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Erschienen in: Neurological Sciences 8/2020

03.03.2020 | Original Article

Association between ZNF184 and symptoms of Parkinson’s disease in southern Chinese

verfasst von: Bei Zhang, Can Cui, Hongxiang Yu, Gang Li

Erschienen in: Neurological Sciences | Ausgabe 8/2020

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Abstract

Study objectives

The aim was to investigate the association between ZNF184 and symptoms of Parkinson’s disease (PD) in southern Chinese.

Methods

A total of 241 PD patients were recruited in this study. All patients were evaluated by Sniffin’ Sticks 16 (SS-16), Hamilton anxiety rating scale and Hamilton depression rating scale, 39-item Parkinson’s disease Questionnaire (PDQ-39) and MDS-Unified PD Rating Scale (MDS-UPDRS). Symptoms were also recorded.

Results

There was association of rapid eye movement sleep behavior disorder (RBD) under additive, dominant and overdominant model (p 0.039, additive; p 0.028, dominant; p 0.044, overdominant). We also found the association of excessive daytime sleepiness under the dominant model, the association of urgent urination or urinary incontinence under the recessive model and the association of sensitive to hot under the overdominant model (excessive daytime sleepiness: p 0.032, dominant; p 0.038, dominant; urgent urination or urgent incontinence: p 0.027, recessive; sensitive to hot: p, 0.027, overdominant).

