AI Article Synopsis

  • Abnormal uterine bleeding (AUB) significantly impacts women's health and is associated with genetic factors; this study aimed to investigate the link between specific genes (PTGFR, MMP9, MMP2, TGFB3, and VEGFB) and AUB.
  • The study involved blood samples from 212 AUB patients and healthy controls, using qPCR analysis to evaluate gene expression across different demographic groups.
  • Results showed that gene expression was generally downregulated in AUB patients, with variations based on bleeding duration, history of miscarriage, and body weight, suggesting these genes may serve as potential biomarkers for early AUB diagnosis.

Article Abstract

Background: Abnormal uterine bleeding (AUB) is irregular menstrual bleeding which has great impact on female health and life style. Various genetic factors are involved in etiology and pathology of AUB. Present study was designed to explore the association of PTGFR, MMP9, MMP2, TGFB3 and VEGFB with AUB.

Methods: Blood samples of 212 females with AUB were collected along with age-matched healthy control. Expression variation of targeted genes was evaluated using qPCR. Present study cohort was divided into different groups based on demographic parameters and all targeted genes were correlated with study demographics.

Results: Expression of targeted genes was significantly (P < 0.001) downregulated in females with AUB compared to control. Reduced (P < 0.01) expression of targeted genes was observed in all age groups (21-30, 31-40, 41-50 year) of AUB patients compared to respective control. Expression of VEGFB increased (P < 0.05) in AUB females with > 9 days bleeding compared to AUB patient had < 9 days bleeding. AUB women with miscarriage history showed upregulation in MMP2, TGFB3 (P < 0.05), and downregulation in MMP9 and VEGFB (P < 0.05) expression compared to AUB group with no miscarriage history. Expression of MMP2 increased (P < 0.05) in AUB females with > 60 kg body weigh compared to AUB patient with < 60 kg weight.

Conclusion: Present study open a new window for diagnosis of AUB at early stages and suggested a possible involvement of PTGFR, MMP9, MMP2, TGFB3 and VEGFB as candidate biomarkers in AUB.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784108PMC
http://dx.doi.org/10.1186/s12905-022-02132-yDOI Listing

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