Urinary symptoms decrease quality of life in patients with Parkinson’s disease – R

Urinary symptoms decrease quality of life in patients with Parkinson’s disease – R

Esmeralda Gracián-Castro 1, Nancy R. Bertado-Ramírez 2 , Arturo García-Galicia 2 , Daniel Núñez-Corona 3, Gisela Alonso-Torres 4, Álvaro J. Montiel-Jarquín 5 , Jorge Loría-Castellanos 6

1 Facultad de Medicina, Universidad Popular Autónoma del Estado de Puebla, Puebla, México; 2 Dirección de Educación e Investigación en Salud. Hospital de Especialidades de Puebla, Instituto Mexicano del Seguro Social, Puebla, Pue., México; 3 Departamento Clínico de Urología, Centro Médico Nacional, Hospital de Especialidades Gral. de Div. Manuel Ávila Camacho, Instituto Mexicano del Seguro Social, Puebla, México; 4 Facultad de Medicina, Benemérita Universidad Autónoma de Puebla, Puebla, México; 5 Dirección de Educación e Investigación en Salud, Centro Médico Nacional Gral. de Div. Manuel Ávila Camacho, Hospital de Especialidades de Puebla, Instituto Mexicano del Seguro Social (IMSS) Puebla, México; 6 Coordinación de Proyectos Especiales en Salud, Instituto Mexicano del Seguro Social, Ciudad de México, México

*Correspondence: Arturo García-Galicia. Email: neurogarciagalicia@yahoo.com.mx

Date of reception: 15-01-2024

Date of acceptance: 17-01-2024

DOI: 10.24875/AMH.M24000069

Available online: 27-05-2024

An Med ABC 2024;69(1):1-6




PARTIAL RETRACTION

Abstract

Introduction: Parkinson’s disease (PD) is a progressive neurodegenerative disorder that affects multiple systems manifesting with motor and non-motor symptoms. Urinary symptoms are the most prevalent non-motor manifestations.

Objective: To compare the quality of life (QoL) in patients with PD according to their urinary symptomatology in a tertiary care hospital.

Methods: Comparative, cross-sectional, prospective study in a third level hospital in Puebla, Mexico. Patients with a diagnosis of PD, older than 30 years, both sexes, were included. The IPSS and SF-36 scales were applied. Descriptive statistics, Kruskal-Wallis and Spearman’s rho were used.

Results: Thirty-seven patients were evaluated, 59.5% male, mean age 62.3 years (range: 43-84; SD: 10.79). Differences in SF-36 and IPSS were significant in the pain and social function domains (p < 0.05). The correlation between the domain’s physical role, pain, social function, and vitality from IPSS was significant with rho scores from 0.28 to 0.4. The correlation between the impact on QoL by SF-36 and IPSS was not significant (p > 0.05) except in the emotional role domain.

Conclusions: Urinary symptoms affect QoL in the domains pain, social function, physical role, and vitality.

Keywords: Quality of life. Parkinson disease. Lower urinary tract symptoms.

Contents

Introduction

Parkinson’s disease (PD) is a progressive neurodegenerative disorder that affects multiple systems, manifesting with motor and non-motor symptoms. PD is characterized by the loss of dopaminergic cells1,2.

In most cases, the etiology of PD is idiopathic (85-90%), while in the remaining cases, PD has a genetic cause3,4. Age is the most important risk factor: it begins between 60 and 70 years of age. It is more common in men versus women, with a ratio of 1.4:15.

The clinical signs can be divided into motor and non-motor symptoms. The former includes tremor, postural instability, rigidity, and bradykinesia, while the latter includes GI, genitourinary, and cognitive symptoms, among others, which all have a negative impact on the patients’ the quality of life (QoL)6,7.

Urinary symptoms are the most prevalent non-motor manifestations of PD. They affect QoL by interfering with daily activities and health status, causing concern and discomfort. The most frequently observed symptoms are urinary urgency and frequency.

