Contribution of Visceral Fat Accumulation to the Risk Factors for Atherosclerosis in Non-Obese Japanese

Similar documents
Fat Accumulation and Obesity-related Cardiovascular Risk Factors in Middle-aged Japanese Men and Women

ORIGINAL ARTICLE. Abstract. Introduction

Waist Circumference can Predict the Occurrence of Multiple Metabolic Risk Factors in Middle-aged Japanese Subjects

Changes and clinical significance of serum vaspin levels in patients with type 2 diabetes

Obesity, Metabolic Syndrome, and Diabetes: Making the Connections

ORIGINAL ARTICLE. Abstract. Introduction

Relationship between Hyperuricemia and Body Fat Distribution

Development of the Automated Diagnosis CT Screening System for Visceral Obesity

A study of waist hip ratio in identifying cardiovascular risk factors at Government Dharmapuri College Hospital

Metabolic syndrome and insulin resistance in an urban and rural adult population in Sri Lanka

The Metabolic Syndrome Update The Metabolic Syndrome: Overview. Global Cardiometabolic Risk

The Metabolic Syndrome Prof. Jean-Pierre Després

Journal: J. Jpn. Assoc. Dietary Fiber Res., 2000, 4 (2), (Original paper is in Japanese)

ATHEROSCLEROTIC cardiovascular complications are the leading cause of. Diabetes Mellitus Has an Additional Effect on Coronary Artery Disease

Cut-Off Values of Visceral Fat Area and Waist-to-Height Ratio: Diagnostic Criteria for Obesity-Related Disorders in Korean Children and Adolescents

Metabolic Syndrome in Asians

New Criteria for Obesity Disease in Japan

3/20/2011. Body Mass Index (kg/[m 2 ]) Age at Issue (*BMI > 30, or ~ 30 lbs overweight for 5 4 woman) Mokdad A.H.

Original Contributions. Close Correlation of Intra-abdominal Fat Accumulation to Hypertension in Obese Women

The Metabolic Syndrome Update The Metabolic Syndrome Update. Global Cardiometabolic Risk

Roadmap. Diabetes and the Metabolic Syndrome in the Asian Population. Asian. subgroups 8.9. in U.S. (% of total

The investigation of serum lipids and prevalence of dyslipidemia in urban adult population of Warangal district, Andhra Pradesh, India

Visceral Fat Area Evaluation by Computed Tomography Correlates with Visceral Fat Volume

Waist Circumference Measurements in Special Metabolic Syndrome Medical Checkups for Employees of a Japanese University: A Follow-up Study

Total risk management of Cardiovascular diseases Nobuhiro Yamada

Impact of Physical Activity on Metabolic Change in Type 2 Diabetes Mellitus Patients

An evaluation of body mass index, waist-hip ratio and waist circumference as a predictor of hypertension across urban population of Bangladesh.

Metabolic Syndrome.

PREVALENCE OF METABOLİC SYNDROME İN CHİLDREN AND ADOLESCENTS

HSN301 REVISION NOTES TOPIC 1 METABOLIC SYNDROME

Cardiometabolics in Children or Lipidology for Kids. Stanley J Goldberg MD Diplomate: American Board of Clinical Lipidology Tucson, Az

Predictive value of overweight in early detection of metabolic syndrome in schoolchildren

UMHS-PUHSC JOINT INSTITUTE

Carol Davila University of Medicine and Pharmacy, Bucharest, Romania

3/25/2010. Age-adjusted incidence rates for coronary heart disease according to body mass index and waist circumference tertiles

EPIDEMIOLOGICAL studies often report an association

902 Biomed Environ Sci, 2014; 27(11):

Metabolic Syndrome Update The Metabolic Syndrome: Overview. Global Cardiometabolic Risk

Nomogram of the Relation of Brachial-Ankle Pulse Wave Velocity with Blood Pressure

Plasma fibrinogen level, BMI and lipid profile in type 2 diabetes mellitus with hypertension

Effective waist circumference reduction rate necessary to avoid the development of type 2 diabetes in Japanese men with abdominal obesity

Subcutaneous and Visceral Adipose Tissue: Their Relation to the Metabolic Syndrome

MOLINA HEALTHCARE OF CALIFORNIA

Metabolic Syndrome among Type-2 Diabetic Patients in Benghazi- Libya: A pilot study. Arab Medical University. Benghazi, Libya

AUTONOMIC FUNCTION IS A HIGH PRIORITY

CHAPTER 3 DIABETES MELLITUS, OBESITY, HYPERTENSION AND DYSLIPIDEMIA IN ADULT CENTRAL KERALA POPULATION

High sensitive C-reactive protein, an independent and early novel inflammatory marker in healthy obese women.

