Kawaguchi Hideki, Masuo Kazuko, Katsuya Tomohiro, Sugimoto Ken, Rakugi Hiromi, Ogihara Toshio, Tuck Michael L
Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
Hypertens Res. 2006 Dec;29(12):951-9. doi: 10.1291/hypres.29.951.
High blood pressure (BP) is a major determinant of cardiovascular events in obesity. The beta2- and beta3-adrenoceptor polymorphisms are associated with obesity and hypertension. In the present study, we examine the relationships of beta2- and beta3-adrenoceptor polymorphisms with further weight gain-induced BP elevation in obese subjects. Changes in BP, body weight, total body fat-mass, waist-to-hip ratio, plasma norepinephrine (NE) and leptin levels, and beta2(Arg16Gly)- and beta3(Trp64Arg)-adrenoceptor polymorphisms were measured periodically over a 5-year period in 55 entry obese (body mass index [BMI]> or =25.0 kg/m(2)) normotensive (BP<140/90 mmHg) men. BP elevation and weight gain were defined as > or =10% increases from entry levels over 5 years in mean BP or BMI. Obese subjects with weight gain, BP elevation or weight gain-induced BP elevation had higher frequencies of the Gly16 allele of Arg16GIy and Arg64 allele of Trp64Arg. Subjects carrying the Gly16 or Arg64 alleles had significantly greater total fat-mass and waist-to-hip ratio at entry and over a 5-year period compared to the subjects who did not carry these polymorphisms. Subjects carrying the Gly16 allele had similar levels of plasma NE, higher levels of plasma leptin and a lower slope of the regression lines between plasma leptin and NE levels. Those carrying the Arg64 allele had higher plasma NE levels at entry and over a 5-year period compared to the subjects without the Arg64 allele, but plasma leptin levels and slopes were similar. The findings demonstrate that the Arg64 allele of the beta3-adrenoceptor polymorphisms relates to weight gain-induced BP elevation accompanying high plasma NE (heightened sympathetic activity) in obese men. The Gly16 allele of the beta2-adrenoceptor polymorphisms links to weight gain-induced BP elevation associated with leptin resistance. beta2- and beta3-adrenoceptor polymorphisms could predict the future BP elevation and further weight gain-induced BP elevation in originally obese subjects.
高血压是肥胖人群心血管事件的主要决定因素。β2-和β3-肾上腺素能受体基因多态性与肥胖和高血压有关。在本研究中,我们检测了肥胖受试者中β2-和β3-肾上腺素能受体基因多态性与体重进一步增加导致的血压升高之间的关系。在55名初诊时肥胖(体重指数[BMI]≥25.0 kg/m²)且血压正常(血压<140/90 mmHg)的男性中,在5年期间定期测量血压、体重、全身脂肪量、腰臀比、血浆去甲肾上腺素(NE)和瘦素水平,以及β2(Arg16Gly)-和β3(Trp64Arg)-肾上腺素能受体基因多态性。血压升高和体重增加定义为平均血压或BMI较初诊水平在5年内升高≥10%。体重增加、血压升高或体重增加导致血压升高的肥胖受试者,其Arg16GIy的Gly16等位基因和Trp64Arg的Arg64等位基因频率较高。与未携带这些基因多态性的受试者相比,携带Gly16或Arg64等位基因的受试者在初诊时以及5年期间的总脂肪量和腰臀比显著更高。携带Gly16等位基因的受试者血浆NE水平相似,血浆瘦素水平较高,血浆瘦素与NE水平之间的回归线斜率较低。与未携带Arg64等位基因的受试者相比,携带Arg64等位基因者在初诊时以及5年期间血浆NE水平较高,但血浆瘦素水平和斜率相似。研究结果表明,β3-肾上腺素能受体基因多态性的Arg64等位基因与肥胖男性体重增加导致的血压升高以及高血浆NE(交感神经活动增强)有关。β2-肾上腺素能受体基因多态性的Gly16等位基因与体重增加导致的血压升高以及瘦素抵抗有关。β2-和β3-肾上腺素能受体基因多态性可以预测肥胖受试者未来的血压升高以及体重进一步增加导致的血压升高。