Taghizadeh Mohsen, Tamtaji Omid Reza, Dadgostar Ehsan, Daneshvar Kakhaki Reza, Bahmani Fereshteh, Abolhassani Javad, Aarabi Mohammad Hossein, Kouchaki Ebrahim, Memarzadeh Mohammad Reza, Asemi Zatollah
Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Islamic Republic of Iran.
Physiology Research Center, Kashan University of Medical Sciences, Kashan, Islamic Republic of Iran.
Neurochem Int. 2017 Sep;108:183-189. doi: 10.1016/j.neuint.2017.03.014. Epub 2017 Mar 22.
The current research was performed to evaluate the effects of omega-3 fatty acids and vitamin E co-supplementation on clinical signs and metabolic status in people with Parkinson's disease (PD). This randomized double-blind placebo-controlled clinical trial was conducted in 60 patients with PD. Participants were randomly assigned into two groups to receive either 1000 mg omega-3 fatty acids from flaxseed oil plus 400 IU vitamin E supplements (n = 30) or placebo (n = 30) for 12 weeks. Unified Parkinson's disease rating stage (UPDRS) were recorded at baseline and the after 3-month intervention. After 12 weeks' intervention, compared with the placebo, omega-3 fatty acids and vitamin E co-supplementation led to a significant improve in UPDRS (-3.3 ± 10.0 vs. +4.4 ± 14.9, P = 0.02). Furthermore, co-supplementation decreased high-sensitivity C-reactive protein (hs-CRP) (-0.3 ± 0.6 vs. +0.3 ± 0.3 μg/mL, P < 0.001), and increased total antioxidant capacity (TAC) (+65.2 ± 68.7 vs. +16 ± 52.4 μmol/L, P = 0.003) and glutathione (GSH) concentrations (+41.4 ± 80.6 vs. -19.6 ± 55.9 μmol/L, P = 0.001) compared with the placebo. Additionally, co-supplementation meaningfully decreased insulin (-2.1 ± 4.9 vs. +1.4 ± 6.2 μIU/mL, P = 0.01), homeostasis model of assessment-estimated insulin resistance (-0.7 ± 1.8 vs.+0.3 ± 1.6, P = 0.02) and Beta cell function (-5.9 ± 13.9 vs. +5.7 ± 25.5, P = 0.03), and increased quantitative insulin sensitivity check index (+0.009 ± 0.02 vs. -0.006 ± 0.03, P = 0.03) compared with the placebo. Overall, our study demonstrated that omega-3 fatty acids and vitamin E co-supplementation in people with PD had favorable effects on UPDRS, hs-CRP, TAC, GSH and markers of insulin metabolism.
本研究旨在评估ω-3脂肪酸与维生素E联合补充对帕金森病(PD)患者临床症状及代谢状态的影响。本随机双盲安慰剂对照临床试验纳入了60例PD患者。参与者被随机分为两组,一组接受来自亚麻籽油的1000毫克ω-3脂肪酸加400国际单位维生素E补充剂(n = 30),另一组接受安慰剂(n = 30),为期12周。在基线及3个月干预后记录统一帕金森病评定量表(UPDRS)。干预12周后,与安慰剂组相比,ω-3脂肪酸与维生素E联合补充使UPDRS有显著改善(-3.3±10.0 vs. +4.4±14.9,P = 0.02)。此外,联合补充降低了高敏C反应蛋白(hs-CRP)(-0.3±0.6 vs. +0.3±0.3μg/mL,P < 0.001),并提高了总抗氧化能力(TAC)(+65.2±68.7 vs. +16±52.4μmol/L,P = 0.003)和谷胱甘肽(GSH)浓度(+41.4±80.6 vs. -19.6±55.9μmol/L,P = 0.001)。与安慰剂组相比,联合补充还显著降低了胰岛素(-2.1±4.9 vs. +1.4±6.2μIU/mL,P = 0.01)、稳态模型评估估算的胰岛素抵抗(-0.7±1.8 vs. +0.3±1.6,P = 0.02)和β细胞功能(-5.9±13.9 vs. +5.7±25.5,P = 0.03),并提高了定量胰岛素敏感性检查指数(+0.009±0.02 vs. -0.006±0.03,P = 0.03)。总体而言,我们的研究表明,PD患者联合补充ω-3脂肪酸与维生素E对UPDRS、hs-CRP、TAC、GSH及胰岛素代谢指标有有益影响。