Association of the Apolipoprotein B/Apolipoprotein A-I Ratio, Metabolic Syndrome Components, Total Cholesterol, and Low-Density Lipoprotein Cholesterol with Insulin Resistance in the Population of Georgia

Makaridze, Zaza; Giorgadze, Elene; Asatiani, Ketevan

doi:https://doi.org/10.1155/2014/925650

International Journal of Endocrinology

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Research Article | Open Access

Volume 2014 | Article ID 925650 | https://doi.org/10.1155/2014/925650

Association of the Apolipoprotein B/Apolipoprotein A-I Ratio, Metabolic Syndrome Components, Total Cholesterol, and Low-Density Lipoprotein Cholesterol with Insulin Resistance in the Population of Georgia

Zaza Makaridze,¹Elene Giorgadze,²and Ketevan Asatiani²

Academic Editor: Alexander Schreiber

Received11 Mar 2014

Revised17 Apr 2014

Accepted17 Apr 2014

Published13 May 2014

Abstract

The study was designed to assess the association between insulin resistance (IR) and apolipoprotein B/apolipoprotein A-I ratio (ApoB/ApoA-I ratio), metabolic syndrome (MetS) components, total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C) in the nondiabetic population of Georgia. The subjects were 1522 Georgians of Caucasian origin (mean age = 45 years, 653 women) without diabetes who had visited the clinics for a related health checkup between 2012 and 2013. IR was calculated using the computer homeostasis model assessment (HOMA2-IR) and was defined as the upper quartile. MetS was diagnosed using the updated ATP-III definition of the metabolic syndrome. Logistic and multiple regression models were used to estimate the association between IR and other components. IR was positively correlated with age, ApoB, ApoB/ApoA-I ratio, MetS components (excluding high-density lipoprotein cholesterol—HDL-C), LDL-C, fasting insulin, and TC and negatively correlated with HDL-C and ApoA-I in both sexes (all ). In the logistic regression models, gender, age, ApoB/ApoA-I ratio, diastolic pressure, HDL-C, LDL-C, fasting glucose, and triglycerides were the covariates significantly associated with IR (OR: 8.64, 1.03, 17.95, 1.06, 0.13, 1.17, 3.75, and 2.29, resp.; all ). Multiple regression models demonstrated that these components (except for HDL-C) made an independent contribution to the prediction of HOMA2 (all ).

1. Introduction

Insulin resistance (IR) is a metabolic disorder independently associated with cardiovascular disease [1–3]. IR is associated with aging and a cluster of important cardiometabolic risk factors (dyslipidemia, arterial hypertension, hyperglycemia, and obesity) and is believed to be the common shared pathophysiological disturbance [4–8]. Thus, accurate and early prediction and detection of IR are very important in clinical practice so as to identify patients at high risk for cardiovascular disorders. Evaluation and revealing of the potential additional metabolic markers can help predict cardiovascular risk better.

Prospective risk studies, such as AMORIS [9–11], INTERHEART [12], EPIC-Norfolk study [13, 14], and ULSAM [15], indicate that apolipoprotein B/apolipoprotein A-I ratio (ApoB/ApoA-I ratio) is a strong predictor of risk of myocardial infarction (MI). A recent review of existing evidence by Walldius supports the use of ApoB/ApoA-I ratio as a strong predictor of cardiovascular risk [16].

Some studies have indicated that IR was significantly associated with ApoB/ApoA-I ratio, metabolic syndrome (MetS), and lipid indices. Sierra-Johnson et al. studied 2.955 adults (mean age 47 years, 1.457 women) without diabetes from the US NHANS III population. The ApoB/ApoA-I ratio was an independent predictor of insulin resistance after adjustment for age and race and remained significant after further adjustment for MetS components and traditional and inflammatory risk factors [17]. Ying et al. investigated 3.945 men and 2.141 women with abdominal obesity. Both low-density lipoprotein cholesterol (LDL-C) and ApoB/ApoA-I ratio were independent risk factors for Mets, and ApoB/ApoA-I ratio was stronger in this regard for obese population [18].

