Increase of Metabolic Syndrome Score is an Independent Determinant of Increasing Pulse Pressure

Jae-Youn Moon; Sungha Park; Chul Min Ahn; Jung Rae Cho; Chan Mi Park; Young-Guk Ko; Donghoon Choi; Myung Ho Jeong; Yangsoo Jang; Namsik Chung

doi:10.3349/ymj.2008.49.1.63

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Moon, Park, Ahn, Cho, Park, Ko, Choi, Jeong, Jang, and Chung: Increase of Metabolic Syndrome Score is an Independent Determinant of Increasing Pulse Pressure

Original Article

Yonsei Medical Journal

Yonsei Medical Journal 2008; 49(1): 63-70.

Published online: 20 February 2008

DOI: https://doi.org/10.3349/ymj.2008.49.1.63

Increase of Metabolic Syndrome Score is an Independent Determinant of Increasing Pulse Pressure

Jae-Youn Moon¹, Sungha Park^2,³, Chul Min Ahn², Jung Rae Cho², Chan Mi Park³, Young-Guk Ko², Donghoon Choi², Myung Ho Jeong¹, Yangsoo Jang^2,³, Namsik Chung²

¹The Heart Center, Chonnam National University Hospital, Gwangju, Korea.

²Division of Cardiology, Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.

³Cardiovascular Genome Center, Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.

Reprint address: requests to Dr. Sungha Park, Division of Cardiology, Yonsei Cardiovascular Center, Yonsei University College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul 120-752, Korea. Tel: 82-2-2228-8455, Fax: 82-2-393-2041, shpark0530@yuhs.ac

Received 18 July 2007 Accepted 13 September 2007

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

The objective of this study was to determine whether the progressive increase of metabolic syndrome (MetS) score, the number of components of MetS, is correlated significantly with increasing pulse pressure (PP).

Materials and Methods

4,034 subjects were enrolled from the Cardiovascular Genome Center of Yonsei University (M : F = 2344 : 1690, 55.2 ± 10.5). Most of the study population were recruited from hypertension clinics, controlled with medications according to JNC7 guidelines. The Asian modified criteria of MetS were applied and MetS score was estimated. The HOMA index for insulin resistance, cholesterol profiles, and anthropometric measurements were assessed.

Results

Among 4034 participants, 1690 (41.9%) were classified as MetS. Progressive increase in PP was demonstrated for increasing components of the MetS score. Multiple linear regression analysis with PP as the dependent variable showed that age (β = 0.311, p < 0.001), MetS score (β = 0.226, p < 0.001), male gender (β = -0.093, p < 0.001) and HOMA index IR (β = 0.033, p = 0.03) are significantly associated with PP (R² = 0.207, p < 0.001).

Conclusion

The present results from this study demonstrate that increasing MetS score is an independent determinant of increasing PP. The results also demonstrate the independent role of MetS in increasing arterial stiffness and PP.

Keywords: Metabolic syndrome, pulse pressure, arterial stiffness, metabolic syndrome scores

INTRODUCTION

The pulse pressure (PP), the difference between systolic blood pressure (SBP) and diastolic blood pressure (DBP), is known to be an important predictor of cardiovascular and cerebrovascular mortality in both hypertensive and normotensive populations.1-3

PP is determined by ventricular interaction with the elastic properties of the large arteries and the magnitude of wave reflection.1,2,4 Therefore, the increase in PP is determined primarily by the increase in large arterial stiffness.3 Recent epidemiologic studies have demonstrated that the increase in PP is independently associated with adverse cardiovascular events.1-3 Therefore, clinical determinants associated with increasing PP may have clinical significance.

Studies have shown that obesity and the presence of MetS are associated with increasing arterial stiffness.5-9 Endothelial dysfunction, insulin resistance, atherogenic alterations, neurohormonal abnormalities and hypercoagulability are some of the factors that contribute to the increased arterial stiffness in MetS.5

Therefore, the objective of this study was to determine whether the progressive increase in MetS score, the number of components of metabolic syndrome, is significantly correlated with increase in PP.

