4.5 Article

Genetic polymorphisms of Vascular Endothelial Growth Factor (VEGF) associated with endometriosis in Nigerian women

期刊

HUMAN GENOMICS
卷 15, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40246-021-00364-x

关键词

Endometriosis; Vascular endothelial growth factor; Ascites; Genetic polymorphism; Nigeria

资金

  1. National Institute of Health (NIH)/Fogarty Grant [D43TW010134]
  2. Fogarty International Centre (FIC)
  3. NIH Common Fund
  4. Office of Strategic Coordination, Office of the Director (OD/OSC/CF/NIH)
  5. Office of AIDS Research, Office of the Director (OAR/NIH)
  6. Office of Research on Women's Health
  7. Office of the Director (ORWH/NIH)
  8. National Institute on Minority Health and Health Disparities (NIMHD/NIH)
  9. National Institute of Neurological Disorders and Stroke (NINDS/NIH)

向作者/读者索取更多资源

The study aimed to investigate the association between VEGF gene polymorphisms and endometriosis in Nigerian women. Results showed no significant difference in VEGF levels between cases and controls, and the distribution of VEGF gene polymorphisms was also not significantly different between endometriosis patients and controls.
Objective To determine if genetic polymorphism of VEGF is associated with the development of endometriosis in Nigerian women. Study design Case control study of 100 women (50 healthy controls and 50 with endometriosis). Serum VEGF concentration of participants were determined using enzyme-linked immunosorbent assay (ELISA) technique. Genomic DNAs were isolated from peripheral blood samples and quantified by nanodrop spectrophotometer one. Single nucleotide polymorphisms genotyping was carried out by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP). Results Mean age of participants was 32.96 +/- 6.91 years for control and 32.04 +/- 7.56 years for cases. VEGF levels in case and control groups were not statistically different (82.68 pg/ml [69.11-121.11 pg/ml] vs. 82.81 pg/ml [72.90-113.82 pg/ml] respectively; p = 0.967). All four genotypes examined were in Hardy-Weinberg equilibrium. Minor allele frequency of - 460T > C, - 1154G > A, + 936C > T and + 2578C > A were 24%, 8%, 6% and 10% in the control and 19%, 9%, 5% and 14% in endometriosis patients. However, allele and genotype distributions of - 460T > C, - 1154G > A, + 936C > T and + 2578C > A VEGF polymorphisms in endometriosis patients and control were not significantly different (p > 0.05). Conclusion Our preliminary findings revealed no association between endometriosis and - 460T > C, - 1154G > A, + 936C > T and + 2578C > A of VEGF genes among Nigerian women.

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