Skip to main content
  • Research article
  • Open access
  • Published:

Urological dysfunctions in patients with Parkinson’s disease: clues from clinical and non-invasive urological assessment



Autonomic nervous system dysfunction, common in patients with Parkinson’s disease (PD), causes significant morbidity and it is correlated with poor quality of life. To assess frequency of urinary symptoms in patients with PD, without conditions known to interfere with urinary function.


Non-demented PD patients were consecutively enrolled from the outpatients clinic of our department. Scales investigating motor and non-motor symptoms were carried out. Evaluation of urinary dysfunctions was carried out using the AUTonomic Scale for Outcomes in Parkinson’s disease (SCOPA-AUT) questionnaire. Patients underwent noninvasive urological studies (nUS), including uroflowmetry and ultrasound of the urinary tract.


Forty-eight (20 women, 42%) out of 187 PD patients met the inclusion criteria and were enrolled in the study. Mean SCOPA-AUT score was 14.1 ± 6.9 (urinary symptoms subscore 5.2 ± 3.8). Among those evaluated by the SCOPA-AUT scale, the urinary symptoms were among the most common complaints (93.8%). At nUS mean maximum flow rate (Qmax) was 17.9 ± 9.1 ml/s, and mean postvoid residual (PVR) urine volume was 24.4 ± 44.1 ml. Ultrasound investigation documented prostate hypertrophy in 12 male patients (42.8%). Urinary items of the SCOPA-AUT (SCOPA-U subscore) correlated with measures of disease severity only in female patients.


Urinary symptoms and abnormal findings in nUS are common in PD. Though nigrostriatal degeneration might be responsible for urinary symptoms also in the early-intermediate stage of the disease, when urinary dysfunction occurs other medical conditions need to be excluded.

Peer Review reports


Growing evidence suggests that non-motor symptoms (NMS) play a very important, and sometimes a decisive role, in influencing the management of Parkinson’s disease (PD).

Autonomic dysfunction affects up to 70–80% of PD patients, including cardiovascular (orthostatic hypotension, cardiac arrhythmias, lower limb edemas), gastrointestinal (constipation, sialorrhea, heartburn), sudomotor (sweating, seborrhea), thermoregulatory (heat or cold intolerance), and urogenital (urgency, incontinence, erectile dysfunction) symptoms [1]. Urinary symptoms (US) may occur even from the earliest premotor stages of PD and are associated with higher motor disability, more severe dopaminergic denervation, and poorer quality of life [2, 3].

The reported frequency of US in patients with PD varies considerably among studies, mainly due to the use of different and often non-validated questionnaires. Moreover, an important issue that has not always received enough attention is that most PD patients are in the age group in which concomitant pathological conditions might affect urinary function, the most common of which in men is an outflow obstruction due to prostatic enlargement.

Despite these considerations, all authors agree that the urinary symptoms are very common in PD, with recent evidence that prevalence of lower urinary tract symptoms may range from 25 to 50% [4]. In the PRIAMO study [5], US were very common (57.3%), and a follow-up study showed their role as early markers of more severe disease progression [3].

The pathophysiological basis of the urinary dysfunction, that mainly consists in a bladder overactivity, is supposed to rely on a dysfunction of the dopamine basal ganglia circuit, which normally suppresses the micturition reflex [4].

In this study we aimed to assess the occurrence of urinary symptoms in a group of patients suffering from PD who did not suffer from diseases known to influence the urinary function. To this aim, we used a validated questionnaire, i.e. the AUTonomic Scale for Outcomes in Parkinson’s disease (SCOPA-AUT) [6], and we performed a urological examination including noninvasive urological investigation (nUS).


Diagnosis of PD was made according to the U.K. PD Brain Bank criteria. PD patients suffering from diseases known to influence the urinary function, i.e. cognitive impairment, major depression and other psychiatric disorders, previous stroke, diabetes mellitus, spondylosis, prostate hypertrophy, urinary tract infections, as well as subjects receiving any medication for urinary problems, were excluded from the study. Clinical assessment of PD patients was performed by SCOPA-AUT questionnaire, Hoehn and Yahr (H&Y) scale, Unified Parkinson’s disease rating scale (UPDRS), Beck Depression Inventory (BDI), Neuropsychiatric Inventory (NPI), Parkinson’s Disease Questionnaire (PDQ-39) and Parkinson’s disease sleep scale (PDSS).

