Genome-Wide Association Study for Urinary and Fecal Incontinence in Women.
Adaptor Proteins, Signal Transducing
/ genetics
Adult
Aged
DNA
/ genetics
Fecal Incontinence
/ genetics
Female
Follow-Up Studies
Genome-Wide Association Study
/ methods
Genotype
Humans
Middle Aged
Nerve Tissue Proteins
/ genetics
Polymorphism, Single Nucleotide
Quality of Life
Repressor Proteins
/ genetics
Retrospective Studies
Risk Factors
Time Factors
Urinary Incontinence
/ genetics
fecal incontinence
genome-wide association study
urinary incontinence
Journal
The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
pubmed:
16
11
2019
medline:
17
4
2020
entrez:
16
11
2019
Statut:
ppublish
Résumé
Urinary incontinence and fecal incontinence are common disorders in women that negatively impact quality of life. In addition to known health and lifestyle risk factors, genetics may have a role in continence. Identification of genetic variants associated with urinary incontinence and fecal incontinence could result in a better understanding of etiologic pathways, and new interventions and treatments. We previously generated genome-wide single nucleotide polymorphism data from Nurses' Health Studies participants. The participants provided longitudinal urinary incontinence and fecal incontinence information via questionnaires. Cases of urinary incontinence (6,120) had at least weekly urinary incontinence reported on a majority of questionnaires (3 or 4 across 12 to 16 years) while controls (4,811) consistently had little to no urinary incontinence reported. We classified cases of urinary incontinence in women into stress (1,809), urgency (1,942) and mixed (2,036) subtypes. Cases of fecal incontinence (4,247) had at least monthly fecal incontinence reported on a majority of questionnaires while controls (11,634) consistently had no fecal incontinence reported. We performed a genome-wide association study for each incontinence outcome. We identified 8 single nucleotide polymorphisms significantly associated (p <5×10 Few studies have collected genetic data and detailed urinary incontinence and fecal incontinence information. This genome-wide association study provides initial evidence of genetic associations for urinary incontinence and merits further research to replicate our findings and identify additional risk variants.
Identifiants
pubmed: 31729902
doi: 10.1097/JU.0000000000000655
pmc: PMC7659982
mid: NIHMS1621446
doi:
Substances chimiques
Adaptor Proteins, Signal Transducing
0
DAB1 protein, human
0
Nerve Tissue Proteins
0
Repressor Proteins
0
TRPS1 protein, human
0
DNA
9007-49-2
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
978-983Subventions
Organisme : NICHD NIH HHS
ID : R21 HD089502
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA067262
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA176726
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK120945
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA186107
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA049449
Pays : United States
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