Sulfotransferase 1A3/4 copy number variation is associated with neurodegenerative disease

No Thumbnail Available
File version
Author(s)
Butcher, NJ
Horne, MK
Mellick, GD
Fowler, CJ
Masters, CL
Minchin, RF
Griffith University Author(s)
Primary Supervisor
Other Supervisors
Editor(s)
Date
2018
Size
File type(s)
Location
License
Abstract

The cytosolic aryl sulfotransferase genes SULT1A3 and SULT1A4 are located on chromosome 16p11.2 in a region of chromosomal instability. SULT1A3/4 are important enzymes in the metabolism of catecholamines linked to neurodegenerative diseases such as Parkinson’s and Alzheimer’s. In the present study, copy number variation of the SULT1A3/4 genes in healthy individuals, as well as a cohort of Parkinson’s disease and Alzheimer’s disease patients was examined. In all subjects, SULT1A3/4 copy number varied from 1 to 10. In Alzheimer’s disease patients, there was a significantly lower copy number compared to controls, and a positive correlation between copy number and age of disease onset. By contrast, there were no differences in Parkinson’s disease patients. However, when early-onset Parkinson’s disease was evaluated separately, there appeared to be an association with gene copy number and risk. The current study shows that these neurodegenerative diseases may be related to SULT1A3/4 copy number.

Journal Title

The Pharmacogenomics Journal

Conference Title
Book Title
Edition
Volume

18

Issue
Thesis Type
Degree Program
School
Publisher link
Patent number
Funder(s)
Grant identifier(s)
Rights Statement
Rights Statement
Item Access Status
Note
Access the data
Related item(s)
Subject

Pharmacology and pharmaceutical sciences

Pharmacology and pharmaceutical sciences not elsewhere classified

Persistent link to this record
Citation
Collections