
|
作者
Kamal, Manal [1 ,2 ]
Fathy, Mona M. [1 ,2 ]
Taher, Eman [3 ]
Hasan, Manal [4 ]
Tolba, May [5 ]
机构
[1] Cairo Univ, Dept Clin & Chem Pathol, Cairo, Egypt
[2] Cairo Univ, Dept Community Med, Cairo, Egypt
[3] Cairo Univ, Dept Ind Med & Occupat Dis, Cairo, Egypt
[4] Cairo Univ, Dept Internal Med, Cairo, Egypt
[5] Cairo Univ, Fac Med, Cairo, Egypt
关键词
LOW-DENSITY-LIPOPROTEIN; CARDIOVASCULAR-DISEASE; NORTHERN NIGERIA; LIPID PROFILES; RISK; CHOLESTEROL; INHIBITION; OXIDATION; METALS; PLASMA;
D O I
10.4103/0256-4947.84625
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND AND OBJECTIVE: Lead exposure is a well known cause of cardiovascular damage, including atherosclerosis. Paraoxonase 1 (PON1), a high-density lipoprotein-associated antioxidant enzyme, is capable of hydrolyzing oxidized lipids and thus it protects against atherosclerosis. The mechanism by which heavy metals inhibit serum PON1 activity is still not clear. Our aim was to detect the association between lead exposure and serum PON1 activity and lipid profile and also to study the polymorphism of the PON1 gene. DESIGN AND SETTING: A case-control, cross-sectional study conducted from June 2008 until May 2009. SUBJECTS AND METHODS: Male workers (n= 100) in a lead battery manufactory were recruited for this study. They were compared with 100 male age-matched workers not exposed to lead (control group). Serum lipid profile, paraoxonase activity and lead were measured in blood samples. The DNA was extracted for detecting the Q192R polymorphism of the PON1 gene by polymerase chain reaction followed by restriction fragment length polymorphism. RESULTS: There was significant difference in triglycerides, total cholesterol and high-density lipoprotein cholesterol (HDL-C) (P=. 01,. 05 and. 04, respectively) between cases and controls. Multiple linear regression analysis showed that blood lead levels were significantly associated with decreased serum paraoxonase activity (P=. 03) in lead workers. The paraoxonase genotype QR was the most prevalent in 34/53 subjects (64%) among the lead-exposed groups, while the genotype QQ was more prevalent in the control group, in 15/25 subjects (60%), with a significant difference between the control and other groups (P <. 05). CONCLUSION: Lead exposure is associated with increased triglycerides, total cholesterol and low-density lipoprotein cholesterol and decreased HDL-C. Because of the protective role of PON1 in the development of atherosclerosis, a decrease in serum PON1 activity due to lead exposure may render individuals more susceptible to atherosclerosis.
引用
收藏
页码:481 / 487
页数:7
相关论文
共 50 条
  • [41] Paraoxonase 192 Q/R gene polymorphism, enzyme activity and coronary heart disease in type 2 diabetes
    Gorshunska, M.
    Karachentsev, I.
    Atramentova, L.
    Krasova, N.
    Tyzhnenko, T.
    Pochernyaev, A.
    Leshchenko, Z.
    Fedorova, G.
    Gladkih, A.
    Kravchun, N.
    Khizhnyak, O.
    Poltorak, V.
    DIABETOLOGIA, 2009, 52 : S522 - S523
  • [42] PARAOXONASE ACTIVITY AND PON1 (Q/R192) GENE POLYMORPHISM IN ISCHEMIC STROKE PATIENTS
    Murugan, Magesh Mugundan
    Alagirisamy, Renuka
    Manokaran, Sharmila
    Balakrishnan, Anandan
    INTERNATIONAL JOURNAL OF LIFE SCIENCE AND PHARMA RESEARCH, 2012, 2 (04): : L169 - L176
  • [43] Paraoxonase (Pon1) Q192R polymorphism and serum Pon1 activity in diabetic patients on maintenance hemodialysis
    Zhang, B
    Eto, S
    Fan, P
    Bian, C
    Shimoji, E
    Saito, T
    Saku, K
    CLINICAL NEPHROLOGY, 2003, 60 (04) : 257 - 265
  • [44] The paraoxonase L55M and Q192R gene polymorphisms and myocardial infarction in a Tunisian population
    Kallel, Amani
    Sediri, Yousra
    Sbai, Mohamed Hedi
    Mourali, Mohamed Sami
    Feki, Moncef
    Elasmi, Monia
    Taieb, Samah Haj
    Sanhaji, Haifa
    Souheil, Omar
    Mechmeche, Rachid
    Jemaa, Riadh
    Kaabachi, Naziha
    CLINICAL BIOCHEMISTRY, 2010, 43 (18) : 1461 - 1463
  • [45] Association of L55M and Q192R Polymorphisms of Paraoxonase-1 Gene with Preeclampsia
    Yaghmaei, Minoo
    Hashemi, Mohammad
    Azarian, Azin
    Moazeni-Roodi, Abdolkarim
    Mokhtari, Mojgan
    Naghavai, Anoosh
    Salimi, Saeideh
    Mohammadi, Mandi
    Taheri, Mohsen
    Ghavami, Saeid
    ARCHIVES OF MEDICAL RESEARCH, 2011, 42 (04) : 324 - 328
  • [46] Paraoxonase-1 Q192R Polymorphism and Lipid Peroxidation and Antioxidant Defense State in Russian Healthy Teenagers
    Bairova, Tatjana A.
    Ershova, Oksana A.
    Darenskaya, Marina
    Rychkova, Lyubov V.
    Grebenkina, Lyudmila
    Kolesnikova, Lyubov
    FREE RADICAL BIOLOGY AND MEDICINE, 2022, 180 : 60 - 60
  • [47] 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
    Luu, Hung N.
    Kingah, Pascal L.
    North, Kari
    Boerwinkle, Eric
    Volcik, Kelly A.
    ANNALS OF EPIDEMIOLOGY, 2011, 21 (11) : 815 - 823
  • [48] Association of Paraoxonase1 Gene Q192R Polymorphism and Apolipoprotein B in Asian Indian Women with Coronary Artery Disease Risk
    Deshpande, Chetana S.
    Singhal, Rekha S.
    Mukherjee, Manjari S.
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2013, 17 (02) : 140 - 146
  • [49] Synergistic effects between Q192R polymorphism of paraoxonase I gene and some conventional risk factors in premature coronary artery disease
    Balcerzyk, Anna
    Zak, Iwona
    Krauze, Jolanta
    ARCHIVES OF MEDICAL RESEARCH, 2007, 38 (05) : 545 - 550
  • [50] Association between Q192R Polymorphism of Paraoxonase-1 Gene and Risk of Coronary Artery Disease: A Case-control Study
    Kaur, Harleen
    Kaur, Jaskiran
    Mohan, Gurinder
    Sharma, Nishant
    Kukreja, Sahiba
    JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2023, 17 (08) : BC5 - BC8