An examination of biochemical parameters and their association with response to ketogenic dietary therapies

Summary Objective In the absence of specific metabolic disorders, accurate predictors of response to ketogenic dietary therapies (KDTs) for treating epilepsy are largely unknown. We hypothesized that specific biochemical parameters would be associated with the effectiveness of KDT in humans with epi...

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Veröffentlicht in:Epilepsia (Copenhagen) 2017-05, Vol.58 (5), p.893-900
Hauptverfasser: Schoeler, Natasha E., Bell, Gail, Yuen, Alan, Kapelner, Adam D., Heales, Simon J. R., Cross, J. Helen, Sisodiya, Sanjay
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container_end_page 900
container_issue 5
container_start_page 893
container_title Epilepsia (Copenhagen)
container_volume 58
creator Schoeler, Natasha E.
Bell, Gail
Yuen, Alan
Kapelner, Adam D.
Heales, Simon J. R.
Cross, J. Helen
Sisodiya, Sanjay
description Summary Objective In the absence of specific metabolic disorders, accurate predictors of response to ketogenic dietary therapies (KDTs) for treating epilepsy are largely unknown. We hypothesized that specific biochemical parameters would be associated with the effectiveness of KDT in humans with epilepsy. The parameters tested were β‐hydroxybutyrate, acetoacetate, nonesterified fatty acids, free and acylcarnitine profile, glucose, and glucose‐ketone index (GKI). Methods Biochemical results from routine blood tests conducted at baseline prior to initiation of KDT and at 3‐month follow‐up were obtained from 13 adults and 215 children with KDT response data from participating centers. One hundred thirty‐two (57%) of 228 participants had some data at both baseline and 3 months; 52 (23%) of 228 had data only at baseline; 22 (10%) of 228 had data only at 3 months; and 22 (10%) of 228 had no data. KDT response was defined as ≥50% seizure reduction at 3‐month follow‐up. Results Acetyl carnitine at baseline was significantly higher in responders (p < 0.007). It was not associated with response at 3‐month follow‐up. There was a trend for higher levels of free carnitine and other acylcarnitine esters at baseline and at 3‐month follow‐up in KDT responders. There was also a trend for greater differences in levels of propionyl carnitine and in β‐hydroxybutyrate measured at baseline and 3‐month follow‐up in KDT responders. No other biochemical parameters were associated with response at any time point. Significance Our finding that certain carnitine fractions, in particular baseline acetyl carnitine, are positively associated with greater efficacy of KDT is consistent with the theory that alterations in energy metabolism may play a role in the mechanisms of action of KDT.
doi_str_mv 10.1111/epi.13729
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One hundred thirty‐two (57%) of 228 participants had some data at both baseline and 3 months; 52 (23%) of 228 had data only at baseline; 22 (10%) of 228 had data only at 3 months; and 22 (10%) of 228 had no data. KDT response was defined as ≥50% seizure reduction at 3‐month follow‐up. Results Acetyl carnitine at baseline was significantly higher in responders (p &lt; 0.007). It was not associated with response at 3‐month follow‐up. There was a trend for higher levels of free carnitine and other acylcarnitine esters at baseline and at 3‐month follow‐up in KDT responders. There was also a trend for greater differences in levels of propionyl carnitine and in β‐hydroxybutyrate measured at baseline and 3‐month follow‐up in KDT responders. No other biochemical parameters were associated with response at any time point. Significance Our finding that certain carnitine fractions, in particular baseline acetyl carnitine, are positively associated with greater efficacy of KDT is consistent with the theory that alterations in energy metabolism may play a role in the mechanisms of action of KDT.</description><identifier>ISSN: 0013-9580</identifier><identifier>EISSN: 1528-1167</identifier><identifier>DOI: 10.1111/epi.13729</identifier><identifier>PMID: 28369834</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Acetylcarnitine - blood ; Adolescent ; Adult ; Age Factors ; Biochemistry ; Biomarkers - blood ; Carnitine ; Child ; Child, Preschool ; Children ; Diet, Ketogenic ; Energy metabolism ; Epilepsy ; Epilepsy - blood ; Epilepsy - diet therapy ; Epilepsy - genetics ; Esters ; Fatty acids ; Female ; Follow-Up Studies ; High‐fat ; Humans ; Low‐carbohydrate ; Male ; Metabolic disorders ; Predictor ; Seizures ; Treatment Outcome ; Young Adult</subject><ispartof>Epilepsia (Copenhagen), 2017-05, Vol.58 (5), p.893-900</ispartof><rights>Wiley Periodicals, Inc. © 2017 International League Against Epilepsy</rights><rights>Wiley Periodicals, Inc. © 2017 International League Against Epilepsy.</rights><rights>Copyright © 2017 International League Against Epilepsy</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3889-2c3b27e7406cad63b5d3ee68e739074930ae20db5403935bf37b59f19d727dc43</citedby><cites>FETCH-LOGICAL-c3889-2c3b27e7406cad63b5d3ee68e739074930ae20db5403935bf37b59f19d727dc43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fepi.13729$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fepi.13729$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,1435,27931,27932,45581,45582,46416,46840</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28369834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schoeler, Natasha E.</creatorcontrib><creatorcontrib>Bell, Gail</creatorcontrib><creatorcontrib>Yuen, Alan</creatorcontrib><creatorcontrib>Kapelner, Adam D.</creatorcontrib><creatorcontrib>Heales, Simon J. R.