Urinary symptoms are the most prevalent non-motor manifestations of PD. They affect QoL by interfering with daily activities and health status, causing concern and discomfort. Their frequency ranges from 17% up to 27% for voiding symptoms and from 57% up to 83% for storage symptoms. The most frequently observed symptoms are urinary urgency (33% up to 54%) and urinary frequency (16% up to 36%)8,9.

The World Health Organization defines QoL as “an individual’s perception of their position in life in the context of the culture and value systems in which they live and in relation to their goals, expectations, standards, and concerns”8,10.

The objective of this study is to compare the QoL of PD patients based on their urinary symptomatology in a tertiary referral hospital.

Materials and methods

This was a comparative, observational, cross-sectional, and prospective study conducted on patients treated from a tertiary referral hospital during 2023. Patients clinically diagnosed with PD, > 30 years, of both sexes, were included. No patient was excluded or removed from the study.

The diagnosis of PD was considered in patients with at least three of the following signs: bradykinesia, resting tremor, rigidity, or postural instability, with response to dopaminergic drug11.

Patients were interviewed in outpatient consultation. Age, sex, marital status, occupation, academic degree, and comorbidities were collected. The following instruments were applied:

  • Hoehn and Yahr scale, to identify the severity of the disease in terms of mobility impairment, postural reflexes, laterality, and disability. The scoring ranges from 0 to 5, with 0 being asymptomatic, 1 indicating unilateral motor involvement, 2 indicating bilateral involvement without balance impairment, 3 indicating bilateral involvement with altered postural reflexes, 4 indicating severe disability with the ability to walk or stand unassisted, and 5 indicating confinement to bed or wheelchair11.
  • International prostate symptoms score (IPSS), to evaluate urinary symptoms caused by the prostate. It consists of seven questions that assess urgency, straining, hesitancy, nocturia, urinary frequency, decreased urine stream, and intermittency of urine flow. Each question is scored from 0 up to 5 points, with a total score ranging from 0 up to 35 points. The options for scoring are never, < 1 in 5 times, less than half of the time, about half of the time, more than half of the time, and almost always. Questions 1, 3, 5, and 6 evaluate obstructive symptoms, while questions 2, 4, and 7 assess storage symptoms. Based on the result, symptoms are categorized as mild (0 to 7 points), moderate (8 to 19 points), or severe (20 to 35 points). A lower score indicates lower symptomatology, and vice versa. An eighth question assesses the impact on QoL and is scored from 0 up to 6; this is analyzed separately. Although its primary use is in men, it is also useful for evaluating the severity of lower urinary tract symptoms in women12,13.
  • SF-36 Health Survey (SF-36), to evaluate QoL. It consists of 36 questions that assess a total of 8 domains: physical functioning, physical role, bodily pain, general health perceptions, vitality, social functioning, role limitations, and mental health. Each domain is scored from 0 up to 100, with a higher score indicating better QoL14,15.

Based on the results of the ISPSS, patients were categorized into 3 groups: with mild, moderate, and severe urinary symptomatology. The groups were compared in terms of the domains of the SF-36 scale for QoL.

Descriptive statistics was used for data analysis. To compare QoL among the groups with different urinary symptomatology, the Kruskal–Wallis test was used. Spearman’s rho coefficient was used for correlation analysis. Data were processed using the statistical software SPSS v. 25 for Windows. p ≤ 0.05 was considered statistically significant.

Patients signed an informed consent form. The data obtained were used solely for scientific purposes, and participants’ anonymity was preserved at all times. The protocol was approved by the Local Health Research Committee No. 2101 of the Instituto Mexicano del Seguro Social.

Results

A total of 37 PD patients were evaluated, including 22 (59.5%) men and 15 (40.5%) women. The mean age was 62.3 years (range, 43-84; standard deviation, 10.79). A total of 75.7% of the patients were married, 29.7% had completed primary education, 31.6% were engaged in household work, and 67.6% did not exhibit any comorbidities during the study. The details of the clinical and sociodemographic characteristics of the patients are shown in Table 1.