There is no Georgian report available about this subject. The aim of our study was to assess the association between insulin resistance and apolipoprotein B/apolipoprotein A-I ratio, MetS components, total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C) in the population of Georgia. We also analyzed the independence of these associations.

2. Materials and Methods

2.1. Subjects

We analyzed 1522 Georgians of Caucasian origin, who had visited the National Institute of Endocrinology (Tbilisi State University Affiliated Clinic) and “Medicore” Ltd. (Tbilisi State Medical University Affiliated Clinic) for a related health checkup between 2012 and 2013. Subjects were men and nonpregnant women aged ≥18 years and <80 years (653 women and 869 men), who attended the morning medical examination and who had fasted ≥8 h. Exclusion criteria used were missing readings for ApoB, ApoA-I, MetS components, low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), and all self-reported diabetics and/or subjects on medication for this disease and/or those with fasting glucose ≥7 mmol/l (126 mg/dL) and/or postprandial glucose ≥11.1 mmol/l (200 mg/dL).

2.2. Anthropometric Measurements and Laboratory Data

Height and weight were obtained using standardized techniques and equipment. Waist circumference (WC) was measured in the erect position with a soft tape at the middle between the lowest rib and the iliac crest. Body mass index (BMI) was calculated as weight (kg)/(height[m])².

Systolic blood pressure (SP) and diastolic blood pressure (DP) were measured twice in the sitting position after at least 15 minutes of rest. The mean of the two measurements was used in the analyses. Insulin sensitivity index was determined using the updated computer homeostasis model assessment (HOMA2-IR) index. Venous blood samples were drawn after a minimum of 8 h of fasting. ApoB and ApoA-I levels were measured by the immunoturbidimetric assay with Roche Diagnostics kit, using Roche/Hitachi C311 analyzer. Glucose was measured after enzymatic oxidation in the presence of glucose oxidase with HUMAN Diagnostics kit (Germany), using HUMALYZER 2000 analyzer. Total cholesterol (TC) was measured after enzymatic hydrolysis and oxidation with enzymatic colorimetric test for cholesterol with lipid clearing factor (HUMAN Diagnostics kit, Germany), using HUMALYZER 2000 analyzer. High-density cholesterol lipoprotein (HDL-C) was measured in the supernatant after precipitating the other lipoproteins with phosphotungstic acid and magnesium chloride and centrifugation with HUMAN Diagnostics kit (Germany), using HUMALYZER 2000 analyzer. The triglycerides (TG) were measured after enzymatic hydrolysis with lipases by enzymatic colorimetric test for triglycerides with lipid clearing factor (HUMAN Diagnostics kit, Germany), using HUMALYZER 2000 analyzer. LDL-C was calculated by Friedewald formula. When TG level was greater than or equal to 200 mg/dL (2.3 mmol/l), LDL-C level was measured by direct method with HUMALYZER 2000 analyzer. Insulin was measured by ELISA method with HUMAN Diagnostics kit (Germany), using ELISYS UNO analyzer.

2.3. Metabolic Syndrome Definition

The updated ATP-III definition of MetS [19] was used when any three or more criteria were present: waist circumference (WC) ≥ 102 cm in men and ≥88 cm in women; impaired fasting glucose-fasting blood glucose (FG) of ≥5.6 mmol/l (100 mg/dL); systolic blood pressure (SP) ≥ 130 mmHg and/or diastolic blood pressure (DP) ≥ 85 mmHg or treatment of previously diagnosed hypertension; fasting levels of triglycerides (TG) ≥ 1.7 mmol/l (150 mg/dL) or treatment for this abnormality; fasting high-density lipoprotein cholesterol (HDL-C) < 1.03 mmol/l (40 mg/dL) for men and <1.30 mmol/l (50 mg/dL) for women or treatment for this abnormality.

