Acosta Andres, Camilleri Michael, Shin Andrea, Vazquez-Roque Maria I, Iturrino Johanna, Burton Duane, O'Neill Jessica, Eckert Deborah, Zinsmeister Alan R
Clinical Enteric Neuroscience Translational and Epidemiological Research, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota.
Clinical Enteric Neuroscience Translational and Epidemiological Research, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota.
Gastroenterology. 2015 Mar;148(3):537-546.e4. doi: 10.1053/j.gastro.2014.11.020. Epub 2014 Dec 6.
BACKGROUND & AIMS: Weight loss after pharmacotherapy varies greatly. We aimed to examine associations of quantitative gastrointestinal and psychological traits with obesity, and to validate the ability of these traits to predict responses of obese individuals to pharmacotherapy.
In a prospective study, we measured gastric emptying of solids and liquids, fasting and postprandial gastric volume, satiation by nutrient drink test (volume to fullness and maximal tolerated volume), satiety after an ad libitum buffet meal, gastrointestinal hormones, and psychological traits in 328 normal-weight, overweight, or obese adults. We also analyzed data from 181 previously studied adults to assess associations betwecen a subset of traits with body mass index and waist circumference. Latent dimensions associated with overweight or obesity were appraised by principal component analyses. We performed a proof of concept, placebo-controlled trial of extended-release phentermine and topiramate in 24 patients to validate associations between quantitative traits and response to weight-loss therapy.
In the prospective study, obesity was associated with fasting gastric volume (P = .03), accelerated gastric emptying (P < .001 for solids and P = .011 for liquids), lower postprandial levels of peptide tyrosine tyrosine (P = .003), and higher postprandial levels of glucagon-like peptide 1 (P < .001). In a combined analysis of data from all studies, obesity was associated with higher volume to fullness (n = 509; P = .038) and satiety with abnormal waist circumference (n = 271; P = .016). Principal component analysis identified latent dimensions that accounted for approximately 81% of the variation among overweight and obese subjects, including satiety or satiation (21%), gastric motility (14%), psychological factors (13%), and gastric sensorimotor factors (11%). The combination of phentermine and topiramate caused significant weight loss, slowed gastric emptying, and decreased calorie intake; weight loss in response to phentermine and topiramate was significantly associated with calorie intake at the prior satiety test.
Quantitative traits are associated with high body mass index; they can distinguish obesity phenotypes and, in a proof of concept clinical trial, predicted response to pharmacotherapy for obesity. ClinicalTrials.gov Number: NCT01834404.
药物治疗后的体重减轻差异很大。我们旨在研究胃肠道和心理定量特征与肥胖的关联,并验证这些特征预测肥胖个体对药物治疗反应的能力。
在一项前瞻性研究中,我们测量了328名体重正常、超重或肥胖成年人的固体和液体胃排空、空腹和餐后胃容积、通过营养饮料测试的饱腹感(达到饱腹感的体积和最大耐受体积)、随意自助餐餐后的饱腹感、胃肠激素和心理特征。我们还分析了181名先前研究的成年人的数据,以评估一部分特征与体重指数和腰围之间的关联。通过主成分分析评估与超重或肥胖相关的潜在维度。我们在24名患者中进行了一项概念验证性、安慰剂对照的缓释苯丁胺和托吡酯试验,以验证定量特征与减肥治疗反应之间的关联。
在前瞻性研究中,肥胖与空腹胃容积相关(P = 0.03)、胃排空加速(固体P < 0.001,液体P = 0.011)、餐后肽YY水平降低(P = 0.003)以及餐后胰高血糖素样肽1水平升高(P < 0.001)。在所有研究数据的综合分析中,肥胖与达到饱腹感的较高体积相关(n = 509;P = 0.038)以及腰围异常时的饱腹感相关(n = 271;P = 0.016)。主成分分析确定了潜在维度,这些维度占超重和肥胖受试者变异的约81%,包括饱腹感或饱足感(21%)、胃动力(14%)、心理因素(13%)和胃感觉运动因素(11%)。苯丁胺和托吡酯的联合使用导致显著体重减轻、胃排空减慢以及卡路里摄入量减少;对苯丁胺和托吡酯的体重减轻反应与先前饱腹感测试时的卡路里摄入量显著相关。
定量特征与高体重指数相关;它们可以区分肥胖表型,并且在一项概念验证性临床试验中,预测了对肥胖药物治疗的反应。ClinicalTrials.gov编号:NCT01834404。