Metabolic syndrome (MetS), a complex of interrelated risk factors for cardiovascular disease (CVD), includes elevated fasting plasma glucose (FPG) levels, elevated blood pressure (BP), elevated triglyceride (TG) levels, reduced highdensity lipoprotein cholesterol (HDL-C) levels, and obesity [1]. Obesity seems to be a central metabolic risk factor (MetRF) because insulin resistance, which is generally related to obesity, is a potential pathophysiologic link among MetRF. In this context, obesity, as measured by abdominal adiposity and increased waist circumference, is included as an essential factor for diagnosis of MetS by the International Diabetes Federation (IDF) and the Japanese Examination Committee for Criteria of Metabolic Syndrome [2, 3]. However MetRF were frequently clustered, even among non-obese subjects. Subjects with clustering of MetRF are often insulin-resistant compared with subjects without clustering of MetRF, even though they were not obese. Thus, non-obese subjects with a clustering of MetRF are at increased risk of CVD, as are obese subjects with a clustering of MetRF, or subjects with MetS. Thus, evaluation of MetRF seems to be important for finding such individuals. Recently, Hiraoka et al. reported an association of fatty liver with MetRF and such insulin-resistance indices as HOMA-R among non-obese subjects with normal waist circumference none of whom met the MetS criteria [4]. Blood pressure, serum triglyceride, and HOMA-R levels were significantly elevated among non-obese subjects with normal waist circumference and fatty liver compared to those without (males: 122/78 vs. 120/76 mmHg, 161.5 vs. 105.5 mg/dl, 1.9 vs. 1.3, respectively; females: 120/73 vs. 116/71 mmHg, 115.2 vs. 82.0 mg/dl, 1.7 vs. 1.3, respectively). This result indicated that those with fatty liver were at risk of clustering of MetRF and, thus, of developing MetS, even though they were not obese or did not meet the MetS criteria. Therefore, evaluation of fatty liver, which can be detected easily by ultrasonography in ordinary clinical settings, seems to be important for non-obese and obese individuals. Furthermore, because the authors excluded those who regularly drank 20 g or more alcohol per day from their study population, the fatty liver described in the report seems to be non-alcoholic fatty liver disease (NAFLD) [4]. Studies of MetS have revealed a J-shaped relationship between alcohol intake and the risk of MetS [5–7]. Indeed, light alcohol consumption was actually associated with a lower risk of MetS [6–8] whereas very heavy alcohol consumption was associated with a substantial increase in the risk of MetS [9]. However, the different relationships between alcohol intake and the risk of clustering of MetRF might be related to the different obesity of the subjects, i.e. non-obese versus obese. We recently reported that alcohol intake by non-obese males with a clustering of MetRF was significantly higher than by those without, but such differnce was not observed in obese males [10]. Furthermore, analysis of non-obese males stratified into the four groups on the basis of alcohol consumption (none, light (1–139 g/ week), heavy (140–279 g/week), and very heavy (]280 g/ week)) revealed a positive linear association between amount of alcohol intake and clustering of MetRF [10], i.e., increasing alcohol intake seemed to increase the risk of clustering of MetRF among non-obese Japanese males whereas non-obese individuals with no or light alcohol & Makoto Daimon mdaimon@hirosaki-u.ac.jp
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