Pregled bibliografske jedinice broj: 1115760
A preliminary study of immunoglobulin G glycosylation in people with Down syndrome
A preliminary study of immunoglobulin G glycosylation in people with Down syndrome // Zbornik radova: 11th ISABS conference on forensic and anthropologic genetics and MAYO clinic lectures in individualized medicine
Zagreb, Hrvatska, 2019. str. x-x (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1115760 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A preliminary study of immunoglobulin G
glycosylation in people with Down syndrome
Autori
Cindrić, Ana ; Krištić, Jasminka ; Mačkić-Đurović, Mirela ; Lauc, Gordan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Zbornik radova: 11th ISABS conference on forensic and anthropologic genetics and MAYO clinic lectures in individualized medicine
/ - , 2019, X-x
Skup
Eleventh ISABS conference on forensic and anthropologic genetics and MAYO clinic lectures in individualized medicine
Mjesto i datum
Zagreb, Hrvatska, 17.06.2019. - 22.06.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
Down syndrome, immunoglobulin G, glycosylation
Sažetak
Immunoglobulin G (IgG) is among the most abundant glycoproteins in human serum and is also a very important effector molecule of the immune system. The composition of glycans bound to IgG is crucial for its structure and function. Changes in IgG glycosylation are correlated to age and to various diseases. An important symptom of trisomy 21, also known as Down syndrome (DS), are premature signs of aging, which have many notable consequences for the entire organism, especially for the central nervous system and for the immune system. The goal of this preliminary research was to determine whether people with DS show a different IgG glycan composition to their healthy peers and, if so, using IgG glycans as biomarkers of age, to see if these changes are connected to premature aging. The comparison of glycosylation profiles of 13 people with DS and their healthy peers using ultra performance liquid chromatography (UPLC) revealed that there are significant differences in the percentage of certain IgG glycans in DS compared to healthy controls. It was also established that the observed differences in IgG glycan percentages reflect the presence of premature aging in people with DS. Conclusively, in order to see the full effect of DS on IgG glycosylation, more extensive research is needed. This research would be done on larger DS cohorts consisting of individuals with characterized symptoms, so the onset and severity of specific symptoms could be correlated to IgG glycosylation. As a result, IgG glycans may potentially find a use in clinical prognostics for DS.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
GENOS d.o.o.