</creatorcontrib><creatorcontrib>Cross, J. Helen</creatorcontrib><creatorcontrib>Sisodiya, Sanjay</creatorcontrib><title>An examination of biochemical parameters and their association with response to ketogenic dietary therapies</title><title>Epilepsia (Copenhagen)</title><addtitle>Epilepsia</addtitle><description>Summary Objective In the absence of specific metabolic disorders, accurate predictors of response to ketogenic dietary therapies (KDTs) for treating epilepsy are largely unknown. We hypothesized that specific biochemical parameters would be associated with the effectiveness of KDT in humans with epilepsy. The parameters tested were β‐hydroxybutyrate, acetoacetate, nonesterified fatty acids, free and acylcarnitine profile, glucose, and glucose‐ketone index (GKI). Methods Biochemical results from routine blood tests conducted at baseline prior to initiation of KDT and at 3‐month follow‐up were obtained from 13 adults and 215 children with KDT response data from participating centers. One hundred thirty‐two (57%) of 228 participants had some data at both baseline and 3 months; 52 (23%) of 228 had data only at baseline; 22 (10%) of 228 had data only at 3 months; and 22 (10%) of 228 had no data. KDT response was defined as ≥50% seizure reduction at 3‐month follow‐up. Results Acetyl carnitine at baseline was significantly higher in responders (p &lt; 0.007). It was not associated with response at 3‐month follow‐up. There was a trend for higher levels of free carnitine and other acylcarnitine esters at baseline and at 3‐month follow‐up in KDT responders. There was also a trend for greater differences in levels of propionyl carnitine and in β‐hydroxybutyrate measured at baseline and 3‐month follow‐up in KDT responders. No other biochemical parameters were associated with response at any time point. 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Helen ; Sisodiya, Sanjay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3889-2c3b27e7406cad63b5d3ee68e739074930ae20db5403935bf37b59f19d727dc43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acetylcarnitine - blood</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Biochemistry</topic><topic>Biomarkers - blood</topic><topic>Carnitine</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Diet, Ketogenic</topic><topic>Energy metabolism</topic><topic>Epilepsy</topic><topic>Epilepsy - blood</topic><topic>Epilepsy - diet therapy</topic><topic>Epilepsy - genetics</topic><topic>Esters</topic><topic>Fatty acids</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>High‐fat</topic><topic>Humans</topic><topic>Low‐carbohydrate</topic><topic>Male</topic><topic>Metabolic disorders</topic><topic>Predictor</topic><topic>Seizures</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schoeler, Natasha E.</creatorcontrib><creatorcontrib>Bell, Gail</creatorcontrib><creatorcontrib>Yuen, Alan</creatorcontrib><creatorcontrib>Kapelner, Adam D.</creatorcontrib><creatorcontrib>Heales, Simon J. R.</creatorcontrib><creatorcontrib>Cross, J. Helen</creatorcontrib><creatorcontrib>Sisodiya, Sanjay</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Epilepsia (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schoeler, Natasha E.</au><au>Bell, Gail</au><au>Yuen, Alan</au><au>Kapelner, Adam D.</au><au>Heales, Simon J. R.</au><au>Cross, J. Helen</au><au>Sisodiya, Sanjay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An examination of biochemical parameters and their association with response to ketogenic dietary therapies</atitle><jtitle>Epilepsia (Copenhagen)</jtitle><addtitle>Epilepsia</addtitle><date>2017-05</date><risdate>2017</risdate><volume>58</volume><issue>5</issue><spage>893</spage><epage>900</epage><pages>893-900</pages><issn>0013-9580</issn><eissn>1528-1167</eissn><abstract>Summary Objective In the absence of specific metabolic disorders, accurate predictors of response to ketogenic dietary therapies (KDTs) for treating epilepsy are largely unknown. We hypothesized that specific biochemical parameters would be associated with the effectiveness of KDT in humans with epilepsy. The parameters tested were β‐hydroxybutyrate, acetoacetate, nonesterified fatty acids, free and acylcarnitine profile, glucose, and glucose‐ketone index (GKI). Methods Biochemical results from routine blood tests conducted at baseline prior to initiation of KDT and at 3‐month follow‐up were obtained from 13 adults and 215 children with KDT response data from participating centers. One hundred thirty‐two (57%) of 228 participants had some data at both baseline and 3 months; 52 (23%) of 228 had data only at baseline; 22 (10%) of 228 had data only at 3 months; and 22 (10%) of 228 had no data. KDT response was defined as ≥50% seizure reduction at 3‐month follow‐up. Results Acetyl carnitine at baseline was significantly higher in responders (p &lt; 0.007). It was not associated with response at 3‐month follow‐up. There was a trend for higher levels of free carnitine and other acylcarnitine esters at baseline and at 3‐month follow‐up in KDT responders. There was also a trend for greater differences in levels of propionyl carnitine and in β‐hydroxybutyrate measured at baseline and 3‐month follow‐up in KDT responders. No other biochemical parameters were associated with response at any time point. Significance Our finding that certain carnitine fractions, in particular baseline acetyl carnitine, are positively associated with greater efficacy of KDT is consistent with the theory that alterations in energy metabolism may play a role in the mechanisms of action of KDT.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28369834</pmid><doi>10.1111/epi.13729</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Acetylcarnitine - blood
Adolescent
Adult
Age Factors
Biochemistry
Biomarkers - blood
Carnitine
Child
Child, Preschool
Children
Diet, Ketogenic
Energy metabolism
Epilepsy
Epilepsy - blood
Epilepsy - diet therapy
Epilepsy - genetics
Esters
Fatty acids
Female
Follow-Up Studies
High‐fat
Humans
Low‐carbohydrate
Male
Metabolic disorders
Predictor
Seizures
Treatment Outcome
Young Adult
title An examination of biochemical parameters and their association with response to ketogenic dietary therapies
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