Hypertriglyceridemia and the Related Factors in Middle-aged Adults in Taiwan

Dual Bioelectrical Impedance Analys. Restriction( Dissertation_ 全文 ) /doctor.k18

Retrospective Cohort Study for the Evaluation of Life- Style Risk Factors in Developing Metabolic Syndrome under the Estimated Abdominal Circumference

Diabetes in Asian Americans

Visceral Fat Area, Waist Circumference and Metabolic Risk Factors in Abdominally Obese Chinese Adults*

Relationships between the Visceral Fat Area on CT and Coronary Risk Factor Markers

Impact of Body Mass Index and Metabolic Syndrome on the Characteristics of Coronary Plaques Using Computed Tomography Angiography

PIEDMONT ACCESS TO HEALTH SERVICES, INC. Guidelines for Screening and Management of Dyslipidemia

2.5% of all deaths globally each year. 7th leading cause of death by % of people with diabetes live in low and middle income countries

Obesity has become a alarming public health problem

The Impact Of Adiposity And Insulin Resistance On Endothelial Function In Middle-Aged Subjects

Risk Factors for Heart Disease

Prediction of Homeostasis Model Assessment of Insulin Resistance in Japanese Subjects

ORIGINAL INVESTIGATION. C-Reactive Protein Concentration and Incident Hypertension in Young Adults

Short stature is an inflammatory disadvantage among middle-aged Japanese men

Atherosclerosis 206 (2009) Contents lists available at ScienceDirect. Atherosclerosis

Objectives. Objectives. Alejandro J. de la Torre, MD Cook Children s Hospital May 30, 2015

Relationships Between Indices of Obesity and Its Cardiovascular Comorbidities in a Chinese Population

Combination of BMI and Waist Circumference for Identifying Cardiovascular Risk Factors in Whites

Screening Results. Juniata College. Juniata College. Screening Results. October 11, October 12, 2016

Cardiovascular Complications of Diabetes

Non alcoholic fatty liver disease and atherosclerosis Raul Santos, MD

The IDF consensus worldwide definition of the metabolic syndrome

Know Your Number Aggregate Report Single Analysis Compared to National Averages

300 Biomed Environ Sci, 2018; 31(4):

Relationship between Abdominal Fat Area Measured by Screening Abdominal Fat CT and Metabolic Syndrome

Relationship of Waist Circumference and Lipid Profile in Children

Relationship between Arterial Stiffness and the Risk of Coronary Artery Disease in Subjects with and without Metabolic Syndrome

Insulin resistance and its associated comorbidities in young individuals: a HOMA study

HDL-C. J Jpn Coll Angiol, 2008, 48: NIPPON DATA80, MEGA study, JELIS, dyslipidemia, risk assessment chart

Department of Internal Medicine and Molecular Science, Graduate School of Medicine, Osaka University, Osaka, Japan. 4

PAPER Optimal cut-off values for obesity: using simple anthropometric indices to predict cardiovascular risk factors in Taiwan

Appropriate waist circumference cut off level for hypertension screening among admission students at Chiang Mai University

Metabolic Syndrome: What s in a name?

Associations between White Blood Cell Count and Features of the Metabolic Syndrome in Japanese Male Office Workers

Figure S1. Comparison of fasting plasma lipoprotein levels between males (n=108) and females (n=130). Box plots represent the quartiles distribution

Abnormality of risk factors for atherosclerotic disease among young Japanese aged years old: an evaluation of health checkup data

Metabolic Syndrome. Shon Meek MD, PhD Mayo Clinic Florida Endocrinology

THE EFFECT OF SECONDHAND SMOKE EXPOSURE ON HIGH MOLECULAR WEIGHT ADIPONECTIN LEVELS IN ADULT WOMEN: A PRELIMINARY REPORT

Metabolic syn and CVD. Dr : dehestani Imam reza hospital

METABOLIC SYNDROME IN TYPE-2 DIABETES MELLITUS

Correlation between fasting insulin and blood pressure in obese and non-obese middle aged Indian diabetic adults

Effects of Exercise and Physical Activity on Diabetes Mellitus and Obesity

Waist Circumference and Waist-to-Height Ratio as Predictors of Cardiovascular Disease Risk in Korean Adults

Andrejs Kalvelis 1, MD, PhD, Inga Stukena 2, MD, Guntis Bahs 3 MD, PhD & Aivars Lejnieks 4, MD, PhD ABSTRACT INTRODUCTION. Riga Stradins University

Association of urine acidification with visceral obesity and the metabolic syndrome

Association of serum adipose triglyceride lipase levels with obesity and diabetes

Obesity and the Metabolic Syndrome in Developing Countries: Focus on South Asians

