LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han‐Chinese from mainland China
Identifieur interne : 000A55 ( Main/Exploration ); précédent : 000A54; suivant : 000A56LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han‐Chinese from mainland China
Auteurs : Zijuan Zhang [République populaire de Chine] ; Jean-Marc Burgunder [République populaire de Chine, Suisse, Singapour] ; Xingkai An [République populaire de Chine] ; Yan Wu [République populaire de Chine] ; Wenjun Chen [République populaire de Chine] ; Jinhong Zhang [République populaire de Chine] ; Yingcheng Wang [République populaire de Chine] ; Yanming Xu [République populaire de Chine] ; Yingru Gou [République populaire de Chine] ; Guanggu Yuan [République populaire de Chine] ; Xueye Mao [République populaire de Chine] ; Rong Peng [République populaire de Chine]Source :
- Movement Disorders [ 0885-3185 ] ; 2009-10-15.
English descriptors
- KwdEn :
Abstract
Mutations in LRRK2, the gene that encodes leucine‐rich repeat kinase 2 (LRRK2), are associated with autosomal dominant and sporadic forms of Parkinson's disease (PD) and are the most common genetic causes of PD. Recently, a R1628P variant has been reported as a risk factor for PD in Taiwan and Singapore. To determine the association of this variant and PD in the Han‐Chinese population from mainland China, we analyzed its frequency in a cohort of 600 patients and 459 unrelated healthy controls. Forty (6.7%) patients were heterozygous and 3 (0.5%) homozygous for the R1628P variant, which was significantly more frequent than in the controls [2.4% heterozygous and 0.0% homozygous, Odds ratio = 3.14, 95%CI: 1.60–6.17, P < 0.01]. Considering the age at onset, this difference was found only in late‐onset PD (older than 50) [Odds ratio = 3.76, 95% CI: 1.90–7.45, P < 0.01]. Our data confirms that the LRRK2 R1628P variant is associated with an increased risk to develop late onset PD in the ethnic Han‐Chinese population. © 2009 Movement Disorder Society
Url:
DOI: 10.1002/mds.22371
Affiliations:
- République populaire de Chine, Singapour, Suisse
- Canton de Berne
- Berne
- Université de Berne, Université nationale de Singapour
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Mutations in LRRK2, the gene that encodes leucine‐rich repeat kinase 2 (LRRK2), are associated with autosomal dominant and sporadic forms of Parkinson's disease (PD) and are the most common genetic causes of PD. Recently, a R1628P variant has been reported as a risk factor for PD in Taiwan and Singapore. To determine the association of this variant and PD in the Han‐Chinese population from mainland China, we analyzed its frequency in a cohort of 600 patients and 459 unrelated healthy controls. Forty (6.7%) patients were heterozygous and 3 (0.5%) homozygous for the R1628P variant, which was significantly more frequent than in the controls [2.4% heterozygous and 0.0% homozygous, Odds ratio = 3.14, 95%CI: 1.60–6.17, P < 0.01]. Considering the age at onset, this difference was found only in late‐onset PD (older than 50) [Odds ratio = 3.76, 95% CI: 1.90–7.45, P < 0.01]. Our data confirms that the LRRK2 R1628P variant is associated with an increased risk to develop late onset PD in the ethnic Han‐Chinese population. © 2009 Movement Disorder Society</div>
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