-
Je něco špatně v tomto záznamu ?
Circulating lipopolysaccharide-binding protein and carotid intima-media thickness in obstructive sleep apnea
I. Trojova, M. Kozarova, D. Petrasova, Z. Malachovska, I. Paranicova, P. Joppa, R. Tkacova
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- biologické markery krev MeSH
- dospělí MeSH
- endotoxemie krev diagnóza patofyziologie MeSH
- intimomediální šíře tepenné stěny * trendy MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- membránové glykoproteiny krev MeSH
- obstrukční spánková apnoe krev diagnóza patofyziologie MeSH
- polysomnografie metody trendy MeSH
- proteiny akutní fáze MeSH
- průřezové studie MeSH
- rizikové faktory MeSH
- transportní proteiny krev MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Circulating lipopolysaccharide-binding protein (LBP), a metabolic endotoxemia marker, was identified as an independent predictor of atherosclerosis. Although increases in carotid intima-media thickness (CIMT) were repeatedly reported in obstructive sleep apnea (OSA), neither the role of OSA in metabolic endotoxemia nor of LBP in early atherosclerosis were explored in patients with OSA. At a tertiary university hospital we investigated the relationships between OSA, LBP and CIMT in 117 men who underwent full polysomnography and CIMT assessment by B-mode ultrasound. Circulating LBP concentrations and average CIMT increased from patients without OSA to those with mild-moderate and severe OSA (from 32.1+/-10.3 to 32.3+/-10.9 to 38.1+/-10.3 microg.ml(-1), p=0.015; from 0.52+/-0.09 to 0.58+/-0.06 to 0.62+/-0.10 mm, p=0.004, respectively). Oxygen desaturation index (ODI) was a predictor of serum LBP levels independent of age, waist-to-hip ratio (WHR), smoking, hypertension, HDL cholesterol, triglycerides and fasting glucose [p (ANOVA)=0.002, r(2)=0.154], with no independent effect of the ODI*WHR interaction term on LBP. Furthermore, serum LBP predicted CIMT independently of known risk factors of atherosclerosis including obesity (p<0.001, r(2)=0.321). Our results suggest that OSA severity contributes to metabolic endotoxemia in patients with OSA independently of obesity, and that LBP might represent a contributing factor promoting early atherosclerosis in such patients.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18031095
- 003
- CZ-PrNML
- 005
- 20180930143821.0
- 007
- ta
- 008
- 180914s2018 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.933632 $2 doi
- 035 __
- $a (PubMed)29137477
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Trojová, Ivana. $u Department of Respiratory Medicine, P. J. Safarik University, Medical Faculty and L. Pasteur University Hospital, Kosice, Slovakia $7 xx0232068
- 245 10
- $a Circulating lipopolysaccharide-binding protein and carotid intima-media thickness in obstructive sleep apnea / $c I. Trojova, M. Kozarova, D. Petrasova, Z. Malachovska, I. Paranicova, P. Joppa, R. Tkacova
- 520 9_
- $a Circulating lipopolysaccharide-binding protein (LBP), a metabolic endotoxemia marker, was identified as an independent predictor of atherosclerosis. Although increases in carotid intima-media thickness (CIMT) were repeatedly reported in obstructive sleep apnea (OSA), neither the role of OSA in metabolic endotoxemia nor of LBP in early atherosclerosis were explored in patients with OSA. At a tertiary university hospital we investigated the relationships between OSA, LBP and CIMT in 117 men who underwent full polysomnography and CIMT assessment by B-mode ultrasound. Circulating LBP concentrations and average CIMT increased from patients without OSA to those with mild-moderate and severe OSA (from 32.1+/-10.3 to 32.3+/-10.9 to 38.1+/-10.3 microg.ml(-1), p=0.015; from 0.52+/-0.09 to 0.58+/-0.06 to 0.62+/-0.10 mm, p=0.004, respectively). Oxygen desaturation index (ODI) was a predictor of serum LBP levels independent of age, waist-to-hip ratio (WHR), smoking, hypertension, HDL cholesterol, triglycerides and fasting glucose [p (ANOVA)=0.002, r(2)=0.154], with no independent effect of the ODI*WHR interaction term on LBP. Furthermore, serum LBP predicted CIMT independently of known risk factors of atherosclerosis including obesity (p<0.001, r(2)=0.321). Our results suggest that OSA severity contributes to metabolic endotoxemia in patients with OSA independently of obesity, and that LBP might represent a contributing factor promoting early atherosclerosis in such patients.
- 650 _2
- $a proteiny akutní fáze $7 D000209
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a biologické markery $x krev $7 D015415
- 650 12
- $a intimomediální šíře tepenné stěny $x trendy $7 D059168
- 650 _2
- $a transportní proteiny $x krev $7 D002352
- 650 _2
- $a kohortové studie $7 D015331
- 650 _2
- $a průřezové studie $7 D003430
- 650 _2
- $a endotoxemie $x krev $x diagnóza $x patofyziologie $7 D019446
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a membránové glykoproteiny $x krev $7 D008562
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a polysomnografie $x metody $x trendy $7 D017286
- 650 _2
- $a rizikové faktory $7 D012307
- 650 _2
- $a obstrukční spánková apnoe $x krev $x diagnóza $x patofyziologie $7 D020181
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kozárová, Miriam $7 xx0306259 $u Fourth Department of Internal Medicine, P. J. Safarik University in Kosice, Medical Faculty and L. Pasteur University Hospital, Kosice, Slovakia
- 700 1_
- $a Petrášová, Darina $7 xx0076347 $u Laboratory of Research Biomodels, P. J. Safarik University in Kosice, Medical Faculty, Kosice, Slovakia
- 700 1_
- $a Malachovská, Zuzana $7 xx0227629 $u Fourth Department of Internal Medicine, P. J. Safarik University in Kosice, Medical Faculty and L. Pasteur University Hospital, Kosice, Slovakia
- 700 1_
- $a Paraničová, Ivana. $7 xx0232050 $u Department of Respiratory Medicine, P. J. Safarik University, Medical Faculty and L. Pasteur University Hospital, Kosice, Slovakia
- 700 1_
- $a Joppa, Pavol $7 xx0106183 $u Department of Respiratory Medicine, P. J. Safarik University, Medical Faculty and L. Pasteur University Hospital, Kosice, Slovakia
- 700 1_
- $a Tkáčová, Ružena $7 xx0052690 $u Department of Respiratory Medicine, P. J. Safarik University, Medical Faculty and L. Pasteur University Hospital, Kosice, Slovakia
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 67, č. 1 (2018), s. 69-78
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/29137477 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20180914 $b ABA008
- 991 __
- $a 20180930144304 $b ABA008
- 999 __
- $a ok $b bmc $g 1335338 $s 1028068
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 67 $c 1 $d 69-78 $e 20171110 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $b NLK118 $a Pubmed-20180914