The Open Neurology Journal

ISSN: 1874-205X ― Volume 13, 2019

The Insertion/Deletion Polymorphism of the Angiotensin Converting Enzyme (ACE) in Parkinson’s Disease

Spiridon Papapetropoulos*, 1, 2, Kostantinos Glynos3, Zongmin Zhou3, Stylianos E Orfanos3, Georgia Mitsi4, Andreas Papapetropoulos5
1 Department of Neurology University of Miami, Miller School of Medicine, USA
2 Department of Neurology, Regional University Hospital of Patras, Greece
3 George P. Livanos-Marianthi Simou Laboratories, Department of Critical Care and Pulmonary Services, Evangelismos Hospital, University of Athens School of Medicine, Athens, Greece
4 University of Miami/Humana Health Research Services, USA
5 Laboratory of Molecular Pharmacology, Department of Pharmacy, University of Patras, Patras, Greece


Parkinson’s disease (PDI is a neurodegenerative disorder of unknown etiology. Both genetic and environmental factors are thought to be implicated to some extent. The ACE gene insertion/deletion (I/D) polymorphism has been associated with common neurodegenerative disorders that share similar clinical and neuropathological features with PD (Alzheimer’s disease). In this study we set out to examine the role of the ACE gene insertion/deletion (I/D) polymorphism in Parkinson’s disease (PD).

We conducted a case-control association study among 77 PD patients and 50 non-PD controls from Greece.

The genotype frequencies for II, ID, and DD were 39, 48, and 13%, respectively, in the PD group and 32, 50, and 18% in the control group. Although the DD frequency was higher in the case group statistical significance was not reached.

We conclude that although disease modifying effects cannot be excluded, the ACE insertion/deletion polymorphism is unlikely to be an important determinant of susceptibility to PD in this population.

Keywords: Angiotensin Converting Enzyme, ACE, Polymorphism, Insertion-deletion, Parkinson’s disease, Association study.

Article Information

Identifiers and Pagination:

Year: 2008
Volume: 2
First Page: 66
Last Page: 70
Publisher Id: TONEUJ-2-66
DOI: 10.2174/1874205X00802010066

Article History:

Received Date: 16/4/2008
Revision Received Date: 17/9/2008
Acceptance Date: 19/9/2008
Electronic publication date: 31/10/2008
Collection year: 2008

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© Papapetropoulos et al.; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

* Address correspondence to this author at the Department of Neurology, University of Miami, Miller School of Medicine, Clinical Research Building 1120 N.W. 14th Street, 13th Floor Room 1349, Miami, FL 33136, USA; Tel: (+1)(305) 243-8461/(+1)(305) 243-9620; Fax: (+1)(305) 243-3321; E-mail:


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