Hernández Carlos F, Villaman Camilo, Leu Costin, Lal Dennis, Mata Ignacio, Klein Andrés D, Pérez-Palma Eduardo
Universidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, 7610658, Santiago, Chile.
Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Sci Rep. 2025 Apr 3;15(1):11407. doi: 10.1038/s41598-025-95755-8.
Alzheimer's disease (AD) is usually accompanied by comorbidities such as type 2 diabetes (T2D), epilepsy, major depressive disorder (MDD), and migraine headaches (MH) that can significantly affect patient management and progression. As AD, these comorbidities have their own cumulative common genetic risk component that can be explored in a single individual through polygenic scores. Utilizing data from the UK Biobank, we investigated the correlation between polygenic scores (PGS) for these comorbidities and their actual presentation in AD patients. We show that individuals with higher PGS values showed an elevated risk of developing T2D (OR 2.1, p = 1.07 × 10) and epilepsy (OR 1.5, p = 0.0176). High T2D-PGS is also associated with an earlier AD onset in individuals at high genetic risk for AD (AD-PGS). In contrast, no significant genetic associations were found for MDD and MH. Our findings show distinct common genetic risk factors for T2D and epilepsy carried by AD patients that are associated with increased prevalence and earlier disease onset. These results highlight the contribution of common genetic variation to the broader clinical landscape of AD and will contribute to future tailored patient management strategies for individuals at high genetic risk.
阿尔茨海默病(AD)通常伴有2型糖尿病(T2D)、癫痫、重度抑郁症(MDD)和偏头痛(MH)等合并症,这些合并症会显著影响患者的管理和病情进展。与AD一样,这些合并症都有其累积的共同遗传风险成分,可通过多基因评分在个体中进行探究。利用英国生物银行的数据,我们研究了这些合并症的多基因评分(PGS)与其在AD患者中的实际表现之间的相关性。我们发现,PGS值较高的个体患T2D(优势比2.1,p = 1.07×10)和癫痫(优势比1.5,p = 0.0176)的风险升高。高T2D-PGS也与AD高遗传风险个体(AD-PGS)的AD发病较早有关。相比之下,未发现MDD和MH有显著的遗传关联。我们的研究结果表明,AD患者携带的T2D和癫痫存在不同的共同遗传风险因素,这些因素与患病率增加和疾病发病较早有关。这些结果突出了常见基因变异对AD更广泛临床情况的影响,并将有助于未来为高遗传风险个体制定量身定制的患者管理策略。