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Advanced Neurology





                                        SHORT COMMUNICATION
                                        Associations of common variants in TAAR5,

                                        OR6C70, and GBA with hyposmia in Han Chinese
                                        individuals with Parkinson’s disease



                                                              1†
                                                1†
                                        Yi-Lun Ge , Pu-Zhi Wang , Jia-Hui Yan , Wen Li , Jin-Ru Zhang , Hong Jin ,
                                                                          1
                                                                                                        1
                                                                                              1
                                                                                 1
                                                             2
                                                   1
                                        Ya-Ping Yang , Fen Wang , Dan Li , Jing Chen , Kai Li *, Cheng-Jie Mao *, and
                                                                     3
                                                                                                     1,3
                                                                                     1
                                                                               1
                                        Chun-Feng Liu 1,2,3
                                        1 Department of Neurology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China
                                        2 Institute of Neuroscience, Soochow University, Suzhou, Jiangsu, China
                                        3 Department of Neurology, Suqian First Hospital, Suqian, China
                                        Abstract
                                        Hyposmia is one of the cardinal symptoms of Parkinson’s disease (PD), with a
                                        considerably high prevalence rate in PD individuals. However, some individuals still
                                        retain normal olfactory function. Recent studies have shown that genetic factors
                                        may play a role in such a phenomenon. This study aimed to explore the potential
                                        genetic factors underlying the variation of olfactory function among PD individuals.
                                        Two hundred and three Han Chinese individuals with PD were recruited into this
            † These authors contributed equally   study. All the individuals underwent detailed clinical assessment conducted by
            to this work.               experienced neurologists. High-throughput sequencing was performed to identify
            *Corresponding authors:     gene variants associated with  PD.  TAAR5,  OR6C70, and  GBA were included  in the
            Kai Li (liskai@126.com)
            Cheng-Jie Mao               association analysis. In our study, 85 out of 203 individuals (41.9%) reported normal
            (drchengjiemao@163.com)     olfaction, and the other 118  (58.1%) reported hyposmia. Genotype and allele
                                        logistic regression models were applied to association analysis. We did not find any
            Citation: Ge Y-L, Wang P-Z,
            Yan J-H, et al., 2022, Associations   significant association of TAAR5 and OR6C70 with hyposmia. However, we found that
            of common variants in TAAR5,   GBA rs762488 was associated with increased hyposmia risk (P = 0.036, OR = 3.05,
            OR6C70 and GBA with hyposmia   95% CI = 1.08–8.63), while GBA rs1800438 was associated with decreased hyposmia
            in Han Chinese individuals with
            Parkinson’s disease. Adv Neuro,   risk (P = 0.032, OR = 0.47, 95% CI = 0.24–0.94). In conclusion, this study revealed the
            1(2): 71.                   association of GBA with hyposmia, indicating the genetic involvement in PD hyposmia
            https://doi.org/10.36922/an.v1i2.71  variation. However, we did not replicate previous results (TAAR5 and OR6C70) in this
            Received: April 17, 2022    study. Further studies with larger sample sizes in different populations are warranted.
            Accepted: May 31, 2022
            Published Online: July 27, 2022  Keywords: Parkinson’s disease; Olfaction; TAAR5; OR6C70; GBA
            Copyright: © 2022 Author(s).
            This is an Open Access article
            distributed under the terms of the
            Creative Commons Attribution   1. Introduction
            License, permitting distribution,
            and reproduction in any medium,   The olfactory system is the bodily structures that serve the sense of smell and enable
            provided the original work is   animals to identify the environmental information from specific odors . Hyposmia is
                                                                                                 [1]
            properly cited.
                                        characterized by the loss of odor detection, identification, or memory  and is a common
                                                                                              [2]
            Publisher’s Note: AccScience                                          [2,3]
            Publishing remains neutral with   symptom in a plethora of neurodegenerative diseases  .
            regard to jurisdictional claims in   More than half of Parkinson’s disease (PD) individuals reported hyposmia , which
                                                                                                      [4]
            published maps and institutional
            affiliations.               precedes the occurrence of motor symptoms. However, olfactory function remains
            Volume 1 Issue 2 (2022)                         1                        https://doi.org/10.36922/an.v1i2.71
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