2.4. Arterial Hypertension Definition

Subjects were considered having hypertension if they were taking antihypertensive medications and/or having systolic blood pressure ≥ 140 mmHg and/or having diastolic blood pressure ≥ 90 mmHg, as defined by the recent Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure guidelines.

2.5. Dyslipidemia Definition

Subjects were considered to have dyslipidemia if they had fasting levels of triglycerides (TG) ≥ 1.7 mmol/l (150 mg/dL) and/or fasting levels of high-density lipoprotein cholesterol (HDL-C) < 1.03 mmol/l (40 mg/dL) in men and <1.30 mmol/l (50 mg/dL) in women and/or fasting level of total cholesterol (TC) ≥ 5.2 mmol/l (200 mg/dL) and/or fasting level of low-density lipoprotein cholesterol (LDL-C) ≥ 4.10 mmol/l (160 mg/dL) and/or used medications for this abnormality.

2.6. Statistical Analysis

All the analyses were performed using IBM SPSS Statistics for Windows (version 22.0).

IR was defined as the gender-specific upper quartile of HOMA2-IR and insulin sensitivity (IS) as the remaining three quartiles. We used the Mann-Whitney test to compare related data between sexes and between IR and IS subjects. Chi-square test was used to compare the prevalence of MetS, AH, and dyslipidemia between sexes and between IR and IS subjects.

Spearman partial correlation analysis of HOMA2-IR with ApoB/ApoA-I ratio, MetS components, BMI, TC, and LDL-C in men and women (controlling by age) was done. Further partial correlation analysis of ApoB/ApoA-I ratio with HOMA2-IR in both sexes was performed, after adjustment for age, MetS components, BMI, TC, and LDL-C.

A logistic regression was carried out to assess the association between IR and ApoB/ApoA-I ratio, MetS components, and LDL-C. Because of high correlation of HOMA2-IR with TC (), WC (), and SP (), these variables were not included into the regression models. Selection of predictor variables was done by entry (blockwise selection) method. To analyze the additional contribution of ApoB/ApoA-I and MetS components to IR, multiple linear regression was used (stepwise method). The predictive value of each variable was assessed by comparing values obtained from each model.

3. Results

Descriptive characteristics between sexes are shown in Table 1.

The ApoB/ApoA-I ratio, ApoB, blood pressure levels, WC, BMI, LDL-C, FG, FIns, TG, TC, HOMA2-IR, the prevalence of MetS, AH, and dyslipidemia were all significantly higher but HDL-C and ApoA-I levels were significantly lower in men than in women (all ).

Therefore, we stratified the analysis by sex.

Insulin resistant subjects in both sexes were older and had greater mean values for ApoB/ApoA-I ratio, ApoB, blood pressure levels, WC, BMI, LDL-C, FG, FIns, TG, TC, and HOMA2-IR than insulin sensitive subjects. On the contrary, IR subjects had significantly lower HDL-C and ApoA-I levels than IS subjects (all ). The prevalence of MetS, AH, and dyslipidemia was significantly higher in IR subjects (all ) (Tables 2 and 3).

ApoB level, ApoB/ApoA-I ratio, and LDL-C level increased significantly and gradually among HOMA2-IR quartiles (Table 4).

Results of spearman partial correlation analysis of HOMA2-IR with ApoB/ApoA-I ratio, MetS components, BMI, TC, and LDL-C in men and women are shown in Figure 1. Further partial correlation of ApoB/ApoA-I ratio with IR in men and women was done (Figure 2). There was still significant positive correlation between them ( for women and 0.209 for men, both ).

