Department of Geriatrics, Center for Ageing Brain, Memory Unit, University of Bari, Policlinico, Piazza Giulio Cesare, 11-70124 Bari, Italy.
J Neurol Neurosurg Psychiatry. 2010 Apr;81(4):433-40. doi: 10.1136/jnnp.2009.181743. Epub 2009 Dec 3.
The authors investigated the relationship of metabolic syndrome (MetS) and its individual components with incident dementia in a prospective population-based study with a 3.5-year follow-up.
A total of 2097 participants from a sample of 5632 subjects (65-84 years old) from the Italian Longitudinal Study on Ageing were evaluated. MetS was defined according to the Third Adults Treatment Panel of the National Cholesterol Education Program criteria. Dementia, Alzheimer disease (AD) and vascular dementia (VaD) were classified using current published criteria.
MetS subjects (N=918) compared with those without MetS (N=1179) had an increased risk for VaD (1.63% vs 0.85%, adjusted hazard ratio (HR) 3.71, 95% CI 1.40 to 9.83). After excluding 338 subjects with baseline undernutrition, MetS subjects compared with those without MetS had an elevated risk of VaD (adjusted HR, 3.82; 95% CI 1.32 to 11.06). Moreover, those with MetS and high inflammation had a still further higher risk of VaD (multivariate adjusted HR, 9.55; 95% CI 1.17 to 78.17) compared with those without MetS and high inflammation. On the other hand, those with MetS and low inflammation compared with those without MetS and low inflammation did not exhibit a significant increased risk of VaD (adjusted HR, 3.31, 95% CI 0.91 to 12.14). Finally, a synergistic MetS effect versus its individual component effects was verified on the risk of VaD.
In our population, MetS subjects had an elevated risk of VaD that increased after excluding patients with baseline undernutrition and selecting MetS subjects with high inflammation.
作者通过一项前瞻性的基于人群的研究,对代谢综合征(MetS)及其各组分与发病性痴呆的关系进行了研究,随访时间为 3.5 年。
共有 5632 名受试者的样本中抽取了 2097 名参与者(年龄 65-84 岁)参与了意大利老龄化纵向研究。根据美国国家胆固醇教育计划第三次成人治疗专家组的标准来定义 MetS。使用当前发表的标准对痴呆、阿尔茨海默病(AD)和血管性痴呆(VaD)进行分类。
与无 MetS 的受试者(N=1179)相比,有 MetS 的受试者(N=918)患 VaD 的风险增加(1.63%比 0.85%,调整后的风险比(HR)3.71,95%置信区间(CI)1.40 至 9.83)。排除 338 名基线营养不良的受试者后,与无 MetS 的受试者相比,有 MetS 的受试者患 VaD 的风险仍较高(调整后的 HR,3.82;95%CI 1.32 至 11.06)。此外,与无 MetS 和高炎症的受试者相比,MetS 且炎症较高的受试者患 VaD 的风险更高(多变量调整后的 HR,9.55;95%CI 1.17 至 78.17)。另一方面,与无 MetS 和低炎症的受试者相比,有 MetS 和低炎症的受试者患 VaD 的风险没有显著增加(调整后的 HR,3.31,95%CI 0.91 至 12.14)。最后,还验证了 MetS 对 VaD 风险的影响与各组成部分的影响之间存在协同作用。
在我们的人群中,MetS 患者患 VaD 的风险增加,在排除基线营养不良的患者并选择炎症较高的 MetS 患者后,这种风险进一步增加。