J 2024

Serum autoantibodies against hexokinase 1 manifest secondary to diabetic macular edema onset

ŠIMČÍKOVÁ, Daniela, Jana IVANČINOVÁ, Miroslav VEITH, Jaroslava DUSOVÁ, Veronika MATUŠKOVÁ et. al.

Základní údaje

Originální název

Serum autoantibodies against hexokinase 1 manifest secondary to diabetic macular edema onset

Autoři

ŠIMČÍKOVÁ, Daniela (203 Česká republika), Jana IVANČINOVÁ (203 Česká republika), Miroslav VEITH (203 Česká republika), Jaroslava DUSOVÁ (203 Česká republika), Veronika MATUŠKOVÁ (203 Česká republika, domácí), Jan NĚMČANSKÝ (203 Česká republika), Přemysl KUNČICKÝ (203 Česká republika), Oldřich CHRAPEK (203 Česká republika, domácí), Naďa JIRÁSKOVÁ (203 Česká republika), Jan GOJDA (203 Česká republika) a Petr HENEBERG (203 Česká republika)

Vydání

Diabetes Research and Clinical Practice, CLARE, ELSEVIER IRELAND LTD, 2024, 0168-8227

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30207 Ophthalmology

Stát vydavatele

Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 5.100 v roce 2022

Organizační jednotka

Lékařská fakulta

UT WoS

001263613100001

Klíčová slova anglicky

Autoimmunity; Glycolysis; Disease marker; Disease prediction; Tissue damage; Vitreous fluid

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 5. 8. 2024 13:37, Mgr. Tereza Miškechová

Anotace

V originále

Aims Autoantibodies against hexokinase 1 (HK1) were recently proposed to be associated with diabetic macular edema (DME). We hypothesized that anti-HK1 autoantibodies can be used as DME markers and to predict DME onset. Materials and methods Serum from patients with 1) DME, 2) diabetes mellitus (DM), 3) allergies or autoimmunities, and 4) control subjects was tested for anti-HK1 and anti-hexokinase 2 (HK2) autoantibodies by immunoblotting. Patients with DM were prospectively followed for up to nine years, and the association of anti-HK1 antibodies with new-onset DME was evaluated. The vitreous humor was also tested for autoantibodies. Results Among patients with DME, 32 % were positive for anti-HK1 autoantibodies (42 % of those with underlying type 1 DM and 31 % of those with underlying type 2 DM), and 12 % were positive for anti-HK2 autoantibodies, with only partial overlap of these two groups of patients. Anti-HK1 positive were also 7 % of patients with DM, 6 % of patients with allergies and autoimmunities, and 3 % of control subjects. The latter three groups were anti-HK2 negative. Only one of seven patients with DM who were initially anti-HK1 positive developed DME. Conclusions Anti-HK1 autoantibodies can be used as DME markers but fail to predict DME onset.