Figure 1

Spearman partial correlation () analysis of HOMA2-IR with ApoB/ApoA-I ratio, MetS components, BMI (body mass index), TC, and LDL-C in men and women (controlling by age). Partial correlation: Spearman partial correlation coefficient ; (2-tailed) <.0001. ApoB/ApoA-I ratio: apolipoprotein B/apolipoprotein A-I ratio, SP: systolic blood pressure, DP: diastolic blood pressure, WC: waist circumference, BMI: body mass index, HDL-C: high-density lipoprotein cholesterol, LDL-C: low-density lipoprotein cholesterol, FG: fasting glucose, TG: triglyceride, TC: total cholesterol, and HOMA2-IR: homeostasis model assessment of insulin resistance.

Figure 2

Partial correlation () of ApoB/ApoA-I ratio with HOMA2-IR (controlling by age, SP, DP, WC, BMI, HDL-C, LDL-C, FG, TG, and TC). Partial correlation: Spearman partial correlation coefficient ; (2-tailed) <.0001. ApoB/ApoA-I ratio: apolipoprotein B/apolipoprotein A-I ratio, IR: insulin resistance, SP: systolic blood pressure, DP: diastolic blood pressure, WC: waist circumference, BMI: body mass index, HDL-C: high-density lipoprotein cholesterol, LDL-C: low-density lipoprotein cholesterol, FG: fasting glucose, TG: triglyceride, TC: total cholesterol, and HOMA2-IR: homeostasis model assessment of insulin resistance.

Logistic regression models demonstrated that gender, age, ApoB/ApoA-I ratio, diastolic blood pressure, HDL-C, LDL-C, fasting glucose, and triglycerides were the covariates significantly associated with the presence of IR (OR: 8.64, 1.03, 17.95, 1.06, 0.13, 1.17, 3.75, and 2.29, resp.; all ) (Table 5).

Multiple regression models demonstrated that ApoB/ApoA-I ratio, FG, DP, gender, LDL-C, age, and TG made a significant and independent contribution to the prediction of HOMA2-IR ( change: 0.421, 0.133, 0.039, 0.026, 0.014, 0.004, and 0.002, resp.; all ), with ApoB/ApoA-I ratio being the strongest predictor (Table 6). HDL-C was considered nonsignificant.

4. Discussion

ApoB and ApoA-I are the two major apolipoproteins involved in lipid transport and in the processes causing atherosclerosis and its complications [16]. ApoB is the major protein in very low-density lipoproteins (VLDL), intermediate-density lipoproteins (IDL), and low-density lipoproteins (LDL), one protein per particle [20]. ApoA-I is the major protein in high-density lipoprotein (HDL) particles. The ApoB number indicates the total number of atherogenic particles; the higher the number the higher the cardiovascular (CV) risk. ApoA-I reflects the antiatherogenic potential in HDL particles; the higher the value the better the protection against CV risk. The ApoB/ApoA-I ratio indicates the balance between atherogenic and antiatherogenic particles; the higher the value, the higher the CV risk.

Many authors have reviewed the importance of ApoB, ApoA-I, and ApoB/ApoA-I ratio as markers of atherogenic risk [9, 11, 21–27]. Prospective risk studies, such as AMORIS [9–11], INTERHEART [12], EPIC-Norfolk study [13, 14], and ULSAM [15], indicate that ApoB/ApoA-I ratio is a very useful predictor of risk of myocardial infarction (MI). In the AMORIS study it was found that ApoB was significantly better to predict risk than LDL-C, especially for those with low values of LDL-C, and ApoB/ApoA-I ratio had a significantly stronger relation with MI than any other lipid-based ratio. INTERHEART case-control study showed that, in all 52 countries investigated, ApoB/ApoA-I ratio was not only the strongest factor in explaining risk of acute MI, but also the most prevalent risk factor of all the nine conventional risk factors investigated irrespective of age, sex, race, and other lipids or lipid ratios. In the ULSAM study a risk prediction score for MI including proinsulin and the ApoB/ApoA-I ratio was developed in middle-aged men. This score was highly predictive for future fatal and nonfatal MI and proved to be at least as good as the Framingham and the PROCAM scores.

