Plasma Short‐Chain Fatty Acids in Patients With Parkinson's Disease

丁酸盐 内科学 脂肪酸 丙酸盐 化学 醋酸 丁酸 短链脂肪酸 单胺氧化酶B 内分泌学 生物化学 单胺氧化酶 医学 发酵
作者
Chaewon Shin,Yunsook Lim,Hyewon Lim,Tae‐Beom Ahn
出处
期刊:Movement Disorders [Wiley]
卷期号:35 (6): 1021-1027 被引量:84
标识
DOI:10.1002/mds.28016
摘要

Abstract Background Short‐chain fatty acids are exclusively produced by gut microbiota and are reduced in feces of patients with Parkinson's disease (PD). The objective of this study was to conduct a case–control study on peripheral concentration of short‐chain fatty acids based on evidence of pathologic changes in the blood–brain barrier in PD and the possible role of short‐chain fatty acids in blood–brain barrier permeability. Methods The plasma short‐chain fatty acid concentration was measured in 38 PD and 33 normal controls using gas chromatography. The clinical characteristics of patients with PD and controls were evaluated, and dietary information was obtained using a food frequency questionnaire. Short‐chain fatty acid concentrations were further compared after adjusting for age, sex, and significant food frequency questionnaire items. Results The concentrations of acetate, propionate, and butyrate did not differ between patients with PD and controls in unadjusted comparison. Dietary intakes of fibers, carbohydrates, lipids (total and fatty acids), and proteins did not differ between groups. After correction of covariates, acetic acid concentration was higher in patients with PD than in controls (116.47 ± 16.83 vs 108.20 ± 18.37 μmol/L; P = 0.010). In correlation analyses, acetic acid concentration was positively correlated ( R = 0.374, P = 0.021) with age, propionic acid concentration was negatively correlated with UPDRS part III score ( R = −0.376, P = 0.020) and use of entacapone ( R = −0.325, P = 0.047), and butyric acid concentration was correlated with monoamine oxidase inhibitor use ( R = 0.382, P = 0.018) and anticholinergic use ( R = −0.385, P = 0.024). Conclusions Plasma short‐chain fatty acids were paradoxically increased in PD and were associated with disease severity and antiparkinsonian medications. Further studies are warranted to elucidate the relationships of gut dysbiosis and inflammation with plasma short‐chain fatty acids. © 2020 International Parkinson and Movement Disorder Society
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