JMSCR Volume 03 Issue 04 Page April 2015

CORRELATION OF OBESITY, INSULIN RESISTANCE AND LIPID PROFILE IN WOMEN WITH PCOS IN KIMS HOSPITAL BANGALORE Shashikala H. Gowda 1, Mansi Dhingra 2

Accelerated atherosclerosis begins years prior to the diagnosis of diabetes

The Effects of Moderate Intensity Exercise on Lipoprotein-Lipid Profiles of Haramaya University Community

Metabolic Syndrome. Bill Roberts, M.D., Ph.D. Professor of Pathology University of Utah

Transcription:

ORIGINAL ARTICLE Contribution of Visceral Fat Accumulation to the Risk Factors for Atherosclerosis in Non-Obese Japanese Takashi MIYAWAKI, Megumi ABE, Kensei YAHATA, Noboru KAJIYAMA, Hirokazu KATSUMA and Nobuo SAITO Abstract Objective To clarify the contributions of visceral fat tissue (VAT) mass deposition to the accumulation of risk factors for atherosclerosis in normal weight subjects. Subjects and Methods We investigated the relationship between VAT accumulation and both risk factors and waist circumference in non-obese subjects. In the 955 normal weight Japanese subjects (782 men and 173 women), visceral fat area (VFA), subcutaneous fat area (SFA) and waist circumference were measured through computed tomography. Total cholesterol, high-density lipoprotein (HDL) cholesterol, triglyceride, uric acid, fasting blood glucose, and 2-hour postprandial glucose in the oral glucose tolerance test (OGTT) were measured to assess the risk factors for atherosclerosis. Results In both men and women with normal body weight, VFA was correlated with total cholesterol (r=0.78 and r=0.71, respectively), HDL cholesterol (r= 0.89 and r= 0.82, respectively), triglyceride (r=0.72 and r=0.91, respectively), uric acid (r=0.71 and r=0.69, respectively), fasting blood glucose (r=0.84 and r=0.82, respectively), OGTT 2-hour postprandial glucose (r=0.75 and r=0.50, respectively), and systolic (r=0.93 and r=0.73, respectively) and diastolic (r=0.91 and r=0.73, respectively) blood pressure. The average number of risk factors was also correlated with VFA both in men (r=0.88, p=0.005) and women (r=0.91, p=0.003) with normal body weight. Based on the results of the multiple regression analyses, among VFA, SFA, body mass index (BMI) and age, VFA was considered to be the most important predictor for explaining the average number of risk factors. We also demonstrated that VFA was correlated with the waist circumference in normal weight men (r=0.74) and women (r=0.59). In normal weight subjects, the waist circumference equivalent to more than 1.0 of the average number of risk factors was 81 cm in men and 89 cm in women. Conclusion VAT accumulation itself plays a role as a risk factor for atherosclerosis irrespective of BMI, and measurement of VFA may be more important than that of BMI for predicting the presence of risk factors in normal weight subjects. Measurement of waist circumference also might be important for assessing the possibility of VAT accumulation leading to atherosclerosis. (Internal Medicine 43: 1138 1144, 2004) Key words: visceral fat, risk factor for atherosclerosis, nonobese Japanese Introduction Several studies have shown that obesity is a risk factor for type 2 diabetes, hypertension, dyslipidemia and hyperuricemia, which lead to atherosclerotic disorders such as cardiovascular disease (1). Particularly, visceral fat obesity, known to be caused by excess accumulation of visceral adipose tissue (VAT), has been found to be related to the appearance of atherosclerotic-related disorders including dyslipidemia, hypertension, impaired glucose tolerance and hyperuricemia (2). The disproportionate accumulation of VAT can cause metabolic and cardiovascular diseases more frequently than the excess accumulation of subcutaneous adipose tissue (3). For the analysis of VAT, visceral fat area (VFA) measured through computed tomography (CT) is most popularly used (4). Recently, excess accumulation of VAT itself has been re- For editorial comment, see p 1095. From the Health Administration Center, NTT West Kyoto Hospital, Kyoto Received for publication February 2, 2004; Accepted for publication June 28, 2004 Reprint requests should be addressed to Dr. Takashi Miyawaki, Health Administration Center, NTT West Kyoto Hospital, 1 Nishikujo Nanden-cho, Minami-ku, Kyoto 601-8441 1138

Visceral Fat in Non-Obese Japanese ported to be a risk factor for atherosclerosis, irrespective of body weight (4 6). However, in these studies, the subjects consisted of a small number of men and women, or only men or women. There have been few reports in which the relationship between VAT accumulation in normal weight subjects and risk factors for atherosclerosis were precisely investigated in both genders. Furthermore, few reports are available which determine the cut-off points of VFA and waist circumference for atherosclerosis in non-obese subjects. In the present cross-sectional study, we investigated the relationship between VAT accumulation and the risk factors for atherosclerosis such as dyslipidemia, hypertension, impaired glucose tolerance and hyperuricemia in normal weight Japanese subjects. We also investigated the relationship between VAT accumulation and the waist circumference to explore the cut-off points of waist circumference for atherosclerosis in non-obese Japanese subjects. Subjects and Methods We reviewed data of normal body mass index (BMI) [BMI of less than 25 (kg/m 2 )] in 955 middle-aged Japanese subjects [782 men and 173 women at the age of 49.8±6.7 and 48.9±5.8 years, respectively (mean±sd)]. All subjects were from a general population who were undergoing a yearly health screening or participating in a precise health check-up program performed in our hospital, and also desired a VFA measurement by CT. Subjects who had any history of endocrinological or metabolic disease or who were regularly taking any drugs were excluded in advance. The health screening included a physical check-up, routine collection of biochemical data, a 75-g oral glucose tolerance test (OGTT), and a CT evaluation of body-fat distribution. All subjects showed normal body mass index (BMI) [BMI of less than 25 (kg/m 2 )] according to the criteria of the Japan Society for the Study of Obesity (7), had no history of endocrinological or metabolic disease, and were not regularly taking any drugs. Body weight in light clothes was measured by 0.1 kg and height by 0.1 cm. BMI was calculated as weight (kg) divided by the square of height (m 2 ). Morning blood pressure was recorded using a mercury sphygmomanometer in the sitting position. Abdominal fat distribution was examined at the umbilicus level in the spine position using CT (Toshiba X Vision scanner, Tokyo, Japan), according to the previously described procedure (8). VFA, subcutaneous fat area (SFA), total fat area (TFA) and waist circumference were measured using a commercial software package (Fat Scan, N2 System, Osaka, Japan). VFA, SFA and TFA were calculated as follows. A region of interest of the subcutaneous fat was defined by tracing its contour on each scan, and the attenuation range of CT numbers for the fat tissue was calculated and expressed as the mean±2sd. Total and intra-peritoneal tissues with attenuation within the mean±2sd were considered to be TFA and VFA, respectively. SFA was calculated as TFA minus VFA. To measure serum total cholesterol, high-density lipoprotein (HDL) cholesterol, triglyceride, uric acid and glucose levels, blood samples were obtained at 9 : 00 AM after an overnight fast. Subsequently, all subjects underwent the standard oral glucose tolerance test (OGTT) proposed by WHO (9) between 9: 00 AM and 11: 00 AM. Serum total cholesterol and triglyceride levels were measured by enzymatic methods. HDL cholesterol, uric acid, and glucose levels in serum were measured by the direct method using a proprietary detergent, the uricase method, and the hexokinase method, respectively. This study was approved by the ethical committee of NTT West Kyoto Hospital. The average number of risk factors for atherosclerosis We regarded glucose impairment, dyslipidemia, hyperuricemia and hypertension as the risk factors for atherosclerosis (7). Dyslipidemia was defined by a total cholesterol level of not less than 220 mg/dl, a triglyceride level of not less than 150 mg/dl, and/or an HDL cholesterol level of less than 40 mg/dl. Glucose impairment was defined by a fasting glucose level of not less than 126 mg/dl and/or a 2-h postprandial glucose level in OGTT of not less than 200 mg/dl, and hyperuricemia by a uric acid level of not less than 7 mg/dl. Hypertension was defined by systolic blood pressure of not less than 140 mmhg and/or diastolic blood pressure of not less than 90 mmhg. In consideration of interobserver variation, the levels of VFA were grouped by every 10 cm 2 and the average number of risk factors in each group was calculated (8). Statistical analysis Data were expressed as means±sem. Correlations were assessed using Spearman s rank correlation test. Multiple regression analyses were performed using a model in which the dependent variable was the average number of risk factors for atherosclerosis, with the following explanatory variables: VFA, SFA, BMI and age. All variables were entered into the analysis simultaneously. Analyses of covariance (ANCOVA) were performed to examine the differences between the ratio of waist circumference to VFA in men and that in women. P values of less than 0.05 were considered to be significant. The statistical software SPSS for Windows (Version 8.0) was used for the analyses. Results The baseline characteristics for all subjects are shown in Table 1. In both men and women, BMI showed almost normal distribution with a mode value in the range of 22.5 kg/m 2 in men, and 21.3 kg/m 2 in women. The VFA values in men showed almost a normal distribution with a mode value in the range of 60 100 cm 2, while those in women showed a peak at a lower portion of the distribution with a mode value in the range of 20 40 cm 2. Figure 1 shows the relationship between VFA and meta- 1139

