Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
Faculty of Medicine, Biomedical Center, Lund University, Room No. C1112a, Sölvegatan 19, 22362, Lund, Sweden.
Sci Rep. 2021 Oct 6;11(1):19853. doi: 10.1038/s41598-021-99310-z.
Cognitive decline in early-stage Alzheimer's disease (AD) may depend on genetic variability. In the Swedish BioFINDER study, we used polygenic scores (PGS) (for AD, intelligence, and educational attainment) to predict longitudinal cognitive change (measured by mini-mental state examination (MMSE) [primary outcome] and other cognitive tests) over a mean of 4.2 years. We included 260 β-amyloid (Aβ) negative cognitively unimpaired (CU) individuals, 121 Aβ-positive CU (preclinical AD), 50 Aβ-negative mild cognitive impairment (MCI) patients, and 127 Aβ-positive MCI patients (prodromal AD). Statistical significance was determined at Bonferroni corrected p value < 0.05. The PGS for intelligence (beta = 0.1, p = 2.9e-02) was protective against decline in MMSE in CU and MCI participants regardless of Aβ status. The polygenic risk score for AD (beta = - 0.12, p = 9.4e-03) was correlated with the rate of change in MMSE and was partially mediated by Aβ-pathology (mediation effect 20%). There was no effect of education PGS on cognitive measures. Genetic variants associated with intelligence mitigate cognitive decline independent of Aβ-pathology, while effects of genetic variants associated with AD are partly mediated by Aβ-pathology.
早期阿尔茨海默病(AD)的认知能力下降可能取决于遗传变异性。在瑞典 BioFINDER 研究中,我们使用多基因评分(PGS)(用于 AD、智力和教育程度)来预测纵向认知变化(通过迷你精神状态检查(MMSE)[主要结果]和其他认知测试来衡量),平均随访时间为 4.2 年。我们纳入了 260 名β-淀粉样蛋白(Aβ)阴性认知正常(CU)个体、121 名 Aβ 阳性 CU(临床前 AD)、50 名 Aβ 阴性轻度认知障碍(MCI)患者和 127 名 Aβ 阳性 MCI 患者(前驱 AD)。统计学意义采用 Bonferroni 校正后 p 值 < 0.05。智力的 PGS(beta = 0.1,p = 2.9e-02)对 CU 和 MCI 参与者的 MMSE 下降具有保护作用,无论 Aβ 状态如何。AD 的多基因风险评分(beta = -0.12,p = 9.4e-03)与 MMSE 的变化率相关,部分由 Aβ-病理学介导(中介效应 20%)。教育 PGS 对认知测量没有影响。与智力相关的遗传变异独立于 Aβ-病理学减轻认知下降,而与 AD 相关的遗传变异的影响部分由 Aβ-病理学介导。