Gorostidi A, Ruiz-Martínez J, Lopez de Munain A, Alzualde A, Martí Massó J F
Neurogenetics Laboratory, Hospital Donostia, Donostia-San Sebastián, Gipuzkoa, Spain.
Neurogenetics. 2009 Apr;10(2):157-9. doi: 10.1007/s10048-008-0162-0. Epub 2008 Nov 20.
Mutations in LRRK2 gene are the most frequent cause of Parkinson's disease (PD) described, but their prevalence varies between populations. Patients, 418, with PD and 138 unrelated controls from the Basque Country were screened for LRRK2 G2019S and R1441G mutations. Of the patients, 3.82% were heterozygous carriers of G2019S and 13.15% of R1441G. G2019S frequency was higher in non-Basque population (6.0%), while R1441G was more common in Basque origin population (22.4%). Our conclusion is that both G2019S and R1441G mutations' frequency varies markedly between Basque and non-Basque origin population reinforcing the importance of ethnicity consideration when establishing mutation prevalence.
LRRK2基因的突变是已描述的帕金森病(PD)最常见的病因,但其在不同人群中的患病率有所不同。对来自巴斯克地区的418例帕金森病患者和138例无关对照进行了LRRK2基因G2019S和R1441G突变筛查。在患者中,3.82%是G2019S杂合携带者,13.15%是R1441G杂合携带者。G2019S在非巴斯克人群中的频率较高(6.0%),而R1441G在巴斯克裔人群中更为常见(22.4%)。我们的结论是,G2019S和R1441G突变的频率在巴斯克裔和非巴斯克裔人群之间存在显著差异,这进一步强调了在确定突变患病率时考虑种族因素的重要性。