Del Bo Roberto, Comi Giacomo Pietro, Giorda Roberto, Crimi Marco, Locatelli Federica, Martinelli-Boneschi Filippo, Pozzoli Uberto, Castelli Enrico, Bresolin Nereo, Scarlato Guglielmo
Dipartimento di Scienze Neurologiche, Padiglione Ponti, I. R. C. S. S. Ospedale Maggiore Policlinico, Via F. Sforza, 35, 20122 Milan, Italy.
J Neurol. 2003 Jun;250(6):688-92. doi: 10.1007/s00415-003-1057-5.
Recently, a frequent prion protein gene (PRNP) polymorphism consisting of a methionine (M) for valine (V) substitution at codon 129 has been associated with cognitive impairment in elderly individuals. Down syndrome (DS) is associated with mental retardation and development of Alzheimer-like brain abnormalities. In the present study, we investigated the role of the PRNP polymorphism in 122 relatively young Italian DS patients. Allele frequencies of DS subjects did not differ from those in the general population. However, we found a significantly faster rate of decline in intellectual ability in the subgroup of DS patients carrying at least one V allele compared with the M/M DS subjects. An additive deleterious effect of apolipoprotein E epsilon 4 allele was detected after stratifying by APOE gene status. Our findings provide evidence that variability of the PRNP gene at codon 129 might contribute to accelerating the rate of earlier cognitive decline in DS subjects.
最近,一种常见的朊蛋白基因(PRNP)多态性,即密码子129处的缬氨酸(V)被甲硫氨酸(M)取代,已被发现与老年人的认知障碍有关。唐氏综合征(DS)与智力发育迟缓以及类似阿尔茨海默病的脑部异常发展有关。在本研究中,我们调查了PRNP多态性在122名相对年轻的意大利DS患者中的作用。DS受试者的等位基因频率与一般人群没有差异。然而,我们发现与M/M型DS受试者相比,携带至少一个V等位基因的DS患者亚组的智力能力下降速度明显更快。在按载脂蛋白E基因状态分层后,检测到载脂蛋白E ε4等位基因的累加有害效应。我们的研究结果提供了证据,表明密码子129处PRNP基因的变异性可能有助于加速DS受试者早期认知能力下降的速度。