Abstract
Depressive symptoms in Parkinson’s disease (PD) are multifactorial and are partly linked to the underlying dopaminergic deficit. However, at least a subset of PD patients may exhibit an unspecific depressive reaction to chronic illness. Here, we compared the prevalence and severity of depressive symptoms in PD patients and disease controls (DC). PD patients reported depressive symptoms at similar frequencies as DC but were on antidepressants, especially Mirtazapine, more frequently. Still, in both groups, a high proportion of patients with clinically significant depressive symptoms was not receiving medication. Diagnosis and treatment of depressive symptoms both in PD and DC should be improved.
Similar content being viewed by others
Depression worsens the prognosis and quality of life of individuals with Parkinson’s disease (PD) but remains underdiagnosed and undertreated1,2,3,4. Depression has been reported to occur in PD more frequently than in the general population5. However, the prevalence of depression in patients with other chronic conditions has also been reported to be higher than in the general population6. To our knowledge, only a few studies compared the prevalence of depression in PD with other diseases causing motor impairment, such as arthritis, essential tremor, and dystonia, and report similar frequencies of depression in these conditions as in PD7,8.
Diagnosing depression in PD is challenging due to the overlap of symptoms of both conditions, fluctuating mood states and off-periods9,10. The pathophysiology of depression in PD is likely attributable to disturbances in dopaminergic, serotonergic, and noradrenergic pathways and is linked to the underlying biologic processes of neuronal cell loss11. However, some patients may exhibit more general depressive reactions due to chronic illness. Differentiation of subtypes of depressed PD patients has been proposed with a prevalence of 10.2% of PD patients suffering from depressive symptoms specifically associated with PD in contrast to 6.8% of PD patients with an unspecific depressive reaction due to a chronic progressive illness12.
We aimed to analyze whether depressive symptoms in PD are sufficiently recognized and treated. In addition, we investigated the prevalence and severity of depressive symptoms in PD compared to patients with motor impairment due to other chronic conditions.
Results
Frequency of depressive symptoms
PD and DC most frequently reported prior episodes of depression compared to the HC (lifetime self-report question) (Fig. 1b, Table 1). PD patients were more likely (45.8%) to have current depressive symptoms (BDI Ia≥ 10) compared to HC (29.8%), but not DC (48.6%). Stratification of BDI Ia scores into severities indicated depressive symptoms in the PD group to be predominantly mild to moderate (10–18 points) (Table 1). Severe depressive symptoms (BDI Ia≥ 18; n = 8 in the PD group, n = 13 in the DC group) were too rare for meaningful conclusions. We found no significant difference in the prevalence of depressive symptoms between PD patients receiving dopaminergic medication or not (BDI Ia ≥ 10: 173/354 (48.9%) vs. 23/43 (53.5%); p = 0.567).
Use of antidepressants
Patients with PD were more likely to be on antidepressants (145/570 (25%)) than individuals from the other groups, with a particularly large difference in the range of mild to moderate depressive symptoms (BDI Ia = 10–18). Dosages in the therapeutic range were administered to 17% of the PD group but less than 5% of the study participants in the control groups (Table 1). In the PD group, 42/145 (29%) individuals on antidepressants received Mirtazapine (7.5 mg: n = 4; 15 mg: n = 22) and four Amitriptyline. In the DC group, only 2/33 (6%) took Mirtazapine 15 mg, and 5/33 (15%) Amitriptyline.
Comorbidities
Patients with PD exhibited vertigo/dizziness, essential tremor, restless legs syndrome, joint diseases, back pain, thyroid disease, hyperlipidemia and cardiac arrhythmia more often than DC, whereas epilepsy, migraine, stroke, polyneuropathy, coronary heart disease and diabetes mellitus showed similar frequencies in both groups. Arterial hypertension and cancer appeared more often in the PD group compared to the DC group, however, this effect was no longer present after adjustment for age and sex (Table 2).