The SCOPA-AUT questionnaire [6] includes 6 items investigating bladder storage and voiding dysfunctions. Storage symptoms include urinary urgency, increased daytime and night-time urinary frequency (nocturia), and urge/stress/mixed incontinence. Increased urinary frequency was defined as passing urine 8 or more times per daytime and twice or more per night. Voiding symptoms consist of hesitancy, slow stream, intermittency, straining, feeling of incomplete emptying and urinary retention. Non-invasive urological studies included uroflowmetry and ultrasound of the urinary tract. The quantitative parameters measured during the voiding phase were maximum flow rate (Qmax) and postvoid residual (PVR) urine volume. Qmax values lower than 10 ml/s and PVR values higher that 50 ml were considered abnormal according to reference values of our laboratory, which were also similar to those used in a previous study conducted in PD patients to assess the urinary function [7]. All PD patients completed a 24-h bladder diary before performing nUS. The 24-h diary included recording of the volume and time of each void, as well as the frequency of incontinence following prompted voiding.

The study was approved by the Ethics Committee of the University of Palermo and all participants gave their informed consent to participate to the study.

Data analysis

Correlations between clinical/instrumental measures and SCOPA-AUT score and urinary items of the SCOPA-AUT (SCOPA-U subscore) were investigated by means of Pearson’s correlation coefficient. Patients were divided into two groups according to the SCOPA-AUT score (above and below the mean).

In order to investigate the unique role of Parkinson’s disease in determining US, we also divided patients in two groups according to the mean SCOPA-U subscore (below and above the mean value) after we excluded those who showed at nUS organic/structural causes responsible of urinary dysfunction. In both cases, differences between groups were assessed by T test. All analyses were performed with 9.2 SAS version.


At the end of the enrollment period (from January 2013 to December 2015), 187 PD patients (103 males, 59.9%) were screened. Due to inclusion criteria, thirty-eight PD patients with cognitive impairment, 27 patients receiving medication for urinary problems, and 47 patients suffering from diseases known to influence the urinary function were excluded.

Twenty-seven patients refused to participate to the study, mainly because they declined to undergo instrumental investigations required by the study protocol.

Finally, 48 patients (28 males and 20 females) were included in the study (mean age at interview 62.7 ± 10.6; mean disease duration: 6.2 ± 4.2 years). Most of the patients (84%) were on HY stage 1–2 (33.3% stage 1, 51% stage 2, 8.9% stage 3, 6.7% stage 4 and none stage 5). Demographic and clinical characteristics of the patients enrolled are shown in Table 1. Mean SCOPA-AUT score was 14.1 ± 6.9 while mean SCOPA-U subscore was 5.2 ± 3.8.

Table 1 demographic and clinical data (means ± SD) of patients with Parkinson’s disease

At least one clinical symptom of dysautonomia was found in all PD patients. The most frequently involved SCOPA-AUT domains referred to the gastrointestinal (95.8%) and the urinary (93.8%) system, followed by cardiovascular (43.7%), thermoregulatory (50%), sexual (31.2%), and pupillomotor (25%) dysfunctions. Only three patients did not complain of urinary problems. Most of the patients with urinary symptoms had a storage disorder (91%), i.e. urgency, nocturia and urinary frequency, while few had a voiding disorder (9%). The instrumental examination showed mean Qmax of 17.9 ± 9.1 SD ml/s and mean PVR of 24.4 ± 44.1 SD ml. Ultrasound documented structural abnormalities of the urinary tract due to prostate hypertrophy in 12 out of 28 (42.8%) male patients, while non-significant alterations were found in the group of female subjects (only in a single subject we found leiomyomas of the uterus).

