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 |
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