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Identification of bidirectional causal links between gut microbiota and narcolepsy type 1 using Mendelian randomization.
Sheng, Dandan; Li, Peihong; Xiao, Zheng; Li, Xinru; Liu, Jing; Xiao, Bo; Liu, Weiping; Zhou, Luo.
Afiliación
  • Sheng D; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Li P; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Xiao Z; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Li X; Department of Pathology, First Hospital of Changsha, Changsha, Hunan, China.
  • Liu J; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Xiao B; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Liu W; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Zhou L; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Sleep ; 47(3)2024 Mar 11.
Article en En | MEDLINE | ID: mdl-38174762
ABSTRACT
STUDY

OBJECTIVES:

Narcolepsy type 1 (NT1), characterized by cataplexy and orexin deficiency, is a rare and frequently debilitating neurological disorder. It has been noted to have connections with the gut microbiota, yet the exact causal relationships remain unclear.

METHODS:

We conducted a comprehensive bidirectional Mendelian randomization (MR) study to rigorously investigate the causal links between the gut microbiota and NT1, utilizing genetic datasets from the MiBioGen consortium and FinnGen consortium, respectively. The inverse-variance weighted (IVW) method was employed to obtain the primary MR estimates, supplemented by several alternative methods as well as sensitivity analyses including Cochran's Q, MR-Egger, MR pleiotropy residual sum and outlier, leave-one-out, and genetic colocalization.

RESULTS:

Our findings indicated that an increased relative abundance of five genera including Blautia (p = 4.47E-5), Collinsella (p = 0.036), Gordonibacter (p = 0.047), Hungatella (p = 0.015), and Lachnospiraceae UCG010 (p = 0.027) may be associated with a decreased risk of NT1. Conversely, an increased relative abundance of class Betaproteobacteria (p = 0.032), genus Alloprevotella (p = 0.009), and genus Ruminiclostridium6 (p = 0.029) may potentially heighten the risk of NT1. The onset of NT1 may lead to a decrease in the relative abundance of genus Eubacterium eligens group (p = 0.022), while a increase in the family Family XI (p = 0.009), genus Hungatella (p = 0.005), genus Prevotella (p = 0.013), and unknown genus id.2001 (p = 0.019). These findings remained robust under all sensitivity analyses.

CONCLUSIONS:

Our results offer robust evidence for the bidirectional causal links between particular gut microbial taxa and NT1, underscoring the significance of the microbiota-gut-brain axis in the pathological process of NT1.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cataplejía / Microbioma Gastrointestinal / Narcolepsia Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Idioma: En Revista: Sleep Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cataplejía / Microbioma Gastrointestinal / Narcolepsia Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Idioma: En Revista: Sleep Año: 2024 Tipo del documento: Article