Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease

被引:90
作者
Clark, Joanne [1 ,2 ]
Reddy, Sonika [1 ,2 ]
Zheng, Kangni [1 ,2 ]
Betensky, Rebecca A. [3 ]
Simon, David K. [1 ,2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02215 USA
关键词
GAMMA COACTIVATOR-1-ALPHA PGC-1-ALPHA; MITOCHONDRIAL-DNA POLYMORPHISMS; IMPAIRED GLUCOSE-TOLERANCE; GLY482SER POLYMORPHISM; GENE POLYMORPHISMS; DIABETES-MELLITUS; PPARGC1A; MUTATIONS; SUSCEPTIBILITY; HYPERTENSION;
D O I
10.1186/1471-2350-12-69
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Peroxisome proliferator-activated receptor-g co-activator (PGC)-1 alpha is a transcriptional co-activator of antioxidant genes and a master regulator of mitochondrial biogenesis. Parkinson's disease (PD) is associated with oxidative stress and mitochondrial dysfunction and recent work suggests a role for PGC-1 alpha. We hypothesized that the rs8192678 PGC-1 alpha single nucleotide polymorphism (SNP) may influence risk or age of onset of PD. The A10398G mitochondrial SNP has been inversely associated with risk of PD in some studies. In the current study we analyzed whether rs8192678 or other PGC-1 alpha SNPs affect PD risk or age of onset, singularly or in association with the A10398G SNP. Methods: Genomic DNA samples from 378 PD patients and 173 age-matched controls were analyzed by multiplexed probe sequencing, followed by statistical analyses of the association of each SNP, alone or in combination, with risk or age of onset of PD. Adjustments were made for age of onset being less than the age of sampling, and for the observed dependence between these two ages. The PD samples were obtained as two separate cohorts, therefore statistical methods accounted for different sampling methods between the two cohorts, and data were analyzed using Cox regression adjusted for sampling in the risk set definition and in the model. Results: The rs8192678 PGC-1 alpha SNP was not associated with the risk of PD. However, an association of the PGC-1 alpha rs8192678 GG variant with longevity was seen in control subjects (p = 0.019). Exploratory studies indicated that the CC variant of rs6821591 was associated with risk of early onset PD (p = 0.029), with PD age of onset (p = 0.047), and with longevity (p = 0.022). The rs2970848 GG allele was associated with risk of late onset PD (p = 0.027). Conclusions: These data reveal possible associations of the PGC-1 alpha SNPs rs6821591 and rs2970848 with risk or age of onset of PD, and of the PGC-1 alpha rs8192678 GG and the rs6821591 CC variants with longevity. If replicated in other datasets, these findings may have important implications regarding the role of PGC-1 alpha in PD and longevity.
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页数:9
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