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首页> 外文期刊>Molecular neurodegeneration >Heart fatty acid binding protein and Aβ-associated Alzheimer’s neurodegeneration
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Heart fatty acid binding protein and Aβ-associated Alzheimer’s neurodegeneration

机译:心脏脂肪酸结合蛋白和与Aβ相关的阿尔茨海默氏症的神经变性

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摘要

Background Epidemiological and molecular findings suggest a relationship between Alzheimer’s disease (AD) and dyslipidemia, although the nature of this association is not well understood. Results Using linear mixed effects models, we investigated the relationship between CSF levels of heart fatty acid binding protein (HFABP), a lipid binding protein involved with fatty acid metabolism and lipid transport, amyloid-β (Aβ), phospho-tau, and longitudinal MRI-based measures of brain atrophy among 295 non-demented and demented older individuals. Across all participants, we found a significant association of CSF HFABP with longitudinal atrophy of the entorhinal cortex and other AD-vulnerable neuroanatomic regions. However, we found that the relationship between CSF HABP and brain atrophy was significant only among those with low CSF Aβ1–42 and occurred irrespective of phospho-tau181p status. Conclusions Our findings indicate that Aβ-associated volume loss occurs in the presence of elevated HFABP irrespective of phospho-tau. This implicates a potentially important role for fatty acid binding proteins in Alzheimer’s disease neurodegeneration.
机译:背景流行病学和分子学发现提示阿尔茨海默氏病(AD)与血脂异常之间存在关联,尽管这种关联的性质尚未得到很好的理解。结果使用线性混合效应模型,我们研究了心脏脂肪酸结合蛋白(HFABP),参与脂肪酸代谢和脂质转运的脂质结合蛋白,淀粉样蛋白β(Aβ),磷酸化tau蛋白和纵向蛋白的脑脊液水平之间的关系。基于MRI的295名非痴呆和痴呆老年人的大脑萎缩测量。在所有参与者中,我们发现脑脊液HFABP与内嗅皮层和其他易受AD损害的神经解剖区域的纵向萎缩之间存在显着关联。然而,我们发现脑脊液HABP与脑萎缩之间的关系仅在脑脊液Aβ1-42低的患者中才有意义,并且与磷tau181p状态无关。结论我们的研究结果表明,存在高水平HFABP的情况下,与Aβ相关的体积损失发生,而与磷τ无关。这暗示着脂肪酸结合蛋白在阿尔茨海默氏病神经变性中可能具有重要作用。

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