| Naslov: | Mutations of the CYP21A2 Gene : association of p.V28IL mutation with polycystic ovarian syndrome (PCOS) |
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| Avtorji: | ID Stangler Herodež, Špela (Avtor)
ID Fijavž, Lusien (Avtor)
ID Zagradišnik, Boris (Avtor)
ID Došen, Marko (Avtor)
ID Takač, Iztok (Avtor)
ID Kokalj-Vokač, Nadja (Avtor) |
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| Datoteke: |  https://journals.um.si/index.php/amb/article/view/1578
 RAZ_Stangler_Herodez_Spela_2018.pdf (166,31 KB)
MD5: 9A85B533539EF8D73125699ADB96D3DE
https://www.dlib.si/details/URN:NBN:SI:doc-V286W9G7
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| Jezik: | Angleški jezik |
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| Vrsta gradiva: | Znanstveno delo |
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| Tipologija: | 1.01 - Izvirni znanstveni članek |
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| Organizacija: | MF - Medicinska fakulteta
UZUM - Univerzitetna založba Univerze v Mariboru
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| Opis: | Purpose: The CYP21A2 gene encodes the enzyme 21–hydroxilase, which is responsible for the production of steroids. These hormones are key mediators of sexual development and conception. Patients with 21–hydroxilase deficiency tend to be affected in different stages of life. The purpose of this study was to compare the genetic profiles of women with unexplained infertility problems with the genetic profiles of healthy controls. Furthermore, were analyzed associations between mutations of the CYP21A2 gene and various clinical and laboratory parameters.
Methods: We enrolled 300 women, diagnosed with unexplained infertility problems, into this retrospective study. For each subject, we recorded important clinical and laboratory parameters during different phases of the menstrual cycle. In the control group, we enrolled 100 samples. Each subject provided a blood sample, which was used to isolate DNA for subsequent polymerase chain reaction (PCR).
Results: In total, 11.6% of the test subjects exhibited significant hormonal deviations (HD) (estrogens and/ or progestins and/or total testosterone) and 5.3% were diagnosed with polycystic ovarian syndrome (PCOS). We identified a significant association between the p.V281L mutation and the frequency of test subjects with significant HD (x2=6.99, p=0.01). A similar association was also observed between p.V281L mutation and the frequency of test subjects with PCOS (x2=16.78, p=0.00). However, we did not establish any associations between the frequency of mutations in test subjects when compared with controls. In addition, we did not find any significance in the frequency of CYP21A2 gene mutations and any of the laboratory parameters tested. |
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| Ključne besede: | p.V281L mutation, CYP21A2 gene, polycystic ovarian syndrome, PCOS |
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| Datum objave: | 01.01.2018 |
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| Kraj izida: | Maribor |
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| Založnik: | Univerza v Mariboru, Univerzitetna založba |
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| Leto izida: | 2018 |
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| Št. strani: | 10 |
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| Številčenje: | Letn. 11, št. 2 |
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| PID: | 20.500.12556/DKUM-97108  |
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| UDK: | 618.11-006 |
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| COBISS.SI-ID: | 6554175 |
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| DOI: | 10.18690/actabiomed.169 |
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| ISSN pri članku: | 1855-5640 |
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| Datum objave v DKUM: | 18.02.2026 |
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| Število ogledov: | 187 |
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| Število prenosov: | 3 |
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| Metapodatki: |    |
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| Področja: | Ostalo
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