Institute of Applied Health Sciences, University of Aberdeen, Polwarth Building, Foresterhill, Aberdeen, Scotland, AB25 2ZH, UK,
Eur J Nutr. 2014 Feb;53(1):277-85. doi: 10.1007/s00394-013-0526-6. Epub 2013 Apr 27.
To distinguish between contributions to dementia made by homocysteine, folate, B12 and antioxidant micronutrients.
This is a follow-up study of a sample reported in 2002. Homocysteine was measured at baseline in 201 individuals born in 1921 and without dementia at age 77 years and followed up to age 88 years. Baseline macro- and micronutrient status was estimated from BMI, the MONICA food frequency questionnaire, plasma folate, B12 and, in a subgroup (N = 173), plasma antioxidant micronutrients. Time to dementia onset during follow-up was compared between participants grouped by homocysteine concentration using Cox regression. Model 1 adjusted for age, sex, childhood IQ, education, socioeconomic deprivation, presence of heart disease, hypertension, plasma folate and B12. In model 2 plasma, antioxidants were added to these covariables.
During a mean follow-up of about 5 years, there were 39 incident dementia cases among 201 participants. In model 1, being in the highest homocysteine group (>14 μmol/L) was associated with a 234 % increased risk (HR 3.34, 95 % CI 1.16-9.57) of any dementia. After inclusion of plasma antioxidants in model 2, there were 32 incident dementia cases from a subsample (N = 173). Homocysteine >14 μmol was associated with a 272 % increased dementia risk (HR = 3.72, 95 % CI 1.06-13.08).
High homocysteine increases the risk of dementia. The association between tHcy and dementia is independent of plasma folate, B12 and antioxidant micronutrient status.
区分同型半胱氨酸、叶酸、B12 和抗氧化微量营养素对痴呆的贡献。
这是 2002 年报告的样本的随访研究。在 201 名 1921 年出生且在 77 岁时无痴呆的人群中测量了基线同型半胱氨酸,并随访至 88 岁。基线宏量和微量营养素状况由 BMI、MONICA 食物频率问卷、血浆叶酸、B12 以及亚组(N=173)的血浆抗氧化微量营养素来估计。使用 Cox 回归比较在随访期间按同型半胱氨酸浓度分组的参与者之间痴呆发病时间。模型 1 调整了年龄、性别、儿童智商、教育、社会经济贫困、心脏病、高血压、血浆叶酸和 B12。在模型 2 中,将血浆抗氧化剂添加到这些协变量中。
在大约 5 年的平均随访期间,201 名参与者中有 39 例发生了痴呆事件。在模型 1 中,处于同型半胱氨酸最高组(>14 μmol/L)与任何痴呆的风险增加 234%相关(HR 3.34,95%CI 1.16-9.57)。在模型 2 中包含血浆抗氧化剂后,从亚组(N=173)中发生了 32 例痴呆事件。同型半胱氨酸>14 μmol 与痴呆风险增加 272%相关(HR=3.72,95%CI 1.06-13.08)。
高同型半胱氨酸增加痴呆风险。tHcy 与痴呆之间的关联独立于血浆叶酸、B12 和抗氧化微量营养素状况。