Sex-Related Longitudinal Change of Motor, Non-Motor, and Biological Features in Early Parkinson’s Disease

Author:

Picillo Marina1,LaFontant David-Erick2,Bressman Susan3,Caspell-Garcia Chelsea2,Coffey Christopher2,Cho Hyunkeun Ryan2,Burghardt Elliot L.2,Dahodwala Nabila4,Saunders-Pullman Rachel3,Tanner Caroline M.5,Amara Amy W.6,

Affiliation:

1. Center for Neurodegenerative Diseases (CEMAND), Department of Medicine, Surgery and Dentistry, Neuroscience Section, University of Salerno, Italy

2. Department of Biostatistics, The University of Iowa, Iowa City, IA, USA

3. Department of Neurology, Icahn School of Medicine at Mount Sinai and Mount Sinai Beth Israel, New York, NY, USA

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

5. Weill Institute for Neuroscience, Department of Neurology, University of California–San Francisco, & Parkinson’s Disease Research Education and Clinical Center, San Francisco Veterans Affairs Health Care System, San Francisco, CA, USA

6. Department of Neurology, University of Alabama at Birmingham, Birmingham, AL, USA

Abstract

Background: Investigation of sex-related motor and non-motor differences and biological markers in Parkinson’s disease (PD) may improve precision medicine approach. Objective: To examine sex-related longitudinal changes in motor and non-motor features and biologic biomarkers in early PD. Methods: We compared 5-year longitudinal changes in de novo, untreated PD men and women (at baseline N = 423; 65.5%male) of the Parkinson’s Progression Markers Initiative (PPMI), assessing motor and non-motor manifestations of disease; and biologic measures in cerebrospinal fluid (CSF) and dopamine transporter deficit on DaTscanTM uptake. Results: Men experienced greater longitudinal decline in self-reported motor (p < 0.001) and non-motor (p = 0.009) aspects of experiences of daily living, such that men had a yearly increase in MDS-UPDRS part II by a multiplicative factor of 1.27 compared to women at 0.7, while men had a yearly increase in MDS-UPDRS part I by a multiplicative factor of 0.98, compared to women at 0.67. Compared to women, men had more longitudinal progression in clinician-assessed motor features in the ON medication state (p = 0.010) and required higher dopaminergic medication dosages over time (p = 0.014). Time to reach specific disease milestones and longitudinal changes in CSF biomarkers and DaTscanTM uptake were not different by sex. Conclusion: Men showed higher self-assessed motor and non-motor burden of disease, with possible contributions from suboptimal dopaminergic therapeutic response in men. However, motor features of disease evaluated with clinician-based scales in the OFF medication state, as well as biological biomarkers do not show specific sex-related progression patterns.

Publisher

IOS Press

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

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