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首页> 外文期刊>BMC Neurology >Association between cytomegalovirus end-organ diseases and moderate-to-severe dementia: a population-based cohort study
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Association between cytomegalovirus end-organ diseases and moderate-to-severe dementia: a population-based cohort study

机译:cytomegalovirus末端器官疾病与中度至严重痴呆之间的关联:基于人群的队列研究

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摘要

The association between cytomegalovirus (CMV) and dementia remains controversial. Previous studies have suggested that CMV serostatus, as assessed by serum immunoglobulin G, plays a role in neurodegeneration with cognitive impairment. We aimed to evaluate the association between CMV tissue-invasive end-organ diseases and moderate-to-severe dementia. The ICD 10th revision codes from the National Health Insurance Database covering the entire population of the Republic of Korea were used to classify patients into exposed (n?=?687, age?≥?40?years, with CMV disease) and unexposed (n?=?3435, without CMV disease) groups, matched by age and sex at a 1:5 ratio of exposed: unexposed. All non-HIV-1-infected subjects selected during 2010–2014 with a washout period of the previous 4?years were followed up until December 2016 to identify newly diagnosed cases of moderate-to-severe dementia. Multivariate regression model (M3) adjusted for age, sex, low income, body mass index, transplantation status, malignant neoplasms, end-stage renal disease on dialysis, type 2 diabetes mellitus, hypertension, and dyslipidaemia showed a significantly higher incidence of dementia (odds ratio: 1.9; 95% confidence interval: 1.2–2.8) in the exposed group than that in the unexposed group. The risk of vascular dementia (2.9, 1.1–7.5) was higher than that of Alzheimer’s disease (1.6, 1.0–2.6) in the exposed group in M3. In M3, patients aged 40–59?years with CMV diseases had a significantly higher risk of all kinds of dementia than those aged 60–79 and?≥?80?years (11.7, 2.5–49.4 vs. 1.8, 1.1–3.2 vs. 1.3, 0.5–2.8; P?=?0.025). CMV diseases may be associated with the risk of moderate-to-severe dementia.
机译:cytomegalovirus(CMV)和痴呆之间的关联仍然存在争议。以前的研究表明,如血清免疫球蛋白G评估的CMV Serostatus在具有认知障碍的神经变性中发挥作用。我们的目标是评估CMV组织侵袭性终生物疾病和中度至严重的痴呆之间的关联。来自国民健康保险数据库的ICD第10次修订码,涵盖大韩民国的全国人口的人员被揭露(n?= 687,年龄≥10岁,患有CMV疾病)和未曝光(n ?=?3435,没有CMV疾病)组,匹配年龄和性别在1:5的曝光比例:未曝光。所有非HIV-1感染的受试者在2010-2014期间选择的所有非HIV-1感染的受试者在2016年12月到2016年12月之前随访时间,以确定新诊断的中度至严重痴呆症病例。多变量回归模型(M3)调整为年龄,性别,低收入,体重指数,移植地位,恶性肿瘤,透析的末期肾病,2型糖尿病,高血压和血脂血症表现出明显较高的痴呆发病率(赔率比率:1.9; 95%置信区间:1.2-2.8)在暴露组中,比未暴露的群体中的置型组。血管痴呆(2.9,1.1-7.5)的风险高于M3的暴露组中的阿尔茨海默病(1.6,1.0-2.6)。在M3中,40-59岁的患者患有CMV疾病的年龄较高的痴呆风险明显高于60-79岁的痴呆症风险明显较高,并且≥?80?年(11.7,2.5-49.4与1.8,1.1-3.2 vs 。1.3,0.5-2.8; p?= 0.025)。 CMV疾病可能与中度至严重痴呆的风险有关。

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