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. Author manuscript; available in PMC: 2024 Feb 1.
Published in final edited form as: Parkinsonism Relat Disord. 2023 Jan 16;107:105285. doi: 10.1016/j.parkreldis.2023.105285

Table 3.

Gaps and Research Opportunities Relating to Sex and Gender in DLB

Knowledge or Care
Gap
Potential Research Opportunities
Differences in presenting phenotype and clinicopathological correlations Large-scale clinicopathologic studies with assessment of both sex and gender
Risk Factors - Studies examining genetic risk factors (e.g. APOE, GBA)
- Studies investigating hormonal influences (pregnancy, menopause, estrogen/hormone replacement therapy, androgen-deprivation treatment, transgender health, etc.)
- Evaluation of environmental exposures, comorbidities (cerebrovascular risk factors, etc.), demographics (education, ethnicity/race, age, etc.) and how they may differ by sex/gender
Under- or misdiagnosis Studies of pragmatic approaches to increase recognition of DLB generally and with sex- and gender-specific considerations
Biomarker differences by sex/gender Targeted recruitment of diverse populations for biomarker studies and subanalyses by sex and gender
Progression Natural history studies with diverse recruitment (including by sex/gender) and associated subanalyses
Treatment - Stratifying by sex/gender during randomization
- Inclusion of biomarkers in DLB treatment trials (as this may be different by sex and affect treatment response)
- Assessment of treatment response by sex/gender
Caregiving - Research on differential caregiver experiences by sex and gender, access to healthcare/resources, and potential value of specific interventions