Table 1. Clinical and sociodemographic characteristics of the patients (n = 37)

Sex
Female Male
40.5% 59.5%
Age (years)
40-49 50-59 60-69 70-79 80-89
16.2% 21.6% 37.8% 18.9% 5.4%
Civil status
Single Married Widow Coupled
5.4% 75.7% 8.1% 10.8%
Education
Primary or lower Secondary or higher
45.94% 54.05%
Occupation
Housewife Retiree Other
31.6% 26.3% 40.54%
Comorbidities
Diabetes Hypertension Both None
2.6% 13.2% 15.8% 65.8%
Hoehn Yahr Scale
0 1 2 3 4 5
5.3% 5.3% 21.1% 50% 10.5% 5.3%

Regarding clinical stage, 50% (19 patients) were in stage 3, 21.1% (8 patients) in stage 2, and 10.5% (4 patients) in stage 4 of the Hoehn and Yahr scale.

Patients were on dopaminergic therapy as follows: 21 (56.75%) on levodopa-carbidopa and pramipexole, 10 (27%) on levodopa-carbidopa and biperiden, 3 (8.1%) on levodopa-carbidopa only, 2 (5.4%) on pramipexole and biperiden, and 1 (2.7%) on levodopa-carbidopa, pramipexole, and rasagiline.

Reported side effects included dyskinesias in 18 (48.64%) patients and behavioral changes in 2 (5.4%) (one aggression and inappropriate behaviors, and 1 emotional lability).

Regarding obstructive urinary symptoms, between 13.2% and 34.2% of patients reported discomfort approximately half the time to almost always. The most frequent urinary sign was decreased caliber of the urinary stream (34.2%). As for storage symptoms, between 23.7% and 28.9% reported impairment approximately half the time and almost always. The most common storage symptom was urinary frequency (28.9%). In question 8, 31.6% of patients reported feeling rather dissatisfied to very unhappy.

The comparison between groups with mild, moderate, and severe urinary symptomatology in the physical nature domains of the SF-36 scale is illustrated in Table 2. The comparison in mental nature domains is shown in Table 3. Significant differences were found only in the domains of pain and social function (p < 0.05). Only correlations between the physical role, pain, physical function, and vitality domains with urinary symptoms were significant (p ≤ 0.05), with rho ranging from 0.28 up to 0.4 (Tables 2 and 3).

Table 2. Quality of life and urinary symptom comparison. Physical Domains of SF-36

Quality of life domains (SF-36) Urinary symptoms (%) International prostate symptoms score p Kruskal–Wallis test Spearman Rho
Mild (n = 13) Moderate (n = 17) Severe (n = 7)
Physical Role 0.116 −0.283 (p = 0.0445)
 No impairment 30.76 0 14.28
 Mild 15.38 29.41 0
 Very mild 0 0 0
 Moderate 0 0 0
 Severe 7.69 17.64 0
 Very severe 46.15 52.94 85.71
Pain 0.027 −0.400 (p = 0.007)
 No impairment 30.76 11.76 14.28
 Mild 23.07 23.52 0
 Very mild 7.69 5.88 0
 Moderate 15.38 11.76 0
 Severe 7.69 11.76 14.28
 Very severe 15.38 35.2 71.42
General state of health 0.176 −0.151 (p = 0.187)
 No impairment 0 0 0
 Mild 0 5.88 0
 Very mild 7.69 0 0
 Moderate 15.38 29.41 14.28
 Severe 23.07 11.76 0
 Very severe 53.84 52.94 85.57
Physical function 0.086 −0.310 (p = 0.031)
 No impairment 7.69 5.88 14.28
 Mild 15.38 11.76 0
 Very mild 15.38 0 0
 Moderate 0 23.52 0
 Severe 30.76 5.88 0
 Very severe 30.76 52.94 85.71

SF: Short form.