Quality of life
The WHO-QoL showed an equally reduced quality of life for PD and DC compared to HC. Only the physical limitations domain score was lowest in the PD group (Table 1). The strongest predictor of poor QoL in a group-spanning analysis was the presence of at least mild depressive symptoms (BDI Ia ≥ 10) (OR = 6.416; B = 1.859, 95% CI = 4.712–8.737, p < 0.001).
Symptom profiles
We compared the relative contribution of individual BDI items to the total BDI score between the DC and PD groups. The PD group exhibited higher proportions of the items “tiredness” (p = 0.012) and “loss of weight” (p = 0.010) and lower contributions of the items “feelings of failure” (p = 0.002), “feelings of guilt” (p < 0.001), “self-hate” (p < 0.001), “self-accusation” (p = 0.008), “suicidal thoughts” (p = 0.021), “loss of libido” (p < 0.001) than the DC group.
One-year follow-up
In total, 149 DC and 211 PD patients appeared for follow-up (mean time interval 11.9 ± 0.8 months). A similar number of persons newly developed a BDI Ia> 10 in both groups (DC: 6/75 (8.0%), p = 0.115; PD: 14/97 (14.4%), p = 0.310). Most of the PD patients on antidepressant medication during the first visit continued its use (23/34 (67.6%)), whereas 11/34 (32.4%) discontinued it. Out of 123 PD patients unmedicated during the first visit, 9 (7.3%) started antidepressant medication within the follow-up period. In the DC group, 2/7 (28.6%) on medication during the first visit discontinued the medication, and 0/31 patients who had not been on medication started it until the second visit.
Discussion
We did not find any differences in the prevalence of depressive symptoms in PD compared to DC while confirming the higher prevalence of depressive symptoms in PD than in HC. More frequent use of antidepressants in PD may indicate partially successful treatment of depressive symptoms in PD, resulting in lower current prevalences and severities. On the other hand, PD and DC patients in our study reported similar lifetime prevalences of depression, arguing against this possible explanation. It seems more likely that neurologists address and treat depressive symptoms more often than other physicians treating DC.
Only part of the study participants received medication in the recommended therapeutic dosage. Although low dosages of antidepressants may be effective in elderly study participants, we observed low dosages more frequently in the PD group than in the DC group. Low dosages of Mirtazapine or Amitriptyline are often prescribed as a sleeping aid. Our study participants reported similar prevalences and severities of sleeping problems. Therefore, we may see an effect of low dosages of Mirtazapine prescribed as a sleeping aid in PD. Furthermore, the use of antidepressants for minimal or mild depressive symptoms is debatable as it is not supported by sufficient data.
Conflicting reports exist concerning the effect of dopaminergic medication on depressive symptoms. Previously, Pramipexole has been found to improve depressive symptoms11,13. However, a recent study showed no independent effect of dopaminergic medication on mood in PD when adjusted for motor improvement14. In our sample, we also did not find a significant difference in the prevalence of depressive symptoms between PD patients receiving dopaminergic therapy or not. Further, the quality of depressive symptoms in PD was nonspecific, with the highest contribution of “tiredness” and “loss of weight” to the total BDI in the PD group. These results may be attributable to the different subgroups of depression in PD, arguing that, at least in part, depressive symptoms in PD are not specific to the disease.
PD patients exhibited a higher burden of comorbidities than DC. Out of those, joint diseases, back pain15 and vertigo/dizziness16 have known associations with PD, and restless legs syndrome is considered a clinical manifestation in both the prodromal and the manifest phase of the disease17. Further, an association of PD with essential tremor has also been established18. In previous reports, PD patients have been found to exhibit accompanying other conditions more often than participants with other diseases presenting to primary care19. Similar to our results, these conditions were mostly known to be related to PD. In our analysis, after adjustment for age and sex, we found thyroid disease, hyperlipidemia and cardiac arrhythmia to be more common in the PD group than in DC. In a recent meta-analysis, thyroid disease has been found to increase the risk of PD20, which would explain the higher prevalence of thyroid disease in the PD group in our analysis. However, hyperlipidemia seems to be protective against developing PD21 and cardiac arrhythmias have rarely been reported in PD22. It is possible that the assessment of previous diseases is imprecise as they were self-reported by the study participants. Further, ascertainment bias is possible, as the PD group has been recruited through an outpatient and inpatient setting, but the DC group from the general population. This could partly explain the heavier burden of disease in the PD group. However, despite the higher burden of disease in PD compared to DC in our sample, PD patients showed similar prevalences of depressive symptoms as DC. This result further supports the view that depressive symptoms in PD are at least in part not specifically attributable to PD.