As shown in Table 2, SCOPA-AUT scores significantly correlated with total (Rho 0.40, p = 0.005) and motor section (Rho 0,39, p = 0.006) UPDRS scores, levodopa dosage (Rho 0.30, p = 0.03), PDSS score (Rho − 0,46, p = 0.001), BDI score (Rho 0.31, p = 0.03), NPI score (Rho 0.35, p = 0.01), and with the following dimensions of the PDQ-39 scale: mobility (Rho 0.34, p 0.002), cognition (Rho 0.37, p = 0.01) and communication (Rho 0.30, p = 0.004). No correlations with findings of nUS (Qmax and PVR) were found. SCOPA-U subscore significantly correlated only with age at enrollment (Rho 0.41, p = 0.003) and with the two following dimensions of the PDQ-39: mobility (Rho 0.29, p = 0.04) and cognition (Rho 0.30, p = 0.04). No significant correlations with other clinical variables were found. In the hypothesis that this was mainly due to the high frequency of prostate hypertrophy in the male population, we also carried out the correlation analysis considering only female patients. In this group of patients, we found that SCOPA-U subscore significantly correlated along with age at study enrollment (Rho 0.48, p = 0.03), also with PDSS score (Rho − 0,55, p = 0.01), mobility (Rho 0.54, p = 0.01) and cognition (Rho 0.44, p = 0.05) of the PDQ-39, and total (Rho 0.46, p = 0.04) and motor section (Rho 0,52, p = 0.02) UPDRS scores.

Table 2 Correlation between clinical/instrumental measures, SCOPA-AUT score and SCOPA-U (urinary items) subscore


In our study, though we enrolled patients with PD without documented history of urinary problems, almost all patients complained of urinary symptoms as shown by the SCOPA-U subscore. Noteworthy, the ultrasound investigation revealed a prostatic hypertrophy as a possible cause of urinary symptoms in a considerable number of male patients.

It is now well established that urinary symptoms can be a troublesome aspect of the non-motor spectrum affecting PD patients. Notwithstanding, there is not yet consensus on the nature, severity and temporal occurrence of urinary symptoms among PD patients [3]. This is also due to the difficulty to make a direct comparison between findings of various studies using different and often non-validated questionnaires and scales.

In this study we used the SCOPA-AUT scale, which is an instrument specifically designed for detection of dysautonomic symptoms in PD including 6 items exploring the urinary function [6]. Though questionnaires and scales evaluating non-motor symptoms [8] such as US can be easily applied in PD patients to address important disease-related issues, these tools are unsuitable to detect bladder dysfunctions with sufficient sensitivity and specificity [6]. Thus, all our patients underwent an in-depth urological clinical and instrumental examination to exclude coexistence of other pathological conditions that could be responsible for urological dysfunctions. As a matter of fact, in our study population the ultrasound investigation revealed a prostate hypertrophy in almost half of males. This benign and treatable pathological condition is often underdiagnosed and undertreated in middle and advanced age male population [9]. Therefore, also on the bases of our results, all male patients with PD and urinary symptoms should underwent a careful urological assessment to exclude conditions responsible for bladder outlet obstruction, and avoid the risk to attribute the urinary symptoms exclusively to the PD.

In our study, almost all patients had an autonomic system involvement, though most of them presented with mild to moderate disease severity (33.3% stage 1, 51% stage 2). This is in line with previous literature showing that autonomic dysfunctions may develop also in early stage of disease and, sometimes, can also precede the diagnosis of PD [10]. We also found that the SCOPA-AUT scores significantly correlated with different measures of motor and non-motor impairment according to the evidence that patients with autonomic symptoms may have higher motor and non-motor burden [11]. It is to note, however, that no significant correlations between SCOPA-U subscores and clinical and instrumental measures were found when considering the whole study population, with the exception of PDSS and PDQ-39 mobility and cognition.

This was likely due to the presence of prostate hypertrophy in a significant number of male patients, that could have acted as a confounding factor. Indeed, correlations between SCOPA-U subscore and total and motor UPDRS scores were found when considering exclusively female patients, in accord to the evidence that prevalence and severity of US in PD patients increases with disease severity [4]. Moreover, the finding that the SCOPA-U subscores significantly correlated with age at enrollment, agrees with other reports showing that PD patients with US are significantly older than patients without US [11, 12].