MATERIALS AND METHODS

Patient population

The study group consisted of 4,034 subjects who were enrolled at the Yonsei Cardiovascular Genome center (men: 2,344. women: 1,690. mean age: 55.2 ± 10.5). The Cardiovascular Genome Center is a Korean government-sponsored research project, whose objective is to determine the genetic factors that are associated with the development of cardiovascular disease in a large prospective Korean cohort. Most of the study populations were recruited from the hypertension outpatient clinic, and their blood pressure was controlled with medications according to JNC7 guidelines.10 The rest of subjects were composed of populations who presented for a routine health status check up at Yonsei Cardiovascular Center. The blood pressure of hypertension patients was presented as normal subjects because of proper medications. Our database contained information about all the constituents of the MetS, and biochemical risk factors for coronary artery disease (CAD). Subjects were asked to refrain from performing strenuous exercise or drinking alcoholic beverages 24 hours before the laboratory test. They were also instructed to avoid eating or drinking anything during the test except water. Written informed consent was obtained from all subjects, and the protocol was approved by the Institutional Review Board of Yonsei University College of Medicine.

Blood collection and assessment of insulin resistance

Blood samples were taken from the forearm after at least 12 hours of fasting and collected into EDTA-treated and plain tubes. The serum glucose levels were determined by using the enzymatic method (Hitach 7600 - 110, Hitachi Co., Tokyo, Japan), and the insulin concentration with an immunoradiometric assay (Biosource, Nivelles, Belgium) with intra- and inter-assay coefficients of variation of 2.1 - 4.5% and 4.7 - 12.2%, respectively. The status of insulin resistance was measured using the homeostasis model assessment of insulin resistance index (HOMA index) with the following formula;

HOMA (homeostasis model assessment of insulin resistance) index = Fasting insulin (µIU/mL) × Fasting glycemia (mmol/L) / 22.5

The serum apolipoprotein A1 and B were determined by using Immuno-turbidometric analyzer at 340 nm with a specific antiserum (Cobas Integra Roche, USA, Rotkreuz, Switzerland).

The analysis of total cholesterol and triglycerides was based on an enzymatic method (Hitachi 7600 - 110, Hitachi Co., Tokyo, Japan). After precipitation of serum chylomicron, low density lipoprotein-cholesterol (LDL-C), and very low density lipoprotein (VLDL) with dextran sulfate-magnesium, and high density lipoprotein-cholesterol (HDL-C) remaining in the supernatant fluid was measured by using an enzymatic method (Hitachi 7600-110, Hitachi Co., Tokyo, Japan). The LDL-C level was calculated using the Friedewald formula with serum triglyceride concentrations < 4.52 mol/L (400 mg/dL).11

Anthropometric and blood pressure measurements

The body weight, waist circumferences and height were measured in the morning. Body mass index (BMI) was calculated by dividing body weight (in kg) by height² (in m). Blood pressure was read from the left arm while subjects remained seated. Readings of SBP and DBP were taken in the supported left arm of the seated subject after 5 minutes of quiet rest, with a mercury column sphygmomanometer with cuff-size adjustment based on arm circumference. Baseline of each SBP and DBP each was average of 3 separate measurements taken by the examining physician.

Classification of metabolic status (modified NCEP criteria for Asian)

The National Cholesterol Education Program (NCEP) Adult Treatment Panel III (ATP III) guidelines12,13 classify individuals as having the MetS if they possess three or more of the following criteria:

Central obesity: The World Health Organization (WHO) has recognized the disproportionate contribution of obesity to the development of cardiovascular risk factors in Asians and has provisionally lowered the classification of central obesity to > 80 or > 90 cm in females and males

High blood pressure: If patient's systolic and/or diastolic blood pressures were ≥ 130/85 mmHg or patients were receiving blood pressure lowering drugs.

Hyperglycemia: Fasting plasma glucose ≥ 6.1 mmol/L (110 mg/dL) or patients were receiving glucose lowering drugs.

Low HDL-cholesterol (HDL-C): Fasting HDL-C < 1.04 or 1.29 mmol/L (40 or 50 mg/dL) in males and females, respectively.

Hypertriglyceridemia: Fasting plasma triglycerides ≥ 1.69 mmol/L (150 mg/dL).