MIYAWAKI et al Table 1. Baseline Characteristics of Subjects Weight (kg) BMI (kg/m 2 ) Waist circumference (cm) Total fat area (cm 2 ) Visceral fat area (cm 2 ) Subcutaneous fat area (cm 2 ) Fasting glucose (mg/dl) 2-h postprandial glucose (mg/dl) Total cholesterol (mg/dl) HDL cholesterol (mg/dl) Triglyceride (mg/dl) Uric acid (mg/dl) Systolic blood pressure (mmhg) Diastolic blood pressure (mmhg) Men 64.9±0.2 22.5±0.1 85.3±0.2 196.9±2.2 86.1±1.3 110.0±1.2 103.9±0.7 119.0±1.8 216.1±1.2 57.4±0.5 138.3±3.8 6.2±0.1 127.0±0.6 79.5±0.4 Women 52.2±0.4 21.3±0.1 80.7±0.5 177.8±4.8 42.7±1.8 136.0±3.6 97.8±1.0 108.2±4.2 220.1±2.9 67.0±1.1 87.0±3.8 4.4±0.1 119.5±1.2 73.5±0.8 bolic or circulatory parameters. In both men and women with normal weight, VFA was positively correlated with the average levels of total cholesterol (r=0.78, p=0.005; r=0.71, p=0.026, respectively), triglyceride (r=0.72, p=0.005; r=0.91, p=0.003, respectively), uric acid (r=0.71, p=0.001; r=0.69, p=0.022, respectively), fasting glucose (r=0.84, p=0.0005; r=0.82, p=0.007, respectively) and OGTT 2-h postprandial glucose (r=0.75, p=0.001; r=0.50, p=0.04, respectively), and was inversely correlated with HDL cholesterol (r= 0.89, p=0.001; r= 0.82, p=0.006, respectively). VFA in men and women was also positively correlated with the average levels of systolic (r=0.93, p=0.001; r=0.73, p=0.01, respectively) and diastolic (r=0.91, p=0.0002; r=0.67, p=0.001, respectively) blood pressure. Total cholesterol, triglyceride, and fasting glucose levels tended to exceed the upper limit of normal ranges (220 mg/dl, 150 mg/dl, and 110 mg/dl, respectively) as VFA increased. Meanwhile, in both normal weight men and women, BMI and the level of each metabolic or circulatory parameter was slightly or not correlated (Total cholesterol r=0.07, p=0.048; r=0.16, p=0.038, respectively: triglyceride r=0.11 p=0.003; r=0.26, p=0.001, respectively: uric acid r=0.08, p=0.020; r=0.19, p=0.011, respectively: fasting glucose r=0.07, p= 0.051; r=0.16, p=0.034, respectively: OGTT 2-h postprandial glucose r=0.11, p=0.048; r=0.08, p=0.059, respectively: HDL cholesterol r= 0.26, p<0.0001: r= 0.18, p=0.018, respectively: systolic blood pressure r=0.19, p<0.0001; r=0.23, p=0.024, respectively: diastolic blood pressure r=0.21, p<0.0001; r=0.20, p=0.009, respectively). Figure 2 shows that VFA was correlated with the average number of risk factors for atherosclerosis, in both men (r=0.88 p=0.005) and women (r=0.91 p=0.003). The VFA that was equivalent to 1.0 of the average number of risk factors on the regression line was about 68 cm 2 in men and 59 cm 2 in women. Multiple regression analyses were performed to determine the variables among VFA, SFA, BMI and age contributing to the average number of risk factors (Table 2). In both men and women with normal weight, the regression procedure indicated VFA as the most important predictive variable (r=0.28, p<0.0001; r=0.35, p<0.0001, respectively) for explaining the average number of risk factors for atherosclerosis, while BMI had a slight correlation to the number of risk factors (r= 0.14, p=0.78; r= 0.03, p=0.79, respectively). Figure 3 shows the relationship between VFA and waist circumference calculated through CT. In both men and women, VFA was closely correlated with waist circumference (r=0.74, p<0.0001; r=0.59, p<0.0001, respectively). VFA in men was more strongly correlated with waist circumference than that in women, and men had a VFA about 2.2 times larger than that of women with the same waist circumference. ANCOVA was conducted using waist circumference as a covariate, and revealed significant gender differences in VFA (p<0.001). Calculated from the regression line, the waist circumferences which were equivalent to 68 cm 2 and 59 cm 2 of the VFA in men and women, respectively (equivalent to 1.0 of the average number of risk factors, calculated in Fig. 2), were about 81 cm and 89 cm, respectively. Discussion In this study, we demonstrated that, in both men and women with normal body weight, the levels of measured parameters of risk factors for atherosclerosis and the average number of risk factors were highly correlated with VFA, compared with BMI. To our knowledge, this is the first study to investigate the precise relationship between VFA and the risk factors for atherosclerosis in both non-obese men and women. Using multiple regression analyses, among VFA, SFA, BMI and age, VFA was the most predictive variable for explaining the number of risk factors. We also demonstrated that VFA was correlated with the waist circumference 1140

