Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Severity-adjusted evaluation of liver transplantation on health outcomes in urea cycle disorders

R. Posset, SF. Garbade, F. Gleich, S. Scharre, JG. Okun, AL. Gropman, SCS. Nagamani, AC. Druck, F. Epp, GF. Hoffmann, S. Kölker, M. Zielonka, Urea Cycle Disorders Consortium (UCDC), European registry and network for Intoxication type Metabolic...

. 2024 ; 26 (4) : 101039. [pub] 20231203

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc24014502

Grantová podpora
U54 HD061221 NICHD NIH HHS - United States
U54 HD090257 NICHD NIH HHS - United States
P50 HD103555 NICHD NIH HHS - United States

PURPOSE: Liver transplantation (LTx) is performed in individuals with urea cycle disorders when medical management (MM) insufficiently prevents the occurrence of hyperammonemic events. However, there is a paucity of systematic analyses on the effects of LTx on health-related outcome parameters compared to individuals with comparable severity who are medically managed. METHODS: We investigated the effects of LTx and MM on validated health-related outcome parameters, including the metabolic disease course, linear growth, and neurocognitive outcomes. Individuals were stratified into "severe" and "attenuated" categories based on the genotype-specific and validated in vitro enzyme activity. RESULTS: LTx enabled metabolic stability by prevention of further hyperammonemic events after transplantation and was associated with a more favorable growth outcome compared with individuals remaining under MM. However, neurocognitive outcome in individuals with LTx did not differ from the medically managed counterparts as reflected by the frequency of motor abnormality and cognitive standard deviation score at last observation. CONCLUSION: Whereas LTx enabled metabolic stability without further need of protein restriction or nitrogen-scavenging therapy and was associated with a more favorable growth outcome, LTx-as currently performed-was not associated with improved neurocognitive outcomes compared with long-term MM in the investigated urea cycle disorders.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc24014502
003      
CZ-PrNML
005      
20240905134242.0
007      
ta
008      
240725s2024 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.gim.2023.101039 $2 doi
035    __
$a (PubMed)38054409
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Posset, Roland $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany. Electronic address: roland.posset@med.uni-heidelberg.de
245    10
$a Severity-adjusted evaluation of liver transplantation on health outcomes in urea cycle disorders / $c R. Posset, SF. Garbade, F. Gleich, S. Scharre, JG. Okun, AL. Gropman, SCS. Nagamani, AC. Druck, F. Epp, GF. Hoffmann, S. Kölker, M. Zielonka, Urea Cycle Disorders Consortium (UCDC), European registry and network for Intoxication type Metabolic Diseases (E-IMD) Consortia Study Group
520    9_
$a PURPOSE: Liver transplantation (LTx) is performed in individuals with urea cycle disorders when medical management (MM) insufficiently prevents the occurrence of hyperammonemic events. However, there is a paucity of systematic analyses on the effects of LTx on health-related outcome parameters compared to individuals with comparable severity who are medically managed. METHODS: We investigated the effects of LTx and MM on validated health-related outcome parameters, including the metabolic disease course, linear growth, and neurocognitive outcomes. Individuals were stratified into "severe" and "attenuated" categories based on the genotype-specific and validated in vitro enzyme activity. RESULTS: LTx enabled metabolic stability by prevention of further hyperammonemic events after transplantation and was associated with a more favorable growth outcome compared with individuals remaining under MM. However, neurocognitive outcome in individuals with LTx did not differ from the medically managed counterparts as reflected by the frequency of motor abnormality and cognitive standard deviation score at last observation. CONCLUSION: Whereas LTx enabled metabolic stability without further need of protein restriction or nitrogen-scavenging therapy and was associated with a more favorable growth outcome, LTx-as currently performed-was not associated with improved neurocognitive outcomes compared with long-term MM in the investigated urea cycle disorders.
650    _2
$a lidé $7 D006801
650    12
$a transplantace jater $7 D016031
650    12
$a vrozené poruchy cyklu močoviny $x genetika $x chirurgie $7 D056806
650    _2
$a proteiny $7 D011506
650    _2
$a hodnocení výsledků zdravotní péče $7 D017063
655    _2
$a časopisecké články $7 D016428
655    _2
$a Research Support, N.I.H., Extramural $7 D052061
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Garbade, Sven F $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Gleich, Florian $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Scharre, Svenja $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Okun, Jürgen G $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Gropman, Andrea L $u Children's National Health System and The George Washington School of Medicine, Washington, DC
700    1_
$a Nagamani, Sandesh C S $u Department of Molecular and Human Genetics, Baylor College of Medicine and Texas Children's Hospital, Houston, TX
700    1_
$a Druck, Ann-Catrin $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Epp, Friederike $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Hoffmann, Georg F $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Kölker, Stefan $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany
700    1_
$a Zielonka, Matthias $u Heidelberg University, Medical Faculty Heidelberg, and Center for Pediatric and Adolescent Medicine, Department I, Division of Pediatric Neurology and Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany. Electronic address: matthias.zielonka@med.uni-heidelberg.de
710    2_
$a Urea Cycle Disorders Consortium (UCDC)
710    2_
$a European registry and network for Intoxication type Metabolic Diseases (E-IMD) Consortia Study Group
773    0_
$w MED00186213 $t Genetics in medicine $x 1530-0366 $g Roč. 26, č. 4 (2024), s. 101039
856    41
$u https://pubmed.ncbi.nlm.nih.gov/38054409 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20240725 $b ABA008
991    __
$a 20240905134236 $b ABA008
999    __
$a ok $b bmc $g 2143950 $s 1226368
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2024 $b 26 $c 4 $d 101039 $e 20231203 $i 1530-0366 $m Genetics in medicine $n Genet Med $x MED00186213
GRA    __
$a U54 HD061221 $p NICHD NIH HHS $2 United States
GRA    __
$a U54 HD090257 $p NICHD NIH HHS $2 United States
GRA    __
$a P50 HD103555 $p NICHD NIH HHS $2 United States
LZP    __
$a Pubmed-20240725

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...