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Inheritance in overactive bladder syndrome

Nature Reviews Urology volume 20, pages 61–62 (2023)Cite this article

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Despite the high prevalence of overactive bladder (OAB) syndrome, its pathophysiology remains poorly understood. Twin studies offer a unique opportunity for studying the genetics of this disorder, but trials are limited by heterogeneous patient populations. Improved understanding of genetic factors in OAB will be vital to developing targeted management.

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Authors and Affiliations

  1. Department of Urology, Guy’s and St Thomas’ NHS Trust, London, UK

    Nicholas Raison, Sachin Malde & Arun Sahai

  2. Faculty and Life Sciences and Medicine, King’s College London, London, UK

    Nicholas Raison & Arun Sahai

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  1. Nicholas Raison
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  2. Sachin Malde
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  3. Arun Sahai
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Corresponding author

Correspondence to Arun Sahai.

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Competing interests

S.M. declares an educational grant by Medtronic and speaker fees by Medtronic. A.S. declares educational grants by Medtronic, Boston scientific and Saluda Medical and speaker fees by Ferring, Allergan, Medtronic and Boston Scientific. N.R. declares no competing interests.

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Raison, N., Malde, S. & Sahai, A. Inheritance in overactive bladder syndrome. Nat Rev Urol 20, 61–62 (2023). https://doi.org/10.1038/s41585-022-00667-1

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