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Assessing the relationship between single nucleotide polymorphisms in Wingless signaling pathway genes and sella turcica morphology.

Authors :
Brancher, João Armando
Schuh, Rodrigo
Torres, Maria Fernanda Pioli
de Melo Teixeira do Brasil, Jordanna
Hueb, Maria Angélica
dos Santos Haemmerle, Carlos Alexandre
Proff, Peter
Alam, Mohammad Khursheed
Kirschneck, Christian
Küchler, Erika Calvano
Source :
Journal of Anatomy; Jul2023, Vol. 243 Issue 1, p167-173, 7p
Publication Year :
2023

Abstract

Sella turcica development involves molecular factors and genes responsible for ossification. It is possible that single nucleotide polymorphisms (SNPs) in key genes are involved in morphological variation of sella turcica. Genes belonging to the WNT signaling pathway are involved in the ossification process and are candidates of sella turcica morphology. This study aimed to evaluate if SNPs in WNT6 (rs6754599) and WNT10A (rs10177996 and rs3806557) genes are associated with the calcification and patterns of the sella turcica. Nonsyndromic individuals were included in the research. Cephalometric radiographs were examined and the sella calcification was evaluated and classified according to the calcification of the interclinoid ligament (no calcification, partial calcification, and incomplete calcification) and sella turcica pattern (normal sella turcica, bridge type A—ribbon‐like fusion, bridge type B—extension of the clinoid processes, incomplete bridge, hypertrophic posterior clinoid process, hypotrophic posterior clinoid process, irregularity in the posterior part, pyramidal shape of the dorsum, double contour of the floor, oblique anterior wall, and oblique contour of the floor). DNA samples were used to evaluate SNPs in the WNT genes (rs6754599, rs10177996, and rs3806557) using real‐time PCR. Chi‐square test or Fisher's exact test were used to compare the allele and genotype distributions according to sella turcica phenotypes. The alpha was set as 5% for all comparisons. A total of 169 individuals were included, 133 (78.7%) present sella turcica partially or completely calcified. Sella turcica anomalies were found in 131 individuals (77.5%). Sella turcica bridge type A (27.8%), posterior hypertrophic clinoid process (17.1%), and sella turcica bridge type B (11.2%) were the most prevalent morphological patterns observed. Individuals carrying the TT genotype in rs10177996 (TT vs. CT + CC) had higher chance to present a partially calcified sella turcica (p = 0.047; Odds ratio = 2.27, Confidence Interval 95% 1.01–5.13). In conclusion, the SNP in WNT10A is associated with the calcification phenotype of the sella turcica, the pleiotropic effect of this gene should be taken into consideration in future studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00218782
Volume :
243
Issue :
1
Database :
Complementary Index
Journal :
Journal of Anatomy
Publication Type :
Academic Journal
Accession number :
164370096
Full Text :
https://doi.org/10.1111/joa.13855