The prevalence of IR is increasing worldwide [28–31]. Studies have indicated that IR was significantly associated with ApoB/ApoA-I ratio, metabolic syndrome (MetS), and lipid indices. Sierra-Johnson et al. studied 2.955 adults (mean age 47 years; 1.457 women) without diabetes from the US NHANS III population. The ApoB/ApoA-I ratio was an independent predictor of insulin resistance after adjustment for age and race and remained significant after further adjustment for MetS components and traditional and inflammatory risk factors [17]. Similar results were found in our study.

Ying et al. investigated 3.945 men and 2.141 women with abdominal obesity. The study showed that the correlation coefficient between ApoB/ApoA-I ratio and HOMA2-IR was higher than between LDL-C and HOMA2-IR in both sexes (with more differences in females), as it was found in our study. Both LDL-C and ApoB/ApoA-I ratio were independent risk factors for MetS, and ApoB/ApoA-I ratio was stronger in this regard for obese population [18].

Belfki et al. have shown in a Tunisian population (330 adults aged 35–74) that ApoB/ApoA-I ratio was strongly associated with MetS, with each of the components, and with increasing number of components, as well as with IR [32]. Another study reported that subjects with higher levels of ApoB had a higher proportion of the MetS components in comparison with patients having higher LDL-C and normal level of ApoB [33]. Some studies have shown that measurement of the ApoB/ApoA-I ratio may improve vascular risk prediction. Higher ApoB/ApoA-I ratio has been associated with increased cardiac events [24].

Head to head analysis (Table 4) of ApoB, ApoB/ApoA-I ratio, and LDL-C among HOMA2-IR quartiles showed that in IR subjects emphasis in risk evaluation and therapy should be made on ApoB and ApoB/ApoA-I ratio rather than on LDL-C, because LDL-C level might be in “optimal” or “near optimal” range. The study showed the possibility of focusing patients at “high risk” of having IR according to ApoB/ApoA-I ratio (≥1.12 in men and ≥1.0 in women, ). These findings correlate well with other authors [18, 34]. Carnevale et al. enrolled 616 patients with normal glucose tolerance (NGT) and found that, in NGT with LDL-C < 100 mg/dL, a higher ApoB/ApoA-I exhibited an atherogenic lipid profile, indicating that LDL-C alone is insufficient to define CV risk. Independent from LDL-level, when ApoB/ApoA-I is lower, the lipid profile is, in fact, less atherogenic. This study demonstrates that ApoB/ApoA-I is at least complementary to LDL-C in identifying the “effective” CV risk profile of asymptomatic NGT subjects [34].

Enkhmaa et al. have studied several ethnic groups of European and African Americans and developed a CV risk score which was found to be significantly increased across tertiles of ApoB/ApoA-I ratio. They concluded that ApoB/ApoA-I ratio differed across ethnicities and was associated with the presence of MetS in both groups. Among African Americans, an elevated ApoB/ApoA-I ratio independently predicted a greater risk of CAD [35].

Based on these findings, Sniderman and Faraj recommended that the dyslipidemia be redefined to include ApoB and ApoA-I as stronger risk marker especially compared to LDL-C (often low in MetS), TG, and HDL-C [36].

This study has several limitations. Calculated HOMA index is well, but not perfectly correlated with values of insulin sensitivity from the euglycemic clamp, which is considered the gold standard for measurement of insulin sensitivity. Another limitation is that the subjects were not a general population but visitors to the clinic.