Statistical analysis

Values were expressed as mean ± SD. Statistical analysis was performed with SPSS version 13.0 for WINDOWS (SPSS Inc, Chicago, IL, USA) for descriptive statistics. Linear regression analysis was performed using the variables significant in bivariate analysis as the candidate variables and PP as a dependent variable.

In model 1, the MetS score (the number of components) was entered along with age, gender, smoking habits, and LDL cholesterol. In model 2, the MetS score was entered with age, gender, smoking habits, LDL cholesterol, and HOMA index. A two-tailed value of p < 0.05 was considered statistically significant.

RESULTS

Clinical characteristics in relation to MetS score

The study population consisted of 4,034 subjects (men: 2,344. women: 1,690. mean age: 55.2 ± 10.5). Table 1 describes the general clinical features of subjects included in the study and the distribution of subjects with a 0 to 5 MetS score [MetS score 0 (n = 525), 1 (n = 833), 2 (n = 986), 3 (n = 968), 4 (n = 572), 5 (n = 150)]. As expected, the values of all of the anthropometric, metabolic, serum lipoprotein and marker of insulin resistance variables, except LDL cholesterol levels, were significantly different between the subjects with different MetS scores. Subjects with increasing MetS scores were associated with an increase in age, waist line, BMI, SBP, DBP, TG, apoB, fasting glucose, insulin, and HOMA index. A clear relation was evident between the MetS score and the degree of insulin resistance and hyperglycemia.

As MetS score increased, so did HOMA index, which is a marker of increased insulin resistance. As the number of components of the MetS rose, the prevalence of hypertension also increased. No difference was noted in the serum levels of LDL cholesterol and the prevalence of current smokers. The prevalence of NCEP Asian modified MetS (≥ 3 metabolic components) was 41.9% (men: 35.5%, women: 50.8%) in the study group. PP was different between the subjects with and without MetS (without MetS: 42.2 ± 12.0 mmHg vs with MetS: 49.1 ± 14.6 mmHg, p < 0.001). The prevalence of MetS according to age group is shown in Table 2.

Effects of MetS score on pulse pressure

Fig. 1 shows the significant difference in the level of PP for subjects with different MetS score (Score 0: 36.8 ± 7.6 mmHg, Score 1: 42.0 ± 12.1 mmHg, Score 2: 45.2 ± 12.8 mmHg, Score 3: 47.8 ± 14.2 mmHg, Score 4: 50.5 ± 14.3 mmHg, Score 5: 52.3 ± 16.9 mmHg, p < 0.001 by one-way ANOVA analysis). When the subjects were divided into 5 groups according to age and MetS score, PP showed a progressive increase as the MetS score increased within each age group (Fig. 2). The slope of the elevation showed steep increase in the patients over the age of 50. Also, the HOMA index demonstrated a pattern of increase according to increasing PP in each age groups as well (Fig. 3). After adjustment for age and hypertension, insulin resistance, which was measured by HOMA index, was also correlated with PP (correlation coefficient = 0.074, p < 0.01). We investigated whether increased MetS scores were independently associated with an increase in PP. Linear regression was performed using the variables significant in bivariate analysis as the candidate variables and PP as a dependent variable, and we found associations of MetS score with PP while controlling for classical cardiovascular risk factors (smoking, age, gender, LDL-C). Cardiovascular risk factors that are components of MetS, such as the presence of hypertension, triglycerides, HDL and obesity, were not entered in the analysis due to collinearity.

When age, gender, smoking history, serum LDL-C, MetS score, and HOMA index were entered into the model, the independent predictors of PP were age (β = 0.311, p < 0.001), MetS score (β = 0.226, p < 0.001), male gender (β = - 0.093, p < 0.001) and HOMA index (β = 0.033, p = 0.03) with a model R² = 0.207 (p < 0.001)(Table 3).

DISCUSSION

The main finding from this study is that an increase in MetS score is correlated with an increase in PP. Furthermore, we found that MetS score itself was an independent predictor of increase in PP, and that an increasing degree of MetS score is associated with an increase in the parameter of insulin resistance, such as HOMA index.

