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Apolipoprotein E ε4 and risk of freezing of gait in early Parkinson’s disease

R. Kim, J.S Jun, H.J Kim, B.S Jeon (Incheon, Republic of Korea)

Meeting: MDS Virtual Congress 2020

Abstract Number: 479

Keywords: Parkinsonism

Category: Parkinson's Disease: Genetics

Objective: To investigate the association between Apolipoprotein E (APOE) genotype and freezing of gait (FOG) in Parkinson’s disease (PD).

Background: This cohort study using the PPMI data included 339 early PD patients who were divided into APOE ε4-positive (n=88) and ε4-negative (n=251) groups. They were followed-up over up to 6 years to identify the development of FOG. To investigate the influence of CSF β‐amyloid 1-42 (Aβ42) on their association, the patients were additionally dichotomized into “high-level” and “low-level” groups according to CSF Aβ42 levels (cutoff=258 pg/ml).

Method: This cohort study using the PPMI data included 339 early PD patients who were divided into APOE ε4-positive (n=88) and ε4-negative (n=251) groups. They were followed-up over up to 6 years to identify the development of FOG. To investigate the influence of CSF β‐amyloid 1-42 (Aβ42) on their association, the patients were additionally dichotomized into “high-level” and “low-level” groups according to CSF Aβ42 levels (cutoff=258 pg/ml).

Results: At baseline, the APOE ε4-positive group had lower CSF Aβ42 levels than the APOE ε4-negative group. During a median follow-up of 5.0 years, the APOE ε4-positive group had a higher incidence of FOG than the APOE ε4-negative group. In the multivariable Cox model excluding CSF Aβ42, APOE ε4 was a significant predictor of FOG. However, after adding CSF Aβ42 in the model, APOE ε4 did not survive, whereas lower CSF Aβ42 levels were associated with FOG. In subgroup analyses according to CSF Aβ42 levels, the effect of APOE ε4 allele was not found in the “low-level” group. However, in the “high-level” group, the APOE ε4 allele independently increased the risk of FOG, and this association was stronger than the association with CSF Aβ42.

Conclusion: We found the APOE ε4 allele as a novel genetic risk factor for FOG in early PD. This association seemed to be mainly mediated by Aβ-dependent pathways, but its Aβ-independent effects might also contribute to the development of FOG.

To cite this abstract in AMA style:

R. Kim, J.S Jun, H.J Kim, B.S Jeon. Apolipoprotein E ε4 and risk of freezing of gait in early Parkinson’s disease [abstract]. Mov Disord. 2020; 35 (suppl 1). https://www.mdsabstracts.org/abstract/apolipoprotein-e-%ce%b54-and-risk-of-freezing-of-gait-in-early-parkinsons-disease/. Accessed June 15, 2025.
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