Conclusions

ZNF184 rs9468199 was associated with the presence of RBD, excessive daytime sleepiness, urgent urination or urgent incontinence and sensitive to hot.
Literatur
2.
Zurück zum Zitat Bene R, Antic S, Budisic M, Lisak M, Trkanjec Z, Demarin V, Podobnik-Sarkanji S (2009) Parkinson’s disease. Acta Clin Croat 48(3):377–380PubMed Bene R, Antic S, Budisic M, Lisak M, Trkanjec Z, Demarin V, Podobnik-Sarkanji S (2009) Parkinson’s disease. Acta Clin Croat 48(3):377–380PubMed
7.
Zurück zum Zitat Chang D, Nalls MA, Hallgrimsdottir IB, Hunkapiller J, van der Brug M, Cai F, Kerchner GA, Ayalon G, Bingol B, Sheng M, Hinds D, Behrens TW, Singleton AB, Bhangale TR, Graham RR (2017) A meta-analysis of genome-wide association studies identifies 17 new Parkinson’s disease risk loci. Nat Genet 49(10):1511–1516. https://doi.org/10.1038/ng.3955 CrossRefPubMedPubMedCentral Chang D, Nalls MA, Hallgrimsdottir IB, Hunkapiller J, van der Brug M, Cai F, Kerchner GA, Ayalon G, Bingol B, Sheng M, Hinds D, Behrens TW, Singleton AB, Bhangale TR, Graham RR (2017) A meta-analysis of genome-wide association studies identifies 17 new Parkinson’s disease risk loci. Nat Genet 49(10):1511–1516. https://​doi.​org/​10.​1038/​ng.​3955 CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Postuma RB, Berg D, Stern M, Poewe W, Olanow CW, Oertel W, Obeso J, Marek K, Litvan I, Lang AE, Halliday G, Goetz CG, Gasser T, Dubois B, Chan P, Bloem BR, Adler CH, Deuschl G (2015) MDS clinical diagnostic criteria for Parkinson’s disease. Mov Disord 30(12):1591–1601. https://doi.org/10.1002/mds.26424 CrossRefPubMed Postuma RB, Berg D, Stern M, Poewe W, Olanow CW, Oertel W, Obeso J, Marek K, Litvan I, Lang AE, Halliday G, Goetz CG, Gasser T, Dubois B, Chan P, Bloem BR, Adler CH, Deuschl G (2015) MDS clinical diagnostic criteria for Parkinson’s disease. Mov Disord 30(12):1591–1601. https://​doi.​org/​10.​1002/​mds.​26424 CrossRefPubMed
11.
Zurück zum Zitat Goetz CG, Tilley BC, Shaftman SR, Stebbins GT, Fahn S, Martinez-Martin P, Poewe W, Sampaio C, Stern MB, Dodel R, Dubois B, Holloway R, Jankovic J, Kulisevsky J, Lang AE, Lees A, Leurgans S, LeWitt PA, Nyenhuis D, Olanow CW, Rascol O, Schrag A, Teresi JA, van Hilten JJ, LaPelle N (2008) Movement disorder society-sponsored revision of the unified Parkinson’s disease rating scale (MDS-UPDRS): scale presentation and clinimetric testing results. Mov Disord 23(15):2129–2170. https://doi.org/10.1002/mds.22340 CrossRefPubMed Goetz CG, Tilley BC, Shaftman SR, Stebbins GT, Fahn S, Martinez-Martin P, Poewe W, Sampaio C, Stern MB, Dodel R, Dubois B, Holloway R, Jankovic J, Kulisevsky J, Lang AE, Lees A, Leurgans S, LeWitt PA, Nyenhuis D, Olanow CW, Rascol O, Schrag A, Teresi JA, van Hilten JJ, LaPelle N (2008) Movement disorder society-sponsored revision of the unified Parkinson’s disease rating scale (MDS-UPDRS): scale presentation and clinimetric testing results. Mov Disord 23(15):2129–2170. https://​doi.​org/​10.​1002/​mds.​22340 CrossRefPubMed
14.
Zurück zum Zitat Mandaviya PR, Joehanes R, Aissi D, Kuhnel B, Marioni RE, Truong V, Stolk L, Beekman M, Bonder MJ, Franke L, Gieger C, Huan T, Ikram MA, Kunze S, Liang L, Lindemans J, Liu C, McRae AF, Mendelson MM, Muller-Nurasyid M, Peters A, Slagboom PE, Starr JM, Tregouet DA, Uitterlinden AG, van Greevenbroek MMJ, van Heemst D, van Iterson M, Wells PS, Yao C, Deary IJ, Gagnon F, Heijmans BT, Levy D, Morange PE, Waldenberger M, Heil SG, van Meurs JBJ (2017) Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes. PLoS One 12(10):e0182472. https://doi.org/10.1371/journal.pone.0182472 CrossRefPubMedPubMedCentral Mandaviya PR, Joehanes R, Aissi D, Kuhnel B, Marioni RE, Truong V, Stolk L, Beekman M, Bonder MJ, Franke L, Gieger C, Huan T, Ikram MA, Kunze S, Liang L, Lindemans J, Liu C, McRae AF, Mendelson MM, Muller-Nurasyid M, Peters A, Slagboom PE, Starr JM, Tregouet DA, Uitterlinden AG, van Greevenbroek MMJ, van Heemst D, van Iterson M, Wells PS, Yao C, Deary IJ, Gagnon F, Heijmans BT, Levy D, Morange PE, Waldenberger M, Heil SG, van Meurs JBJ (2017) Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes. PLoS One 12(10):e0182472. https://​doi.​org/​10.​1371/​journal.​pone.​0182472 CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Garcia S, Cano-Martinez LJ, Coral-Vazquez RM, Coronel-Perez A, Gomez-Diaz B, Toledo-Lozano CG, Gallegos-Arreola MP, Davila-Maldonado L, Jimenez-Hernandez DA, Alcaraz-Estrada SL, Lopez-Hernandez LB (2017) Analysis of the rs13306560 functional variant in the promoter region of the MTHFR gene in sporadic Parkinson’s disease. Neuro Endocrinol Lett 38(4):257–260PubMed Garcia S, Cano-Martinez LJ, Coral-Vazquez RM, Coronel-Perez A, Gomez-Diaz B, Toledo-Lozano CG, Gallegos-Arreola MP, Davila-Maldonado L, Jimenez-Hernandez DA, Alcaraz-Estrada SL, Lopez-Hernandez LB (2017) Analysis of the rs13306560 functional variant in the promoter region of the MTHFR gene in sporadic Parkinson’s disease. Neuro Endocrinol Lett 38(4):257–260PubMed
21.
Zurück zum Zitat Hashida H, Goto J, Zhao N, Takahashi N, Hirai M, Kanazawa I, Sakaki Y (1998) Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA). Genomics 54(1):50–58. https://doi.org/10.1006/geno.1998.5516 CrossRefPubMed Hashida H, Goto J, Zhao N, Takahashi N, Hirai M, Kanazawa I, Sakaki Y (1998) Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA). Genomics 54(1):50–58. https://​doi.​org/​10.​1006/​geno.​1998.​5516 CrossRefPubMed
Metadaten
Titel
Association between ZNF184 and symptoms of Parkinson’s disease in southern Chinese
verfasst von
Bei Zhang
Can Cui
Hongxiang Yu
Gang Li
Publikationsdatum
03.03.2020
Verlag
Springer International Publishing
Erschienen in
Neurological Sciences / Ausgabe 8/2020
Print ISSN: 1590-1874
Elektronische ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-020-04309-5

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