-
Something wrong with this record ?
Bactericidal permeability increasing protein gene variants in children with sepsis
J. Michálek, P. Světlíková, M. Fedora, M. Klimovič, L. Klapačová, D. Bartošová, L. Elbl, H. Hrstková, J.A. Hubáček
Language English Country United States
NLK
ProQuest Central
from 1997-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2000-01-01 to 1 year ago
Nursing & Allied Health Database (ProQuest)
from 1997-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-01-01 to 1 year ago
- MeSH
- Child MeSH
- Adult MeSH
- Financing, Organized MeSH
- Gram-Negative Bacterial Infections genetics complications mortality MeSH
- Antimicrobial Cationic Peptides genetics MeSH
- Infant MeSH
- Blood Proteins genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Membrane Proteins genetics MeSH
- Adolescent MeSH
- Infant, Newborn MeSH
- Polymorphism, Genetic MeSH
- Child, Preschool MeSH
- Prospective Studies MeSH
- Sepsis genetics complications mortality MeSH
- Severity of Illness Index MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Infant MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Female MeSH
- Geographicals
- Czech Republic MeSH
OBJECTIVE: To evaluate the role of genetic polymorphisms of the bactericidal permeability increasing protein (BPI) in pediatric patients with sepsis. DESIGN: Prospective, single-center, case-control study at the pediatric intensive care unit (PICU) of a university hospital. PATIENTS: 345 consecutive pediatric patients admitted to the PICU with fever, systemic inflammatory response syndrome (SIRS), sepsis, severe sepsis, septic shock, or multiple organ distress syndrome (MODS). INTERVENTIONS: DNA was isolated and two BPI gene polymorphisms BPI (G545 > C) Taq and BPI (A645[ > G) 216 were studied in patients and compared with healthy controls. MEASUREMENTS AND RESULTS: Genetic analysis of the BPI Taq gene revealed significant differences between healthy controls and the subgroup of febrile patients (p = 0.0243), the subgroup of SIRS and sepsis (p = 0.0101), and the subgroup of severe sepsis, septic shock, and MODS (p = 0.0027), respectively. No statistically significant differences for the BPI 216 gene polymorphism were found between patient and healthy control groups. A statistically significant predisposition to Gram-negative sepsis in patients carrying the BPI Taq GG variant together with the BPI 216 AG or GG variant was revealed (p = 0.0081), and these haplotypes were also associated with death due to sepsis-related complications. CONCLUSION: BPI Taq gene polymorphism is the accurate predictor of the severity of sepsis in children admitted to the PICU.
- 000
- 02222naa 2200577 a 4500
- 001
- bmc11003039
- 003
- CZ-PrNML
- 005
- 20121105125331.0
- 008
- 110225s2007 xxu e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Michálek, Jaroslav $7 xx0071617
- 245 10
- $a Bactericidal permeability increasing protein gene variants in children with sepsis / $c J. Michálek, P. Světlíková, M. Fedora, M. Klimovič, L. Klapačová, D. Bartošová, L. Elbl, H. Hrstková, J.A. Hubáček
- 314 __
- $a University Hospital Brno, First Department of Pediatrics, Cernopolni 9, 61300 Brno, Czech Republic. jmichalek@fnbrno.cz
- 520 9_
- $a OBJECTIVE: To evaluate the role of genetic polymorphisms of the bactericidal permeability increasing protein (BPI) in pediatric patients with sepsis. DESIGN: Prospective, single-center, case-control study at the pediatric intensive care unit (PICU) of a university hospital. PATIENTS: 345 consecutive pediatric patients admitted to the PICU with fever, systemic inflammatory response syndrome (SIRS), sepsis, severe sepsis, septic shock, or multiple organ distress syndrome (MODS). INTERVENTIONS: DNA was isolated and two BPI gene polymorphisms BPI (G545 > C) Taq and BPI (A645[ > G) 216 were studied in patients and compared with healthy controls. MEASUREMENTS AND RESULTS: Genetic analysis of the BPI Taq gene revealed significant differences between healthy controls and the subgroup of febrile patients (p = 0.0243), the subgroup of SIRS and sepsis (p = 0.0101), and the subgroup of severe sepsis, septic shock, and MODS (p = 0.0027), respectively. No statistically significant differences for the BPI 216 gene polymorphism were found between patient and healthy control groups. A statistically significant predisposition to Gram-negative sepsis in patients carrying the BPI Taq GG variant together with the BPI 216 AG or GG variant was revealed (p = 0.0081), and these haplotypes were also associated with death due to sepsis-related complications. CONCLUSION: BPI Taq gene polymorphism is the accurate predictor of the severity of sepsis in children admitted to the PICU.
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a kationické antimikrobiální peptidy $x genetika $7 D023181
- 650 _2
- $a krevní proteiny $x genetika $7 D001798
- 650 _2
- $a dítě $7 D002648
- 650 _2
- $a předškolní dítě $7 D002675
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a gramnegativní bakteriální infekce $x genetika $x komplikace $x mortalita $7 D016905
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a kojenec $7 D007223
- 650 _2
- $a novorozenec $7 D007231
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a membránové proteiny $x genetika $7 D008565
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a polymorfismus genetický $7 D011110
- 650 _2
- $a prospektivní studie $7 D011446
- 650 _2
- $a sepse $x genetika $x komplikace $x mortalita $7 D018805
- 650 _2
- $a stupeň závažnosti nemoci $7 D012720
- 650 _2
- $a financování organizované $7 D005381
- 651 _2
- $a Česká republika $7 D018153
- 700 1_
- $a Vydržalová, Petra $7 xx0105235
- 700 1_
- $a Fedora, Michal, $d 1964- $7 xx0051260
- 700 1_
- $a Klimovič, Michal, $d 1962- $7 mzk2005300713
- 700 1_
- $a Klapačová, Lenka $7 xx0127848
- 700 1_
- $a Bartošová, Drahomíra, $d 1944-2012 $7 mzk2003204103
- 700 1_
- $a Elbl, Lubomír, $d 1956- $7 nlk20000083642
- 700 1_
- $a Hrstková, Hana, $d 1944- $7 jn20000401084
- 700 1_
- $a Hubáček, Jaroslav, $d 1966- $7 nlk20050169367
- 773 0_
- $t Intensive Care Medicine $w MED00002258 $g Roč. 33, č. 12 (2007), s. 2158-2164 $x 0342-4642
- 910 __
- $a ABA008 $b x $y 1
- 990 __
- $a 20110413114050 $b ABA008
- 991 __
- $a 20121105125339 $b ABA008
- 999 __
- $a ok $b bmc $g 830437 $s 695031
- BAS __
- $a 3
- BMC __
- $a 2007 $b 33 $c 12 $d 2158-2164 $i 0342-4642 $m Intensive care medicine $n Intensive Care Med $x MED00002258
- LZP __
- $a 2011-2B/dkme