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Oral Microbiome and Serum Metabolome Alterations in Epilepsy and after Seizure Controloral Microbiome and Serum Metabolome Alterations in Epilepsy and after Seizure Control

54 Pages Posted: 16 Aug 2022

See all articles by Zhigang Ren

Zhigang Ren

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Zhenguo Liu

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Liwen Liu

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Tianwen Wu

Zhengzhou University - Department of Neurology

Jiamin Lou

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Chao Liu

Shanghai Mobio Biomedical Technology Co., Ltd.

Yuan Chen

Zhengzhou University - Department of Neurology

Shanshuo Liu

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Haiyu Wang

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Limin Jin

Zhengzhou University - Department of Neurology

Mengfan Jiao

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Zenghan Wang

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease

Shuang Li

Zhengzhou University - Department of Neurology

Yajun Lian

Zhengzhou University - Department of Neurology

Yan Jiang

Zhengzhou University - Department of Neurology

More...

Abstract

Background: The existing diagnostic methods of epilepsy such as history collection and EEG has great limitations in practice, so more reliable and less difficult diagnostic methods are needed.

Methods: 16S rRNA sequencing was performed on 480 tongue swabs (157 EPs, 22 EPRs, and 301healthy controls (HCs)). Untargeted metabolomics analysis was performed on 432 serum samples (131 EPs, 19 EPRs, and 282 HCs).

Findings: At the genus level, Streptococcus and Leptotrichia increased in EP, though Neisseria and Schaalia decreased. In serum metabolomics, d-glutamine and d-glutamate metabolism and cutin, suberine and wax biosynthesis were altered in EP and EPR. Compared with EP, sphingolipid metabolism was enhanced in EPR. The diagnostic efficacy of oral microbial markers in training cohort and validation cohort was 98.85% and 97.23%, respectively. Importantly, the biomarker set achieved a diagnostic efficacy of 92.44% in additional independent validation sets. The diagnostic ability of the 4-metabolite model was 99.4% in the training cohort and 100% in the validation cohort.

Interpretation: In conclusion, this study describes the characterization of oral microbiome and serum metabolites in EP and EPR and demonstrates the potential of specific microbiome and metabolites as non-invasive diagnostic tools for epilepsy.

Funding Information: This study was sponsored by grants from National Key Research and Development Program of China (2018YFC2000501), National Natural Science Foundation of China (U2004121, 82070643, and U1904164), and Research Project of Jinan Microecological Biomedicine Shandong Laboratory (JNL-2022001A).

Declaration of Interests: All authors declare that they have no competing interests.

Ethics Approval Statement: This study was approved by the Institutional Review Board from the First Affiliated Hospital of Zhengzhou University (2019-039). The study was performed in accordance with the Helsinki Declaration and Rules of Good Clinical Practice. All participants signed written informed consent after the study protocol was fully explained.

Keywords: Keywords: Epilepsy, Seizure control, Oral microbiome, Serum metabolome, Diagnostic model

Suggested Citation

Ren, Zhigang and Liu, Zhenguo and Liu, Liwen and Wu, Tianwen and Lou, Jiamin and Liu, Chao and Chen, Yuan and Liu, Shanshuo and Wang, Haiyu and Jin, Limin and Jiao, Mengfan and Wang, Zenghan and Li, Shuang and Lian, Yajun and Jiang, Yan, Oral Microbiome and Serum Metabolome Alterations in Epilepsy and after Seizure Controloral Microbiome and Serum Metabolome Alterations in Epilepsy and after Seizure Control. Available at SSRN: https://ssrn.com/abstract=4191373 or http://dx.doi.org/10.2139/ssrn.4191373

Zhigang Ren (Contact Author)

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

No. 1, Jianshe East Road
Zhengzhou
China

Zhenguo Liu

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Liwen Liu

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Tianwen Wu

Zhengzhou University - Department of Neurology ( email )

Jiamin Lou

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Chao Liu

Shanghai Mobio Biomedical Technology Co., Ltd. ( email )

Yuan Chen

Zhengzhou University - Department of Neurology ( email )

Shanshuo Liu

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Haiyu Wang

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Limin Jin

Zhengzhou University - Department of Neurology ( email )

Mengfan Jiao

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Zenghan Wang

Zhengzhou University, First Affiliated Hospital, Department of Infectious Disease ( email )

Shuang Li

Zhengzhou University - Department of Neurology ( email )

Yajun Lian

Zhengzhou University - Department of Neurology ( email )

Yan Jiang

Zhengzhou University - Department of Neurology ( email )