Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events

Beginning in 2006, the Urea Cycle Disorders Consortium (UCDC) has conducted a longitudinal study of eight inherited deficiencies of enzymes and transporters of the urea cycle, including 444 individuals with ornithine transcarbamylase deficiency (OTCD), of whom 300 (67 males, 233 females) received ps...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Bürger, Corinna (VerfasserIn) , Garbade, Sven (VerfasserIn) , Kölker, Stefan (VerfasserIn) , Burgard, Peter (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2019
In: Journal of inherited metabolic disease
Year: 2018, Jahrgang: 42, Heft: 2, Pages: 243-253
ISSN:1573-2665
DOI:10.1002/jimd.12013
Online-Zugang:Verlag, Volltext: https://doi.org/10.1002/jimd.12013
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/jimd.12013
Volltext
Verfasserangaben:Corinna Buerger, Sven F. Garbade, Fabienne Dietrich Alber, Susan E. Waisbren, Robert McCarter, Stefan Kölker, Peter Burgard, on behalf of the Urea Cycle Disorders Consortium

MARC

LEADER 00000caa a2200000 c 4500
001 1665030771
003 DE-627
005 20230426130914.0
007 cr uuu---uuuuu
008 190509r20192018xx |||||o 00| ||eng c
024 7 |a 10.1002/jimd.12013  |2 doi 
035 |a (DE-627)1665030771 
035 |a (DE-599)KXP1665030771 
035 |a (OCoLC)1341212464 
040 |a DE-627  |b ger  |c DE-627  |e rda 
041 |a eng 
084 |a 33  |2 sdnb 
100 1 |a Bürger, Corinna  |d 1983-  |e VerfasserIn  |0 (DE-588)1050013832  |0 (DE-627)783136692  |0 (DE-576)404276237  |4 aut 
245 1 0 |a Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events  |c Corinna Buerger, Sven F. Garbade, Fabienne Dietrich Alber, Susan E. Waisbren, Robert McCarter, Stefan Kölker, Peter Burgard, on behalf of the Urea Cycle Disorders Consortium 
264 1 |c 2019 
300 |a 11 
336 |a Text  |b txt  |2 rdacontent 
337 |a Computermedien  |b c  |2 rdamedia 
338 |a Online-Ressource  |b cr  |2 rdacarrier 
500 |a First published: 27 December 2018 
500 |a Gesehen am 09.05.2019 
520 |a Beginning in 2006, the Urea Cycle Disorders Consortium (UCDC) has conducted a longitudinal study of eight inherited deficiencies of enzymes and transporters of the urea cycle, including 444 individuals with ornithine transcarbamylase deficiency (OTCD), of whom 300 (67 males, 233 females) received psychological evaluation. In a cross-sectional study (age range, 3-71 years), analysis of covariance (ANCOVA) determined the association between outcomes in five cognitive domains (global intelligence, executive functions, memory, visuomotor integration, visual perception) and sex, age at testing and timing of disease onset defined as early onset (≤28 days; EO), late onset (LO), or asymptomatic (AS). The dataset of 183 subjects with complete datasets (31 males, 152 females) revealed underrepresentation of EO subjects (2 males, 4 females), who were excluded from the ANCOVA. Although mean scores of LO and AS individuals were within 1 SD of the population norm, AS subjects attained significantly higher scores than LO subjects and males higher scores than females. Correlations between cognitive domains were high, particularly intelligence proved to be a distinguished indicator for cognitive functioning. Maximum plasma ammonium concentration and intelligence correlated significantly higher in EO (r = −0.47) than in LO subjects (r = 0.04). Correlation between the number of hyperammonemic events and intelligence scores were similar for EO (r = −0.30) and LO (r = −0.26) individuals. The number of clinical symptoms was significantly associated with intelligence (r = −0.28) but not with scores in other domains. Results suggest that OTCD has a global impact on cognitive functioning rather than a specific effect on distinct cognitive domains. 
534 |c 2018 
650 4 |a cognitive outcome 
650 4 |a ornithine transcarbamylase deficiency 
650 4 |a urea cycle disorders 
