Neuropsychiatric Disease and Treatment (Jul 2019)

Apolipoprotein E e4 allele is associated with extrapyramidal symptoms in Alzheimer’s disease

  • Chang YP,
  • Chou MC,
  • Lai CL,
  • Chien I,
  • Yang YH

Journal volume & issue
Vol. Volume 15
pp. 1915 – 1919

Abstract

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Yang-Pei Chang,1 Mei-Chuan Chou,1–3 Chiou-Lian Lai,2,4–5 I Chien,1 Yuan-Han Yang1,21Department of Neurology, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan; 2Department of Neurology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan; 3Graduate Institute of Clinical Medicine, Kaohsiung Medical University, Kaohsiung City, Taiwan; 4Department of Neurology, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan; 5Department of Neurology, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung Medical University, Kaohsiung, TaiwanBackground: Extrapyramidal symptoms (EPS) are not uncommon in Alzheimer’s disease (AD). As apolipoprotein E(APOE) e4 allele is a major risk factor for late-onset AD, we intend to examine the association between APOE genotype and the development of EPS in AD.Method: This study describes two hundred and fifty-five clinically diagnosed AD patients aged 72 to 80 years from 2010 to 2014. We reviewed the medical charts to determine the development of EPS. APOE genotypes were also confirmed.Results: APOE e4 allele was detected in 74 patients (29%) and rigidity was among the most common EPS (61%). After adjusting the age, gender, baseline clinical dementia rating, we found AD patients carrying APOE e4 allele are more likely to develop EPS (OR: 4.515, p=0.033).Conclusion: This study demonstrates the higher coexistence of EPS in AD patients with APOE e4 allele. Furthermore, the identification of APOE e4 allele in the development of EPS in AD patients supports the hypothesis that EPS may be partially attributed to AD pathology.Keywords: Alzheimer’s disease, extrapyramidal symptoms, apolipoprotein e e4

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