학술논문
Metabolome analysis using cerebrospinal fluid from narcolepsy type 1 patients
ORIGINAL ARTICLE
ORIGINAL ARTICLE
Document Type
Report
Author
Source
SLEEP. November 2020, Vol. 43 Issue 11, p1i, 9 p.
Subject
Language
English
ISSN
0161-8105
Abstract
Introduction Narcolepsy type 1 (NT1) is a sleep disorder with a prevalence of 0.16%-0.18% in Japan and 0.02%-0.06% in the United States and Europe [1]. NT1 is characterized by excessive [...]
Narcolepsy type 1 (NT1) is a hypersomnia characterized by excessive daytime sleepiness and cataplexy. Inappropriate regulation of fatty acid metabolism has been suggested to be involved in the pathophysiology of NT1, but the detailed mechanisms remain uncertain. Here we performed a metabolomic analysis of cerebrospinal fluid samples from 14 NT1 and 17 control subjects using a novel capillary electrophoresis coupled with Fourier transform mass spectrometry. A total of 268 metabolites were identified and the amount of histidine was the most significantly increased in NT1 patients (p = 4.0 * [10.sup.-4]). Validation analysis using highperformance liquid chromatography (HPLC) including independent replication samples also identified the association of histidine (p = 2.02 * [10.sup.-3]). Further, levels of histamine, which is synthesized from histidine, were also examined using HPLC and were found to be significantly decreased in NT1 patients (p = 6.12 * [10.sup.-4]). Pathway analysis with nominally significant metabolites identified several pathways related to the metabolism of glycogenic amino acids, suggesting that glycogenesis is enhanced in NT1 as a compensatory mechanism for fatty acid metabolism. We performed further exploratory analysis, searching for metabolites associated with sleep variables from polysomnography and the multiple sleep latency test. As a result, [5.sup.']-deoxy-[5.sup.']-methylthioadenosine showed a significant association with apnea-hypopnea index (p = 2.66 * [10.sup.-6]). Moreover, gamma aminobutyric acid displayed a negative correlation with rapid eye movement sleep latency (REML), and thus might represent an intriguing target for future studies to elucidate how the controlling circuit of REM sleep is associated with abnormally short REML in NT1. Key words: narcolepsy; metabolome; CSF; histidine; MSLT
Narcolepsy type 1 (NT1) is a hypersomnia characterized by excessive daytime sleepiness and cataplexy. Inappropriate regulation of fatty acid metabolism has been suggested to be involved in the pathophysiology of NT1, but the detailed mechanisms remain uncertain. Here we performed a metabolomic analysis of cerebrospinal fluid samples from 14 NT1 and 17 control subjects using a novel capillary electrophoresis coupled with Fourier transform mass spectrometry. A total of 268 metabolites were identified and the amount of histidine was the most significantly increased in NT1 patients (p = 4.0 * [10.sup.-4]). Validation analysis using highperformance liquid chromatography (HPLC) including independent replication samples also identified the association of histidine (p = 2.02 * [10.sup.-3]). Further, levels of histamine, which is synthesized from histidine, were also examined using HPLC and were found to be significantly decreased in NT1 patients (p = 6.12 * [10.sup.-4]). Pathway analysis with nominally significant metabolites identified several pathways related to the metabolism of glycogenic amino acids, suggesting that glycogenesis is enhanced in NT1 as a compensatory mechanism for fatty acid metabolism. We performed further exploratory analysis, searching for metabolites associated with sleep variables from polysomnography and the multiple sleep latency test. As a result, [5.sup.']-deoxy-[5.sup.']-methylthioadenosine showed a significant association with apnea-hypopnea index (p = 2.66 * [10.sup.-6]). Moreover, gamma aminobutyric acid displayed a negative correlation with rapid eye movement sleep latency (REML), and thus might represent an intriguing target for future studies to elucidate how the controlling circuit of REM sleep is associated with abnormally short REML in NT1. Key words: narcolepsy; metabolome; CSF; histidine; MSLT