Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Nov 2:5:15492.
doi: 10.1038/srep15492.

Differential effect of caffeine intake in subjects with genetic susceptibility to Parkinson's Disease

Affiliations

Differential effect of caffeine intake in subjects with genetic susceptibility to Parkinson's Disease

Prakash M Kumar et al. Sci Rep. .

Abstract

We examined if caffeine intake has a differential effect in subjects with high and low genetic susceptibility to Parkinson's disease (PD), a common neurodegenerative disorder. A case control study involving 812 subjects consisting of PD and healthy controls were conducted. Caffeine intake assessed by a validated questionnaire and genotyping of PD gene risk variant (LRRK2 R1628P) was carried out. Compared to caffeine takers with the wild-type genotype (low genetic susceptibility), non-caffeine takers with R1628P variant (high genetic susceptibility) had a 15 times increased risk of developing PD (OR = 15.4, 95% CI = (1.94, 122), P = 0.01), whereas caffeine takers with R1628P (intermediate susceptibility) had a 3 times risk (OR = 3.07, 95% CI = (2.02, 4.66), P < 0.001). Caffeine intake would significantly reduce the risk of PD much more in those with high genetic susceptibility compared to those with low genetic susceptibility.

PubMed Disclaimer

References

    1. Tan E. K. & Skipper L. M. Pathogenic Mutations in Parkinson Disease. Hum Mutat 28, 641–53 (2007). - PubMed
    1. Zimprich A. et al. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 44, 601–7 (2004). - PubMed
    1. Tan E. K. et al. Multiple LRRK2 Variants Modulate Risk of Parkinson Disease: A Chinese Multicenter Study. Hum Mutat 31, 561–8 (2010). - PubMed
    1. Ross O. A. et al. Analysis of LRRK2 R1628P as a risk factor for Parkinson’s Disease. Annals of Neurology 64, 88–96 (2008). - PubMed
    1. Costa J., Lunet N., Santos C., Santos J. & Vaz-Carneiro A. Caffeine exposure and the risk of Parkinson’s disease: a systematic review and meta-analysis of observational studies. Journal of Alzheimer’s disease 20, S221–38 (2010). - PubMed

Publication types