Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

Matthew J. Farrer, Jeremy T. Stone, Chin Hsien Lin, Justus C. Dächsel, Mary M. Hulihan, Kristoffer Haugarvoll, Owen A. Ross, Ruey Meei Wu

Research output: Contribution to journalArticle

154 Scopus citations

Abstract

The goal of genetic association studies is to identify common (>5%) risk factors in complex disease traits. Herein we describe the first replicable 'functional' risk allele for Parkinson's disease. The leucine-rich repeat kinase 2 (Lrrk2) G2385R substitution is associated with familial parkinsonism, late-, and early-onset Parkinson's disease in ethnic Chinese Taiwanese. Crucially, we provide evidence of identity-by-descent and suggest that Lrrk2 G2385R carriers originate from one ancestor some 4800 years ago, at the start of Chinese civilization. Moreover, our findings demonstrate that common genetic coding variants contribute to Parkinson's disease in a population specific manner which may have important implications for future genome-wide association studies.

Original languageEnglish (US)
Pages (from-to)89-92
Number of pages4
JournalParkinsonism and Related Disorders
Volume13
Issue number2
DOIs
StatePublished - Mar 1 2007

Keywords

  • Asia
  • Lrrk2
  • Parkinson's disease

ASJC Scopus subject areas

  • Neurology
  • Geriatrics and Gerontology
  • Clinical Neurology

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    Farrer, M. J., Stone, J. T., Lin, C. H., Dächsel, J. C., Hulihan, M. M., Haugarvoll, K., Ross, O. A., & Wu, R. M. (2007). Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia. Parkinsonism and Related Disorders, 13(2), 89-92. https://doi.org/10.1016/j.parkreldis.2006.12.001