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CDKL5 缺乏症患者的肠道微生物群特征。

Gut microbiota profile in CDKL5 deficiency disorder patients.

机构信息

Department of Health Sciences, Università Degli Studi di Milano, Milan, Italy.

Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.

出版信息

Sci Rep. 2024 Mar 28;14(1):7376. doi: 10.1038/s41598-024-56989-0.

Abstract

CDKL5 deficiency disorder (CDD) is a neurodevelopmental condition characterized by global developmental delay, early-onset seizures, intellectual disability, visual and motor impairments. Unlike Rett Syndrome (RTT), CDD lacks a clear regression period. Patients with CDD frequently encounter gastrointestinal (GI) disturbances and exhibit signs of subclinical immune dysregulation. However, the underlying causes of these conditions remain elusive. Emerging studies indicate a potential connection between neurological disorders and gut microbiota, an area completely unexplored in CDD. We conducted a pioneering study, analyzing fecal microbiota composition in individuals with CDD (n = 17) and their healthy relatives (n = 17). Notably, differences in intestinal bacterial diversity and composition were identified in CDD patients. In particular, at genus level, CDD microbial communities were characterized by an increase in the relative abundance of Clostridium_AQ, Eggerthella, Streptococcus, and Erysipelatoclostridium, and by a decrease in Eubacterium, Dorea, Odoribacter, Intestinomonas, and Gemmiger, pointing toward a dysbiotic profile. We further investigated microbiota changes based on the severity of GI issues, seizure frequency, sleep disorders, food intake type, impairment in neuro-behavioral features and ambulation capacity. Enrichment in Lachnoclostridium and Enterobacteriaceae was observed in the microbiota of patients with more severe GI symptoms, while Clostridiaceae, Peptostreptococcaceae, Coriobacteriaceae, Erysipelotrichaceae, Christensenellaceae, and Ruminococcaceae were enriched in patients experiencing daily epileptic seizures. Our findings suggest a potential connection between CDD, microbiota and symptom severity. This study marks the first exploration of the gut-microbiota-brain axis in subjects with CDD. It adds to the growing body of research emphasizing the role of the gut microbiota in neurodevelopmental disorders and opens doors to potential interventions that target intestinal microbes with the aim of improving the lives of patients with CDD.

摘要

CDKL5 缺乏症(CDD)是一种神经发育障碍,其特征为全面发育迟缓、早发性癫痫发作、智力障碍、视力和运动损伤。与雷特综合征(RTT)不同,CDD 缺乏明确的退行期。CDD 患者常伴有胃肠道(GI)紊乱,并表现出亚临床免疫失调的迹象。然而,这些病症的根本原因仍难以捉摸。新兴研究表明,神经紊乱与肠道微生物群之间存在潜在联系,而这一领域在 CDD 中尚未得到探索。我们开展了一项开创性研究,分析了 17 名 CDD 患者及其健康亲属(n=17)的粪便微生物群组成。值得注意的是,在 CDD 患者中发现了肠道细菌多样性和组成的差异。特别是,在属水平上,CDD 微生物群落的特征是相对丰度增加了 Clostridium_AQ、Eggerthella、链球菌和 Erysipelatoclostridium,减少了 Eubacterium、Dorea、Odoribacter、Intestinomonas 和 Gemmiger,指向一种失调的特征。我们进一步根据 GI 问题的严重程度、癫痫发作频率、睡眠障碍、饮食类型、神经行为特征和步行能力受损情况,研究了微生物群的变化。在胃肠道症状更严重的患者中,观察到 Lachnoclostridium 和肠杆菌科的富集,而 Clostridiaceae、Peptostreptococcaceae、Coriobacteriaceae、Erysipelotrichaceae、Christensenellaceae 和 Ruminococcaceae 在每天癫痫发作的患者中富集。我们的发现表明 CDD、微生物群和症状严重程度之间存在潜在联系。这项研究标志着首次在 CDD 患者中探索肠道微生物群-大脑轴。它增加了越来越多的强调肠道微生物群在神经发育障碍中的作用的研究,并为针对肠道微生物的潜在干预措施开辟了道路,目的是改善 CDD 患者的生活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3422/10978852/feb43b26a4ad/41598_2024_56989_Fig1_HTML.jpg

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