Gut Bacterial Dysbiosis in Children with Intractable Epilepsy
A few published clinical studies have evaluated the association between gut microbiota in intractable epilepsy, but with inconsistent results. We hypothesized that the factors associated with the gut bacterial composition, such as age and geography, contributed to the discrepancies. Therefore, we us...
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description | A few published clinical studies have evaluated the association between gut microbiota in intractable epilepsy, but with inconsistent results. We hypothesized that the factors associated with the gut bacterial composition, such as age and geography, contributed to the discrepancies. Therefore, we used a cohort that was designed to minimize the effects of possible confounding factors and compared the gut microbiota between children with intractable epilepsy and healthy controls. Eight children with intractable epilepsy aged 1 to 7 years and 32 age-matched healthy participants were included. We collected stool samples and questionnaires on their diet and bowel habits at two time points and analyzed the gut microbiota compositions. In the epilepsy group, the amount of Bacteroidetes was lower (Mann-Whitney test, false discovery rate (FDR) < 0.01) and the amount of Actinobacteria was higher (FDR < 0.01) than in the healthy group. The epilepsy subjects were 1.6- to 1.7-fold lower in microbiota richness indices (FDR < 0.01) and harbored a distinct species composition (
< 0.01) compared to the healthy controls. Species biomarkers for intractable epilepsy included the
group,
group, and
, while the strongest functional biomarker was the ATP-binding cassette (ABC) transporter. Our study identified gut bacterial dysbiosis associated with intractable epilepsy within the cohort that was controlled for the factors that could affect the gut microbiota. |
doi_str_mv | 10.3390/jcm10010005 |
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< 0.01) compared to the healthy controls. Species biomarkers for intractable epilepsy included the
group,
group, and
, while the strongest functional biomarker was the ATP-binding cassette (ABC) transporter. Our study identified gut bacterial dysbiosis associated with intractable epilepsy within the cohort that was controlled for the factors that could affect the gut microbiota.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm10010005</identifier><identifier>PMID: 33375063</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alzheimer's disease ; Antibiotics ; Anticonvulsants ; Biomarkers ; Body mass index ; Chronic illnesses ; Clinical medicine ; Convulsions & seizures ; Discriminant analysis ; Epilepsy ; Feces ; Genes ; Microbiota ; Nervous system ; Nutrition research ; Ostomy ; Patients ; Phylogenetics ; Taxonomy</subject><ispartof>Journal of clinical medicine, 2020-12, Vol.10 (1), p.5</ispartof><rights>2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-d6e722964d957e654b585aad734bfe800385d793d223940ada18689c0cd0e15e3</citedby><cites>FETCH-LOGICAL-c409t-d6e722964d957e654b585aad734bfe800385d793d223940ada18689c0cd0e15e3</cites><orcidid>0000-0001-6449-7819 ; 0000-0001-9608-9924 ; 0000-0001-5175-0029</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792797/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792797/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33375063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Kihyun</creatorcontrib><creatorcontrib>Kim, Namil</creatorcontrib><creatorcontrib>Shim, Jung Ok</creatorcontrib><creatorcontrib>Kim, Gun-Ha</creatorcontrib><title>Gut Bacterial Dysbiosis in Children with Intractable Epilepsy</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>A few published clinical studies have evaluated the association between gut microbiota in intractable epilepsy, but with inconsistent results. We hypothesized that the factors associated with the gut bacterial composition, such as age and geography, contributed to the discrepancies. Therefore, we used a cohort that was designed to minimize the effects of possible confounding factors and compared the gut microbiota between children with intractable epilepsy and healthy controls. Eight children with intractable epilepsy aged 1 to 7 years and 32 age-matched healthy participants were included. We collected stool samples and questionnaires on their diet and bowel habits at two time points and analyzed the gut microbiota compositions. In the epilepsy group, the amount of Bacteroidetes was lower (Mann-Whitney test, false discovery rate (FDR) < 0.01) and the amount of Actinobacteria was higher (FDR < 0.01) than in the healthy group. The epilepsy subjects were 1.6- to 1.7-fold lower in microbiota richness indices (FDR < 0.01) and harbored a distinct species composition (
< 0.01) compared to the healthy controls. Species biomarkers for intractable epilepsy included the
group,
group, and
