Pregled bibliografske jedinice broj: 437219
K469E polymorphism of the intracellular adhesion molecule 1 gene is associated with proliferative diabetic retnopathy in Caucasians with type 2 diabetes
K469E polymorphism of the intracellular adhesion molecule 1 gene is associated with proliferative diabetic retnopathy in Caucasians with type 2 diabetes // Clinical and experimental ophthalmology, 36 (2008), 5; 468-472 doi:10.1111/j.1442-9071.2008.01785.x (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 437219 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
K469E polymorphism of the intracellular adhesion molecule 1 gene is associated with proliferative diabetic retnopathy in Caucasians with type 2 diabetes
Autori
Globočnik Petrović, Mojca ; Osredkar, Joško ; Saraga-Babić, Mirna ; Petrović, Danijel
Izvornik
Clinical and experimental ophthalmology (1442-6404) 36
(2008), 5;
468-472
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
G241A polymorphism; genetic marker; intercellular adhesion molecule 1 gene; K469E polymorphism; proliferative diabetic retinopathy
Sažetak
Background: In proliferative diabetic retinopathy (PDR) increased levels of cytokines, inflammatory cells and angiogenic factors are present. These factors increase the expression of cellular adhesion molecules (CAMs) The objective of this study was to investigate the association between the polymorphisms of the ICAM-1 gene (K469E, G241A) and the development of PDR among patients with type 2 diabetes in the Slovenian population (Caucasians). Methods: For the purpose, 195 subjects with type 2 diabetes with PDR were compared with 143 subjects with type 2 diabetes of duration of more than 10 years who had no clinical signs of diabetic retinopathy. We analysed serum ICAM levels in 54 subjects with type 2 diabetes and 25 subjects without diabetes. Results: A significantly higher frequency of the EE genotype of the K469E polymorphism of the ICAM-1 was found in the patients with PDR compared with those without diabetic retinopathy (OR = 2.0, 95% confidence interval [CI] = 1.1–3.5 ; P = 0.013), whereas the G241A polymorphism of the ICAM-1 gene failed to yield an association with PDR. Moreover, significantly higher sICAM-1 serum levels were demonstrated in diabetics with the EE genotype compared with those with the other (EK + KK) genotypes (918 ± 104 vs. 664 ± 209 µg/L ; P = 0.001). The G241A polymorphism of the ICAM-1 gene, on the other hand, failed to affect sICAM-1 serum levels in diabetics. Conclusions: We may conclude that the EE genotype of the K469E polymorphism of the ICAM-1 might be a risk factor for PDR in the Slovenian population (Caucasians) with type 2 diabetes.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
216-2160528-0507 - Genski izražaj u ranom razvoju čovjeka (Saraga-Babić, Mirna) ( CroRIS)
Ustanove:
Medicinski fakultet, Split
Profili:
Mirna Saraga-Babić
(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