Cognitive profile of LRRK2‐related Parkinson's disease. Issue 5 (4th February 2015)
- Record Type:
- Journal Article
- Title:
- Cognitive profile of LRRK2‐related Parkinson's disease. Issue 5 (4th February 2015)
- Main Title:
- Cognitive profile of LRRK2‐related Parkinson's disease
- Authors:
- Srivatsal, Sindhu
Cholerton, Brenna
Leverenz, James B.
Wszolek, Zbigniew K.
Uitti, Ryan J.
Dickson, Dennis W.
Weintraub, Daniel
Trojanowski, John Q.
Van Deerlin, Vivianna M.
Quinn, Joseph F.
Chung, Kathryn A.
Peterson, Amie L.
Factor, Stewart A.
Wood‐Siverio, Cathy
Goldman, Jennifer G.
Stebbins, Glenn T.
Bernard, Bryan
Ritz, Beate
Rausch, Rebecca
Espay, Alberto J.
Revilla, Fredy J.
Devoto, Johnna
Rosenthal, Liana S.
Dawson, Ted M.
Albert, Marilyn S.
Mata, Ignacio F.
Hu, Shu‐Ching
Montine, Kathleen S.
Johnson, Catherine
Montine, Thomas J.
Edwards, Karen L.
Zhang, Jing
Zabetian, Cyrus P.
… (more) - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="mds26161-sec-0001" sec-type="section"> <title>Background</title> <p>Increasing evidence suggests that genetic factors play a role in the variability associated with cognitive performance in Parkinson's disease (PD). Mutations in the <italic>LRRK2</italic> gene are the most common cause of monogenic PD; however, the cognitive profile of <italic>LRRK2</italic>‐related PD is not well‐characterized.</p> </sec> <sec id="mds26161-sec-0002" sec-type="section"> <title>Methods</title> <p>A cohort of 1, 447 PD patients enrolled in the PD Cognitive Genetics Consortium was screened for <italic>LRRK2</italic> mutations and completed detailed cognitive testing. Associations between mutation carrier status and cognitive test scores were assessed using linear regression models.</p> </sec> <sec id="mds26161-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>LRRK2</italic> mutation carriers (n = 29) demonstrated better performance on the Mini Mental State Examination (<italic>P</italic> = 0.03) and the Letter‐Number Sequencing Test (<italic>P</italic> = 0.005). A smaller proportion of <italic>LRRK2</italic> carriers were demented (<italic>P</italic> = 0.03).</p> </sec> <sec id="mds26161-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Our cross‐sectional study demonstrates better performance on certain cognitive tests, as well as lower rates of dementia in <italic>LRRK2</italic>‐related PD. Future<abstract abstract-type="main"> <title>Abstract</title> <sec id="mds26161-sec-0001" sec-type="section"> <title>Background</title> <p>Increasing evidence suggests that genetic factors play a role in the variability associated with cognitive performance in Parkinson's disease (PD). Mutations in the <italic>LRRK2</italic> gene are the most common cause of monogenic PD; however, the cognitive profile of <italic>LRRK2</italic>‐related PD is not well‐characterized.</p> </sec> <sec id="mds26161-sec-0002" sec-type="section"> <title>Methods</title> <p>A cohort of 1, 447 PD patients enrolled in the PD Cognitive Genetics Consortium was screened for <italic>LRRK2</italic> mutations and completed detailed cognitive testing. Associations between mutation carrier status and cognitive test scores were assessed using linear regression models.</p> </sec> <sec id="mds26161-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>LRRK2</italic> mutation carriers (n = 29) demonstrated better performance on the Mini Mental State Examination (<italic>P</italic> = 0.03) and the Letter‐Number Sequencing Test (<italic>P</italic> = 0.005). A smaller proportion of <italic>LRRK2</italic> carriers were demented (<italic>P</italic> = 0.03).</p> </sec> <sec id="mds26161-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Our cross‐sectional study demonstrates better performance on certain cognitive tests, as well as lower rates of dementia in <italic>LRRK2</italic>‐related PD. Future longitudinal studies are needed to determine whether <italic>LRRK2</italic> mutation carriers exhibit slower cognitive decline. © 2015 International Parkinson and Movement Disorder Society</p> </sec> </abstract> … (more)
- Is Part Of:
- Movement disorders. Volume 30:Issue 5(2015)
- Journal:
- Movement disorders
- Issue:
- Volume 30:Issue 5(2015)
- Issue Display:
- Volume 30, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 30
- Issue:
- 5
- Issue Sort Value:
- 2015-0030-0005-0000
- Page Start:
- 728
- Page End:
- 733
- Publication Date:
- 2015-02-04
- Subjects:
- Movement disorders -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mds.26161 ↗
- Languages:
- English
- ISSNs:
- 0885-3185
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5980.317200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3279.xml