International Journal of Clinical Biochemistry and Research

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Online ISSN: 2394-6377

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International Journal of Clinical Biochemistry and Research (IJCBR) open access, peer-reviewed quarterly journal publishing since 2014 and is published under auspices of the Innovative Education and Scientific Research Foundation (IESRF), aim to uplift researchers, scholars, academicians, and professionals in all academic and scientific disciplines. IESRF is dedicated to the transfer of technology and research by publishing scientific journals, research content, providing professional’s membership, and conducting conferences, seminars, and award more...

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Get Permission Vasanthan, Birundha. S, Lalitha.S, Rajalakshmi K, and Balasubramanian. A: Studying atherogenic index of plasma and lipoprotein (A) for better cardiac risk stratification in public health


Introduction

The most important risk factors for Cardio-vascular disease (CVD) consist of dyslipidemia, hypertension, obesity and physical inactivity. Dyslipidemia being is the major predictor for CVD.1 By 2020, global CVD prevalence will rise by 75% in developing countries.2

Hyperlipidemia is the most common type of dyslipidemia which includes increased Triglycerides (TGL), Total Cholesterol, Low Density Lipoprotein (LDL), and decreased High Density Lipoprotein (HDL). This is supported by a study conducted in urban population of south India.3 The study states, that the prevalence of CV D is increased in Hyperlipidemia.

The commonly known fact that, obese individuals are more prone to cardiovascular events is questioned by a study which says hyperlipidemia can also be seen in non-obese individuals.4 Lipoprotein(a) [Lp (a)], an individual parameter and a type of LDL has shown its specificity on the CVD.5

To understand more as a predictor of CVD, the two most important lipid profile parameters, LDL and HDL taken together to calculate the Atherogenic Index of Plasma (AIP) and the single most significant parameter were compared among diabetic patients.

Estimating Lp(a) is costlier and not a routine parameter. This study was also aimed to highlight the importance of the ratio of the usually estimated lipid parameters, LDL and HDL on the single effective and costlier parameter, Lp(a).

Table 1
Parameter Method
TGL Enzymatic GPO-POD
HDL Direct antibody inhibition
Lp(a) Immunoturbidimetry

Parameters with their methods of estimation

Table 2
Group Parameter N Min Max Mean Std. Deviation
A TGL 30 116 188 155.43 19.611
HDL 30 30 60 44.00 10.072
B TGL 30 180 282 209.63 24.848
HDL 30 18 55 35.03 9.936

Values of TGL and HDL among group A & B

Table 3
Group A N Mean Std. Deviation df t - Statistics P - Value
Lp(a) 30 10.2867 1.29075 58 40.459 0.000*
AIP 30 0.7464 0.04552

Comparison of Lp( a) and AIP among the subjects in group A

[i] p– value < 0.05 is considered statistically significant.

Table 4
Group B N Mean Std. Deviation df t - Statistics P - Value
Lp(a) 30 22.1200 4.31544 58 27.250 0.000*
AIP 30 0.6447 0.09865

Comparison of Lp( a) and AIP among the controls in group B

[i] p – value < 0.05 is considered statistically significant.

Materials and Methods

The study included 30 non-diabetic subjects as Group A and 30 diabetic patients as Group B from Sree Balaji Medical College Hospital, Chennai. Blood samples were drawn from the participants after overnight fasting. Lipoprotein(a) was estimated by Immunoturbidimetry by Respons 910 analyzer and the parameters, TGL and H DL by their respective methods in Erba MI-150 Auto-analyzer.

The sample collection was in accordance to the ethical criteria of the institute.

AIP was calculated with the help of the formula, AIP = log (TGL/HDL).

Results

The results of the parameters of group A and B are as follows. The parameters, Lp(a) and the calculated parameter AIP, were compared within their group A & B with the help of Independent t test under the guidance of the statistician.

Discussion

The study reveals a positive correlation of AIP with the Lp(a). When the TG L/HDL and Lp(a) values were compared by the difference in the mean values among the patients in Group A who are non-diabetic subjects, it showed a highly significant value p<0.001. It was also highly significant with p< 0.001 when the same variables were compared among the Group B, diabetic patients.

A study conducted by Kanthe PS et al, atherogenic index was the best indicator of CVD next to dyslipidemia.6 This was in accordance with a study, which concludes that serum triglyceride level has a predicting ability along with HDL.7 The above mentioned studies highlight the importance of commonly tested lipid parameters and correlation of these lipid parameters among each other has a very good predicting capacity of CVD. From this study, the calculated parameter AIP, obtained from TGL and HDL, had a mean of 0.74 among the control group A and a mean of 0.64 among the study group B [Table 4, Table 3 ].

Considering the variation in prevalence and prognosis of CVD based on different races , based on the Lp(a), a study conducted by Dahlen GH et al among the white patients concludes Lp (a) as a n important risk factor for CVD.8 Another study conducted by Heyden S, et al compared Lp (a) levels between black and white races. The study concluded that, Lp( a) levels are important in black race people than the white race. Lp( a) levels were also significantly increased in Cerebrovascular disease, apart from CVD.9 This is supported by a study conducted by Howard BV et al among two ethnic groups, which showed a relation of Lp(a) with LDL and fibrinogen.10 Increase in LDL and fibrinogen are considered to be important causes for CVD. The study also suggested alongitudinal data to understand Lp(a) as a predict or in CVD disease among various ethnic groups. The present study was hence conducted to study the significance of Lp(a) in Asian population. From this study, the parameter Lp(a) had a mean of 10.29 among the control group A and a mean of 22.12 a mong the study group B [Table 4, Table 3 ].

