J 2023

Association between polymorphism rs2421943 of the insulin-degrading enzyme and schizophrenia: Preliminary report

AMBROZOVÁ, Laura, Tomáš ZEMAN, Vladimír JANOUT, Jana JANOUTOVÁ, Jan LOCHMAN et. al.

Základní údaje

Originální název

Association between polymorphism rs2421943 of the insulin-degrading enzyme and schizophrenia: Preliminary report

Autoři

AMBROZOVÁ, Laura (703 Slovensko, domácí), Tomáš ZEMAN (203 Česká republika, domácí), Vladimír JANOUT, Jana JANOUTOVÁ, Jan LOCHMAN (203 Česká republika, domácí) a Omar ŠERÝ (203 Česká republika, garant, domácí)

Vydání

Journal of Clinical Laboratory Analysis, Wiley, 2023, 0887-8013

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30210 Clinical neurology

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 2.700 v roce 2022

Kód RIV

RIV/00216224:14310/23:00134349

Organizační jednotka

Přírodovědecká fakulta

UT WoS

001036281600001

Klíčová slova anglicky

candidate gene analyses; genetic association study; insulin-degrading enzyme (IDE); miRNA; schizophrenic disorder; single nucleotide polymorphism (SNP)

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 3. 1. 2024 11:28, Mgr. Marie Šípková, DiS.

Anotace

V originále

Background Insulin-degrading enzyme (IDE) is an important gene in studies of the pathophysiology of type 2 diabetes mellitus (T2DM). Recent studies have suggested a possible link between type 2 diabetes mellitus (T2DM) and the pathophysiology of schizophrenia (SZ). At the same time, significant changes in insulin-degrading enzyme (IDE) gene expression have been found in the brains of people with schizophrenia. These findings highlight the need to further investigate the role of IDE in schizophrenia pathogenesis. Methods We enrolled 733 participants from the Czech Republic, including 383 patients with schizophrenia and 350 healthy controls. Our study focused on the single nucleotide polymorphism (SNP) rs2421943 in the IDE gene, which has previously been associated with the pathogenesis of Alzheimer's disease. The SNP was analyzed using the PCR-RFLP method. Results The G allele of the rs2421943 polymorphism was found to significantly increase the risk of developing SZ (p < 0.01) when a gender-based analysis showed that both AG and GG genotypes were associated with a more than 1.55 times increased risk of SZ in females (p < 0.03) but not in males. Besides, we identified a potential binding site at the G allele locus for has-miR-7110-5p, providing a potential mechanism for the observed association. Conclusion Our results confirm the role of the IDE gene in schizophrenia pathogenesis and suggest that future research should investigate the relationship between miRNA and estrogen influence on IDE expression in schizophrenia pathogenesis.

Návaznosti

GP309/09/P361, projekt VaV
Název: Vztah interakce polymorfismů kandidátních genů k patogenezi schizofrenie
Investor: Grantová agentura ČR, Vztah interakce polymorfismů kandidátních genů k patogenezi schizofrenie