Table 3. Quality of life and urinary symptom comparison. Mental Domains of SF-36

Quality of life domains (SF-36) Urinary symptoms (%) International prostate symptoms score p Kruskal–Wallis test Spearman Rho
Mild (n = 13) Moderate (n = 17) Severe (n = 7)
Vitality 0.077 −0.322 (p = 0.026)
 No impairment 0 0 14.28
 Mild 23.07 11.76 0
 Very mild 7.69 0 0
 Moderate 7.69 17.64 0
 Severe 30.76 17.64 0
 Very severe 30.76 52.94 85.71
Social function 0.021 −0.240 (p = 0.076)
 No impairment 0 0 0
 Mild 7.69 11.76 0
 Very mild 7.69 0 0
 Moderate 7.69 23.52 0
 Severe 38.46 35.29 14.28
 Very severe 38.46 29.41 85.71
Emotional role 0.099 −0.270 (p = 0.080)
 No impairment 15.38 17.64 0
 Mild 0 0 0
 Very mild 0 0 0
 Moderate 46.15 41.17 14.28
 Severe 0 0 0
 Very severe 38.46 41.17 85.71
Mental health 0.1515 −0.220 (p = 0.095)
 No impairment 0 0 0
 Mild 15.38 11.76 0
 Very mild 7.69 0 0
 Moderate 15.38 17.64 0
 Severe 15.38 23.52 28.57
 Very severe 46.15 47.05 71.42

SF: Short form.

The correlation between the impact on QoL (question 8 of the IPSS) and the SF-36 domains was not significant (p > 0.05), except for the emotional role domain (r = −0.404; p = 0.013).

Discussion

PD is a chronic and progressive disorder affecting multiple systems, being a heterogeneous disease1.

In this study, a predominance of males over females was observed at a ratio of 1.5:1, very similar to other reports16.

PD affects individuals > 60 years, with peaks around 85 years16,17. We should mention that in this population, 75% of patients were < 70 years, with a mean age of 62.3 years. Only 2 patients were reported > 80 years.

Up to about 46% of our patients reported primary level education or lower, which is similar to what former studies have reported in Latin America18.

We should mention that the diagnoses identified in this study were diabetes and arterial hypertension. Most did not report other diagnoses. Other reports identify sleep disturbances (81.3%) and depression (37.1%) as the most frequent comorbidities18,19. This is an area of opportunity to improve the study and management of these patients.

Most patients in this study are on levodopa along with a dopaminergic agonist, which is consistent with other reports from Mexico and Latin America20,21.

A total of 51% of patients manifest motor complications associated with levodopa22. The results presented today show a very similar percentage (52.6%).

Regarding the severity reported in this study according to the Hoehn-Yahr scale, 73% of patients were in stages 2 and 3. In other Mexican studies, similar severity has been reported in up to 93% of cases. There seems to be a greater impact on QoL within physical and mobility areas, but in the present study, the most affected domains are pain, social function, and emotional role22,23.

The most common urinary symptoms in this study were urinary frequency (storage) and decreased caliber of the urinary stream (obstructive), while other studies report nocturia in up to 60% and urinary urgency in 54% as the most frequent symptoms9,24.

The presence of urinary symptoms affects social relationships, intimacy, and participation in social activities, as it causes embarrassment, resulting in a negative impact on QoL25,26. The findings of the present study corroborate this, as the assessment of QoL in the IPSS corresponds to the rating of domains of the SF-36 instrument specific to that construct.

Storage symptoms have a greater impact on QoL particularly as PD progresses27,28. In this study, no differentiation was made by the intensity of obstructive or storage symptoms, yet significant impairment was found in five of the eight SF-36 domains.

QoL assessed by the SF-36 scale did not correlate significantly with question 8 of the IPSS, except for the emotional role domain, with moderately high figures (0.404). A construct as complex as QoL will hardly be properly evaluated with a single question. These results suggest that the emotional aspect has the greatest impact on QoL.