Findings regarding quality of sleep showed that PD patients with urinary dysfunction had lower scores at PDSS scale, and 75% (27/36) of them complained of nocturia. This supports the concept that nocturnal US are possible determinants of worst quality of sleep [13] and is in line with evidence that patients with US have overall higher non-motor burden [11]. Nonetheless, the coexistence of urinary dysfunction with sleep disorders might also be consistent with the brainstem involvement that may occur early in the course of the disease as demonstrated by neuropathological studies [14].

Main limitations of the study are the relatively low numbers of subjects enrolled and the absence of a control group. Indeed, though several studies have yet reported that PD patients have significantly more US than healthy age-matched control subjects [15, 16] the exact role of age-related changes in the urinary function in PD patients deserves to be investigated in future studies. In many clinical situations, it is difficult to determine to what extent PD is contributing to urinary dysfunction in any given individual. Effective treatment of urologic symptoms in these patients it is often difficult.


In conclusion, our findings suggest that urinary symptoms are common in PD patients, occurring also in early stages of the disease. It is essential however not to forget that abnormal findings in nUS might alternatively explain symptoms that often are erroneously attributed to Parkinson’s disease. Though autonomic dysfunction might be related to nigrostriatal degeneration, urinary dysfunction in patients with PD could be attributed to other medical conditions.



Beck Depression Inventory


Hoehn and Yahr


Neuropsychiatric Inventory


Non invasive urological studies


Parkinson’s disease


Parkinson’s Disease Questionnaire


Parkinson’s disease sleep scale


Postvoid residual


Maximum flow rate


AUTonomic SCale for Outcomes in Parkinson’s disease


Urinary items of the AUTonomic SCale for Outcomes in Parkinson’s disease


Unified Parkinson’s disease rating scale


  1. Jost WH. Autonomic dysfunctions in idiopathic Parkinson’s disease. J Neurol. 2003;250(Suppl. 1):I28–30.

    Article  Google Scholar 

  2. Liu Z, Uchiyama T, Sakakibara R, Yamamoto T. Underactive and overactive bladders are related to motor function and quality of life in Parkinson’s disease. Int Urol Nephrol. 2015;47:751–7.

    Article  PubMed  Google Scholar 

  3. Picillo M, Palladino R, Barone P, Erro R, Colosimo C, Marconi R, Morgante L, Antonini A, on behalf of the PRIAMO Study Group. The PRIAMO study: urinary dysfunction as a marker of disease progression in early Parkinson’s disease. Eur J Neurol. 2017;24:788–95.

    Article  CAS  PubMed  Google Scholar 

  4. Winge K. Lower urinary tract dysfunction in patients with parkinsonism and other neurodegenerative disorders. Handb Clin Neurol. 2015;130:335–56.

    Article  PubMed  Google Scholar 

  5. Barone P, Antonini A, Colosimo C, Marconi R, Morgante L, Avarello TP, Bottacchi E, Cannas A, Ceravolo G, Ceravolo R, Cicarelli G, Gaglio RM, Giglia RM, Iemolo F, Manfredi M, Meco G, Nicoletti A, Pederzoli M, Petrone A, Pisani A, Pontieri FE, Quatrale R, Ramat S, Scala R, Volpe G, Zappulla S, Bentivoglio AR, Stocchi F, Trianni G, Dotto PD, PRIAMO study group. The PRIAMO study: a multicenter assessment of nonmotor symptoms and their impact on quality of life in Parkinson's disease. Mov Disord. 2009;24:1641–9.

    Article  PubMed  Google Scholar 

  6. Visser M, Marinus J, Stiggelbout AM, van Hilten JJ. Assessment of autonomic dysfunction in Parkinson’s disease: the SCOPA-AUT. Mov Disord. 2004;19:1306–12.

    Article  Google Scholar 

  7. Uchiyama T, Sakakibara R, Yamamoto T, Ito T, Yamaguchi C, Awa Y, Yanagisawa M, Higuchi Y, Sato Y, Ichikawa T, Yamanishi T, Hattori T, Kuwabara S. Urinary dysfunction in early and untreated Parkinson’s disease. J Neurol Neurosurg Psychiatry. 2011;82:1382–6.

