Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200, Copenhagen N, Denmark.
Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Cardiovasc Diabetol. 2023 Feb 25;22(1):41. doi: 10.1186/s12933-023-01765-z.
Identifying and reducing cardiometabolic risks driven by obesity remains a healthcare challenge. The metabolic syndrome is associated with abdominal obesity and inflammation and is predictive of long-term risk of developing type 2 diabetes and cardiovascular disease in otherwise healthy individuals living with obesity. Therefore, we investigated the effects of adherent exercise, a glucagon-like peptide 1 receptor agonist (GLP-1 RA), or the combination on severity of metabolic syndrome, abdominal obesity, and inflammation following weight loss.
This was a randomized, double-blinded, placebo-controlled trial. During an 8-week low-calorie diet (800 kcal/day), 195 adults with obesity and without diabetes lost 12% in body weight. Participants were then evenly randomized to four arms of one-year treatment with: placebo, moderate-to-vigorous exercise (minimum of 150 min/week of moderate-intensity or 75 min/week of vigorous-intensity aerobic physical activity or an equivalent combination of both), the GLP-1 RA liraglutide 3.0 mg/day, or a combination (exercise + liraglutide). A total of 166 participants completed the trial. We assessed the prespecified secondary outcome metabolic syndrome severity z-score (MetS-Z), abdominal obesity (estimated as android fat via dual-energy X-ray absorptiometry), and inflammation marker high-sensitivity C-reactive protein (hsCRP). Statistical analysis was performed on 130 participants adherent to the study interventions (per-protocol population) using a mixed linear model.
The diet-induced weight loss decreased the severity of MetS-Z from 0.57 to 0.06, which was maintained in the placebo and exercise groups after one year. MetS-Z was further decreased by liraglutide (- 0.37, 95% CI - 0.58 to - 0.16, P < 0.001) and the combination treatment (- 0.48, 95% CI - 0.70 to - 0.25, P < 0.001) compared to placebo. Abdominal fat percentage decreased by 2.6, 2.8, and 6.1 percentage points in the exercise, liraglutide, and combination groups compared to placebo, respectively, and hsCRP decreased only in the combination group compared with placebo (by 43%, P = 0.03).
The combination of adherent exercise and liraglutide treatment reduced metabolic syndrome severity, abdominal obesity, and inflammation and may therefore reduce cardiometabolic risk more than the individual treatments. Trial registration EudraCT number: 2015-005585-32, ClinicalTrials.gov: NCT04122716.
识别和降低肥胖引起的心脏代谢风险仍然是一个医疗挑战。代谢综合征与腹部肥胖和炎症有关,并且可以预测健康肥胖个体长期患 2 型糖尿病和心血管疾病的风险。因此,我们研究了坚持运动、胰高血糖素样肽 1 受体激动剂(GLP-1RA)或两者联合应用对减肥后代谢综合征严重程度、腹部肥胖和炎症的影响。
这是一项随机、双盲、安慰剂对照试验。在 8 周的低热量饮食(800 千卡/天)期间,195 名肥胖但无糖尿病的成年人体重减轻了 12%。然后,参与者被平均随机分配到为期一年的四种治疗组之一:安慰剂、中等到剧烈运动(每周至少 150 分钟中等强度或 75 分钟剧烈强度有氧运动,或两者等效组合)、GLP-1RA 利拉鲁肽 3.0 毫克/天或联合治疗(运动+利拉鲁肽)。共有 166 名参与者完成了试验。我们评估了预设的次要结局代谢综合征严重程度 z 评分(MetS-Z)、腹部肥胖(通过双能 X 射线吸收法估计为安卓脂肪)和炎症标志物高敏 C 反应蛋白(hsCRP)。使用混合线性模型对 130 名遵守研究干预措施的参与者(意向治疗人群)进行了统计分析。
饮食诱导的体重减轻使 MetS-Z 严重程度从 0.57 降低至 0.06,在一年后安慰剂和运动组中保持不变。与安慰剂相比,利拉鲁肽(-0.37,95%CI-0.58 至-0.16,P<0.001)和联合治疗(-0.48,95%CI-0.70 至-0.25,P<0.001)进一步降低了 MetS-Z。与安慰剂相比,运动、利拉鲁肽和联合治疗组的腹部脂肪百分比分别降低了 2.6、2.8 和 6.1 个百分点,而 hsCRP 仅在联合治疗组中与安慰剂相比有所降低(降低 43%,P=0.03)。
坚持运动和利拉鲁肽治疗的联合应用降低了代谢综合征严重程度、腹部肥胖和炎症,因此可能比单独治疗更能降低心脏代谢风险。试验注册 EudraCT 编号:2015-005585-32,ClinicalTrials.gov:NCT04122716。