The findings may have been affected by the relatively small sample size. Studies with a larger sample will contribute to filling the existing gap in current reports on the topic.

Conclusions

The most frequent urinary symptoms were urinary frequency and decreased caliber of the urinary stream. The pain and social function domains of QoL showed a significant decrease according to urinary symptoms. Physical role, pain, social function, and vitality showed a significant correlation with urinary symptomatology.

Funding

The authors declare that they have not received funding.

Conflicts of interest

The authors declare no conflicts of interest.

Ethical disclosures

Protection of human and animal subjects. The authors declare that no experiments were performed on humans or animals for this study.

Confidentiality of data. The authors declare that they have followed the protocols of their work center on the publication of patient data.

Right to privacy and informed consent. The authors have obtained the written informed consent of the patients or subjects mentioned in the article. The corresponding author is in possession of this document.

Use of artificial intelligence for generating text. The authors declare that they have not used any type of generative artificial intelligence for the writing of this manuscript nor for the creation of images, graphics, tables, or their corresponding captions.

References

1. Jameson JL, Fauci AS, Kasper DL, Hauser SL, Longo DL, Loscalzo J, editors. Harrison. Principios de Medicina Interna. 20ªed. México:McGraw Hill Education;2018. 3120-9.

2. Cheon M, Kim SM, Ha SW, Kang MJ, Yang HE, Yoo J. Diagnostic performance for differential diagnosis of atypical Parkinsonian syndromes from Parkinson's disease using quantitative indices of 18F-FP-CIT PET/CT. Diagnostics (Basel). 2022;12:1402.

3. Khwaounjoo P, Singh G, Grenfell S, Özsoy B, MacAskill MR, Anderson TJ, et al. Non-contact hand movement analysis for optimal configuration of smart sensors to capture Parkinson's disease hand tremor. Sensors (Basel). 2022;22:4613.

4. Armstrong MJ, Okun MS. Diagnosis and treatment of Parkinson disease:a review. JAMA. 2020;323:548-60.

5. Russillo MC, Andreozzi V, Erro R, Picillo M, Amboni M, Cuoco S, et al. Sex differences in Parkinson's disease:from bench to bedside. Brain Sci. 2022;12:917.

6. Balestrino R, Schapira AH. Parkinson disease. Eur J Neurol. 2020;27:27-42.

7. Pérez-Sánchez JR, Martínez-Álvarez R, Martínez-Moreno NE, Torres-Díaz C, Rey G, Pareés I, et al. Radiocirugía estereotáctica con Gamma Knife®como tratamiento del temblor esencial y parkinsoniano:experiencia a largo plazo. Neurologia. 2023;38:188-96.

8. Jalón-Monzón A, Fernández-Gómez JM, Rodríguez-Faba O, García-Rodríguez J, Rodríguez-Martínez JJ, González-Álvarez RC, et al. Relación entre síntomas del tracto urinario inferior y calidad de vida. Arch Esp Urol. 2005;58:109-13.

9. Jaramillo D, Ortiz MJ, Pérez S, Vásquez-Builes S, Rojas IC. Disfunción urinaria en la enfermedad de Parkinson:una revisión práctica. Rev Chil Neuro Psiquiatr. 2022;60:62-74.

10. The World Health Organization quality of life assessment (WHOQOL):position paper from the World Health Organization. Soc Sci Med. 1995;41:1403-9.

11. Palacios-Sánchez E, Virginia-González A, Vicuña JA, Villamizar L. Calidad de vida en los pacientes con enfermedad de Parkinson valorados en un hospital universitario de Bogotá, Colombia. Neurol Arg. 2019;11:151-8.

12. Arlandis-Guzmán S, García-Matres MJ, González-Segura D, Rebollo P. Prevalencia de síntomas del tracto urinario inferior en pacientes con síndrome de vejiga hiperactiva:manejo del paciente en la práctica clínica habitual. Actas Urol Esp. 2009;33:902-8.

