Specific Nutritional Biomarker Profiles in Mild Cognitive Impairment and Subjective Cognitive Decline Are Associated With Clinical Progression: The NUDAD Project

被引:17
作者
de Leeuw, Francisca A. [1 ]
van der Flier, Wiesje M. [1 ,2 ]
Tijms, Betty M. [1 ]
Scheltens, Philip [1 ]
Mendes, Vera M. [3 ]
Manadas, Bruno [3 ]
Bierau, Jorgen [4 ]
van Wijk, Nick [5 ]
van den Heuvel, Ellen G. H. M. [6 ]
Mohajeri, M. Hasan [7 ]
Teunissen, Charlotte E. [8 ,9 ]
Kester, Maartje, I [1 ]
机构
[1] Vrije Univ Amsterdam, Alzheimer Ctr Amsterdam, Dept Neurol, Amsterdam UMC,Amsterdam Neurosci, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Amsterdam UMC, Amsterdam Publ Hlth Res, Dept Epidemiol & Biostat, Amsterdam, Netherlands
[3] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Coimbra, Portugal
[4] Maastricht UMC, Dept Clin Genet, Maastricht, Netherlands
[5] Nutricia Res, Nutricia Adv Med Nutr, Utrecht, Netherlands
[6] FrieslandCampina, Amersfoort, Netherlands
[7] DSM Nutr Prod Ltd, R&D Human Nutr & Hlth, Basel, Switzerland
[8] VU Univ Med Ctr Amsterdam, Dept Clin Chem, Neurochem Lab, Amsterdam Neurosci, Amsterdam, Netherlands
[9] VU Univ Med Ctr Amsterdam, Dept Clin Chem, Biobank, Amsterdam Neurosci, Amsterdam, Netherlands
关键词
Nutrients; nutritional biomarker profiles; subjective cognitive decline; mild cognitive impairment; cognitive decline; clinical progression; nutritional biomarker; TOTAL CHOLESTEROL LEVELS; ALZHEIMERS-DISEASE; S-ADENOSYLMETHIONINE; CEREBROSPINAL-FLUID; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; DEMENTIA; SERUM; RISK; PLASMA;
D O I
10.1016/j.jamda.2019.12.009
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objectives: Nutritional insufficiencies have been associated with cognitive impairment. Understanding whether nutritional biomarker levels are associated with clinical progression could help to design dietary intervention trials. This longitudinal study examined a panel of nutritional biomarkers in relation to clinical progression in patients with subjective cognitive decline (SCD) or mild cognitive impairment (MCI). Design, setting and participants: We included 299 patients without dementia (n = 149 SCD; age 61 +/- 10 years, female 44%, n = 150 MCI; age 66 +/- 8 years, female 38%). Median (interquartile range) follow-up was 3 (2-5) years. Methods: We measured 28 nutritional biomarkers in blood and 5 in cerebrospinal fluid (CSF), associated with 3 Alzheimer's disease pathologic processes: vascular change (lipids), synaptic dysfunction (homocysteine-related metabolites), and oxidative stress (minerals and vitamins). Nutritional biomarker associations with clinical progression to MCI/dementia and cognitive decline based on the Mini-Mental State Examination score were evaluated using Cox proportional hazard models and linear mixed models. We used partial least squares Cox models (PLS-Cox) to examine nutritional biomarker profiles associated with clinical progression. Results: In the total group, high high-density lipoprotein (HDL) levels were associated with clinical progression and cognitive decline. In SCD, high folate and low bilirubin levels were associated with cognitive decline. In MCI, low CSF S-adenosylmethionine (SAM) and high theobromine were associated with clinical progression to dementia and high HDL, cholesterol, iron, and 1,25(OH)(2) vitamin D were associated with cognitive decline. PLS-Cox showed 1 profile for SCD, characterized by high betaine and folate and low zinc associated with clinical progression. In MCI, a profile with high theobromine and HDL and low triglycerides and a second profile with high plasma SAM and low cholesterol were associated with risk of dementia. Conclusion and Implications: High HDL was most consistently associated with clinical progression. Moreover, different nutritional biomarker profiles for SCD and MCI showed promising associations with clinical progression. Future dietary (intervention) studies could use nutritional biomarker profiles to select patients, taking into account the disease stage. (C) 2019 The Author(s). Published by Elsevier Inc. on behalf of AMDA - The Society for Post-Acute and Long-Term Care Medicine. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1513.e1 / 1513.e17
页数:17
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