Senior Scientist Group Nutrition, Immunity and Metabolism, Department of Nutrition and Gerontology, German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany.
Institute of Nutritional Science, University of Potsdam, 14558 Nuthetal, Germany.
Nutrients. 2020 Nov 26;12(12):3636. doi: 10.3390/nu12123636.
Nutritional interventions in morbidly obese individuals that effectively reverse a pro-inflammatory state and prevent obesity-associated medical complications are highly warranted. Our aim was to evaluate the effect of high (HP) or low (LP) protein diets on circulating immune-inflammatory biomarkers, including C-reactive protein (CRP), interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-a), interleukin-10 (IL-10), monocyte chemoattractant protein-1 (MCP-1), chemerin, omentin, leptin, total adiponectin, high molecular weight adiponectin, and fetuin-A. With this aim, 18 people with morbid obesity were matched into two hypocaloric groups: HP (30E% protein, = 8) and LP (10E% protein, = 10) for three weeks. Biomarkers were measured pre and post intervention and linear mixed-effects models were used to investigate differences. Consuming HP or LP diets resulted in reduced CRP (HP: -2.2 ± 1.0 mg/L, LP: -2.3 ± 0.9 mg/L) and chemerin (HP: -17.9 ± 8.6 ng/mL, LP: -20.0 ± 7.4 ng/mL), with no statistically significant differences by diet arm. Participants following the LP diet showed a more pronounced decrease in leptin (-19.2 ± 6.0 ng/mL) and IL-6 (-0.4 ± 0.1 pg/mL) and an increase in total adiponectin (1.6 ± 0.6 µg/mL). Changes were also observed for the remaining biomarkers to a smaller degree by the HP than the LP hypocaloric diet, suggesting that a LP hypocaloric diet modulates a wider range of immune inflammatory biomarkers in morbidly obese individuals.
需要有效的逆转促炎状态并预防肥胖相关并发症的病态肥胖个体的营养干预措施是非常有必要的。我们的目的是评估高蛋白(HP)或低蛋白(LP)饮食对循环免疫炎症生物标志物的影响,包括 C 反应蛋白(CRP)、白细胞介素 6(IL-6)、肿瘤坏死因子-α(TNF-α)、白细胞介素 10(IL-10)、单核细胞趋化蛋白 1(MCP-1)、chemerin、网膜素、瘦素、总脂联素、高分子量脂联素和胎球蛋白 A。为此,我们将 18 名病态肥胖患者匹配到两个低热量组:HP(30E% 蛋白质,n=8)和 LP(10E% 蛋白质,n=10),持续 3 周。在干预前后测量生物标志物,并使用线性混合效应模型来研究差异。食用 HP 或 LP 饮食导致 CRP(HP:-2.2±1.0mg/L,LP:-2.3±0.9mg/L)和 chemerin(HP:-17.9±8.6ng/mL,LP:-20.0±7.4ng/mL)减少,但饮食组之间无统计学差异。遵循 LP 饮食的患者的瘦素(-19.2±6.0ng/mL)和 IL-6(-0.4±0.1pg/mL)下降更为明显,总脂联素增加(1.6±0.6µg/mL)。与 LP 低热量饮食相比,HP 低热量饮食对其余生物标志物的变化程度较小,这表明 LP 低热量饮食可调节病态肥胖个体更广泛的免疫炎症生物标志物。