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

J Parkinsons Dis. 2022;12(1):421-436. doi: 10.3233/JPD-212892.

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.

Keywords: DaTScan; Parkinson’s disease; motor; non-motor; sex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products*
  • Biomarkers / cerebrospinal fluid
  • Disease Progression
  • Female
  • Humans
  • Male
  • Parkinson Disease* / cerebrospinal fluid
  • Parkinson Disease* / diagnosis

Substances

  • Biological Products
  • Biomarkers