Pregled bibliografske jedinice broj: 973035
Genetic variants in the ST6GAL1 gene are associated with thyroglobulin plasma level in healthy individuals.
Genetic variants in the ST6GAL1 gene are associated with thyroglobulin plasma level in healthy individuals. // Thyroid, / (2019) doi:10.1089/thy.2018.0661 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 973035 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetic variants in the ST6GAL1 gene are associated with thyroglobulin plasma level in healthy individuals.
Autori
Matana, Antonela ; Popović, Marijana ; Boutin, Thibaud ; Torlak, Vesela ; Brdar, Dubravka ; Gunjača, Ivana ; Kolčić, Ivana ; Boraska Perica, Vesna ; Punda, Ante ; Rudan, Igor ; Polašek, Ozren ; Barbalić, Maja ; Hayward, Caroline ; Zemunik, Tatijana
Izvornik
Thyroid (1050-7256)
(2019);
0
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
genome-wide association study ; thyroglobulin ; thyroid ; ST6GAL1
Sažetak
Background: Thyroglobulin (Tg) is a 660 kDa iodoglycoprotein that serves as a precursor for thyroid hormone synthesis. Although a twin study showed that variability of serum Tg levels has a substantial genetic basis, no genome-wide association study (GWAS) of serum/plasma Tg levels has been performed to date. The aim of this study was to identify genetic variants associated with plasma Tg levels among healthy individuals. Methods: We conducted GWAS on two Croatian cohorts and performed a combined analysis. The analyses included 1094 individuals. A total of 7 597 379 variants, imputed using the 1000 Genomes reference panel, were analysed for association. GWAS was performed under an additive model, controlling for age, sex, and relatedness within each data set. Combined analysis was conducted using the inverse- variance fixed- effects method. Results: Sixteen variants located on chromosome 3, within the ST6GAL1 gene, reached genome-wide significance. The lead SNP was rs4012172 (P=1.29×〖10〗^(-10)), which explained 3.19% of the variance in Tg levels. ST6GAL1 belongs to the sialyltransferase protein family which has a fundamental role in the synthesis of specific sialylated structures on various glycoproteins, including Tg. It is known that only immature Tg (poorly sialylated or desialylated) can be transferred to the bloodstream. Conclusions: We identified a highly biologically plausible locus that could have a role in the regulation of plasma Tg levels in healthy individuals.
Izvorni jezik
Engleski
POVEZANOST RADA
Ustanove:
KBC Split,
Medicinski fakultet, Split
Profili:
Maja Barbalić
(autor)
Ivana Gunjača
(autor)
Antonela Matana
(autor)
Vesela Torlak
(autor)
Marijana Popovic
(autor)
Tatijana Zemunik
(autor)
Ozren Polašek
(autor)
Vesna Boraska Perica
(autor)
Igor Rudan
(autor)
Ivana Kolčić
(autor)
Ante Punda
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE