Association of Baseline Depression and Anxiety with Longitudinal Health Outcomes in Parkinson's Disease

Author:

Shi Yiwen1ORCID,Dobkin Roseanne2,Weintraub Daniel134ORCID,Cho Hyunkeun R.5,Caspell‐Garcia Chelsea5,Bock Meredith6ORCID,Brown Ethan6ORCID,Aarsland Dag78,Dahodwala Nabila19

Affiliation:

1. Department of Neurology, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

2. Department of Psychiatry Rutgers University, Robert Wood Johnson Medical School New Brunswick New Jersey USA

3. Department of Psychiatry, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

4. Department of Veterans Affairs Parkinson's Disease Research, Education and Clinical Center Philadelphia Pennsylvania USA

5. Department of Biostatistics, College of Public Health University of Iowa Iowa City Iowa USA

6. Department of Neurology, The San Francisco Veterans Affairs Medical Center University of California, San Francisco San Francisco California USA

7. Department of Old Age Psychiatry Institute of Psychiatry, Psychology & Neuroscience, King's College London London UK

8. Centre for Age‐Related Diseases Stavanger University Hospital Stavanger Norway

9. Leonard Davis Institute of Health Economics University of Pennsylvania Philadelphia Pennsylvania USA

Abstract

AbstractBackgroundAnxiety and depression are common non‐motor symptoms in Parkinson's disease (PD) but remain under‐recognized and under‐treated.ObjectivesTo evaluate functional outcomes associated with baseline anxiety or depression and effects related to the initiation of new psychiatric treatment.MethodsWe analyzed 7 years of data from patients with de novo PD enrolled in the Parkinson's Progression Markers Initiative. Longitudinal regression models evaluated the association between baseline anxiety and depression with Schwab and England (SE) and MDS‐UPDRS total scores over time. Cox proportional hazard models assessed effects of baseline anxiety and depression on time to initiation of dopaminergic therapy. Piecewise linear regression models examined the association of treatment initiation for anxiety and depression with SE and MDS‐UPDRS.Results490 participants with baseline depression and anxiety data were included. Anxiety and depression were associated with lower SE (anxiety: β = −1.31, P = 0.038, depression: β = −1.96, P = 0.012, co‐morbid: β = −2.70, P = 0.003) and higher MDS‐UPDRS scores (anxiety: β = 5.37, P < 0.001, depression: β = 9.17, P < 0.001, co‐morbid: β = 10.50, P < 0.001) longitudinally. Anxiety was associated with faster time to dopamine replacement therapy initiation (HR 1.30, 95% CI 1.03–1.66, P = 0.03). 16 participants with anxiety initiated treatment for anxiety, which was associated with subsequent lower levodopa daily dose (slope change = −218.49, P = 0.018). 10 participants with depression initiated treatment of depression, which was associated with reduced MDS‐UPDRS total scores (slope change = −8.3, P < 0.001) and higher SE scores (slope change = 5.99, P = 0.004).ConclusionsAnxiety and depression at PD onset are associated with multiple negative longitudinal trajectories. However, preliminary findings suggest that anxiety and depression treatment may be linked with improved motor and non‐motor outcomes.

Publisher

Wiley

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