5. Conclusion

ApoB/ApoA-I ratio, MetS components, LDL-C, TC, gender, and age were all found to be associated with IR in the Georgian population. But ApoB/ApoA-I ratio was stronger in this regard, highlighting the fact that in IR patients emphasis in risk evaluation and therapy should be made on ApoB/ApoA-I ratio rather than on LDL-C level. The independent and significant association of the ApoB/ApoA-I ratio with IR demonstrates the usefulness of using this ratio as a valuable predictor of IR and an important risk factor in the cardiovascular risk assessment.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

G. Hu, “Plasma insulin and cardiovascular mortality in non-diabetic European men and women: a meta-analysis of data from eleven prospective studies,” Diabetologia, vol. 47, no. 7, pp. 1245–1256, 2004.
View at: Google Scholar
M. Pyörälä, H. Miettinen, P. Halonen, M. Laakso, and K. Pyörälä, “Insulin resistance syndrome predicts the risk of coronary heart disease and stroke in healthy middle-aged men: the 22-year follow-up results of the Helsinki Policemen Study,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 20, no. 2, pp. 538–544, 2000.
View at: Google Scholar
E. Ferrannini, S. M. Haffner, B. D. Mitchell, and M. P. Stern, “Hyperinsulinaemia: the key feature of cardiovascular and metabolic syndrome,” Diabetologia, vol. 34, no. 6, pp. 416–422, 1991.
View at: Google Scholar
R. H. Eckel, K. Alberti, S. M. Grundy, and P. Z. Zimmet, “The metabolic syndrome,” The Lancet, vol. 375, no. 9710, pp. 181–183, 2010.
View at: Publisher Site | Google Scholar
E. S. Ford, “Risks for all-cause mortality, cardiovascular disease, and diabetes associated with the metabolic syndrome: a summary of the evidence,” Diabetes Care, vol. 28, no. 7, pp. 1769–1778, 2005.
View at: Publisher Site | Google Scholar
A. M. McNeill, W. D. Rosamond, C. J. Girman et al., “The metabolic syndrome and 11-year risk of incident cardiovascular disease in the atherosclerosis risk in communities study,” Diabetes Care, vol. 28, no. 2, pp. 385–390, 2005.
View at: Publisher Site | Google Scholar
B. Balkau, T. Drivsholm, K. Borch-Johnsen et al., “Frequency of the who metabolic syndrome in European cohorts, and an alternative definition of an insulin resistance syndrome,” Diabetes and Metabolism, vol. 28, no. 5, pp. 364–376, 2002.
View at: Google Scholar
K. G. M. M. Alberti and P. Zimmet, “Metabolic syndrome—a new world-wide definition. A consensus statement from the International Diabetes Federation,” Diabetic Medicine, vol. 23, no. 5, pp. 469–480, 2006.
View at: Publisher Site | Google Scholar
A. D. Sniderman, C. D. Furberg, A. Keech et al., “Apolipoproteins versus lipids as indices of coronary risk and as targets for statin treatment,” The Lancet, vol. 361, no. 9359, pp. 777–780, 2003.
View at: Publisher Site | Google Scholar
A. D. Sniderman, I. Junger, I. Holme, A. Aastveit, and G. Walldius, “Errors that result from using the TC/HDL C ratio rather than the apoB/apoA-I ratio to identify the lipoprotein-related risk of vascular disease,” Journal of Internal Medicine, vol. 259, no. 5, pp. 455–461, 2006.
View at: Publisher Site | Google Scholar
G. Walldius and I. Jungner, “The apoB/apoA-I ratio: a strong, new risk factor for cardiovascular disease and a target for lipid-lowering therapy—a review of the evidence,” Journal of Internal Medicine, vol. 259, no. 5, pp. 493–519, 2006.
View at: Publisher Site | Google Scholar