Visceral Fat in Non-Obese Japanese Figure 1. Correlation between VAT accumulation and the average values of risk factors for atherosclerosis in non-obese subjects. Closed circles, men; open circles, women. The broken line represents the upper limits (except lower limits in HDL cholesterol) of the normal range in each parameter. 1141

MIYAWAKI et al Figure 2. Relationship between VFA and the average number of risk factors for atherosclerosis in non-obese subjects. Closed circles, men; open circles, women. Risk factors were defined as dyslipidemia, hyperuricemia, glucose intolerance and hypertension. The horizontal and vertical dotted lines represent the average number of risk factors for atherosclerosis of 1.0 and the VFA equivalent to the risk factors of 1.0, respectively. Men VAT SAT BMI Age Women VAT SAT BMI Age Table 2. Multiple Regression Analyses Standardized partial regression coefficient 0.28 0.02 0.14 0.11 0.35 0.1 0.03 0.23 P value <0.0001 0.75 0.78 0.01 <0.0001 0.35 0.79 0.01 Explanatory variables: VAT, SAT, BMI and age. Dependent variables: The average number of risk factors for atherosclerosis (risk factors: glucose impairment, dyslipidemia, hyperuricemia and hypertension). in both men and women with normal body weight. VFA in men was more strongly correlated with waist circumference than that in women, and men had a VFA about 2.2 times larger than that of women with the same waist circumference. Furthermore, we demonstrated that the waist circumferences in non-obese Japanese subjects, which were equivalent to more than 1.0 of the average number of risk factors, were 81 cm in men and 89 cm in women. Recent studies have revealed that inappropriate VAT accumulation itself may cause the multiple risk factor syndrome, irrespective of BMI (4, 10, 11). The concept of the multiple risk factor syndrome has been referred to as syndrome X (12), the deadly quartet (13), metabolic syndrome (14) and visceral fat syndrome (10). The mechanisms responsible for these metabolic disorders are not fully understood, but some investigators have reported that insulin resistance due to inappropriate accumulation of VAT may in part cause these metabolic risks in both humans (15 18) and animals (19). One of the mechanisms of insulin resistance by VAT accumulation may be due to an overload of liver free fatty acids (FFA) produced by the high lipolytic activity of VAT. Overexposure of hepatic and extrahepatic tissues to FFA leads to the promotion of aberrations in insulin action and dynamics, and may cause insulin resistance (4, 20). The other possible mechanism responsible for insulin resistance related to VAT is the contribution of bioactive substances (adipocytokine) such as tumor necrotizing factor (TNF ), adiponectin, and resistin. Previous reports have demonstrated that TNF- levels are essentially dependent on VAT amount (21) and inversely correlated with insulin sensitivity in obese type 2 diabetic patients (22). Adiponectin, which may increase insulin sensitivity, decreases as VAT increases (23), and hypoadiponectinemia in patients with VAT accumulation may be closely related to insulin resistance and hyperinsulinemia (24). Resistin may also contribute to insulin resistance and its expression in human VAT enhances the expression in abdominal fat (25). The humoral regulators of adipocytokine and neuroendocrine perturbations may play a crucial role in insulin resistance, which leads to atherosclerosis. We also demonstrated that VFA was an important predictor for explaining the number of risk factors for atherosclerosis in subjects with a normal weight, while BMI had a slight correlation to the number of risk factors. Taken together, these results suggested that, in normal weight sub- 1142

