Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's disease. (December 2018)

• Record Type: Journal Article
• Authors: Xu, Yuming; Liu, Chunfeng; Wang, Zhenyu; Wang, Ping; Hu, Guohua; Wang, Weizhi; Zhang, Baorong; Liang, Zhanhua; Xie, Anmu; Luo, Benyan; Lü, Wen; Sun, Shenggang; Shao, Ming; Liu, Zhuolin; Liu, Yiming; Ye, Qinyong; Chen, Haibo; Wan, Xinhua; Sheng, Xia; Liu, Shu-Ying; Zheng, Zheng; Gu, Zhu-Qin; Wang, Chao-Dong; Tang, Bei-Sha; Xu, Yan-Ming; Ma, Jing-Hong; Zhou, Yong-Tao; Feng, Tao; Chen, Sheng-Di; Chan, Piu
• Is Part Of: Parkinsonism & related disorders. Volume 57(2018)
• Page Start: 72
• Page End: 76
• Publication Date: 2018-12
• Subjects: Parkinson's disease -- Pre-diagnostic -- LRRK2 -- GBA; Parkinson's disease -- Periodicals; Movement disorders -- Periodicals; Movement Disorders -- Periodicals; Nerve Degeneration -- Periodicals; Nervous System Diseases -- Periodicals; Parkinson Disease -- Periodicals; Tremor -- Periodicals; Parkinson, Maladie de -- Périodiques; Parkinson's disease; 616.833
• DOI: 10.1016/j.parkreldis.2018.08.007
• Languages: English
• ISSNs: 1353-8020

Abstract

Abstract: Introduction: Glucocerebrosidase ( GBA ) mutations and leucine-rich repeat kinase 2 ( LRRK2 ) variants are the most common genetic risk factors for late-onset Parkinson's disease (PD). In this study, we aimed to investigate the differences in pre-diagnostic symptoms of PD associated with the variants. Methods: The participants were recruited from 24 centers across China and genotyped for LRRK2 G2385R and R1628P variants and GBA L444P mutation. Participants were surveyed with structural questionnaires for history of environmental exposure and living habits and interviewed to collect the time at onset of each symptoms before diagnosis. We compared the cumulative prevalence and manifestation pattern of symptoms between groups using multiple logistic regression, adjusting age and gender. Results: Total 1799 PD patients were recruited, including 226 patients with LRRK2 G2385R or R1628P variant, 44 with GBA L444P mutation, three with both LRRK2 and GBA mutation, and 1526 idiopathic patients. The cumulative prevalence of non-motor and typical motor symptoms did not differ between groups before diagnosis (P > 0.05). The manifestation sequences of non-motor symptoms were indistinguishable between the LRRK2 -carriers, GBA -carriers, and idiopathic PD subjects, and followed the sequence of constipation, hyposmia, sleep disorders, anxiety and depression, sexual dysfunction, urinary incontinency, dizziness and cognition. Slightly higher prevalence of hypomimia and micrographia were detected in the GBA -carriers. Conclusions: The prevalence of pre-diagnostic symptoms is almost indistinguishable between the LRRK2 -carriers, GBA -carriers, and idiopathic PD before diagnosis; the sequence of the manifestation of non-motor symptoms largely conforms to the Braak stage for both genetic-related and idiopathic late-onset PD. Highlights: GBA -, LRRK2 - and iPD had similar prevalence of pre-diagnostic symptoms. Manifestation of PD symptoms conforms to Braak stage regardless of gene factors. GBA -PD had slightly more micrographia and hypomimia before diagnosis.