Mitochondrial DNA A4336G mutation in Alzheimer's and Parkinson's diseases

被引:16
作者
García-Lozano, JR
Mir, P
Alberca, R
Aguilera, I
Néciga, EG
Fernández-López, O
Cayuela, A
Núñez-Roldan, A
机构
[1] Hosp Univ Virgen del Rocio, Serv Inmunol, E-41013 Seville, Spain
[2] Hosp Univ Virgen del Rocio, Neurol Serv, E-41013 Seville, Spain
[3] Hosp Univ Virgen del Rocio, Unidad Apoyo Invest, E-41013 Seville, Spain
[4] Hosp Univ Virgen del Rocio, Serv Andaluz Salud, E-41013 Seville, Spain
关键词
Alzheimer's disease; Parkinson's disease; mitochondrial mutation; genetics;
D O I
10.1159/000064955
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: 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). Material and Methods: 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 chi(2) and Fisher's exact tests. p < 0.05 was established as a statistically significant differential value. Results: 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 (11.4%). These differences were not statistically significant. Conclusion: 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.
引用
收藏
页码:34 / 36
页数:3
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