Visceral Fat in Non-Obese Japanese Figure 3. Relationship between waist circumference and VFA in non-obese subjects. The horizontal and vertical dotted lines represent the VFA calculated in Fig. 2 and the waist circumference equivalent to the VFA, respectively. jects, measurement of VAT is more important than that of BMI for predicting the presence of risk factors for atherosclerosis. Therefore, lifestyles that may develop VAT, such as taking a high-sucrose diet (26) and alcohol (27), psychosocial stress (27), decreased exercise (28), and smoking (29), should be avoided even in subjects with normal weight. Though VFA was the most predictive variable in total for explaining the number of risk factors in the multiple regression analyses, it was less predictive in women than in men. It was speculated that variables that were not investigated in the present analysis such as physical activity and diet might also contribute to the risk factors. Further study is needed to clarify these confounding factors. In the present study, it was shown that VAT was closely correlated with waist circumference in normal weight Japanese subjects, and that waist circumferences which were equivalent to more than 1.0 of the average number of risk factors for atherosclerosis were over 81 cm in men and over 89 cm in women. Previous studies have indicated a close relationship between a larger waist circumference and deposition of VAT or cardiovascular risks in obesity, and suggested that subjects with a waist circumference which is over approximately 94 102 cm in Western men and 80 100 cm in Western women (not limited to normal weight subjects) have a likelihood of developing atherosclerotic metabolic disturbances (30 32). In addition, the WHO has reported that Asians with a waist circumference of not less than 90 cm in men and not less than 80 cm in women are at high risk (33). The reasons why the cut-off points obtained in this study were different from those described in previous reports might include racial differences in body shape, differences in study population (subjects were limited to those with normal weight in our study), and the measurement method of waist circumference (measurement was made using CT in our study). In the present study, non-obese Japanese men had a VFA 2.2 times larger than that of non-obese Japanese women with the same waist circumference. It has been reported that the VFA in obese men is 2.6 times larger than that in obese women (34). Based on these results, measurement of the waist circumference in men with normal body weight might be more important than that in women for assessing the accumulation of VAT. Measurement of the waist circumference is a useful and convenient method (35), though the anthropometric measurements comprise both abdominal subcutaneous fat and intra-abdominal visceral fat. When there is insufficient time to measure waist circumference at a medical examination, asking for the size of trousers or skirt of the subjects or patients may be useful for exploring the possibility of VAT accumulation. 1143