, while the strongest functional biomarker was the ATP-binding cassette (ABC) transporter. Our study identified gut bacterial dysbiosis associated with intractable epilepsy within the cohort that was controlled for the factors that could affect the gut microbiota.</description><subject>Alzheimer's disease</subject><subject>Antibiotics</subject><subject>Anticonvulsants</subject><subject>Biomarkers</subject><subject>Body mass index</subject><subject>Chronic illnesses</subject><subject>Clinical medicine</subject><subject>Convulsions & seizures</subject><subject>Discriminant analysis</subject><subject>Epilepsy</subject><subject>Feces</subject><subject>Genes</subject><subject>Microbiota</subject><subject>Nervous system</subject><subject>Nutrition research</subject><subject>Ostomy</subject><subject>Patients</subject><subject>Phylogenetics</subject><subject>Taxonomy</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkdFLwzAQxoMobsw9-S4FXwSpXpO0aR4UdM45GPiizyFtMpeRtjNplf33ZmyOKRzcwf34-O4-hM4TuCGEw-2yrBKAUJAeoT4GxmIgOTk-mHto6P0yEJDnFCfsFPUIISyFjPTR3aRro0dZttoZaaOntS9M442PTB2NFsYqp-vo27SLaFq3LnCysDoar4zVK78-Qydzab0e7voAvT-P30Yv8ex1Mh09zOKSAm9jlWmGMc-o4inTWUqLNE-lVIzQYq5zCC5TxThRGBNOQSqZ5FnOSygV6CTVZIDut7qrrqi0KvXGixUrZyrp1qKRRvzd1GYhPpovwRjHjLMgcLUTcM1np30rKuNLba2sddN5gSkL3wSe4YBe_kOXTefqcJ7AGU2AJpiTQF1vqdI13js935tJQGySEQfJBPri0P-e_c2B_AAeOofE</recordid><startdate>20201222</startdate><enddate>20201222</enddate><creator>Lee, Kihyun</creator><creator>Kim, Namil</creator><creator>Shim, Jung Ok</creator><creator>Kim, Gun-Ha</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6449-7819</orcidid><orcidid>https://orcid.org/0000-0001-9608-9924</orcidid><orcidid>https://orcid.org/0000-0001-5175-0029</orcidid></search><sort><creationdate>20201222</creationdate><title>Gut Bacterial Dysbiosis in Children with Intractable Epilepsy</title><author>Lee, Kihyun ; Kim, Namil ; Shim, Jung Ok ; Kim, Gun-Ha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-d6e722964d957e654b585aad734bfe800385d793d223940ada18689c0cd0e15e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alzheimer's disease</topic><topic>Antibiotics</topic><topic>Anticonvulsants</topic><topic>Biomarkers</topic><topic>Body mass index</topic><topic>Chronic illnesses</topic><topic>Clinical medicine</topic><topic>Convulsions & seizures</topic><topic>Discriminant analysis</topic><topic>Epilepsy</topic><topic>Feces</topic><topic>Genes</topic><topic>Microbiota</topic><topic>Nervous system</topic><topic>Nutrition research</topic><topic>Ostomy</topic><topic>Patients</topic><topic>Phylogenetics</topic><topic>Taxonomy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Kihyun</creatorcontrib><creatorcontrib>Kim, Namil</creatorcontrib><creatorcontrib>Shim, Jung Ok</creatorcontrib><creatorcontrib>Kim, Gun-Ha</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Kihyun</au><au>Kim, Namil</au><au>Shim, Jung Ok</au><au>Kim, Gun-Ha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gut Bacterial Dysbiosis in Children with Intractable Epilepsy</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2020-12-22</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>5</spage><pages>5-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>A few published clinical studies have evaluated the association between gut microbiota in intractable epilepsy, but with inconsistent results. We hypothesized that the factors associated with the gut bacterial composition, such as age and geography, contributed to the discrepancies. Therefore, we used a cohort that was designed to minimize the effects of possible confounding factors and compared the gut microbiota between children with intractable epilepsy and healthy controls. Eight children with intractable epilepsy aged 1 to 7 years and 32 age-matched healthy participants were included. We collected stool samples and questionnaires on their diet and bowel habits at two time points and analyzed the gut microbiota compositions. In the epilepsy group, the amount of Bacteroidetes was lower (Mann-Whitney test, false discovery rate (FDR) < 0.01) and the amount of Actinobacteria was higher (FDR < 0.01) than in the healthy group. The epilepsy subjects were 1.6- to 1.7-fold lower in microbiota richness indices (FDR < 0.01) and harbored a distinct species composition (
< 0.01) compared to the healthy controls. Species biomarkers for intractable epilepsy included the
group,
group, and
, while the strongest functional biomarker was the ATP-binding cassette (ABC) transporter. Our study identified gut bacterial dysbiosis associated with intractable epilepsy within the cohort that was controlled for the factors that could affect the gut microbiota.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>33375063</pmid><doi>10.3390/jcm10010005</doi><orcidid>https://orcid.org/0000-0001-6449-7819</orcidid><orcidid>https://orcid.org/0000-0001-9608-9924</orcidid><orcidid>https://orcid.org/0000-0001-5175-0029</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer's disease Antibiotics Anticonvulsants Biomarkers Body mass index Chronic illnesses Clinical medicine Convulsions & seizures Discriminant analysis Epilepsy Feces Genes Microbiota Nervous system Nutrition research Ostomy Patients Phylogenetics Taxonomy |
title | Gut Bacterial Dysbiosis in Children with Intractable Epilepsy |
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