700 1 |a Garbade, Sven  |d 1971-  |e VerfasserIn  |0 (DE-588)129234362  |0 (DE-627)707186889  |0 (DE-576)297554263  |4 aut 
700 1 |a Kölker, Stefan  |e VerfasserIn  |0 (DE-588)1022937758  |0 (DE-627)717335771  |0 (DE-576)366197568  |4 aut 
700 1 |a Burgard, Peter  |e VerfasserIn  |0 (DE-588)1050864808  |0 (DE-627)785218416  |0 (DE-576)160485630  |4 aut 
773 0 8 |i Enthalten in  |t Journal of inherited metabolic disease  |d Hoboken, NJ : Wiley, 1978  |g 42(2019), 2, Seite 243-253  |h Online-Ressource  |w (DE-627)320457753  |w (DE-600)2006875-X  |w (DE-576)105704652  |x 1573-2665  |7 nnas  |a Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events 
773 1 8 |g volume:42  |g year:2019  |g number:2  |g pages:243-253  |g extent:11  |a Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events 
856 4 0 |u https://doi.org/10.1002/jimd.12013  |x Verlag  |x Resolving-System  |3 Volltext 
856 4 0 |u https://onlinelibrary.wiley.com/doi/abs/10.1002/jimd.12013  |x Verlag  |3 Volltext 
951 |a AR 
992 |a 20190509 
993 |a Article 
994 |a 2019 
998 |g 1050864808  |a Burgard, Peter  |m 1050864808:Burgard, Peter  |d 910000  |d 910500  |e 910000PB1050864808  |e 910500PB1050864808  |k 0/910000/  |k 1/910000/910500/  |p 7  |y j 
998 |g 1022937758  |a Kölker, Stefan  |m 1022937758:Kölker, Stefan  |d 910000  |d 910500  |e 910000PK1022937758  |e 910500PK1022937758  |k 0/910000/  |k 1/910000/910500/  |p 6 
998 |g 1050013832  |a Bürger, Corinna  |m 1050013832:Bürger, Corinna  |d 910000  |d 910500  |e 910000PB1050013832  |e 910500PB1050013832  |k 0/910000/  |k 1/910000/910500/  |p 1  |x j 
998 |g 129234362  |a Garbade, Sven  |m 129234362:Garbade, Sven  |d 910000  |d 910500  |e 910000PG129234362  |e 910500PG129234362  |k 0/910000/  |k 1/910000/910500/  |p 2 
999 |a KXP-PPN1665030771  |e 3472334835 
BIB |a Y 
SER |a journal 
JSO |a {"type":{"media":"Online-Ressource","bibl":"article-journal"},"relHost":[{"id":{"eki":["320457753"],"doi":["10.1002/(ISSN)1573-2665"],"issn":["1573-2665"],"zdb":["2006875-X"]},"physDesc":[{"extent":"Online-Ressource"}],"title":[{"title":"Journal of inherited metabolic disease","title_sort":"Journal of inherited metabolic disease","subtitle":"JIMD ; official journal of the Society for the Study of Inborn Errors of Metabolism"}],"type":{"bibl":"periodical","media":"Online-Ressource"},"part":{"extent":"11","volume":"42","text":"42(2019), 2, Seite 243-253","year":"2019","pages":"243-253","issue":"2"},"disp":"Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic eventsJournal of inherited metabolic disease","titleAlt":[{"title":"JIMD"}],"pubHistory":["1.1978 -"],"note":["Gesehen am 11.03.20","Ungezählte Beil.: Suppl"],"language":["eng"],"recId":"320457753","origin":[{"publisherPlace":"Hoboken, NJ ; Dordrecht [u.a.] ; Dordrecht [u.a.]","publisher":"Wiley ; Kluwer ; Springer Science + Business Media B.V","dateIssuedDisp":"1978-","dateIssuedKey":"1978"}]}],"title":[{"title_sort":"Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events","title":"Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events"}],"physDesc":[{"extent":"11 S."}],"id":{"eki":["1665030771"],"doi":["10.1002/jimd.12013"]},"person":[{"family":"Bürger","display":"Bürger, Corinna","role":"aut","given":"Corinna"},{"family":"Garbade","display":"Garbade, Sven","role":"aut","given":"Sven"},{"role":"aut","given":"Stefan","family":"Kölker","display":"Kölker, Stefan"},{"role":"aut","given":"Peter","family":"Burgard","display":"Burgard, Peter"}],"name":{"displayForm":["Corinna Buerger, Sven F. Garbade, Fabienne Dietrich Alber, Susan E. Waisbren, Robert McCarter, Stefan Kölker, Peter Burgard, on behalf of the Urea Cycle Disorders Consortium"]},"origin":[{"dateIssuedKey":"2019","dateIssuedDisp":"2019"}],"language":["eng"],"note":["First published: 27 December 2018","Gesehen am 09.05.2019"],"recId":"1665030771"} 
SRT |a BUERGERCORIMPAIRMENT2019