P. S. Yusuf, S. Hawken, S. Ôunpuu et al., “Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study,” The Lancet, vol. 364, no. 9438, pp. 937–952, 2004.
View at: Publisher Site | Google Scholar
S. F. C. Vaessen, F. G. Schaap, J.-A. Kuivenhoven et al., “Apolipoprotein A-V, triglycerides and risk of coronary artery disease: the prospective Epic-Norfolk Population Study,” Journal of Lipid Research, vol. 47, no. 9, pp. 2064–2070, 2006.
View at: Publisher Site | Google Scholar
W. A. Van Der Steeg, S. M. Boekholdt, E. A. Stein et al., “Role of the apolipoprotein B-apolipoprotein A-I ratio in cardiovascular risk assessment: a case-control analysis in EPIC-Norfolk,” Annals of Internal Medicine, vol. 146, no. 9, pp. 640–648, 2007.
View at: Google Scholar
K. Dunder, L. Lind, B. Zethelius, L. Berglund, and H. Lithell, “Evaluation of a scoring scheme, including proinsulin and the apolipoprotein B/apolipoprotein A1 ratio, for the risk of acute coronary events in middle-aged men: uppsala Longitudinal Study of Adult Men (ULSAM),” The American Heart Journal, vol. 148, no. 4, pp. 596–601, 2004.
View at: Publisher Site | Google Scholar
G. Walldius, “The apoB/apoA-I ratio is a strong predictor of cardiovascular risk,” Lipoproteins in Health and Diseases, Article ID 39545, pp. 95–148, 2012.
View at: Publisher Site | Google Scholar
J. Sierra-Johnson, A. Romero-Corral, V. K. Somers et al., “ApoB/apoA-I ratio: an independent predictor of insulin resistance in US non-diabetic subjects,” European Heart Journal, vol. 28, no. 21, pp. 2637–2643, 2007.
View at: Publisher Site | Google Scholar
X. Ying, Y. Qian, Y. Jiang, Z. Jiang, Z. Song, and C. Zhao, “Association of the apolipoprotein B/apolipoprotein A-I ratio and low-density lipoprotein cholesterol with insulin resistance in a Chinese population with abdominal obesity,” Acta Diabetologica, vol. 49, no. 6, pp. 465–472, 2012.
View at: Google Scholar
S. M. Grundy, J. I. Cleeman, S. R. Daniels et al., “Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute scientific statement,” Circulation, vol. 112, no. 17, pp. 2735–2752, 2005.
View at: Publisher Site | Google Scholar
J. Elovson, J. E. Chatterton, G. T. Bell et al., “Plasma very low density lipoproteins contain a single molecule of apolipoprotein B,” Journal of Lipid Research, vol. 29, no. 11, pp. 1461–1473, 1988.
View at: Google Scholar
G. Walldius and I. Jungner, “Apolipoprotein B and apolipoprotein A-I: risk indicators of coronary heart disease and targets for lipid-modifying therapy,” Journal of Internal Medicine, vol. 255, no. 2, pp. 188–205, 2004.
View at: Publisher Site | Google Scholar
G. Walldius and I. Jungner, “Is there a better marker of cardiovascular risk than LDL cholesterol? Apolipoproteins B and A-I - new risk factors and targets for therapy,” Nutrition, Metabolism and Cardiovascular Diseases, vol. 17, no. 8, pp. 565–571, 2007.
View at: Publisher Site | Google Scholar
D. J. Rader, J. M. Hoeg, and H. B. Brewer Jr., “Quantitation of plasma apolipoproteins in the primary and secondary prevention of coronary artery disease,” Annals of Internal Medicine, vol. 120, no. 12, pp. 1012–1025, 1994.
View at: Google Scholar
A. Thompson and J. Danesh, “Associations between apolipoprotein B, apolipoprotein AI, the apolipoprotein B/AI ratio and coronary heart disease: a literature-based meta-analysis of prospective studies,” Journal of Internal Medicine, vol. 259, no. 5, pp. 481–492, 2006.
View at: Publisher Site | Google Scholar
E. Di Angelantonio, N. Sarwar, P. Perry et al., “Major lipids, apolipoproteins, and risk of vascular disease,” JAMA—Journal of the American Medical Association, vol. 302, no. 18, pp. 1993–2000, 2009.
