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Povezava genetskih polimorfizmov v dopaminergični poti s poznimi zapleti pri bolnikih s sladkorno boleznijo tipa 2
ID Bohorč, Leila (Author), ID Klen, Jasna (Mentor) More about this mentor... This link opens in a new window, ID Dolžan, Vita (Comentor)

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Abstract
Dopaminergični sistem ima pomembno vlogo v patofiziologiji sladkorne bolezni tipa 2 (SB2) in pri razvoju poznih zapletov SB2, saj uravnava fiziološke procese v trebušni slinavki, ledvicah, mrežnici in simpatičnem živčevju. Preučevali smo potencialen vpliv izbranih polimorfizmov v genih COMT, DRD1, DRD2 in DRD3 na razvoj poznih zapletov, ki se pogosto pojavljajo pri bolnikih z neurejeno SB2. V raziskavo smo vključili 344 klinično dobro opredeljenih bolnikov s SB2. Z metodo KASP smo izvedli genotipizacijo ter rezultate statistično analizirali. Statistično značilnih povezav z urejenostjo sladkorne bolezni ali krvnim tlakom nismo potrdili, kar pripisujemo majhnemu vzorcu, vplivu zdravljenja z antihipertenzivi, širšemu genetskemu ozadju in okoljskim dejavnikom. Med poznimi zapleti smo statistično značilno povezavo potrdili le za polimorfizem DRD1 rs4532 in diabetično retinopatijo, kar potrjuje ugotovitve predhodnih raziskav o vplivu sprememb aktivnosti receptorja D1 na patološke spremembe mrežnice.

Language:Slovenian
Keywords:sladkorna bolezen tipa 2, pozni zapleti, dopaminergična pot, COMT, dopaminski receptorji
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Year:2026
PID:20.500.12556/RUL-184364 This link opens in a new window
COBISS.SI-ID:286554371 This link opens in a new window
Publication date in RUL:06.07.2026
Views:179
Downloads:79
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Secondary language

Language:English
Title:Association of genetic polymorphisms in the dopaminergic pathway with late complications in patients with type 2 diabetes
Abstract:
Dopaminergic system has a major role in the pathophysiology of type 2 diabetes mellitus (T2DM) and its associated late complications by regulating physiological processes in the pancreas, kidneys, retina, and the sympathetic nervous system. We investigated the potential influence of selected COMT, DRD1, DRD2 and DRD3 polymorphisms on the development of late complications frequently observed in patients with poorly controlled T2DM. The study included a cohort of 344 clinically well-defined patients with T2DM. After statistical analysis of the results from KASP genotyping, we found no significant associations with glycemic control or blood pressure, which is likely attributable to the size of the cohort, the effects of antihypertensive therapy, as well as the broader genetic and environmental background. The key finding of this study is a statistically significant association between DRD1 rs4532 polymorphism and diabetic retinopathy. This result supports previous findings regarding the impact of altered D1 receptor activity on pathological changes in the retina. No significant associations were found for other complications.

Keywords:type 2 diabetes, late complications, dopaminergic pathway, catechol-O-methyltransferase, dopamine receptors

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