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Limb-shaking transient ischemic attacks: case report and review of literature
Authors:Saad Ali  Muhib Alam Khan  Bhojo Khealani
Institution:1. Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, 199 Tung-Hwa North Road, 10591, Taipei, Taiwan
2. Laboratory of Neurogenetics, National Institute on Aging Porter Neuroscience Building, 35, Convent Drive, 20892, Bethesda, MD, USA
3. Reta Lila Weston Institute of Neurological Studies, University College London, 1 WakefieldStreet, WC1 N1PJ, London, UK
4. Molecular Genetics Unit, National Institute on Aging, National Institutes of Health, 20892, Bethesda, MD, USA
Abstract:

Background

Parkinson's disease (PD) is the most common neurodegenerative movement disorder, characterized clinically by resting tremor, bradykinesia, postural instability and rigidity. The prevalence of PD is approximately 2% of the population over 65 years of age and 1.7 million PD patients (age ≥ 55 years) live in China. Recently, a common LRRK2 variant Gly2385Arg was reported in ethnic Chinese PD population in Taiwan. We analyzed the frequency of this variant in our independent PD case-control population of Han Chinese from Taiwan.

Methods

305 patients and 176 genetically unrelated healthy controls were examined by neurologists and the diagnosis of PD was based on the published criteria. The region of interest was amplified with standard polymerase chain reaction (PCR). PCR fragments then were directly sequenced in both forward and reverse directions. Differences in genotype frequencies between groups were assessed by the X 2 test, while X 2 analysis was used to test for the Hardy-Weinberg equilibrium.

Results

Of the 305 patients screened we identified 27 (9%) with heterozygous G2385R variant. This mutation was only found in 1 (0.5%) in our healthy control samples (odds ratio = 16.99, 95% CI: 2.29 to 126.21, p = 0.0002). Sequencing of the entire open reading frame of LRRK2 in G2385R carriers revealed no other variants.

Conclusion

These data suggest that the G2385R variant contributes significantly to the etiology of PD in ethnic Han Chinese individuals. With consideration of the enormous and expanding aging Chinese population in mainland China and in Taiwan, this variant is probably the most common known genetic factor for PD worldwide.
Keywords:
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