MetS and increasing arterial stiffness

MetS is recognized as a cluster of cardiovascular risk factors that frequently coincides with insulin resistance and hyperglycemia. Previous studies showed that obesity and the presence of MetS are associated with increasing arterial stiffness.5-9 Moreover, the independent association between vascular structure with function and each component of MetS has previously been reported.8 In the present study, regression analysis revealed that an increase of MetS score was proportionately related to an increase in PP, demonstrating that increasing component of MetS is a determinant of increasing PP, irrespective of age. Because traditional risk factors of cardiovascular disease are known to be associated with increasing degree of arteriosclerosis, the clustering of risk factors in patients with MetS may be one of the important factors for the elevation in arterial stiffness and subsequent increase in PP.14-16 However, the effect of MetS is more than the sum of its parts, with each components acting synergistically in the development of cardiovascular disesase.17,18 In a cross sectional analysis of the Baltimore Longitudinal Study of Aging (BLSA), the clustering of components of MetS exerted a synergistic effect on vascular stiffness that was more than the effect of individual components of MetS.8 MetS is associated with an increase in sympathetic and neurohormonal activation, endothelial dysfunction and increasing degree of insulin resistance which may act in concert to increase arterial stiffness and PP.5,19,20

Vascular inflammation is also an important determinant of increasing arterial stiffness with an increase in serum high sensitivity C-reactive protein (hsCRP) that is associated with increase in pulse wave velocity.21 Inflammation plays a key role in the development of complications in metabolic syndrome, and hsCRP is known to be significantly correlated with each component of metabolic syndrome as well as degree of insulin resistance.22-24 Therefore, an increasing degree of vascular inflammation may be important in increasing arterial stiffness and PP in patients with MetS.

Mechanisms of correlations between insulin resistance and arterial stiffness

An interesting finding from this study is the progressive increase in insulin resistance that is associated with increase in PP. This finding was demonstrated in all age groups, except for the subgroup of patients over 70 years. Insulin resistance is known to be associated with increasing arterial stiffness.25 Although the mechanism underlying this association is not clearly defined, insulin resistance state is associated with decreased endothelial dependent arterial compliance.25 Also, insulin is known to diminish wave reflection the effect of which is blunted in obese, insulin resistance state,26 and regression analysis which HOMA index in the equation demonstrated that insulin resistance is independently associated with increase in PP. (Table 3, model 2) However, the addition of HOMA index to the regression model resulted in weak contribution of insulin resistance to pulse pressure with an increase of R² from 0.206 to 0.207 (Table 3). Therefore, the clustering of components of MetS that exerts a synergistic effect on vascular stiffness may be more important in increasing pulse pressure than insulin resistance itself.

The prevalence of MetS in this study population was relatively high due to the fact that the study population consisted of a high proportion of patients with a history of cardiovascular disease and hypertension. Also, many patients consented to enroll at the cardiovascular genome center due to health concerns. Therefore, the prevalence of MetS in our data does not reflect that of the general population. Furthermore, blood pressure and PP in this study were relatively low, and the reason appeared to be that many of the patients in the study group were being administered with antihypertensive medications. Nevertheless, this would not diminish the clinical impact of this study since PP is a significant predictor for cardiovascular risk in treated hypertensive patients as well.27

Figures and Tables

Fig. 1

Difference of pulse pressure in relation to metabolic syndrome score (Score 0: 36.8 ± 7.6; Score 1: 42.0 ± 12.1; Score 2: 45.2 ± 12.8; Score 3: 47.8 ± 14.2; Score 4: 50.5 ± 14.3; Score 5: 52.3 ± 16.9).

Fig. 2

Difference of pulse pressure in relation to metabolic syndrome score (in age groups).

Fig. 3

Difference of pulse pressure between HOMA 4 quartiles.

Table 1

Clinical Characteristics of Subjects in Relation to MetS Score

^*p value < 0.05 between groups.

BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure; PP, pulse pressure; TG, triglycerides; LDL-C, LDL-cholesterol; HDL-C, HDL-cholesterol; apoA1, apolipoproteinA1; apoB, apolipoproteinB; fasting glc, fasting glucose.

Table 2

Prevalence of Metabolic Syndrome (Total and Women Group)

Table 3

Multiple Regression Models Evaluating the Independent Determinants of PP

Notes

This work was supported by grant (A000385) from the Ministry of Health and Welfare, Republic of Korea, and by a grant of the Seoul R &BD Program, Republic of Korea (10526).

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