首页> 外文期刊>European archives of psychiatry and clinical neuroscience >The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study
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The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study

机译:BDNF Val66Met多态性在从主观认知能力下降到轻度认知障碍和阿尔茨海默病进展中的意义:一项为期9年的随访研究

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摘要

Brain-derived natriuretic factor (BDNF) Val66Met polymorphism has been frequently reported to be associated with Alzheimer's disease (AD) with contrasting results. Numerous studies showed that Met allele increased the risk of AD only in women, while other studies have found worse cognitive performance in Val/Val carriers. We aimed to inquire the effects of Val66Met polymorphism on the progression from subjective cognitive decline (SCD) to mild cognitive impairment (MCI) and from MCI to AD and to ascertain if this effect is modulated by demographic and cognitive variables. For this purpose, we followed up 74 subjects (48 SCD, 26 MCI) for a mean time of 9 years. All participants underwent extensive neuropsychological assessment, cognitive reserve estimation, BDNF and apolipoprotein E (ApoE) genotype analysis at baseline. Personality traits and leisure activities were assessed in a subgroup. Each patient underwent clinical-neuropsychological follow-up, during which 18 out of 48 SCD subjects progressed to MCI and 14 out of 26 MCI subjects progressed to AD. We found that Val66Met increased the risk of progression from SCD to MCI and from MCI to AD only in women. Nevertheless, Val/Val carriers who progressed from SCD to MCI had a shorter conversion time compared to Met carriers. We concluded that Val66Met polymorphism might play different roles depending on sex and stage of the disease.
机译:脑源性利钠因子 (BDNF) Val66Met 多态性经常被报道与阿尔茨海默病 (AD) 相关,结果截然不同。大量研究表明,Met 等位基因仅增加女性患 AD 的风险,而其他研究发现 Val/Val 携带者的认知表现较差。我们旨在探究Val66Met多态性对从主观认知能力下降(SCD)到轻度认知障碍(MCI)以及从MCI到AD的进展的影响,并确定这种影响是否受到人口统计学和认知变量的调节。为此,我们随访了 74 名受试者(48 名 SCD,26 名 MCI),平均时间为 9 年。所有参与者在基线时都接受了广泛的神经心理学评估、认知储备估计、BDNF 和载脂蛋白 E (ApoE) 基因型分析。在亚组中评估人格特质和休闲活动。每位患者均接受临床神经心理学随访,在此期间,48 名 SCD 受试者中有 18 名进展为 MCI,26 名 MCI 受试者中有 14 名进展为 AD。我们发现,Val66Met仅在女性中增加了从SCD进展为MCI和从MCI进展为AD的风险。然而,与Met载体相比,从SCD进展为MCI的Val/Val载体的转换时间更短。我们得出结论,Val66Met多态性可能根据性别和疾病阶段发挥不同的作用。

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