• E Sidransky, M A Nalls, J O Aasly, J Aharon-Peretz, G Annesi, E R Barbosa, A Bar-Shira, D Berg, J Bras, A Brice, C-M Chen, L N Clark, C Condroyer, E V De Marco, A Dürr, M J Eblan, S Fahn, M J Farrer, H-C Fung, Z Gan-Or, T Gasser, R Gershoni-Baruch, N Giladi, A Griffith, T Gurevich, C Januario, P Kropp, A E Lang, G-J Lee-Chen, S Lesage, K Marder, I F Mata, A Mirelman, J Mitsui, I Mizuta, G Nicoletti, C Oliveira, R Ottman, A Orr-Urtreger, L V Pereira, A Quattrone, E Rogaeva, A Rolfs, H Rosenbaum, R Rozenberg, A Samii, T Samaddar, C Schulte, M Sharma, A Singleton, M Spitz, E-K Tan, N Tayebi, T Toda, A R Troiano, S Tsuji, M Wittstock, T G Wolfsberg, Y-R Wu, C P Zabetian, Y Zhao, and S G Ziegler.
• Section on Molecular Neurogenetics, Medical Genetics Branch, NHGRI, National Institutes of Health, Bethesda, MD 20892-3708, USA. sidranse@mail.nih.gov
• N. Engl. J. Med. 2009 Oct 22; 361 (17): 165116611651-61.

BackgroundRecent studies indicate an increased frequency of mutations in the gene encoding glucocerebrosidase (GBA), a deficiency of which causes Gaucher's disease, among patients with Parkinson's disease. We aimed to ascertain the frequency of GBA mutations in an ethnically diverse group of patients with Parkinson's disease.MethodsSixteen centers participated in our international, collaborative study: five from the Americas, six from Europe, two from Israel, and three from Asia. Each center genotyped a standard DNA panel to permit comparison of the genotyping results across centers. Genotypes and phenotypic data from a total of 5691 patients with Parkinson's disease (780 Ashkenazi Jews) and 4898 controls (387 Ashkenazi Jews) were analyzed, with multivariate logistic-regression models and the Mantel-Haenszel procedure used to estimate odds ratios across centers.ResultsAll 16 centers could detect two GBA mutations, L444P and N370S. Among Ashkenazi Jewish subjects, either mutation was found in 15% of patients and 3% of controls, and among non-Ashkenazi Jewish subjects, either mutation was found in 3% of patients and less than 1% of controls. GBA was fully sequenced for 1883 non-Ashkenazi Jewish patients, and mutations were identified in 7%, showing that limited mutation screening can miss half the mutant alleles. The odds ratio for any GBA mutation in patients versus controls was 5.43 across centers. As compared with patients who did not carry a GBA mutation, those with a GBA mutation presented earlier with the disease, were more likely to have affected relatives, and were more likely to have atypical clinical manifestations.ConclusionsData collected from 16 centers demonstrate that there is a strong association between GBA mutations and Parkinson's disease.2009 Massachusetts Medical Society

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