Opstad Trine B, Sundfør Tine, Tonstad Serena, Seljeflot Ingebjørg
Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Oslo, Norway; Faculty of Medicine, University of Oslo, Norway.
Section of Preventive Cardiology, Department of Endocrinology, Morbid Obesity and Preventive Medicine, Oslo University Hospital Aker, Oslo, Norway.
Nutr Metab Cardiovasc Dis. 2021 Jun 7;31(6):1871-1878. doi: 10.1016/j.numecd.2021.03.005. Epub 2021 Mar 19.
BACKGROUND & AIMS: The favorable effect of caloric restriction (CR) on health span is well known and partly mediated by the sirtuin system. Sirtuin1, a regulator of energy homeostasis in response to nutrient availability, is activated by CR. We therefore investigated effects of two different CR regimens on Sirtuin1 concentrations.
METHODS & RESULTS: The study included 112 abdominally obese subjects, randomized to intermittent or continuous CR for 1 year. Blood samples and anthropometric measures were collected at baseline and after 12 months. Sirtuin1 concentrations were measured by ELISA. Sirtuin1 correlated significantly to BMI at baseline (r = .232, p = 0.019). Mean reduction in body-weight was 8.0 and 9.0 kg after intermittent and continuous CR, respectively. After 1 year, no significant between-group differences in Sirtuin1 levels were observed according to regimen (p = 0.98) and sex (p = 0.41). An increase in median Sirtuin1 concentrations (pg/mL) [25, 75 percentiles] from baseline was observed after intermittent CR in the total population (884 [624, 1285] vs.762 [530, 1135]; p = 0.041), most marked in men (820 [623, 1250] vs. 633 [524, 926]; p = 0.016). Improvement in BMI after 1 year correlated to Sirtuin1 changes, but varied according to sex. In women, Spearman's rho = .298, p = 0.034, with stronger correlation in the intermittent CR group (r = .424, p = 0.049). In men, there was an inverse relation to Sirtuin1 changes, only in the intermittent CR group (r = -.396, p = 0.045).
Effects on Sirtuin1 concentrations after 1 year of CR are sex and BMI-related. Intermittent CR regimen affected Sirtuin1 to a stronger extent than continuous CR, suggesting individualized dietary intervention.
热量限制(CR)对健康寿命的有益影响众所周知,且部分是由沉默调节蛋白系统介导的。沉默调节蛋白1是一种响应营养可利用性的能量稳态调节因子,可被热量限制激活。因此,我们研究了两种不同热量限制方案对沉默调节蛋白1浓度的影响。
该研究纳入了112名腹部肥胖受试者,随机分为间歇性或连续性热量限制组,为期1年。在基线和12个月后采集血样和人体测量数据。采用酶联免疫吸附测定法(ELISA)测量沉默调节蛋白1浓度。基线时,沉默调节蛋白1浓度与体重指数显著相关(r = 0.232,p = 0.019)。间歇性和连续性热量限制后,体重平均分别减轻了8.0千克和9.0千克。1年后,根据方案(p = 0.98)和性别(p = 0.41),两组间沉默调节蛋白1水平无显著差异。在总人口中,间歇性热量限制后,沉默调节蛋白1浓度中位数(pg/mL)[第25、75百分位数]较基线有所增加(884 [624, 1285] 对 762 [530, 1135];p = 0.041),在男性中最为明显(820 [623, 1250] 对 633 [524, 926];p = 0.016)。1年后体重指数的改善与沉默调节蛋白1的变化相关,但因性别而异。在女性中,斯皮尔曼等级相关系数rho = 0.298,p = 0.034,在间歇性热量限制组相关性更强(r = 0.424,p = 0.049)。在男性中,仅在间歇性热量限制组与沉默调节蛋白1的变化呈负相关(r = -0.396,p = 0.045)。
热量限制1年后对沉默调节蛋白1浓度的影响与性别和体重指数有关。间歇性热量限制方案对沉默调节蛋白1的影响程度强于连续性热量限制,提示应进行个体化饮食干预。