Evidence map›Paper›PMID 42078903›Full record

ArticleResearch square2026

Phenome-wide association study of uterine fibroid subtypes reveals symptoms of fibroid severity and subtype-specific comorbidities.

Digna Velez Edwards, Jeewoo Kim, Elizabeth Jasper, Sarah Jones, Todd Edwards, Jacklyn Hellwege

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In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Digna Velez EdwardsVanderbilt University Medical Center.ORCID 0000-0001-5293-0056
Jeewoo KimVanderbilt University Medical Center.
Elizabeth JasperVanderbilt University.
Sarah JonesVanderbilt University Medical Center.
Todd EdwardsDepartment of Veterans Affairs.ORCID 0000-0003-4318-6119
Jacklyn HellwegeVanderbilt University Medical Center.ORCID 0000-0001-7479-0920

Funding

Building Interdisciplinary Research Careers in Women's HealthK12HD043483 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARTMANN, KATHERINE E, MAJOR, AMY S · 2002 to 2023
$10.3M
NRSA Training CoreTL1TR002244 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Julie A. Bastarache · 2017 to 2026
$4.6M
Large-scale studies in eMERGE to discover the genetic determinants of uterine fibroidsR01HD093671 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI EDWARDS, TODD L, VELEZ EDWARDS, DIGNA R · 2017 to 2021
$3.3M
Training Program on Genetic Variation and Human PhenotypesT32GM080178 · NIGMS · VANDERBILT UNIVERSITY · PI COX, NANCY J, SAMUELS, DAVID C · 2007 to 2021
$3.1M
Understanding the genetic risk underlying racial disparities in uterine fibroids - Diversity SupplementR01HD074711 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI VELEZ EDWARDS, DIGNA R · 2013 to 2017
$2.9M
Evaluating the impact of altered gene expression on uterine fibroid risk in African ancestry populationsR01HD112169 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Todd L Edwards, Digna R Velez Edwards · 2024 to 2026
$2.1M
Building Interdisciplinary Research Careers in Women's HealthK12AR084232 · NIAMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI AMY S MAJOR, Digna R Velez Edwards · 2023 to 2026
$1.3M
Transdisciplinary approaches for maternal-child health: a focus on gestational weight gainK01DK140644 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Elizabeth A Jasper · 2025 to 2026
$285k
Using the Exome to Discover Genetic Determinants of Fibroids in African AmericansR03HD078567 · NICHD · VANDERBILT UNIVERSITY · PI VELEZ EDWARDS, DIGNA R · 2014 to 2015
$155k
NCATS NIH HHS TL1 TR002244NIAMS NIH HHS K12 AR084232NICHD NIH HHS K12 HD043483NICHD NIH HHS R01 HD074711NICHD NIH HHS R01 HD093671NICHD NIH HHS R01 HD112169NICHD NIH HHS R03 HD078567NIDDK NIH HHS K01 DK140644NIGMS NIH HHS T32 GM080178
6 · The paper itself

Abstract

Background: Uterine leiomyomata (or fibroids) are common benign tumors of the uterus. Fibroids are classified into subtypes by location: submucosal, intramural, subserosal. Although the symptomology and comorbidities associated with fibroids have been extensively assessed, there is less knowledge regarding factors associated with fibroid subtypes. We tested the associations between fibroid subtypes and a broad range of clinical diagnoses to characterize their shared and unique comorbidity profiles. Methods: Using billing codes and clinical note text from the Vanderbilt University Medical Center's electronic health record (EHR) system, we identified individuals with three common fibroid subtypes (cases/controls): submucosal (2,445/28,746), intramural (4,877/20,315), subserosal (3,472/24,447). Using multivariate logistic regression, we performed a phenome-wide association study (PheWAS) for each subtype with over 1,800 constructed clinical diagnoses (phecodes) as predictors. Results: We identified 149 significant phecode associations with submucosal fibroids, 218 with intramural fibroids, and 178 with subserosal fibroids. The most significant submucosal fibroid associations were "disorders of menstruation" (odds ratio [OR][95% Confidence Interval] = 5.35[4.79-5.97]) and "iron deficiency anemia secondary to blood loss (chronic)" (OR = 5.20[4.53-5.97]). The most significant association with intramural fibroids was also "disorders of menstruation" (OR = 4.68[4.31-5.08]). The most significant association in the subserosal analysis was with "other benign neoplasm of connective and other soft tissue" (OR = 5.35[4.74-6.04]). We performed sensitivity analyses to narrow down subtype-specific associations. From these, only submucosal fibroids had multiple anemia-, irregular menstruation-, and dysmenorrhea-related phecodes remain significant, and only submucosal and intramural fibroids remained significantly associated with infertility. Conclusions: We identified multiple factors that were more strongly or uniquely associated with having a specific fibroid subtype. We demonstrated a greater severity of fibroid symptoms in individuals with a subtype-level fibroid diagnosis.

Identifiers

PMID42078903
PMCPMC13131860

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