de van der Schueren Marian A E, Lonterman-Monasch Sabine, van der Flier Wiesje M, Kramer Mark H, Maier Andrea B, Muller Majon
Department of Nutrition and Dietetics, Internal Medicine, VU University Medical Center, Amsterdam, The Netherlands.
Department of Nutrition, Sports and Health, Faculty of Health and Social Studies, HAN University of Applied Sciences, Nijmegen, The Netherlands.
J Am Geriatr Soc. 2016 Dec;64(12):2457-2463. doi: 10.1111/jgs.14385. Epub 2016 Oct 28.
To study the associations between protein energy malnutrition, micronutrient malnutrition, brain atrophy, and cerebrovascular lesions.
Cross-sectional.
Geriatric outpatient clinic.
Older adults (N = 475; mean age 80 ± 7).
Nutritional status was assessed using the Mini Nutritional Assessment (MNA) and according to serum micronutrient levels (vitamins B1, B6, B12, D; folic acid). White matter hyperintensities (WMHs), global cortical brain atrophy, and medial temporal lobe atrophy on magnetic resonance imaging (MRI) were rated using visual rating scales. Logistic regression analyses were performed to assess associations between the three MNA categories (<17, 17-23.5, ≥23.5) and micronutrients (per SD decrease) and WMHs and measures of brain atrophy.
Included were 359 participants. Forty-eight participants (13%) were malnourished (MNA <17), and 197 (55%) were at risk of malnutrition (MNA = 17-23.5). Participants at risk of malnutrition (odds ratio (OR) = 1.93, 95% confidence interval (CI) = 1.01-3.71) or who were malnourished (OR = 2.80, 95% CI = 1.19-6.60) had a greater probability of having severe WMHs independent of age and sex than those with adequate nutritional status. Results remained significant after further adjustments for cognitive function, depressive symptoms, cardiovascular risk factors, history of cardiovascular disease, smoking and alcohol use, and micronutrient levels. Lower vitamin B1 (OR = 1.51, 95% CI = 1.11-2.08) and B12 (OR = 1.45, 95% CI = 1.02-2.04) levels were also related to greater risk of severe WMHs, independent of age and sex. Results remained significant after additional adjustments. MNA and vitamin levels were not associated with measures of brain atrophy.
Malnutrition and lower vitamin B1 and B12 levels were independently associated with greater risk of WMHs. Underlying mechanisms need to be further clarified, and whether nutritional interventions can modify these findings also needs to be studied.
研究蛋白质能量营养不良、微量营养素营养不良、脑萎缩和脑血管病变之间的关联。
横断面研究。
老年门诊。
老年人(N = 475;平均年龄80±7岁)。
使用微型营养评定法(MNA)并根据血清微量营养素水平(维生素B1、B6、B12、D;叶酸)评估营养状况。通过视觉评定量表对磁共振成像(MRI)上的白质高信号(WMH)、全脑皮质萎缩和内侧颞叶萎缩进行评分。进行逻辑回归分析以评估MNA的三个类别(<17、17 - 23.5、≥23.5)与微量营养素(每标准差降低)以及WMH和脑萎缩测量指标之间的关联。
纳入359名参与者。48名参与者(13%)营养不良(MNA <17),197名(55%)有营养不良风险(MNA = 17 - 23.5)。有营养不良风险的参与者(比值比(OR)= 1.93,95%置信区间(CI)= 1.01 - 3.71)或营养不良的参与者(OR = 2.80,95% CI = 1.19 - 6.60)与营养状况良好的参与者相比,在不考虑年龄和性别的情况下,发生严重WMH的可能性更大。在进一步调整认知功能、抑郁症状、心血管危险因素、心血管疾病史、吸烟和饮酒情况以及微量营养素水平后,结果仍然显著。较低的维生素B1(OR = 1.51,95% CI = 1.11 - 2.08)和B12(OR = 1.45,95% CI = 1.02 - 2.04)水平也与发生严重WMH的较高风险相关,且与年龄和性别无关。在进一步调整后结果仍然显著。MNA和维生素水平与脑萎缩测量指标无关。
营养不良以及较低的维生素B1和B12水平与WMH的较高风险独立相关。潜在机制需要进一步阐明,营养干预是否能改变这些结果也需要进行研究。