4.6 Article

Evidence that geographic variation in genetic ancestry associates with uterine fibroids

Journal

HUMAN GENETICS
Volume 140, Issue 10, Pages 1433-1440

Publisher

SPRINGER
DOI: 10.1007/s00439-021-02322-y

Keywords

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Funding

  1. Vanderbilt CTSA grant from NCATS/NIH [ULTR000445]
  2. National Institute of Health [R01HD074711, R01HD093671, R03HD078567]
  3. National Human Genome Research Institute training grant [5T32HG008341]
  4. [K12HD04348]

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The study found that different ancestral proportions are associated with fibroid risk and traits in Black women, while protective ancestral proportions are negatively correlated with fibroid risk and traits in White women. These findings suggest that genetic differences between geographic groups contribute to racial disparities in fibroid risk and traits.
Uterine fibroids disproportionately impact Black women. Evidence suggests Black women have earlier onset and higher cumulative risk. This risk disparity may be due an imbalance of risk alleles in one parental geographic ancestry subgroup relative to others. We investigated ancestry proportions for the 1000 Genomes phase 3 populations clustered into six geographic groups for association with fibroid traits in Black women (n = 583 cases, 797 controls) and White women (n = 1195 cases, 1164 controls). Global ancestry proportions were estimated using ADMIXTURE. Dichotomous (fibroids status and multiple fibroid status) and continuous outcomes (volume and largest dimension) were modeled for association with ancestry proportions using logistic and linear regression adjusting for age. Effect estimates are reported per 10% increase in genetically inferred ancestry proportion. Among Black women, West African (WAFR) ancestry was associated with fibroid risk, East African ancestry was associated with risk of multiple fibroids, Northern European (NEUR) ancestry was protective for multiple fibroids, Southern European ancestry was protective for fibroids and multiple fibroids, and South Asian (SAS) ancestry was positively associated with volume and largest dimension. In White women, NEUR ancestry was protective for fibroids, SAS ancestry was associated with fibroid risk, and WAFR ancestry was positively associated with volume and largest dimension. These results suggest that a proportion of fibroid risk and fibroid trait racial disparities are due to genetic differences between geographic groups. Further investigation at the local ancestry and single variant levels may yield novel insights into disease architecture and genetic mechanisms underlying ethnic disparities in fibroid risk.

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