13. Preciado-Estrella DA, Kaplan SA, Iturriaga-Goyón E, Ramón-Trejo E, Mayorga-Gómez E, Auza-Benavides A, et al. Comparación del índice internacional de síntomas prostáticos versus escala visual análoga Gea®para la evaluación de los síntomas de la vía urinaria inferior. Rev Mex Urol. 2017;77:372-82.

14. Vilagut G, Ferrer M, Rajmil L, Rebollo P, Permanyer-Miralda G, Quintana JM, et al. El Cuestionario de salud SF-36 español:una década de experiencia y nuevos desarrollos. Gac Sanit. 2005;19:135-50.

15. Trujillo BW, Román JJ, Lombard AM, Remior E, Arredondo OF, Martínez E, et al. Adaptación del cuestionario SF-36 para medir calidad de vida relacionada con la salud en trabajadores cubanos. Rev Cubana Salud Trab. 2014;15:62-70.

16. Saavedra-Moreno JS, Millán PA, Buriticá-Henao OF. Introducción, epidemiología y diagnóstico de la enfermedad de Parkinson. Acta Neurol Colomb. 2019;35:2-10.

17. Martínez-Fernández R, Gasca-Salas C, Sánchez-Ferro A, Obeso JA. Actualización en la enfermedad de Parkinson. Rev Med Clin Condes. 2016;27:363-79.

18. Condor IR, Atencio-Paulino JI, Contreras-Cordova CR. Características clínico epidemiológicas de la enfermedad de Parkinson en un hospital nacional de la sierra peruana. Rev Fac Med Hum. 2019;19:14-21.

19. Pohar SL, Jones AC. The burden of Parkinson disease (PD) and concomitant comorbidities. Arch Gerontol Geriatr. 2009;49:317-21.

20. Rodríguez-Violante M, Villar-Velarde A, Valencia-Ramos C, Cervantes-Arriaga A. Características epidemiológicas de pacientes con enfermedad de Parkinson de un hospital de referencia en México. Arch Neurocien. 2011;16:64-8.

21. Moreira-Díaz LR, Palenzuela-Ramos Y, Maciñeira-Lara IE, Díaz-González L, Torres-Martínez Y. Variables clínicas y epidemiológicas de pacientes diagnosticados con enfermedad de Parkinson. Univ Méd Pinareña. 2019;15:320-8.

22. Navarro-Peternella FM, Marcon SS. Calidad de vida de las personas con enfermedad de Parkinson y su relación con la evolución en el tiempo y la gravedad de la enfermedad. Rev Latino Am Enferm. 2012;20:1-8.

23. Berganzo K, Tijero B, González-Eizaguirre A, Somme J, Lezcano E, Gabilondo I. Síntomas no motores y motores en la enfermedad de Parkinson y su relación con la calidad de vida y los distintos subgrupos clínicos. Neurologia. 2016;31:585-91.

24. Martínez-Martín P, Rodríguez-Blázquez C, Kurtis MM, Chaudhuri KR. The impact of non-motor symptoms on health-related quality of life of patients with Parkinson's disease. Mov Disord. 2011;26:399-406.

25. Argandoña-Palacios L, Perona-Moratalla AB, Hernández-Fernández F, Díaz-Maroto I, García-Muñozguren S. Trastornos no motores de la enfermedad de Parkinson:introducción y generalidades. Rev Neurol. 2010;50:S1-5.

26. Chen Z, Li G, Liu J. Autonomic dysfunction in Parkinson's disease:implications for pathophysiology, diagnosis, and treatment. Neurobiol Dis. 2020;134:104700.

27. Vaughan CP, Burgio KL, Googe PS, Juncos JL, McGwin G, Muirhead L. Behavioral therapy for urinary symptoms in Parkinson's disease:a randomized clinical trial. Neurourol Urodyn. 2019;38:1737-44.

28. Sveinbjornsdottir S. The clinical symptoms of Parkinson's disease. J Neurochem. 2016;139:318-24.