    Article  PubMed  Google Scholar 

  8. Chaudhuri KR, Martinez-Martin P, Brown RG. The metric properties of a novel non-motor symptoms scale for Parkinson’s disease: reults from a international pilot study (2007) Mov. Disorders. 22:1901–11.

    Article  Google Scholar 

  9. M. Speakman, R. Kirby, S. Doyle, C. Ioannou (2015) Burden of male lower urinary tract symptoms (LUTS) suggestive of benign prostatic hyperplasia (BPH) – focus on the UK BJU Int BJU International 115, 508–519. doi:

    Article  Google Scholar 

  10. Violante MR, Zeron-Martınez R, Arriaga A, Corona T. Who can diagnose Parkinson’s disease first? Role of pre-motor symptoms. Arch Med Res. 2017;48:221–7.

    Article  Google Scholar 

  11. Erro R, Picillo M, Amboni M, Moccia M, Vitale C, Longo K, Pellecchia MT, Santangelo G, Martinez-Martin P, Chaudhuri KR, Barone P. Nonmotor predictors for levodopa requirement in De novo patients with Parkinson’s disease. Mov Disord. 2015;30:373–8.

    Article  CAS  PubMed  Google Scholar 

  12. Chaudhuri KR, Schapira AH. Non-motor symptoms of Parkinson’s disease: dopaminergic pathophysiology and treatment. Lancet Neurol. 2009;8:464–74.

    Article  CAS  PubMed  Google Scholar 

  13. Arnao V, Cinturino A, Valentino F, Perini V, Mastrilli S, Bellavia G, Savettieri G, Realmuto S, D’Amelio M. In patients with Parkinson disease, autonomic symptoms are frequent and associated with other non-motor symptoms. Clin Auton Res. 2015;(5):301–7.

    Article  Google Scholar 

  14. Braak H, Del Tredici K, Rüb U, de Vos RAI, Jansen Steur ENH, Braak E. Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging. 2003;24:197–210.

    Google Scholar 

  15. Campos-Sousa RN, Quagliato E, Silva BBd, Jr de Carvalho RM, Ribeiro SC, de Carvalho DF. Urinary symptoms in Parkinson‘disease: prevalence and associated factors. Arq Neuropsiquiatr. 2003;61:359–63.

    Article  Google Scholar 

  16. A.V. Badri, R.S. Purohit, J. Skenazy, .J.P. Weiss, J.G. Blaivas (2014) A review of lower urinary tract symptoms in patients with Parkinson’s disease Curr Urol Rep. 15, 435. doi:

    Article  PubMed  Google Scholar 

Download references

Availability of data and materials

The datasets on which the conclusions of our manuscript rely are stored in our institutional database. We did not obtain permission to deposit these data on publicly available repositories from our institutional Ethics Committee and we cannot therefore share them.

Author information

Authors and Affiliations



FV, and MD gave substantial contributions to the conception and design of the work, acquisition and analysis of data; FV, TVB, GC, SM, VA, PA, SC, AP, CP and MD interpreted data; all authors drafted the work or revised it critically for important intellectual content; all authors gave their final approval of the version to be published; all authors agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy and integrity of any part of the work are appropriately investigated and resolved.

Corresponding author

Correspondence to Marco D’Amelio.

Ethics declarations

Ethics approval and consent to participate

The study was approved by local ethical committee (Comitato Etico Palermo 1, University Hospital P. Giaccone of Palermo) and written informed consent to participate was obtained by all participants to the study. The form of the informed consent was approved by the local ethic committee of the Palermo University Hospital “Paolo Giaccone”.

Consent for publication

All patients gave their consent to participate to the study and for the publication of the results.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Valentino, F., Bartolotta, T.V., Cosentino, G. et al. Urological dysfunctions in patients with Parkinson’s disease: clues from clinical and non-invasive urological assessment. BMC Neurol 18, 148 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: