PO.PR01.04 · 预防研究

橄榄油副产品多酚富集提取物对肌肉功能、肌少症相关参数及皮肤健康的影响

Effects of olive oil byproducts polyphenol reach extract on muscle function, sarcopenia-related parameters and skin health

海报缩略图:橄榄油副产品多酚富集提取物对肌肉功能、肌少症相关参数及皮肤健康的影响
编号 3634 展板 20 时间 4/20 02:00–05:00 区域 Section 36 主讲 Adriana Albini, PhD
分会场 Metabolism and Microbiome in Cancer Initiation and Prevention
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作者与单位 Authors & Affiliations

Adriana Albini1, Sara Nofri2, Danilo Morelli3, Paola Corradino1, Gianni Lo Franco4, Calogero Caruso5, Anna Aiello5

1IEO - European Institute of Oncology, Milan, Italy,2University of Florence, Firenze, Italy,3Fondazione IRCCS Istituto Tumori di Milano, Milan, Italy,4Fattoria la Vialla, Castiglion Fibocchi (AR), Italy,5Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, Palermo, Italy

摘要 Abstract

中文摘要
肌少症,即与年龄相关的骨骼肌质量、力量和功能的丧失,是老年人衰弱和残疾的主要决定因素。针对炎症和氧化应激的营养保健策略已被提出作为辅助对策。橄榄油生产的副产品橄榄油磨坊废水(OMWW)富含羟基酪醇和其他多酚,具有强大的抗氧化和抗炎作用。一项为期30天的单臂初步试验评估了摄入OMWW提取物OMWW-OL(Oliphenolia®)后的若干生物计量和人体测量参数,结果显示在患有代谢综合征(肌肉衰退风险升高的人群)的成人中,改善肌少症相关指标的趋势呈阳性。共纳入29名参与者,23名(15名男性,8名女性)完成研究。评估内容包括基于生物电阻抗的肌肉质量指数、人体测量、握力、小腿围、水合状态以及炎症/代谢标志物,分别在基线(T0)、补充后(T1)和干预后30天(T2)进行。OMWW-OL耐受性良好。参与者在T1时表现出向无脂质量指数(FFMI)、四肢骨骼肌质量(ASMM)和握力改善的适度但一致的趋势,并在T2时部分持续。小腿围在整个观察期内稳步增加。在生化标志物中,氧化型LDL(oxLDL)——一种与肌肉分解相关的脂质过氧化指标——从T0到T2呈现小幅但渐进的下降,与OMWW多酚的抗氧化特征一致,而CRP在T1时短暂升高,随后在T2时回落至接近基线水平。尽管由于样本量小和研究设计的限制,统计学显著性有限,但观察到的趋势与临床前证据一致,即OMWW多酚可减轻氧化应激、抑制促炎细胞因子并促进肌肉蛋白稳态。这些探索性发现为开展更大规模的随机试验以评估OMWW作为肌少症预防和管理营养保健策略提供了依据。肌少症也与癌症相关,在患有代谢综合征的肿瘤患者中更为常见,并会恶化治疗反应。使用OMWW-OL的药妆制剂也显示出对皮肤的保护特性。OMWW-OL中主要的多酚之一是羟基酪醇,目前正在研究这种纯化物质的作用。
查看英文原文 English abstract
Sarcopenia, the age-related loss of skeletal muscle mass, strength, and function, represents a major determinant of frailty and disability in older adults. Nutraceutical strategies targeting inflammation and oxidative stress have been proposed as adjunctive countermeasures. Olive mill wastewater (OMWW), a byproduct of olive oil production, is rich in hydroxytyrosol and other polyphenols with potent antioxidant and anti-inflammatory effects. Results from a 30-day, single-arm pilot trial to evaluate several biometric and anthropometric parameters, after assumption of the OMWW extract, OMWW-OL (Oliphenolia®), revealed a positive trends to ameliorate sarcopenia-related values in adults with metabolic syndrome, a population at elevated risk for muscle decline. Twenty-nine participants were enrolled, and 23 (15 men, 8 women) completed the study. Assessments included bioimpedance-derived indices of muscle mass, anthropometry, handgrip strength, calf circumference, hydration, and inflammatory/metabolic markers at baseline (T0), after supplementation (T1), and 30 days post-intervention (T2). OMWW-OL was well tolerated. Participants showed modest but consistent trends toward improved fat-free mass index (FFMI), appendicular skeletal muscle mass (ASMM), and handgrip strength at T1, with partial persistence at T2. Calf circumference increased steadily across the observation period. Among biochemical markers, oxidized LDL (oxLDL), a lipid peroxidation indicator linked to muscle catabolism, showed a small but progressive reduction from T0 to T2, consistent with the antioxidant profile of OMWW polyphenols, whereas CRP exhibited a transient rise at T1 before returning near baseline at T2.Although statistical significance was limited by small sample size and study design, the observed trends align with preclinical evidence that OMWW polyphenols mitigate oxidative stress, suppress pro-inflammatory cytokines, and promote muscle protein homeostasis. These exploratory findings justify larger randomized trials to evaluate OMWW as a nutraceutical strategy for sarcopenia prevention and management. Sarcopenia has been also associated with cancer, is higher in oncology patients with metabolic syndrome and worsens response to therapy. Cosmeceutical preparations using OMWW-OL also reveal protective properties for the skin. One of the major polyphenols in OMWW-Ol is hydroxytyrosol, and investigations are ongoing oh the role of the purified substance.
利益披露 Disclosure
A. Albini, None.. S. Nofri, None.. D. Morelli, None.. P. Corradino, None.. G. Lo Franco, None.. C. Caruso, None.. A. Aiello, None.

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