At a follow-up examination after one year, we observed similar proportions of patients in both groups converting to higher BDI scores and starting to take antidepressant medication. However, other study participants scored lower during the second visit and discontinued antidepressant medication, indicating a fluctuating course of depressive symptoms in PD and DC as observed in non-PD-related depression.
Mild depressive symptoms seem to be common in PD patients and are clinically relevant. This is further supported by the finding that depressive symptoms are the strongest predictor of reduced quality of life. It would thus be essential to define markers of subthreshold depression in PD and develop therapeutic recommendations.
In conclusion, DC exhibit a similar prevalence of depressive symptoms as PD patients despite the higher burden of comorbidities in PD. The prevalence of depressive symptoms in PD does not seem to be influenced by the intake of dopaminergic medication. However, PD patients use antidepressants more frequently, suggesting neurologists' awareness of depressive mood as a non-motor feature in PD. Still, many patients remain underdiagnosed and undertreated, as evidenced by a high proportion of patients with clinically significant depressive symptoms not receiving medication. Therefore, there remains room for improvement in diagnosing and treating depressive symptoms in PD and DC.
Methods
Study design
We analyzed data from the first two visits of a prospective, population-based cohort to study non-motor symptoms in parkinsonism (EPIPARK)23. We recruited non-PD participants via a mailed survey sent to 10,000 inhabitants of Lübeck, Germany, aged 50–79 years. Based on age, the residents’ registration office created a random sample from all inhabitants and provided the addresses. PD patients were recruited from the Department of Neurology at the University Medical Center Schleswig-Holstein, Campus Lübeck, Germany, and from the Neurological Center of Segeberg Clinics in Bad Segeberg, Germany (Fig. 1a).
Ethics approval
All participants gave written informed consent after approval by the local ethics committee of the University of Lübeck (AZ22-409; AZ09-069). The study was conducted in accordance with the Declaration of Helsinki.
Clinical examination
Neurological examinations using the Unified Parkinson’s Disease Rating Scale (UPDRS) were performed by movement disorder specialists24. PD was diagnosed according to the established clinical criteria for PD (United Kingdom Brain Bank Society (UKBBS) and Movement Disorder Society (MDS))25. Non-PD participants were classified into two groups: disease controls (DC) and healthy controls (HC) (Fig. 1a)26,27,28. The examination further included assessments of comorbidities (Table 2), medication, Levodopa equivalent daily dose29, and the Montreal Cognitive Assessment (MoCA). No participant in the DC group reported having dementia or other neurodegenerative conditions. We used the Beck Depression Inventory Ia (BDI Ia) to assess depressive symptoms and considered a BDI Ia score of 0–9 an indicator of none to minimal, 10–18 mild to moderate, 19–29 moderate to severe, and ≥ 30 severe depressive symptoms30. Participants were asked whether they had ever received a diagnosis of depression (lifetime self-report question). Subjective quality of life was assessed using the World Health Organization Quality of Life (WHO QoL) questionnaire using the 26-item version31. The scores of four domains (physical health, psychological, social relationships, and environment) were calculated, with higher scores corresponding to a higher quality of life. We differentiated between therapeutic and non-therapeutic doses of antidepressants according to the recommended therapeutic dosages to treat depression in adults.
Statistical analysis
Statistical analyses using SPSS28 (IBM SPSS Statistics for Macintosh, Armonk, NY: IBM Corp) comprised chi-square tests for categorical, Mann-Whitney U tests for ordinal, and t-tests or ANOVA for continuous variables. In addition, a multivariable logistic regression model was built to define factors (age, sex, group) associated with comorbidities and quality of life. A significance threshold of p < 0.05 was applied.
Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
References
Soh, S. E. et al. Determinants of health-related quality of life in people with Parkinson’s disease: A path analysis. Qual. Life Res. 22, 1543–1553 (2013).
Papapetropoulos, S., Ellul, J., Argyriou, A. A., Chroni, E. & Lekka, N. P. The effect of depression on motor function and disease severity of Parkinson’s disease. Clin. Neurol. Neurosurg. 108, 465–469 (2006).
Orayj, K. et al. Trend of recognizing depression symptoms and antidepressants use in newly diagnosed Parkinson’s disease: Population-based study. Brain Behav. 11, 1–8 (2021).
Reijnders, J. S. A. M., Ehrt, U., Weber, W. E. J., Aarsland, D. & Leentjens, A. F. G. A systematic review of prevalence studies of depression in Parkinson’s disease. Mov. Disord. 23, 183–189 (2008).
Lubomski, M., Davis, R. L. & Sue, C. M. Depression in Parkinson’s disease: Perspectives from an Australian cohort. J. Affect. Disord. 277, 1038–1044 (2020).
Cong, S. et al. Prevalence and clinical aspects of depression in Parkinson’s disease: a systematic review and meta‑analysis of 129 studies. Neurosci. Biobehav. Rev. 104749 (2022). https://doi.org/10.1016/j.neubiorev.2022.104749.
Gotham, A. M., Brown, R. G. & Marsden, C. D. Depression in Parkinson’s disease: A quantitative and qualitative analysis. J. Neurol. Neurosurg. Psychiatry 49, 381–389 (1986).
Miller, K. M. et al. Depression symptoms in movement disorders: Comparing Parkinson’s disease, dystonia, and essential tremor. Mov. Disord. 22, 666–672 (2007).
Marsh, L. Depression and Parkinson’s Disease: Current Knowledge. Curr. Neurol. Neurosci. Rep. 13, 409 (2013).
Reiff, J. et al. Subthreshold depression in Parkinson’s disease. Mov. Disord. 26, 1740–1743 (2011).
Prange, S., Klinger, H., Laurencin, C., Danaila, T. & Thobois, S. Depression in Patients with Parkinson’s Disease: Current Understanding of its Neurobiology and Implications for Treatment. Drugs Aging 39, 417–439 (2022).
Even, C. & Weintraub, D. Is depression in Parkinson’s Disease (PD) a specific entity? J. Affect. Disord. 139, 103–112 (2012).
Seppi, K. et al. Update on treatments for nonmotor symptoms of Parkinson’s disease—an evidence-based medicine review. Mov. Disord. 34, 180–198 (2019).
Espay, A. J. et al. Lack of independent mood-enhancing effect for dopaminergic medications in early Parkinson’s disease. J. Neurol. Sci. 402, 81–85 (2019).
Rabin, M. L., Earnhardt, M. C., Patel, A., Ganihong, I. & Kurlan, R. Postural, Bone, and Joint Disorders in Parkinson’s Disease. Mov. Disord. Clin. Pract. 3, 538 (2016).
Park, J. H. & Kang, S. Y. Dizziness in Parkinson’s disease patients is associated with vestibular function. Sci. Rep. 11, 1–6 (2021).
Heinzel, S. et al. Update of the MDS research criteria for prodromal Parkinson’s disease. Mov. Disord. 34, 1464–1470 (2019).
Laroia, H. & Louis, E. D. Association between essential tremor and other neurodegenerative diseases: what is the epidemiological evidence? Neuroepidemiology 37, 1–10 (2011).
McLean, G., Hindle, J. V., Guthrie, B. & Mercer, S. W. Co-morbidity and polypharmacy in Parkinson’s disease: Insights from a large Scottish primary care database. BMC Neurol. 17, 1–8 (2017).
Charoenngam, N., Rittiphairoj, T., Ponvilawan, B. & Prasongdee, K. Thyroid Dysfunction and Risk of Parkinson’s Disease: A Systematic Review and Meta-Analysis. Front. Endocrinol. (Lausanne) 13, 705 (2022).
