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. 2019 Mar;14(1):24-30.
doi: 10.1007/s11884-019-00503-0. Epub 2019 Feb 8.

Functional brain imaging in voiding dysfunction

Affiliations

Functional brain imaging in voiding dysfunction

Rose Khavari et al. Curr Bladder Dysfunct Rep. 2019 Mar.

Abstract

Purpose of review: Voiding dysfunction (VD) is morbid, costly, and leads to urinary tract infections, stones, sepsis, and permanent renal failure. Evaluation and diagnosis of VD in non-obstructed patients can be challenging. Potential diagnostic and therapeutic options beyond the bladder, such as brain centers involved in voiding have been proposed as promising targets. This review focuses on current and future applications of functional neuroimaging in human in voiding and in patients with VD.

Recent findings: The current understanding of brain centers, and their roles in initiating, maintaining and/or modulating voiding, is rudimentary in humans and in patients with VD. With the advent and advancement in functional neuroimaging we are gaining more insight into specific brain regions involved in the voiding phase of micturition. In healthy individuals, right dorsomedial pontine tegmentum, periaqueductal grey, hypothalamus, and the inferior, medial and superior frontal gyrus have been identified as regions of interest in voiding.

Summary: Functional neuroimaging could suggest new diagnostic methods and provides crucial steps towards therapeutic options for the morbid and intractable VD condition, in patients with neurogenic (e.g. MS or Strokes) or non-neurogenic VD (e.g. underactive bladder or Fowler's syndrome).

Keywords: bladder dysfunction; fMRI; micturition; neuroimaging; voiding.

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Conflict of interest statement

Conflict of Interest Dr. Boone has nothing to disclose.

Figures

Figure 1.
Figure 1.
Unpublished data of the author. Anterior thalamic radiation (ATR) and the Superior longitudinal fasiculus (FSL) are the main two white matter tracts in the brain involved in proper lower urinary tract function. This image shows that these WMTs, especially the Left ATR are damaged in a female patient with Multiple Sclerosis and lower urinary tract dysfunction. Authors’ personal image.

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