Progranulin protein levels are differently regulated in plasma and CSF
Citation Manager Formats
Make Comment
See Comments
This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased.
Abstract
Objective: We aimed to investigate the relationship between plasma and CSF progranulin (PGRN) levels.
Methods: Plasma and CSF PGRN were measured in a cohort of 345 subjects from the Mayo Clinic Study of Aging by ELISA. Single nucleotide polymorphism genotyping was performed using TaqMan assays. Associations between PGRN and sex, age at sample collection, diagnosis, single nucleotide polymorphism genotypes (GRN, SORT1, and APOE), and Pittsburgh compound B score were explored separately in CSF and plasma using single variable linear regression models. Pearson partial correlation coefficient was used to estimate the correlation of PGRN in CSF and plasma.
Results: Plasma (p = 0.0031) and CSF (p = 0.0044) PGRN significantly increased with age, whereas plasma PGRN levels were 7% lower (p = 0.0025) and CSF PGRN levels 5% higher (p = 0.0024) in male compared with female participants. Correcting for age and sex, higher plasma PGRN was associated with higher CSF PGRN (partial r = 0.17, p = 0.004). In plasma, both rs5848 (GRN; p = 0.002) and rs646776 (SORT1; p = 3.56E-7) were associated with PGRN, while only rs5848 showed highly significant association in CSF (p = 5.59E-14). Age, sex, rs5848 genotype, and plasma PGRN together accounted for only 18% of the variability observed in CSF PGRN.
Conclusions: While some correlation exists between plasma and CSF PGRN, age, sex, and genetic factors differently affect PGRN levels. Therefore, caution should be taken when using plasma PGRN to predict PGRN changes in the brain. These findings further highlight that plasma PGRN levels may not accurately predict clinical features or response to future frontotemporal lobar degeneration therapies.
GLOSSARY
- Aβ=
- β-amyloid;
- AD=
- Alzheimer disease;
- DAT=
- dementia of the Alzheimer type;
- FTLD=
- frontotemporal lobar degeneration;
- MCI=
- mild cognitive impairment;
- MCSA=
- Mayo Clinic Study of Aging;
- mRNA=
- messenger RNA;
- PGRN=
- progranulin;
- PiB=
- Pittsburgh compound B;
- SNP=
- single nucleotide polymorphism;
- SORT1=
- sortilin 1;
- TDP=
- TAR DNA-binding protein
Footnotes
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
- Received June 25, 2013.
- Accepted in final form February 20, 2014.
- © 2014 American Academy of Neurology
AAN Members
We have changed the login procedure to improve access between AAN.com and the Neurology journals. If you are experiencing issues, please log out of AAN.com and clear history and cookies. (For instructions by browser, please click the instruction pages below). After clearing, choose preferred Journal and select login for AAN Members. You will be redirected to a login page where you can log in with your AAN ID number and password. When you are returned to the Journal, your name should appear at the top right of the page.
AAN Non-Member Subscribers
Purchase access
For assistance, please contact:
AAN Members (800) 879-1960 or (612) 928-6000 (International)
Non-AAN Member subscribers (800) 638-3030 or (301) 223-2300 option 3, select 1 (international)
Sign Up
Information on how to subscribe to Neurology and Neurology: Clinical Practice can be found here
Purchase
Individual access to articles is available through the Add to Cart option on the article page. Access for 1 day (from the computer you are currently using) is US$ 39.00. Pay-per-view content is for the use of the payee only, and content may not be further distributed by print or electronic means. The payee may view, download, and/or print the article for his/her personal, scholarly, research, and educational use. Distributing copies (electronic or otherwise) of the article is not allowed.
Letters: Rapid online correspondence
- Low plasma PGRN levels due to neutralizing PGRN-antibodies in patients with autoimmune diseases might lead to misdiagnosis of FTLD
- Lorenz Thurner, Saarland University Medical School, Jose Carreras Center for Immuno- and Gene Therapy and Internal Mlorenz.thurner@uks.eu
- Lorenz Thurner; Klaus-Dieter Preuss and Michael Pfreundschuh
Submitted May 22, 2014
REQUIREMENTS
You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
Dr. Victoria Leavitt and Dr. Laura Hancock
► Watch
Related Articles
- No related articles found.
Topics Discussed
Alert Me
Recommended articles
-
Articles
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN. Finch, M.M. Carrasquillo, M. Baker et al.Neurology, December 22, 2010 -
Articles
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degenerationR. Ghidoni, L. Benussi, M. Glionna et al.Neurology, September 03, 2008 -
Articles
APOE modifies the association between Aβ load and cognition in cognitively normal older adultsK. Kantarci, V. Lowe, S.A. Przybelski et al.Neurology, December 21, 2011 -
Articles
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRNJ. L. Whitwell, C. R. Jack, Jr, B. F. Boeve et al.Neurology, March 02, 2009