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DOI 10.1097/ju.0000000000004187

Медицинская библиотека · The Journal of urology · 2024

Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study.

Breinbjerg Anders, Jørgensen Cecilie Siggaard, Walters G Bragi, Grove Jakob, Als Thomas D, Kamperis Konstantinos, Stéfansdóttir Lilja, Thirstrup Janne P, Borg Britt, Albiñana Clara, Vilhjálmsson Bjarni J, Eðvarðsson Viðar Ö, Stefánsson Hreinn, Mortensen Preben B, Agerbo Esben, Werge Thomas, Børglum Anders, Demontis Ditte, Stefánsson Kári, Rittig Søren, Christensen Jane Hvarregaard

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Аннотация

PURPOSE: Childhood incontinence is stigmatized and underprioritized, and a basic understanding of its pathogenesis is missing. Our goal was to identify risk-conferring genetic variants in daytime urinary incontinence (DUI).

MATERIALS AND

METHODS

We conducted a genome-wide association study in the Danish iPSYCH2015 cohort. Cases (3024) were identified through DUI diagnosis codes and redeemed prescriptions for DUI medication in individuals aged 5 to 20 years. Controls (30,240), selected from the same sample, were matched to cases on sex and psychiatric diagnoses, if any, and down-sampled to a 1:10 case:control ratio. Replication was performed in the Icelandic deCODE cohort (5475 cases/287,773 controls). Single-nucleotide polymorphism heritability was calculated using the genome-based restricted maximum likelihood method. Cross-trait genetic correlation was estimated using linkage disequilibrium score regression. Polygenic risk scores generated with LDpred2-auto and BOLT-LMM were assessed for association.

RESULTS

Variants on chromosome 6 (rs12210989, odds ratio [OR] 1.24, 95% CI 1.17-1.32, P = 3.21 × 10-12) and 20 (rs4809801, OR 1.18, 95% CI 1.11-1.25, P = 3.66 × 10-8) reached genome-wide significance and implicated the PRDM13 and RIPOR3 genes. Chromosome 6 findings were replicated (P = .024, OR 1.09, 95% CI 1.01-1.16). Liability scale heritability ranged from 10.20% (95% CI 6.40%-14.00%) to 15.30% (95% CI 9.66%-20.94%). DUI and nocturnal enuresis showed positive genetic correlation (rg = 1.28 ± 0.38, P = .0007). DUI was associated with attention-deficit/hyperactivity disorder (OR 1.098, 95% CI 1.046-1.152, P < .0001) and BMI (OR 1.129, 95% CI 1.081-1.178, P < .0001) polygenic risk.

CONCLUSIONS

Common genetic variants contribute to the risk of childhood DUI, and genes important in neuronal development and detrusor smooth muscle activity were implicated. These findings may help guide identification of new treatment targets.

Для цитирования: Breinbjerg Anders, Jørgensen Cecilie Siggaard, Walters G Bragi, Grove Jakob, Als Thomas D, Kamperis Konstantinos, Stéfansdóttir Lilja, Thirstrup Janne P, Borg Britt, Albiñana Clara, Vilhjálmsson Bjarni J, Eðvarðsson Viðar Ö, Stefánsson Hreinn, Mortensen Preben B, Agerbo Esben, Werge Thomas, Børglum Anders, Demontis Ditte, Stefánsson Kári, Rittig Søren, Christensen Jane Hvarregaard. Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study.. The Journal of urology. 2024. DOI: 10.1097/ju.0000000000004187.

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