Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran.
Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran.
J Clin Neurosci. 2024 Nov;129:110845. doi: 10.1016/j.jocn.2024.110845. Epub 2024 Sep 30.
The aim of designing this clinical trial is to investigate the impact of a nicotine-rich diet with/without protein redistribution on the motor indices of patients with Parkinson's disease (PD).
We randomly divided 45 patients (age > 50) with PD into three groups including: nicotine-rich diet (20 µg per day) group (group N; n = 15), nicotine-rich diet with protein redistribution group (group N + P; n = 15), and control group (group C; n = 15). In all group, the diet was isocaloric, and participants received six meals and snacks. After 12 weeks, the Unified Parkinson's Disease Rating Scale part III (UPDRS), serum alpha-synuclein levels, serum apolipoprotein A1, serum cotinine, and anthropometric parameters were measured in the three groups before and 12 weeks after the beginning of the study.
All of the enrolled patients completed the study. The UPDRS score was improved by 1.47 and 1.95 units in the N and N + P groups compared to the placebo (P < 0.001). On the other hand, effect size of N and N + P diets for α-synuclein were -52.82 and -175.85, respectively. The differences were significant compared to the control group (P < 0.05). Also, the effect of the both diets on serum cotinine compared to the control group was significant (P < 0.05). Although the effect size for UPDRS, α-synuclein, and cotinine in N + P diet were higher than N group, the differences were not statistically significant (P > 0.05). Also, the obtained results showed that there were no significant effects on anthropometric variables and serum levels of Apolipoprotein A1 in diet-receiving groups (P > 0.05).
The results of our study indicated that nicotine consumption in an isocaloric diet, while preventing a decrease in anthropometric indices, leads to improvements in motor indices and a reduction in alpha-synuclein levels. Additional and larger controlled trials are required to validate these findings.
本临床试验旨在研究富含尼古丁的饮食与/或蛋白质重分配对帕金森病(PD)患者运动指标的影响。
我们将 45 名(年龄>50 岁)PD 患者随机分为三组:富含尼古丁的饮食(每天 20μg)组(组 N;n=15)、富含尼古丁的饮食加蛋白质重分配组(组 N+P;n=15)和对照组(组 C;n=15)。在所有组中,饮食均为等热量,参与者接受六餐和零食。在研究开始后 12 周,测量三组患者的统一帕金森病评定量表第三部分(UPDRS)、血清α-突触核蛋白水平、血清载脂蛋白 A1、血清可替宁和人体测量学参数。
所有入组患者均完成了研究。与安慰剂相比,N 组和 N+P 组的 UPDRS 评分分别改善了 1.47 和 1.95 分(P<0.001)。另一方面,N 和 N+P 饮食对α-突触核蛋白的作用大小分别为-52.82 和-175.85。与对照组相比,差异有统计学意义(P<0.05)。此外,与对照组相比,两种饮食对血清可替宁的影响也有显著差异(P<0.05)。尽管 N+P 饮食组的 UPDRS、α-突触核蛋白和可替宁的作用大小高于 N 组,但差异无统计学意义(P>0.05)。此外,研究结果表明,接受饮食的两组患者的人体测量学变量和血清载脂蛋白 A1 水平无显著变化(P>0.05)。
本研究结果表明,在等热量饮食中摄入尼古丁可防止人体测量学指标下降,同时改善运动指标并降低α-突触核蛋白水平。需要进一步进行更大规模的对照试验来验证这些发现。