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Turkish Journal of Medical Sciences

Author ORCID Identifier

MERT POLAT: 0000-0002-9555-4932

FERİDE ŞAHİN: 0000-0001-7308-9673

ESRA BASKIN: 0000-0003-4361-8508

UĞUR TOPRAK: 0000-0002-2949-9189

KAAN GÜLLEROĞLU: 0000-0003-1434-3824

MEHMET HABERAL: 0000-0002-3462-7632

YUNUS TERZİ: 0000-0001-5612-9696

DOI

10.55730/1300-0144.5911

Abstract

Background/aimCongenital anomalies of the kidney and urinary tract (CAKUT) are characterized by renal developmental disorders in the embryonic period. STAT3 is a member of the STAT protein family. The members of this protein family play roles in various cellular mechanisms, such as the early stages of embryonic development, kidney development, and renal diseases. This study aims to determine the frequency of STAT3 rs1053004, rs744166, rs3816769, and rs4796793 polymorphisms in individuals with CAKUT disease.Materials and methodsTwo of the four polymorphisms, rs744166 (c.-1-13666T>C, NM_001369512.1) and rs4796793 ( c.-1915C>G, NM_001369512.1), were analyzed by a polymerase chain reaction and restriction fragment length polymorphism method (PCR-RFLP). Two other polymorphisms, rs1053004 (c.*1671C>T, NM_001369512.1) and rs3816769 (c.273+314A>G, NM_001369512.1), were analyzed by real-time PCR-melting curve analysis.ResultsOur research indicates that individuals with the TT allele for rs1053004 SNP have a 1.23 times greater risk of disease than those with the CC allele, and the CC allele for rs3816769 has a 1.41 times greater risk of disease than those with the TT allele. These findings suggest a potential genetic predisposition to CAKUT. Furthermore, our research has identified significant connections between rare haplotypes and CAKUT (p=0.041). The CCTC haplotype for rs744166, rs4796793, rs1053004, and rs3816769 polymorphism was exclusively present in the CAKUT group, while the CGTT haplotype for the same polymorphisms was solely detected in the control group.ConclusionThe presence of rare haplotypes for the rs1053004, rs3816769, rs4796793, and rs744166 polymorphisms may significantly affect the onset or prevention of CAKUT. These findings could potentially have important clinical implications, providing a deeper understanding of the genetic basis of CAKUT and potentially influencing future diagnostic and treatment strategies.

Keywords

CAKUT, Congenital anomaly, kidney, STAT3, urinary tract

First Page

1286

Last Page

1294

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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