Low-fat yogurt consumption maintains biomarkers of immune function relative to nondairy control food in women with elevated BMI: A randomized controlled crossover trial

IF 3.4 3区 医学 Q2 NUTRITION & DIETETICS
Yu Hasegawa , Andrea L. Noll , David J. Lang , Elizabeth M. Akfaly , Zhenhua Liu , Bradley W. Bolling
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引用次数: 0

Abstract

Yogurt consumption may help reduce chronic inflammation associated with obesity. However, the underlying mechanism(s) by which yogurt consumption modulates the immune system have not been validated in human intervention studies. We hypothesized that 4-week yogurt consumption (12 oz/day) attenuates systemic inflammation by modulating the proportion of circulating T helper (Th) 17 and regulatory T (Treg) cells in adult women with elevated body mass index (BMI). To test the hypothesis, we conducted a randomized crossover dietary intervention study consisted of a 4-week dietary intervention in which participants consumed 12 oz of either low-fat dairy yogurt or a soy pudding control snack per day, with a 4-week washout between treatments. Thirty-nine healthy adult women with a BMI between 25 and 40 kg/m2 were enrolled and 20 completed the study. Changes in the biometrics, circulating T cells, and markers of systemic and colonic inflammation were assessed between the 2 treatment groups, as well as 24-hour diet recalls were conducted at baseline and following each treatment. The primary study outcome, the change in the proportion of circulating Th17 cells, was unaffected by the treatments. Secondary outcome measures, circulating Treg, Th17, and markers of chronic inflammation, were maintained by yogurt treatment, whereas circulating Treg was increased and interleukin-10 was reduced by control snack treatment. However, circulating Treg changes were not associated with changes to other biomarkers of inflammation, implying other immune cells and/or tissues may mediate circulating biomarkers of chronic inflammation. This study was approved by the University of Wisconsin-Madison institutional review board and registered at ClinicalTrials.gov NCT04149418.

与非乳制品对照食品相比,饮用低脂酸奶可维持体重指数升高妇女的免疫功能生物标志物:一项随机对照交叉试验
饮用酸奶有助于减少与肥胖有关的慢性炎症。然而,饮用酸奶调节免疫系统的基本机制尚未在人体干预研究中得到验证。我们假设,在体重指数(BMI)升高的成年女性中,连续 4 周饮用酸奶(12 盎司/天)可通过调节循环 Th17 细胞和 Treg 细胞的比例来减轻全身炎症。为了验证这一假设,我们进行了一项随机交叉饮食干预研究,其中包括为期4周的饮食干预,参与者每天食用12盎司低脂乳制品酸奶或大豆布丁对照零食,并在两次治疗之间进行为期4周的冲洗。39 名体重指数在 25-40 公斤/米之间的健康成年女性参加了这项研究,其中 20 人完成了研究。研究人员评估了两个治疗组之间生物计量学、循环 T 细胞、全身和结肠炎症标志物的变化,并在基线和每个治疗后进行了 24 小时饮食回顾。主要研究结果是循环 Th17 细胞比例的变化,不受治疗方法的影响。酸奶疗法维持了次要结果指标,即循环Treg、Th17和慢性炎症指标,而对照零食疗法则增加了循环Treg,减少了IL-10。然而,循环 Treg 的变化与其他炎症生物标志物的变化无关,这意味着其他免疫细胞和/或组织可能介导慢性炎症的循环生物标志物。本研究已获得威斯康星大学麦迪逊分校机构审查委员会批准,并在 ClinicalTrial.gov NCT04149418 网站注册。
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来源期刊
Nutrition Research
Nutrition Research 医学-营养学
CiteScore
7.60
自引率
2.20%
发文量
107
审稿时长
58 days
期刊介绍: Nutrition Research publishes original research articles, communications, and reviews on basic and applied nutrition. The mission of Nutrition Research is to serve as the journal for global communication of nutrition and life sciences research on diet and health. The field of nutrition sciences includes, but is not limited to, the study of nutrients during growth, reproduction, aging, health, and disease. Articles covering basic and applied research on all aspects of nutrition sciences are encouraged, including: nutritional biochemistry and metabolism; metabolomics, nutrient gene interactions; nutrient requirements for health; nutrition and disease; digestion and absorption; nutritional anthropology; epidemiology; the influence of socioeconomic and cultural factors on nutrition of the individual and the community; the impact of nutrient intake on disease response and behavior; the consequences of nutritional deficiency on growth and development, endocrine and nervous systems, and immunity; nutrition and gut microbiota; food intolerance and allergy; nutrient drug interactions; nutrition and aging; nutrition and cancer; obesity; diabetes; and intervention programs.
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