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Karger Publishers, European Neurology, 1(48), p. 34-36, 2002

DOI: 10.1159/000064955

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Mitochondrial DNA A4336G Mutation in Alzheimer’s and Parkinson’s Diseases

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

<i>Objectives:</i> To determine whether the mitochondrial DNA (mtDNA) A4336G mutation represents a risk factor for Spanish patients with both Alzheimer’s disease (AD) and Parkinson’s disease (PD). <i>Material and Methods:</i> One hundred and sixty-one AD and 106 PD unrelated patients were included in the study. Seventy-eight age-matched and 144 randomly chosen healthy subjects served as controls. The frequency of the A4336G mutation in these groups was compared using the χ<sup>2</sup> and Fisher’s exact tests. p < 0.05 was established as a statistically significant differential value. <i>Results: </i>The mtDNA A4336G mutation was present in 1/161 of AD patients (0.6%), in 3/106 of PD patients (2.8%), in 1/78 of age-matched controls (1.3%) and in 2/144 of the randomly chosen controls (1.4%). These differences were not statistically significant. <i>Conclusion:</i> Our results do not support the hypothesis that this mutation represents a risk factor for either AD or PD patients, at least in the case of this Spanish sample.