The need to predict CVD at an early age and in non-obese younger population is growing recently. This fact is supported by a study conducted by Cunningham TE et al , Chu NF et al and Herd SL et al among various ethnic groups , which concluded that Lp(a) to be estimated in children with a family history of premature CVD and more effective than anthropometry.13, 12, 11

Lp(a) is being considered as a better prediction marker of CVD in various other studies. Increased Lp(a) concentration is related to vascular events like CVD and stroke, a study says.14

The pathogenesis of Lp(a) in CVD was explained genetically by studies conducted by Clarke R et al and Spence JD.16, 15 The former study identified two Lp (a) variants and according to the the latter study, strong correlation between Lp (a) and kringle IV type 2 genotype atherosclerotic stenosis in the coronary, carotid, and femoral arteries. These facts are supported by a study conducted by Phan BAP et al, suggesting the involvement of Lp(a) in commencement and development of atherosclerosis.17

According to a study conducted by Oladipo A et al, women had increased AIP than men with high significance.18

A study conducted by Anupama Kamath et al had decreased HDL levels with increased BMI in women , similar to our study [Table 2].19

AIP as a risk predictor for CVD was also proved by a study conducted by CJ Ikewuchi.20

Our study shows a higher significance of p<0.001 when Lp(a) and AIP were compared within the control group and the study group, revealing the importance of these parameters in predicting a case of CVD.

Hence, there is an increase in the AIP among diabetics when compared to the non-diabetics, which correlated with the Lp(a) values with high significance.

Conclusion

It is summarized that, the Atherogenic index of plasma will have to be accepted as a better indicator of cardio-vascular risks other than taking into account one of the lipoproteins as such. Estimating Lipoprotein(a) is costlier compared to the other lipoproteins, which makes it an objectionable parameter by the patients themselves. In the future, we would thereby, insist the rationale behind estimating the lipoprotein ratios as better markers of assessing cardio-vascular risks.

Source of funding

None.

Conflicts of interest

None.

References

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R Gupta Burden of coronary heart disease in IndiaIndian Heart J200557632638

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Viswanathan Mohan Raj Deepa Subramaniam Shanthi Rani Gopal Premalatha Prevalence of coronary artery disease and its relationship to lipids in a selected population in South IndiaJ Am Coll Cardiol200138368268710.1016/s0735-1097(01)01415-2

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K Parinita Study of serum lipid profile in individuals residing in and around NalgondaInt J pharm Bio Sci20122110116

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J K Gambhir H Kaur D S Gambhir K M Prabhu Lipoprotein (a) as an independent risk factor for coronary artery disease in patients below 40 years of ageIndian Heart J200052411416

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P S Kanthe B S Patil Bagali Sh A Deshpande G Shaikh M Aithala Atherogenic Index as a Predictor of Cardiovascular Risk among Women with Different Grades of ObesityIJCRIMPH2012410176717743

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V Manninen L Tenkanen P Koskinen J K Huttunen M Mänttäri O P Heinonen Joint effects of serum triglyceride and LDL cholesterol and HDL cholesterol concentrations on coronary heart disease risk in the Helsinki Heart Study. Implications for treatment.Circ1992851374510.1161/01.cir.85.1.37

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G H Dahlen J R Guyton M Attar J A Farmer J A Kautz A M Gotto Association of levels of lipoprotein Lp(a), plasma lipids, and other lipoproteins with coronary artery disease documented by angiography.Circ198674475876510.1161/01.cir.74.4.758

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S Heyden Raised Lipoprotein(a) in Hypercholesterolemic Black-Students Compared to Age-Matched Whites in North and South-CarolinaInt J Epidemiol1994232301306

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B V Howard Concentrations of Lp(a) in black and white young adults: relations to risk factors for cardiovascular diseaseAnn Epidemiol199445341350

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Teresa E Cunningham Susan M Sayers Gurmeet R Singh Lipoprotein(a) identifies cardiovascular risk in childhood: The Australian Aboriginal Birth Cohort StudyJ Paediat Child Health201147525726110.1111/j.1440-1754.2010.01955.x

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N F Chu Lipoprotein profiles, not anthropometric measures, correlate with serum lipoprotein(a) values in children: the Taipei children heart studyEur J Epidemiol2000161512

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S L Herd Body fat, fat distribution and serum lipids, lipoproteins and apolipoproteins in African-American and Caucasian-American prepubertal childrenInt J Obes Relat Metab Disord2001252198204

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S Erqou S Kaptoge P L Perry Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortalityJAMA2009302412423

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R Clarke J F Peden J C Hopewell Genetic variants associated with Lp(a) lipoprotein level and coronary diseaseN Engl J Med200936125182528

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J D Spence M Koschinsky Mechanisms of lipoprotein(a) pathogenicity: prothrombotic, proatherosclerotic, or both?Arterioscler Thromb Vasc Biol20123215501551

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Bap Phan P P Toth Lipoprotein(a): epidemiology, atherogenic activity and impact on cardiovascular riskClin Lipidol20138195203

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A Oladipo Plasma lipid profile, atherogenic and coronary risk indices in some residents of Abeokuta in south-western NigeriaBIOKEMISTRI20082028591

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K Anupama Relation of anthropometry to CVD risk factors in young obese womenBiomed Res2005162137141

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C J Ikewuchi Alteration of Plasma Lipid Profile and Atherogenic Indices of Cholesterol Loaded Rats by Tridax Procumbens Linn: Implications for the Management of Obesity and Cardiovascular DiseasesBiokemist20092129599



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76-79


Authors Details

M Vasanthan, Birundha. S, Shenbaga Lalitha.S, Rajalakshmi K, Balasubramanian. A


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