Evidence map›Paper›PMID 38548767›Full record

ArticleScientific reports2024

Gut microbiota profile in CDKL5 deficiency disorder patients.

Elisa Borghi, Ornella Xynomilakis, Emerenziana Ottaviano, Camilla Ceccarani, Ilaria Viganò, Paola Tognini, Aglaia Vignoli

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06448663 (Targeting the Gut to Improve Seizure Control in CDD), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06448663 naunknown statusnot on this map

Targeting the Gut to Improve Seizure Control in CDD

TypeinterventionalSponsorUniversity of MilanRan2024 to 2025Enrolled20ConditionsCDKL5Armsalpha-lactalbumin, fructooligosaccharides, inulin, alpha-lactalbumin, sodium butyrate, fructooligosaccharides, inulin
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 1 country.

Elisa BorghiDepartment of Health Sciences, Università Degli Studi di Milano, Milan, Italy.
Ornella XynomilakisDepartment of Health Sciences, Università Degli Studi di Milano, Milan, Italy.
Emerenziana OttavianoDepartment of Health Sciences, Università Degli Studi di Milano, Milan, Italy.
Camilla CeccaraniInstitute of Biomedical Technologies, National Research Council, Segrate, Milan, Italy.
Ilaria ViganòEpilepsy Center-Child Neuropsychiatric Unit, ASST Santi Paolo e Carlo, Milan, Italy.
Paola TogniniDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy. paola.tognini@santannapisa.it.
Aglaia VignoliDepartment of Health Sciences, Università Degli Studi di Milano, Milan, Italy.
University of Milan · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITAzienda Socio Sanitaria Territoriale Santi Paolo e CarloNational Research Council · ITScuola Superiore Sant'Anna · ITUniversity of Pisa · IT

Funding

Fondazione Telethon GSP21001Ministero dell'Università e della Ricerca PNRR YOUNG MSCA_0000081
6 · The paper itself

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.

Indexed as

Epileptic SyndromesGastrointestinal MicrobiomeRett SyndromeSpasms, InfantileHumansProtein Serine-Threonine KinasesSeizuresCDKL5 protein, humanProtein Serine-Threonine KinasesCDKL5 deficiency disorderGastrointestinal disturbancesGut-brain-axisGut microbiota

Identifiers

PMID38548767
PMCPMC10978852
OpenAlexW4393260467

What Socratic holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.