School of Public Health, College of Public Health, Taipei Medical University, Taipei, Taiwan.
Department of Internal Medicine, Chang Gung Memorial Hospital, Keelung, Taiwan.
J Am Heart Assoc. 2017 Sep 12;6(9):e004749. doi: 10.1161/JAHA.116.004749.
The relationship of alteration of metabolic syndrome (MetS) with dementia remains unclear. The purpose of study was to evaluate the association between dynamic change in MetS status around a 5-year period and dementia.
The cohort study was conducted from the Taiwanese Survey on Prevalence of Hypertension, Hyperglycemia, and Hyperlipidemia in 2002, with follow-up in 2007. The sample was subsequently linked to the National Health Insurance Research Database. Participants were divided into 3 groups: persistent MetS (MetS both in 2002 and 2007); nonpersistent MetS (MetS either in 2002 or 2007); and non-MetS (MetS neither in 2002 nor 2007). Furthermore, the individuals with nonpersistent MetS were categorized as improved MetS (MetS in 2002 but not in 2007) and worsened MetS (MetS not in 2002 but in 2007). Each participant was tracked until the end of 2011 to identify the development of dementia. In total, 3458 participants aged 40 to 80 years were included. Up to 10 years and 31 741 person-years of follow-up, 76 patients developed dementia. Only a relationship was found between the nonpersistent MetS and dementia (adjusted hazard ratio=1.93; 95% confidence interval =1.17-3.19; =0.010). Moreover, a significantly higher dementia risk was observed in patients with worsened MetS (adjusted hazard ratio=2.22; 95% confidence interval=1.32-3.72; =0.003), but not those with persistent (=0.752) or improved (=0.829) MetS. Similar results were detected in participants aged ≥65 years.
Patients with worsened MetS had an increased dementia risk during the 10-year follow-up period in a population-based sample.
代谢综合征(MetS)改变与痴呆的关系尚不清楚。本研究旨在评估 5 年内 MetS 状态的动态变化与痴呆之间的关系。
该队列研究来自 2002 年台湾高血压、高血糖和高血脂患病率调查,随访至 2007 年。随后,该样本与国家健康保险研究数据库相关联。参与者被分为 3 组:持续 MetS(2002 年和 2007 年均存在 MetS);非持续 MetS(2002 年或 2007 年存在 MetS);非 MetS(2002 年和 2007 年均不存在 MetS)。此外,非持续 MetS 的个体被分为改善 MetS(2002 年存在 MetS,但 2007 年不存在)和恶化 MetS(2002 年不存在 MetS,但 2007 年存在)。每位参与者都被跟踪至 2011 年底,以确定痴呆的发展情况。共纳入 3458 名 40 至 80 岁的参与者。随访时间长达 10 年和 31741 人年,有 76 名患者发生痴呆。仅发现非持续 MetS 与痴呆之间存在关系(调整后的危险比=1.93;95%置信区间=1.17-3.19;=0.010)。此外,在 MetS 恶化的患者中,痴呆的风险显著增加(调整后的危险比=2.22;95%置信区间=1.32-3.72;=0.003),但在持续存在(=0.752)或改善(=0.829)MetS 的患者中未观察到这种情况。在≥65 岁的参与者中也检测到了类似的结果。
在基于人群的样本中,在 10 年随访期间,MetS 恶化的患者痴呆风险增加。