-
Something wrong with this record ?
Transcriptional activity of tumour necrosis factor α (TNF-α) in patients with subclinical coronary atherosclerosis - preliminary results
J. Dabek, R. Swiderski, J. Głogowska-Ligus, P. Pysz
Language English Country Czech Republic
Document type Journal Article
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
ProQuest Central
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
- MeSH
- Adult MeSH
- Genetic Predisposition to Disease MeSH
- Transcription, Genetic * MeSH
- Coronary Vessels metabolism pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Coronary Artery Disease genetics MeSH
- Receptors, Tumor Necrosis Factor, Type I genetics metabolism MeSH
- Receptors, Tumor Necrosis Factor, Type II genetics metabolism MeSH
- Gene Expression Regulation MeSH
- Risk Factors MeSH
- Aged MeSH
- Tumor Necrosis Factor-alpha genetics MeSH
- Calcium metabolism MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
The most frequent cause of ischaemic heart disease is coronary arteriosclerosis. This study was aimed at assessing gene expression of TNFA and its two receptors (TNFR1, TNFR2), as well as determining coronary artery calcium score (CACS) in the context of occurrence of classical risk factors in patients with subclinical atherosclerosis of coronary vessels. The study involved 47 subjects with complaints of chest pain and suspicion of acute coronary syndrome or stable coronary disease. Additionally, CACS was assessed by 64-slice computerized tomography. QRT-PCR molecular studies were performed using RNA isolated from peripheral blood mononuclear cells. Preliminary results of molecular studies on patients with subclinical coronary atherosclerosis revealed a significantly lower numbers of TNFR1 and TNFR2 gene copies as compared with healthy subjects. In addition, it can be demonstrated that among classical risk factors hypertension is of substantial importance in the progression of coronary arteries' calcification, and that in the examined group CACS increases together with the rising number of classical risk factors involved. No correlation was observed, however, between expression of TNFA, TNFR1 and TNFR2 genes and the value of CACS. Conclusions: 1. The occurrence of hypertension facilitates initiation and progression of arteriosclerotic lesions in blood vessels including the coronary ones; the raised number of circulatory disease classical risk factors involved correlates with elevated calcification of coronary arteries as shown by 64-slice computerized tomography scans. 2. Significantly decreased numbers of TNFR1 and TNFR2 gene copies observed in the investigated group may play a significant role in initiation and progression of arteriosclerosis.
Department of Cardiology Medical University of Silesia in Katowice Poland
Department of Epidemiology Medical University of Silesia in Katowice Poland
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13033280
- 003
- CZ-PrNML
- 005
- 20131106152510.0
- 007
- ta
- 008
- 131015s2012 xr d f 000 0|eng||
- 009
- AR
- 035 __
- $a (PubMed)23249640
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Dabek, J. $u Department of Cardiology, Medical University of Silesia in Katowice, Poland
- 245 10
- $a Transcriptional activity of tumour necrosis factor α (TNF-α) in patients with subclinical coronary atherosclerosis - preliminary results / $c J. Dabek, R. Swiderski, J. Głogowska-Ligus, P. Pysz
- 520 9_
- $a The most frequent cause of ischaemic heart disease is coronary arteriosclerosis. This study was aimed at assessing gene expression of TNFA and its two receptors (TNFR1, TNFR2), as well as determining coronary artery calcium score (CACS) in the context of occurrence of classical risk factors in patients with subclinical atherosclerosis of coronary vessels. The study involved 47 subjects with complaints of chest pain and suspicion of acute coronary syndrome or stable coronary disease. Additionally, CACS was assessed by 64-slice computerized tomography. QRT-PCR molecular studies were performed using RNA isolated from peripheral blood mononuclear cells. Preliminary results of molecular studies on patients with subclinical coronary atherosclerosis revealed a significantly lower numbers of TNFR1 and TNFR2 gene copies as compared with healthy subjects. In addition, it can be demonstrated that among classical risk factors hypertension is of substantial importance in the progression of coronary arteries' calcification, and that in the examined group CACS increases together with the rising number of classical risk factors involved. No correlation was observed, however, between expression of TNFA, TNFR1 and TNFR2 genes and the value of CACS. Conclusions: 1. The occurrence of hypertension facilitates initiation and progression of arteriosclerotic lesions in blood vessels including the coronary ones; the raised number of circulatory disease classical risk factors involved correlates with elevated calcification of coronary arteries as shown by 64-slice computerized tomography scans. 2. Significantly decreased numbers of TNFR1 and TNFR2 gene copies observed in the investigated group may play a significant role in initiation and progression of arteriosclerosis.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a vápník $x metabolismus $7 D002118
- 650 _2
- $a nemoci koronárních tepen $x genetika $7 D003324
- 650 _2
- $a koronární cévy $x metabolismus $x patologie $7 D003331
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a regulace genové exprese $7 D005786
- 650 _2
- $a genetická predispozice k nemoci $7 D020022
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a receptory TNF - typ I $x genetika $x metabolismus $7 D047888
- 650 _2
- $a receptory TNF - typ II $x genetika $x metabolismus $7 D047889
- 650 _2
- $a rizikové faktory $7 D012307
- 650 12
- $a genetická transkripce $7 D014158
- 650 _2
- $a TNF-alfa $x genetika $7 D014409
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Swiderski, R. $u Department of Cardiology, Medical University of Silesia in Katowice, Poland
- 700 1_
- $a Głogowska-Ligus, J. $u Department of Epidemiology, Medical University of Silesia in Katowice, Poland
- 700 1_
- $a Pysz, P. $u Department of Cardiology, Medical University of Silesia in Katowice, Poland
- 773 0_
- $w MED00011004 $t Folia biologica $x 0015-5500 $g Roč. 58, č. 5 (2012), s. 209-214
- 856 41
- $u https://fb.cuni.cz/file/5658/FB2012A0031.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 970 $c 89 $y 4 $z 0
- 990 __
- $a 20131015 $b ABA008
- 991 __
- $a 20131106101957 $b ABA008
- 999 __
- $a ok $b bmc $g 999614 $s 831734
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 58 $c 5 $d 209-214 $i 0015-5500 $m Folia biologica (Praha) $n Folia biol. (Praha) $x MED00011004
- LZP __
- $b NLK138 $a Pubmed-20131015