Pregled bibliografske jedinice broj: 507769
Genetic interactions in the renin-angiotensin system confer increased risk of stroke.
Genetic interactions in the renin-angiotensin system confer increased risk of stroke. // Abstracts of the 78th European Atherosclerosis Society Congress ; U: Atherosclerosis Supplements 11 (2010) (2) 1-246.
Hamburg, Njemačka, 2010. str. 221-221 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 507769 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetic interactions in the renin-angiotensin system confer increased risk of stroke.
Autori
Bazina, Antonela ; Božina, Tamara ; Lovrić, Jasna ; Poljaković, Zdravka ; Božina, Nada ; Sertić, Jadranka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstracts of the 78th European Atherosclerosis Society Congress ; U: Atherosclerosis Supplements 11 (2010) (2) 1-246.
/ - , 2010, 221-221
Skup
78th European Atherosclerosis Society Congress
Mjesto i datum
Hamburg, Njemačka, 20.06.2010. - 23.06.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
renin-angiotensin system; stroke
Sažetak
Background: Stroke is a polygenic and multifactorial atherothrombotic disease. The renin-angiontensin system has an importan role in cerebrovascular disease through a variety of processes. The angiotensin-converting enzyme converts angiotensin I into angiotensin II, which binds the angiotensin II type-1 receptor and is a potent vasoconstrictor. Both ACE I/D and AT1R A1166C polymorphisms lead to an enhanced activity of the angiotensin II-AT1R axis, thereby possibly contributing to circulatory disturbances. The aim of our study was to investigate ACE I/D and AT1R A1166C polymorphism and the risk of stroke. Methods and materials: Clinical data and genetic and biochemical parameters of 84 patients, aged 30 to 60 years, with acute ischemic stroke were analyzed. A total of 76 controls matched for antropometric parameters, but were carotide ultrasonography alterations-free, older at lest ten years than patients and without history of stroke before age of 70 in two generations. DNA was genotyped for ACE I/D and AT1R A1166C polymorphism. Results: 51, 45 and 41 % of patients had elevated cholesterol, triglycerides and blood pressure respectively. The ACE D allele combined with the AT1R 1166C allele did not yield a risk of ischemic stroke. However, the co-occurrence of the homozygous ACE D/D and at least one AT1R 1166C allele was more frequent in the ischemic stroke group of patients under the age of forty than in the control group (22.4 vs 11%, p < 0.03, OR, 2.33 ; 95% CI, 1.46-3.7). Conclusion: ACE D/D and AT1R 1166C polymorphism could be risk factor for early occurance of stroke.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-1080134-0136 - Funkcijska genomika i proteomika rizičnih čimbenika ateroskleroze (Sertić, Jadranka, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Zdravka Poljaković
(autor)
Jasna Lovrić
(autor)
Nada Božina
(autor)
Tamara Božina
(autor)
Jadranka Sertić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE