Frontiers in Neurology (Jul 2023)

Sex differences in alpha-synucleinopathies: a systematic review

  • Kausar Raheel,
  • Gemma Deegan,
  • Gemma Deegan,
  • Irene Di Giulio,
  • Irene Di Giulio,
  • Diana Cash,
  • Diana Cash,
  • Diana Cash,
  • Katarina Ilic,
  • Katarina Ilic,
  • Katarina Ilic,
  • Valentina Gnoni,
  • Valentina Gnoni,
  • K. Ray Chaudhuri,
  • Panagis Drakatos,
  • Panagis Drakatos,
  • Rosalyn Moran,
  • Ivana Rosenzweig,
  • Ivana Rosenzweig

DOI
https://doi.org/10.3389/fneur.2023.1204104
Journal volume & issue
Vol. 14

Abstract

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BackgroundPast research indicates a higher prevalence, incidence, and severe clinical manifestations of alpha-synucleinopathies in men, leading to a suggestion of neuroprotective properties of female sex hormones (especially estrogen). The potential pathomechanisms of any such effect on alpha-synucleinopathies, however, are far from understood. With that aim, we undertook to systematically review, and to critically assess, contemporary evidence on sex and gender differences in alpha-synucleinopathies using a bench-to-bedside approach.MethodsIn this systematic review, studies investigating sex and gender differences in alpha-synucleinopathies (Rapid Eye Movement (REM) Behavior Disorder (RBD), Parkinson’s Disease (PD), Dementia with Lewy Bodies (DLB), Multiple System Atrophy (MSA)) from 2012 to 2022 were identified using electronic database searches of PubMed, Embase and Ovid.ResultsOne hundred sixty-two studies were included; 5 RBD, 6 MSA, 20 DLB and 131 PD studies. Overall, there is conclusive evidence to suggest sex-and gender-specific manifestation in demographics, biomarkers, genetics, clinical features, interventions, and quality of life in alpha-synucleinopathies. Only limited data exists on the effects of distinct sex hormones, with majority of studies concentrating on estrogen and its speculated neuroprotective effects.ConclusionFuture studies disentangling the underlying sex-specific mechanisms of alpha-synucleinopathies are urgently needed in order to enable novel sex-specific therapeutics.

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