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The association of KEAP1 and NFE2L2 polymorphisms with glycemic control and late complications in patients with type 2 diabetes
ID
Vraničar, Zala
(
Avtor
),
ID
Goričar, Katja
(
Avtor
),
ID
Blagus, Tanja
(
Avtor
),
ID
Dolžan, Vita
(
Avtor
),
ID
Klen, Jasna
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(753,66 KB)
MD5: 5EF28AFDFB56794E9086ECBD2AD530D8
URL - Izvorni URL, za dostop obiščite
https://www.sciencedirect.com/science/article/pii/S0378111925004202
Galerija slik
Izvleček
To investigate the association of KEAP1 rs1048290, rs9676881 and NFE2L2 rs6706649, rs6721961, rs35652124 polymorphisms with glycemic control and development of late complications in patients with type 2 diabetes mellitus (T2DM), a total of 316 T2DM patients were included in the retrospective genetic association study. Genotyping was performed using competitive allele-specific PCR. Data on HbA1c levels as a measure of glycemic control, and information on late complications, including ischemic heart disease, retinopathy, and nephropathy, was obtained from the medical records. Logistic regression analysis was used to assess the association between selected genetic polymorphisms and patients outcomes. Significant associations were observed between KEAP1 rs9676881 (p < 0.001) and NFE2L2 rs6721961 (p = 0.006) polymorphisms and elevated HbA1c levels. Additionally, NFE2L2 rs35652124 polymorphism was linked to a nominally higher risk of late complications, including ischemic heart disease (p = 0.036), retinopathy (p = 0.032), and nephropathy (p = 0.026). Results indicate that polymorphisms in the KEAP1 and NFE2L2 genes may influence glycemic control and the development of late complications in T2DM patients. These findings provide valuable insights into the genetic factors underlying T2DM progression and its complications in European populations, highlighting the potential role of genetic markers in optimizing personalized treatment strategies.
Jezik:
Angleški jezik
Ključne besede:
diabetes mellitus type 2
,
oxidative pathway
,
genetic polymorphism
,
microvascular complications
,
macrovascular complications
,
personalized medicine
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
BF - Biotehniška fakulteta
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2025
Št. strani:
7 str.
Številčenje:
Vol. 964, art. 149631
PID:
20.500.12556/RUL-182545
UDK:
616.3
ISSN pri članku:
1879-0038
DOI:
10.1016/j.gene.2025.149631
COBISS.SI-ID:
240248579
Datum objave v RUL:
15.05.2026
Število ogledov:
172
Število prenosov:
150
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Gene
Skrajšan naslov:
Gene
Založnik:
Elsevier
ISSN:
1879-0038
COBISS.SI-ID:
23394309
Licence
Licenca:
CC BY-NC 4.0, Creative Commons Priznanje avtorstva-Nekomercialno 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc/4.0/deed.sl
Opis:
Licenca Creative Commons, ki prepoveduje komercialno uporabo, vendar uporabniki ne rabijo upravljati materialnih avtorskih pravic na izpeljanih delih z enako licenco.
Projekti
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P3-0298
Naslov:
Geni, hormonske in osebnostne spremembe pri metabolnih motnjah
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