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      Altered brain high-energy phosphate metabolism in mild Alzheimer's disease: A 3-dimensional 31P MR spectroscopic imaging study

      research-article
      a , b , * , c , d , a , b , a , b , 1 , c , 1
      NeuroImage : Clinical
      Elsevier
      1H, proton, 31P–MRS, phosphorus magnetic resonance spectroscopy, AC, anterior commissure, ACC, anterior cingulate cortex, AD, Alzheimer's disease, ADP, adenosine diphosphate, ATP, adenosine triphosphate, CK, creatine kinase, Cr, creatine, CSF, cerebrospinal fluid, GM, grey matter, GPCh, glycerophosphocholine, GPEth, glycerophosphoethanolamine, HL, left hippocampus, HR, right hippocampus, LS, least square, MCI, mild cognitive impairment, MMSE, Mini Mental State Examination, MRSI, magnetic resonance spectroscopic imaging, NAD(H), nicotinamide adenine dinucleotide, OXPHOS, oxidative phosphorylation, PC, posterior commissure, PCh, phosphocholine, PCr, phosphocreatine, PDE, phosphodiesters, PEth, phosphoethanolamine, Pi, inorganic phosphate, PME, phosphomonoesters, ROI, region of interest, RSC, retrosplenial cortex, WM, white matter, Dementia, Alzheimer's disease, Phospholipid metabolism, Energy metabolism, Phosphorus magnetic resonance spectroscopic imaging

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          Abstract

          In Alzheimer's disease (AD), defects in essential metabolic processes for energy supply and phospholipid membrane function have been implicated in the pathological process. However, post-mortem investigations are generally limited to late stage disease and prone to tissue decay artifacts. In vivo assessments of high energy phosphates, tissue pH and phospholipid metabolites are possible by phosphorus MR spectroscopy ( 31P–MRS), but so far only small studies, mostly focusing on single brain regions, have been performed. Therefore, we assessed phospholipid and energy metabolism in multiple brain regions of 31 early stage AD patients and 31 age- and gender-matched controls using 31P–MRS imaging. An increase of phosphocreatine (PCr) was found in AD patients compared with controls in the retrosplenial cortex, and both hippocampi, but not in the anterior cingulate cortex. While PCr/inorganic phosphate and pH were also increased in AD, no changes were found for phospholipid metabolites. This study showed that PCr levels are specifically increased in regions that show early degeneration in AD. Together with an increased pH, this indicates an altered energy metabolism in mild AD.

          Highlights

          • Phosphocreatine and pH are increased in mild Alzheimer's disease.

          • Phosphocreatine increase occurs in early affected brain regions.

          • Brain energy metabolism may be altered in mild Alzheimer's disease.

          • Phospholipid and energy metabolites as well as pH, differ across brain regions.

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          Most cited references45

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          Inflammation and Alzheimer's disease.

          Inflammation clearly occurs in pathologically vulnerable regions of the Alzheimer's disease (AD) brain, and it does so with the full complexity of local peripheral inflammatory responses. In the periphery, degenerating tissue and the deposition of highly insoluble abnormal materials are classical stimulants of inflammation. Likewise, in the AD brain damaged neurons and neurites and highly insoluble amyloid beta peptide deposits and neurofibrillary tangles provide obvious stimuli for inflammation. Because these stimuli are discrete, microlocalized, and present from early preclinical to terminal stages of AD, local upregulation of complement, cytokines, acute phase reactants, and other inflammatory mediators is also discrete, microlocalized, and chronic. Cumulated over many years, direct and bystander damage from AD inflammatory mechanisms is likely to significantly exacerbate the very pathogenic processes that gave rise to it. Thus, animal models and clinical studies, although still in their infancy, strongly suggest that AD inflammation significantly contributes to AD pathogenesis. By better understanding AD inflammatory and immunoregulatory processes, it should be possible to develop anti-inflammatory approaches that may not cure AD but will likely help slow the progression or delay the onset of this devastating disorder.
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            Oxidative stress hypothesis in Alzheimer's disease.

