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dc.contributor.authorRaj, S.
dc.contributor.authorThalamuthu, A.
dc.contributor.authorArmstrong, Nicola
dc.contributor.authorWright, M.J.
dc.contributor.authorKwok, J.B.
dc.contributor.authorTrollor, J.N.
dc.contributor.authorAmes, D.
dc.contributor.authorSchofield, P.R.
dc.contributor.authorBrodaty, H.
dc.contributor.authorSachdev, P.S.
dc.contributor.authorMather, K.A.
dc.date.accessioned2021-11-18T02:06:56Z
dc.date.available2021-11-18T02:06:56Z
dc.date.issued2021
dc.identifier.citationRaj, S. and Thalamuthu, A. and Armstrong, N.J. and Wright, M.J. and Kwok, J.B. and Trollor, J.N. and Ames, D. et al. 2021. Investigating olfactory gene variation and odour identification in older adults. Genes. 12 (5): Article No. 669.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/86406
dc.identifier.doi10.3390/genes12050669
dc.description.abstract

Ageing is associated with a decrease in odour identification. Additionally, deficits in olfaction have been linked to age-related disease and mortality. Heritability studies suggest genetic variation contributes to olfactory identification. The olfactory receptor (OR) gene family is the largest in the human genome and responsible for overall odour identification. In this study, we sought to find olfactory gene family variants associated with individual and overall odour identification and to examine the relationships between polygenic risk scores (PRS) for olfactory-related phenotypes and olfaction. Participants were Caucasian older adults from the Sydney Memory and Ageing Study and the Older Australian Twins Study with genome-wide genotyping data (n = 1395, mean age = 75.52 ± 6.45). The Brief-Smell Identification Test (BSIT) was administered in both cohorts. PRS were calculated from independent GWAS summary statistics for Alzheimer’s disease (AD), white matter hyperintensities (WMH), Parkinson’s disease (PD), hippocampal volume and smoking. Associations with olfactory receptor genes (n = 967), previously identified candidate olfaction-related SNPs (n = 36) and different PRS with BSIT scores (total and individual smells) were examined. All of the relationships were analysed using generalised linear mixed models (GLMM), adjusted for age and sex. Genes with suggestive evidence for odour identification were found for 8 of the 12 BSIT items. Thirteen out of 36 candidate SNPs previously identified from the literature were suggestively associated with several individual BSIT items but not total score. PRS for smoking, WMH and PD were negatively associated with chocolate identification. This is the first study to conduct genetic analyses with individual odorant identification, which found suggestive olfactory-related genes and genetic variants for multiple individual BSIT odours. Replication in independent and larger cohorts is needed.

dc.languageEnglish
dc.publisherMDPI
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectGenetics & Heredity
dc.subjectolfaction
dc.subjectodour identification
dc.subjectgenetics
dc.subjectageing
dc.subjectSYDNEY MEMORY
dc.subjectASSOCIATION
dc.subjectPOPULATION
dc.subjectIMPAIRMENT
dc.subjectCOHORT
dc.subjectSMELL
dc.titleInvestigating olfactory gene variation and odour identification in older adults
dc.typeJournal Article
dcterms.source.volume12
dcterms.source.number5
dcterms.source.issn2073-4425
dcterms.source.titleGenes
dc.date.updated2021-11-18T02:06:55Z
curtin.note

© 2021 The Authors. Published by MDPI Publishing.

curtin.departmentSchool of Elec Eng, Comp and Math Sci (EECMS)
curtin.accessStatusOpen access
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidArmstrong, Nicola [0000-0002-4477-293X]
curtin.identifier.article-numberARTN 669
dcterms.source.eissn2073-4425
curtin.contributor.scopusauthoridArmstrong, Nicola [14631735000]


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