Samenvatting
In a previous study it was shown that lower factor XI (FXI) levels in women with heavy menstrual bleeding (HMB). Our aim was to determine the single-nucleotide variants (SNVs) in the F11 gene in women with HMB. In addition, an extensive literature search was performed to determine the clinical significance of each SNV. Patients referred for HMB (PBAC-score >100) were included. With direct sequencing analysis of all 15 exons and flanking introns of the F11 gene, 29 different non-structural SNVs were detected in 49 patients with HMB. Interestingly, most of these SNVs have previously been associated with venous thrombosis instead of bleeding. These findings have not helped to elucidate the molecular basis of HMB. They also question the specificity of previously reported F11 variations in patients with thrombosis. More studies are needed to explain the lower FXI levels seen in patients with HMB.
Originele taal-2 | English |
---|---|
Pagina's (van-tot) | 912-918 |
Aantal pagina's | 7 |
Tijdschrift | Journal of obstetrics and gynaecology |
Volume | 37 |
Nummer van het tijdschrift | 7 |
DOI's | |
Status | Published - 2017 |
Vingerafdruk
Duik in de onderzoeksthema's van 'Factor 11 single-nucleotide variants in women with heavy menstrual bleeding'. Samen vormen ze een unieke vingerafdruk.Datasets
-
Factor 11 single-nucleotide variants in women with heavy menstrual bleeding
Wiewel - Verschueren, S. (Creator), Mulder, A. B. (Creator), Meijer, K. (Creator) & Mulder, R. (Creator), figshare, 2017
DOI: 10.6084/m9.figshare.5104897
Dataset
-
Factor 11 single-nucleotide variants in women with heavy menstrual bleeding
Wiewel-Verschueren, S. (Contributor), Mulder, A. B. (Contributor), Meijer, K. (Contributor) & Mulder, R. (Contributor), University of Groningen, 13-jun.-2017
DOI: 10.6084/m9.figshare.5104897.v1
Dataset