Introduction

High-density lipoproteins (HDL) have received increasing attention because they have been shown to retard the oxidation of LDL. The HDL-associated enzyme, paraoxonase 1 (PON1), is one of the enzymes located on HDL particles responsible for preventing the accumulation of lipid peroxides on LDL.^{1 2 3 4} The anti-atherogenic properties of HDL are mainly related to reverse cholesterol transport, stabilization of atherosclerotic plaque, and anti-inflammatory and anti-oxidant effects.^{5 6} Apolipoprotein A-I (apoA-I) accounts for approximately 70% of the total protein mass of HDL, and the remaining protein components mainly include apoA-II, apoC, apoA-IV, and paraoxonase (PON).⁷ PON1 has been shown to effectively hydrolyze the oxidized phospholipids present in LDL, thus retarding the oxidation of these lipoproteins, attenuating their pro-inflammatory effects and protecting vessels from atherosclerosis progression.^{2 8 9} Moreover Aviram et al.,³ have shown that PON1 also reduces HDL lipid oxidation. Serum PON1 activity and concentration are decreased in subjects who have had a myocardial infarction compared with controls¹⁰ and low serum PON1 activity represent an independent risk factor for coronary events.⁸ Other diseases associated with alterations in circulating PON1 concentrations are Alzheimer's disease, chronic renal failure, chronic liver impairment, and type I and type II diabetes mellitus.^{11 12} PON1, aryldialkylphosphatase (EC 3.1.8.1) is a Ca²⁺-dependent serum esterase synthesized mainly by the liver¹³ catalyzes the hydrolysis of many highly toxic xenobiotics.¹⁴ PON1 gene is localized at q21-q22 on the long arm of chromosome 7 in humans.¹⁵ Genetic variations of the PON1 gene modify serum PON1 properties^{15 16} affecting its catalytic efficiency. The most studied polymorphisms of the PON1 gene are the glutamine to arginine substitution (Q/R) at codon 192 and the leucine to methionine substitution (L/M) at codon 55.^{16 17} The activity of the polymorphism at position 192 (QR192) is substrate dependent. For instance, paraoxon and fenitroxon are hydrolyzed faster by the R allele, while both isoforms hydrolyze chlorpyrifos-oxon and phenylacetate at approximately the same rate. The Q allele, on the other hand, hydrolyze more rapidly substrates such as soman, sarin and diazoxon.¹⁸ Polymorphism at position 55 (LM55) has a much smaller, but significant, effect on PON1 activity than the QR192 polymorphism.^{19 20} Therefore, there is a variation in the catalytic sites for different substrates and has been proposed that in humans, PON1 activity resides in the hydrolysis of the organophosphates paraoxon and phenylacetate.³ Taking into account the growing importance of PON1 as a risk factor of atherosclerosis, the purpose of this study was to evaluate the association of two single nucleotide polymorphisms in the PON1 gene with the serum activities of paraoxonase and arylesterase and the risk factors associated with atherosclerosis progression, the lipid profile and glycemia, in non diabetics subjects with a cardiovascular event (cases) and controls from the city of Buenos Aires, Argentina to get a better understanding of the role of the PON1 Q192R and L55M polymorphisms in the development of atherosclerosis and coronary artery disease (CAD).

Materials and methods

A case-control study was carried out for a period of one year between 2012 and 2013. A total of 329 subjects were included (randomized) from patients admitted and hospitalized to the Coronary Care Unit of the Cardiology Department with suspicion of acute coronary syndrome. Subjects who had liver diseases, renal diseases, thyroid diseases, diabetes and those on current therapy on antioxidant supplementation were excluded. The rest was intended to the case group if they met the following inclusion criteria: previous or current diagnosis of myocardial infarction or CAD. This diagnosis was made on the basis of the history, physical assessment, ECG patterns compatible with CAD (e.g.: presence of Q waves, ST elevation or depression, inverted T-waves, left bundle branch block, LBBB), biomarkers of myocardial injury (CPK that doubled the normal upper limit and CK-MB representing more than 6% of the amount of CPK or an absolute value greater than 28 according to the method used) or by coronary angiography that showed at least 75% obstruction of at least one coronary artery or 50% obstruction of the left main vessel. In all cases the final diagnosis was established according to the diagnostic algorithm in use and the medical judgment. Those individuals who did not meet the inclusion criteria were assigned to the control group. Based on the inclusion and exclusion criteria, a total number of 126 CAD cases and 203 age and sex matched controls were selected for the present study. Patients were consecutively selected as and when they presented to us. Both cases and controls were interviewed to obtain relevant data. Informed consents were obtained from all the subjects who were involved in the study. The patients and controls voluntarily participated in the study. Protocol was approved by the Ethical Committee of the University Hospital, UAI.

Results

Discussion

The heterogeneity of the Argentinean population, particularly in the metropolitan area, which results in cultural, socioeconomic, and ethnic diversities, may represent a interesting factor for epidemiological and biomarkers studies. It is important to take into account that large differences in frequency between ethnic populations are known in the PON1 genotype distribution which may be the reason for differences among studies.²³ Our data on risk factors of atherosclerosis (Table 1) indicated that in the overall sample, cases had higher serum triglycerides and glycemia, and lower HDL cholesterol than controls, though total cholesterol, LDL cholesterol, and PON1 paraoxonase and arylesterase activities did not show significant differences between both groups. The development of CAD is believed to be largely under genetic control.²⁴ Alterations in circulating in PON1 concentrations have been reported in CAD. Many case-control studies have addressed, in particular, the putative role of the polymorphisms in the PON1 gene regarding the enzymatic activities.²⁵ Several studies found associations between one or more polymorphisms of the PON genes, but the strongest associations were found with PON1 Q192R and L55M polymorphisms.²⁶ PON1 has antioxidant, antiatherosclerotic and anti-inflammatory functions by inhibiting LDL oxidative modification and suppressing the differentiation of monocytes into macrophages, which is the first stage in the development of atherosclerosis. Furthermore, PON1 prevents the accumulation of oxidized LDL and stimulates cholesterol efflux from macrophages.²⁴ One molecular basis of the paraoxonase polymorphisms is a missense mutation in the coding region of PON1 resulting in a glutamine (Q)/arginine (R) substitution at codon 192.¹⁵ The PON1 Q192 alloform hydrolyzes paraoxon much less efficiently than does PON1 R192, while the opposite is true in case of soman or sarin. PON1 Q192 is also more efficient at metabolizing oxidized HDL or LDL than PON1 R192.³ Another coding region polymorphism, resulting in aminoacid substitution at position 55 Leu(L)/Met(M), has been associated with plasma PON1 protein levels, specifically with PON1 M55 being associated with a low plasma PON1 level. In QR192 variant an excess of homozygotes was detected, leading to a H-WE deviation both in cases and controls. This fenomenom can be due to the presence of subgroups that may lead to Wahlunds’ effect, namely, if two or more subpopulations have different allele frequencies then the overall heterozygosity is reduced, even if the subpopulations themselves are in a H-WE. With respect to LM55 variant it can observe in cases but not controls a H-WE deviation. This may indicate that the polymorphism may be associated with the disease. According to our data, we have not found a statistically significantly different level of allele distribution of PON 192 and PON 55 genotypes between patients and controls (Table 2). Only a slight correlation with more cases with the allele 192Q and less with the 55L were found. These two polymorphisms were associated with paraoxonase activity, which increased, as we corroborated in CAD patients and healthy population (Table 3) in the order of QQ < QR < RR genotype in the PON1 192 polymorphism and MM < ML < LL genotype in the PON1 55 polymorphism. In both patients and controls, 192 QQ and 55 MM homozygotes have the lowest PON1 activity and 192RR and 55LL the highest. With respect to arylesterase activity, the Q192R polymorphism did not show any influence in cases and controls, but this activity increased in the order MM < ML < LL due to the L55M polymorphism in both populations, having the 55MM homozygote the lowest and the 55LL the highest. These results accord with other studies.²⁶ Only one article²⁷ reported that the 192R allele decrease arylesterase activity, although to a lesser extent to that of paraoxonase activity. Our results support the idea that lipid protection against oxidation by PON1 may be reduced in CAD patients because of lower enzyme activity as reported by Bayrak et al.,.