Paz-Y-Miño César A, García-Cárdenas Jennyfer M, López-Cortés Andrés, Salazar Carolina, Serrano Marcos, Leone Paola E
Instituto de Investigaciones Biomédicas (CAP, JMG-C, AL-C, CS, PEL), Facultad de Ciencias de la Salud, Universidad de las Américas, Quito, Ecuador; Carrera de Ingeniería en Biotecnología, Facultad de Ciencias de la Vida, Escuela Politécnica del Ejército, Sangolquí, Ecuador; and Servicio de Neurología (MS), "Hospital Carlos Andrade Marín," Quito, Ecuador.
Am J Med Sci. 2015 Oct;350(4):296-301. doi: 10.1097/MAJ.0000000000000555.
Alzheimer's disease (AD) is the most common cause of senile dementia. In Ecuador, the number of deaths caused by AD increases each year. Epidemiologically, the Ecuadorian population is composed of a mixture of several genetic backgrounds along with environmental factors, that make it unique and ideal for population studies. The main objective of this study was to determine the prevalence of Cystatin C (CST3), Cathepsin D (CTSD) and Manganese superoxide dismutase (MnSOD) amino acid-altering polymorphisms and their influence on the development of AD in the Ecuadorian population.
This is a case-control study consisting of 56 patients with AD, from the Department of Neurology at Carlos Andrade Marín Hospital. The control group (n = 55) comprised healthy elderly adults. The inclusion period was from January to August of 2012. Peripheral blood was collected from both groups for DNA extraction, polymerase chain reaction and capillary sequencing.
There was a positive association between a CTSD polymorphism (Ala224Val) and the development of AD (odds ratio = 8.1, 95% confidence interval: 0.9-85.7; P < 0.025). However, the 3 other polymorphisms investigated did not show significant associations with AD.
Variations in CTSD and MnSOD showed no association with the development of AD, whereas the presence of the Ala224Val polymorphism in CTSD had a positive association with the development of AD.
阿尔茨海默病(AD)是老年痴呆最常见的病因。在厄瓜多尔,由AD导致的死亡人数逐年增加。从流行病学角度来看,厄瓜多尔人口由多种遗传背景与环境因素混合构成,这使其具有独特性,成为人群研究的理想对象。本研究的主要目的是确定胱抑素C(CST3)、组织蛋白酶D(CTSD)和锰超氧化物歧化酶(MnSOD)氨基酸改变多态性的患病率及其对厄瓜多尔人群AD发病的影响。
这是一项病例对照研究,包括来自卡洛斯·安德拉德·马林医院神经科的56例AD患者。对照组(n = 55)由健康老年人组成。纳入期为2012年1月至8月。从两组采集外周血用于DNA提取、聚合酶链反应和毛细管测序。
CTSD多态性(Ala224Val)与AD发病之间存在正相关(优势比 = 8.1,95%置信区间:0.9 - 85.7;P < 0.025)。然而,所研究的其他3种多态性与AD无显著关联。
CTSD和MnSOD的变异与AD发病无关联,而CTSD中Ala224Val多态性的存在与AD发病呈正相关。