View at: Publisher Site | Google Scholar
J. H. Contois, G. R. Warnick, and A. D. Sniderman, “Reliability of low-density lipoprotein cholesterol, non-high-density lipoprotein cholesterol, and apolipoprotein B measurement,” Journal of Clinical Lipidology, vol. 5, no. 4, pp. 264–272, 2011.
View at: Publisher Site | Google Scholar
S.-O. Olofsson, O. Wiklund, and J. Borén, “Apolipoproteins A-I and B: biosynthesis, role in the development of atherosclerosis and targets for intervention against cardiovascular disease,” Vascular Health and Risk Management, vol. 3, no. 4, pp. 491–502, 2007.
View at: Google Scholar
M. P. Bahíllo-Curieses, F. Hermoso-López, M. J. Martínez-Sopena et al., “Prevalence of insulin resistance and impaired glucose tolerance in a sample of obese spanish children and adolescents,” Endocrine, vol. 41, no. 2, pp. 289–295, 2012.
View at: Publisher Site | Google Scholar
P. Kocelak, J. Chudek, and M. Olszanecka-Glinianowicz, “Prevalence of metabolic syndrome and insulin resistance in overweight and obese women according to the different diagnostic criteria,” Minerva Endocrinologica, vol. 37, no. 3, pp. 247–254, 2012.
View at: Google Scholar
J. M. Lee, M. J. Okumura, M. M. Davis, W. H. Herman, and J. G. Gurney, “Prevalence and determinants of insulin resistance among U.S. adolescents: a population-based study,” Diabetes Care, vol. 29, no. 11, pp. 2427–2432, 2006.
View at: Publisher Site | Google Scholar
K. H. Yi, J. S. Hwang, E. Y. Kim, S. H. Lee, D. H. Kim, and J. S. Lim, “Prevalence of insulin resistance and cardiometabolic risk in Korean children and adolescents: a population-based study,” Diabetes Research and Clinical Practice, vol. 103, no. 1, pp. 106–113, 2014.
View at: Google Scholar
H. Belfki, S. Ben Ali, S. Bougatef et al., “The Apolipoprotein B/Apolipoprotein A 1 ratio in relation to metabolic syndrome and its components in a sample of the Tunisian population,” Experimental and Molecular Pathology, vol. 91, no. 2, pp. 622–625, 2011.
View at: Publisher Site | Google Scholar
N. Sattar, K. Williams, A. D. Sniderman, R. D'Agostino Jr., and S. M. Haffner, “Comparison of the associations of apolipoprotein B and non-high-density lipoprotein cholesterol with other cardiovascular risk factors in patients with the metabolic syndrome in the insulin resistance atherosclerosis study,” Circulation, vol. 110, no. 17, pp. 2687–2693, 2004.
View at: Publisher Site | Google Scholar
G. P. Carnevale Schianca, R. Pedrazzoli, S. Onolfo et al., “ApoB/apoA-I ratio is better than LDL-C in detecting cardiovascular risk,” Nutrition, Metabolism and Cardiovascular Diseases, vol. 21, no. 6, pp. 406–411, 2011.
View at: Publisher Site | Google Scholar
B. Enkhmaa, E. Anuurad, Z. Zhang, T. A. Pearson, and L. Berglund, “Usefulness of apolipoprotein B/apolipoprotein A-I ratio to predict coronary artery disease independent of the metabolic syndrome in African Americans,” The American Journal of Cardiology, vol. 106, no. 9, pp. 1264–1269, 2010.
View at: Publisher Site | Google Scholar
A. D. Sniderman and M. Faraj, “Apolipoprotein B, apolipoprotein A-I, insulin resistance and the metabolic syndrome,” Current Opinion in Lipidology, vol. 18, no. 6, pp. 633–637, 2007.
View at: Publisher Site | Google Scholar

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Copyright © 2014 Zaza Makaridze et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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