Effects of a community-based weight loss intervention on adipose tissue circulating factors

SummaryAimsObesity is associated with metabolic dysfunctions, which may be mediated by changes in adipose tissue signaling factors. These molecules are denoted as Adipose Tissue Generated Mediators of CardioVascular Risk (ATGMCVR) here, and include leptin, adiponectin, C-reactive protein (CRP), interleukin 6 (IL-6), tumor necrosis factor alpha (TNFα), and plasminogen activator inhibitor 1 (PAI-1). This study examined the effect of a weight loss program on ATGMCVR in obese adults with prediabetes.Materials and methodsSubjects were randomized to usual care (UC; n = 15) or lifestyle weight loss groups (LWL; n = 15). LWL was a community-based weight loss intervention to promote physical activity and healthy eating. ATGMCVR at 1-year were compared between groups by analysis of covariance; baseline value of the mediator was the covariate. Baseline means for ATGMCVR were compared between those with (n = 21) and without (n = 9) metabolic syndrome (MetS).ResultsAt baseline, subjects were 58 ± 9 (SD) years, 70% female, with a BMI of 34 ± 4 kg/m2. One-year weight loss (%) was 7.8 ± 6.0% for LWL and 1.7 ± 4.5% for UC. Group differences at 1-year were noted (adjusted means [95%CI] for UC and LWL, respectively) for adiponectin (8526.3 [7397.7, 9827]; 10,870.9 [9432.0, 12,529.3] ng/ml; p = 0.02), leptin (30.4 [26.1, 35.4]; 23.7 [20.3, 27.5] ng/ml; p = 0.02), IL-6 (0.4 [0.3, 0.5]; 0.2 [0.1, 0.2] pg/ml; p = 0.001), and PAI-1 (50 [42.7, 58.7]; 36.2 [30.8, 42.4] pg/ml; p = 0.01). No differences in baseline ATGMCVR were seen between subjects with and without MetS.ConclusionThese findings suggest ATGMCVR can be improved with weight loss; larger studies are needed to determine if improvements in metabolic dysfunction are related to changes in ATGMCVR.