Gut microbiota has important roles in the obstructive sleep apnea-induced inflammation and consequent neurocognitive impairment

Front Microbiol. 2024 Dec 6:15:1457348. doi: 10.3389/fmicb.2024.1457348. eCollection 2024.

Abstract

Obstructive sleep apnea (OSA) is a state of sleep disorder, characterized by repetitive episodes of apnea and chronic intermittent hypoxia. OSA has an extremely high prevalence worldwide and represents a serious challenge to public health, yet its severity is frequently underestimated. It is now well established that neurocognitive dysfunction, manifested as deficits in attention, memory, and executive functions, is a common complication observed in patients with OSA, whereas the specific pathogenesis remains poorly understood, despite the likelihood of involvement of inflammation. Here, we provide an overview of the current state of the art, demonstrating the intimacy of OSA with inflammation and cognitive impairment. Subsequently, we present the recent findings on the investigation of gut microbiota alteration in the OSA conditions, based on both patients-based clinical studies and animal models of OSA. We present an insightful discussion on the role of changes in the abundance of specific gut microbial members, including short-chain fatty acid (SCFA)-producers and/or microbes with pathogenic potential, in the pathogenesis of inflammation and further cognitive dysfunction. The transplantation of fecal microbiota from the mouse model of OSA can elicit inflammation and neurobehavioral disorders in naïve mice, thereby validating the causal relationship to inflammation and cognitive abnormality. This work calls for greater attention on OSA and the associated inflammation, which require timely and effective therapy to protect the brain from irreversible damage. This work also suggests that modification of the gut microbiota using prebiotics, probiotics or fecal microbiota transplantation may represent a potential adjuvant therapy for OSA.

Keywords: gut microbiota; intermittent hypoxia; neurocognitive dysfunction; obstructive sleep apnea; systematic inflammation.

Publication types

  • Review

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was funded by the Medical Research Foundation of GuangDong Province (A2022046 and B2022097), the Outstanding Young Researcher program (NSZD2023011), the general project (2020072) and the key program (NS2022005) granted by the Science and Technology Key Research Program in Nanshan District Health Care System, the Shenzhen Science and Technology Innovation Commission for Research and Development Projects (JCYJ20210324112607020, JCYJ20220530141616037, and JCYJ20230807115827057), Shenzhen University ENT Discipline Development Project sponsored by Shenzhen Huaqiang Holdings Co., Ltd., and the GuangDong Basic and Applied Basic Research Foundation (2023A1515110855).