Peri-Okonny Poghni A, Ayers Colby, Maalouf Naim, Das Sandeep R, de Lemos James A, Berry Jarett D, Turer Aslan T, Neeland Ian J, Scherer Philipp E, Vongpatanasin Wanpen
Hypertension Section, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Department of Clinical Science, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Diabetes Metab Res Rev. 2017 Feb;33(2). doi: 10.1002/dmrr.2840. Epub 2016 Aug 18.
Excess adipose tissue has been implicated in the pathogenesis of insulin resistance and atherosclerosis and is a key risk factor for blood pressure (BP) elevation. However, circulating levels of adiponectin, a protein produced by adipose tissue and widely implicated in the pathogenesis of insulin resistance and atherosclerosis, are inversely proportional to adiposity. The relationship between adiponectin and incident hypertension has not been determined in the general US population.
Normotensive participants (n = 1233) enrolled in the Dallas Heart Study, a multiethnic, probability-based population sample of Dallas County adults were followed for median of 7 years. Retroperitoneal, intraperitoneal, visceral, and subcutaneous adipose tissue were measured at baseline by magnetic resonance imaging. Liver fat content was measured by H-magnetic resonance spectroscopy. Relative risk regression was used to determine the association of adiponectin with incident hypertension after adjustment for age, race, sex, BMI, smoking, diabetes, baseline systolic BP, total cholesterol, and regional fat depot.
Of the 1233 study participants (median age 40 years, 40% black, and 56% women), 391 (32%) had developed hypertension over a median follow-up of 7 years. Adiponectin levels were associated with reduced risk of incident hypertension (RR 0.81, 95% CI [0.68-0.96]) in the fully adjusted model, which included liver fat. Similar results were observed after adjustment for subcutaneous or visceral fat depots when tested individually or simultaneously in the model.
Our study suggested a protective role of adiponectin against incident hypertension independent of body fat distribution.
过多的脂肪组织与胰岛素抵抗和动脉粥样硬化的发病机制有关,是血压升高的关键危险因素。然而,脂联素是一种由脂肪组织产生的蛋白质,广泛参与胰岛素抵抗和动脉粥样硬化的发病机制,其循环水平与肥胖程度成反比。在美国普通人群中,脂联素与新发高血压之间的关系尚未确定。
达拉斯心脏研究纳入了血压正常的参与者(n = 1233),这是一个基于概率的达拉斯县成年多民族人群样本,随访时间中位数为7年。通过磁共振成像在基线时测量腹膜后、腹腔内、内脏和皮下脂肪组织。通过氢磁共振波谱测量肝脏脂肪含量。在调整年龄、种族、性别、体重指数、吸烟、糖尿病、基线收缩压、总胆固醇和局部脂肪储存后,使用相对风险回归来确定脂联素与新发高血压之间的关联。
在1233名研究参与者(中位年龄40岁,40%为黑人,56%为女性)中,391人(32%)在中位随访7年期间发生了高血压。在包括肝脏脂肪的完全调整模型中,脂联素水平与新发高血压风险降低相关(风险比0.81,95%置信区间[0.68 - 0.96])。在模型中单独或同时调整皮下或内脏脂肪储存后,观察到类似结果。
我们的研究表明脂联素对新发高血压具有保护作用,且独立于体脂分布。