            The major hurdle in understanding Alzheimer's disease (AD) is a lack of knowledge about the etiology and pathogenesis of selective neuron death. In recent years, considerable data have accrued indicating that the brain in AD is under increased oxidative stress and this may have a role in the pathogenesis of neuron degeneration and death in this disorder. The direct evidence supporting increased oxidative stress in AD is: (1) increased brain Fe, Al, and Hg in AD, capable of stimulating free radical generation; (2) increased lipid peroxidation and decreased polyunsaturated fatty acids in the AD brain, and increased 4-hydroxynonenal, an aldehyde product of lipid peroxidation in AD ventricular fluid; (3) increased protein and DNA oxidation in the AD brain; (4) diminished energy metabolism and decreased cytochrome c oxidase in the brain in AD; (5) advanced glycation end products (AGE), malondialdehyde, carbonyls, peroxynitrite, heme oxygenase-1 and SOD-1 in neurofibrillary tangles and AGE, heme oxygenase-1, SOD-1 in senile plaques; and (6) studies showing that amyloid beta peptide is capable of generating free radicals. Supporting indirect evidence comes from a variety of in vitro studies showing that free radicals are capable of mediating neuron degeneration and death. Overall, these studies indicate that free radicals are possibly involved in the pathogenesis of neuron death in AD. Because tissue injury itself can induce reactive oxygen species (ROS) generation, it is not known whether this is a primary or secondary event. Even if free radical generation is secondary to other initiating causes, they are deleterious and part of a cascade of events that can lead to neuron death, suggesting that therapeutic efforts aimed at removal of ROS or prevention of their formation may be beneficial in AD.
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              Correlations between apolipoprotein E epsilon4 gene dose and brain-imaging measurements of regional hypometabolism.

              Patients with Alzheimer's disease (AD) have abnormally low positron emission tomography (PET) measurements of the cerebral metabolic rate for glucose (CMRgl) in regions of the precuneus and the posterior cingulate, parietotemporal, and frontal cortex. Apolipoprotein E (APOE) epsilon4 gene dose (i.e., the number of epsilon4 alleles in a person's APOE genotype) is associated with a higher risk of AD and a younger age at dementia onset. We previously found that cognitively normal late-middle-aged APOE epsilon4 carriers have abnormally low CMRgl in the same brain regions as patients with probable Alzheimer's dementia. In a PET study of 160 cognitively normal subjects 47-68 years of age, including 36 epsilon4 homozygotes, 46 heterozygotes, and 78 epsilon4 noncarriers who were individually matched for their gender, age, and educational level, we now find that epsilon4 gene dose is correlated with lower CMRgl in each of these brain regions. This study raises the possibility of using PET as a quantitative presymptomatic endophenotype to help evaluate the individual and aggregate effects of putative genetic and nongenetic modifiers of AD risk.
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                Author and article information

                Contributors
                Journal
                Neuroimage Clin
                Neuroimage Clin
                NeuroImage : Clinical
                Elsevier
                2213-1582
                28 February 2018
                2018
                28 February 2018
                : 18
                : 254-261
                Affiliations
                [a ]Department of Geriatric Medicine, Radboud university medical center, Nijmegen, The Netherlands
                [b ]Radboudumc Alzheimer Center, Donders Institute for Brain, Cognition and Behaviour, Radboud university medical center, Nijmegen, The Netherlands
                [c ]Department of Radiology and Nuclear Medicine, Radboud university medical center, Nijmegen, The Netherlands
                [d ]Department of Paediatrics, Radboud university medical center, Nijmegen, The Netherlands
                Author notes
                [* ]Corresponding author at: Radboud University Medical Center, Dep. Geriatric Medicine, - hp 925, P.O.Box 9101, 6500 HB Nijmegen, the Netherlands. Anne.Rijpma@ 123456radboudumc.nl
                [1]

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                Article
                S2213-1582(18)30031-7
                10.1016/j.nicl.2018.01.031
                5987799
                29876246
                c9f3f6cd-3750-45cc-8a0e-a6bf0a9d2b48
                © 2018 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 30 June 2017
                : 15 December 2017
                : 24 January 2018
                Categories
                Regular Article

                1h, proton,31p–mrs, phosphorus magnetic resonance spectroscopy,ac, anterior commissure,acc, anterior cingulate cortex,ad, alzheimer's disease,adp, adenosine diphosphate,atp, adenosine triphosphate,ck, creatine kinase,cr, creatine,csf, cerebrospinal fluid,gm, grey matter,gpch, glycerophosphocholine,gpeth, glycerophosphoethanolamine,hl, left hippocampus,hr, right hippocampus,ls, least square,mci, mild cognitive impairment,mmse, mini mental state examination,mrsi, magnetic resonance spectroscopic imaging,nad(h), nicotinamide adenine dinucleotide,oxphos, oxidative phosphorylation,pc, posterior commissure,pch, phosphocholine,pcr, phosphocreatine,pde, phosphodiesters,peth, phosphoethanolamine,pi, inorganic phosphate,pme, phosphomonoesters,roi, region of interest,rsc, retrosplenial cortex,wm, white matter,dementia,alzheimer's disease,phospholipid metabolism,energy metabolism,phosphorus magnetic resonance spectroscopic imaging

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