²⁸ Indeed, triglycerides were higher in cases with the 192QQ genotype or the 55M allele, though the decrease in PON1 activity was not manifested in cholesterol, LDL and HDL in our population of cases. In our study, the decrease of HDL observed in cases L55M with respect to controls is not due to the less PON1 activity because it was observed in patients with any of the three genotypes. The increased HDL concentration observed in controls with the 192R allele and the reduced triglycerides concentration in controls with the 55M allele are not explained considering only PON1 activity. There is controversy about the influence of the several PON1 genetic polymorphisms on CAD. In a recent review, Abelló et al.,²⁶ aim to update and clarify the scientific evidence available on PON enzymes and their roles in CAD. They found that the strongest correlation resides in a protective role of the 192Q allele and the negative effect of the 192R allele. Nevertheless some manuscripts reported that the 192Q allele was more frequent in CAD patients. The 55M allele of PON1 has also been associated with CAD but others suggested that the 55M allele of PON1 has a protective effect against CAD.²⁹ In spite that diabetic subjects were excluded for the study, after the biochemical determinations, those presenting fasting glucose serum values up to 7.3 mmol/L were included. We found in cases higher glycemia concentrations in 192QQ homozygotes as compared with homo- and heterozygous carriers of the mutant R allele and in homo and heterozygous carriers of the M allele as compared with 55LL homozygotes, correlating with low activities of paraoxonase for the Q192R genotype and of paraoxonase and arylesterase for the L55M genotype. These results are consistent with the greater antioxidant efficiency attributed to the R allele as insulin resistance is affected by oxidative stress³⁰ while polymorphism at position 55 (LM55) has also been shown to have an effect on PON1 concentrations and activities.¹⁹ As a consequence the increased amount of ROS and oxidized LDL-C synergize to impair insulin signaling.³¹ Then, PON1 polymorphisms could be associated with the two hyperglycemic generators in glucose metabolism, impaired glucose utilization for skeletal muscle and uninhibited hepatic glucose output, both insulin-mediated pathways and sensitive to oxidative stress.³⁰ In this work patients are not diabetics and it is very stochastic that PON1 activity was decreased by protein glycosylation, as other authors had argued,^{12 32 33} based on several works that report that glycation of proteins including enzymes may decrease their activities in diabetes.^{34 35} Our results suggest on the contrary that primary low PON1 activities has high probability to determine the higher levels of blood glucose observed in subjects with a cardiovascular event. Metabolic syndrome is a set of common metabolic disorders that is strictly linked to CAD. Low-grade chronic inflammation, characterized by the production of abnormal cytokines such as IL-6, TNF-α, IL-1, leptin and resistin, is associated with insulin resistance in the liver. These factors inhibit insulin signaling in hepatocytes by activating the suppressor proteins of cytokine signaling, several kinases such as JNK, IKK-β and PKC and protein tyrosine phosphatases such as PTP1B and PTEN that in turn impair insulin signaling at the insulin receptor and insulin receptor substrate level. Hepatic insulin resistance in turn causes impaired suppression of glucose production by insulin in hepatocytes leading to hyperglycemia. Our results suggest that the decrease in antioxidant protection due to the lower activity of 192QQ genotype and 55M allele would increase inflammatory cytokines capable to increase blood glucose generated by peripherical insulin resistance, causing the evolution of the atherosclerotic plaque.^{36 37 38} In spite of the fact of the several limitations of the present study such as the relatively small size of the cohorts, and that the PON1 protein concentration, the insulin and the glycosylated hemoglobin were not measured, it constitutes a strong preliminary report in patients, about the contribution of PON1 polymorphism on the variations in glycemia associated with tryglyceridemia and CAD, enriched besides, for the heterogenicity of Buenos Aires population. It is known the association of diabetes with the bad CAD prognosis, but intrinsic metabolic mechanisms are in discussion. Our findings contribute to put in agenda the role of PON1 polymorphisms related with glucose metabolism.

Conclusions

Increase triglycerides observed in cases confirm the relationship between variations in PON1 activities and lipid metabolism described by other works. PON1 low activities, determined by genetic polymorphism, result in a decrease in anti-inflammatory and antioxidant protection in CAD, characterized by increased levels of cytokines, which would determine an increase in blood glucose. The concomitant increase in triglycerides and blood glucose contribute to the aggravation of atherosclerotic disease and CAD.

Ethical responsibilities

Funding

No endorsement of any kind received to conduct this study/article.

Conflict of interest

The authors declare no conflict of interest.