Evidence map›Paper›PMID 38272482›Full record

ArticleCentral European journal of public health2023

Initial screening of the rs104893657 variant of the PAX8 gene in women with hypothyroidism from Northeastern Slovakia.

Marta Mydlárová Blaščáková, Barbora Homjáková, Melinda Nagy, Janka Poráčová, Zuzana Lörinczová, Pavol Makovický, Tatiana Kimáková, Vincent Sedlák, Mária Konečná

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Article in Central European journal of public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Marta Mydlárová BlaščákováDepartment of Biology, Faculty of Humanities and Natural Sciences, University of Presov, Presov, Slovak Republic.
Barbora HomjákováDepartment of Biology, Faculty of Humanities and Natural Sciences, University of Presov, Presov, Slovak Republic.
Melinda NagyDepartment of Biology, Faculty of Education, J. Selye University, Komarno, Slovak Republic.
Janka PoráčováDepartment of Biology, Faculty of Humanities and Natural Sciences, University of Presov, Presov, Slovak Republic.
Zuzana LörinczováAGEL Hospital Kosice-Saca, Kosice, Slovak Republic.
Pavol MakovickýDepartment of Biology, Faculty of Education, J. Selye University, Komarno, Slovak Republic.
Tatiana KimákováDepartment of Public Health and Hygiene, Faculty of Medicine, Pavol Jozef Safarik University, Kosice, Slovak Republic.
Vincent SedlákDepartment of Biology, Faculty of Humanities and Natural Sciences, University of Presov, Presov, Slovak Republic.
Mária KonečnáDepartment of Biology, Faculty of Humanities and Natural Sciences, University of Presov, Presov, Slovak Republic.
University of Prešov · SKSelye János University · SKUniversity of Pavol Jozef Šafárik · SKUniversity of Veterinary Medicine in Košice · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThyroid diseases are among the most common endocrinopathies and metabolic disorders. Hypothyroidism is caused by insufficient production of thyroid hormones with a higher prevalence in women. Causes for the development of endocrine diseases may be mutations in genes that encode peptide hormones. The aim of this scientific study was to determine the genotype and allele frequencies of the rs104893657 variant of the PAX8 gene and to determine the genotype versus phenotype association.

methodsThe study population consisted of 135 women from northeastern Slovakia who were divided on the basis of screening into two groups: a control group without diagnosed hypothyroidism (CG = 67) and a group of women with hypothyroidism (HY = 68). Biochemical markers - thyroid-stimulating hormone (TSH), prealbumin (PREA), calcium (Ca), phosphorus (P), and alkaline phosphatase (ALP) were determined using Cobas Integra 400 plus, Cobas e411 analysers (Roche). Genotyping was performed using TaqMan

resultsStudent's t-test revealed a statistically significant difference between CG and HY in biochemical parameters: TSH (p < 0.001), P (p = 0.008). By Chi-square test we found no statistically significant difference in the representation of genotypes (p = 0.788) in the rs104893657 polymorphism of PAX8 gene. The T allele was not associated with hypothyroidism in Slovak women (p = 0.548). In CC genotype we found statistically significant difference between CG and HY in parameters TSH (p < 0.001) and P (p = 0.006).

conclusionThe mutant T allele was detected at low frequency in both groups of women studied. The association of the T allele with the development of hypothyroidism in Slovak women was not confirmed. The results of this work provide initial information on the distribution of genotypes and alleles in the studied variant of PAX8 gene in the Slovak female population.

Indexed as

HypothyroidismFemaleGenotypeHumansPAX8 Transcription FactorPolymorphism, GeneticSlovakiaThyrotropinPAX8 protein, humanPAX8 Transcription FactorThyrotropinhypothyroidismmarkerPAX8 genephenotypewomen

Identifiers

PMID38272482
OpenAlexW4391235672

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