MIYAWAKI et al In conclusion, in normal weight Japanese subjects, the levels of measured parameters of the risk factors for atherosclerosis and the average number of risk factors were correlated with VAT accumulation. Measurement of VFA was more important than that of BMI for predicting the presence of risk factors in normal weight subjects. VFA was correlated with waist circumference in non-obese Japanese. Therefore, measurement of waist circumference in normal weight subjects, especially in men, might be important for assessing the possibility of VAT accumulation leading to atherosclerosis. Acknowledgements: We thank the clinical staff of the Department of Radiology and the Health Administration Center for their assistance. References 1) Anderson KM, Kannel WB. Obesity and disease. in: Obesity. Björntorp P, Brodoff BN, Eds. JB. Lippincott Company, Philadelphia, 1992: 465 473. 2) Peiris AN, Sothmann MS, Hoffmann RG, et al. Adiposity, fat distribution, and cardiovascular risk. Ann Intern Med 110: 867 872, 1989. 3) Fujioka S, Matsuzawa Y, Tokunaga K, Tarui S. Contribution of intraabdominal fat accumulation to the impairment of glucose and lipid metabolism in human obesity. Metabolism 36: 54 59, 1987. 4) Matsuzawa Y. Pathophysiology and molecular mechanisms of visceral fat syndrome: The Japanese experience. Diabetes Metab Rev 13: 3 13, 1997. 5) Kobayashi H, Nakamura T, Miyaoka K, et al. Visceral fat accumulation contributes to insulin resistance, small-sized low density lipoprotein, and progression of coronary artery disease in middle-aged non-obese Japanese men. Jpn Circ J 65: 193 199, 2001. 6) Yamamoto M, Egusa G, Hara H, Yamakido M. Association of intraabdominal fat and carotid atherosclerosis in non-obese middleaged men with normal glucose tolerance. Int J Obes Relat Metab Disord 21: 948 951, 1997. 7) Examination Committee of Criteria for Obesity Disease in Japan, Japan Society for the Study of Obesity. New Criteria for Obesity Disease in Japan. Circ J 66: 987 992, 2002. 8) Yoshizumi T, Nakamura T, Yamane M, et al. Abdominal fat: Standardized technique for measurement at CT. Radiology 211: 283 286, 1999. 9) World Health Organizaiton. Diabetes Mellitus: Report of a WHO Study Group. Techinical Report Series no. 727. Geneva, 1985. 10) Nakamura T, Tokunaga K, Shimomura I, et al. Contribution of visceral fat accumulation to the development of coronary artery disease in nonobese men. Atherosclerosis 107: 239 246, 1994. 11) Matsuzawa Y, Shimomura I, Nakamura T, Keno Y, Kotani K, Tokunaga K. Pathophysiology and pathogenesis of visceral fat obesity. Obes Res 3 suppl 2: 187S 194S, 1995. 12) Reaven GM. Banting lecture 1988. Role of insulin resistance in human disease. Diabetes 37: 1595 1607, 1988. 13) Kaplan NM. The deadly quartet: upper-body obesity, glucose intolerance, hypertriglyceridemia, and hypertension. Arch Intern Med 149: 1514 1520, 1989. 14) Park YW, Zhu S, Palaniappan L, Heshka S, Carnethon MR, Heymsfield SB. The metabolic syndrome: prevalence and associated risk factor findings in the US population from the Third National Health and Nutrition Examination Survey, 1988 1994. Arch Intern Med 163: 427 436, 2003. 15) DeFronzo RA, Ferrannini E. Insulin resistance. A multifaceted syndrome responsible for NIDDM, obesity, hypertension, dyslipidemia, and atherosclerotic cardiovascular disease. Diabetes Care 14: 173 194, 1991. 16) Pouliot MC, Després JP, Nadeau A, et al. Visceral obesity in men. Associations with glucose tolerance, plasma insulin, and lipoprotein levels. Diabetes 41: 826 834, 1992. 17) Yamashita S, Nakamura T, Shimomura I, et al. Insulin resistance and body fat distribution; Contribution of visceral fat accumulation to the development of insulin resistance and atherosclerosis. Diabetes Care 19: 287 291, 1996. 18) Kahn BB, Flier JS. Obesity and insulin resistance. J Clin Invest 106: 473 481, 2000. 19) Masuzaki H, Paterson J, Shinyama H, et al. A transgenic model of visceral obesity and the metabolic syndrome. Science 294: 2166 2170, 2001. 20) Björntorp P. Portal adipose tissue as a generator of risk factors for cardiovascular disease and diabetes. Arteriosclerosis 10: 493 496, 1990. 21) Bertin E, Nguyen P, Guenounou M, Durlach V, Potron G, Leutenegger M. Plasma levels of tumor necrosis factor-alpha (TNF- ) are essentially dependent on visceral fat amount in type 2 diabetic patients. Diabetes Metab 26: 178 182, 2000. 22) Katsuki A, Sumida Y, Murashima S, et al. Serum levels of tumor necrosis factor- are increased in obese patients with noninsulindependent diabetes mellitus. J Clin Endocrinol and Metab 83: 859 862, 1998. 23) Hotta K, Funahashi T, Bodkin NL, et al. Circulating concentrations of the adipocyte protein adiponectin are decreased in parallel with reduced insulin sensitivity during the progression to type-2 diabetes in rhesus monkeys. Diabetes 50: 1126 1133, 2001. 24) Weyer C, Funahashi T, Tanaka S, et al. Hypoadiponectinemia in obesity and type 2 diabetes: close association with insulin resistance and hyperinsulinemia. J Clin Endocrinol and Metab 86: 1930 1935, 2001. 25) McTernan PG, McTernan CL, Chetty R, et al. Increased resistin gene and protein expression in human abdominal adipose tissue. J Clin Endocrinol Metab 87: 2407, 2002. 26) Keno Y, Matsuzawa Y, Tokunaga K, et al. High sucrose diet increases visceral fat accumulation in VMH-lesioned obese rats. Int J Obes 15: 205 211, 1991. 27) Marniemi J, Kronholm E, Aunola S, et al. Visceral fat and psychosocial stress in identical twins discordant for obesity. J Intern Med 251: 35 43, 2002. 28) Shimomura I, Tokunaga K, Kotani K, et al. Marked reduction of acyl- CoA synthetase activity and mrna in intra-abdominal visceral fat by physical exercise. Am J Physiol 265: E44 50, 1993. 29) Shimokata H, Muller DC, Andres R. Studies in the distribution of body fat. III. Effects of cigarette smoking. JAMA 261: 1169 1173, 1989. 30) Pouliot MC, Després JP, Lemieux S, et al. Waist circumference and abdominal sagittal diameter: best simple anthoropometric indexes of abdominal visceral adipose tissue accumulation and related cardiovascular risk in men and women. Am J Cardiol 73: 460 468, 1994. 31) Han TS, van Leer EM, Seidell JC, Lean ME. Waist circumference action levels in the dentification of cardiovascular risk factors: prevalence study in a random sample. BMJ 311: 1401 1405, 1995. 32) Lean ME, Han TS, Seidell JC. Impairment of health and quality of life in people with large waist circumference. Lancet 351: 853 856, 1998. 33) World Health Organizaiton. The Asia-Pacific perspective; Redefining obesity and its treatment. Steering Committee of the Western Pacific Region of the WHO, the Internaitonal Association for the Study of Obesity, and the International Obesity Task Force. Melbourne. Australia, 2000. 34) Kotani K, Tokunaga K, Fujioka S, et al. Sexual dimorphism of agerelated changes in whole-body fat distribution in the obese. Int J Obes Relat Metab Disord 18: 207 212, 1994. 35) Han TS, Lean MEJ. Self-reported waist circumference compared with the Waist Watcher tape-measure to identify individuals at increased health risk through intra-abdominal fat accumulation. Br J Nutr 80: 81 88, 1998. 1144