Fu, X. et al. A systematic review and meta-analysis of serum cholesterol and triglyceride levels in patients with Parkinson’s disease. Lipids Health Dis. 19, 1–10 (2020).
Scorza, F. A., Fiorini, A. C., Scorza, C. A. & Finsterer, J. Cardiac abnormalities in Parkinson’s disease and Parkinsonism. J. Clin. Neurosci. 53, 1–5 (2018).
Kasten, M. et al. Cohort profile: A population-based cohort to study non-motor symptoms in Parkinsonism (EPIPARK). Int. J. Epidemiol 42, 128–128k (2013).
Goetz, C. G. et al. Teaching tape for the motor section of the unified Parkinson’s disease rating scale. Mov. Disord. 10, 263–266 (1995).
Postuma, R. B. et al. MDS clinical diagnostic criteria for Parkinson’s disease. Mov. Disord. 30, 1591–1601 (2015).
Tunc, S. et al. A population-based study on combined markers for early Parkinson’s disease. Mov. Disord. (2015). https://doi.org/10.1002/mds.26100.
Hughes, A. J., Daniel, S. E., Kilford, L. & Lees, A. J. Accuracy of clinical diagnosis of idiopathic Parkinson’s disease: A clinico-pathological study of 100 cases. J. Neurol. Neurosurg. Psychiatry 55, 181–184 (1992).
Louis, E. D. & Bennett, D. A. Mild Parkinsonian signs: An overview of an emerging concept. Mov. Disord. 22, 1681–1688 (2007).
Schade, S., Mollenhauer, B. & Trenkwalder, C. Levodopa Equivalent Dose Conversion Factors: An Updated Proposal Including Opicapone and Safinamide. Mov. Disord. Clin. Pract. 7, 343–345 (2020).
Beck, A. T., Ward, C. H., Mendelson, M., Mock, J. & Erbaugh, J. An Inventory for Measuring Depression. Arch. Gen. Psychiatry 4, 561–571 (1961).
Harper, A. et al. Development of the World Health Organization WHOQOL-BREF Quality of Life Assessment. Psychol. Med. 28, 551–558 (1998).
Funding
Open Access funding enabled and organized by Projekt DEAL.
Author information
Authors and Affiliations
Consortia
Contributions
1) Research project: A. Conception, B. Organization, C. Execution; 2) Statistical Analysis: A. Design, B. Execution, C. Review and Critique; 3) Manuscript: A. Writing of the first draft, B. Review and Critique. TU: 1B, 1 C, 2 A, 2B, 3 A, BH: 1B, 2 C, 3B; HH: 1B, 1 C, 2 C, 3B, JP: 1B, 1 C, 2 C, 3B, AB: 1B, 1 C, 2 C, 3B, MB: 1B, 1 C, 2 C, 3B, VT: 1B, 1 C, 2 C, 3B, AK: 1B, 1 C, 2 C, 3B, GNS: 2 C, 3B, EJV: 1B, 1 C, 2 C, 3B, CK: 1 A, 1B, 2 C, 3B, NB: 1 A,1B, 2 C, 3B. MK: 1 A,1B, 1 C, 2 C, 3B. All authors contributed to the article and approved the submitted version.
Corresponding author
Ethics declarations
Competing interests
T.U., B.H., A.B., M.B., H.H., J.P., V.T., A.K., G.N.S., E.J.V., and M.K. report no competing interests. C.K. reports a Medical advisor role to CENTOGENE GmbH for genetic testing of movement disorders excluding Parkinson’s disease, and to Retromer Therapeutics; N.B. reports consultancies to Abbott, Zambon, CENTOGENE GmbH, Bridgebio, Biomarin, Biogen, receiving honoraria from Abbott, Zambon, CENTOGENE GmbH, Bridgebio, Biomarin, and Biogen.
Additional information
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 licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Usnich, T., Hauptmann, B., Hanssen, H. et al. Depressive symptoms in Parkinson’s disease are insufficiently but more often treated than in other chronic conditions. npj Parkinsons Dis. 9, 113 (2023). https://doi.org/10.1038/s41531-023-00551-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41531-023-00551-8